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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Форма поиска

Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 3169. Отображено 192.
06-02-2019 дата публикации

Способы стерильной хроматографии и производства

Номер: RU2679133C2

Изобретение относится к способам осуществления хроматографии с использованием гамма-облученной хроматографической смолы, включающим получение хроматографической колонки, включающей гамма-облученную хроматографическую смолу; осуществление первого цикла хроматографии с помощью колонки, где цикл включает восстановление связывающей способности гамма-облученной анионообменной хроматографической смолы путем подвергания гамма-облученной анионообменной хроматографической смолы воздействию денатурирующего буфера; и осуществление по меньшей мере одного дополнительного цикла хроматографии с помощью колонки. Кроме того, изобретение относится к интегрированным, замкнутым, или, по существу, замкнутым, и непрерывным способам производства рекомбинантного белка, включающим применение по меньшей мере одной хроматографической колонки, включающей гамма-облученную хроматографическую смолу, где гамма-облученную хроматографическую смолу подвергают воздействию денатурирующего буфера в течение каждого цикла способа ...

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25-01-2021 дата публикации

Номер: RU2019113872A3
Автор:
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10-12-2014 дата публикации

СТРУКТУРЫ СЛИТОГО БЕЛКА ШЕЛКА ПАУКОВ ДЛЯ СВЯЗЫВАНИЯ С ОРГАНИЧЕСКОЙ МИШЕНЬЮ

Номер: RU2013123270A
Принадлежит:

... 1. Белковая структура, способная к селективному взаимодействию с органической мишенью, выбранной из группы, состоящей из области кристаллизующегося фрагмента (F) IgG и молекул, содержащих IgG или его производные, где указанная белковая структура представляет собой полимер, содержащий в качестве повторяющегося структурного элемента рекомбинантный слитый белок, который способен к селективному взаимодействию с органической мишенью, и содержащий части B, REP и CT, где полимер содержит более 100 структурных элементов слитого белка и где:B представляет собой неспидроиновую часть из более чем 30 аминокислотных остатков, которая обеспечивает способность к селективному взаимодействию с органической мишенью, где часть B выбрана из группы, состоящей из Z-домена белка A стафилококков, белка A стафилококков и его доменов E, D, A, B и C; и белковых фрагментов, имеющих по меньшей мере 70% идентичность с любой из этих аминокислотных последовательностей;части REP и CT обеспечивают способность образовывать ...

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03-09-2015 дата публикации

Verfahren zur Beschleunigung des thermischen Gleichgewichts in einer Chromatographiesäule

Номер: DE112013003406T5

Beschrieben sind Techniken zur Beschleunigung des thermischen Gleichgewichts in einer Chromatographiesäule. Eine Vorrichtung weist eine Chromatographiesäule auf und eine Vielzahl von Temperatursteuereinheiten in thermischem Kontakt mit der Chromatographiesäule. Ein Verfahren zur Durchführung von Flüssigkeitschromatographie umfasst das Einstellen eines Eingangs einer Chromatographiesäule auf eine erste Temperatur unter Verwendung einer ersten Temperatursteuereinheit in thermischem Kontakt mit dem Eingang auf, sowie die Einstellung eines Ausgangs der Chromatographiesäule auf eine zweite Temperatur unter Verwendung einer zweiten Temperatursteuereinheit in thermischem Kontakt mit dem Ausgang, wobei die erste Temperatur geringer als die zweite Temperatur ist; und das Injizieren einer Probe in einen Flüssigkeitsstrom, der durch die Chromatographiesäule fließt, nachdem der Eingang auf die erste Temperatur und der Ausgang auf die zweite Temperatur eingestellt wurden.

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01-06-2011 дата публикации

Номер: DE602007014099D1

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29-07-2004 дата публикации

ADSOPTIONSCHROMATOGRAPHIE

Номер: DE0069911754T2
Принадлежит: GENENTECH INC, GENENTECH, INC.

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26-03-2014 дата публикации

Chromatography column

Номер: GB0002506166A
Принадлежит:

A chromatography column 50 containing a bed of packed particles comprising fused core particles. The bed comprises a plurality of bed sections 51,53 and each bed section has an average particle diameter calculated from the particles in that section. There are at least two different average particle diameter bed sections, wherein the particles of each bed are separated from particles of an adjacent bed by a partition 78 that is liquid permeable to allow through a flow of mobile phase. Preferably each partition is a frit and the partition prevents particles from one section from mixing with particles of an adjacent section. In use, a liquid mobile phase containing a sample to be separated into components is flowed through the packed column. Advantageously a high column efficiency can be provided with lower pressure drop per unit length of the column.

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02-05-2007 дата публикации

Method and apparatus for forming an homogeneous mixture of chromatography media in a vessel

Номер: GB0000705436D0
Автор:
Принадлежит:

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05-03-2014 дата публикации

Apparatus and method for waste treatment

Номер: GB0201400833D0
Автор:
Принадлежит:

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16-01-2019 дата публикации

Apparatus for obtaining liquid from a solid phase

Номер: GB0002561425B

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15-09-2008 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT0000408142T
Принадлежит:

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15-11-2010 дата публикации

CHROMATOGRAPHY COLUMN

Номер: AT0000487523T
Принадлежит:

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15-09-2011 дата публикации

COLUMN AND PROCEDURE FOR CHROMATOGRAPHY WITHOUT LIFTING APPARATUS

Номер: AT0000523783T
Принадлежит:

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15-04-2011 дата публикации

STERILISATION PROCEDURE FOR CHROMATOGRAPHI PARTING AGENT

Номер: AT0000505209T
Принадлежит:

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23-05-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00036168917T
Принадлежит:

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02-07-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00035242888T
Принадлежит:

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03-05-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00030026431T
Принадлежит:

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13-02-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00031527515T
Принадлежит:

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24-12-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00031516848T
Принадлежит:

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02-04-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00035630630T
Принадлежит:

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15-05-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00037314942T
Принадлежит:

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10-07-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00033816836T
Принадлежит:

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07-03-2019 дата публикации

Separator

Номер: AU2019201090A1
Принадлежит: Spruson & Ferguson

... 'J-t A separator for separating one or more components selected from particulate material, hydrophobic material, non-polar material, microorganisms, or viruses from a mixture of water and the one or more components or from a mixture of a polar liquid and the one or more components, the separator comprising a layer of a metal hydroxide hydrate.

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21-01-2021 дата публикации

Molecularly Imprinted Polymer beads for extraction of metals and uses thereof

Номер: AU2016297956B2
Принадлежит:

The present disclosure provides Molecularly Imprinted Polymer (MIP) technology for selectively sequestering one or more target molecules from chemical mixtures. Also disclosed herein are MIP beads and methods of making and using thereof.

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14-09-2006 дата публикации

METHOD OF STERILIZATION

Номер: CA0002599650A1
Принадлежит:

The present invention relates to a method of sterilizing a chromatography column which is packed with a separation matrix, which method comprises passing a super-heated aqueous liquid through the packing of the column to obtain at least one substantially sterile packed chromatography column. The method may also comprise a preceding heating. In the most advantageous embodiment, the superheated aqueous liquid is passed in a substantially uniform flow through the packing of the column, resulting in a sterility of the packed column.

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11-02-2014 дата публикации

METHOD OF PREPARING A COMPOSITION USING ARGENTATION CHROMATOGRAPHY

Номер: CA0002633509C

The present invention is directed to a method of preparing compositions enriched in compounds containing carbon chains of varying degrees of unsaturation using argentation chromatography. The present method utilizes an argentized cationic resin or a conditioned argentized alumina to separate compounds containing saturated or mono-unsaturated carbon chains from compounds having polyunsaturated carbon chains present in a starting composition. The invention is particularly useful for preparing a composition enriched in polyunsaturated fatty acid alkyl esters from mixtures of fatty acid esters in a starting composition derived from vegetable oils. The present invention is also directed to a method of preparing a conditioned argentized alumina adsorbent having increased selectivity for compounds containing one or more polyunsaturated carbon chains.

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21-08-2018 дата публикации

METHODS OF EVALUATING QUALITY OF A CHROMATOGRAPHY MEDIA WHICH BINDS ANTI-A OR ANTI-B ANTIBODIES

Номер: CA0002938549C
Принадлежит: MERCK PATENT GMBH

Embodiments described herein relate to methods of evaluating quality of a chromatography media far removal of anti-A or anti-B antibodies from a sample, where the methods employ use of purified monoclonal IgM-A and IgM-B antibodies.

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23-07-2015 дата публикации

STERILE CHROMATOGRAPHY RESIN AND USE THEREOF IN MANUFACTURING PROCESSES

Номер: CA0002936969A1
Принадлежит:

Provided herein are methods of reducing bioburden of (e.g., sterilizing) a chromatography resin that include exposing a container including a composition including a chromatography resin and at least one antioxidant agent and/or chelator to a dose of gamma-irradiation sufficient to reduce the bioburden of the container and the chromatography resin, where the at least one antioxidant agent and/or chelator are present in an amount sufficient to ameliorate the loss of binding capacity of the chromatography resin after/upon exposure to the dose of gamma-irradiation. Also provided are reduced bioburden chromatography columns including the reduced bioburden chromatography resin, compositions including a chromatography resin and at least one chelator and/or antioxidant agent, methods of performing reduced bioburden column chromatography using one of these reduced bioburden chromatography columns, and integrated, closed, and continuous processes for reduced bioburden manufacturing of a purified ...

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17-02-2011 дата публикации

METHODS OF SYNTHESIS AND PURIFICATION BY USE OF A SOLID SUPPORT

Номер: CA0002805849A1
Принадлежит:

Disclosed herein are novel methods of using polymeric adsorbent resin for chemical synthesis and the purification of product therefrom. Also disclosed herein is a novel method of using silica gel for the combination of chemical reaction and chromatography into a single step. The methods disclosed herein increase the efficiency of chemical synthesis processes. Accordingly, the utility of the methods disclosed herein includes the ability to automate chemical synthesis and purification of the resulting products.

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18-04-2013 дата публикации

TREATMENT OF CONTAMINATED LIQUIDS

Номер: CA0002852037A1
Принадлежит:

Apparatus and method for the treatment of a contaminated liquid to remove contaminants from said liquid. The apparatus comprises a bed of a carbon based adsorbent material capable of electrochemical regeneration, at least one pair of electrodes operable to pass an electric current through said bed to regenerate the adsorbent material, and means to admit contaminated liquid into said bed to contact said adsorbent material at a flow rate which is sufficiently high to pass the liquid through the bed but below the flow rate required to fluidise the bed of adsorbent material.

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06-01-1994 дата публикации

Passivated and Stabilized Porous Supports and Methods for the Preparation and Use of Same

Номер: CA0002138520A1
Принадлежит:

This invention relates generally to modified porous solid supports and processes for the preparation and use of same. In particular, passivated porous mineral oxide, polymeric, or polymer-coated mineral oxide supports are disclosed which are characterized by a reversible high sorptive capacity substantially unaccompanied by non-specific adsorption of or interaction with biomolecules. Passivation is achieved by use of a passivation mixture comprising a main monomer, a passivating monomer and a crosslinking agent, which mixture upon polymerization results in the substantial elimination of the undesirable non-specific interaction with biomolecules.

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31-01-2018 дата публикации

FIELD OF ALKALI FLUSHING SOLUTIONS DURING CHROMATOGRAPHY FOR REMOVAL OF ADMIXTURES

Номер: EA0201792012A1
Автор:
Принадлежит:

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30-11-2016 дата публикации

SEPARATOR

Номер: EA0201691163A1
Автор:
Принадлежит:

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13-09-2016 дата публикации

멸균 크로마토그래피 및 제조 공정

Номер: KR1020160107325A
Принадлежит:

... 본원에서는, 감마선 조사 크로마토그래피 수지로 크로마토그래피를 수행하는 방법으로서, 감마선 조사 크로마토그래피 수지를 포함하는 크로마토그래피 컬럼을 제공하는 단계; 컬럼을 통해 크로마토그래피의 제1 사이클을 수행하되, 이 사이클은 크로마토그래피 수지를 변성 완충액에 노출시키는 단계를 포함하는 단계; 및 컬럼을 통해 크로마토그래피의 적어도 하나의 추가 사이클을 수행하는 단계를 포함하는, 방법이 제공된다. 또한, 재조합 단백질의 제조를 위한 통합형, 닫힌 또는 실질적으로 닫힌, 연속 공정으로서, 감마선 조사 크로마토그래피 수지를 포함하는 적어도 하나의 크로마토그래피 컬럼의 사용을 포함하되, 감마선 조사 크로마토그래피 수지는 공정의 각 사이클 동안 변성 완충액에 노출되고, 저감된 바이오버든 완충액이 공정에 사용되는, 공정이 제공된다.

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09-01-2014 дата публикации

TECHNIQUES FOR ACCELERATING THERMAL EQUILIBRIUM IN A CHROMATOGRAPHIC COLUMN

Номер: WO2014008059A1
Принадлежит:

Techniques are described for accelerating thermal equilibrium in a chromatographic column. An apparatus comprises a chromatography column, and a plurality of temperature control units in thermal contact with the chromatography column. A method of performing liquid chromatography comprises setting an inlet of a chromatography column to a first temperature using a first temperature control unit in thermal contact with said inlet, setting an outlet of the chromatography column to a second temperature using a second temperature control unit in thermal contact with the outlet, wherein the first temperature is less than the second temperature; and injecting a sample into a liquid stream that flows through the chromatography column after the inlet is set at the first temperature and the outlet is at the second temperature.

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22-08-2013 дата публикации

IONIC LIQUID SEPARATIONS

Номер: WO2013121220A1
Принадлежит:

A process for the separation of inorganic compounds comprises centrifugal partitioning of at least one inorganic compound between a mobile liquid phase and an immiscible stationary liquid phase. At least one of the mobile liquid phase and the stationary liquid phase comprises or consists of an ionic liquid. A rotary coil centrifuge for counter current chromatography and a liquid-liquid chromatography or liquid-liquid extraction apparatus may be used in the process.

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26-08-2010 дата публикации

NOVEL USE OF POLYMERS

Номер: WO2010094976A1
Принадлежит:

The invention provides a method for the removal of bacteria from media, the method comprising the steps of : (a) providing a stimulus responsive polymer adapted to be capable of binding bacteria; (b) applying said functionalised polymer to the medium so as to facilitate binding of the polymer to bacteria; and (c) removing the polymer and polymer-bound bacteria from the medium. In preferred embodiments the method provides for the use of thermoresponsive polymers functionalised by the incorporation of bacteria-binding ligands in the removal of bacteria from wounds. The invention also envisages the use of the disclosed polymers for the removal of bacteria from media.

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23-03-2010 дата публикации

Method of sterilization

Номер: US0007682510B2

The present invention relates to a method of sterilizing a chromatography column which is packed with a separation matrix, which method comprises passing a superheated aqueous liquid through the packing of the column to obtain at least one substantially sterile packed chromatography column. The method may also comprise a preceding heating. In the most advantageous embodiment, the superheated aqueous liquid is passed in a substantially uniform flow through the packing of the column, resulting in a sterility of the packed column.

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15-02-2018 дата публикации

Modified Walnut Shell and Use

Номер: US20180044203A1
Принадлежит: Polymer Ventures Inc.

Herein are described compositions useful in the purification of hydrocarbon-contaminated liquids (e.g., oil-contaminated water), methods of their manufacture, and methods of their use. In one instance, the composition can include a porous agricultural substrate selected from the group consisting of walnut shell, pecan shell, apricot pit, peach pit, corn cob, and a mixture thereof; the porous agricultural substrate having an external surface and pores, wherein the external surface is hydrophilic; and an organo-amine carried within the pores of the porous agricultural substrate. These compositions are utilized as regenerable filter media in place of, for example, ground walnut media.

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25-02-2010 дата публикации

Меthоd оf stеrilizаtiоn

Номер: US0020258234B2

Тhе prеsеnt invеntiоn rеlаtеs tо а mеthоd оf stеrilizing а сhrоmаtоgrаphу соlumn whiсh is pасkеd with а sеpаrаtiоn mаtriх, whiсh mеthоd соmprisеs pаssing а supеrhеаtеd аquеоus liquid thrоugh thе pасking оf thе соlumn tо оbtаin аt lеаst оnе substаntiаllу stеrilе pасkеd сhrоmаtоgrаphу соlumn. Тhе mеthоd mау аlsо соmprisе а prесеding hеаting. In thе mоst аdvаntаgеоus еmbоdimеnt, thе supеrhеаtеd аquеоus liquid is pаssеd in а substаntiаllу unifоrm flоw thrоugh thе pасking оf thе соlumn, rеsulting in а stеrilitу оf thе pасkеd соlumn.

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25-10-2006 дата публикации

Methods for purifying highly anionic proteins

Номер: EP0001714982A2
Принадлежит:

The present invention is directed to a method for dissociating Fc containing molecules from complexes of Protein A/Fc containing molecules in a mixture comprising contacting the mixture with a metal chelate chromatographic column (IMAC) under pH conditions between 5.0 and 5.7, wherein the pH conditions are established by the addition of ethylene glycol to said mixture to dissociate Fc containing molecules from complexes of Protein A/Fc containing molecules.

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11-06-2008 дата публикации

Intelligent system and method for automated packing of chromatography columns

Номер: EP0001710005B1
Принадлежит: MILLIPORE CORPORATION

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07-11-2019 дата публикации

Номер: RU2018104571A3
Автор:
Принадлежит:

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06-07-2006 дата публикации

Controllable several storage cell system for e.g. material delivery, comprises a polymer storage cell, which has a hydrogel structure, a cell carrier, and a media

Номер: DE102004061732A1
Принадлежит:

A controllable several storage cell system, comprises a polymer storage cell, which has a hydrogel structure, cell carrier, and a media, where conditions of cells are controlled by heat resistor/light/radiation effect. A controllable several storage cell system, comprises a polymer storage cell, which has a hydrogel structure, cell carrier, and a media, where conditions of cells are controlled by heat resistor/light/radiation effect. The carrier is provided with thermal resistances for heat uncoupling the storage cells, where the thermal resistances are material dilutions, materials/material combinations with a high thermal resistance, louvers or cavities. The controlling factor is organic solvents, biologically pharmaceutical materials, enzymes, proteins, antibody, antigens or genes. The hydrogel structure has cells or large porous molecules.

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30-01-1992 дата публикации

HPLC-KOLONNE.

Номер: DE0003775360D1
Автор: RITACCO P, HAMPTON W
Принадлежит: SEPARATIONS TECHNOLOGY INC

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12-10-2016 дата публикации

Superficially porous particles with precisely controlled particle density, and methods of preparation and use thereof

Номер: GB0002537207A
Принадлежит:

The invention relates superficially porous particles, wherein each particle comprises a hollow core, a non-porous inner shell, and a porous outer shell. The hollow core has a radius ranging from 20% to 90% of the radius of the entire particle, the particles have a median size range from about 0.5 μm to 100 μm, with a particle size distribution (one standard deviation) of no more than 15% of the median particle size, the particles have a specific surface area of from 5 to 1000 m2 /g, and the particles comprise a metal oxide selected from silica alumina, titania or zirconia. The particles may constitute a stationary phase in a separation device such as a chromatographic column. Further, a method for making these superficially porous particles is disclosed.

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22-08-2007 дата публикации

Axial chromatography colums and method

Номер: GB0000713572D0
Автор:
Принадлежит:

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18-02-2015 дата публикации

Techniques for thermally insulating a liquid chromatographic column

Номер: GB0002517373A
Принадлежит:

An apparatus for performing liquid chromatography includes a chromatography column, and an insulating member surrounding the chromatography column wherein the insulating member is formed from a vacuum chamber surrounding the chromatography column. Another apparatus for performing liquid chromatography includes a chromatography column, and an insulating member surrounding the chromatography column, wherein the insulating member includes aerogel. Also described is a method of insulating a chromatography column comprising forming a jacket surrounding the chromatography column, and creating a vacuum chamber in an area between the jacket and the chromatography column.

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15-01-1992 дата публикации

HPLC COLUMN.

Номер: AT0000070465T
Принадлежит:

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15-12-2000 дата публикации

PASSIVATED AND STABILIZED CARRIERS AND METHODS TO THEIR PRODUCTION AND USE

Номер: AT0000197556T
Принадлежит:

Подробнее
15-06-2006 дата публикации

GRANULATED CHROMATOGRAPHY MATERIAL

Номер: AT0000324976T
Принадлежит:

Подробнее
05-05-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00035838380T
Принадлежит:

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21-01-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00038620731T
Принадлежит:

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19-05-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00039793578T
Принадлежит:

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10-06-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00031890956T
Принадлежит:

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03-09-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00034085168T
Принадлежит:

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17-07-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00038164591T
Принадлежит:

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12-01-2000 дата публикации

CHROMATOGRAPHY DEVICE

Номер: AT00035651859T
Принадлежит:

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02-07-1987 дата публикации

FILTRATION PROCESS

Номер: AU0000563290B2
Принадлежит:

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02-11-2017 дата публикации

Use of alkaline washes during chromatography to remove impurities

Номер: AU2016233557A1
Принадлежит: AJ Park IP Pty Ltd

In certain embodiments, the invention provides a method of purifying a protein of interest from a mixture which comprises the protein of interest and one or more contaminants, said method comprising: a) subjecting the mixture to a first chromatography matrix, wherein the protein of interest binds to the first chromatography matrix; b) contacting the first chromatography matrix with a first wash solution which has a pH of at least 9.0, and does not comprise arginine or an arginine derivative; and c) eluting the protein of interest from the first chromatography matrix into an elution solution.

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23-03-2017 дата публикации

Methods of evaluating quality of media suitable for removing anti-A or anti-B antibodies

Номер: AU2016219568A1
Принадлежит: Shelston IP Pty Ltd.

Abstract [00109] Embodiments described herein relate to methods of evaluating quality of a chromatography media for removal of anti-A or anti-B antibodies from a sample, where the methods employ use of purified Lectins.

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24-10-2019 дата публикации

CHROMATOGRAPHY COLUMN QUALIFICATION IN MANUFACTURING METHODS FOR PRODURING ANTI-TNF ANTIBODY COMPOSITIONS

Номер: CA0003097776A1

The present disclosure is directed to a method of operating a chromatography column in methods of manufacture for producing anti-TNF antibodies, e.g., the anti-TNFa antibody SIMPONI® (golimumab), and specific pharmaceutical compositions of the antibody. This method involves collecting column outlet signal and accumulated flow parameters at two or more intervals of at least one mobile phase transition front during operation of the chromatography column comprising column packing. A model gamma cumulative distribution curve is determined based on the collected column outlet signal and accumulated flow parameters for the at least one mobile phase transition front. The height equivalent theoretical plate (HETP) value is calculated for the at least one mobile phase transition front using parameters of the model gamma cumulative distribution curve and the quality of the chromatography column packing is assessed based on the calculated HETP value. If during routine column monitoring, an adverse ...

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25-06-2019 дата публикации

SPIDER SILK FUSION PROTEIN STRUCTURES FOR BINDING TO AN ORGANIC TARGET

Номер: CA0002815267C
Принадлежит: SPIBER TECH AB, SPIBER TECHNOLOGIES AB

A protein structure capable of selective interaction with an organic target is provided. The protein structure is a polymer comprising as a repeating structural unit a recombinant fusion protein that is capable of selective interaction with the organic target. The fusion protein is comprising the moieties B, REP and CT, and optionally NT. B is a non-spidroin moiety of more than 30 amino acid residues, which provides the capacity of selective interaction with the organic target. REP is a moiety of from 70 to 300 amino acid residues and is derived from the repetitive fragment of a spider silk protein. CT is a moiety of from 70 to 120 amino acid residues and is derived from the C-terminal fragment of a spider silk protein. NT is an optional moiety of from 100 to 160 amino acid residues and is derived from the N-terminal fragment of a spider silk protein. The fusion protein and protein structure thereof is useful as an affinity medium and a cell scaffold material.

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16-08-2012 дата публикации

FILTERING MEDIUM FOR FLUID PURIFICATION

Номер: CA0002825350A1
Принадлежит:

The present invention concerns a filtering medium, a method for the production thereof, the use of said filtering medium and a method for reducing the content of multiple contaminants simultaneously in fluids by means of said filtering medium, wherein said filtering medium consists of or comprises at least one of the following: a mixture (A) containing a major part of an iron-based powder and a minor part of a silver powder, an iron-silver powder alloy (B), and an iron-based porous and permeable composite containing silver (C).

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08-05-2001 дата публикации

COLLAPSIBLE APPARATUS FOR COMPRESSING PACKING MATERIAL IN LIQUID CHROMATOGRAPHY COLUMNS AND METHODS OF USE

Номер: CA0002219680C

Longitudinally collapsible apparatus for compacting packing material within a tubular liquid chromatography column. The apparatus includes a first support member, a second support member and a movable support member. The movable support member is releasably connectable to the second support member for support thereby. When released from the second support member, the movable member is adapted to ride on guide members extending between the first and second support members. A compression mechanism is supported on the movable support member to move therewith to a longitudinally collapsed position for the apparatus. The compression mechanism comprises a reversible drive for an axially movable rod carrying a movable piston. With the movable support memb er secured to the second support member, the piston of the compression mechanis m is movable in an end of the tubular column when the column is supported on t he first support member. Movement of the movable piston within the column axial ly ...

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18-12-2014 дата публикации

MONOLITHIC POROUS BODY COLUMN

Номер: WO2014199444A1
Принадлежит:

A monolithic porous body column is configured from a monolithic porous body rod (2) having a cylindrical external shape and a framework with a three-dimensional network structure and from a metal pipe (3) for covering the monolithic porous body rod (2). In at least a portion of a plurality of sections partitioned along the axial direction, the initial diameter of the uncovered monolithic porous body rod (2) is larger than the internal diameter of the metal pipe (3) at the corresponding section, the compression of the covered framework within the range of elastic deformation causes the covered monolithic porous body rod (2) to have a covered diameter that is smaller than the initial diameter, the framework on the peripheral surface of the monolithic porous body rod (2) is dispersed throughout the entire periphery and touches the inner wall surface of the metal pipe (3), the diameter compression amount obtained by subtracting the covered diameter from the initial diameter is at least 0.01 ...

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09-04-2009 дата публикации

FRACTIONATION PURIFICATION APPARATUS

Номер: WO000002009044425A1
Принадлежит:

A solution containing a target compound is flowed through trap column (14) so as to have the target compound trapped in the column (14). Thereafter, water is introduced in the trap column (14) for washing. Then, 6-way valve (7) is switched and opening or closing valve (6) is opened so as to introduce nitrogen gas through supply-side channel (8) in the trap column (14). In this stage, by means of heat exchange block (10), the nitrogen gas is warmed, and the trap column (14) is warmed by column rack (15). Any water remaining in the trap column (14) is first pushed up by the nitrogen gas, going out from exit edge (14b) and discharged through discharge-side channel (20). Further, any water adhering to adsorbent and internal wall surface of the trap column (14) is promptly evaporated and carried away by the nitrogen gas. Accordingly, as any water remaining in the trap column (14) can be rapidly removed, water mixing can be avoided in the ensuing eluate recovery by introduction of a solvent with ...

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04-09-2018 дата публикации

Antimicrobial capture system with carbon container

Номер: US0010065869B2

According to one embodiment, a container for removing antimicrobials from an antimicrobial composition includes a container body having an exterior and an interior. The interior is at least partially filled with carbon granules configured to remove a portion of the antimicrobials in the antimicrobial composition. The interior is further filled with a liquid to at least a level that completely submerges each of the carbon granules. The container further includes an agitator configured to agitate at least a portion of the carbon granules. The container further includes a drain and a drainage valve. The location of the drainage valve is configured to prevent the drainage valve from lowering a current level of the liquid below the level that completely submerges each of the carbon granules.

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01-06-2017 дата публикации

Method of Preparing Adsorbent for Phosphorus Adsorption and Adsorbent Prepared by the Same

Номер: US20170151550A1
Принадлежит:

The present invention relates to a method for preparing an adsorbent for phosphorus adsorption and an adsorbent prepared by the method. Specifically, according to the present invention, the surface of conventional expanded vermiculite, which is effective for removal of cations but is not effective for removal of anions, is coated with sulfate to modify the surface, thereby preparing an adsorbent for phosphorus adsorption. Namely, the surface of expanded vermiculite is ionized by sulfate to thereby significantly increase the efficiency with which the anion phosphorus is removed by the expanded vermiculite. In addition, a floating-type adsorbent can be prepared using the expanded vermiculite as described above, and thus it can be quickly separated from water after adsorption without requiring a process for separating the absorbent from water.

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01-12-2005 дата публикации

Processing of chemicals in flow-through device with porous media

Номер: US20050263455A1
Принадлежит:

A method of processing a sample comprising introducing a sample into a flow-through device containing a porous solid media therein, and thereafter subjecting the device to microwave energy.

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20-10-2016 дата публикации

SEPARATOR

Номер: US20160304358A1
Принадлежит:

A separator for separating one or more components selected from particulate material, hydrophobic material, non-polar material, microorganisms, or viruses from a mixture of water and the one or more components or from a mixture of a polar liquid and the one or more components, the separator comprising a layer of a metal hydroxide hydrate.

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16-09-2009 дата публикации

SEPARATION MEDIA SLURRY TANK

Номер: EP2100136A1
Принадлежит:

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14-05-2014 дата публикации

Номер: JP0005491501B2
Автор:
Принадлежит:

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20-10-2023 дата публикации

СТЕРИЛЬНАЯ ХРОМАТОГРАФИЧЕСКАЯ СМОЛА И ЕЕ ПРИМЕНЕНИЕ В СПОСОБАХ ПРОИЗВОДСТВА

Номер: RU2805607C2

Изобретение относится к способам снижения бионагрузки (например, стерилизации) хроматографической смолы. Предложена композиция для снижения бионагрузки аффинной хроматографической смолы, содержащей белковый лиганд, после воздействия дозы гамма-излучения, содержащая (i) аффинную хроматографическую смолу, содержащую белковый лиганд, и (ii) жидкость, содержащую от приблизительно 15 мМ и до приблизительно 35 мМ аскорбата натрия, от приблизительно 15 мМ до приблизительно 35 мМ метионина, от приблизительно 15 мМ и до приблизительно 35 маннита и от приблизительно 15 мМ до приблизительно 35 мМ гистидина. Также предложен контейнер для снижения бионагрузки аффинной хроматографической смолы, содержащей белковый лиганд, после воздействия дозы гамма-излучения, содержащий указанную композицию. 2 н. и 6 з.п. ф-лы, 17 ил., 4 табл., 5 пр.

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25-10-2018 дата публикации

Poröser Monolith für chromatographische Anwendungen

Номер: DE102017108561A1
Принадлежит:

Es wird ein Trägermaterial für die Chromatographie, bevorzugt Affinitätschromatographie, vorgeschlagen, wobei das Trägermaterial monolithisch in Form einer Fritte ausgebildet ist und wobei wenigstens an einem Teil der Porenoberflächen der Fritte ein Ligand für eine Wechselwirkung mit einer Zielsubstanz gebunden ist.

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03-02-2021 дата публикации

Techniques for accelerating thermal equilibrium in a chromatographic column

Номер: GB0002586096A
Принадлежит:

Apparatus for liquid chromatography, comprising: a liquid chromatography column 128 having inlet 10 for receiving mobile phase and outlet 20 for the mobile phase to exit column 128; heater 310 in thermal contact with column 128 for adjusting the temperature of the mobile phase; outlet temperature sensor P2 for measuring temperature of mobile phase exiting column 128 at outlet 20; and a processor for executing programming instructions to control heater 310, the processor: determining a desired set point for the temperature of the mobile phase exiting column 128 at outlet 20; receiving the measured temperature of the mobile phase exiting column 128 at outlet 20 from temperature sensor P2; determining a difference between the received measured temperature of the mobile phase exiting column 128 at outlet 20 and the desired set point; and based on the determined difference, controlling heater 310 to impart heat to the mobile phase to attempt to reach the desired set point.

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09-06-2010 дата публикации

Fractional purification apparatus

Номер: GB0002465956A
Принадлежит:

Mixed liquid channel (31) is connected to trapping channel (22) upstream of trap column (23). A mixed liquid of diluent and additive suctioned/emitted by respective liquid feed pumps (35,36) is fed to the mixed liquid channel (31). At the flow of eluate containing a target compound through the trap column (23), the eluate is diluted with the diluent, so that the elution power is lowered to thereby ease trapping of the target compound in the trap column (23). On the other hand, although lowering of the solubility of mobile phase in the eluate would ease precipitation of not only the target compound but also foreign matter, the precipitation can be inhibited by the action of the additive to thereby enable prevention of clogging of the trap column (23) and piping.

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26-01-2012 дата публикации

Preparative chromatography column and methods

Номер: US20120018380A1
Автор: Sarfaraz K. Niazi
Принадлежит: Therapeutic Proteins Inc

A chromatography column that captures components in a process liquid in a free flow state and allows elution in steps is described.

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16-02-2012 дата публикации

Hydrophobic monomers, hydrophobically-derivatized supports, and methods of making and using the same

Номер: US20120039920A1
Принадлежит: 3M Innovative Properties Co

A composition is disclosed comprising a hydrophobic monomer having the structure: CH 2 ═CR 4 C(O)NHC(R 1 R 1 )(C(R 1 R 1 )) n C(O)XR 3 wherein n is an integer of 0 or 1; R 1 is independently selected from at least one of: a hydrogen atom, alkyls aryls, and alkylaryls, wherein the alkyls, aryls, and alkylaryls have a total of 10 carbon atoms or less; R 3 is a hydrophobic group selected from at least one of: alkyls, aryls, alkylaryls and ethers, wherein the alkyls, aryls, alkylaryls and ethers have a total number of carbon atoms ranging from 4 to 30; R 4 H or CH 3 ; X is O or NH. In some embodiments the hydrophobic monomer is derived from an amine or an alcohol (HXR 3 ) that has a hydrophilicity index of 25 or less. A polymerizable composition comprising the hydrophobic monomer is disclosed, which optionally may comprise a cross-linking monomer and/or a non-cross-linking monomer. This polymerizable mixture may be used to from hydrophobically-derivatized supports, which may be used in applications such as hydrophobic interaction chromatography.

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13-09-2012 дата публикации

Adsorption of contaminants from liquid and electrochemical regeneration of adsorbent

Номер: US20120228230A1
Принадлежит: Arvia Technology Ltd

A method for the treatment of a liquid. The method comprises contacting the liquid within a treatment zone with an adsorbent material, which is then electrochemically regenerated within a regeneration zone following contact with said liquid. A disinfectant precursor species is provided within the regeneration zone and then electrochemically converted to a disinfectant species which can then contact adsorbent material and/or liquid within the regeneration zone effecting in-situ disinfection and resulting in the presence of residual disinfectant species in the treated liquid. There is further provided apparatus for carrying out such a method.

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14-03-2013 дата публикации

PACKING SYSTEM AND METHOD FOR CHROMATOGRAPHY COLUMNS

Номер: US20130061941A1
Автор: Gebauer Klaus
Принадлежит: GE HEALTHCARE BIO-SCIENCES AB

The invention relates to a system for packing chromatography columns with a chromatography medium and packing method for use in such columns. In particular, the invention relates to a method and system for packing chromatography columns where the column and chromatography media are pre-sterilized. 1. A method for packing an axial flow chromatography column with a bed of particulate medium of a target bed height ,said column comprising:a housing comprising an elongated tubular side wall;opposed, axially spaced first and second end units separated by said side wall, wherein at least one said unit is axially movable by drive means relative to the other said unit;a first filter adjacent to said first unit and a second filter adjacent to said second unit which together with the side wall define an enclosed bed space for containing a bed of particulate medium and wherein relative movement of the first and/or second filter alters the bed height;said first end unit comprising a first valve means for filling of the bed space with said particulate medium; and a first port for adding a liquid to or removing a liquid from the bed space; said method comprising:', 'i. adjusting the axial spacing between the first and second filters to a distance greater than that of the target bed height;', 'ii. introducing a suspension of the particulate medium into the bed space via the first valve means to provide a bed of particulate medium therein;', 'iii. compressing said bed of particulate medium to produce the target bed height by axial movement of the first and/or second end filters;, 'the second end unit comprising a second port for adding a liquid to or removing a liquid from the bed space;'}wherein said axial flow chromatography column and said suspension of particulate medium are pre-sterilized.2. The method of claim 1 , wherein step iii) is achieved by said drive means which is non-integral to and is external to the column.3. The method of claim 2 , wherein said drive means is ...

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14-03-2013 дата публикации

PACKING SYSTEM AND METHOD FOR CHROMATOGRAPHY COLUMNS

Номер: US20130062267A1
Автор: Gebauer Klaus
Принадлежит: GE HEALTHCARE BIO-SCIENCES AB

The invention relates to a method for providing an aseptic chromatography column, said method comprising the steps of: 1. A method for providing an aseptic chromatography column , said method comprising the steps of:pre-sterilize an empty chromatography column;pre-sterilize a chromatography medium;introducing the pre-sterilized chromatography medium into the pre-sterilized chromatography column using aseptic equipment, thereby providing an aseptic chromatography column comprising chromatography medium.2. The method according to claim 1 , wherein the method for pre-sterilization of the chromatography column and the method for pre-sterilisation of the chromatography medium can be selected from at least one of the different methods of sterilization such as heat sterilization by autoclaving or steaming (in place) claim 1 , chemical sterilization (i.e. ethylene oxide) claim 1 , gamma irradiation or eBeam irradiation.3. The method according to claim 2 , wherein the method for sterilization used for the pre-sterilization of the chromatography column is different from the method for sterilization used for the pre-sterilization of the chromatography medium.4. The method according to claim 2 , wherein the method for pre-sterilization of the chromatography column and the method for pre-sterilisation of the chromatography medium are the same whereby the intensity of protocol for performing the pre-sterilisation using said method are different.5. An aseptic chromatography column comprising chromatography medium wherein the chromatography column has been pre-sterilized separately and the chromatography medium has been pre-sterilized separately before introduction into the chromatography column.6. The aseptic chromatography column according to claim 5 , wherein the pre-sterilization of chromatography medium is performed on dry chromatography medium.7. The aseptic chromatography column according to claim 5 , wherein one method for sterilization has been used for the pre- ...

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21-03-2013 дата публикации

Sample detection method by thin-layer chromatography, thin-layer chromatography plate, and method for producing same

Номер: US20130067996A1
Принадлежит: Daicel Corp

The present invention provides a thin-layer chromatography plate and a thin-layer chromatography that can detect the separation of a component in a sample by a separating agent layer that does not permit the detection of the separation of the component in the sample by an optical response. For a sample that has an optical response to ultraviolet light or a coloring agent, the present invention uses a thin-layer chromatography plate that has a first separating agent layer, which has the same optical response as the sample, and a second separating agent layer, which is disposed adjacent thereto and has an optical response that is different from the aforementioned optical response; carries out development of the sample in the first separating agent layer; thereafter carries out further development of the spots from the first separating agent layer toward the second separating agent layer; and detects the spots in the second separating agent layer through exposure to ultraviolet radiation or a color-development treatment with a coloring agent. In addition, the development axis in the first separating agent layer is maintained approximately perpendicular, and spot broadening at the boundary surface is prevented by adjusting the binder blending ratio.

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18-04-2013 дата публикации

TUBE AND FLOAT SYSTEMS AND METHODS OF USING THE SAME

Номер: US20130095008A1
Принадлежит: RareCyte, Inc.

This disclosure is directed to systems for analyzing target materials of a suspension. In one aspect, the systems include a tube and a float that is at least partially coated with a coating having a high affinity for target analytes of a suspension. The coating provides an adhesion or an attraction force with the target analytes through chemical means. In another aspect, the coating can be a changeable material that when stimulated by application of an appropriate stimulus attracts and/or attaches the target analytes to the coated surface of the float. In another aspect, a coating applied to the float may also be used to form a sealing engagement between the float and the inner surface of the tube in order to inhibit fluids from flowing past the coated float in the tube. 1. A float for separating a suspension suspected of containing a target analyte , the float comprising:a main body; anda coating applied to at least a portion of the main body, wherein the coating has an affinity for the target analyte.2. The float of claim 1 , wherein the coating attracts the target analyte.3. The float of claim 1 , wherein the coating forms a chemical bond with the target analyte.4. The float of claim 1 , wherein the coating is a changeable material that is changeable upon application of a stimulus.5. The float of claim 4 , wherein the stimulus further comprises one or more of thermal claim 4 , electromagnetic claim 4 , optical claim 4 , light claim 4 , or sound energy.6. A float for separating a suspension suspected of containing a target analyte claim 4 , comprising:a main body; and,a coating, wherein the float is sized to fit within a tube, and wherein the coating forms a sealing engagement between the float and the tube.7. The float of claim 6 , further comprising at least one structural element extending radially from the main body.8. The float of claim 7 , wherein the at least one structural element is coated with the coating.9. The float of claim 8 , wherein the coating is ...

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09-05-2013 дата публикации

COMPOSITE MATERIAL

Номер: US20130112623A1
Принадлежит: JACOBS UNIVERSITY BREMEN GGMBH

The invention describes a composite microfiber, which is comprising a polysaccharide polymer selected from the group consisting of cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, methyl cellulose, ethyl cellulose, n-propyl cellulose, isopropyl cellulose, cellulose acetate and combinations of two or more of these substances, and combinations of two or more of these substances, thereby the polysaccharide polymer further comprising substituents comprising a given formula, wherein k is 1 or greater, and wherein each moiety Ris independently selected from H and methyl, and wherein each moiety Ris independently selected from —H, —OH, —NH, —SH, —OR, —NHRand —NRR, —SR, and wherein each moiety Rand Rare chemical groups independently selected from C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkoxy halide and C1-C4 heteroalkyl substituents, and is preferably selected from —CH, —CH—CH, —CH—OH, —CH—CH—OH, —CH—CH—NH, —CH—CH(OH)—CH—OH, —CH—CH(OH)—CH, glycidyl, anhydride, sulfonic acid and hydroxysuccinimide, said substituents forming a hydrogel in the presence of water, and said composite microfiber having a swelling factor of at least 10%, preferably of 10-400%. 3. The method as recited in claim 2 , wherein:a) the monomers for gamma radiation induced polymerization are vinyl monomers, such as glycidyl methacrylate (GMA) and dimethyl acrylamide (DMAA) and/orb) the liquid medium is a polar liquid medium and such as water and optionally one or more of methanol, ethanol, n-propanol, iso-propanol, butanol, ter-butanol, acetonitrile, dimethylsulfoxide, acetone, dimethylformamide, and mixtures thereof.4. The method as recited in claim 2 , wherein the gamma radiation induced polymerization is performed in the absence of a polymerization initiator substance claim 2 , such as in the absence of peroxides and/or azo compounds.5. The method as recited in claim 2 , wherein the gamma radiation induced polymerization is performed witha) a radiation dose of 5-15 kGy, and/orb) a dose velocity of ...

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01-08-2013 дата публикации

METHOD OF PACKING CHROMATOGRAPHIC COLUMNS

Номер: US20130193051A1
Принадлежит: PURDUE RESEARCH FOUNDATION

Improved methods for packing a chromatographic column and columns packed by these methods are provided. The methods include introducing a packing material into a chromatographic column, while simultaneously ultrasonicating and applying pressure to the packing material to form a packed column with radial homogeneity. 1. A method for packing a chromatographic column comprising the steps ofa) introducing a packing material into a chromatographic column;b) ultrasonicating the chromatographic column; andc) applying pressure to the packing material, wherein steps a)-c) are performed simultaneously and wherein a packed chromatographic column with an eddy diffusion term of less than 1 μm is formed.2. The method of claim 1 , wherein the packing material comprises silica particles.3. The method of claim 2 , wherein all or at least a portion of the silica particles have a diameter range from about 100 nm to 2 μm.4. The method of claim 3 , wherein the silica particles have a diameter range from about 150 nm to 1 μm.5. The method of claim 1 , wherein the packing material comprises nonporous silica particles claim 1 , porous silica particles claim 1 , core-shell silica particles claim 1 , nonporous polystyrene particles claim 1 , or combinations thereof.6. The method of claim 1 , wherein the chromatographic column comprises fused silica claim 1 , glass claim 1 , ceramic claim 1 , stainless steel claim 1 , aluminum claim 1 , PEEK claim 1 , acrylic claim 1 , or polystyrene.7. The method of claim 6 , wherein the chromatographic column comprises fused silica.8. The method of claim 6 , wherein the chromatographic column comprises glass.9. The method of claim 6 , wherein the chromatographic column comprises stainless steel.10. The method of claim 1 , wherein the chromatographic column has an inner diameter within the range of 10 μm to 1 meter.11. The method of claim 10 , wherein the chromatographic column has an inner diameter within the range of 10 μm to 1 cm.12. The method of claim 1 ...

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15-08-2013 дата публикации

SUPERFICIALLY POROUS MATERIALS COMPRISING A SUBSTANTIALLY NONPOROUS HYBRID CORE HAVING NARROW PARTICLE SIZE DISTRIBUTION; PROCESS FOR THE PREPARATION THEREOF; AND USE THEREOF FOR CHROMATOGRAPHIC SEPARATIONS

Номер: US20130206665A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for its preparation and separations devices containing the chromatographic material; separations devices, chromatographic columns and kits comprising the same; and methods for the preparation thereof. The chromatographic materials of the invention are chromatographic materials comprising having a narrow particle size distribution. 1. A superficially porous material comprising a substantially nonporous inorganic/organic hybrid core and one or more layers of a porous shell material surrounding the core.2. The superficially porous material of claim 1 , wherein the material is comprised of superficially porous particles.3. The superficially porous material of claim 1 , wherein the material is a superficially porous monolith.4. The superficially porous material of claim 2 , wherein the material has a substantially narrow particle size distribution.5. The superficially porous material of claim 2 , wherein the core has a substantially narrow particle size distribution.6. The superficially porous material of claim 2 , wherein the 90/10 ratio of particle sizes is from 1.00-1.55 claim 2 , from 1.00-1.10 claim 2 , from 1.05-1.10 claim 2 , from 1.10-1.55 claim 2 , from 1.10-1.50 or from 1.30-1.45.711-. (canceled)12. The superficially porous material of claim 1 , wherein the material has chromatographically enhancing pore geometry.13. The superficially porous material of claim 12 , wherein the material has a small population of micropores.19. The superficially porous material of wherein the porous shell material is a porous inorganic/organic hybrid material.20. The superficially porous material of wherein the porous shell material is a porous silica.21. The superficially porous material of wherein the porous shell material is a porous composite material.22. The superficially porous material of comprising more than one layer of porous shell material wherein each layer ...

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29-08-2013 дата публикации

METHOD OF PRE-TREATING AN ADSORBENT FOR A CHROMATOGRAPHIC SEPARATION

Номер: US20130220928A1
Автор: OELSNER Steve
Принадлежит: NORDION (CANADA) INC.

A method of treating an adsorbent for a chromatographic separation. The method involves sonicating particles of an inorganic metal oxide having fragile edges in the absence of any alkylating or acylating agent to form smoothened particles of the inorganic metal oxide and washing the smoothened particles of the inorganic metal oxide to remove fine particulate matter to produce a treated adsorbent. The treated adsorbent can be used in a method of isolating a daughter radioisotope from a daughter radioisotope that is produced from the parent radioisotope by radioactive decay. 1. A method of treating an adsorbent for a chromatographic separation , comprising:sonicating particles of an inorganic metal oxide having fragile edges in the absence of any alkylating or acylating agent to form smoothened particles of the inorganic metal oxide, andwashing the smoothened particles of the inorganic metal oxide to remove fine particulate matter, thereby producing a washed, treated adsorbent.2. The method according to claim 1 , wherein the particles of the inorganic metal oxide are sonicated for a period of about 1 to about 4 hours.3. The method according to claim 1 , wherein the particles of the inorganic metal oxide are sonicated for a period of about 1 to about 2 hours.4. The method according to claim 1 , wherein the inorganic metal oxide has a particle size of from about 10 μm to about 300 μm.5. The method according to claim 1 , wherein the particles of the inorganic metal oxide are irregularly-shaped.6. The method according to claim 1 , further comprising a step of baking the particles of the inorganic metal oxide having fragile edges or the washed claim 1 , smoothened particles of the inorganic metal oxide at a temperature of from about 400 to about 600° C. for about 1 to about 2 hours.7. The method according to claim 1 , wherein the inorganic metal oxide is titanium oxide claim 1 , aluminum oxide claim 1 , tin oxide claim 1 , zirconium oxide or silicon dioxide.8. The method ...

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26-09-2013 дата публикации

EXPANDED BED CHROMATOGRAPHIC SEPARATION COLUMN FOR BIOCHEMICAL SEPARATION PROCESS AND TECHNICAL PROCESS THEREOF

Номер: US20130248430A1
Автор: Gu Xiongyi

An expanded bed chromatographic adsorption (EBA) column for a biochemical separation process comprises a pressure equalization liquid distributor having a self-cleaning function below a porous blocking sieve plate at the bottom of the expanded bed, an upper part nozzle assembly having a backflush cleaning function at the top of the expanded bed, a better distribution of the feedstock liquor added into the expanded bed ensuring that the fluid passed through the expanded bed layer displays a state of piston flow. The expanded bed layer displays a state of piston flow. The expanded bed chromatographic separation column has advantages of increasing the separation efficiency of the expanded bed. 1. A column for expanded bed adsorption (EBA) chromatography for biopharmaceutical purification and bioprocessing , comprising a first mesh and an outlet on the top adaptor , and a second mesh and an inlet on the bottom adaptor , characterized by:the top adaptor includes a bypass valve that allows back flush of the mesh, a feed outlet, a waste outlet, a movable plug, and sealing o-rings;the bottom adaptor includes a self cleanable even flow distributor, which is comprised of a feed inlet, radial injection holes, a distribution inner core, and a feed outlet;when aggregation or clogging is happening underneath the top mesh and flow resistance increases, a back flush flow can be applied from above the top mesh through the feed outlet to push the aggregates or clogging away from the mesh, in the meantime the plug is moved down and opens the bypass valve, which allows the aggregates or clogging to be pushed out to the waste, after the back flush, the plug moves up and closes the bypass valve and the normal operation resumes;said distribution inner core and the first mesh on the bottom adaptor form the flow distribution channels from the center out along the radial directions;the feed is injected into the distribution channels in the radial directions by the nozzle, sweeping underneath ...

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10-10-2013 дата публикации

COLUMN PACKING METHOD

Номер: US20130263968A1
Принадлежит:

A method for packing a media bed in a column (). According to the invention the method comprises the steps of: providing data to a control unit () connected to the column (), said data comprising at least a measured slurry concentration, a target bed height, a target packing factor or compression factor and minimum and maximum acceptable values for at least one of target bed height and target packing or compression factor; forcing a movable adapter () along a longitudinal axis of the column () in order to pack the media; detecting when the media bed is consolidated; the control unit () processing the provided data and the information about the consolidated bed height in order to present to the user acceptable bed heights, if there are any, giving acceptable packing or compression factors. 13. A method for packing a media bed in a column () from a slurry being a dispersion of said media particles and a liquid , comprising the steps of:{'b': 15', '3, 'providing data to a control unit () connected to the column (), said data comprising at least a measured slurry concentration, a target bed height, a target packing factor or compression factor and minimum and maximum acceptable values for at least one of target bed height and target packing or compression factor;'}{'b': '3', 'filling the column () with correct amount of slurry according to the column dimensions and the provided data;'}{'b': 9', '3, 'forcing a movable adapter () along a longitudinal axis of the column () in order to pack the media;'}detecting when the media bed is consolidated; and{'b': '15', 'using the control unit () processing the provided data and the information about the consolidated bed height in order to present to the user acceptable bed heights, if there are any, giving acceptable packing or compression factors.'}215. The method of claim 1 , wherein the control unit () further is adapted to present to the user windows in time or distance as to when to stop the packing such that both bed height ...

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17-10-2013 дата публикации

METHODS FOR OBTAINING LIQUID FROM A SOLID PHASE

Номер: US20130274454A1
Автор: Chua Yii Leng
Принадлежит:

A method for obtaining a liquid from a porous solid phase is described. The method comprises forming a liquid seal at a first end of a porous solid phase to which a liquid is bound, wherein liquid of the liquid seal is immiscible with the liquid bound to the solid phase, and applying a pressure differential across the porous solid phase to cause the immiscible liquid to move through the porous solid phase towards a second end of the porous solid phase, thereby displacing the liquid bound to the porous solid phase towards the second end and releasing this liquid from the second end. Recovery of liquid from the solid phase using such methods is increased compared with corresponding methods in which no liquid seal is formed. In preferred embodiments, the liquid used to form the liquid seal is a mineral oil. The methods have particular application in nucleic acid extractions which utilise capture of nucleic acid to a solid phase. Kits and apparatus for performing the methods are also described.

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23-01-2014 дата публикации

Filtration System

Номер: US20140021138A1
Автор: Osterhoudt Lewis E.
Принадлежит:

A filtration system and methods for using same are disclosed. The filtration system can include a frame, and a plurality of filters coupled to the frame and coupled to each other in series. A pump can provide a pressure differential that causes fluid to flow through the filters in series. The first filter can be provided as a pre-filter, and one or more additional filters can include pleated, calendared, micro-fiber filters. Another filter can be a percentage removal nano-filter that is adapted to remove sub-micron particles from the fluid. The nano-filter can include three pleated filter layers. Each pleated filter layer can be oriented approximately concentrically about a common longitudinal axis. 1. A fountain solution filtration system configured to remove particles from a fountain solution fluid of a printing or lithographic system , the fluid filtration system comprising:a first mechanical filter comprising a first outer housing and a filter media disposed in the first outer housing, the filter media having a first particle size rating to remove particles from the fountain solution when the fountain solution flows through the filter media, the particles removed by the filter material having a dimension greater than the first particle size;an electropositive filter disposed downstream of the first mechanical filter and configured to receive the fountain solution fluid from the first mechanical filter, the the electropositive filter including a second outer housing that is separate from the first outer housing, the electropositive filter further including a web of electro-positive fibers disposed in the second outer housing, wherein the electropositive filter defines a flow path through the web of electro-positive fibers, the electropositive fibers having an electro-positive electrokinetic charge that attracts and filters negatively charged material from the fountain solution so as to remove the negatively charged material from the fountain solution fluid when ...

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27-03-2014 дата публикации

HYDROLYTICALLY STABLE ION-EXCHANGE STATIONARY PHASES AND USES THEREOF

Номер: US20140083946A1
Автор: ANDREI BORDUNOV
Принадлежит: AGILENT TECHNOLOGIES, INC.

The invention provides novel ion-exchange media and related methods for their preparation and use. Ion-exchange stationary phases according to the invention are suitable for chromatographic separation of a variety of biomolecules. Distinguishing characteristics of ion-exchange media according to this invention includes, for example, their ability to separate variants of monoclonal antibodies via cation-exchange liquid chromatography using porous substrates with particle sizes <5 μm. The ion-exchange stationary media include a hydrolytically stable layer, which inhibits surface degradation of the particles in 100% aqueous media. Another unique feature is low molecular weight building blocks used to functionalize the particles with ion-exchange groups. 2. The ion-exchange medium of claim 1 , wherein the particulate substrate is porous.3. The ion-exchange medium of claim 1 , wherein the particulate substrate comprises a non-porous core and a porous shell.4. The ion-exchange medium of claim 1 , wherein the particulate substrate is non-porous.5. The ion-exchange medium of claim 2 , wherein the particulate substrate has an average pore size of about 60 Å to about 2 claim 2 ,000 Å.9. The ion-exchange medium of claim 1 , wherein the ion-exchange layer of one or more ion-exchange organic compounds covalently bond to the hydrolytically stable monolayer comprises one or more cation-exchange organic compounds covalently bond to the hydrolytically stable monolayer.10. The ion-exchange medium of claim 1 , wherein the ion-exchange layer of one or more ion-exchange organic compounds covalently bond to the hydrolytically stable monolayer comprises one or more anion-exchange organic compounds covalently bond to the hydrolytically stable monolayer.12. The method of claim 11 , wherein the particulate substrate is porous claim 11 , comprises a non-porous core and a porous shell claim 11 , or is non-porous.13. The method of claim 11 , wherein the biological analyte is selected from ...

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07-01-2016 дата публикации

SORBENT

Номер: US20160001258A1
Принадлежит: JOHNSON MATTHEY PLC

A method for preparing a sorbent composition includes the steps of: 1. A sorbent composition comprising an eggshell layer on the exterior surface of a support material , the layer comprising at least one copper compound and having a thickness in the range 1-200 μm , and the sorbent composition comprises 0.5 to 20% by weight of copper.2. A sorbent composition according to claim 1 , wherein the at least one copper compound comprises copper (II) sulphide.3. A sorbent composition according to claim 1 , wherein the at least one copper compound is selected from the group consisting of basic copper carbonate and copper (II) oxide.4. A sorbent composition according to claim 1 , wherein the support material comprises an alumina claim 1 , hydrated alumina claim 1 , titania claim 1 , zirconia claim 1 , silica or aluminosilicate claim 1 , or a mixture of two or more of these.5. A sorbent composition according to claim 1 , wherein the support material is an alumina.6. A sorbent composition according to wherein the support material is in the form of a foam claim 1 , monolith or honeycomb claim 1 , or a coating on a structured packing.7. A sorbent composition according to wherein the support material is in the form of shaped particulate unit selected from the group consisting of spheres claim 1 , rings claim 1 , trilobes claim 1 , quadralobes claim 1 , and cylinders8. A sorbent composition according to claim 7 , wherein the support material has between 2 and 10 holes extending therethrough.9. A sorbent composition according to claim 1 , wherein the support material has a BET surface area of 10-330 m·gand a pore volume in the range 0.3-0.9 cm·g.10. A sorbent composition according to claim 1 , wherein the thickness of the layer is in the range 1 to 150 μm.11. A sorbent composition according to claim 1 , wherein the sorbent comprises 0.75-10% by weight of copper.12. A sorbent composition according to wherein the support material is in the form of a shaped particulate unit with a ...

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02-01-2020 дата публикации

A Method in Continuous Chromatography

Номер: US20200001203A1
Принадлежит:

The present invention relates to a method for purifying a target product in a flow-through chromatography system comprises at least a first column loaded with feed material from a feed source. The at least first column is purged after binding of impurities and wherein the outlet of purged material from the column is subsequently passed to the feed source. 1. A method for purifying a target product in a flow-through chromatography system comprising at least a first column loaded with feed material from a feed source , wherein the at least first column is purged after binding of impurities to produce purged material and wherein the purged material from the column is passed upstream of the at least one column to be re-purified.2. The method according to claim 1 , wherein said upstream passing of the purged material is passing to the feed source.3. The method according to further including the steps of:providing an outlet sensor arranged downstream of at least the first column;loading the first column with feed material from the feed source,detecting impurity breakthrough based on a signal detected by the outlet sensor of the first column,when a predetermined impurity breakthrough is detected, disconnecting the first column from the feed source,purging partly purified feed material from the first column using a purging buffer, andpassing the purged partly purified feed material to the feed source.4. The method according to claim 3 , wherein the or each outlet sensor is a UV sensor and the predetermined impurity breakthrough corresponds to a predetermined percentage of impurities in a target product downstream of the or each column.5. The method according to claim 4 , wherein the predetermined percentage of impurities in the target product is about 1% claim 4 , 10% claim 4 , 20% claim 4 , 50% or 70%.6. The method according to or claim 4 , wherein a UV sensor is provided upstream each column claim 4 , and the method further comprises dynamically controlling the impurity ...

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02-01-2020 дата публикации

Method and System for Transferring Separation Resin

Номер: US20200001204A1
Принадлежит:

A method and a system and a container system for transferring separation resin from at least one first container (′) to a second container (′), wherein said first container is a deformable, single-use separation resin storage container, said method comprising the steps of:—preparing (S1) the at least one first container by providing a deformable, single-use container comprising an outlet port (′) with a predefined volume of separation resin in a storage solution;—fluidizing (S3) the separation resin in the at least one first container to provide a resin slurry, said fluidizing being performed by mechanical interaction to the first container from an outside of the first container to provide a deformation of said first container;—fluidically connecting (S5) the outlet port (′) of the at least one first container to an inlet port () of the second container;—transferring (S7) separation resin from the at least one first container to the second container by generating a pressure difference between an interior of the second container and an interior of the first container where the pressure is lower in the second container. 1. A method for transferring separation resin from at least one first container to a second container , wherein said first container is a deformable , single-use separation resin storage container , said method comprising the steps of:preparing the at least one first container by providing a deformable, single-use container comprising an outlet port with a predefined volume of separation resin in a storage solution;fluidizing the separation resin in the at least one first container to provide a resin slurry, said fluidizing being performed by mechanical interaction to the first container from an outside of the first container to provide a deformation of said first container;fluidically connecting the outlet port of the at least one first container to an inlet port of the second container;transferring separation resin from the at least one first ...

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04-01-2018 дата публикации

CHROMATOGRAPHY MEDIA AND ION EXCHANGE RESIN PERFORMANCE RESTORATION

Номер: US20180001314A1
Принадлежит:

An ion exchange resin rejuvenation system includes a vessel, a source of a first cleaning solution including an enzyme fluidly connected to the vessel, a source of a second cleaning solution fluidly connected to the vessel, a source of rinse solution connected to the vessel, and a source of a resin regeneration solution fluidly connected to the vessel. 113.-. (canceled)14. A method of rejuvenating ion exchange resin , the method comprising:treating an ion exchange resin contaminated with a protein layer with a first cleaning solution including an enzyme to provide a stripped ion exchange resin and protein fragments.15. The method of claim 14 , wherein treating the ion exchange resin with the first cleaning solution includes treating the ion exchange resin with a protease.16. The method of claim 15 , wherein treating the ion exchange resin with the first cleaning solution includes treating the ion exchange resin with subtilisin.17. The method of claim 14 , wherein treating the ion exchange resin with the first cleaning solution includes treating the ion exchange resin with the first cleaning solution at a temperature of about 55° C.18. The method of claim 14 , wherein treating the ion exchange resin with the first cleaning solution includes treating the ion exchange resin with the first cleaning solution at a pH of about 9.19. The method of claim 14 , further comprising backwashing the protein fragments.20. The method of claim 14 , further comprising treating the stripped ion exchange resin with a second cleaning solution to provide a cleaned ion exchange resin.21. The method of claim 20 , wherein treating the stripped ion exchange resin with the second cleaning solution comprises treating the stripped ion exchange resin with an acid.22. The method of claim 20 , wherein treating the stripped ion exchange resin with the second cleaning solution includes treating the stripped ion exchange resin with at least one of a caustic solution claim 20 , a base solution claim 20 ...

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14-01-2016 дата публикации

POROUS INORGANIC/ORGANIC HYBRID MATERIALS WITH ORDERED DOMAINS FOR CHROMATOGRAPHIC SEPARATIONS AND PROCESSES FOR THEIR PREPARATION

Номер: US20160008737A1
Принадлежит:

Porous hybrid inorganic/organic materials comprising ordered domains are disclosed. Methods of making the materials and use of the materials for chromatographic applications are also disclosed. 1. A porous hybrid inorganic/organic material comprising ordered domains wherein the ordered domains are ordered radially , and having formula I , II or III below:{'br': None, 'sub': x', 'y', 'z, '(A)(B)(C)\u2003\u2003(Formula I)'}wherein the order of repeat units A, B, and C may be random, block, or a combination of random and block;A is an organic repeat unit which is covalently bonded to one or more repeat units A or B via an organic bond;B is an organosiloxane repeat unit which is bonded to one or more repeat units B or C via an inorganic siloxane bond and which may be further bonded to one or more repeat units A or B via an organic bond;C is an inorganic repeat unit which is bonded to one or more repeat units B or C via an inorganic bond; andx, y are positive numbers and z is a non negative number, whereinwhen z=0, then 0.002≦x/y≦210, and when z≠0, then {'br': None, 'sub': x', 'y', 'y', 'z, '(A)(B)(B*)*(C)\u2003\u2003(Formula II)'}, '0.0003≦y/z≦500 and 0.002≦x/(y+z)≦210;'}wherein the order of repeat units A, B, B*, and C may be random, block, or a combination of random and block;A is an organic repeat unit which is covalently bonded to one or more repeat units A or B via an organic bond;B is an organosiloxane repeat units which is bonded to one or more repeat units B or B* or C via an inorganic siloxane bond and which may be further bonded to one or more repeat units A or B via an organic bond;B* is an organosiloxane repeat unit which is bonded to one or more repeat units B or B* or C via an inorganic siloxane bond, wherein B* is an organosiloxane repeat unit that does not have reactive (i.e., polymerizable) organic components and may further have a protected functional group that may be deprotected after polymerization;C is an inorganic repeat unit which is bonded to ...

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12-01-2017 дата публикации

SYNTHESIS OF AMMONIUM DINITRAMIDE, ADN

Номер: US20170008768A1
Принадлежит: TOTALFORSVARETS FORSKNINGSINSTITUT

The invention concerns a method for making ADN from GUDN in one single process step. GUDN is reacted with an ammonium. source (ammonium-sulfamate, ammonium-sulfate, ammonia) and an ion-change gives ADN from GUDN in one process stage. The advantages are that the process gives pure ADN without potassium contaminants and that a smaller amount of solvent is necessary. 1. Method for producing ammonium dinitramidecharacterized in that guanylureadinitramide is reacted with an ammonium source so that an ion-change takes place and ammonium dinitramide is formed.2. Method for producing ammonium dinitramide according tocharacterized in that guanylurea dinitramide is reacted with an ammonium source in a solution of water and alcohol.3. Method for producing ammonium dinitramide according tocharacterized in that the alcohol is methanol.4. Method for producing ammonium dinitramide according tocharacterized in that the alcohol is ethanol.5. Method for producing ammonium-dinitramide according tocharacterized in that the alcohol is a propanol.6. Method for producing ammonium dinitramide according tocharacterized in that the alcohol is a butanol.7. Method for producing ammonium dinitramide according tocharacterized in that the ammonium source is ammonium-sulfamate.8. Method for producing ammonium dinitramide according tocharacterized in that the ammonium source is ammonium sulfate.9. Method for producing ammonium dinitramide according tocharacterized in that the reaction of guanylurea-dinitramide is reacted an ammonium source in a solution of alcohol.10. Method for producing ammonium dinitramide according tocharacterized in that the ammonium source is ammonium sulfate.11. Method for producing ammonium dinitramide according tocharacterized in that the ammonium source is ammonium sulfamate.129. Method for producing ammonium dinitramide according to demandcharacterized in that the alcohol is methanol.13. Method for producing ammonium dinitramide according tocharacterized in that the ...

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11-01-2018 дата публикации

CHROMATOGRAPHIC MATERIAL HAVING IMPROVED PH STABILITY, METHOD FOR PREPARATION THEREOF AND USES THEREOF

Номер: US20180008959A1
Принадлежит: Dionex Corporation

A chromatographic material including a substrate having a surface and having a polymeric layer covalently bound to the surface; the polymeric layer comprising polymer molecules covalently attached to the surface of the substrate, each polymer molecule being attached to the surface via multiple siloxane bonds and each polymer molecule being connected to one or more functionalizing compounds that each comprise a functional group, wherein the polymeric layer is formed by covalently attaching polymer molecules to the surface of the substrate via multiple siloxane bonds, each polymer molecule containing multiple first reactive groups, and reacting the first reactive groups of the attached polymer molecules with at least one functionalizing compound that comprises a second reactive group that is reactive with the first reactive groups and that further comprises a functional group. Preferred conditions of reacting the polymer with the substrate include elevated temperature and reduced pressure. 1. A chromatographic material comprising:a substrate having a surface and the substrate having a polymeric layer covalently bound to the surface;the polymeric layer comprising polymer molecules covalently attached to the surface of the substrate, each polymer molecule being attached to the surface via multiple siloxane bonds and each polymer molecule being connected to one or more functionalizing compounds that each comprise a functional group.2. The chromatographic material according to claim 1 , wherein the polymeric layer is formed by covalently attaching polymer molecules to the surface of the substrate via multiple siloxane bonds claim 1 , each polymer molecule containing multiple first reactive groups claim 1 , and reacting the first reactive groups of the attached polymer molecules with at least one functionalizing compound that comprises a second reactive group that is reactive with the first reactive groups and that further comprises a functional group.3. The ...

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27-01-2022 дата публикации

FILTERING MEDIUM FOR FLUID PURIFICATION

Номер: US20220023825A1
Автор: Gore Avinash, Hu Bo, Luk Sydney
Принадлежит: Höganas AB (publ)

A filtering medium, a method for the production thereof, the use of said filtering medium and a method for reducing the content of multiple contaminants simultaneously in fluids by means of said filtering medium, wherein said filtering medium has or includes at least one of the following: a mixture (A) containing a major part of an iron-based powder and a minor part of a silver powder, an iron-silver powder alloy (B), and an iron-based porous and permeable composite containing silver (C). 1. A filtering medium for reducing the content of contaminants in fluids , wherein said filtering medium comprises an iron-silver powder alloy ,wherein the iron-silver powder alloy contains 0.01-5% of silver, by weight of the alloy, obtained by thermal bonding or thermal alloying atomized iron powder particles with silver powder particles, wherein atomized iron powder particles have a Fe-content of at least 90% by weight of the iron powder,wherein the iron-silver powder alloy has an average particle size between 1 μm and 10 mm, andwherein said contaminants are selected from the group consisting of chlorine containing compounds, nitrates, nitrites, heavy metals, toxic inorganic substances, toxic organic compounds, microorganisms and/or combinations thereof.2. The filtering medium according to claim 1 , wherein the iron-silver powder alloy contains 0.05-1% of silver claim 1 , by weight of the alloy.3. The filtering medium according to claim 1 , wherein the iron-silver powder alloy has an average particle size between 20 μm and 5 mm.4. The filtering medium according to claim 1 , wherein the iron-silver powder alloy has an average particle size between 45 μm and 2 mm.5. The filtering medium according to claim 1 , wherein the iron-silver powder alloy is obtained by thermal alloying atomized iron powder particles with silver powder particles.6. The filtering medium according to claim 1 , wherein the iron-silver powder alloy is obtained by thermal bonding atomized iron powder particles ...

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14-01-2021 дата публикации

Multi-Column Continuous Resin Regeneration System

Номер: US20210008539A1
Принадлежит:

A continuous resin regeneration system includes a process by which resin in need of being recharged is continuously recharged and cleaned with a plurality of two-set filtration columns so that resin regeneration and the flow of influent is continuous and interrupted. Downstream filtration columns also undergo this cycling but at slower and related rates as the first column with the dirtiest water will naturally degrade resin faster than the downstream columns. Contaminated influent is cleaned by the continuously recharged resin in multiple column sets. The degree of cleaning of earlier filtration columns affects the resin flow rate of later filtration columns. 1. A continuous resin regeneration system for use in cleaning a water stream from a contaminated water reservoir , comprising:a first anion resin set having a first anion column and a second anion column in fluid communication with the first anion column, said first anion column and said second anion column of said first anion resin set including an anion resin;a first cation resin set having a first cation column and a second cation column in fluid communication with the first cation column, said first cation column and said second cation column of said first cation resin set including a cation resin;a first set control valve in fluid communication with the water reservoir, with said first anion column of said first anion resin set, and with said second anion column of said first anion resin set;a second set control valve in fluid communication with the water reservoir, said first cation column of said first cation resin set, and with said second cation column of said first cation resin set; anda controller in data communication with said first set control valve, said controller configured to determine if said anion resin associated with said first anion column of said first anion resin set is greater than a predetermined parameter and, if so, to actuate said first set control valve to direct the water stream ...

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14-01-2016 дата публикации

Process for isolation of plasma or serum proteins

Номер: US20160009757A1
Автор: Allan Otto Fog Lihme
Принадлежит: Therapure Biopharma Inc

The present invention provides a process for the isolation of one or more proteins) from a protein solution. The process comprising the steps of: a) providing a protein solution comprising one or more specific proteins) and having a preset pH and a preset ionic strength or conductivity, b) applying the protein solution to a packed bed or expanded bed column comprising an adsorbent, and c) obtaining one or more proteins) from the column; wherein the protein solution has been supplemented with an alcohol.

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10-01-2019 дата публикации

A MICROFLUIDIC DEVICE AND METHODS FOR MANUFACTURING SAME

Номер: US20190009190A1
Принадлежит:

The present invention relates generally to a sample processing device, such as a microfluidic device, comprising a substrate, wherein the substrate comprises a plurality of channels configured to transport a fluid, and wherein the plurality of channels are substantially coated with lubricin, or a functional variant thereof. Also disclosed herein are methods of manufacturing such devices, methods of preventing fouling of a channel in a device using lubricin, or a functional variant thereof and methods of controlling the electrokinetic flow of an analyte through a channel that is substantially coated with lubricin, or a functional variant thereof. Also disclosed herein is chromatographic material for the electrophoretic and/or chromatographic separation of an analyte, wherein the chromatographic material is substantially coated with lubricin, or a functional variant thereof. 1. A microfluidic device comprising a substrate , wherein the substrate comprises a plurality of channels configured to transport a fluid , and wherein the plurality of channels are substantially coated with lubricin , or a functional variant thereof.2. The device of claim 1 , wherein the plurality of channels comprise a surface selected from the group consisting of a hydrophobic surface claim 1 , an anionic surface claim 1 , a polar surface and combinations thereof.3. The device of claim 2 , wherein the plurality of channels comprise a hydrophobic surface.4. The device of claim 3 , wherein the hydrophobic surface is a gold surface.5. The device of claim 3 , wherein the hydrophobic surface is a thiol-modified hydrophobic surface.6. The device of claim 5 , wherein the thiol is a OH-thiol or a CH-thiol.7. The device of claim 1 , wherein the plurality of channels comprise a COOH-thiol-modified surface.8. The device of claim 1 , wherein the plurality of channels comprise a polystyrene-modified surface.9. The device of claim 1 , wherein at least one of the plurality of channels is a capillary.10. The ...

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10-01-2019 дата публикации

DEIONIZATION DEVICE

Номер: US20190010063A1
Автор: SCHMIDT Harald
Принадлежит:

A deionization device for liquids includes a first chamber for a first ion exchange agent that has a first intake opening and a first discharge opening. A second chamber for a second ion exchange agent has a second intake opening and a second discharge opening. A line connects the first chamber and the second chamber that has a third intake opening and a third discharge opening. The third intake opening is dedicated to the first discharge opening of the first chamber and the third discharge opening is dedicated to the second intake opening of the second chamber. The line also has a first regeneration opening for a first regeneration liquid, wherein the first regeneration opening can be closed for deionization, and wherein the line can be closed for regenerating the deionization device such that the third intake opening can be isolated from the third discharge opening. 1. A deionization device for liquids , comprising:a first chamber for a first ion exchange agent that has a first intake opening and a first discharge opening, a second chamber for a second ion exchange agent that has a second intake opening and a second discharge opening, a line for connecting the first chamber and the second chamber, that has a third intake opening and a third discharge opening, wherein the third intake opening is dedicated to the first discharge opening of the first chamber and the third discharge opening is dedicated to the second intake opening of the second chamber, wherein the line also has a first regeneration opening for a first regeneration liquid, wherein the first regeneration opening is closed for deionization, and wherein the line is closed for regenerating the deionization device such that the third intake opening can be is isolated from the third discharge opening.2. The deionization device according to claim 1 , wherein the line has a second regeneration opening for a second regeneration liquid claim 1 , wherein the second regeneration opening is closed for ...

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14-01-2016 дата публикации

METHOD FOR FRACTIONATING DIOXINS

Номер: US20160011163A1
Принадлежит: MIURA CO., LTD.

The interior of a fractionating tool for fractionating dioxins is packed with a purification layer and an adsorption layer. The adsorption layer includes a first adsorption layer including an activated carbon-containing silica gel layer and a graphite-containing silica gel layer, and a second adsorption layer including an alumina layer. When a solution of dioxins is injected into the purification layer and is supplied with an aliphatic hydrocarbon solvent, the solvent dissolves dioxins in the solution of dioxins and passes through the purification layer and the adsorption layer. In this process, non-ortho PCBs, PCDDs and PCDFs among dioxins are adsorbed to the first adsorption layer, and mono-ortho PCBs among dioxins are adsorbed to the second adsorption layer. As a result, dioxins are fractionated into a group including non-ortho PCBs, PCDDs and PCDFs, and mono-ortho PCBs. 1. A method for fractionating dioxins , comprising the step of:passing an aliphatic hydrocarbon solvent solution of dioxins through an activated carbon-containing silica gel layer and a graphite-containing silica gel layer in this order.2. The method for fractionating dioxins according to claim 1 , wherein the aliphatic hydrocarbon solvent solution having passed through the graphite-containing silica gel layer is further passed through an alumina layer.3. The method for fractionating dioxins according to claim 2 , further comprising the steps of:supplying the activated carbon-containing silica gel layer and the graphite-containing silica gel layer through which the aliphatic hydrocarbon solvent solution has passed with a solvent capable of dissolving dioxins, to secure the solvent having passed through the activated carbon-containing silica gel layer and the graphite-containing silica gel layer; andsupplying the alumina layer through which the aliphatic hydrocarbon solvent solution has passed with a solvent capable of dissolving dioxins, to secure the solvent having passed through the alumina ...

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03-02-2022 дата публикации

SOLID SUPPORT COMPRISING CARBON NANOTUBES, SYSTEMS AND METHODS TO PRODUCE IT AND TO ADSORBE ORGANIC SUBSTANCES ON IT

Номер: US20220032264A1
Автор: VUONO Danilo
Принадлежит:

Method for manufacturing an inert solid support with optionally functionalised carbon nanotubes (CNTs), comprising the steps of: i) providing an inert solid support and at least one catalytic metal associated with, or absorbed in, or adsorbed/deposited on, said support, said metal being optionally selected from among the group consisting of iron, cobalt, nickel, molybdenum and combinations thereof; ii) supplying a source of gaseous, liquid or solid carbon to the catalytic metal; iii) through chemical vapor deposition (CVD), depositing at least part of the carbon source at the catalytic metal as CNTs, stably connected to the inert solid support. The present invention further regards an inert solid support and a separation method. 1. Method for manufacturing inert solid supports with optionally functionalised carbon nanotubes (CNTs) , comprising steps of:i) providing inert solid supports and at least one catalytic metal absorbed in, or adsorbed or deposited on, said supports, said metal being optionally selected from among the group consisting of iron, cobalt, nickel, molybdenum and combinations thereof;ii) supplying a gaseous, liquid or solid carbon source to the catalytic metal;iii) through chemical vapor deposition (CVD), depositing at the catalytic metal at least part of the carbon source as CNTs, stably connected to the inert solid supports;wherein the inert solid supports are in the form of particulate, granule or pellet with an over-nanometric particle size distribution, that is inert solid supports having an average size distribution comprised from 0.1 mm to 5 mm, and wherein the CNTs are in the form of scattered bundles or tangle, grouped at the catalytic metal.2. The method according to claim 1 , wherein the inert solid supports are selected from among the group consisting of aluminium silicate (for example: mullite) claim 1 , silico-aluminates claim 1 , quartz sand claim 1 , quartz claim 1 , alumina or aluminium oxide (for example: corundum) claim 1 , ...

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03-02-2022 дата публикации

METHOD FOR PRODUCING ZERO-VALENT METALS IN FILTERING MEDIA

Номер: US20220033283A1
Принадлежит: POLITECNICO DI TORINO

A method for producing microparticles and/or nanoparticles based on zero-valent metals directly inside a filtering media and/or for creating covering layers based on the zero-valent metals for covering. The filleting media includes the steps of introducing at least one solution containing metal salts in the filtering medium, introducing at least one solution containing inorganic reducing agents into the filtering medium. The steps of introducing the at least one solution containing metal salts and the at least one solution containing inorganic reducing agents inside the filtering medium is carried out in a way separated in time and/or in space to realize, in the filtering medium, a mixture of metal ions with the inorganic reducing agents as well as a chemical reduction of the zero-valent metals to form the microparticles and/or the nanoparticles and/or coverings based on the zero-valent metals inside of the filtering medium. 1. A method for producing microparticles and/or nanoparticles and/or coverings containing at least one zero-valent metal inside a filtering medium , comprising the following steps:{'b': '100', 'step ) providing a first aqueous solution of at least one metal or a salt of the at least one metal;'}{'b': '101', 'step ) providing a second aqueous solution of at least one inorganic reducing agent;'}{'b': 102', '101', '102, 'step ) preparing the filtering medium for introducing the first aqueous solution of the step and the second aqueous solution of the step ;'}{'b': '103', 'i': 'a', 'step ) introducing the first aqueous solution inside the filtering medium;'}{'b': '103', 'i': 'b', 'step ) introducing the second aqueous solution inside the filtering medium;'}{'b': 103', '103', '103, 'i': a', 'b, 'step ) amounts of the first aqueous solution of the step and the second aqueous solution of the step are in a predetermined mutual ratio;'}{'b': '104', 'step ) allowing or inducing a mixing of the first aqueous solution with the second aqueous solution inside ...

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21-01-2021 дата публикации

METHODS AND SYSTEMS FOR PRODUCING LOW SUGAR BEVERAGES

Номер: US20210015127A1
Принадлежит:

Methods and systems are disclosed for selectively removing naturally-occurring sugars in beverages in an effective, affordable and scalable manner. 1. A method of lowering the sugar content of a fruit juice , the method comprising:(a) separating at least part of solid components from the juice; and(b) contacting a first adsorbent with the juice, the first adsorbent being active so as to have a higher relative selectivity for disaccharides than for monosaccharides and organic acids, wherein the first adsorbent comprises a zeolite, to treat the juice and obtain a treated juice having at least 30% less sugar than the untreated form of the juice and a ratio of disaccharides to total sugars below at least 30 percent.2. The method of claim 1 , further comprising the steps of:hydrolyzing the disaccharides bound to the first adsorbent into monosaccharides after the juice has contacted the first adsorbent; wherein the hydrolyzing is performed by heating the first absorbent;washing the first adsorbent with a solution to remove the hydrolyzed monosaccharides, wherein the solution comprises at least one of: water, water in a mixture with at least one of fructose, glucose and galactose, and a solution of at least one of fructose, glucose and galactose; andregulating the acidity of the treated juice to have a pH of at least about 4.3. The method of claim 1 , wherein a Brix/acidity ratio of the treated juice is decreased to be less than about 20% claim 1 , when compared to the untreated form of the juice.45.-. (canceled)6. The method of claim 1 , wherein the first adsorbent is in a column.78.-. (canceled)9. The method of claim 1 , wherein the zeolite is selected from zeolites having a Si/Al molar ratio of at least about 10:1 and up to about 30:1.10. The method of claim 1 , wherein the zeolite comprises at least one of: Y Zeolite H claim 1 , and Y Zeolite Ca.1114.-. (canceled)15. The method of claim 1 , wherein the first adsorbent is associated with a carrier claim 1 , wherein the ...

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19-01-2017 дата публикации

ELECTRO-SPUN FIBERS AND APPLICATIONS THEREOF

Номер: US20170016144A1
Принадлежит:

A supported nanofiber medium useful for segregating chemical species is provided by selecting a polymer, selecting a substrate; and electrospinning the polymer to form a nanofiber medium on the supporting substrate. When the substrate is a planar surface, the nanofiber medium will be a mat suitable for conducting chromatographic separation. When the substrate is a filament, the nanofiber medium is an annular mat suitable for solid phase microextraction. The nanofiber media formed may be selectively cross-linked and at least partially carbonized to carbon nanofibers. The nanofiber medium is supported on the substrate without the use of binder material. 1. A method for analytically separating at least two chemical species , comprising the steps of:providing a separation medium, comprising a mat of nanofibers disposed on a surface of a substrate;providing at least two chemical species, mixed together in an appropriate solvent; andseparating the at least two chemical species from each other through contact of the mixture with the separation medium.2. The method of claim 1 , wherein:the separating step is achieved by ultrathin layer chromatography (UTLC);the substrate surface is planar and the mat of nanofibers on the planar surface has a thickness in the range of from about 11.5 to about 17.4 microns and has an average fiber diameter in the range of from about 150 to about 400 nm, such that the separation medium is a UTLC stationary phase; andthe mixture of the at least two chemical species in the appropriate solvent is a UTLC mobile phase.3. The method of claim 2 , wherein: placing the UTLC mobile phase onto the UTLC stationary phase; and', 'drawing the UTLC mobile phase upward by capillary action., 'the ultra-thin chromatography separating step is achieved by the steps of4. The method of claim 1 , wherein: placing the UTLC mobile phase onto the UTLC stationary phase; and', 'drawing the UTLC mobile phase upward by capillary action., 'the ultra-thin chromatography ...

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17-01-2019 дата публикации

SUPERFICIALLY POROUS MATERIALS COMPRISING A COATED CORE HAVING NARROW PARTICLE SIZE DISTRIBUTION; PROCESS FOR THE PREPARATION THEREOF; AND USE THEREOF FOR CHROMATOGRAPHIC SEPARATIONS

Номер: US20190015815A1
Принадлежит:

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for its preparation and separations devices containing the chromatographic material; separations devices, chromatographic columns and kits comprising the same; and methods for the preparation thereof. The chromatographic materials of the invention are chromatographic materials comprising having a narrow particle size distribution. 1. A superficially porous material comprising a coated core and one or more layers of a porous shell material surrounding the coated core , wherein said coated core comprises a substantially nonporous core material coated with a core-coating material.2. The superficially porous material of claim 1 , wherein the material is comprised of superficially porous particles.3. The superficially porous material of claim 1 , wherein the material is a superficially porous monolith.4. The superficially porous material of claim 2 , wherein the material has a substantially narrow particle size distribution.5. The superficially porous material of claim 2 , wherein the substantially nonporous core material has a substantially narrow particle size distribution.6. The superficially porous material of claim 2 , wherein the 90/10 ratio of particle sizes is from 1.00-1.55.7. The superficially porous material of claim 6 , wherein the 90/10 ratio of particle sizes is from 1.00-1.10.8. The superficially porous material of claim 7 , wherein the 90/10 ratio of particle sizes is from 1.05-1.10.9. The superficially porous material of claim 6 , wherein the 90/10 ratio of particle sizes is from 1.10-1.55.10. The superficially porous material of claim 9 , wherein the 90/10 ratio of particle sizes is from 1.10-1.50.11. The superficially porous material of claim 10 , wherein the 90/10 ratio of particle sizes is from 1.30-1.45.12. The superficially porous material of claim 1 , wherein the material has chromatographically enhancing pore geometry.13. The ...

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21-01-2021 дата публикации

PROCESS FOR REMOVING METHOXYETHANOL FROM A MIXTURE COMPRISING METHOXYETHANOL AND MORPHOLINE

Номер: US20210016204A1
Принадлежит:

A method for removing methoxyethanol from a mixture comprising methoxyethanol and morpholine makes use of the selective adsorption of methoxyethanol onto a mixed oxide comprising a spinel phase. The mixed oxide comprises 20 to 30% by weight MgO and 80 to 70% by weight AlO. The spinel phase has the formula MgAlO. The mixture is a pre-purified reaction output of the reaction of diethylene glycol with ammonia in the presence of an amination catalyst. 1. A method for removing methoxyethanol from a mixture comprising methoxyethanol and morpholine by selective adsorption of methoxyethanol onto a mixed oxide comprising a spinel phase.2. The method according to claim 1 , wherein the spinel phase has the formula{'br': None, 'sub': 2', '4, 'ABO'}in whichA is a divalent cation; andB is a trivalent or tetravalent cation.3. The method according to claim 2 , wherein the spinel phase has the formula MgAlO.4. The method according to claim 3 , wherein the mixed oxide comprises 20 to 30% by weight MgO and 80 to 70% by weight AlO.5. The method according to claim 1 , wherein the mixture is passed over a bed of the mixed oxide.6. The method according to claim 1 , wherein the mixture comprises in addition at least one component selected from 1 claim 1 ,2-ethylenediamine claim 1 , methoxyethylmorpholine and formylmorpholine.7. The method according to claim 1 , wherein the mixture is dried prior to the selective adsorption.8. The method according to claim 7 , wherein the mixture is dried by bringing it into contact with a molecular sieve.9. The method according to claim 1 , wherein the mixed oxide is regenerated by treatment with water.10. The method according to claim 9 , wherein coadsorbed morpholine is desorbed prior to the regeneration of the mixed oxide.11. The method according to claim 10 , wherein coadsorbed morpholine is desorbed by passing over an inert gas or an inert gas containing steam.12. The method according to claim 11 , wherein the desorbed coadsorbed morpholine is ...

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21-01-2021 дата публикации

FUNCTIONALIZED POLYOLEFIN CAPILLARIES FOR OPEN TUBULAR ION CHROMATOGRAPHY

Номер: US20210016266A1
Принадлежит:

Open tubular capillary columns for liquid and ion chromatography, based upon an ionically impermeable polyolefin capillary having a bore with a sulfonate-group- or amine-group-functionalized internal surface. The capillary columns may include a coating of ion exchanging nanoparticles electrostatically bound to the functionalized internal surface. The capillary columns may be made by exposing the interior surface to a sulfonating reagent comprising chlorosulfonic acid (CISOH), preferably from 85 wt % to 95 wt % chlorosulfonic acid at a process temperature of 20 to 25° C. The interior surface may be subsequently exposed to an asymmetrical diamine to form a sulfonic mid-linkage to the diamine, i.e., to form a sulfonamide-linked, amine-group-functionalized internal surface. The coating may be provided by subsequently exposing the interior surface to an aqueous suspension of ion exchanging nanoparticles to electrostatically bond the ion exchanging nanoparticles to the functionalized internal surface. 1. An open tubular capillary column for liquid and ion chromatography , the column comprising:an ionically impermeable capillary of a polyolefin material;{'sub': '3', 'the capillary having a bore with an internal surface that has been exposed to a sulfonating reagent comprising chlorosulfonic acid (ClSOH) to sulfonate the polyolefin material to a sulfonated polyolefin material, wherein, after exposure to the sulfonating reagent, the internal surface has been exposed to an asymmetrical diamine aminating agent to form a sulfonamide-linked, amine-group-functionalized internal surface.'}2. The open tubular capillary column of claim 1 , wherein the aminating reagent comprised N—N-dimethylethylenediamine.3. The open tubular capillary column of claim 1 , wherein claim 1 , after exposure to the aminating agent claim 1 , the internal surface has been exposed to a methylating agent to form a sulfonamide-linked claim 1 , quaternary-amine-group-functionalized internal surface.4. The ...

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21-01-2016 дата публикации

METHOD FOR TREATING PRINTING PLATE DEVELOPER LIQUID AND SYSTEM FOR TREATING PRINTING PLATE DEVELOPER LIQUID

Номер: US20160018778A1
Автор: MATSUOKA Koki
Принадлежит: Sumitomo Riko Company Limited

Provided is a method for treating a printing plate developer liquid by which a developer waste liquid can be reused by also removing components that are dissolved in the developer waste liquid, and a system for treating a printing plate developer liquid.

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16-01-2020 дата публикации

ELECTROCHEMICAL ADSORBTION WITH GRAPHENE NANOCOMPOSITES

Номер: US20200017374A1
Принадлежит: UITI Limited Partnership

In alternative aspects, the invention provides processes for cyclic electrochemical adsorption of aqueous contaminants using nanocomposites of graphene with tin oxide or antimony doped tin oxide. 1. A process for treating a liquid , comprising:contacting the liquid with a solid adsorbent nanocomposite of graphene with tin oxide (TO) or antimony doped tin oxide (ATO), so that a contaminant in the liquid is adsorbed onto the nanocomposite to provide a treated liquid; and,passing a current through the nanocomposite to regenerate the nanocomposite by electrochemical conversion of the adsorbed contaminant so as to remove the contaminant from the nanocomposite and thereby provide a regenerated nanocomposite.2. The process of claim 1 , wherein the liquid is aqueous and the contaminant is an organic compound.3. The process of or claim 1 , wherein the electrochemical conversion comprises electrochemical oxidation of the contaminant.4. The process of any one of to claim 1 , wherein the current is 3-50 mA per cmof a current feeder for the nanocomposite.5. The process of claim 4 , wherein the current is 5-15 mA per cmof the current feeder.6. The process of or claim 4 , wherein the current feeder is graphite claim 4 , and a bed of the nanocomposite sits on the current feeder.7. The process of claim 6 , wherein the bed of the nanocomposite is from about 0.2 mm to 2 mm thick.8. The process of or claim 6 , wherein a salt is added to the bed of nanocomposite.9. The process of claim 8 , wherein the salt is NaCl or NaSO.10. The process of any one of to claim 8 , wherein the process is a batch treatment process.11. The process of any one of to claim 8 , wherein the process is a continuous treatment process.12. The process of any one of to claim 8 , wherein the process further comprises contacting the liquid with the regenerated nanocomposite.13. The process of claim 12 , wherein the process further comprises a plurality of cycles of contacting the liquid and regenerating the ...

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28-01-2016 дата публикации

One-way drier filter

Номер: US20160023129A1
Автор: DING Xiaohong
Принадлежит:

A one way drier filter includes: an input end cap with an input opening provided thereon; an output end cap with an output opening provided thereon; a cylinder shell having an inner space, wherein an input end and an output end of the cylinder shell are respectively covered by the input end cap and the output end cap; a granular molecular sieve provided in the inner space of the cylinder shell for dehydrating refrigerating fluid; parallel punched nets; filtering nets; glass fibers; a spring mounted at the input end of the cylinder shell; a hot air pump connected to an air inlet of the output end cap through an air tube; an air inlet valve mounted on the air inlet of the output end cap; and an air outlet valve mounted on an air outlet of the input end cap. 13-. (canceled)4. A one-way drier filter , comprising:an input end cap with an input opening provided thereon;an output end cap with an output opening provided thereon;a cylinder shell having an inner space, wherein an input end and an output end of said cylinder shell are respectively covered by said input end cap and said output end cap;a granular molecular sieve provided in said inner space of said cylinder shell for dehydrating refrigerating fluid;parallel punched nets;filtering nets;glass fibers;wherein said parallel punched nets, said filtering nets and said glass fibers are provided in said inner space of said cylinder shell for filtering the refrigerating fluid;a spring mounted at said input end of said cylinder shell for compressing said granular molecular sieve, said parallel punched net, said filtering nets and said glass fibers;a hot air pump connected to an air inlet of said output end cap through an air tube, wherein said hot air pump heats air and drives heated air into said cylinder shell for regenerating said granular molecular sieve;an air inlet valve mounted on said air inlet of said output end cap, wherein when dehydrating and filtering the refrigerating fluid, said air inlet valve is closed for ...

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25-01-2018 дата публикации

AMINOGLYCOSIDE HYDROGEL MICROBEADS AND MACROPOROUS GELS WITH CHEMICAL CROSSLINK, METHOD OF PREPARATION AND USE THEREOF

Номер: US20180021753A1
Принадлежит:

Methods and materials for the generation of amikacin antibiotic-derived microbeads, (FIG. ). These beads may function as anion-exchange resins for use in pDNA purification as well as in situ capture of DNA from mammalian cells. New microresin and macroporous monolith based materials also are disclosed and may function for plasmid DNA binding and purification, mammalian whole cell genomic DNA extraction, and in-vitro cell culture. 1. A method to prepare a macroporous column , comprising:providing a chromatographic column packed with salt;mixing an aminoglycoside and a cross-linker in an organic solvent;disposing said aminoglycoside/cross-linker/organic solvent in said chromatographic column;after said aminoglycoside reacts with said cross-linker to form a macroporous porous, cross-linked resin, adding water to said column to dissolve said salt;draining said water from said chromatographic column,2. The method of claim 1 , wherein said aminoglycoside is selected from the group consisting of Amikacin claim 1 , Neomycin claim 1 , Streptomycin claim 1 , Tobramycin claim 1 , Sisomicin claim 1 , Paromomycin claim 1 , Apramycin claim 1 , Framecytin claim 1 , Ribostamycin claim 1 , Kanamycin claim 1 , Arbekacin claim 1 , Beckanamycin claim 1 , Dibekacin claim 1 , Astromicin claim 1 , Spectinomycin claim 1 , Hygromycin b claim 1 , Gentamicin claim 1 , Netilmicin claim 1 , Isepamicin claim 1 , and Verdamicin.3. The method of claim 1 , wherein said cross-linker comprises a di-epoxide.4. The method of claim 1 , wherein said cross-linker is selected from the group consisting of Poly (ethylene glycol) diglycidyl ether claim 1 , Ethylene glycol diglycidyl ether claim 1 , 1 claim 1 , 4-Cyclohexane dimethanol diglycidyl ether claim 1 , Neopentyl glycol diglycidyl ether claim 1 , 1 claim 1 ,4-Butanediol diglycidyl ether claim 1 , Resorcinol diglycidyl ether claim 1 , Poly (propylene glycol) diglycidyl ether claim 1 , Glycerol diglycidyl ether claim 1 , Polyethylene glycol) diacrylate ...

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25-01-2018 дата публикации

Apatite pretreatment

Номер: US20180022608A1
Автор: Larry Cummings
Принадлежит: Bio Rad Laboratories Inc

Apatite pretreatment methods are provided. The method is applied to the apatite solid surface prior to first chromatographic use. In one embodiment, the method may be achieved by contacting an apatite solid surface with a phosphate buffered solution at a pH of at least about 6.5 and contacting the apatite solid surface with a solution having a hydroxide.

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22-01-2015 дата публикации

Regeneration of olefin treating adsorbents for removal of oxygenate contaminants

Номер: US20150025285A1
Принадлежит: Chevron USA Inc

Processes for eliminating oxygenates and water from a light hydrocarbon processing system, wherein oxygenates are removed from a light hydrocarbon stream by adsorption of the oxygenates on an oxygenate adsorption unit to provide a deoxygenated hydrocarbon stream, the oxygenate adsorption unit is regenerated via a regenerant stream to provide an oxygenated regenerant stream comprising the oxygenates, and the oxygenated regenerant stream is subjected to hydro-deoxygenation to convert the oxygenates into paraffins and water, wherein the water may also be permanently removed from the system.

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23-01-2020 дата публикации

METHOD AND SYSTEM FOR TRANSFERRING SEPARATION RESIN

Номер: US20200023290A1
Автор: Avallin Johan Fredrik
Принадлежит:

A method and a system for transferring a slurry of a separation resin, from at least one first container to a second container, said method comprising the steps of: 1. A method for transferring a slurry of a separation resin , from at least one first container to a second container , said method comprising the steps of:connecting the at least one first container to the second container by a transferring connection;providing a degree of vacuum to the second container by a vacuum production device connected to the second container;allowing the vacuum in the second container to affect the content in the at least one first container through the transferring connection such that the slurry initially provided in the at least one first container is transferred to the second container through the transferring connection.2. A method according to claim 1 , wherein the step of connecting the at least one first container to the second container comprises connecting the two containers by disposable claim 1 , pre-sterilized connecting parts.3. A method according to claim 1 , wherein the step of allowing the vacuum in the second container to affect the content in the at least one first container comprises opening at least one valve provided in the transferring connection between the at least one first container and the second container.4. A method according to claim 1 , further comprising the step of:rinsing the at least one first container by transferring a rinsing solution through the at least one first container and further to the second container, said rinsing solution coming from a rinse bag connected to the at least one first container, said transferring of a rinsing solution being accomplished by the same vacuum as provided to the second container for transferring the slurry.5. A method according to claim 3 , wherein the step of rinsing the at least one first container comprises opening a rinsing valve provided in the connection between the at least one first container and ...

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28-01-2021 дата публикации

Systems and Methods for Separating Radium from Lead, Bismuth, and Thorium

Номер: US20210024365A1
Автор: OHara Matthew J.
Принадлежит: BATTELLE MEMORIAL INSTITUTE

Systems for separating Ra from a mixture comprising at least Ra, Pb, Bi, and Th are provided. The systems can include: a first vessel housing a first media and Th or Bi; a second vessel in fluid communication with the first vessel, the second vessel housing a second media and Pb; and a third vessel in fluid communication with the second vessel, the third vessel housing a third media and Ra, wherein at least one of the first, second, or third medias are different from the other media. 1. A system for separating Ra from a mixture comprising at least Ra , Pb , Bi , and Th , the system comprising:a first vessel housing a first media and either Pb or Bi and/or Th; anda second vessel in fluid communication with the first vessel, the second vessel housing a second media and Ra, wherein the first media is different from the second media.2. The system of wherein the first media is associated with Bi and/or Th and comprises a quaternary amine on a polystyrene divinylbenzene copolymer.3. The system of wherein the second media is associated with Ra and comprises a silica support.4. The system of wherein the first media is associated with Pb and comprises 18-crown-6 and 1-octanol on Amberchrom CG-71 polymer support.5. The system of wherein the second media is associated with Ra comprises a on silica support.6. The system of wherein the first media size is less than 100 μm.7. The system of wherein the second media size is greater than 100 μm.8. A system for separating Ra from a mixture comprising at least Ra claim 1 , Pb claim 1 , Bi claim 1 , and Th claim 1 , the system comprising:a first vessel housing a first media and Th and/or Bi; anda second vessel in fluid communication with the first vessel, the second vessel housing a first media and Pb, wherein the first media is different from the second media.9. The system of wherein the first vessel is in fluid communication with raw material supply.10. The system of wherein the first vessel is in fluid communication with a wash ...

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01-02-2018 дата публикации

SOLID-LIQUID SEPARATION DEVICE

Номер: US20180028935A1
Принадлежит: Hitachi, Ltd.

A solid-liquid separation device performs dehydration/deoiling from a mixture of water and/or oil and a solid. Substance A is capable of dissolving water and oil. The device includes substance B circulated while generating phase change in a closed system; a compressor; a first heat exchanger exchanging condensation heat of substance B and evaporation heat of substance A; a second heat exchanger exchanging evaporation heat of substance B and condensation heat of substance A; and a treatment tank for mixing substance A with an object to be treated; substance A having been evaporated while separated from the water or the oil in the first heat exchanger, and condensed in the second heat exchanger. The first heat exchanger is lower than the treatment tank in a vertical direction, and a connection port of the first heat exchanger and a lower portion of the treatment tank are connected with a flow path. 1. A solid-liquid separation device that performs dehydration or deoiling from an object to be treated that is a mixture of water and a solid , a mixture of oil and a solid , or a mixture of water , oil , and a solid , as the object to be treated , using a substance A capable of dissolving water and oil , the solid-liquid separation device comprising:a substance B that is circulated while generating phase change in a closed system;compression means that compresses the substance B;a first heat exchanger that exchanges heat of condensation of the substance B and heat of evaporation of the substance A;a second heat exchanger that exchanges heat of evaporation of the substance B and heat of condensation of the substance A; anda treatment tank in which the substance A is mixed with the object to be treated, the substance A having been evaporated while separated from the water or the oil in the first heat exchanger, and condensed in the second heat exchanger, whereinthe first heat exchanger is installed in a lower portion than the treatment tank in a vertical direction, anda ...

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02-02-2017 дата публикации

Heparin affinity tag and applications thereof

Номер: US20170029461A1
Принадлежит: University of Arkansas

In one aspect, affinity tags for recombinant protein purification are described herein which, in some embodiments, can mitigate or overcome disadvantages of prior affinity tag systems. In some embodiments, for example, affinity tags described herein permit efficient elution of desired recombinant proteins with simplified solution systems, such as alkali metal salt solutions. An affinity tag described herein comprises an amino acid sequence including a repeating amino acid unit of BXXXBXX, wherein B is an amino acid selected from the group consisting of histidine, lysine and arginine and X is an amino acid selected from the group consisting of amino acids other than histidine, lysine and arginine.

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17-02-2022 дата публикации

Systems and methods for onsite sorbent material reuse

Номер: US20220048021A1

Methods, sorbent cartridges and cleaning devices are disclosed for refurbishing sorbent materials. In one implementation among multiple implementations, a medical fluid delivery method includes: providing a sorbent cartridge including H + ZP within a casing for a treatment; and after the treatment, refurbishing the H + ZP while maintained within the casing via (i) regenerating the non-disinfected H + ZP by flowing an acid solution through the casing, (ii) rinsing the regenerated H + ZP while maintained within the casing, (iii) disinfecting the regenerated and rinsed H + ZP by flowing a disinfecting agent through the casing, and (iv) rinsing the regenerated and disinfected H + ZP while maintained within the casing. Multiple batch sorbent refurbishing implementations are also disclosed.

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01-05-2014 дата публикации

Device and Method for Recovering a Recovering Material from a Recovering Fluid Containing the Recovering Material

Номер: US20140116950A1
Принадлежит: ATOTECH DEUTSCHLAND GMBH

To achieve high efficiency in regeneration of waste fluid from metal plating electrolytes for example, a device and a method for recovering a recovering material from a recovering fluid containing the recovering material are provided. 1. A device for recovering a recovering material from a recovering fluid containing therecovering material,the device comprising at least one container (C),the at least one container (C) comprising at least one sorption material,the at least one sorption material forming at least one sorption bed (SB) in the at least one container (C) and the at least one sorption bed (SB) allowing the recovering fluid to flow there through,characterized in that the at least one container (C) further comprises at least one means for fixing (ML, EP, FM, MO) the at least one sorption bed (SB) to compensate for a volume change (VC) thereof.2. The device according to claim 1 , characterized in that the sorption bed (SB) has a sorption bed height and a sorption bed width claim 1 , an aspect ratio of the sorption bed width to the sorption bed height being at most 1:10.3. The device according to any one of the preceding claims claim 1 , characterized in that the at least one container (C) further comprises at least one first fluid port (FP) allowing a regenerant fluid to enter the at least one container (C) and at least one second fluid (SP) port allowing the regenerant fluid to leave the at least one container (C) and in that the at least one first and second fluid ports are comprised by the at least one container (C) to be claim 1 , irrespective of the volume change (VC) of the at least one sorption bed (SB) claim 1 , in permanent direct contact with the at least one sorption bed (SB).42. The device according to any one of the preceding - claims 1 , characterized in that at least one fixing means comprises a means for locking (ML) at least one sorption bed (SB) in position in at least one container (C) claims 1 , the locking means (ML) being mounted free to ...

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01-05-2014 дата публикации

REDUCED MAINTENANCE WATER TREATMENT APPARATUS INCORPORATING WET AIR REGENERATION

Номер: US20140116952A1
Автор: Ellis Claude E.
Принадлежит:

A water treatment system () incorporating a solubles concentration reduction device () between a powdered activated carbon treatment (PACT) system () and a wet air regeneration (WAR) system (). Soluble components may be removed by sequentially dewatering () then re-slurrying () spent carbon sludge (). The reduced concentration of soluble materials reduces the need for scale removal maintenance and eliminates the necessity for exotic materials of construction of the WAR system components. The solubles concentration reduction device also facilitates active control of the solids concentration being delivered to the WAR system. 1. A water treatment apparatus comprising:a powdered activated carbon treatment (PACT) system;a wet air regeneration (WAR) system in fluid communication with the PACT system and configured to regenerate spent carbon from the PACT system; anda solubles concentration reduction apparatus in fluid communication between the PACT system and the WAR system and configured to reduce a concentration of a soluble material associated with the spent carbon upstream of the WAR system.2. The apparatus of claim 1 , wherein the solubles concentration reduction apparatus comprises:a dewatering device coupled to receive sludge containing the soluble material from the PACT system and to produce dewatered sludge; anda re-slurrying device coupled to receive the dewatered sludge from the dewatering device and to produce re-slurried sludge.3. The apparatus of claim 1 , wherein the solubles concentration reduction apparatus comprises an ion exchange device.4. The apparatus of claim 1 , wherein the WAR system comprises a reactor made of a material sensitive to stress corrosion cracking.5. The apparatus of claim 2 , wherein the dewatering device is selected from the group consisting of a centrifuge claim 2 , a vacuum filter claim 2 , a filter press claim 2 , a screw press claim 2 , a belt press claim 2 , and a washing centrifuge.6. The apparatus of claim 2 , wherein the re ...

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30-01-2020 дата публикации

CONTINUOUS COUNTERCURRENT SPIRAL CHROMATOGRAPHY

Номер: US20200030717A1
Принадлежит:

A system, module and method for continuous countercurrent spiral chromatography are disclosed. The module includes an input port for receiving an input solution, a first mixer for mixing the input solution with a recycled solution to produce a first mixed output, a stage I separator for concentrating the first mixed output to produce a stage I solid fraction, a second mixer for mixing the stage I solid fraction from the stage I separator and an optional buffer solution to produce a second mixed output, and a stage II separator for concentrating the second mixed output to produce a stage II solid fraction which exits the module. At least one separator is a spiral separator. The system includes a plurality of modules, and at least one of the plurality of modules includes a spiral separator. The method includes purifying an unpurified solution with the plurality of modules. 1. A continuous countercurrent spiral chromatography module , comprising:a first input port for receiving an input solution;a first mixer for mixing the input solution with a recycled solution from a second input port to produce a first mixed output;a stage I separator for concentrating the first mixed output to produce a stage I solid fraction, wherein a stage I liquid fraction exits the stage I separator via a first output port;a second mixer for mixing the stage I solid fraction from the stage I separator and an optional buffer solution from a third input port to produce a second mixed output;a stage II separator for concentrating the second mixed output to produce a stage II solid fraction which exits the module from the stage II separator via a second output port, wherein a stage II liquid fraction exits the module from the stage II separator via a third output port; andat least one pump,wherein the recycled solution from the third output port flows countercurrent to the input solution into the second input port, and at least one inlet;', 'a curvilinear channel arranged and disposed to generate ...

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30-01-2020 дата публикации

Use Of Compressed Gas For Moving Eluent Applied To Chromatography

Номер: US20200030718A1
Автор: Boni Jérôme
Принадлежит:

The invention relates to a method for chromatographic separation, comprising at least one step of elution of species held on a stationary phase by means of an eluent, followed by a step of moving the eluent in contact with the stationary phase by means of a compressed gas. Preferably, the movement step takes place after a step of elution of the product(s) of interest and/or after a step of regeneration of the stationary phase. 1. A method for chromatographic separation , comprising at least one step of eluting species retained on a stationary phase by means of an eluent , followed by a step of displacing the eluent in contact with the stationary phase by means of a compressed gas.2. The method of claim 1 , wherein the compressed gas is in a liquid state or a supercritical state.35-. (canceled)6. The method of claim 1 , wherein the eluent is a single compound.7. The method of claim 1 , wherein the eluent is a mixture of at least two compounds.8. The method of claim 1 , wherein the eluent is an aqueous and/or organic solvent claim 1 , or a mixture of aqueous and/or organic solvents.9. The method of claim 1 , wherein the eluent is a mixture of aqueous and/or organic solvent(s) and compressed gas.10. The method of claim 1 , comprising claim 1 , after the step of displacing the eluent claim 1 , collection of a mixture of compressed gas and aqueous and/or organic solvent(s) at the output of the stationary phase claim 1 , and separation of the compressed gas and the aqueous and/or organic solvent(s).11. The method of claim 10 , wherein the aqueous and/or organic solvent(s) are recycled.1213-. (canceled)14. The method of claim 10 , wherein the compressed gas is recycled.1516-. (canceled)17. The method of claim 1 , wherein the step of eluting species retained on a stationary phase by means of an eluent is an elution step of product(s) of interest.18. The method of claim 1 , wherein the step of eluting species retained on a stationary phase by means of an eluent is a step of ...

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04-02-2021 дата публикации

Affinity Chromatography

Номер: US20210031124A1
Принадлежит:

This invention relates to a method of removing a chemical entity from a liquid using affinity chromatography. The method involves passing an elongate solid phase through a conduit through which the liquid also flows. 1. A method comprising: wherein the liquid from which the chemical entity is removed passes along the conduit from the liquid input port to the liquid output port in the opposite direction to the elongate body;', 'wherein the conduit being is configured such that the liquid contacts the elongate body; and', 'wherein attached to the elongate body is an affinity entity having an affinity for the chemical entity; and, 'passing an elongate body comprising a liquid input port and a liquid outlet port through a conduit to remove a chemical entity from a liquid;'}washing the elongate body to remove products present having lower affinity for the affinity entity than the chemical entity.2. The method of claim 1 , wherein one or both the elongate body and the liquid is subjected to sonication as it passes through the conduit.3. The method of claim 1 , wherein washing the elongate body comprises passing the elongate body through a wash conduit to remove the products present on the elongate body having lower affinity for the affinity entity than the chemical entity;wherein the wash conduit comprises a wash liquid input port and a wash liquid outlet port;wherein a wash liquid passes along the wash conduit from the wash liquid input port to the wash liquid output port in the opposite direction to the elongate body; andwherein the wash conduit is configured such that the wash liquid contacts the elongate body.4. The method of claim 3 , wherein one or both the elongate body and the wash liquid is subjected to sonication as it passes through the wash conduit.5. The method of further comprising recovering the chemical entity from the elongate body.6. The method of claim 5 , wherein recovering the chemical entity comprises passing the elongate body through a displacement ...

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04-02-2021 дата публикации

METHOD FOR PRODUCING CELLULOSE PARTICLES USING POROUS MEMBRANE

Номер: US20210032415A1
Принадлежит: JNC CORPORATION

Provided is a method for producing cellulose particles or cellulose acetate particles. By a production method including: (a) dissolving cellulose acetate in an organic solvent and preparing a cellulose acetate solution; (b) obtaining an emulsion of the cellulose acetate solution and an aqueous medium using a porous membrane; and (c) precipitating cellulose acetate particles from the emulsion, cellulose acetate particles are produced. By further saponifying the cellulose acetate obtained by the production method, cellulose particles are produced. 1. A method for producing cellulose acetate particles , comprising:(a) dissolving cellulose acetate in an organic solvent and preparing a cellulose acetate solution;(b) obtaining an emulsion of the cellulose acetate solution and an aqueous medium using a porous membrane; and(c) precipitating cellulose acetate particles from the emulsion.2. The method for producing cellulose acetate particles according to claim 1 , wherein in (a) claim 1 , the organic solvent is ethyl acetate claim 1 , a mixed solvent of ethyl acetate and acetone claim 1 , or cyclohexanone.3. The method for producing cellulose acetate particles according to claim 1 , wherein in (a) claim 1 , the cellulose acetate is cellulose diacetate having a degree of acetylation of 45% to 57%.4. The method for producing cellulose acetate particles according to claim 1 , wherein in (c) claim 1 , the cellulose acetate particles are precipitated by at least one of cooling of the emulsion and addition of a poor solvent to the emulsion.5. The method for producing cellulose acetate particles according to claim 4 , wherein the poor solvent is water claim 4 , alcohols claim 4 , glycols claim 4 , esters claim 4 , or a mixture thereof.6. The method for producing cellulose acetate particles according to claim 1 , wherein in (b) claim 1 , permeation through the porous membrane is performed a plurality of times.7. The method for producing cellulose acetate particles according to claim ...

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11-02-2016 дата публикации

APPARATUS AND METHODS FOR CONTROLLING THE TEMPERATURE OF A CHROMATOGRAPHY COLUMN

Номер: US20160038853A1
Автор: Shreve Joshua A.
Принадлежит: WATERS TECHNOLOGIES CORPORATION

An apparatus for controlling the temperature of a chromatography column includes a thermal-isolation vessel; a heater in thermal communication with the chromatography column and disposed on the thermal-isolation vessel; a temperature sensor disposed to directly measure the temperature of the chromatography column; and a control unit in signal communication with the temperature sensor to control the heater in response to LIGHT the direct measurement. 1. An apparatus for controlling the temperature of a chromatography column , comprising:a thermal-isolation vessel;a heater in thermal communication with the chromatography column, the heater disposed on the thermal-isolation vessel;a temperature sensor disposed to directly measure the temperature of the chromatography column; anda control unit in signal communication with the temperature sensor, the control unit configured to control the heater, in response to direct measurement of the temperature of the column by the temperature sensor.2. The apparatus of claim 1 , wherein the temperature sensor is disposed in contact with the chromatography column.3. The apparatus of claim 1 , wherein the temperature sensor is a non-contact temperature sensor.4. The apparatus of claim 3 , wherein the non-contact temperature sensor is an infrared temperature sensor.5. The apparatus of further comprising a target of known emissivity attached to the chromatography column.6. The apparatus of further comprising an infrared-transmissive material disposed to protect the infrared temperature sensor.7. The apparatus of further comprising additional temperature sensors disposed to directly measure the temperature of the chromatography column.8. The apparatus of claim 1 , wherein the temperature sensor directly measures the temperature at the midpoint of the chromatography column.9. The apparatus of wherein the heater comprises a pre-heater on thermal-isolation vessel.10. The apparatus of further comprising at least one temperature sensor ...

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08-02-2018 дата публикации

Sanitization Method for Affinity Chromatography Matrices

Номер: US20180036445A1
Принадлежит:

The invention discloses a method for cleaning or sanitization of an affinity chromatography matrix, comprising the steps of: a) providing an affinity chromatography matrix having oxidation-tolerant proteinaceous ligands coupled to a support, b) contacting the matrix with a sanitization solution comprising at least one oxidant defined by formula I, R—O—O—H (I) wherein R is hydrogen or an acyl group R′—C(O)—, with R′ being a hydrogen or a methyl, ethyl or propyl group. 2. The method of claim 1 , wherein said proteinaceous ligands comprise or consist essentially of one or more immunoglobulin-binding domains derived from a bacterial protein.3. The method of claim 1 , wherein the concentration of said oxidant in said sanitization solution is 0.01-1 mol/l.4. The method of claim 1 , wherein the pH of said sanitization solution is 2-12 claim 1 , such as 2-4 or 2-3.5. The method of claim 1 , wherein said oxidant is selected from the group consisting of hydrogen peroxide claim 1 , performic acid and peracetic acid.6. The method of claim 1 , wherein said sanitization solution comprises a mixture of at least two oxidants defined by formula I claim 1 , such as a mixture of hydrogen peroxide with performic or peracetic acid.7. The method of claim 1 , wherein the total concentration of oxidants defined by formula I is 0.01-1 mol/l.8. The method of claim 1 , wherein in step b) the matrix is incubated with said sanitization solution for 1 min-24 h claim 1 , such as 5 min-24 h or 15 min-3 h.9. The method of claim 1 , wherein said matrix retains at least 80% claim 1 , such as at least 90% claim 1 , of its binding capacity for a target protein claim 1 , such as an immunoglobulin claim 1 , after step b).10StaphylococcusPeptostreptococcusStreptococcusStreptococcusPeptostreptococcus. The method of claim 2 , wherein said bacterial protein is selected from the group consisting of Protein A claim 2 , Protein L and Protein G claim 2 , such as from the group consisting of Protein A and Protein ...

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07-02-2019 дата публикации

REPLENISHING UREASE IN DIALYSIS SYSTEMS USING UREASE POUCHES

Номер: US20190038997A1
Принадлежит:

An apparatus and method for replenishing urease in a sorbent cartridge for use in sorbent dialysis using urease pouches. The sorbent cartridge is configured to allow insertion of a urease pouch or injection of a urease solution into the sorbent cartridge containing a urease pouch. The sorbent module can also comprise other, rechargeable, sorbent materials for removing toxins other than urea from spent dialysate. 116-. (canceled)17. A method , comprising the steps of:adding either solid urease or urease solution to a sorbent cartridge adapted to replenish urease in the sorbent cartridge.18. The method of claim 17 , wherein the step of adding the solid urease comprises the steps of removing a urease pouch having a reduced amount of urease claim 17 , if present claim 17 , and then adding a fresh urease pouch into the sorbent cartridge.19. The method of claim 17 , wherein the step of adding the urease solution comprises introducing a urease solution into the sorbent cartridge having a concentration between any of 1 mg/mL to 250 mg/mL claim 17 , 15 mg/mL to 150 mg/mL claim 17 , 10 mg/mL to 100 mg/mL claim 17 , or 75 mg/mL to 250 mg/mL of urease.20. The method of claim 17 , further comprising the step of either:recharging an amount of one or more sorbent materials contained in the sorbent cartridge by passing a solution containing an appropriate amount of solutes for recharging the one or more sorbent materials through the sorbent cartridge; orrecharging an amount of one or more sorbent materials by replacing one or more modules of a modular regeneration assembly containing an amount of the one or more of sorbent materials. This application is a divisional of U.S. patent application Ser. No. 14/644,576 filed Mar. 11, 2015, which claims benefit of and priority to U.S. Provisional Application No. 62/077,169 filed Nov. 7, 2014, and U.S. Provisional Application No. 62/016,613 filed Jun. 24, 2014, and the disclosures of each of the above-identified applications are hereby ...

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24-02-2022 дата публикации

METHOD FOR SEPARATING AND PURIFYING RECOMBINANT HUMAN FIBRONECTIN FROM GENETICALLY ENGINEERED RICE SEED

Номер: US20220056071A1
Автор: YANG Daichang, ZHAN Quan
Принадлежит:

Disclosed is a chromatographic method for separating and purifying a recombinant human fibronectin from a genetically engineered rice seed that expresses the human fibronectin. In the method, the genetically engineered rice seed is milled, mixed with an extraction buffer, and then filtered to obtain a crude extract comprising the recombinant human fibronectin; the crude extract comprising the recombinant human fibronectin is subjected to cation exchange chromatography, so as to perform primary separation and purification, thereby obtaining a primary product comprising the recombinant human fibronectin; and the primary product is subjected to anion exchange chromatography so as to perform final separation and purification to obtain the recombinant human fibronectin as a target substance. The method is low cost and easily utilized on an industrial scale. The obtained OsrhFn target substance has a SEC-HPLC purity greater than 95% with excellent bioactivity. 1. A chromatographic method for separating and purifying a recombinant human fibronectin from genetically engineered rice seeds or grains expressing the recombinant human fibronectin , comprising the following steps in sequence:1) extracting the recombinant human fibronectin from the genetically engineered rice seeds or grains containing the recombinant human fibronectin, to obtain a crude protein extract comprising the recombinant human fibronectin;2) subjecting the crude protein extract comprising the recombinant human fibronectin to cation exchange chromatography, to obtain a primary product; and3) subjecting the primary product to anion exchange chromatography, to obtain a purified recombinant human fibronectin;wherein a resin for the cation exchange chromatography comprises a resin selected from the group consisting of Nano Gel 30/50 SP, Uni Gel 30/80 SP, SP Bestarose FF, SP Bestarose HP, Bestarose Diomond MMC, Uniphere S, MacroPrep S, POROS XS, SP-6FF, SP-6HP, and SP Sepharose™ Fast Flow; anda resin for the ...

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07-02-2019 дата публикации

Novel Modified Acid Compositions as Alternatives to Conventional Acids in the Oil and Gas Industry

Номер: US20190040298A1
Принадлежит:

An aqueous modified acid composition for industrial activities, said composition comprising: an alkanolamine and strong acid in a molar ratio of not less than 1:15, preferably not less than 1:10; it can also further comprise a metal iodide or iodate. Said composition demonstrates advantages over known conventional acids and modified acids. 1. An aqueous modified acid composition comprising:a mineral acid and an alkanolamine in a molar ratio of not more than 15:1.2. A aqueous modified acid composition comprising:hydrochloric acid and an alkanolamine in a molar ratio of not more than 15:1.3. The aqueous modified acid composition according to claim 2 , wherein the hydrochloric acid and alkanolamine are present in a molar ratio of not more than 10:1.4. The aqueous modified acid composition according to claim 2 , wherein the hydrochloric acid and alkanolamine are present in a molar ratio of not more than 7.0:1.5. The aqueous modified acid composition according to claim 2 , wherein the hydrochloric acid and alkanolamine are present in a molar ratio of not more than 4.1:1.6. The aqueous modified acid composition according to claim 2 , wherein the hydrochloric acid and alkanolamine are present in a molar ratio of not less than 3:1.7. The aqueous modified acid composition according to any one of to claim 2 , wherein the alkanolamine is selected from the group consisting of: monoethanolamine; diethanolamine; triethanolamine and combinations thereof.8. The aqueous modified acid composition according to any one of to claim 2 , wherein the alkanolamine is monoethanolamine.9. The aqueous modified acid composition according to any one of to claim 2 , wherein the alkanolamine is diethanolamine.10. The aqueous modified acid composition according to any one of to claim 2 , further comprising a metal iodide or iodate.11. The composition according to claim 1 , wherein the mineral acid is selected from the group consisting of: HCl claim 1 , nitric acid claim 1 , sulfuric acid claim 1 , ...

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07-02-2019 дата публикации

Isolation, Detection and Use of Biological Cells

Номер: US20190041306A1
Автор: Gjerde Douglas T.
Принадлежит:

This invention relates to devices and methods for purifying, detecting and using biological cells. A variety of cell types including viable tumor, stem, immune and sperm cells can be purified from a complex biological sample using a column, including a pipette tip column. Methods of the invention can aid research, diagnosis and treatment of cancer. Purified viable cells can be detected on the column or eluted from the column and detected. Cells on a column can be used as a stationary phase for liquid chromatography. Cells may be removed, recovered and analyzed. 1. A column comprised of:a) a column body;b) a bottom frit attached to the open lower end of the column body;c) a bed of medium in contact with the bottom frit, wherein the bed of medium is comprised of water-swollen beads, wherein the beads are compressible, wherein the bed of medium is not compressed, wherein the bed of medium has a packing density, wherein the packing density is in the range of 1.00 to 1.05, wherein the beads are comprised of a capture entity; andd) a top frit attached to the column body, wherein there is a gap between the top frit and the bed of medium;wherein the column is comprised of unconstrained flow channels, wherein the diameters of 98% to 100% of the flow channels are sufficiently large for cells to pass through.2. The column of claim 1 , wherein the column body is a pipette tip.3. A column comprised of:a) a column body;b) a bottom frit attached to the open lower end of the column body;c) a bed of medium in contact with the bottom frit, wherein the bed of medium is not compressed, wherein the bed of medium is comprised of water-swollen beads, wherein the beads are compressible and wherein the beads are comprised of a capture entity; andd) a top frit attached to the column body, wherein there is a gap between the top frit and the bed of medium;wherein the column is comprised of unconstrained flow channels, wherein the minimum flow path diameter is greater than 8 μm.4. The column of ...

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18-02-2016 дата публикации

MATERIAL FOR AND METHOD OF EXTRACTING MYCOTOXINS

Номер: US20160045894A1
Принадлежит:

The present invention relates to a sorbent for extracting polar components from a sample where the sorbent comprises a cross-linked polymer comprising nitrogen containing cyclic compounds, for example 1-vinylimidazole and/or 4-vinylpyridine. The invention further relates to a method of producing said sorbent and the use of the sorbent. 115-. (canceled)16. A solid phase extraction sorbent having a core portion and an outermost portion , and wherein at least the outermost portion of the sorbent comprises a cross-linked polymer partly based on nitrogen-containing conjugated or non-conjugated cyclic compounds.17. The sorbent of wherein the core portion is a bead of a material different from the outermost portion.18. The sorbent of wherein the weight ratio of nitrogen containing cyclic compounds of the outermost portion to the core bead is at least 0.05 claim 16 , or at least 0.10 claim 16 , or at least 0.20 claim 16 , or at least 0.33 or at least 0.50.19. The sorbent according to wherein the core bead is a polymeric bead based on divinyl benzene and styrene.20. The sorbent according to wherein the amount of nitrogen containing cyclic compounds in the cross-linked polymer is at least 20 weight % claim 16 , such as at least 50 weight % claim 16 , and preferably at least 75 weight %.21. The sorbent according to wherein the core portion comprises a cross-linked polymer based on nitrogen containing cyclic compounds.22. The sorbent according to wherein the nitrogen containing cyclic compound is 1-vinylimidazole and/or 4-vinylpyridine or a mixture thereof.23. A method of producing a sorbent having a core portion and an outermost portion claim 16 , and wherein at least the outermost portion of the sorbent comprises a cross-linked polymer partly based on nitrogen-containing conjugated or non-conjugated cyclic compounds claim 16 , comprising:a) providing nitrogen containing conjugated or non-conjugated compounds, a cross-linking agent, a solvent and a polymerisation initiator;b) ...

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18-02-2021 дата публикации

NOVEL AFFINITY CHROMATOGRAPHY MEDIA FOR REMOVAL OF ANTI-A AND/OR ANTI-B ANTIBODIES

Номер: US20210047430A1
Принадлежит:

Embodiments described herein relate to novel chromatography media for removing anti-A and/or anti-B antibodies from a sample, as well as methods of using the same. The media described herein have several advantages over previously described media including, acid and alkaline stability. 1. A method of removing anti-A antibodies from a sample , the method comprising the steps of:(a) providing a sample comprising an amount of anti-A antibodies;(b) incubating the sample with a media comprising a solid support with a blood group A antigen ligand attached thereto, wherein the ligand is attached to the solid support at a ligand loading of at least 0.8 mg/ml of solid support, and wherein the media is stable under acid and/or alkaline conditions and wherein the solid support comprises a polymer selected from the group consisting of polyvinylether, polyvinylalcohol, polymethacrylate, polyacrylate, polystyrene, polyacrylamide, polymethacrylamide and polycarbonate and the blood group A antigen ligands are attached via pAA tentacle chemistry to a solid support, for the media to bind anti-A antibodies;(c) recovering portion of the sample which is not bound to the media; and(d) measuring amount of anti-A antibodies in the portion of the sample in (c), wherein the amount of anti-A antibodies in (d) is at least 80% less than the amount of anti-A antibodies in the sample in (a).2. A method of removing anti-B antibodies from a sample , the method comprising the steps of:(a) providing a sample comprising an amount of anti-B antibodies;(b) incubating the sample with a media for removing anti-B antibodies from a sample, the media comprising a solid support with a blood group B antigen ligand attached thereto, wherein the ligand is attached to the solid support at a ligand loading of at least 0.8 mg/ml of solid support, and wherein the media is stable under acid and/or alkaline conditions and wherein the solid support comprises a polymer selected from the group consisting of ...

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16-02-2017 дата публикации

METHODS FOR THE PURIFICATION OF PROTEINS USING CAPRYLIC ACID

Номер: US20170044210A1
Принадлежит:

A protein purification process with virus inactivation or removal uses caprylic acid (octanoic acid) at acidic pH. The method comprises caprylic acid treatment as part of the chromatographic step so as to perform viral inactivation without a discontinuous process and without the requirement of attention by personnel, particularly when the pH adjustment of the eluate is performed automatically by eluting into buffer. The method of the invention further results in mycoplasmas being inactivated, and reduced impurities like Host Cell Protein (HCP). 1. A method for the purification of a target protein from a sample comprising the steps ofi. loading a target protein-containing sample onto a stationary phase, so as to bind the target protein to said stationary phase;ii. subjecting the solid phase with the bound target protein to a caprylic acid solution; wherein the caprylic acid solution is at a pH so as to form free caprylic acid, and wherein the caprylic acid solution is a caprylic acid buffer at a concentration of 1 to 50 mM, as measured in terms of free caprylic acid; andiii. eluting the target protein.2. The method according to claim 1 , wherein purification of a target protein comprises inactivation of virus in said sample.3. A method for the preparation of a virus-free protein solution claim 1 , comprising the steps ofi. loading a target protein-containing sample onto a stationary phase, so as to bind the target protein to said stationary phase;ii. subjecting the solid phase with the bound target protein to a caprylic acid solution; wherein the caprylic acid solution is at a pH so as to form free caprylic acid, and wherein the caprylic acid solution is a caprylic acid buffer at a concentration of 1 to 50 mM, as measured in terms of free caprylic acid; andiii. eluting the target protein.4. The method according to claim 1 , wherein the caprylic acid solution comprises a combination i) a caprylate salt and ii) an inorganic or organic acid in proportions so provide a ...

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16-02-2017 дата публикации

RAPID SOLID PHASE EXTRACTION DEVICE AND METHODS

Номер: US20170044518A1
Принадлежит:

A method and system for solid phase extraction of a compound of interest from a sample matrix using a syringe having a barrel and a plunger, a sorbent for use with the syringe, and a desalting purification column having an end configured to receive liquid from the syringe body. 1. A method for extracting a compound of interest from a sample matrix , comprising the steps of:a. drawing a sample matrix into a syringe having a plunger;b. contacting the sample with a sorbent to bind the compound of interest to the sorbent;c. drawing elution buffer into the syringe containing the sorbent;d. expressing the elution buffer containing the compound of interest through a desalting column.2. The method of claim 1 , further comprising the step of mixing the sample matrix with one or more buffer.3. The method of claim 2 , wherein the syringe is prefilled with one or more buffer solutions before the sample is drawn into the syringe.4. The method of claim 2 , wherein at least one buffer solution is placed in the syringe before the sample matrix is drawn into the syringe.5. The method of claim 2 , wherein at least one buffer solution is placed in the syringe after the sample matrix is drawn into the syringe.6. The method of wherein said one or more buffer comprises a plurality of buffers.7. The method of wherein at least two of the plurality of buffers are placed into the syringe sequentially.8. The method of wherein at least two of the plurality of buffers are placed into the syringe premixed.9. The method of claim 2 , wherein at least one buffer is a lysis buffer.10. The method of further comprising the step of allowing the sample matrix and buffer mixture to incubate for a suitable period of time.11. The method of wherein the sorbent comprises at least one material selected from the group consisting of: silica claim 1 , acid-washed silica claim 1 , glass beads claim 1 , acid-washed glass beads claim 1 , zeolite claim 1 , silica gel claim 1 , filters embedded with silica particles ...

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18-02-2021 дата публикации

NEW METHOD AND APPARATUS FOR THE PRODUCTION OF HIGH PURITY RADIONUCLIDES

Номер: US20210050126A1
Принадлежит:

An apparatus is for the automated production of a daughter radionuclide from a parent radionuclide using a generator comprising a solid medium onto which the parent nuclide is fixed and whereby the daughter nuclide is formed by radioactive decay of the parent nuclide. The apparatus includes a fluid circuit including a chromatography column having a head port and a tail port, at least one connection port for connecting the generator to the fluid circuit, at least one inlet port for connecting fluid sources to the fluid circuit and at least one valve controlled by an electronic control unit for selectively connecting the chromatography column, the connection port and the at least one inlet port in various configurations. The various configurations include a first elution configuration for circulating an A′ solution exiting the generator and containing the daughter radionuclide, through the chromatography column from the head port to the tail port for loading the chromatography column with the daughter radionuclide; a first washing configuration for circulating an A washing solution from a solution inlet through the chromatography column from the head port to the tail port; and a second washing configuration for circulating an A′ washing solution from a solution inlet through the chromatography column from the tail port to the head port. 1. An apparatus for the automated production of a daughter radionuclide from a parent radionuclide using a generator comprising a solid medium onto which the parent nuclide is fixed and whereby the daughter nuclide is formed by radioactive decay of the parent nuclide , the apparatus comprising a fluid circuit comprising:a chromatography column having a head port and a tail port;at least one connection port for connecting the generator to the fluid circuit;at least one inlet port for connecting fluid sources to the fluid circuit; and [{'b': '1', 'a first elution configuration for circulating an A′ solution exiting the generator and ...

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13-02-2020 дата публикации

Solid phase conditioning

Номер: US20200047158A1
Принадлежит: GE Healthcare Ltd

The present invention relates to a method for conditioning reversed phase SPE cartridges that provides certain advantages compared with known such methods. The method of the invention finds particular use in the automated synthesis of radiolabeled compounds where SPE is used for example in the purification steps.

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23-02-2017 дата публикации

METHOD AND APPARATUS FOR THE EQUILIBRATION OF A PACKED CHROMATOGRAPHY COLUMN

Номер: US20170050120A1
Принадлежит:

Disclosed is a method for equilibrating a chromatography column including the steps of (i) providing a mobile phase; and (ii) passing the mobile phase through a packed chromatography column; wherein the mobile phase includes two liquids, the proportions of which change as it is passed through the column. Also discussed are automated aspects of the method, as well as a system capable of performing such method. 113-. (canceled)14. A method for equilibrating a chromatography column including the steps of (i) providing a packed chromatography column; and (ii) passing a pressurized mobile phase through said column; wherein the mobile phase is obtained by combining at least two liquids , the proportions of which are varied as the mobile phase is passed through the column.15. A method according to claim 14 , wherein the variation of said at least two liquids is achieved by combining an increasing proportion of one liquid and a decreasing proportion of another liquid to provide a linear gradient in the mobile phase as it passes the column.16. A method according to claim 14 , wherein at least one of the liquids is an organic solvent.17. A method according to claim 14 , where the mobile phase is passed through the column at a flow rate in the range of 10-200 ml/min.18. A method according to claim 14 , wherein the column is packed with a media.19. A method according to claim 14 , wherein the surface area of the packing available to the mobile phase is at least 500 m/g (dry weight) or greater.20. A method according to claim 14 , wherein the column and/or the column frits are made of a polymeric material claim 14 , such as polypropylene or polyethylene.21. A method according to claim 14 , wherein the size and material of the column as well as the packing surface area available to the mobile phase are used as parameters to define an equilibration gradient comprised of two liquids claim 14 , the proportions of which are varied as the mobile phase is passed through the column claim ...

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14-02-2019 дата публикации

Isolation, Detection and Use of Biological Cells

Номер: US20190049351A1
Автор: Gjerde Douglas T.
Принадлежит:

This invention relates to devices and methods for purifying, detecting and using biological cells. A variety of cell types including viable tumor, stem, immune and sperm cells can be purified from a complex biological sample using a column, including a pipette tip column. Methods of the invention can aid research, diagnosis and treatment of cancer. Purified viable cells can be detected on the column or eluted from the column and detected. Cells on a column can be used as a stationary phase for liquid chromatography. Cells may be removed, recovered and analyzed. 1. A column comprised of:a) a column body;b) two frits attached to the column body; andc) a bed of medium in contact with the frits, wherein the bed of medium is comprised of water-swollen beads, wherein the beads are compressible, wherein the bed of medium is not compressed, wherein the bed of medium has a packing density, wherein the packing density is in the range of 1.00 to 1.05, wherein the beads are comprised of a capture entity;wherein the column is comprised of unconstrained flow channels, wherein the diameters of 98% to 100% of the flow channels are sufficiently large for cells to pass through.2. The column of claim 1 , wherein the column body is a pipette tip.3. A column comprised of:a) a column body;b) two frits attached to the column body; andc) a bed of medium in contact with the frits, wherein the bed of medium is not compressed, wherein the bed of medium is comprised of water-swollen beads, wherein the beads are compressible and wherein the beads are comprised of a capture entity;wherein the column is comprised of unconstrained flow channels, wherein the minimum flow path diameter is greater than 8 μm.4. The column of claim 3 , wherein the column body is a pipette tip.5. The column of claim 3 , wherein the beads are impervious to reagents or solvents.6. The column of claim 3 , wherein the capture entity is an antibody or an aptamer.7. The column of claim 3 , wherein the bed of medium has a ...

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10-03-2022 дата публикации

MICROENCAPSULATION METHOD FOR IMPROVING STABILITY OF ANTHOCYANIN, PRODUCT THERE-FROM AND USE THEREOF

Номер: US20220071914A1
Принадлежит:

The present invention discloses a microencapsulation method for improving stability of anthocyanin, a product therefrom and use thereof. A preparation method of anthocyanin microcapsules includes: (1) taking sodium alginate as a wall material, adding sodium alginate and calcium carbonate into water, and swelling for 1-2 h to obtain a wall material gel system; (2) taking anthocyanin prepared by a special process as a core material, and fully and uniformly mixing the wall material gel system with an anthocyanin solution to obtain a water phase; (3) mixing Span80 and vegetable oil to obtain an oil phase, mixing the water phase with the oil phase, and magnetically stirring for emulsifying to obtain a W/O emulsion; and (4) adjusting the pH of the W/O emulsion to be acidic, mixing the W/O emulsion with a salt buffer solution, standing for 1-2 h, and then separating the oil phase and the water phase. 1. A microencapsulation method for improving stability of anthocyanin , comprising the following steps:S1, taking sodium alginate as a wall material, respectively preparing sodium alginate, calcium carbonate and water according to a weight ratio of sodium alginate to calcium carbonate to water of (2-4):1:(15-25), and then adding the sodium alginate and the calcium carbonate into water to swell for 1-2 h to obtain a wall material gel system;S2, taking anthocyanin as a core material, and fully and uniformly mixing the wall material gel system with an anthocyanin solution for later use at a weight ratio of the sodium alginate to the anthocyanin of (12-20):1 to obtain a water phase;S3, mixing Span80 with vegetable oil at a volume ratio of (1-2):1 to obtain an oil phase, mixing the water phase with the oil phase at a volume ratio of (3-5):1, and magnetically stirring the mixture for emulsifying to obtain a W/O emulsion; andS4, adjusting the pH of the W/O emulsion to be acidic, mixing the W/O emulsion with a buffer solution at a volume ratio of 1:(3-5), standing for 1-2 h, and ...

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05-03-2015 дата публикации

Porous Adsorptive Or Chromatographic Media

Номер: US20150060342A1
Принадлежит:

A porous substrate capable of adsorptive filtration of a fluid having a porous self-supporting substrate and one or more porous, adsorptive polymeric coatings comprising from about 1 to about 80% of the void volume of the pores of the substrate. The resultant substrate has good convective and diffusive flow and capacity. The substrate may be cross-linked, have one or more capture chemistries attached to it and is useful as a chromatography media for the selective filtration of desired species including biomolecules such as proteins and DNA fragments. 1. A porous coated composite sheet for adsorption based separations comprising:a porous, self-supporting woven or non-woven fabric polyolefin base sheet, coated with one or more porous crosslinked polyallylamine coatings formed on at least a portion of all surfaces of the porous base sheet,wherein the one or more porous coatings have a void volume fraction of the porous base sheet of at least 1%, and wherein said composite sheet comprises a filter selected from a gridded filter, curricular shaped filter, disc shaped filter, pleated filter, depth filter and combinations thereof.2. The composite sheet of claim 1 , wherein the filter is incorporated into a device selected from a holder claim 1 , laboratory device claim 1 , syringe claim 1 , microtiter plate claim 1 , filter cartridge claim 1 , and cartridge.3. The composite sheet of claim 1 , wherein the porous base sheet has a mean flow pore (MFP) rating about 1 micron to 500 microns.4. The composite sheet of claim 1 , wherein the porous base sheet has a pore size about 10 microns to about 300 microns.5. The composite sheet of claim 1 , wherein the porous base sheet has a pore size about 50 microns to about 200 microns.6. The composite sheet of claim 1 , wherein the coating has a thickness about 1 micron to about 100 microns.7. The composite sheet of claim 1 , wherein the coating has a thickness about 2 microns to about 50 microns.8. The composite sheet of claim 1 , ...

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21-02-2019 дата публикации

METHOD FOR CHROMATOGRAPHY REUSE

Номер: US20190054396A1
Принадлежит:

The present invention provides methods for cleaning or regenerating a chromatography materiel for reuse. The methods of the invention can be used for cleaning or regenerating chromatography columns for reuse in the large-scale manufacture of multiple polypeptide products. 1. A method to clean a chromatography material for reuse , the method comprising the steps ofa) passing two or more material volumes of elution buffer through the material, wherein the elution buffer comprises about 0.15 M acetic acid and is about pH 2.9;b) statically holding the material in elution buffer for a time ranging from about 10 minutes to about 30 minutes;c) passing about two or more material volumes of elution buffer through the material; andd) passing about two or more material volumes of regeneration buffer through the material, wherein the regeneration buffer comprises about 0.1 N NaOH and is about pH 13.2. A method to clean a chromatography material for reuse , the method comprising the steps ofa) passing about two material volumes of elution buffer through the material, wherein the elution buffer comprises about 0.15 M acetic acid and is about pH 2.9;b) statically holding the material in elution buffer for about 30 minutes;c) passing about two material volumes of elution buffer through the material; andd) passing about four material volumes of regeneration buffer through the material, wherein the regeneration buffer comprises about 0.1 N NaOH and is about pH 13.3. A method to clean a chromatography material for reuse , the method comprising the steps ofa) passing about two material volumes of elution buffer through the material, wherein the elution buffer comprises about 0.15 M acetic acid and is about pH 2.9,b) statically holding the material in elution buffer for about 30 minutes,c) passing about two material volumes of elution buffer through the material, andd) passing about two and one-half material volumes of regeneration buffer through the material, wherein the regeneration ...

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21-02-2019 дата публикации

Recovery and precipitation of various elements and compounds

Номер: US20190054458A1
Принадлежит: MESTENA OPERATING Ltd

Systems and methods are disclosed for extracting a plurality of materials from a solution. These include a plurality of extraction devices. The extraction devices use a resin suspended above at least one screen, and the resin is used to extract at least one material from a fluid. A liquid is forced through the plurality of extraction devices and a separate material is extracted in each of the extraction devices. The resin is selected for each of the extraction devices and is based upon the material for which that extraction device is designed to remove from the fluid. Each of the extraction devices operate in series to remove at least one material from the fluid.

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04-03-2021 дата публикации

COMPOSITIONS AND DEVICES FOR REMOVAL OF ENDOTOXINS AND CYTOKINES FROM FLUIDS

Номер: US20210060232A1
Принадлежит:

Provided are sorption materials and devices using the sorption materials, and methods of using the sorption materials and devices containing the sorption materials. In various examples, the sorption materials bind to various inflammation stimulating and/or mediating molecules, which are often associated with systemic infections and systemic inflammation associated with conditions such as, for example, sepsis. 2. The method of claim 1 , wherein the contacting comprises passing a biological fluid through a housing claim 1 , wherein the housing includes an inlet and an outlet claim 1 , wherein the inlet and the outlet are in fluid communication claim 1 , and the housing is configured such that the fluid enters the housing through the inlet and exits the housing through the outlet claim 1 , wherein the at least one sorption material is disposed in the housing.3. The method of claim 1 , wherein the method further comprises returning the biological fluid to the subject.4. The method of claim 1 , wherein the biological fluid is blood claim 1 , serum claim 1 , culture media claim 1 , or a combination thereof.5. The method of claim 1 , wherein the substrate is a hydrogel network or solid substrate.6. The method of claim 5 , wherein the solid substrate is porous.7. A device for removing inflammation stimulating and/or mediating molecules from a fluid comprising:a housing defining an inlet and an outlet, wherein the inlet and the outlet are in fluid communication with one another, and the housing is configured such that the fluid enters the housing through the inlet and exits the housing through the outlet; and {'br': None, 'sup': 1', '1', '2', '2, 'sub': 'x,y', 'R-L-D-(L-R)'}, 'a sorption material is disposed in the housing, wherein the sorption material comprises at least one compound bound to a substrate, wherein the compound has the following structure{'sup': 1', '1, 'claim-text': [{'sup': 1', '2, 'Land Lindependently at each occurrence are optional and are linker groups ...

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10-03-2022 дата публикации

MICRO-SEPARATOR HAVING STATIONARY PHASE WITH THREE-DIMENSIONAL NANO-STRUCTURE AND METHOD FOR MANUFACTURING THE SAME

Номер: US20220074899A1

A disclosed micro-separator for gas chromatography includes a base substrate having a trench, a channel column disposed in the trench, and a cover member combined with the base substrate and covering the channel column. The channel column includes a stationary phase having pores ordered and three-dimensionally connected to each other. 1. A micro-separator for gas chromatography comprising:a base substrate having a trench;a channel column disposed in the trench; anda cover member combined with the base substrate and covering the channel column,wherein the channel column includes a stationary phase having pores ordered and three-dimensionally connected to each other.2. The micro-separator for gas chromatography of claim 1 , wherein the base substrate includes at least one selected from the group consisting of silicon claim 1 , glass claim 1 , quartz claim 1 , sapphire and a polymer.3. The micro-separator for gas chromatography of claim 1 , wherein the stationary phase includes at least one selected from the group consisting of a polymer claim 1 , a metal and a ceramic.4. The micro-separator for gas chromatography of claim 1 , wherein the stationary phase is disposed on a bottom surface of the trench and is spaced apart from the cover member to define a gas flow path.5. The micro-separator for gas chromatography of claim 1 , wherein the stationary phase includes a lower stationary phase disposed on a bottom surface of the trench claim 1 , and an upper stationary phase combined with a lower surface of the cover member claim 1 , wherein at least a portion of the upper stationary phase is spaced apart from the lower stationary phase to define a gas flow path between the lower stationary phase and the upper stationary phase.6. The micro-separator for gas chromatography of claim 1 , wherein the stationary phase entirely fills the channel column.7. The micro-separator for gas chromatography of claim 1 , wherein a bottom surface of the trench has a concave shape claim 1 , and ...

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21-02-2019 дата публикации

Polymer Compositions with Reduced Volatiles

Номер: US20190055387A1
Принадлежит:

Described herein are polymer compositions comprising a polymer and a molecular sieve having a framework type of AEL, AFO, EUO, FER, HEU, MEL, MTW, MTT, MFI, OFF, or TON. The present polymer composition comprises a toluene content of less than 1.0 mg/mand a C-Cvolatile organic compounds content of less than 3.0 mg/m. Described herein also are a method of reducing the toluene content contained in polymers. 1. A composition comprising:a polymer; anda molecular sieve having a framework type of AEL, MFI, MFS, MEL, MTW, EUO, MTT, HEU, FER, OFF, or TON,{'sup': '3', 'wherein the composition comprises a toluene content of less than 1.0 mg/m, and'}{'sub': 6', '16, 'sup': '3', 'wherein the polymer composition comprises a C-Cvolatile organic compounds content of less than 3.0 mg/m, and'}{'sub': 6', '16, 'wherein each of the toluene content and the C-Cvolatile organic compound content is measured by thermodesorption gas chromatography with mass spectrometric detection method.'}2. The composition of claim 1 , wherein the toluene content is less than 0.1 mg/m.3. The composition of claim 1 , wherein the C-Cvolatile organic compounds content is less than 2.5 mg/m.4. The composition of comprising from 0.5 to 20 wt % the molecular sieve based on the weight of the polymer composition.5. The composition of comprising from 1.5 to 15 wt % the molecular sieve based on the weight of the polymer composition.6. The composition of comprising a cumulative content of benzene claim 1 , toluene claim 1 , xylene claim 1 , ethylbenzene claim 1 , and styrene of less than 0.2 mg/m claim 1 , as measured by high-performance liquid chromatography with diode-array detection method.7. The composition of claim 1 , wherein the polymer composition comprises a cumulative content of formaldehyde claim 1 , acetaldehyde claim 1 , and acrolein of less than 0.15 mg/m.8. The composition of claim 1 , wherein the polymer composition comprises a cumulative content of benzene claim 1 , toluene claim 1 , xylene claim 1 , ...

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02-03-2017 дата публикации

Ion Exchange Regeneration Process Utilizing Membrane Distillation

Номер: US20170057854A1
Принадлежит:

Method for treating effluent waste from a cation-exchange column regeneration cycle, including backwashing the column; regenerating the column using rinse water and a regenerant brine having a temperature warmer than room temperature, thereby forming a waste effluent containing divalent cations; precipitating the divalent cations in a precipitation reactor at a temperature warmer than room temperature; filtering the precipitation effluent; optionally, adjusting the filtered precipitation effluent pH; concentrating the filtered precipitation effluent via membrane-based water recovery, thereby forming separated concentrated salt and pure rinse water; and recirculating the separated concentrated salt and pure rinse water back to the column for a subsequent regeneration cycle. Also, a system including an exhausted cation-exchange column; a chemical precipitation reactor; a filtration unit; an optional pH adjustment unit; and a membrane-based water recovery unit, wherein the system is a closed-loop through which salt and rinse water having a temperature warmer than room temperature recirculate. 1. A method comprisingi) a backwashing step, wherein an exhausted cation-exchange column is backwashed with backwash water;ii) a regeneration step, wherein rinse water having a temperature of from about 40° C. to about 60° C. and a regenerant brine comprising sodium chloride and having a temperature of from about 40° C. to about 60° C. are passed over the exhausted cation-exchange column, thereby forming a waste effluent having a temperature of from about 40° C. to about 60° C. and containing divalent cations and sodium chloride;iii) a precipitation step, wherein the waste effluent is fed at a temperature of from about 30° C. to about 50° C. to a precipitation reactor where the divalent cations are precipitated as carbonates or hydroxides, thereby forming a treated effluent;iv) a filtration step, wherein the treated effluent proceeds through a filtration unit to remove unsettled ...

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04-03-2021 дата публикации

SYSTEMS AND METHODS FOR SELECTIVE RECOVERY OF METALS FROM ION EXCHANGE RESINS

Номер: US20210062296A1
Принадлежит:

Systems and methods for selectively recovering a target metal from an ion exchange resin are generally described. In certain embodiments, such methods and systems can be employed for metal purification and enrichment of target metal species from mixtures containing contaminating or non-target metals. In some embodiments, ion exchange is accomplished in the presence of one or more species that facilitate the recovery of a metal from a composition further comprising one or more other metals. The recovered metal-containing composition may contain the recovered metal at relatively high purity and/or in relatively large amounts. In some embodiments, the conditions present during ion exchange are varied in a manner that facilitates the enrichment of a metal from an initial (e.g. sample) composition further comprising one or more other metals to result in a product that contains the enriched metal at relatively high purity and/or in relatively large amounts 1. A method of selectively recovering a first metal from an ion exchange resin , comprising:{'sup': −5', '4, 'contacting a non-polar fluid and an extractant with the ion exchange resin, the first metal, and a second metal, wherein at least one of the first metal and the second metal are bound to the ion exchange resin, wherein the ion exchange resin comprises a plurality of functional groups having a proton dissociation constant of greater than or equal to 10and less than or equal to 10; and'}selectively eluting the first metal from the ion exchange resin into the non-polar fluid such that a ratio of the first metal to the second metal in the non-polar fluid is greater than a ratio of the first metal to the second metal bound to the ion exchange resin.2. The method of claim 1 , wherein contacting step comprises introducing the non-polar fluid and the extractant into a column containing the ion exchange resin claim 1 , the first metal claim 1 , and the second metal claim 1 , wherein at least one of the first metal and ...

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05-03-2015 дата публикации

Process for purifying a hydrocarbon feed

Номер: US20150065765A1
Принадлежит: Axens SA

A process for purifying a hydrocarbon feed, using a first adsorption unit with first and second adsorption columns respectively filled with first and second adsorbent solids by simultaneously: a) treating the liquid phase hydrocarbon feed in the first adsorption column by contact with the first adsorbent solid to adsorb at least a portion of impurities present and to produce hydrocarbon effluent which is depleted in impurities; b) treating a secondary liquid hydrocarbon feed constituted either by a fraction of the hydrocarbon feed or by a fraction of the hydrocarbon effluent and depleted in impurities to purify the secondary liquid hydrocarbon feed; c) heating the treated secondary liquid hydrocarbon feed from step b); d) regenerating the second adsorbent solid of the second adsorption column which comprises impurities with the secondary hydrocarbon feed heated in step c) to desorb the impurities to produce an effluent with impurities.

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28-02-2019 дата публикации

CHROMATOGRAPHY COLUMN WITH LOCKED PACKED BED AND METHOD OF PACKING THAT COLUMN

Номер: US20190060786A1
Принадлежит:

A chromatography column has a retaining plug permanently fixed to an upstream end of the column and blocks one end of the bore through the column. The plug has a fluid passage therethrough. An upstream end of the passage is preferably but optionally larger in diameter than a downstream end of the passage. An upstream porous member upstream of the retaining plug is held by an upstream end cap and urged toward the plug. Chromatographic media extends from the upstream porous member, through the passage in the retaining plug, to a downstream porous member held by a downstream end cap. The media between the retaining plug and the downstream porous member are under compression to form a bed of packed media. 1. A chromatography column having a tubular body with opposing upstream and downstream ends with upstream and downstream end fittings connected to the tubular body , the tubular body having an internal bore extending along a longitudinal axis of the tubular body and column , the column comprising:a retaining plug blocking an upstream end of the bore and having a passage extending between upstream and downstream ends of the retaining plug and filled with chromatographic media;a downstream porous member blocking the downstream end of the bore, the bore having a continuous wall between the retaining plug and the downstream porous member;a slurry-packed bed of chromatographic media held in compression in the bore by the retaining plug and the downstream porous member;2. The column of claim 1 , wherein the passage contains porous media and further comprising an upstream porous member upstream of the retaining plug located to filter fluid flow through the bore into the at least one passage.3. The column of claim 2 , wherein the passage has a first diameter at the upstream end of the retaining plug and a second diameter at the downstream end of the retaining plug and the first diameter is larger than the second diameter.4. The column of claim 3 , wherein the first diameter is ...

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17-03-2022 дата публикации

PROCESS TECHNOLOGY FOR BIOLOGICAL PRODUCT MANUFACTURING AND DOWNSTREAM PURIFICATION

Номер: US20220081469A1
Принадлежит:

Provided herein are, inter alia, biological manufacturing and downstream purification processes. 1. A process for purifying a biological product , comprising:receiving, via an input line, a heterogeneous mixture containing the biological product;removing impurities from the heterogeneous mixture by filtration in a dynamic filtration module by feeding the biological product from at least one output head in fluid communication with the input line to the dynamic filtration module under negative pressure, thereby producing a filtrate comprising the biological product, the dynamic filtration module comprising a dynamic filtration apparatus having a filter membrane extending between a feed reel and a collection reel with at least one support member having a substantially smooth contact surface, a target region of the filter membrane that is configured to receive the heterogeneous mixture from at least one output head, and a membrane support member with a substantially smooth contact surface that is in communication with a vacuum collection system that is positioned between the feed reel and the collection reel;transferring the filtrate to a first module capable of separating the solution into two or more fractions wherein at least one fraction contains the biological product, the first module comprising an affinity-based purification apparatus, wherein the first module has at least one first inlet and at least one first outlet configured to permit fluid flow between the at least one first inlet and the at least one first outlet via a mechanical rotary system comprising a vessel carousel containing at least one discrete vessel comprising a suspension of beads;transferring the fraction containing the biological product from the at least one outlet of the first module to a second module having at least one inlet for receiving flow from the at least one first outlet of the first module, the second module comprises at least one free-flow electrophoresis apparatus, wherein the ...

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10-03-2016 дата публикации

POLYMER SURFACES HAVING A SILOXANE FUNCTIONAL GROUP

Номер: US20160067631A1
Принадлежит:

An apparatus for collecting mineral particles in a slurry or the tailings is disclosed, including a collection area or tank having one or more collection surfaces configured to contact with a mixture having water and valuable material, the valuable material having a plurality of mineral particles of interest; and a synthetic material provided at least on the one or more collection surfaces, the synthetic material having plurality of molecules with a siloxane functional group configured to attract the mineral particles of interest to the collection surfaces. The one or more collection surfaces includes a conveyor belt that is driven through the collection area or tank, through a release area or tank, back through the collection area or tank. The mixture includes a pulp slurry having ground ore with mineral particles of interest forming part thereof, including mineral particles of interest of about 500 microns or larger. 1. Apparatus comprising:a collection area or tank having one or more collection surfaces configured to contact with a mixture having water and valuable material, the valuable material having a plurality of mineral particles of interest; anda synthetic material provided at least on the one or more collection surfaces, the synthetic material having plurality of molecules with a siloxane functional group configured to attract the mineral particles of interest to the collection surfaces.2. Apparatus according to claim 1 , wherein the one or more collection surfaces includes claim 1 , or forms part of claim 1 , a conveyor belt also that is driven through the collection area or tank claim 1 , through a release area or tank claim 1 , back through the collection area or tank.3. Apparatus according to claim 1 , wherein the mixture includes claim 1 , or takes the form of claim 1 , a pulp slurry having ground ore with mineral particles of interest forming part thereof claim 1 , including mineral particles of interest of about 500 microns or larger.4. Apparatus ...

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08-03-2018 дата публикации

UNIVERSAL BLOOD PRODUCT AND METHODS OF PREPARING AND USING SAME

Номер: US20180065062A1
Принадлежит:

A method of preparing a universal blood product comprising obtaining a blood product; contacting the blood product with (i) hydroxyapatite; (ii) a carbonaceous material comprising at least a mixture of a first carbon particle having macroporous size α and a second carbon particle having macroporous size β; and (iii) at least one support matrix chemically associated with an antigenic determinant.to form a cleansed product; and recovering the cleansed product. A method of preparing a universal blood product comprising obtaining a blood product; contacting the blood product with (i) hydroxyapatite; (ii) a carbonaceous material comprising at least a mixture of a first carbon particle having macroporous size α and a second carbon particle having macroporous size β; and (iii) at least one support matrix chemically associated with an antigenic determinant.to form a cleansed product; wherein at least one of the hydroxyapatite, carbonaceous material and support matrix is functionalized. 1. A method of preparing a universal blood product comprising:obtaining a blood product wherein the blood product comprises whole blood or plasma;contacting the blood product with (i) hydroxyapatite; (ii) a carbonaceous material comprising at least a mixture of a first carbon particle having macroporous size α and a second carbon particle having macroporous size β; and (iii) at least one support matrix chemically associated with an antigenic determinant.to form a cleansed product; andrecovering the cleansed product.2. The method of wherein the hydroxyapatite is naturally-occurring claim 1 , synthetic claim 1 , or combinations thereof3. The method of wherein the hydroxyapatite has a Brunauer Emmett Teller surface area of from about 200 m/g to about 3000 m/g.4. The method of wherein the hydroxyapatite is in the form of beads having a particle size of from about 300 μm to about 1000 μm.5. The method of wherein the hydroxyapatite has a unimodal pore size distribution with a pore size ranging from ...

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17-03-2022 дата публикации

Techniques for system suitability testing of inert liquid chromatography systems and columns

Номер: US20220082531A1
Принадлежит: Waters Technologies Corp

The present disclosure is directed to methods of characterizing a system containing a chromatographic column. The methods can include introducing a sample comprising a positive control and a negative control to the system containing a chromatographic column, wherein the positive control is a sensitive probe that interacts with the system and the negative control is substantially non-interacting with the system; after passing the sample through the chromatographic column, detecting the positive control and the negative control; and determining system suitability by comparing the amount of detected positive control to negative control. In some embodiments, determining system suitability (e.g., inertness of sample to the system) is accomplished by determining a ratio of detected positive control to negative control.

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17-03-2022 дата публикации

INTERCHANGEABLE CHROMATOGRAPHY CARTRIDGEADAPTER SYSTEM

Номер: US20220082536A1
Принадлежит:

A chromatography system has a cartridge adapter that is detachably attachable to enable a chromatography cartridge to be quickly interchanged. Chromatography cartridges are configured with threads for coupling to a corresponding interchangeable coupling component having matching threads. The interchangeable coupling component may be secured to the chromatography system by a coupling retainer. A coupling retainer may have a keyway that is configured for quick interchanging of the interchangeable coupling components. The interchangeable coupling component may have a pair of parallel sides that align with a slot of the keyway to secure the interchangeable coupling components to the coupling retainer. An inlet nipple of the chromatography cartridge may extend through an opening in the coupling components and couple to an inlet conduit for sample gas. Analyte gas may flow back to the chromatography system for detection and collection. 1. A chromatography system comprising: i) an inlet end having an inlet;', 'ii) a threaded cartridge portion comprising threads with a first external diameter;', 'iii) an outlet;, 'a) a first chromatography cartridge comprising i) an inlet end having an inlet;', 'ii) a threaded cartridge portion comprising threads with a second external diameter larger than said first external diameter of the threads of the first chromatography cartridge;', 'iii) an outlet;, 'b) a second chromatography cartridge comprising [ 'a cartridge portion configured on a cartridge end having threads that couple with the threads of the threaded cartridge portion of the first chromatography cartridge;', 'i) a first interchangeable coupling component that is detachably attachable to the chromatography system and comprising, 'a cartridge portion configured on a cartridge end having threads that couple with the threads of the threaded cartridge portion of the second chromatography cartridge;', 'ii) a second interchangeable coupling component that is detachably attachable ...

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09-03-2017 дата публикации

ANTIMICROBIAL SOLUTIONS AND METHODS

Номер: US20170065905A9
Автор: Code Kenneth R.
Принадлежит: BIOLARGO LIFE TECHNOLOGIES, INC.

Contaminants are filtered from a fluid flow stream and the filter is regenerated by a process including steps of: providing a filter material comprising both carbon and potassium iodide; passing a contaminated fluid stream in contact with the filter material; adsorbing contaminants from the fluid stream onto surfaces in the filter material; passing an electric current through the filter material with adsorbed contaminant thereon; disassociating contaminant from the surfaces of the filter material; and removing disassociated contaminant from the filter material by carrying away the disassociated contaminant in a fluid flow mass. 1. An apparatus for removing contamination from a fluid stream comprising: a) a housing containing a filter material having two opposed surfaces , the filter material comprising carbon and an activating agent selected from the group consisting of an alkali metal halogen and an alkaline halogen; b) a fluid inlet port to the housing; c) a fluid outlet port from the housing; d) a source of contaminated fluid available to the fluid inlet port; e) a device for moving fluid through the inlet port and through the outlet port; f) a current source that passes current through the filter material between the two opposed surfaces; and g) a source of fluid flow mass to move fluid mass over the filter material after or during passage of direct current over the filter material.2. The apparatus of wherein the filter material comprises activated carbon and at least 0.05% by total weight of solids of halide salt.3. The apparatus of wherein the halide salt comprises an iodide salt.4. The apparatus of wherein the iodide salt comprises potassium iodide is distributed on at least some surfaces of the activated carbon.5. The apparatus of wherein a source of electric current is provided to be able to apply electric current at a range of voltages at least between 2.0 and 15 volts.6. The apparatus of wherein the current source is located at a position along a path for ...

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11-03-2021 дата публикации

APPARATUS FOR CLARIFICATION OF CHEMICAL COMPOUNDS OF POROUS SILICA FROM AGRICULTURAL WASTE

Номер: US20210069612A1
Принадлежит:

An apparatus to clear and upgrade a quality of native or recovered compounds, paraffinic or naphthenic, and other hydrocarbons containing compounds or polar species, which are to be separated and to adsorb components responsible for dark appearance or darkening of recycling motor oil, vegetable and animal fatty acids through of porous silica obtained from agricultural waste, including a treatment with adsorbent, a porous silica obtained from agricultural waste; one or more containers with different volumes and geometric shape, according to needs of what is going to be treated, configured for the porous silica, the hydrocarbons and other compounds to be treated in contact; an element for temperature control of the mixture of the silica with the compound to be treated; an element for controlling pressure and flow of the mixture of the silica with the compound; and an element that filters and retains the adsorbent inside of the apparatus. 1. An apparatus to clear and upgrade a quality of native or recovered compounds , paraffinic or naphthenic , and other hydrocarbons containing compounds or polar species , which are to be separated and to adsorb components responsible for dark appearance or darkening of recycling motor oil , vegetable and animal fatty acids through of porous silica obtained from agricultural waste , comprising:an adsorbent comprising a porous silica obtained from agricultural waste;one or more containers with different volumes and geometric shape, according to needs of what is going to be treated, configured for the porous silica, the hydrocarbons and other compounds to be treated in contact;an element for temperature control of the mixture of the silica with the compound to be treated;an element for controlling pressure and flow of the mixture of the silica with the compound to be treated; anda filter configured to filter and retain the adsorbent inside the apparatus.2. The apparatus of claim 1 , wherein the porous silica or adsorbent claim 1 , is ...

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11-03-2021 дата публикации

POLYMER FOR SEPARATION OF ANALYTES AND METHODS FOR PREPARATION AND USE OF SAME

Номер: US20210069675A1
Автор: ZHU Fake
Принадлежит:

A polymer for liquid chromatography or solid phase extraction is provided. The polymer is prepared by polymerizing styrene and divinylbenzene to form a styrene-divinylbenzene copolymer; soaking the styrene-divinylbenzene copolymer in a swelling agent to form nano-scale micropores; and soaking the microporous styrene-divinylbenzene copolymer in methanol. When packed in a chromatographic column, the polymer can be used to produce produce natural health or medicinal products from species, for example, industrial hemp. 1. A method for making a polymer for use in liquid chromatography or solid phase extraction , the method comprising:polymerizing styrene and divinylbenzene to form a styrene-divinylbenzene copolymer;soaking the styrene-divinylbenzene copolymer in a swelling agent to form nano-scale micropores; andsoaking the microporous styrene-divinylbenzene copolymer in methanol.2. The method according to claim 1 , wherein polymerizing styrene and divinylbenzene comprises:adding the styrene, the divinylbenzene, a polymerization initiator, and a pore-forming agent to an organic medium to form a mixture; andheating the mixture to initiate a polymerization reaction and to form, by the polymerization reaction, the styrene-divinylbenzene copolymer.3. The method according to claim 1 , wherein the molar ratio of the styrene to the divinylbenzene is in a range of 0.8:1 to 1.2:1.4. The method according to claim 2 , wherein the polymerization initiator comprises one or more of azobisisobutyronitrile and benzoyl peroxide.5. The method according to claim 2 , wherein a number of moles of the polymerization initiator used is 1 to 2% of a number of moles of the styrene.6. The method according to claim 2 , wherein the pore-forming agent comprises polyethylene glycol.7. The method according to claim 2 , wherein the organic medium comprises a mixture of polyethylene glycol and liquid paraffin.8. The method according to claim 7 , wherein the volume ratio of polyethylene glycol and liquid ...

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09-03-2017 дата публикации

NOVEL AFFINITY CHROMATOGRAPHY MEDIA FOR REMOVAL OF ANTI-A AND/OR ANTI-B ANTIBODIES

Номер: US20170066839A1
Принадлежит:

Embodiments described herein relate to novel chromatography media for removing anti-A and/or anti-B antibodies from a sample, as well as methods of using the same. The media described herein have several advantages over previously described media including, acid and alkaline stability. 1. A media for removing anti-A antibodies from a sample , the media comprising a solid support with a blood group A antigen ligand attached thereto , wherein the ligand is attached to the solid support at a ligand loading of at least 0.8 mg/ml of solid support , and wherein the media is stable under acid and/or alkaline conditions.2. A media for removing anti-B antibodies from a sample , the media comprising a solid support with a blood group B antigen ligand attached thereto , wherein the ligand is attached to the solid support at a ligand loading of at least 0.8 mg/ml of solid support , and wherein the media is stable under acid and/or alkaline conditions.3. The media according to claim 1 , wherein the ligand loading is at least 1 mg/ml of solid support or at least 1.5 mg/ml of solid support or at least 1.65 mg/ml of solid support.4. The media according to claim 2 , wherein the ligand loading is at least 1 mg/ml of solid support or at least 1.2 mg/ml of solid support.5. A media for removing anti-A and anti-B antibodies from a sample claim 2 , the media comprising: (a) a solid support with both blood group A antigen ligand and blood group B antigen ligand attached thereto claim 2 , each at a ligand loading of at least 0.8 mg/ml of solid support; or (b) a mixture of two solid supports claim 2 , one comprising blood group A antigen ligand thereto and another comprising blood group B antigen ligand claim 2 , each media having ligand loading of at least 0.8 mg/ml of solid support claim 2 , wherein the media are stable under acid and/or alkaline conditions.6. The media of claims 1 , wherein the solid support comprises a polymer selected from the group consisting of polyvinylether claims 1 ...

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09-03-2017 дата публикации

METHODS OF EVALUATING QUALITY OF MEDIA SUITABLE FOR REMOVING ANTI-A OR ANTI-B ANTIBODIES

Номер: US20170067915A1
Принадлежит:

Embodiments described herein relate to methods of evaluating quality of a chromatography media for removal of anti-A or anti-B antibodies from a sample, where the methods employ use of purified Lectins. 3. The method of claim 1 , wherein the solid support is a porous or non-porous polymeric solid support comprising a polymer selected from the group consisting of polyvinylether claim 1 , polyvinylalcohol claim 1 , polymethacrylate claim 1 , polyacrylate claim 1 , polystyrene claim 1 , polyacrylamide claim 1 , polymethacrylamide and polycarbonate.4. The method of claim 2 , wherein the solid support is a porous or non-porous polymeric solid support comprising a polymer selected from the group consisting of polyvinylether claim 2 , polyvinylalcohol claim 2 , polymethacrylate claim 2 , polyacrylate claim 2 , polystyrene claim 2 , polyacrylamide claim 2 , polymethacrylamide and polycarbonate.5. The method of claim 1 , wherein the solid support is a polyvinylether based porous solid support.6. The method of claim 2 , wherein the solid support is a polyvinylether based porous solid support.7. The method of claim 5 , wherein the polyvinylether based porous solid support is in bead form.8. The method of claim 6 , wherein the polyvinylether based porous solid support is in bead form.9. The method of claim 1 , wherein the binding capacity of the blood group A antigen ligand media for purified HP Lectin correlates with its ability to remove anti-A antibodies from a sample.10. The method of claim 2 , wherein the binding capacity of the blood group B antigen ligand media for purified GSI-B4 Lectin correlates with its ability to remove anti-B antibodies from a sample.11. The method of claim 1 , wherein the two or more affinity chromatography media samples constitute different batches of the same media.12. The method of claim 2 , wherein the two or more affinity chromatography media samples constitute different batches of the same media.13. The method of claim 1 , wherein the ...

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24-03-2022 дата публикации

TRANSITION ANALYSIS METHOD FOR CHROMATOGRAPHY COLUMN QUALIFICATION

Номер: US20220089716A1
Автор: Randolph Paul
Принадлежит:

The present disclosure is directed to a method of operating a chromatography column. This method involves collecting column outlet signal and accumulated flow parameters at two or more intervals of at least one mobile phase transition front during operation of the chromatography column comprising column packing. A model gamma cumulative distribution curve is determined based on the collected column outlet signal and accumulated flow parameters for the at least one mobile phase transition front. The height equivalent theoretical plate (HETP) value is calculated for the at least one mobile phase transition front using parameters of the model gamma cumulative distribution curve and the quality of the chromatography column packing is assessed based on the calculated HETP value. If during routine column monitoring, an adverse trend in HETP is observed or the control limits are exceeded, the eluate product quality, column process performance, and/or impurity removal data should be evaluated to ensure product quality for the identified batch. Should any of the product quality or column performance fail the criteria set, appropriate corrective action, such as conditioning, repacking or replacing the column, and qualification should be performed prior to release for further use. 117-. (canceled)19. The system of claim 18 , wherein the chromatography column is conditioned claim 18 , replaced claim 18 , or repacked based on said assessing.20. The system of claim 18 ,wherein the detector is configured to collect column outlet signals and accumulated flow parameters at two or more intervals of a corresponding mobile phase transition front during one or more subsequent uses of the chromatography column packing;wherein the computing device comprises processor and a non-transitory computer-readable medium with instructions stored thereon, which, when executed by the processor, perform steps comprising:a) said determining and said calculating using the column outlet signal and ...

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05-03-2020 дата публикации

FILTER MODULE FOR WATER TREATMENT APPARATUS, AND WATER TREATMENT APPARATUS COMPRISING SAID FILTER MODULE

Номер: US20200071201A1
Принадлежит:

A filter module for a water treatment apparatus, and a water treatment apparatus comprising the filter module includes: stacked active carbon fiber layers made of active carbon fiber; spacers inserted between the active carbon fiber layers; a pair of current collectors connected to an end of the stacked active carbon fiber layers; and an active carbon fiber filter included stacked one or more active carbon fiber filter units, each active carbon fiber filter unit including a power supply for supplying current to the active carbon fiber layers via the current collectors so that neighboring active carbon fiber layers form cathodes and anodes in alternation. The filter module can lower the hardness of the water while increasing ion removal capability by increasing the specific surface area and water permeability, and can minimize the thickness of the electrodes by eliminating ion exchange membranes and minimizing the volume of current collectors. 1. A filter module for a water treatment apparatus comprising:at least one filter, a plurality of activated carbon fiber layers including activated carbon fiber and stacked in parallel to each other;', 'a plurality of spacers interposed between the activated carbon fiber layers to prevent short;', 'a pair of current collectors connected with one end portion or an opposite end portion of the activated carbon fiber layers stacked; and', 'a power supply unit to apply a current to the activated carbon fiber layer through the current collector such that adjacent activated carbon fiber layers alternately have a positive electrode and a negative electrode., 'wherein the filter is an activated carbon fiber filter including at least one activated carbon fiber filter unit which is stacked and includes2. The filter module of claim 1 , wherein the activated carbon fiber layer is provided in a form of a fabric having flexibility.3. The filter module of claim 1 , wherein the power supply unit applies the current in one direction when ...

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22-03-2018 дата публикации

USE OF ALKALINE WASHES DURING CHROMATOGRAPHY TO REMOVE IMPURITIES

Номер: US20180078876A1
Принадлежит:

In certain embodiments, the invention provides a method of purifying a protein of interest from a mixture which comprises the protein of interest and one or more contaminants, said method comprising: a) subjecting the mixture to a first chromatography matrix, wherein the protein of interest binds to the first chromatography matrix; b) contacting the first chromatography matrix with a first wash solution which has a pH of at least 9.0, and does not comprise arginine or an arginine derivative; and c) eluting the protein of interest from the first chromatography matrix into an elution solution. 1. A method of purifying a protein of interest from a mixture which comprises the protein of interest and one or more contaminants , comprising:a) subjecting the mixture to a first chromatography matrix, wherein the protein of interest binds to the first chromatography matrix;b) contacting the first chromatography matrix with a first wash solution which has a pH of at least 9.0, and does not comprise arginine or an arginine derivative; andc) eluting the protein of interest from the first chromatography matrix into an elution solution.2. The method of claim 1 , wherein the contaminants are selected from host cell proteins claim 1 , host cell metabolites claim 1 , host cell constitutive proteins claim 1 , nucleic acids claim 1 , endotoxins claim 1 , viruses claim 1 , product related contaminants claim 1 , lipids claim 1 , media additives and media derivatives.3. The method of claim 1 , wherein the first chromatography is an affinity chromatography.4. The method of claim 3 , wherein the affinity chromatography is selected from a protein A affinity chromatography and a protein G affinity chromatography.5. The method of claim 4 , wherein the affinity chromatography is a protein A affinity chromatography.6. The method of claim 1 , wherein the protein of interest is selected from an antibody claim 1 , an antibody fragment claim 1 , and an Fc fusion protein.7. The method of claim 6 , ...

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22-03-2018 дата публикации

HPLC COLUMN

Номер: US20180078877A1
Принадлежит:

A slurry chamber is fastened to and held in coaxial alignment with a chromatography column by a V-band. One end of the column has an end cap and frit. A slurry of fluid and chromatographic media is placed in the column and chamber. A piston is forced through the chamber and into the column by a hydraulic ram to expel the fluid and form a media bed in the column. The slurry chamber is removed, and a split end cap is fastened to the column. A threaded recess in the split end cap receives a split, threaded collet. The collet is tightened until it pushes against the piston with the same force as the ram, at which point the ram is released and the column removed for use. 137.-. (canceled)38. A chromatography column having a tubular body with an inner diameter , the column having opposing inlet and outlet ends , the column comprising:a bed of chromatographic media that has just been compressed to its maximum axial compression packing pressure during formation of the chromatographic bed;an upstream and downstream frit inside the tubular body and located on respective upstream and downstream ends of the bed of chromatographic media;a piston having opposing, upstream and downstream ends, the downstream end of the piston urging the upstream frit against the bed of chromatographic media and maintaining the axial compression packing pressure on the bed of chromatographic media, with no spring interposed between the first frit and the piston, the upstream end of the piston having an annular surface encircling a longitudinal axis of the column and facing away from the upstream frit;a fluid seal interposed between the piston and the inner diameter of the tubular body;a locking sleeve with multiple-parts that are connected together to encircle the inlet end of the column, each part of the locking sleeve having sleeve threads located thereon to form a threaded surface encircling the longitudinal axis;an annular locking collet having collet threads located to threadingly engage the ...

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22-03-2018 дата публикации

TREATING SULFURIC ACID

Номер: US20180079645A1
Принадлежит:

Provided is a method for treating sulfuric acid comprising the step (I) of bringing said sulfuric acid into contact with a collection of solid particles (B) having BET surface area of 50 m/g to 5,000 m/g and having volume-average particle diameter of 200 μm or less. 1. A method for treating sulfuric acid comprising the step (I) of bringing said sulfuric acid into contact with a collection of solid particles (B) having BET surface area of 50 m/g to 5 ,000 m/g and having volume-average particle diameter of 200 μm or less.2. The method of claim 1 , wherein said solid particles (B) are activated carbon particles.3. The method of claim 2 , wherein said sulfuric acid claim 2 , prior to said step (I) claim 2 , has undergone a reaction with a copolymer.4. The method of claim 2 , wherein said sulfuric acid is in the form of a solution that comprises sulfuric acid and water.5. The method of claim 2 , wherein said activated carbon particles are powdered activated carbon particles.6. The method of claim 2 , wherein said method further comprises the step claim 2 , after said step (I) claim 2 , of separating said sulfuric acid from said activated carbon particles. It is often desired to react a copolymer with sulfuric acid. A common method for conducting such a reaction is to form a mixture that contains the copolymer and sulfuric acid, to heat the mixture for a time, and then separate the resultant resin from the sulfuric acid. After performance of such a method, the sulfuric acid is known as “spent” sulfuric acid. During reaction with the copolymer, the sulfuric acid often acquires impurities that make the spent sulfuric acid undesirable for further use. Some of those impurities impart color to the sulfuric acid.The publication “Activated Carbons and What They Can Do For You,” by the Cabot Corporation, states that activated carbon is used for treating materials including glycerin, organic acids, and agrochemicals. It is desired to identify a process for removing impurities from ...

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31-03-2022 дата публикации

THERMAL ISOLATION CHAMBERS AND CHROMATOGRAPHY SYSTEMS INCLUDING THEM

Номер: US20220096961A1
Принадлежит:

Thermal isolation chambers that can be used to heat or cool a chromatography column are described. Certain configurations include at least one plate and an insulative barrier. The plate and insulative barrier can form a cyclical air flow path such that air in the cyclical air flow path can be provided to a chromatography column to remove heat from the chromatography column. The heat can be transferred to the plate. Systems including the thermal isolation chambers, and methods of using the thermal isolation chambers to perform chromatographic separations are also described. 1. A thermal isolation chamber comprising:a first plate;a second plate; andan insulative barrier, wherein the thermal isolation chamber is configured to receive a chromatography column and thermally isolate the received chromatography column from other components in the thermal isolation chamber, the thermal isolation chamber comprising a first cyclical air flow path between the insulative barrier and the first plate and between the insulative barrier and the second plate, wherein the first cyclical air flow path is configured to receive an air flow and provide the received air flow to the received chromatography column to remove heat from the received chromatography column and transfer the removed heat to one or both of the first plate and the second plate.2. The thermal isolation chamber of claim 1 , further comprising a cooling device configured as a fan to provide the air flow through the first cyclical air flow path.3. The thermal isolation chamber of claim 2 , further comprising a cooling element in the thermal isolation chamber claim 2 , wherein the fan is thermally coupled to the cooling element to provide cooled air to the first cyclical air flow path.4. The thermal isolation chamber of claim 3 , wherein the cooling element is downstream of the fan.5. The thermal isolation chamber of claim 3 , wherein the cooling element is upstream of the fan.6. The thermal isolation chamber of claim 1 , ...

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31-03-2022 дата публикации

PROCESS FOR REMOVING LEAD, MERCURY, POTASSIUM, AND AMMONIUM IONS FROM BODILY FLUIDS USING RARE-EARTH SILICATE ION EXCHANGE COMPOSITIONS

Номер: US20220096962A1
Принадлежит:

A process for removing Pb, Hg, K and NH toxins from bodily fluids is disclosed. The process involves contacting the bodily fluid with an ion exchange composition to remove the metal toxins in the bodily fluid, including blood and gastrointestinal fluid. Alternatively, blood can be contacted with a dialysis solution which is then contacted with the ion exchange composition. The ion exchange compositions are represented by the following empirical formula: 2. The process of wherein the bodily fluid is selected from the group consisting of whole blood claim 1 , blood plasma claim 1 , or other component of blood claim 1 , gastrointestinal fluids and dialysate solution containing blood claim 1 , blood plasma claim 1 , other component of blood or gastrointestinal fluids.3. The process of where x=0.4. The process of where A is a mixture of calcium and an alkali metal.5. The process of where A is not potassium.6. The process of where A is not ammonium.7. The process of where the ion exchanger is packed into hollow fibers incorporated into a membrane.8. The process of wherein said ion exchanger is contained on particles coated with a coating comprising a cellulose derivative composition.9. The process of wherein said process is a hemoperfusion process wherein said bodily fluid is passed through a column containing said ion exchanger.10. The process of wherein a dialysate solution is introduced into a peritoneal cavity and then is flowed through at least one adsorbent bed containing at least one of said ion exchanger.11. The process of wherein said ion exchanger is formed into a shaped article to be ingested orally claim 1 , followed by ion exchange between said ion exchanger and said Pb claim 1 , Hg claim 1 , K and NH toxins contained in a gastrointestinal fluid in a mammal's intestines and then by excretion of said ion exchanger containing said toxins.12. The process of wherein said shaped article is coated with a coating that is not dissolved by conditions within a stomach. ...

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25-03-2021 дата публикации

Method for refining vasopressin

Номер: US20210087226A1

A method for refining vasopressin, including: subjecting a crude vasopressin solution to reversed-phase enrichment, reversed-phase salt conversion and reversed-phase purification sequentially using reversed-phase high performance liquid chromatography. The crude vasopressin solution is obtained by oxidizing a crude reduced vasopressin prepared by solid phase synthesis. A super water-resistant packing material is used in the reversed-phase high performance liquid chromatography.

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25-03-2021 дата публикации

DEVICES AND METHODS FOR PLASMID PURIFICATION

Номер: US20210087551A1
Принадлежит: PHYNEXUS, INC.

The invention provides columns (including pipette tip columns) and automated methods for the purification of nucleic acids including plasmids. Nucleic acids can be purified from unclarified, clarified or partially-clarified cell lysates that contain cell debris. The columns typically include a bed of medium positioned above a bottom frit and with an optional top frit. Plasmid preparation scales include miniprep, midiprep, maxiprep, megaprep and gigaprep. 119.-. (canceled)20. An automated method for large scale plasmid preparation comprising:(a) providing a cell lysate, the cell lysate comprising cell debris, liquid, and plasmid DNA;(b) providing a column, the column configured to capture plasmid DNA;(c) providing a filter;(d) passing the cell lysate through the filter to produce a filtrate;(e) passing the filtrate through the column such that a portion of the plasmid DNA is captured on the column;(f) passing a wash solution through the column; and(g) eluting the plasmid DNA by passing a desorption solution through the column, wherein an amount of plasmid DNA eluted from the column is between 20 and 200 μg,wherein the passing the filtrate through the column, the passing the wash solution through the column, and the eluting the plasmid DNA are performed at predetermined times.21. The method of claim 20 , wherein at least two cell lysates are processed in parallel.22. The method of claim 20 , where in the filter has a pore size greater than 10 μm.23. The method of claim 20 , wherein the filtrate is passed through the column by aspiration/expulsion claim 20 , vacuum claim 20 , pressure claim 20 , or gravity.24. The method of claim 20 , wherein the passing the cell lysate through the filter claim 20 , the passing the filtrate through the column claim 20 , and the passing the wash solution through the column are performed by vacuum.25. The method of claim 20 , wherein an area of the filter is at least 3 cm. This invention relates to methods and devices for sample ...

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19-06-2014 дата публикации

ANTIMICROBIAL SOLUTIONS AND METHODS

Номер: US20140166565A1
Автор: Code Kenneth R.
Принадлежит: BIOLARGO LIFE TECHNOLOGIES, INC.

Contaminants are filtered from a fluid flow stream and the filter is regenerated by a process including steps of: providing a filter material comprising both carbon and potassium iodide; passing a contaminated fluid stream in contact with the filter material; adsorbing contaminants from the fluid stream onto surfaces in the filter material; passing an electric current through the filter material with adsorbed contaminant thereon; disassociating contaminant from the surfaces of the filter material; and removing disassociated contaminant from the filter material by carrying away the disassociated contaminant in a fluid flow mass. 1. An apparatus for removing contamination from a fluid stream comprising: a) a housing containing a filter material having two opposed surfaces , the filter material comprising carbon and an activating agent selected from the group consisting of an alkali metal halogen and an alkaline halogen; b) a fluid inlet port to the housing; c) a fluid outlet port from the housing; d) a source of contaminated fluid available to the fluid inlet port; e) a device for moving fluid through the inlet port and through the outlet port; f) a current source that passes current through the filter material between the two opposed surfaces; and g) a source of fluid flow mass to move fluid mass over the filter material after or during passage of direct current over the filter material.2. The apparatus of wherein the filter material comprises activated carbon and at least 0.05% by total weight of solids of halide salt.3. The apparatus of wherein the halide salt comprises an iodide salt.4. The apparatus of wherein the iodide salt comprises potassium iodide is distributed on at least some surfaces of the activated carbon.5. The apparatus of wherein a source of electric current is provided to be able to apply electric current at a range of voltages at least between 2.0 and 15 volts.6. The apparatus of wherein the current source is located at a position along a path for ...

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29-03-2018 дата публикации

IN SITU RESTORATION OF APATITE-BASED CHROMATOGRAPHY RESINS

Номер: US20180086638A1
Автор: Cummings Larry J., He Jie
Принадлежит:

Methods and compositions are provided for treatment of an apatite-based resin from which retained solutes have been eluted by an elution buffer that contains an alkali metal salt with solutions of calcium ion, phosphate ion, and hydroxide separately from any sample loading and elution buffers. The treatment solutions restore the resin, reversing the deterioration that is caused by the alkali metal salt in the elution buffer. 2. (canceled)3. The method of claim 1 , wherein target molecules are extracted from a plurality of samples contacted in succession with said resin claim 1 , and steps (i) claim 1 , (ii) claim 1 , and (iii) are performed after each of said samples is contacted with said resin.4. The method of claim 1 , further comprising passing an aqueous wash solution through said resin after each of steps (i) and (ii).5. The method of claim 3 , further comprising passing an aqueous wash solution through said resin after each of steps (i) claim 3 , (ii) claim 3 , and (iii).6. (canceled)7. (Canceled)8. The method of claim 1 , wherein said solution of calcium ion is passed through said resin in an amount of from about 1.0 resin volume to about 10.0 resin volumes.9. The method of claim 1 , wherein said solution of calcium ion has a calcium ion concentration of about 30 ppm to about 1000 ppm claim 1 , and is passed through said resin in an amount of about 1.5 resin volumes to about 6.0 resin volumes.10. The method of claim 1 , wherein said solution of phosphate ion has a pH of about 6.5 to about 9.0 claim 1 , and is passed through said resin in an amount of from about 1.0 resin volume to about 20.0 resin volumes.11. The method of claim 1 , wherein said solution of phosphate ion has a pH of about 6.5 to about 7.5 claim 1 , has a phosphate ion concentration of about 200 mM to about 750 mM claim 1 , and is passed through said resin in an amount of about 1.5 resin volumes to about 10.0 resin volumes.12. The method of claim 1 , wherein said solution of hydroxide ion is ...

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