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

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29-08-2018 дата публикации

Способ получения хроматографического материала

Номер: RU2665442C2

Изобретение относится к способу получения материала для хроматографии. Предложен способ получения материала для хроматографии (ОФХ), включающий следующие стадии: аллилирование частиц пористого полисахаридного материала с помощью аллилглицидилового эфира и прививание стирольных мономеров, выбранных из стирола, трет-бутилстирола и пентафторстирола, на указанные частицы, содержащие аллильную группу. Материал обеспечивает улучшенное разделение пептидов. 4 н. и 3 з.п. ф-лы, 17 ил., 3 табл.

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27-07-2001 дата публикации

ПРОИЗВОДНЫЕ 2,6-ДИГИДРОКСИ-4-АМИНОМЕТИЛБЕНЗОАТА

Номер: RU2171250C2
Принадлежит: ПРОЛИНКС, ИНК. (US)

Изобретение относится к новым соединениям формулы СI, где группа Z обозначает спейсер, выбранный из насыщенной или ненасыщенной цепи, длина которой равна от приблизительно 0 до 6 атомам углерода, неразветвленной насыщенной или ненасыщенной цепи, длина которой равна 6 - 18 атомам углерода, по крайней мере с одним промежуточным амидным или дисульфидным фрагментом и полиэтиленгликолевой цепи, длина которой равна 3 - 12 атомам углерода; R1 обозначает электрофильный или нуклеофильный фрагмент, пригодный для вступления производного в реакцию с биологически активными компонентами и выбранными из группы, включающей такие фрагменты, как акриламид, аминогруппа, бром, дитиопиридил, бромацетамид, гидразид, N-гидроксисукцинимидный эфирный остаток, N-гидроксисульфосукцинимидный эфирный остаток, имидатный эфирный остаток, имидазолил, йод, йодацетамид, малеимид и тиол, R2 обозначает одну из таких групп, как алкильная и метиленовая, несущая электроотрицательный фрагмент с отрицательным дипольным моментом ...

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10-03-2006 дата публикации

МИКРОСФЕРЫ ТЕРМОПЕРЕРАБАТЫВАЕМОГО СОПОЛИМЕРА ТЕТРАФТОРЭТИЛЕНА

Номер: RU2271366C2
Принадлежит: АУСИМОНТ С.П.А. (IT)

Изобретение относится к микросферам термоперерабатываемого сополимера тетрафторэтилена, имеющим в основном сферическую форму для, по меньшей мере, 95% по массе. Средний размер микросфер находится в диапазоне 25 мкм-2 мм, объемная плотность находится в диапазоне 0,5-1,1 г/см3. Изобретение также относится к устройству для коагуляции и способу получения микросфер. Изобретение позволяет получить микросферы термоперерабатываемого сополимера тетрафторэтилена, имеющие хорошо определенную морфологию и регулируемый размер, а также имеющие улучшенную сыпучесть. 3 н. и И 15 з.п. ф-лы, 2 табл., 4 ил.

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27-03-2001 дата публикации

СПОСОБ ПРИГОТОВЛЕНИЯ СОРБЕНТА ДЛЯ ГАЗОЖИДКОСТНОЙ ХРОМАТОГРАФИИ

Номер: RU2164683C2

Изобретение относится к области приготовления колонок для газожидкостной хроматографии, в частности к способам приготовления сорбентов путем нанесения неподвижной жидкой фазы на твердый носитель, и может использоваться для анализа в санитарно-гигиенических лабораторных исследованиях. Сущность изобретения заключается в том, что нанесение неподвижной жидкой фазы осуществляют путем создания пенного слоя пропусканием инертного газа через барботер, на диспергирующей поверхности которого находится неподвижная жидкая фаза, и последующим гашением пены добавлением твердого носителя. Технический результат заключается в уменьшении потерь от измельчения сорбента и сохранении его дисперсного состава. 2 табл.

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25-06-2024 дата публикации

СПОСОБ ИЗВЛЕЧЕНИЯ ИОНОВ СЕРЕБРА ИЗ МНОГОКОМПОНЕНТНЫХ АЗОТНОКИСЛЫХ РАСТВОРОВ ПОСРЕДСТВОМ ИСПОЛЬЗОВАНИЯ ОРГАНИЧЕСКОГО СОРБЕНТА

Номер: RU2821533C1

Изобретение относится к извлечению ионов серебра из многокомпонентных азотнокислых растворов и может быть использовано в практике научно-исследовательских, аналитических и производственных лабораторий. Ионы серебра извлекают из многокомпонентных азотнокислых растворов, показатель кислотности среды которых находится в диапазоне от 1 до 2, посредством использования органического сорбента. Концентрация ионов сопутствующих металлов в многокомпонентном азотнокислом растворе составляет от 1⋅10-5 до 1⋅10-2 моль/дм3. В качестве сорбента используют тиокарбамоилированный полиметилстирол, полная динамическая сорбционная емкость которого составляет 0,16 ммоль/г, а динамическая сорбционная емкость до проскока - 0,10 ммоль/г. Скорость пропускания раствора через сорбент 2 см3/мин. Десорбцию сорбированных ионов серебра осуществляют путем пропускания азотнокислого раствора тиомочевины через слой сорбента. После стадии десорбции сорбент применяют повторно для извлечения ионов серебра. Способ позволяет селективно ...

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30-04-1994 дата публикации

СПОСОБ ГАЗОХРОМАТОГРАФИЧЕСКОГО АНАЛИЗА

Номер: RU2011989C1

Использование: изобретение относится к газовому анализу смесей, в частности газохроматографическому, позволяющему проводить полное разделение компонентов газовой смеси, состоящей из пропана, воздуха и диоксида углерода, в присутствии влаги при комнатной температуре. Сущность: способ основывается на использовании хроматографической колонки, заполненной сорбентом на основе носителя "Полисорб-1", который дополнительно содержит "Силипор-600". Соотношение составляющих, % 25 - 35 - "Полисорб-1", 75 - 65 - "Силипор-600". Колонка заполняется приблизительно на 1/3 длины "Полисорб-1", остальное - "Силипор-600", который расположен по ходу газа за "Полисорбом-1". Анализируемая смесь поступает вначале на "Полисорб-1", затем - на "Силипор-600". 6 ил.

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27-04-2020 дата публикации

СПОСОБ ОЧИСТКИ СМОЛ

Номер: RU2720196C1

Предусматривается способ очистки совокупности гранул смолы, при этом способ предусматривает приведение совокупности гранул смолы в контакт с водным раствором, где водный раствор содержит одно или несколько растворенных аминосоединений, а совокупность гранул смолы содержит полимер, который содержит присоединенные группы, представляющие собой остатки карбоновой кислоты, или группы, представляющие собой остатки сульфоновой кислоты, или их смесь. 6 з.п. ф-лы, 3 табл.

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20-04-2016 дата публикации

КОМПОЗИЦИЯ ДЛЯ ДЕТОКСИКАЦИИ ОРГАНИЗМА

Номер: RU2014139542A
Принадлежит:

... 1. Композиция для очищения организма от токсинов в виде геля, содержащая в качестве активного компонента нерастворимый энтеросорбент, отличающаяся тем, что содержит второй активный компонент в виде растворимого энтеросорбента, при этом растворимый энтеросорбент формирует матрицеобразующую основу для нерастворимого сорбента, нерастворимый сорбент и растворимый сорбент имеют размер частиц не более 150 мкм, при следующем содержании компонентов, в масс %:- нерастворимый энтеросорбент 3-70%;- растворимый энтеросорбент 0,1-70%.2. Композиция по п. 1, отличающаяся тем, что содержит в качестве нерастворимого энтеросорбента компоненты из группы: растительная клетчатка, лигнин гидролизный, отруби, целлюлоза и ее эфиры, микрокристаллическая целлюлоза, высокоэтерифицированный нерастворимый пектин или минеральное вещество из группы: цеолит, смектит, кремнезем (кремния диоксид), активированный уголь.3. Композиция по п. 1, отличающаяся тем, что содержит в качестве растворимого сорбента пищевые волокна ...

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23-11-1991 дата публикации

Способ газохроматографического анализа смеси вода, формальдегид, метанол

Номер: SU1693535A1
Принадлежит:

Изобретение относится к газовой хроматографии , а именно к газохроматографи- ческому разделению и анализу смесей, содержащих воду, формальдегид, метанол. Цель изобретения - повышение эффективности и селективности разделения. Сущность способа заключается в использовании в качестве сорбента для разделения такого рода смесей сополимеров стирола и дивинилбензола, модифицированного цезием. Количество модификатора составляет 20-50% от массы полимерного сорбента. Разделение осуществляют на колонне с сорбентом при 150-190°С, 1 ил., 2 табл.

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07-08-1983 дата публикации

Способ обработки полимерного сорбента для хроматографии

Номер: SU1033181A1
Принадлежит:

СПОСОБ ОБРАБОТКИ ПОЛИМЕРНОГО СОРБЕНТА ДЛЯ ХРОМАТОГРАФИИ, преимущественно на основе сополимера стирола и дивинилбензола путем его нагревания в токе инертного газа, о тл и чают и и с я тем, что, с целью повышения термостойкости сорбента, предварительно сорбент облучают гамма-излучением изото- . па экспозиционной дозой 2«10 :о 3 -10 рентген, ...

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30-06-1976 дата публикации

Способ получения сорбентов

Номер: SU520052A3
Принадлежит: БАЙЕР АГ, (ФИРМА)

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23-08-1984 дата публикации

Способ определения смоляных кислот в хвойных бальзамах и продуктах их переработки

Номер: SU1109633A1
Принадлежит:

СПОСОБ ОПРЕДЕЛЕНИЯ СМОЛЯНЫХ КИСЛОТ В ХВОЙНЫХ БАЛЬЗАМАХ И ПРОДУКТАХ ИХ ПЕРЕРАБОТКИ путем капиллярной газожидкостной хроматографии метиловых эфиров смоляных кислот с использованием неподвижной жидкой фазы, отличающийся тем, что, с целью упрощения анализа , в качестве неподвижной жидкой фазы используют цианозтилметилсиликоновый эластомер ХЕ-60, содержащий 25% цианозтильньгх групп. СО О5 со оо ...

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07-04-1989 дата публикации

Колонка для жидкостной хроматографии и способ ее заполнения

Номер: SU1471958A3

Изобретение относится к аналитическому приборостроению и может быть использовано в химической, медицинской, биологической и других отраслях промышленности для анализа сложных смесей веществ методом высокоэффективной жидкостной хроматографии. Цель изобретения - повышение скорости хроматографирования, разрешающей способности колонки и обеспечение прямого анализа сыворотки и других компонентов крови. Колонка заполнена полностью пористым гидрофильным гелем, в состав которого входят фрагменты винилового спирта. Гель имеет средневесовой диаметр гранул от 4 до 20 мкм, величину влагоудерживания от 0,6 до 2,0 мл/г и концентрацию гидроксильных групп от 3 до 15 мэкв/г. Гельный слой имеет степень однородности от 2,0 до 4,0 определяемую через отношение ВЭП к средневесовому диаметру гранул и упаковочное отношение от 0,66 до 0,78, определяемое по формуле 1 - VOVT,где VO означает объем воды с наружной стороны гранул,VT -общий объем колонки. Колонку заполняют путем продвижения гельной суспензии потоком ...

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04-06-1992 дата публикации

Liq. chromatographic system for determining glycosylated forms of haemoglobin - including sepn. column, automatic sampler, eluent selection system and control elements

Номер: DE0004139683A1
Принадлежит:

Liq. chromatography system comprises (1) device for taking a sample and supplying it, as well as least one eluent, to at least one sepn. column; (2) device for supplying eluent; (3) device for detecting components separated on the column, and (4) control system for (a) calculating the component ratios and other parameters of the detected components, (b) detecting the operational conditions of the working elements of the system and (c) forwarding signals to these working elements. The column is packed with an organic porous material carrying functional (esp. carboxyalkyl) gps. and in the dry state has pore dia. 6-120mm; ion exchange capacity 0.1-0.5 meq/g; particle size 3-4 microns and pore vol. 0.2-0.6 ml/g. USE/ADVANTAGE - The system is used to analyse biological and living compounds, in blood etc. esp. glycosylated forms of haemoglobulin (Hb) to monitor the long term glucose status of diabetics. It allows analysis of all 5 or 6 Hb components an dprovides rapid sepn. of the stable glycosylated ...

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25-09-1986 дата публикации

CHROMATOGRAPHISCHES TRENNMEDIUM FUER DIE SCHNELLE ANALYSE VON KLEINEN PROBEN

Номер: DE0003609021A1
Принадлежит:

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21-04-2011 дата публикации

MONODISPERSE PARTIKEL VERWENDENDE KAPILLARSÄULEN

Номер: DE0060144178D1
Автор: MYERS PETER, MYERS, PETER

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15-03-1978 дата публикации

METHOD FOR PREPARATION OF CATION EXCHANGERS OF HYDROPHILIC POLYMERIC GELS

Номер: GB0001503604A
Автор:
Принадлежит:

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25-01-1978 дата публикации

METHOD FOR THE PREPARATION OF HYDROPHILIC ION EXCHANGERS

Номер: GB0001499134A
Автор:
Принадлежит:

... 1499134 Hydrophilic ion exchange resins CESKOSLOVENSKA AKADEMIE VED 12 Feb 1975 [13 Feb 1974] 5983/75 Heading C3P Macroporous hydrophilic ion exchange resins are obtained by alkylation or hydroxyalkylation - of amino groups in a cross-linked hydroxyalkylacrylate or hydroxyalkylmethacrylate copolymer. The amino groups may be introduced into a pre-formed polymer, or provided by including an aminoalkyl - (meth)acrylate or (meth)acrylamide monomer when preparing the polymer. In Examples (1, 2 and 5) a 2- hydroxyethyl methacrylate/diethylaminoethyl methacrylate/ethylene glycol dimethacrylate copolymer is reacted, respectively, with butyl bromide, ethyl bromide and butyl p-toluene sulphonate; (3) a 2-hydroxyethyl methacrylate/ ethylene glycol dimethacrylate copolymer is activated with cyanogen bromide and then reacted sequentially with ethylene diamine, ethylene oxide and ethyl bromide; and (4) the copolymer used in (3) is reacted sequentially with thionyl chloride, polyethylene imino and ethyl ...

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16-11-1977 дата публикации

PREPARATION OF PARTICULATE CROSS-LINKED POLYMERS

Номер: GB0001492428A
Автор:
Принадлежит:

... 1492428 Porous cross-linked polymer particles SHOWA DENKO KK 4 June 1975 [4 June 1974] 24161/75 Heading C3C Porous cross-linked polymer particles are obtained by polymerizing in aqueous suspension a mixture comprising up to 95% monovinyl aromatic monomer and at least 5% divinyl aromatic monomer, in the presence of paraffin wax and an initiator, removing the paraffin wax from the resulting polymer and, if desired, introducing ion exchange groups into the polymer. In the examples, the monomers comprise (1) divinyl benzene (55%), ethyl vinyl benzene (40%) and other unsaturated compounds (5%) and (2) a mixture of (1) together with about 400% of styrene. Benzoyl peroxide was used as the initiator and sodium dodecyl benzene sulphonate and tricalcium phosphate were also present. Polymerization was effected at 95‹ C. in an autoclave and after washing and drying, the paraffin wax was removed by passing mineral spirit through a column of the particles. Methanol was then passed through and the resultant ...

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26-01-1983 дата публикации

FILLER COMPOSITION FOR USE IN LIQUID CHROMATOGRAPHY

Номер: GB0002042557B
Автор:

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31-12-1979 дата публикации

Method of preparation of sorbing.

Номер: OA0000004296A
Автор:
Принадлежит:

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25-08-1980 дата публикации

HIGH FREQUENCY COAXIAL CABLE FOR ANTENNA LINES AND PROCEDURE FOR ITS PRODUCTION

Номер: AT0000358115B
Автор:
Принадлежит:

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15-04-2009 дата публикации

PROTEIN INTERACTION DIFFERENCE ILLUSTRATION

Номер: AT0000426808T
Принадлежит:

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15-04-2009 дата публикации

PROCEDURE FOR PACKING CAPILLARY AULA WITH PARTIKELFÍRMIGEN MATERIALS

Номер: AT0000427151T
Принадлежит:

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15-03-2009 дата публикации

POLYMERE CARRIER WITH VOID STRUCTURES

Номер: AT0000425195T
Принадлежит:

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15-07-1994 дата публикации

VERFAHREN ZUR TRENNUNG VON NUKLEINSÄUREN

Номер: ATA228592A
Автор:
Принадлежит:

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15-07-1994 дата публикации

PROCEDURE FOR THE SEPARATION FROM NUCLEIC ACIDS

Номер: AT0000228592A
Автор:
Принадлежит:

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15-08-1976 дата публикации

PROCEDURE FOR THE PRODUCTION OF HYDROPHILIC CATION EXCHANGERS FROM POLYMERS GELS

Номер: AT0000079575A
Автор:
Принадлежит:

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15-08-1976 дата публикации

PROCEDURE FOR THE PRODUCTION OF HYDROPHILIC ANION EXCHANGERS FROM POLYMERS GELS

Номер: AT0000099575A
Принадлежит:

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15-09-2008 дата публикации

PROOF OF NUCLEIC ACID HETERO DUPLEX MOLECULES OF MEANS ANION EXCHANGE CHROMATOGRAPHY

Номер: AT0000408026T
Автор: TAYLOR PAUL, TAYLOR, PAUL
Принадлежит:

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15-05-2011 дата публикации

SEPARABLE MEANS FOR OPTICAL ISOMER

Номер: AT0000506118T
Принадлежит:

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15-01-1992 дата публикации

POLYMER MATRIX FUER AFFINITY CHROMATOGRAPHY AND IMMOBILIZATION OF LIGANDS.

Номер: AT0000070539T
Автор: NGO, THAT T.
Принадлежит:

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15-11-2005 дата публикации

CHROMATOGRAPHI DEVICE

Номер: AT0000307333T
Принадлежит:

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15-04-2006 дата публикации

SURFACE-GRAFT-MODIFIED RESINS AND THEIR PRODUCTION

Номер: AT0000321078T
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15-08-2006 дата публикации

POLYMERE ONE OF ANION EXCHANGER RESINS AND THEIR USE IN CHROMATOGRAPHI PROCEDURES

Номер: AT0000334747T
Принадлежит:

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15-01-2007 дата публикации

MAGNETIC IN SITU DILUTIONSVERFAHREN

Номер: AT0000349011T
Принадлежит:

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15-03-1978 дата публикации

VERFAHREN ZUR HERSTELLUNG VON MAKROPOROSEN IONENAUSTAUSCHERMATERIALIEN AUS HYDROPHILEN POLYMEREN GELEN

Номер: ATA67275A
Автор:
Принадлежит:

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15-11-2003 дата публикации

SEPARATION OF THE METALS OF GROUP OF PLATINUM

Номер: AT0000252163T
Принадлежит:

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15-11-2004 дата публикации

WITH MATERIAL FOAMED SUBSTANCE GEFÜLLLTE

Номер: AT0000279978T
Принадлежит:

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17-09-1992 дата публикации

COATED MEDIA FOR CHROMATOGRAPHY

Номер: AU0000628722B2
Принадлежит:

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28-03-1991 дата публикации

HYDROPHILIC ARTICLE AND METHOD OF PRODUCING SAME

Номер: AU0000608315B2
Принадлежит:

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03-12-2001 дата публикации

Molecular imprinting

Номер: AU0006092101A
Принадлежит:

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15-06-2004 дата публикации

Improved hydrophilic monolithic columns for separation of saccharide mixtures

Номер: AU2003286716A8
Принадлежит:

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20-05-1992 дата публикации

MOSAIC MICROCOLUMNS, SLABS, AND SEPARATION MEDIA FOR ELECTROPHORESIS AND CHROMATOGRAPHY

Номер: AU0008949691A
Принадлежит:

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09-11-2006 дата публикации

Polar functionized polymer modified porous substrate for solid phase extraction

Номер: AU2006242643A1
Принадлежит:

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28-08-2014 дата публикации

Chromatography medium

Номер: AU2009238686B2
Принадлежит:

The present invention is within the field of chromatography. More precisely, it relates to a novel chromatography medium, namely a hydrophobic medium provided with different lids excluding molecules over a certain size due to the porosity of the hydrophobic medium and/or the porosity of the lid. The invention also relates to use of the separation mediumfor purification of large molecules, which do not enter the separation medium, as well as small molecules, which enter the separation medium and are eluted from there.

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10-06-2003 дата публикации

SIZE-EXCLUSION FILTERING DEVICE, METHOD FOR MAKING SAME AND RESULTING FILTERING METHOD

Номер: AU2002356258A1
Автор: LESSER JOEL, JOEL LESSER
Принадлежит:

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10-02-1998 дата публикации

Chemical sample treatment cassette and methods

Номер: AU0003653297A
Автор:
Принадлежит:

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29-01-2004 дата публикации

Large-pore chromatographic beads prepared by suspension polymerization

Номер: AU0000769534B2
Принадлежит:

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22-03-2001 дата публикации

NEW MOLECULARLY IMPRINTED POLYMERS GRAFTED ON SOLID SUPPORTS

Номер: CA0002391811A1
Принадлежит:

The invention refers to a molecularly imprinted polymer, a method of preparing a molecularly imprinted polymer material, and the use thereof. According to the invention a support and a composition comprising at least one monomer, and a template, in a polymerisation medium is polymerised with a free radical initiator, whereafter the template is removed from the molecularly imprinted polymer obtained. The polymerisation is confined to the surface of the support, preferably by confining the free radical initiator to the support by bonding or adsorption. The molecularly imprinted polymer may be used in chromatography, for separations, in chemical sensors, in molecular recognition as stationary phase in capillaries, in selective sample enrichment or in catalysis.

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25-03-1997 дата публикации

OLIGONUCLEOTIDE POLYMERIC SUPPORT SYSTEM

Номер: CA0001339010C
Принадлежит: SYNGENE INC, SYNGENE, INC.

A versatile polymeric support system for the synthesis of oligonucleotides is provided featuring a universal primer which allows chain elongation, in either the 3' or 5' direction, with any currently available DNA or RNA synthesis method, by a process which utilizes oxidatively cleaved primers to facilitate chain elongation and release. The support system is capable of withstanding mildly basic and acidic reaction conditions, while still permitting a convenient and quantitative release, either before or after removal of protecting groups from reactive groups, of synthesized oligonucleotides from a single polymeric support. Removal of the protecting groups before cleavage of the oligomer from the support permits the use of the immobilized oligomer as an affinity hybridization support for both isolation and detecting complementary polynucleic acids.

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02-08-1994 дата публикации

ION-EXCHANGE COMPOSITION EMPLOYING RESIN ATTACHMENT TO DISPERSANT AND METHOD FOR FORMING THE SAME

Номер: CA0001331254C
Принадлежит: DIONEX CORP, DIONEX CORPORATION

In accordance with the present invention, an ionexchange composition has been formed which comprises synthetic resin support particles, dispersant capable of suspending the support particles in an aqueous medium to inhibit or prevent agglomeration, and fine synthetic resin layering particles. In a preferred embodiment, the complex can be formed by contacting a suitable dispersant with monomer in an aqueous solution in which the monomer is insoluble. Under suitable conditions for suspension polymerization, the monomer will polymerize to form resin support particles having dispersant irreversibly attached to those particles. The dispersant is irreversibly attached to the synthetic resin support particles, either by covalent bonding or permanent physical entanglement. The dispersant is also attached to the fine layering particles, either by covalent bonding or electrostatic forces. The result is formation of a support particle-dispersant-layering particle complex. The novel ion-exchange composition ...

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25-09-1979 дата публикации

SMALL, POROUS, POLYACRYLATE BEADS

Номер: CA0001063298A1
Принадлежит:

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28-06-2001 дата публикации

SYSTEM AND METHOD FOR AUTOMATED MATCHED ION POLYNUCLEOTIDE CHROMATOGRAPHY

Номер: CA0002393849A1
Принадлежит:

In an extensive Matched Ion Polynucleotide Chromatography (MIPC) system and method, and the computer programs or software associated therewith, the system provides automated options for sample selection, mobile phase gradient selection and control, column and mobile phase temperature control, and fragment collection for a wide variety of MIPC separation processes. MIPC separation processes can be applied to effect size-based separation of DNA fragments, mutation detection, DNA fragment purification, PCR process monitoring and other novel processes. This invention is directed to the system and software which automates many of these procedures, facilitating use of the system to achieve complex separation methods. In one embodiment of the invention, a user specifies a size range of double stranded DNA fragment(s) in a mixture, the software calculates a solvent gradient to elute the fragment(s), and the system performs the chromatographic separation using the calculated gradient. In an embodiment ...

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11-04-2002 дата публикации

ELECTRONIC DETECTION OF INTERACTION AND DETECTION OF INTERACTION BASED ON THE INTERRUPTION OF FLOW

Номер: CA0002424119A1
Автор: BAMDAD, CYNTHIA C.
Принадлежит:

Porous members can be positioned so as to partially or fully span channels in microfluidic systems. The porous members can be assembled and/or disassembled in situ. The porous members can be made such that pores are separated by connections including but a single molecule at one location, allowing for a high level of open area in a very small pore size member. The porous member can be made up of colloid particles interconnected with molecular species. These can be used to detect analytes qualitatively and/or quantitatively, or to selectively bind and/or release agents on command for a variety of purposes including first blocking, then opening a channel, concentrating analyte over time followed by release of analyte and detection downstream, etc. Porous members can define valves in multiple-channel systems and, with controlled binding and release of agents at the porous members, these valves can be opened and closed and fluid flow controlled in a multi-channel system. Fluidic systems of ...

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13-04-1982 дата публикации

POLAR POLYMERIC SORBENTBASED ON GLYCIDYL ESTERS FOR GAS AND LIQUID CHROMATOGRAPHY

Номер: CA0001121944A1
Принадлежит:

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15-04-1993 дата публикации

COVALENTLY REACTIVE PARTICLES INCORPORATED IN A CONTINUOUS POROUS MATRIX

Номер: CA0002114732A1
Принадлежит:

... 2114732 9306925 PCTABS00021 A composite article is provided having covalently reactive particles incorporated in a continuous, porous matrix. The reactive particles have surfaces of covalently reactive functional groups capable of directly forming covalent chemical bonds with ligands without need for an intermediate activation step. An adduct composite article is also provided comprising a continuous, porous matrix and derivatized particles dispersed therein. The derivatized particles comprise a direct, covalent reaction product of ligand with the covalently reactive particles. Methods of making and using the composite articles and adduct composite articles are also provided. Preferred covalently reactive functional groups are azlactone-functional groups of formula (I), wherein R1 and R2 independently can be an alkyl group having 1 to 14 carbon atoms, a cycloalkyl group having 3 to 14 carbon atoms, an aryl group having 5 to 12 ring atoms, an arenyl group having 6 to 26 carbon and 0 to 3 ...

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15-05-1997 дата публикации

ADSORPTION METHOD AND SEPARATION MEDIUM

Номер: CA0002236875A1
Принадлежит:

A population of beads having a density > 1 g/cm-3 and comprising a polymer base matrix in which a particulate filler is incorporated. The beads are characterized in that the filler particles have a density >= 3 g/cm-3 and in that the density and/or size of the beads are distributed within predetermined density and size ranges. Particularly important filler particles are those which have rounded shapes, for instance spheres, ellipsoids or aggregates/agglomerates thereof. The bead population is particularly usable in adsorption processes in fluidized beds, with preference to stable expanded beds.

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04-09-1997 дата публикации

REMOVAL OF BORATE IN CHROMATOGRAPHY

Номер: CA0002247927A1
Принадлежит:

Borate-binding compositions are provided comprising polymers containing covalently attached borate-binding carbohydrates. Methods of making and using the compositions are also provided.

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03-07-1998 дата публикации

CHROMATOGRAPHY COLUMNS WITH CONTINUOUS BEDS FORMED IN SITU FROM AQUEOUS SOLUTIONS

Номер: CA0002225703A1
Принадлежит:

A chromatography column with a continuous solid bed spanning the cross section o f the column, the bed containing channels large enough for hydrodynamic flow, is p repared by polymerizing a mixture of monomers and ammonium sulfate in an aqueous solutio n. The monomers include a monofunctional monomer such as a vinyl, allyl, acrylic, o r methacrylic compound, and a polyfunctional monomer (i.e., a crosslinker), the to tal monomer concentration being in the range of 10% to 20% by weight, the mole ratio of crosslinker to total monomer being in the range of 0.3 to 0.4, and the ammonium sulfate having a concentration in the range of 0.4 M to 0.8 M. Functional groups to impa rt specialized separation capabilities, notably anion and cation exchange, can be i ncluded in the monomer mixture.

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10-01-1992 дата публикации

COATED SINGLE PARTICLES AND THEIR USE IN FLUID BED CHROMATOGRAPHY

Номер: CA0002259061A1
Принадлежит:

A fluidized bed chromatographic process for purification and binding of molecules in a liquid by binding the molecules to an active substance covalently bound to chromatographic adsorbent particles in which process a fluidized bed of the adsorbent particles is formed and the liquid is passed through the fluidized bed, the improvement wherein the chromatographic adsorbent particles comprise a porous composite material having pores allowing access to the interior of the composite material by the molecules, and the porous composite material of each absorbent particle consists of a single density controlling particle which is either (a) a hollow low density particle which is impermeable to the liquid and has a density providing floatation of the adsorbent particle in the liquid or, (b) a high density particle having a density providing sedimentation of the adsorbent particle in the liquid, a matrix formed by consolidating at least one conglomerating agent selected from the group consisting ...

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12-02-1998 дата публикации

BORONIC COMPOUND COMPLEXING REAGENTS AND HIGHLY STABLE COMPLEXES

Номер: CA0002262682A1
Принадлежит: FETHERSTONHAUGH & CO.

Boron compound complexing reagents, intermediate reagents of those reagents and methods of synthesizing these reagents are disclosed. These reagents, including those shown as General Formula (I) and General Formula (II) may be used, after further reactions described herein, to complex with boronic compounds, such as phenylboronic acid or derivatives thereof. Boron compound complexing reagents, boron compound complexes, and methods of synthesizing these reagents and complexes are disclosed. These reagents and complexes include those shown in General Formula (CIII), General formula (CIV), and General Formula (CVI). In one embodiment, the reagents of General formula (CIII) may be used to produce, after condensation with a bioactive species (BAS), the reagent of General Formula (CIV). The reagent of General Formula (CIV) may be used to form a complex with a boron compound, such as a complex shown in General Formula (CVI).

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30-06-1981 дата публикации

PROCEDURE FOR THE PRODUCTION OF HYDROPHILIC CATION EXCHANGERS.

Номер: CH0000623836A5
Принадлежит: CESKOSLOVENSKA AKADEMIE VED

Подробнее
15-09-1978 дата публикации

Номер: CH0000604384A5
Автор: VOSER OTHMAR, OTHMAR VOSER

Подробнее
31-10-1978 дата публикации

Номер: CH0000606153A5
Принадлежит: CESKOSLOVENSKA AKADEMIE VED

Подробнее
31-03-1978 дата публикации

Номер: CH0000597307A5
Принадлежит: BAYER AG

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28-03-2013 дата публикации

Recycling Superabsorbent Polymer Fines

Номер: US20130079221A1
Принадлежит: Evonik Stockhausen, LLC

A process is described for recycling superabsorbent polymer fines into a process that includes treating the superabsorbent polymer fines with caustic and a polymerization step for making the superabsorbent polymer gel. The process requires treating the superabsorbent polymer fines with a caustic, followed by mixture with polymerizable monomer solution, and polymerizing the mixture of the superabsorbent polymer fines and monomer to form the aqueous fluid absorbent polymer. In the process, the fines are incorporated into the new polymer gel and become indistinguishable there from. The gel may then be comminuted into a particulate dried and then separated into a portion having a desired minimum particle size in a fines portion having less than the desired size. The particulate may then be coated with a surface crosslinking agent and surface additives and heated for surface conversion. 186-. (canceled)87. A superabsorbent polymer composition comprising:(i) caustic treated superabsorbent polymer fines treated with from about 1 to about 12 wt % of a caustic solution comprising sodium hydroxide, sodium carbonate or sodium bicarbonate wherein the superabsorbent polymer fines have a particle size of less than about 150 μm.88. The superabsorbent polymer composition of claim 87 , further comprising (ii) a monomer solution comprising acrylic acid wherein from about 0.1 to about 30 wt % of the caustic treated superabsorbent polymer fines of (i) based on the weight of the monomer solution are added to the monomer solution.89. The superabsorbent polymer composition of claim 88 , further comprising (iii) from about 0.001 to about 5.0 wt % based on the monomer of an internal crosslinking agent.90. The superabsorbent polymer composition of claim 88 , wherein the acrylic acid of the monomer solution is neutralized to from about 50 mol % to about 80 mol %.91. The superabsorbent polymer composition of claim 87 , wherein the superabsorbent polymer composition comprises less than 10% ...

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04-07-2013 дата публикации

METHOD FOR PRODUCING POROUS PARTICLES, POROUS PARTICLES, ADSORBENT BODY, AND METHOD FOR PURIFYING PROTEIN

Номер: US20130172538A1
Принадлежит: KANEKA CORPORATION

The objective of the present invention is to provide a method for easily producing a porous cellulose particle which can be used as an adsorbent for various substances in a safe manner without using a highly toxic solvent such as a calcium thiocyanate solution. In addition, the objective of the present invention is to provide a porous particle produced by the production method, an adsorbent which contains the porous particle and by which a highly pure protein can be efficiently purified in a safe manner, and a method for purifying a protein by using the adsorbent. The method for producing a porous particle according to the present invention is characterized in comprising the steps of preparing a solution containing cellulose and an ionic liquid; preparing a dispersion by dispersing the obtained cellulose solution into a liquid, wherein the liquid is not compatible with the ionic liquid; and coagulating the dispersion by bringing into contact with an alcohol or an alcohol aqueous solution in order in order to obtain the porous particle. 1. A method for producing a porous particle , comprising the steps of:preparing a solution containing cellulose and an ionic liquid;preparing a dispersion by dispersing the obtained cellulose solution into a liquid, wherein the liquid is not compatible with the ionic liquid; andcoagulating the dispersion by bringing into contact with an alcohol or an alcohol aqueous solution in order to obtain the porous particle.2. The production method according to claim 1 , wherein water and/or an alcohol is added and an amount of the water and/or alcohol to be added is adjusted to be not less than 2 wt % and not more than 20 wt % relative to a total amount with the ionic liquid in the step for preparing the cellulose solution.3. The production method according to claim 1 , wherein a temperature of the cellulose solution is adjusted to be not less than 0° C. and not more than 70° C.4. The production method according to claim 1 , wherein the ...

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11-07-2013 дата публикации

SUPERABSORBENT POLYMER HAVING A CAPACITY INCREASE

Номер: US20130175472A1
Принадлежит: Evonik Stockhausen, LLC

The present invention relates to a particulate superabsorbent polymer comprising a monomer and an internal crosslinker agent wherein the particulate superabsorbent polymer has a Centrifuge Retention Capacity Increase of 2 g/g or more as set forth herein in the Centrifuge Retention Capacity Increase Test. The present invention further relates to a superabsorbent polymer comprising an internal crosslinker agent comprising a silane compound comprising at least one vinyl group or one allyl group attached to a silicon atom, and at least one Si—O bond. The present invention further relates to an absorbent article that includes such particulate superabsorbent polymers. 136-. (canceled)37. A particulate superabsorbent polymer comprising a polymerized monomer selected from an ethylenically unsaturated carboxylic acid , ethylenically unsaturated carboxylic acid anhydride , salts or derivatives thereof , and an internal crosslinker agent comprising an internal crosslinking agent wherein the internal crosslinker agent comprises a silane compound comprising at least one vinyl group or allyl group and at least one Si—O bond wherein the vinyl group or allyl group is directly attached to a silicon atom.38. The particulate superabsorbent polymer of claim 37 , wherein the particulate superabsorbent polymer has a Centrifuge Retention Capacity of from about 25 g/g to about 55 g/g as set forth herein in the Centrifuge Retention Capacity Test.39. The particulate superabsorbent polymer of claim 37 , wherein the particulate superabsorbent polymer has a Absorbency Under Load at 0.9 psi of about 15 g/g to about 25 g/g as set forth herein in the Absorbency Under Load at 0.9 psi Test.40. The particulate superabsorbent polymer of having a Gel Bed Permeability of from about 10×10cmto about 300×10cmas set forth herein in the Gel Bed Permeability Test.42. The particulate superabsorbent polymer according to wherein said silane compound is selected from vinyltriisopropenoxy silane claim 41 , ...

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11-07-2013 дата публикации

Impregnated nonwoven for degreasing food

Номер: US20130177686A1
Принадлежит:

Various embodiments relate to an impregnated nonwoven for degreasing food, to a process for degreasing food and to a process for manufacturing the impregnated nonwoven. 1. An impregnated nonwoven for degreasing food , the impregnated nonwoven comprising at least a nonwoven and an impregnating composition , wherein the impregnating composition comprises only food grade components and at least an oleophilic substance and an emulsifier.2. The nonwoven according to claim 1 , wherein the oleophilic substance is selected from wax and derivatives claim 1 , silicone and derivatives claim 1 , and mixtures thereof.3. The nonwoven according to claim 2 , wherein the emulsifier is selected from thickeners claim 2 , polysaccharides claim 2 , surfactants claim 2 , polysorbate 20 claim 2 , ceteareth 20 or mixtures thereof.4. The nonwoven according to claim 3 , wherein the ratio of emulsifier to oleophilic substance is in a range from 1:1 to 300 claim 3 ,000.5. The nonwoven according to claim 1 , wherein the impregnated nonwoven comprises 1 to 30 wt. % impregnating composition.6. The nonwoven according to claim 3 , wherein the surfactant is selected from calcium lignin sulfonate or copolymer condesates of ethylene oxide and propylene oxide.7. The nonwoven according to claim 3 , wherein the polysaccharide has a mannose backbone.8. The nonwoven according to claim 1 , wherein the nonwoven is spunbond claim 1 , meltblown or a combination thereof.9. A process for degreasing food claim 1 , wherein the food is contacted with the impregnated nonwoven according to .10. A process for manufacturing the impregnated nonwoven according to claim 1 , wherein the process comprises at least the following processes:a. contacting a thermoplastic nonwoven with a water based emulsion of the oleophilic substance comprising the emulsifier, andb. drying the thermoplastic nonwoven.11. The nonwoven according to claim 1 , wherein the emulsifier is selected from thickeners claim 1 , polysaccharides 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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24-10-2013 дата публикации

WATER-ABSORBENT POLYMER PARTICLES

Номер: US20130281594A1
Принадлежит:

The present invention relates to a process for producing water-absorbent polymer particles by polymerizing droplets of a monomer solution in a surrounding heated gas phase and flowing the gas cocurrent through the polymerization chamber, wherein the temperature of the gas leaving the polymerization chamber is 130° C. or less, the gas velocity inside the polymerization chamber is at least 0.5 m/s, and the droplets are generated by using a droplet plate having a multitude of bores. 1. A process for producing water-absorbent polymer particles by polymerizing droplets of a monomer solution; comprisinga) at least one ethylenically unsaturated monomer which bears acid groups and optionally is at least partly neutralized,b) at least one crosslinker,c) at least one initiator,d) optionally one or more ethylenically unsaturated monomer copolymerizable with the monomer mentioned under a),e) optionally one or more water-soluble polymer, andf) water,in a surrounding heated gas phase and flowing the gas cocurrent through a polymerization chamber, wherein a temperature of the gas leaving the polymerization chamber is 130° C. or less, a gas velocity inside the polymerization chamber is at least 0.5 m/s, and the droplets are generated by using a droplet plate having a multitude of bores.2. A process according to claim 1 , wherein the temperature of the gas leaving the polymerization chamber is from 115 to 125° C.3. A process according to claim 1 , wherein the gas velocity inside the polymerization chamber is from 0.7 to 0.9 m/s.4. A process according to claim 1 , wherein a separation of the bores is from 15 to 30 mm.5. A process according to claim 1 , wherein the diameter of the bores is from 150 to 200 μm.6. A process according to claim 1 , wherein the water-absorbent polymer particles are postcrosslinked with a compound comprising groups which can form at least two covalent bonds with carboxylate groups of the polymer particles.7. A process according to claim 1 , wherein the water ...

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21-11-2013 дата публикации

OXYGEN-ABSORBING FILM, OXYGEN-ABSORBING LAMINATE, OXYGEN-ABSORBING PACKAGING MATERIAL COMPRISING OXYGEN-ABSORBING LAMINATE, AND OXYGEN-ABSORBING RESIN COMPOSITION

Номер: US20130310252A1
Принадлежит: KYODO PRINTING CO., LTD.

An oxygen-absorbing film () is composed of an oxygen-absorbing layer () and thermoplastic resin layers () provided on both surface of the oxygen-absorbing layer (), wherein the oxygen-absorbing layer () comprises both a thermoplastic resin and an oxygen-deficient cerium oxide, and the content of the oxygen-deficient cerium oxide exceeds 50 wt % and is less than 85 wt %. The oxygen-absorbing layer is formed preferably from a resin composition which contains an oxygen-deficient cerium oxide in an amount exceeding 50 wt % and which exhibits a melt flow rate of 1.0 to 18.0 g/10 min. 1. An oxygen-absorbing film , comprising:an oxygen-absorbing layer comprising a thermoplastic resin and an oxygen-deficient cerium oxide; andresin layers arranged on both sides of the oxygen-absorbing layer,wherein the oxygen-absorbing layer comprises the oxygen-deficient cerium oxide in an amount of more than 50% by weight to less than 85% by weight.2. The oxygen-absorbing film according to claim 1 , wherein the oxygen-absorbing layer is formed from a resin composition which comprises said oxygen-deficient cerium oxide in an amount of more than 50% by weight and has a melt flow rate in the range of 1.0 to 18.0 g/10 min.3. An oxygen-absorbing laminate claim 1 , wherein a gas barrier film and/or a base film is/are laminated to the oxygen-absorbing film according to .4. An oxygen-absorbing packaging material claim 3 , which is obtained by forming the oxygen-absorbing laminate according to into a bag.5. A resin composition claim 3 , which comprises:a thermoplastic resin; andan oxygen-deficient cerium oxide,wherein the content of the oxygen-deficient cerium oxide is higher than 50% by weight and said resin composition has a melt flow rate in the range of 1.0 to 18.0 g/10 min.6. An oxygen-absorbing laminate claim 2 , wherein a gas barrier film and/or a base film is/are laminated to the oxygen-absorbing film according to .7. An oxygen-absorbing packaging material claim 6 , which is obtained by ...

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26-12-2013 дата публикации

NOVEL ADSORBENT COMPOSITIONS

Номер: US20130340615A1
Принадлежит:

Adsorbent compositions useful in adsorption and separation processes are made using silicone-derived binding agents. The adsorbent compositions are made from crystallite aluminosilicate particles bound with silicone-derived binding agents, and optionally small amounts of a clay binder, to form agglomerated crystallite particles and are calcined to volatilize the organic components associated with the silicone-derived binding agents. The agglomerated crystallite particles have superior pore structures and superior crush strengths at low binder concentrations and exhibit enhanced Nadsorption rates and capacities when used in air separation processes. 1. A heat treated adsorbent composition comprising a mixture of at least one active material and a silicone-derived binding agent formed as agglomerated particles comprised of 90% or more of the at least one active material calculated on a dry weight final product basis and having:a median pore diameter of equal to or greater than 0.45 μm,10% or less of the macropores and mesopores are of less than or equal to 0.1 μm,a hysteresis factor of equal to or greater than 0.6, anda crush strength value of equal to or greater than that obtained from the value determined by the relationship y=1.2x−0.3 where y is the mean crush strength in lbF and x is the mean particle size in mm.2. The composition of wherein the at least one active material has an average particle size of greater than 1 micron.3. The composition of wherein the one or more zeolites includes a zeolite having a SiO/AlOratio of less than 15.4. The composition of wherein the one or more zeolites includes a zeolite having a SiO/AlOratio of less than or equal to 2.5.5. The composition of wherein the zeolite is LiLSX or LiX.6. The composition of wherein the silicone-derived binding agent is derived from a silicone binder precursor of the general formula [RSiO] claim 1 , where R is one or more organic side groups selected from C1 to C8 organic compounds claim 1 , including ...

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06-02-2014 дата публикации

STABILIZATION OF ONE-POT METHAMPHETAMINE SYNTHESIS SYSTEMS

Номер: US20140034885A1
Автор: Leech Ronald L.
Принадлежит: ACURA PHARMACEUTICALS, INC.

Methods and compositions for stabilizing methamphetamine laboratories, such as by mitigating their explosive potential. 1. An active methamphetamine synthesis laboratory quenching powder mixture comprising:a hygroscopic polymer;a disintegrant;an ion exchange resin; anda water soluble dye.2. The powder mixture of claim 1 , wherein the hygroscopic polymer is present in an amount of about 17 wt % to about 23 wt % of the powder mixture.3. The powder mixture of claim 1 , wherein the hygroscopic polymer comprises polyethylene oxide.4. The powder mixture of claim 1 , wherein the disintegrant is present in an amount of about 35 wt % to about 45 wt % of the powder mixture.5. The powder mixture of claim 1 , wherein the disintegrant comprises crospovidone.6. The powder mixture of claim 1 , wherein the ion exchange resin is present in an amount of about 35 wt % to about 45 wt % of the powder mixture.7. The powder mixture of claim 1 , wherein the ion exchange resin comprises sodium polyacrylate.8. The powder mixture of claim 1 , wherein the water soluble dye is present in an amount of about 0.7 wt % to about 2 wt % of the powder mixture.9. An inactive methamphetamine synthesis laboratory quenching powder mixture comprising:gypsum;a hygroscopic polymer; anda hydrocarbon absorbent polymer.10. The powder mixture of claim 9 , where the gypsum is present in an amount of about 65 wt % to about 80 wt % of the powder mixture.11. The powder mixture of claim 9 , wherein the hygroscopic polymer is present in an amount of about 2 wt % to about 6 wt %.12. The powder mixture of claim 9 , wherein the hygroscopic polymer comprises polyethylene oxide.13. The powder mixture of claim 9 , wherein the hydrocarbon absorbent polymer is present in an amount of about 15 wt % to about 20 wt %.14. The powder mixture of claim 9 , wherein the hydrocarbon absorbent polymer comprises polypropylene hydrocarbon absorbent powder.15. An inactive methamphetamine synthesis laboratory quenching powder mixture ...

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03-04-2014 дата публикации

ABSORBENT STRUCTURE

Номер: US20140094361A1
Принадлежит: Glatfelter Falkenhagen GmbH

An absorbent structure with a sequence of two layers includes at least one liquid absorption layer, a subsequent liquid storage layer with super absorbent polymer particles and super absorbent polymer fibers, and a subsequent liquid distribution layer. The layers are connected and form a sheet structure. The liquid storage layer has its super absorbent polymer extending from the liquid storage layer into the liquid distribution layer in order to generate a return suction effect for the liquid that has passed through the liquid absorption layer and liquid storage layer into the liquid distribution layer. 119-. (canceled)20. A method for producing an absorbent structure , comprising at least the following steps:depositing a first layer for configuring a liquid absorption layer which includes at least cellulose;depositing a second layer which is air laid for configuring a liquid storage layer which includes at least cellulose fibers and super absorbent polymer chosen from the group consisting of super absorbent polymer particles and super absorbent polymer fibers;depositing a third layer which is air laid for forming a liquid distribution layer;moving at least one of the first, second and third layers through a heating device in order to bond the same;supplying at least one of the first, second and third layers to a calender including at least one smooth roller and an opposite roller which form a calender gap; andcompressing the at least one of the first, second and third layers within the calender gap, whereby the super absorbent polymer protrudes from the liquid storage layer into the liquid distribution layer and forms a liquid removing contact between the liquid storage layer and the liquid distribution layer.21. The method according to claim 20 , wherein the first layer is an air laid layer which includes cellulose fibers and bi component fibers.22. The method according to claim 20 , wherein the first layer is air laid layer which includes a highly voluminous ...

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10-04-2014 дата публикации

Porous materials for solid phase extraction and chromatography and processes for preparation and use thereof

Номер: US20140096596A1
Принадлежит: Waters Technologies Corp

The invention provides novel porous materials that are useful in chromatographic processes, e.g., solid phase extraction, and that provide a number of advantages. Such advantages include superior wetting characteristics, selective capture of analytes of interest, and non-retention of interfering analytes. The invention advantageously provides novel porous materials having a large percentage of larger pores (i.e. wide pores). The invention advantageously provides novel porous materials that overcome the problems of SPE of biological samples.

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10-01-2019 дата публикации

METHOD OF CHROMATOGRAPHY ON A POROUS PACKING PRODUCED BY A DRAWING PROCESS

Номер: US20190009251A1
Автор: Parmentier Francois
Принадлежит:

The invention relates to a method of chromatography wherein a gaseous, liquid or supercritical fluid mobile phase, which contains substances to be separated, flows through a porous packing which comprises a plurality of capillary channels which extend in the direction of flow of said mobile phase, 1. A chromatography method wherein a gaseous , liquid or supercritical fluid mobile phase , containing substances to be separated , flows through a porous packing which comprises a plurality of capillary channels which extend in the direction of flow of the mobile phase , a bundle of elementary fibres is assembled, said fibres comprising a core made of a solid, liquid or gaseous material, and a shell made of a drawable material,', 'said bundle is drawn in order to reduce the diameter of the fibres,', 'a porous matrix is made around the core of the drawn fibres, the manufacture of said porous matrix comprising transformation of the shell material, said porous material comprising at least one population of connected pores interconnecting the channels, where the thickness of the porous matrix between two adjacent channels is less than the diameter of the channels, preferably less than half the diameter of the channels,', 'where necessary the core material is removed so as to leave free channels in the porous matrix., 'wherein the packing is manufactured by a method wherein2. The method according to claim 1 , wherein the pores have a diameter greater than twice the molecular diameter of the substances to be separated.3. The method according to claim 1 , wherein the mean diameter of the channels is less than 30 μm claim 1 , and preferably less than 10 μm.4. that the method according to claim 1 , wherein the mobile phase is a gas phase and in that the population of connected pores interconnecting the channels has a mean diameter greater than the mean free path of the species to be separated in the mobile phase.5. that the method according to claim 1 , wherein the bundle is drawn ...

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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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23-01-2020 дата публикации

METHOD FOR MEASURING CONTENT OF WATER-ABSORBING RESIN INCLUDED IN HYGIENIC MATERIAL, ABSORBENT ARTICLE, OR INTERMEDIATE PRODUCT IN MANUFACTURING PROCESS THEREOF, AND METHOD FOR MANUFACTURING HYGIENIC MATERIAL OR ABSORBENT ARTICLE USING THE SAME

Номер: US20200025714A1
Принадлежит: NIPPON SHOKUBAI CO., LTD.

Provided is a convenient, safe, and highly precise method for measuring a content of a water-absorbing resin in a hygienic material or an absorbent article. 1. A method for measuring a content of a water-absorbing resin including a water-soluble cation included in a hygienic material , an absorbent article , or an intermediate product in a manufacturing process thereof , in a form of an ion-dissociating group , the method comprising:A) a step for measuring an amount of a predetermined water-soluble cation in a reference sample including a known amount of the water-absorbing resin and creating a calibration curve indicating a relation between the amount of the water-absorbing resin and the amount of the predetermined water-soluble cation in the reference sample on the basis of the obtained measurement result;B) a step for measuring an amount of the predetermined water-soluble cation in a measurement sample, which includes a portion including the water-absorbing resin, of the hygienic material, the absorbent article, or the intermediate product in the manufacturing process thereof; andC) a step for calculating an amount of the water-absorbing resin in the measurement sample by the calibration curve created in the step A) from the amount of the predetermined water-soluble cation measured in the step B),the step A) and the step B) including measuring the amount of the predetermined water-soluble cation using an ion selective electrode method and including the following steps M1) and M2):M1) a step for immersing a sample in an aqueous solution including a total ionic strength adjusting agent (pre-processing step); andM2) a step for measuring the amount of the predetermined water-soluble cation in a pre-processed supernatant liquid obtained in the step M1).2. The measuring method according to claim 1 , wherein the step B) further includes claim 1 , before the step M1) in the step B) claim 1 , a step B1) for collecting the portion including the water-absorbing resin from ...

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24-04-2014 дата публикации

REGENERATIVE PURIFICATION OF A PRETREATED BIOMASS STREAM

Номер: US20140113812A1
Принадлежит: Beta Renewables S.p.A.

It is disclosed a process for removing at least a portion of the furfural and acetic acid in a first stream comprised of water, at least one compound selected from the group consisting of furfural and acetic acid, C5's and C6's. Such process comprises the steps of contacting the stream with an adsorption media which has been previously contacted with a second stream comprised of the same components and the adsorption media has been regenerated by exposing it to conditions, without being in contact with the second stream, such that at least 70% of the adsorbed furfural and acetic acid have each been desorbed and at least 60% of the C5's and C6's remain adsorbed on the media. 1. An article of manufacture comprised of [ ["wherein the C5's are comprised of the monomers, dimmers, oligomers and polymers of arabinose and xylose,", "and the C6's are comprised of the monomers, dimmers, oligomers and polymers of glucose,"], "contacting the adsorption media, which is an activated carbon or a high surface polymer, with a stream comprised of water, C5's, C6's, furfural and acetic acid"}, "for sufficient time so that the amount of the C5's and the C6's adsorbed onto the media are at least 90% of the maximum level of the C5's and the C6's that can be respectively adsorbed onto the media and the media subsequently regenerated so that the amount of C5's and C6's on the media are at least 76% of the maximum level of the C5's and the C6's that can be respectively adsorbed onto the media, and at least 50% by weight of the total amount of the furfural and acetic acid, respectively is removed from the media."], 'a regenerated adsorption media which has been made by'}2. The article of claim 1 , wherein the amount of C5's and C6's on the media is at least 84% of the maximum level of the C5's and the C6's that can be respectively adsorbed onto the media.3. The article of claim 1 , wherein the amount of C5's and C6's on the media is at least 90% of the maximum level of the C5's and the C6's ...

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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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09-02-2017 дата публикации

METHOD FOR REMOVING BACTERIA FROM BLOOD USING HIGH FLOW RATE

Номер: US20170035956A1
Автор: McCrea Keith, Ward Robert
Принадлежит:

The present invention provides methods for removing a significant amount of bacteria (e.g., gram-negative bacteria and gram-positive bacteria, including bacteria with no or low affinity for heparan sulfate) from whole blood, serum or plasma using an adsorption media. The method can be used in extracorporeal treatments involving high volumetric flow rates and high linear flow rates. 1. An ex vivo method for removing bacteria from a sample taken from a subject who is suspected of being infected with bacteria , the method comprising:contacting a sample taken from the subject with an adsorption media to allow the formation of an adhering complex, wherein the adhering complex comprises bacteria and the adsorption media; andseparating the sample from the adhering complex to produce the sample with a reduced amount of bacteria.2. The method of claim 1 , wherein the sample is selected from the group consisting of whole blood claim 1 , serum and plasma.3. The method of claim 2 , wherein the sample is whole blood.4. The method of claim 1 , wherein the adsorption media is a solid substrate of high surface area having a hydrophilic surface that is free of a polysaccharide adsorbent.5. The method of claim 4 , wherein the solid substrate comprises a plurality of rigid polymer bead.6. The method of claim 5 , wherein the rigid polymer bead is a member selected from the group consisting of polyurethane claim 5 , polymethylmethacrylate claim 5 , polyethylene or co-polymers of ethylene and other monomers claim 5 , polyethylene imine claim 5 , polypropylene claim 5 , and polyisobutylene.7. The method of claim 4 , wherein the solid substrate comprises one or a plurality of hollow fibers.8. The method of claim 4 , wherein the solid substrate comprises solid fibers or woven yarn made from solid fibers.9. The method of claim 4 , wherein the hydrophilic surface is a cationic surface.10. The method of claim 1 , wherein the adsorption media has a high surface area as a result of surface or ...

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15-02-2018 дата публикации

METHOD FOR PRODUCING POROUS CELLULOSE MEDIUM

Номер: US20180043333A1
Принадлежит: Daicel Corporation

Provided are a technique for preparing a porous cellulose medium without using a special gelling agent for a solution in which cellulose acetate serving as a raw material is dissolved; and a porous cellulose medium and the like produced using the technique. A method for producing a porous cellulose medium comprises the step of preparing a flowable homogeneous composition comprising cellulose acetate, a basic compound, and a solvent including water, and gelling the composition by deacetylation reaction of the cellulose acetate. 1. A method for producing a porous cellulose medium comprising the step of preparing a flowable homogeneous composition comprising cellulose acetate , a basic compound , and a solvent including water , and gelling the composition by deacetylation reaction of the cellulose acetate.2. A method for producing spherical porous cellulose particles comprising the step of obtaining a dispersion by dispersing a flowable homogeneous composition comprising cellulose acetate , a basic compound , and a solvent including water in a dispersion medium not miscible with the homogeneous composition , and forming gelled particles composed of the composition by gelling the composition by deacetylation reaction of the cellulose acetate contained in the obtained dispersion.3. The method for producing spherical porous cellulose particles according to claim 2 , which comprises claim 2 , after the preceding step claim 2 , the step of adding a separating solvent for separating the obtained gelled particles to the dispersion in which the gelled particles are formed claim 2 , thereby separating the gelled particles into the separating solvent.4. The method according to claim 3 , wherein the separating solvent is water claim 3 , methanol claim 3 , ethanol claim 3 , 2-propanol claim 3 , acetamide claim 3 , formamide claim 3 , or a mixture of at least two of these solvents.5. A method for producing a porous cellulose monolith comprising the step of placing a flowable ...

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25-02-2016 дата публикации

Method of Forming an Agent and its Use in Desulphurisation

Номер: US20160051974A1
Принадлежит: M-I DRILLING FLUIDS UK LIMITED

The present disclosure is directed to a desulphurisation agent for removing sulphurous species from a diluent or process stream, and a use of such agent. In some examples, the agent may include a compound of manganese, pore forming particles and a compound of copper. The agent may be introduced into or mixed with the diluent or process stream to effectuate removal of sulphurous species from the diluent or process stream. 1. A desulphurisation agent , comprising:pore forming particles;at least one compound of manganese; andat least one compound of copper.2. The agent of claim 1 , further comprising:at least one of a compound of iron and a compound of zinc.3. The agent of claim 1 , wherein a ratio of the compound of manganese to the compound of copper is between 8:1 and 1:8 by weight.4. The agent of claim 1 , wherein a ratio of the compound of manganese to the compound of copper is between 3:1 and 1:3 by weight.5. The agent of claim 2 , wherein a ratio of the compound of manganese to the compound of iron is between 8:1 and 1:8 by weight.6. The agent of claim 2 , wherein a ratio of the compound of manganese to the compound of iron is between 3:1 and 1:3 by weight.7. The agent of claim 2 , wherein a ratio of the compound of manganese to the compound of zinc is between 8:1 and 1:8 by weight.8. The agent of claim 2 , wherein a ratio of the compound of manganese to the compound of zinc is between 3:1 and 1:3 by weight.9. The agent of claim 1 , wherein the pore forming particles comprise at least one of thermoplastic particles and thermoplastic spheres.10. The agent of claim 1 , wherein the pore forming particles comprise hollow particles.11. The agent of claim 1 , where in the pore forming particles comprise at least one of spheres claim 1 , extrudates claim 1 , granules claim 1 , and tablets.12. The agent of claim 1 , wherein pore forming particles comprise between 5% and 95% of a total volume of the agent.13. The agent of claim 1 , wherein pore forming particles comprise ...

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13-02-2020 дата публикации

SEPARATION MATERIAL

Номер: US20200047084A1
Принадлежит:

Disclosed is a separation material comprising hydrophobic polymer particles and a coating layer covering at least a portion of a surface of the hydrophobic polymer particles, wherein the coating layer comprises a hydrophilic polymer having hydroxy groups, and the hydrophilic polymer has a group represented by —NH—R-L or an epoxy group, wherein R represents a hydrocarbon group and L represents a carboxy group or an amino group. 1. A separation material comprising:hydrophobic polymer particles; anda coating layer covering at least a portion of a surface of the hydrophobic polymer particles, whereinthe coating layer comprises a hydrophilic polymer having hydroxy groups, and the hydrophilic polymer has a group represented by —NH—R-L or an epoxy group, wherein R represents a hydrocarbon group and L represents a carboxy group or an amino group.2. The separation material according to claim 1 , wherein the separation material has an elastic modulus at 5% compressive deformation in water of 70 MPa or more.3. The separation material according to claim 1 , wherein when water is passed through a column packed with the separation material such that the column has a pressure of 0.3 MPa claim 1 , a water passing rate is 500 cm/h or more.4. The separation material according to claim 1 , wherein the hydrophobic polymer particles are particles comprising a polymer having a structural unit derived from a styrene monomer.5. The separation material according to claim 1 , wherein the hydrophilic polymer having hydroxy groups is a polysaccharide or a modified product thereof.6. The separation material according to claim 1 , wherein the hydrophilic polymer having hydroxy groups is one or more selected from the group consisting of dextran claim 1 , agarose claim 1 , pullulan claim 1 , a modified product thereof claim 1 , and a mixture thereof.7. The separation material according to claim 1 , wherein the hydrophilic polymer having hydroxy groups is crosslinked.8. The separation material ...

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10-03-2022 дата публикации

METHOD FOR RECYCLING SUPERABSORBENT POLYMER DERIVED FROM USED ABSORBENT ARTICLE AND RECYCLED SUPERABSORBENT POLYMER DERIVED FROM USED ABSORBENT ARTICLE

Номер: US20220072511A1
Принадлежит: Unicharm Corporation

A method of recycling superabsorbent polymers derived from a used absorbent article, the method including: treating the superabsorbent polymers with ozone water after inactivation; reactivating, with an alkaline aqueous solution, the superabsorbent polymers treated with the ozone water; and adding hydrophilic fine particles to the superabsorbent polymers reactivated with the alkaline aqueous solution and then drying the superabsorbent polymers. 1. A method of recycling superabsorbent polymers derived from a used absorbent article , the method comprising:treating the superabsorbent polymers with ozone water after inactivation;reactivating, with an alkaline aqueous solution, the superabsorbent polymers treated with the ozone water; andadding hydrophilic fine particles to the superabsorbent polymers reactivated with the alkaline aqueous solution and then drying the superabsorbent polymers.2. The method according to claim 1 , further comprising:after the reactivating of the superabsorbent polymers and before the adding of the hydrophilic fine particles, dehydrating and washing the superabsorbent polymers with an organic solvent.3. The method according to claim 1 , whereinthe reactivating of the superabsorbent polymers includes:dehydrating and washing the superabsorbent polymers while reactivating the superabsorbent polymers with an aqueous solution containing an organic solvent and an alkali metal ion supply source supplying an alkali metal ion.4. The method according to claim 1 , further comprising:inactivating the superabsorbent polymers with an inactivating agent, whereinin the treating of the superabsorbent polymers, the superabsorbent polymers inactivated with the inactivating agent are treated with the ozone water.5. The method according to claim 4 , whereinthe inactivating agent contains an acidic aqueous solution.6. The method according to claim 1 , whereinthe hydrophilic fine particles include silica fine particles.7. The method according to claim 1 , ...

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01-03-2018 дата публикации

METHOD FOR PRODUCING POROUS CELLULOSE BEADS, AND ADSORBENT USING SAME

Номер: US20180056271A1
Принадлежит: KANEKA CORPORATION

A method for producing porous cellulose beads includes preparing a fine cellulose dispersion by mixing a low temperature alkaline aqueous solution and cellulose; preparing a mixed liquid by adding a crosslinking agent to the fine cellulose dispersion; preparing an emulsion by dispersing the mixed liquid in a dispersion medium; and contacting the emulsion with a coagulating solvent. 1. A method for producing porous cellulose beads , comprising:preparing a fine cellulose dispersion by mixing a low temperature alkaline aqueous solution and cellulose;preparing a mixed liquid by adding a crosslinking agent to the fine cellulose dispersion;preparing an emulsion by dispersing the mixed liquid in a dispersion medium; andcontacting the emulsion with a coagulating solvent.2. The method according to claim 1 , wherein a temperature of the alkaline aqueous solution is 0° C. to 25° C.3. The method according to claim 1 , wherein the crosslinking agent is an epoxy group-containing compound.4. The method according to claim 3 , wherein the epoxy group-containing compound is a glycidyl ether compound.5. The method according to claim 1 , wherein the crosslinking agent is added to the fine cellulose dispersion at a concentration of 3 wt % to lower than 20 wt % in the mixed liquid.6. The method according to claim 1 , wherein a solubility of the crosslinking agent in water is 20% or more.7. The method according to claim 1 , wherein a viscosity of the crosslinking agent is 100 mPa·s to 50000 mPa·s.8. Porous cellulose beads claim 1 , wherein a slope of an approximate straight line in van Deemter Plot prepared by plotting v′: Reduced velocity on x-axis and plotting h′: Reduced HETP on y-axis is 0.022 to lower than 0.040 in a range from 150 through 2000 of v′: Reduced velocity.9. The porous cellulose beads claim 1 , produced by the method according to .10. An adsorbent claim 1 , comprising the porous cellulose beads produced by the method according to and a ligand claim 1 , wherein the ligand ...

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28-02-2019 дата публикации

CHROMATOGRAPHY STATIONARY PHASE

Номер: US20190060871A1
Принадлежит: Daicel Corporation

Provided is a chromatography stationary phase having an excellent molecule discriminating ability. Specifically, provided is a chromatography stationary phase including a carrier carrying a copolymer that has a pyrrolidone backbone or a piperidone backbone, and an imide backbone in a repeating unit of the main chain. 1. A stationary phase for chromatography , the stationary phase comprising a support supporting a polymer including a pyrrolidone skeleton or a piperidone skeleton and an imide skeleton in a repeating unit of a main chain.3. The stationary phase for chromatography according to claim 1 , which is in the form of spherical particles.4. The stationary phase for chromatography according to claim 3 , which has an average particle diameter of 0.1 μm to 1000 μm.5. The stationary phase for chromatography according to claim 1 , which is monolithic.6. The stationary phase for chromatography according to claim 1 , which is a stationary phase for supercritical fluid chromatography.7. A method for separating a target substance claim 1 , the method comprising a step of separating the target substance by using the stationary phase according to claim 1 , and a mobile phase including an eluent or a supercritical fluid.9. The method for producing a stationary phase for chromatography according to claim 8 , wherein the polymerizable functional group is a vinyl group claim 8 , an allyl group claim 8 , an isopropenyl group or an alkenyl group having 4 to 12 carbon atoms and having a double bond at an co position.11. The method for producing a stationary phase for chromatography according to claim 10 , wherein W is a vinyl group claim 10 , X is an amide group or an N-alkylamide group having 1 to 3 carbon atoms claim 10 , Y is an alkylene group having 1 to 5 carbon atoms claim 10 , R are independently a methyl group claim 10 , an ethyl group claim 10 , or a propyl group claim 10 , and Z is an alkoxy group having 1 to 5 carbon atoms claim 10 , a halogen claim 10 , an ...

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27-02-2020 дата публикации

FABRICATION OF HYDROXYAPATITE BASED HYBRID SORBENT MEDIA FOR REMOVAL OF FLUORIDE AND OTHER CONTAMINANTS

Номер: US20200061575A1
Принадлежит:

Fabricating a hybrid sorbent media includes contacting a porous material with a first aqueous solution including phosphate ions to yield a first mixture, contacting the first mixture with a second aqueous solution comprising calcium ions to yield a second mixture, and adjusting a pH of the second mixture to form hydroxyapatite inside the porous media to yield the hybrid sorbent media. 1. A method of fabricating hybrid sorbent media , the method comprising:contacting porous media defining pores with a first aqueous solution comprising phosphate ions to yield a first mixture;contacting the first mixture with a second aqueous solution comprising calcium ions to yield a second mixture; andadjusting a pH of the second mixture to initiate formation of hydroxyapatite on pore surfaces of the pores of the porous media to yield the hybrid sorbent media,wherein contacting the porous media with the first aqueous solution, contacting the first mixture with the second aqueous solution, and adjusting the pH of the second mixture occur at room temperature.2. The method of claim 1 , further comprising removing some of the first aqueous solution from the first mixture before contacting the first mixture with the second aqueous solution.3. The method of claim 1 , further comprising aging the hybrid sorbent media to allow growth of hydroxyapatite nanoparticles inside the pores of the porous media.4. The method of claim 3 , wherein aging comprises aging at room temperature for at least 24 hours.5. The method of claim 1 , wherein the first aqueous solution comprises diammonium hydrogen phosphate claim 1 , ammonium dihydrogen phosphate claim 1 , di-sodium hydrogen phosphate claim 1 , triethyl phosphate claim 1 , phosphorus pentoxide claim 1 , phosphoric acid claim 1 , phosphonoacetic acid claim 1 , or a combination thereof.6. The method of claim 1 , wherein a volume ratio of the first aqueous solution to the porous media is about 2:1.7. The method of claim 1 , wherein the first aqueous ...

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11-03-2021 дата публикации

ORGANIC GEL OR LIQUID CHROMATOGRAPHY METHOD

Номер: US20210069613A1
Автор: Parmentier Francois
Принадлежит:

A chromatography method in which a gaseous, liquid or supercritical mobile phase containing species to be separated is circulated through a packing. The packing includes a plurality of capillary ducts extending in the packing between an upstream face through which the mobile phase enters the packing and a downstream face through which the mobile phase leaves the packing. A continuous medium permeable to molecular diffusion extends between the ducts, including a porous organic gel or an organic liquid with at least one network of connected pores, the size of which is greater than two times the molecular diameter of at least one species to be separated. The at least one species has a diffusive path between the ducts. 1. A packing for chromatography , comprising:a plurality of capillary conduits crossing the packing between an upstream face configured for inflowing of a mobile phase into the packing and a downstream face configured for an outflow of the mobile phase from the packing, anda continuous medium permeable to molecular diffusion extending between said conduits, including a porous organic gel or an organic liquid and including at least one network of connected pores.2. The packing of claim 1 , wherein the diameter of the capillary conduits of the packing is less than or equal to 500 μm claim 1 , preferably less than or equal to 150 μm claim 1 , and even preferably less than or equal to 80 μm.3. The packing of claim 1 , wherein the organic gel forming the continuous medium is selected from:(a) a copolymer of styrene and of divinylbenzene,(b) polymethyl methacrylate, and(c) a copolymer of hydroxyethyl methacrylate and of divinylbenzene.4. The packing of claim 1 , wherein said continuous medium comprises a polyholoside.5. The packing of claim 1 , wherein the organic liquid is selected from:(a) an aliphatic or aromatic hydrocarbon,(b) an aliphatic or aromatic alcohol,(c) an aliphatic or aromatic ketone,(d) an aliphatic or aromatic amine, and(e) a halogenated ...

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12-03-2020 дата публикации

WATER ABSORPTION TREATMENT MATERIAL AND METHOD FOR MANUFACTURING THE SAME

Номер: US20200077618A1
Автор: YOSHINAGA Junji
Принадлежит: DAIKI CO., LTD.

A water absorption treatment material includes a first grain and a second grain that absorb a liquid. The first grain includes a first core portion and a first coating portion. The first core portion has a grain-like shape. The first coating portion contains an adhesive material, and covers the first core portion. The second grain includes a second core portion and a second coating portion. The second core portion has a grain-like shape. The second coating portion contains an adhesive material, and covers the second core portion. The thickness of the second coating portion is smaller than the thickness of the first coating portion. 1. A water absorption treatment material comprising:a first grain that absorbs a liquid, the first grain including a first core portion that has a grain-like shape, and a first coating portion that contains an adhesive material and covers the first core portion; anda second grain that absorbs the liquid, the second grain including a second core portion that has a grain-like shape, and a second coating portion that contains an adhesive material and covers the second core portion,wherein a thickness of the second coating portion is smaller than a thickness of the first coating portion.2. The water absorption treatment material according to claim 1 ,wherein the thickness of the second coating portion is 80% or less of the thickness of the first coating portion.3. The water absorption treatment material according to claim 2 ,wherein the thickness of the second coating portion is 50% or less of the thickness of the first coating portion.4. The water absorption treatment material according to claim 1 ,wherein a plurality of the first grains and a plurality of the second grains are provided.5. The water absorption treatment material according to claim 4 ,wherein the number of the first grains is 30% or more and 70% or less of a total number of the first and second grains.6. The water absorption treatment material according to claim 5 ,wherein ...

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28-03-2019 дата публикации

Polymer Shells

Номер: US20190091646A1
Принадлежит:

The present invention relates to a method for the preparation of polymer shells, preferably composed of cellulose or hemicellulose, comprising the steps of dissolving the polymer component in a first solvent, preferably an organic solvent and precipitating the polymer component by contacting the first solution with a second solvent, which second solvent has a polar character, and in which second solvent the polymer component is essentially insoluble, thereby obtaining polymer shells. Moreover, the invention refers to the polymer shells as such, having permeable and responsive properties, as well as various applications comprising such polymer shells within the fields of drug delivery, separation techniques, and inter alia filling material. 127.-. (canceled)28. A cellulose shell , comprising a shell wall having a thickness from 100 nm to 2 mm and encasing a space comprising a gas , wherein the cellulose shell has an outer diameter between 10 μm and 10 mm.29. The cellulose shell of claim 28 , wherein the outer diameter of the shell is from 10 μm to 5 mm.30. The cellulose shell of claim 28 , wherein the outer diameter of the shell is from 10 μm to 2 mm.31. The cellulose shell of claim 28 , wherein the outer diameter of the shell is from 10 μm to 1 mm.32. The cellulose shell of claim 28 , wherein the shell wall has a thickness from 0.5 μm to 500 μm.33. The cellulose shell of claim 28 , wherein the shell wall has a thickness from 2 μm to 30 μm.34. The cellulose shell of claim 28 , further comprising a molecule comprising xyloglucan attached to the shell.35. A method for preparing the cellulose shell of claim 28 , comprising:(a) dissolving cellulose in a solvent comprising at least one organic solvent to produce a solution of step (a);(b) dissolving a core-forming substance in the solution of step (a) wherein the core-forming substance comprises at least one gas, by feeding said gas into the solution of step (a) or by pressurizing the solution of step (a) with said gas, ...

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03-07-2014 дата публикации

FLOATING TYPE ADSORBENT FOR REMOVAL OF PHOSPHATE IN AQUEOUS SOLUTION AND METHOD FOR FABRICATING THE SAME AND METHOD FOR REGENERATION OF THE SAME

Номер: US20140183405A1

The present disclosure relates to a floating type adsorbent for removal of phosphate that can effectively remove phosphate from aqueous phase through reaction between an amine function attached on the surface of a sponge and phosphate. This adsorbent can be regenerated by desorbing the adsorbed phosphate, a method for fabricating same and a method for regeneration the floating type adsorbent for removal of phosphate. The floating type adsorbent for removal of phosphate according to the present disclosure is fabricated by immersing a sponge in a mixture solution of an amine precursor and anhydrous toluene to form an amine function on the surface of the sponge. The amine precursor may be 3-aminopropyltriethoxysilane (APTES) and the APTES and the anhydrous toluene may be mixed at a volume ratio of 0.5-1:1. 1. A method for fabricating a floating type adsorbent for removal of phosphate , comprising immersing a sponge in a mixture solution of an amine precursor and anhydrous toluene to form an amine function on the surface of the sponge.2. The method for fabricating a floating type adsorbent for removal of phosphate according to claim 1 , wherein the amine precursor is 3-aminopropyltriethoxysilane (APTES).3. The method for fabricating a floating type adsorbent for removal of phosphate according to claim 2 , wherein the APTES and the anhydrous toluene are mixed at a volume ratio of 0.5-1:1.4. The method for fabricating a floating type adsorbent for removal of phosphate according to claim 1 , wherein an inert gas is supplied to the mixture solution of the amine precursor and the anhydrous toluene in order to prevent evaporation of the anhydrous toluene.5. The method for fabricating a floating type adsorbent for removal of phosphate according to claim 1 , wherein the sponge has a porous structure and is foamed from a natural or synthetic resin.6. A floating type adsorbent for removal of phosphate claim 1 , comprising:a sponge; andan amine group provided on the surface of the ...

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10-07-2014 дата публикации

POROUS INORGANIC/ORGANIC HOMOGENOUS COPOLYMERIC HYBRID MATERIALS FOR CHROMATOGRAPHIC SEPARATIONS AND PROCESS FOR THE PREPARATION THEREOF

Номер: US20140194283A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

The present invention relates to porous inorganic/organic homogenous copolymeric hybrid material materials, including particulates and monoliths, methods for their manufacture, and uses thereof, e.g., as chromatographic separations materials. 1140-. (canceled)143. The material according to claim 141 , wherein 0.003≦y/z≦50 and 0.02≦x/(y+z)≦21.144. The material according to claim 141 , wherein said material has a specific surface area of about 50-800 m/g.145. The material according to claim 141 , wherein said material is hydrolytically stable at a pH of about 1 to about 13.146. The material according to claim 142 , wherein 0.003≦y/z≦50 and 0.02≦x/(y+z)≦21.147. The material according to claim 142 , wherein said material has a specific surface area of about 50-800 m/g.148. The material according to claim 142 , wherein said material is hydrolytically stable at a pH of about 1 to about 13.149. A separations device comprising a material according to .150. The separations device according to claim 149 , wherein said device is selected from the group consisting of chromatographic columns claim 149 , thin layer plates claim 149 , filtration membranes claim 149 , sample cleanup devices claim 149 , and microtiter plates.151. A separations device comprising a material according to .152. The separations device according to claim 151 , wherein said device is selected from the group consisting of chromatographic columns claim 151 , thin layer plates claim 151 , filtration membranes claim 151 , sample cleanup devices claim 151 , and microtiter plates. This application claims benefit of and is a continuation of International Application No. PCT/US03/34776, filed Oct. 30, 2003 and designating the United States, which claims benefit of and priority to U.S. Provisional Application No. 60/422,580, filed Oct. 30, 2002. The entire contents of these applications are incorporated herein by reference.Packing materials for liquid chromatography (LC) are generally classified into two types: ...

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27-05-2021 дата публикации

Preparation method and application for a resin-based iron oxide-containing composite phosphate removal adsorbent

Номер: US20210154643A1
Принадлежит:

A preparation method of a resin-based iron oxide-containing composite phosphate removal adsorbent is provided. An alkaline anion resin is taken as a base, a potassium ferrate is used as an iron source, and a characteristics of ferrate ions easily adsorbed on a surface of the anion resin are utilized to prepare resin-based iron oxide-containing composite phosphate removal adsorbent by one-step in-situ hydrolysis precipitation, compared with the related art, a preparation process of the disclosure is relatively simpler, a time period is shorter, and a production cost is lower. It has a strong ability to eliminate interference from other anions in the waste effluents, and it has a strong adsorption capacity, fast adsorption speed and large adsorption capacity for the phosphate. Moreover, it has the advantages of strong regeneration ability and multiple repeated use times. 1. A preparation method of a resin-based iron oxide-containing composite phosphate removal adsorbent , comprising:step (i) adding an alkaline anion resin into a prepared alkaline potassium ferrate solution, and stirring for 1-5 hours at a room temperature to make ferrate ions exchange with anions of the alkaline anion resin;step (ii) discarding a supernatant in a solution obtained in the step (i), adding a water, heating to 50° C.-70° C. and stirring again for 1-3 hours to make the ferrate ions exchanged onto the alkaline anion resin hydrolyze into a ferric hydroxide;{'sup': '−', 'step (iii) adding a 2-10% by mass sodium chloride solution to a solution obtained in the step (ii) to transform a hydroxyl group bonded onto the alkaline anion resin into Cl to thereby obtain a composite resin loaded with nano-sized hydrated iron oxides; and'}step (iv) washing the composite resin loaded with nano-sized hydrated iron oxides to be neutral and then drying to obtain the resin-based iron oxide-containing composite phosphate removal adsorbent;wherein the alkaline potassium ferrate solution has a concentration of 0 ...

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12-05-2016 дата публикации

WATER ABSORBING MATERIAL AND MANUFACTURING METHOD THEREOF

Номер: US20160129419A1
Принадлежит: DAIKI CO., LTD.

A water absorbing material which can reduce burden on the environment in disposal and can be manufactured at low cost, and a manufacturing method thereof are provided. The water absorbing material contains paper obtained by separating polyvinyl chloride from vinyl chloride wallpaper as a raw material. 1. A water absorbing material containing paper obtained by separating polyvinyl chloride from vinyl chloride wallpaper as a raw material.2. The water absorbing material according to claim 1 ,wherein the paper is contained as a main material.3. The water absorbing material according to claim 1 , containing a coloring material.4. The water absorbing material according to claim 1 , comprising:a granular core portion containing the paper as its raw material; anda coating layer portion that covers the granular core portion.5. The water absorbing material according to claim 1 ,wherein the paper is obtained by separating the polyvinyl chloride from the vinyl chloride wallpaper with a separation device, andthe separation device includes:a first shredding unit that shreds the vinyl chloride wallpaper; anda first separation unit that has a first tubular portion in which a large number of first holes that allow the polyvinyl chloride contained in the vinyl chloride wallpaper shredded by the first shredding unit to pass through without allowing the paper to pass through are formed, and that separates the polyvinyl chloride passing through the first holes from the vinyl chloride wallpaper by rotating the first tubular portion in a state in which the vinyl chloride wallpaper shredded by the first shredding unit is accommodated in the first tubular portion.6. The water absorbing material according to claim 5 ,wherein the separation device includes a first ridge that is provided on an inner circumferential surface of the first tubular portion and that extends in a direction in which a central axis of the first tubular portion extends.7. The water absorbing material according to claim ...

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12-05-2016 дата публикации

PREPARATION METHOD OF CHROMATOGRAPHY MEDIUM

Номер: US20160129420A1
Принадлежит: JNC CORPORATION

A method for preparing a chromatography medium having the properties of high virus adsorption and high fluidity, and a method for producing a virus vaccine using the chromatography medium are provided. The chromatography medium is obtained by forming a sulfated polysaccharide bound with porous particles having an exclusion limit molecular weight of 6000 Da or less when pure water is used as mobile phase and standard polyethylene glycol is used and an average particle size in the range of 30-200 μm. 1. A method for preparing a chromatography medium , comprising:step 1: cross-linking porous particles with a polysaccharide by using a cross-linking agent having two or more functional groups, to obtain polysaccharide-binding porous particles, wherein the porous particles have an exclusion limit molecular weight of 6000 Da or less when pure water is used as mobile phase and standard polyethylene glycol is used; and {'br': None, 'sub': 2', '2', '2, 'X—O—CH—C(OH)H—CH—NH—CH—Z\u2003\u2003(1)'}, 'step 2: sulfating the polysaccharide-binding porous particles obtained in step 1 with a sulfating agent to obtain the chromatography medium represented by General Formula (1) belowwherein in Formula (1), X is the porous particle have an average particle size in the range of 30-200 μm, O bonded to X is an oxygen originating from hydroxyl of the porous particle, Z is the sulfated polysaccharide, and C bonded to Z is a carbon originating from the reductive end of the sulfated polysaccharide, wherein the sulfated polysaccharide is a ligand, and a limiting viscosity of the sulfated polysaccharide is in the range of 0.40-0.90 dL/g.2. The method for preparing the chromatography medium according to claim 1 , wherein the porous particles have an average particle size in the range of 40-120 μm.3. The method for preparing the chromatography medium according to claim 1 , wherein the porous particles are cellulose particles.4. The method for preparing the chromatography medium according to claim 1 ...

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10-05-2018 дата публикации

Device for substance separation

Номер: US20180126298A1
Принадлежит: Merck Patent GmBH

The invention relates to a device for substance separation with monolithic sorbents which can be produced by means of 3-D printing. They comprise pressure- and solvent-stable thermoplastics.

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11-05-2017 дата публикации

Materials, apparatuses, and methods for separating immiscible liquids

Номер: US20170129786A1
Принадлежит: PURDUE RESEARCH FOUNDATION

Materials, apparatuses, and methods that are suitable for separating immiscible liquids and make use of a porous host material functionalized with a functionalizing agent such that the host material is superhydrophobic.

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02-05-2019 дата публикации

POROUS FIBER, ADSORBENT MATERIAL, AND PURIFICATION COLUMN

Номер: US20190126239A1
Принадлежит: Toray Industries, Inc.

A solid fiber has a modified cross-section which satisfies the following (a) to (b): (a) a modification degree Do/Di, in a cross section of the solid fiber, is 1.20 to 8.50 when the inscribed circle diameter is denoted by Di and the circumscribed circle diameter is denoted by Do; and (b) a porous specific surface area of the fiber is not less than 30 m/g. An adsorbent material comprises not less than 28 vol % of the porous fiber as a fiber bundle. A purification column is formed by arranging the adsorbent material in the straight form in an axis direction of a plastic casing and by attaching an inlet port and an outlet port of a fluid that is to be treated to both ends of the plastic casing. The porous fiber can efficiently adsorb a removal target substance in the fluid that is to be treated, and a purification column incorporates the porous fiber. 1. A porous fiber comprising a modified solid cross-section , wherein the porous fiber satisfies the following (a) to (b):(a) a modification degree Do/Di, in a cross section of the solid fiber, is 1.20 to 8.50 when the inscribed circle diameter is denoted by Di and the circumscribed circle diameter is denoted by Do; and{'sup': '2', '(b) a porous specific surface area of the fiber is not less than 3 m/g.'}2. The porous fiber according to claim 1 , wherein an average radius of pore is not less than 0.8 nm and not more than 90 nm.3. The porous fiber according to claim 1 , wherein the porous specific surface area is not less than 30 m/g.4. The porous fiber according to claim 1 , wherein an inscribed circle occupancy of the following equation is not less than 0.10:{'br': None, 'Inscribed circle occupancy=Area of the inscribed circle of the cross section of the fiber/Area of the cross section of the fiber.'}5. The porous fiber according to claim 1 , wherein a diameter of pore in the porous fiber is not more than 25 μm and a ratio of an average diameter of pore in the area adjacent to the outer surface of the fiber vs an average ...

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23-04-2020 дата публикации

Air Filters Comprising Polymeric Sorbents for Aldehydes

Номер: US20200122071A1
Принадлежит:

An air filter including a filter support that supports polymeric sorbent particles. The polymeric sorbent particles are the reaction product of a hydrolyzed divinylbenzene/maleic anhydride precursor polymeric material with a nitrogen-containing compound, with the nitrogen-containing compound being ionically attached to the hydrolyzed divinylbenzene/maleic anhydride. 2. The air filter of wherein the filter support comprises a substrate with at least one major surface with at least some polymeric sorbent particles disposed thereon.3. (canceled)4. The air filter of wherein the filter support comprises a porous claim 1 , air-permeable material with polymeric sorbent particles disposed on a major surface thereof and/or with polymeric sorbent particles disposed within the interior of the material at least in a location proximate the major surface of the material.58-. (canceled)9. The air filter of wherein the filter support comprises a fibrous web that exhibits an interior and wherein the polymeric sorbent particles are disposed within at least portions of the interior of the web.10. The air filter of wherein the polymeric sorbent particles are disposed throughout an interior of the fibrous web.11. The air filter of wherein the web is a nonwoven fibrous web.12. (canceled)13. The air filter of wherein at least some fibers of the fibrous web are each bonded to at least one polymeric sorbent particle.14. The air filter of wherein the filter support is one layer of a multilayer claim 1 , air-permeable assembly.15. (canceled)16. The air filter of wherein the particle-filtration layer comprises electret moities.17. The air filter of wherein the filter support is a filter media that exhibits a Percent Penetration of less than 50.18. The air filter of wherein the filter support is pleated.19. The air filter of wherein the air filter is a framed air filter that is configured to be inserted into an air filter receptacle of an air-handling apparatus chosen from the group consisting ...

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07-08-2014 дата публикации

Porous Material And Devices For Performing Separations, Filtrations, And Catalysis And EK Pumps, And Mthods Of Making And Using The Same

Номер: US20140220278A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

Embodiments of the present invention are directed to a porous monolith polymeric composition having utility in catalysis, chromatography, filtration, and electro-kinetic pumps, devices incorporating such composition and methods or making and using such monoliths. The monoliths are characterized by a substantially homogeneous skeletal core with little shrinkage, few voids and few channels. 1. A composition of matter comprising a monolith having a skeletal core and pores , said skeletal core having a substantially homogeneous polymeric composition of two or more organic silane monomers , said pores defining an interstitial volume in the skeletal core and have a pore size distribution in which there are at least macropores and less than 5% of the interstitial volume is mesopores , said macropores allowing fluid movement through the monolith.2. The composition of matter of in which said interstitial volume has fewer than 2% mesopores.3. The composition of matter of wherein said interstitial volume has fewer than 1% mesopores.4. The composition of matter of wherein said skeletal core has polymers which deviate from the substantially homogeneous polymeric composition to form nodules claim 1 , said nodules have a nodule cross-sectional diameter and said skeletal core having a substantially homogeneous polymeric composition without a nodule has a core cross-sectional diameter wherein the ratio of the nodule cross sectional diameter to core cross sectional diameter is less than 80 to 1.5. The composition of matter of wherein said skeletal core has polymers which deviate from the substantially homogeneous polymeric composition to form nodules claim 1 , said nodules have a nodule cross-sectional diameter and said skeletal core claim 1 , having a substantially homogeneous polymeric composition without a nodule claim 1 , has a core cross-sectional diameter wherein the ratio of the nodule cross sectional diameter to core cross sectional diameter is less than 50 to 1.6. The ...

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09-05-2019 дата публикации

POROUS MATERIALS WITH CONTROLLED POROSITY; PROCESS FOR THE PREPARATION THEREOF; AND USE THEREOF FOR CHROMATOGRAPHIC SEPARATIONS

Номер: US20190134604A1
Принадлежит:

The present invention provides novel chromatographic materials. e.g., for chromatographic separations, processes for their preparation and separations devices containing the chromatographic materials. The chromatographic materials of the invention have controlled porosity and comprise a chromatographic core material and one or more layers of chromatographic surface material which each independently provide an average pore diameter, an average pore volume, or a specific surface area such that the combined layers form a chromatographic material having a predetermined or desired pattern of porosity from the core material to the outermost surface. The materials are useful for HPLC separations, normal-phase selarations, reversed-phase separations, chiral separations, HILIC separations, SFC separations, affinity separations, perfusive separations, partially perfusive separations, and SEC separations. 1. A chromatographic material having controlled porosity.2. The chromatographic material of claim 1 , wherein the material is in the form of a particle.3. The chromatographic material of claim 1 , wherein the material is in the form of a monolith.4. The chromatographic material of claim 1 , wherein the material is in the form of a superficially porous material.5. (canceled)6. (canceled)7. The chromatographic material of claim 1 , comprising a chromatographic core material having a primary surface and one or more layers of a chromatographic surface material.8. (canceled)9. The chromatographic material of claim 7 , wherein the chromatographic core material is an inorganic material claim 7 , an organic material claim 7 , or an inorganic/organic hybrid material.10. (canceled)1222-. (canceled)23. The chromatographic material of claim 7 , wherein each layer of the one or more layers of a chromatographic surface material independently has an average pore diameter of 20 to 1500 Angstroms.24. The chromatographic n material of claim 23 , wherein the average pore diameter of the one or ...

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09-05-2019 дата публикации

CONCENTRATING LITHIUM CARBONATE AFTER REGENERATION OF LITHIUM SORBENT

Номер: US20190134607A1
Принадлежит:

A system and method that includes flowing brine containing a metal ion through a reactor that includes porous particles having metal ion imprinted polymer having selective binding sites. The system and method further include discharging the brine from the reactor, contacting the porous particles with water, and pressurizing the reactor with carbon dioxide. The carbon dioxide reacts with the adsorbed metal ions to form a metal carbonate solution, where the metal carbonate solution can then be continuously purified with ion exchange. The method can include recycling eluent from the ion exchange back into the system for re-use. The method further includes depressurizing the reactor to precipitate metal carbonate from the metal carbonate solution and discharging the metal carbonate solution from the reactor. 1. A system comprising: a reactor vessel;', 'a brine inlet through which brine is introduced into the reactor vessel;', 'a brine outlet through which brine is discharged from the reactor vessel;', 'a water inlet through which water is introduced into the reactor vessel;', 'a carbon dioxide inlet configured to receive carbon dioxide from a carbon dioxide source, the carbon dioxide used to pressurize the reactor vessel and depressurize the reactor vessel;', 'a metal bicarbonate solution outlet through which metal bicarbonate is discharged from the reactor vessel;', 'porous particles in the reactor vessel, wherein the porous particles comprise a metal ion imprinted polymer formed from a hydrophilic co-monomer, a cross-linking agent and a metal containing polymerizable compound that includes at least one metal chelating ligand, wherein the metal ion imprinted polymer comprises a plurality of metal ion selective binding sites; and', 'at least a first and a second ion exchange columns in fluid communication with the metal bicarbonate solution outlet configured to work in tandem to remove impurities from the metal carbonate solution, wherein the system is capable of ...

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30-04-2020 дата публикации

PACKED INCOMPRESSIBLE CHROMATOGRAPHY RESINS AND METHODS OF MAKING THE SAME

Номер: US20200129883A1
Принадлежит: REPLIGEN CORPORATION

This disclosure provides chromatography columns that are packed with incompressible media such as ceramic hydroxyapatite particles, which exhibit high separation performance that is robust to transportation and multiple uses. The columns can be made by applying axial compression using rigid bodies, such as porous frits and/or flow regulators. 1. A chromatography column , comprising:a tubular member having first and second ends;a first flow distributor secured to a first end of the tubular member;a second flow distributor secured to a second end of the tubular member; anda packed chromatography medium comprising an incompressible component, the packed chromatography medium being disposed in the tubular member between the first and second flow distributors,wherein the packed chromatography medium is formed by compression between the first and second flow distributors, and{'sub': 'rms', 'wherein a separation performance of the column is characterized by a height-equivalent theoretical plate (HETP) value and an asymmetry value, and wherein (a) the HETP value does not change by more than 10% and/or (b) the asymmetry value does not change by more than 10% following a vibration exposure selected from (I) fixed displacement vibration of 25 mm total fixed displacement or (II) random displacement vibration of an overall Glevel of 1.15.'}2. The column of claim 1 , wherein (a) the HETP value does not change by more than 10% and/or (b) the asymmetry value does not change by more than 10% following a shock exposure selected from (I) a drop of 150 mm claim 1 , (II) an incline impact causing at least a 1.7 m/s velocity change claim 1 , or (III) a horizontal impact causing at least a 1.7 m/s velocity change.3. The column of claim 1 , wherein (a) the HETP value does not change by more than 10% and/or (b) the asymmetry value does not change by more than 10% following a sequence of vibration-shock-vibration exposures claim 1 , wherein the shock exposure is selected from (I) a drop of ...

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14-08-2014 дата публикации

Porous carbon-heteroatom-silicon inorganic/organic materials for chromatographic separations and process for the preparation thereof

Номер: US20140228464A1
Принадлежит: Waters Technologies Corp

The present invention provides porous carbon-heteroatom-silicon inorganic/organic homogenous copolymeric hybrid materials, methods for their preparation, and uses thereof, e.g., as chromatographic separations materials.

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28-08-2014 дата публикации

Sorbent for Lithium Extraction

Номер: US20140239224A1
Принадлежит: Simbol Inc.

This invention relates to a method for preparing a lithium aluminate intercalate (LAI) matrix solid and methods for the selective extraction and recovery of lithium from lithium containing solutions, including brines. The method for preparing the LAI matrix solid includes reacting aluminum hydroxide and a lithium salt for form the lithium aluminate intercalate, which can then be mixed with up to about 25% by weight of a polymer to form the LAI matrix. 1. A method for preparing a composition for the recovery of lithium from a brine , wherein the method comprises the steps of:preparing a lithium aluminate intercalate solid by contacting a lithium salt with alumina under conditions sufficient to infuse the alumina with lithium salt, wherein the mole ratio of lithium to alumina is up to about 0.5:1; andmixing the lithium aluminate intercalate solid with a polymer material in an aqueous medium to form a matrix, wherein said lithium aluminate intercalate solid is present in an amount of at least about 75% by weight and said polymer is present in an amount of between about 1% and 25% by weight, and wherein the said polymer is not an ion-exchange resin.2. The method of claim 1 , wherein the said polymer is selected from a group consisting of polyethylene claim 1 , ultra high molecular weight polyethylene claim 1 , high density polyethylene claim 1 , polypropylene claim 1 , poly vinyl alcohol claim 1 , poly acrylic acid claim 1 , polyvinylidinedifluoride claim 1 , polytetrafluoroethylene claim 1 , and combinations thereof.3. The method of claim 1 , wherein the lithium aluminate intercalate solid is present in the matrix in an amount of at least about 80% by weight and said polymer is present in an amount of between about 1% and 20% by weight.4. The method of claim 1 , wherein the lithium salt is lithium chloride.5. The method of claim 1 , wherein the alumina is selected from gibbsite claim 1 , alumina hydrate claim 1 , bayerite claim 1 , nordstandite claim 1 , bauxite claim ...

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22-09-2022 дата публикации

A chromatography device

Номер: US20220297031A1
Принадлежит: Puridify Ltd

A chromatography device ( 1; 101 ) comprising: —at least one chromatography material unit ( 3 ), wherein said chromatography material unit comprises a convection-based chromatography material; —at least one fluid distribution system ( 7 ) which is configured to distribute fluid into and out from the at least one chromatography material unit ( 3 ); —an inlet ( 15 ); —at least one inlet fluid channel ( 17 a, 17 b ) connecting the inlet ( 15 ) with each chromatography material unit ( 3 ) via the fluid distribution system ( 7 ); —an outlet ( 19 ); and —at least one outlet fluid channel ( 21 ) connecting the outlet ( 19 ) with each chromatography material unit ( 3 ) via the fluid distribution system ( 7 ), wherein at least some parts of said chromatography device ( 1; 101 ) are overmolded and sealed together by plastic or elastomer leaving at least the inlet ( 15 ) and the outlet ( 19 ) open.

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14-06-2018 дата публикации

SEPARATING MEDIUM AND COLUMN FOR LIQUID CHROMATOGRAPHY

Номер: US20180161758A1
Принадлежит:

The present invention provides a separating medium including porous resin particles which has a sufficient pore diameter suitable for liquid chromatography applications and which has high strength, is reduced in pressure loss during liquid passing, has the excellent property of separating a desired substance, and has low nonspecific adsorption properties. The separating medium of the invention is a separating medium obtained by treating porous epoxy resin particles and having an average pore diameter of 10 to 2,000 nm, or a separating medium obtained by treating porous epoxy resin particles and having a water content of 50% or higher. 1. A separating medium obtained by treating porous epoxy resin particles , which has an average pore diameter of 10 to 2 ,000 nm.2. A separating medium obtained by treating porous epoxy resin particles , which has a water content of 50% by weight or higher.3. The separating medium according to claim 2 , which has an average pore diameter of 10 to 2 claim 2 ,000 nm.4. The separating medium according to claim 1 , wherein the porous epoxy resin particles are particles of an epoxy resin corresponding to an addition polymer comprising a polyfunctional compound containing an epoxy group and a polyfunctional compound containing an amino group claim 1 , which has an average particle diameter of 1 to 1 claim 1 ,000 μm.5. The separating medium according to claim 4 , wherein the polyfunctional compound containing an epoxy group is at least one of N claim 4 ,N claim 4 ,N′ claim 4 ,N′-tetraglycidyl-m-xylylenediamine and triglycidyl isocyanurate.6. The separating medium according to claim 1 , wherein the treatment is a hydrophilization treatment wherein a compound having at least one of a hydroxyl group and an amino group is added to epoxy groups remaining in the surface of the porous epoxy resin particles claim 1 , thereby opening the rings of the epoxy groups.7. The separating medium according to claim 1 , wherein the treatment is a grafting ...

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04-09-2014 дата публикации

Thin-layer chromatography plate

Номер: US20140248196A1
Принадлежит: Daicel Corp

An object of the present invention is to provide a TLC plate which allows separation and detection of target substances on one plate. Provided is a TLC plate comprising a substrate, a separating medium layer stacked on the substrate, and a permeation layer stacked on the separating medium layer and allowing permeation of a target substance separated in the separating medium layer, wherein the separating medium layer has separating property for the target substance and optical responsiveness for ultraviolet rays, and the permeation layer has optical responsiveness different from that of the separating medium layer.

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29-09-2022 дата публикации

MIXED MODE CATION EXCHANGE CHROMATOGRAPHY LIGANDS BASED ON 1,3-DIOXOISOINDOLIN-2-YL STRUCTURES

Номер: US20220305460A1
Принадлежит:

The subject invention pertains to proteins are purified by a mixed-mode chromatography system formed by attaching a ligand with cation exchange and hydrophobic 1,3-droxoisoindolin-2-yl group functionalities to a large-pore support matrix, the only linkage between the ligand and the support matrix being a chain having a backbone of one, two, three, four, or five atoms between the hydrophobic group and the support matrix. 1. A mixed-mode chromatography medium comprising one or more ligand coupled to a solid support , said ligand comprising a 1 ,3-droxoisoindolin-2-yl group , said solid support having pores of a median diameter of 0.5 micron or greater with substantially no pores of 0.1 micron or less in diameter , and said ligand coupled to said solid support at a 1 ,3-droxoisoindolin-2-yl group through a chain of one to five atoms.2. The mixed-mode chromatography medium of claim 1 , wherein the solid support comprises particles and said particles have a median particle size of from about 25 microns to about 150 microns.3. The mixed-mode chromatography medium of claim 1 , wherein the ligand is 2-(5-amino-1 claim 1 ,3-dioxoisoindolin-2-yl)acetic acid claim 1 , 4-(5-amino-1 claim 1 ,3-dioxoisoindolin-2-yl)butanoic acid claim 1 , 2-(4-amino-1 claim 1 ,3-dioxoisoindolin-2-yl)acetic acid claim 1 , and/or 4-(4-amino-1 claim 1 ,3-dioxoisoindolin-2-yl)butanoic acid.4. The mixed-mode chromatography medium of claim 1 , wherein the mixed-mode chromatography medium has a dynamic binding capacity of at least about 30 mg of IgG per mL of mixed-mode chromatography medium.5. A composition comprising the mixed-mode chromatography medium of and a source solution or a buffer.6. The composition of claim 5 , wherein the source solution comprises non-antibody target proteins claim 5 , monomeric antibodies and/or antibody aggregates.7. The composition of claim 5 , wherein said source solution or buffer contains a salt selected from alkali metal and alkaline earth metal halides at a ...

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01-07-2021 дата публикации

HONEY PROTEOMICS FOR HONEYBEE DISEASE AND ENVIRONMENTAL BIOMONITORING

Номер: US20210198308A1
Принадлежит:

Methods for isolating proteins from a honey sample are provided. The methods include contacting the honey sample with a substrate functionalized with one or more reactive dyes and recovering proteins associated with the substrate. Methods for detecting proteins in a honey sample and assessing the risk of colony collapse disorder are also provided. 1. A method for isolating proteins from a honey sample , comprising:contacting the honey sample with a substrate functionalized with one or more reactive dyes; andrecovering proteins associated with the substrate.2. The method of claim 1 , wherein the substrate comprises porous nanoparticles.3. The method of claim 2 , wherein the porous nanoparticles are core-shell nanoparticles and the one or more reactive dyes are attached to a surface of the core.4. The method of claim 3 , wherein the porous nanoparticles are formed from a poly(N-isopropylacrylamide-co-acrylic acid) core and a poly(N-isopropylacrylamide-co-vinylsulfonic acid) shell.5. The method of claim 1 , wherein the substrate comprises polymer filaments.6. The method of claim 5 , wherein the polymer filaments are nylon filaments.7. The method of claim 1 , wherein the one or more reactive dyes are selected from the group consisting of oxazine dyes claim 1 , dioxazine dyes claim 1 , benzoxazine dyes claim 1 , azo dyes claim 1 , diazo dyes claim 1 , anthraquinone dyes claim 1 , phathalocyanine dyes claim 1 , and chlorotriazine dyes.8. The method of claim 1 , wherein the recovering step comprises centrifuging the sample containing the substrate to form a pellet and eluting the protein from the pellet.9. A method of detecting proteins in a honey sample claim 1 , comprising:contacting the honey sample with a substrate functionalized with one or more reactive dyes;recovering proteins associated with the substrate; anddetermining an amino acid sequence of the proteins.10. The method of claim 9 , wherein the amino acid sequence is determined using tandem mass spectrometry.11 ...

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02-07-2015 дата публикации

STATIONARY PHASE

Номер: US20150182943A1
Принадлежит:

An object of the present invention is to provide a stationary phase that increases the number of column stages and that exhibits an excellent molecular discrimination ability. It was discovered that the number of column stages can be increased and an excellent molecular discrimination ability can be realized by a stationary phase that contains a polymer having, in main chain repeat units, an aromatic ring that forms a portion of the main chain and a bipolar atomic group that forms a portion of the main chain, wherein the stationary phase has a specific surface area of 5 to 1000 m/g. 1. A stationary phase comprising a polymer having , in main chain repeat units , an aromatic ring that forms a portion of the main chain and a bipolar atomic group that forms a portion of the main chain , wherein{'sup': '2', 'the stationary phase has a specific surface area of 5 to 1000 m/g.'}2. The stationary phase according to claim 1 , wherein the polymer is a polyester claim 1 , a polysulfone claim 1 , a polyethersulfone claim 1 , or a polycarbonate.3. The stationary phase according to claim 2 , wherein the polymer is a polyester.4. The stationary phase according to claim 3 , wherein the polyester is polyethylene terephthalate (PET) claim 3 , polybutylene terephthalate (PBT) claim 3 , polyethylene isophthalate claim 3 , poly(2 claim 3 ,2-dimethylpropan-1 claim 3 ,3-diyl terephthalate) claim 3 , or poly-4-oxymethylbenzoyl.5. The stationary phase according to claim 1 , wherein the polymer is supported on a carrier that has a specific surface area of 5 to 1000 mg.6. The stationary phase according to claim 1 , which is a particulate.7. The stationary phase according to claim 6 , wherein the average particle diameter is 0.1 μm or 1000 μm.8. The stationary phase according to claim 1 , which is a monolith.9. The stationary phase according to claim 1 , which is for supercritical fluid chromatography. The present invention relates to chromatographic technology. The present invention more ...

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22-06-2017 дата публикации

CLEANING METHOD OF IMMERSION LIQUID, IMMERSION LIQUID CLEANING COMPOSITION, AND SUBSTRATE

Номер: US20170176878A1
Принадлежит: JSR Corporation

A cleaning method of an immersion liquid includes supplying an immersion liquid on a surface of a cleaning substrate. The immersion liquid is to be used in a liquid immersion lithography apparatus. The cleaning substrate has a substrate and an organic film laminated on a top face side of the substrate. The immersion liquid is allowed to move on the substrate to remove contaminants from the immersion liquid. 111-. (canceled)13. The cleaning substrate of claim 12 , wherein the compound component comprises of at least two compounds selected from the set consisting of the first compound claim 12 , the second compound and the third compound.18. The cleaning substrate of claim 12 , wherein a content of the compound component is no less than 1 part by mass and no greater than 100 parts by mass with respect to 100 parts by mass of the first polymer.19. The cleaning substrate of claim 12 , wherein a content of the compound component is no less than 1 part by mass and no greater than 50 parts by mass with respect to 100 parts by mass of the first polymer.20. The cleaning substrate of claim 12 , wherein the solvent comprises ketone claim 12 , propylene glycol monoalkyl ether acetate claim 12 , 2-hydroxypropionic acid alkyl claim 12 , 3-alkoxypropionic acid alkyl claim 12 , γ-butyrolactone claim 12 , or a mixture thereof.21. The cleaning substrate of claim 12 , wherein the compound component comprises at least two compounds selected from the set consisting of the second compound and the third compound. The present application is a divisional application of U.S. patent application Ser. No. 13/398,847, filed Feb. 17, 2012, the contents of which are incorporated herein by reference in their entirety.Field of the InventionThe present invention relates to a cleaning method of an immersion liquid, an immersion liquid cleaning composition, and a substrate.Discussion of the BackgroundIn manufacture of semiconductor devices, microfabrication by lithography carried out using a chemically ...

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30-06-2016 дата публикации

MANUFACTURE OF MAGNETIC PARTICLES

Номер: US20160185880A1
Принадлежит:

A method for the production of particles by reacting functional groups on the surface of non-magnetic porous particles with functional groups on the surface of magnetic particles to form a covalent bond, to obtain particles supplemented with magnetic particles covalently bound to the outer part of said particles. Advantages include an increased binding capacity. 1. A method for production of particles (P) , said method comprising the steps of: non-magnetic porous particles (Pp) having an exterior surface, pores and a connected interior surface defined by said pores, the porous particles (Pp) comprising at least one polymer, the porous particles (Pp) comprising at least one type of functional group on said exterior and interior surfaces, and', 'magnetic particles (Mp) comprising at least one type of functional group on their surface wherein the smallest diameter of at least 95 wt % of all magnetic particles (Mp) is larger than the average diameter of the pores of the porous particles (Pp), and wherein a fraction of the magnetic particles (Mp) have such a diameter to enter the porous particles (Pp), and, 'a. providing'} to obtain particles (P) supplemented with magnetic particles (Mp) covalently bound to at least one of the interior surface and the exterior surface of the porous particles (Pp),', 'wherein all of the at least one type of functional groups on the surface of the magnetic particles (Mp) have not reacted to form covalent bonds with the at least one type of functional groups on the exterior and interior surfaces of the porous particles (Pp) so that a fraction of the at least one type of functional groups remain available on at least one of the magnetic particles (Mp) and the porous particles (Pp)., 'b. reacting the functional group(s) on the surface of the non-magnetic porous particle (Pp), with the functional group(s) on the surface of the magnetic particles (Mp) to form a covalent bond,'}2. The method according to claim 2 , wherein the porous particles ( ...

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30-06-2016 дата публикации

DIAGNOSTIC ASSAY USING PARTICLES WITH MAGNETIC PROPERTIES

Номер: US20160187327A1
Принадлежит:

A novel system for the analysis of molecules and cells, comprising clusters where a non-magnetic particle is supplemented with magnetic particles to form a characteristic pattern, fingerprint or bar code. Methods and devices for formation of such particles are also disclosed. 1. A particle comprising a non-magnetic porous particle having an exterior surface , pores and an interior surface defined by said pores , the porous particle comprising at least one polymer , said particle having at least one magnetic particle covalently bound to the outer parts thereof , wherein the smallest diameter of at least 95 percent per weight of all magnetic particles is larger than the largest diameter of at least 95% of the pores of the porous particles , wherein a fraction of the magnetic particles have a diameter such that they enter the non-magnetic porous particle , and wherein said at least one magnetic particle constitutes a feature capable of distinguishing one group of particles from another.2. The particle according to claim 1 , wherein the porous particle comprises at least one material selected from the group consisting of agarose claim 1 , silica claim 1 , cellulose claim 1 , polyvinyl alcohols claim 1 , polyethylene glycols claim 1 , polystyrene claim 1 , and derivatives thereof.3. The particle according to claim 1 , wherein at least one selected from the group consisting of the porous particle and the at least one magnetic particle comprise molecules adapted for detection.4. The particle according to claim 3 , wherein the molecules adapted for detection is at least one selected from the group consisting of an organic molecules claim 3 , an amino acid claim 3 , a peptide claim 3 , a protein claim 3 , a nucleic acid claim 3 , an antigen claim 3 , an enzyme claim 3 , an enzyme inhibitor claim 3 , a cofactor claim 3 , a hormone claim 3 , a toxin claim 3 , a glycoconjugate claim 3 , a lectin claim 3 , and a carbohydrate.5. The particle according to claim 1 , wherein the ...

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13-06-2019 дата публикации

Separation material, column provided with said separation material, and method for producing separation material

Номер: US20190176126A1
Принадлежит: Hitachi Chemical Co Ltd

Disclosed is a separation material comprising: a porous polymer particle containing a crosslinked polymer containing a structural unit derived from a crosslinkable monomer having an aromatic group and two or more vinyl groups bonded to the aromatic group; and a coating layer coating at least part of the surface of the porous polymer. The coating layer contains a first graft chain that is a polymer having a hydroxyl group bonded to the crosslinked polymer, and a second graft chain that is a polymer having a hydroxyl group, bonded to the first graft chain, and being different from the first graft chain.

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20-06-2019 дата публикации

PACKING MATERIAL FOR HILIC COLUMNS, HILIC COLUMN FILLED WITH SAME, AND METHOD FOR ANALYZING OLIGOSACCHARIDE WITH USE OF SAME

Номер: US20190184372A1
Принадлежит: SHOWA DENKO K.K.

Provided is a packing material for HILIC columns for more accurately and more easily performing oligosaccharide analysis by liquid chromatography; an HILIC column which is filled with the packing material for HILIC columns; and a method for analyzing an oligosaccharide with use of this packing material for HILIC columns A packing material for HILIC columns according to the present invention is composed of particles, each of which is obtained by reacting glycidol to a hydroxyl group of a porous cross-linked polymer base material having the hydroxyl group, and which have a hydrophilicity index of 2.30 or more and a surface-pH index of from 0.95 to 1.05. 1. A packing material for HILIC columns , comprising a cross-linked polymer base material having a hydroxyl group ,wherein the cross-linked polymer base material is porous particles;a glycidol is reacted with the hydroxyl group of the cross-linked polymer base material;a hydrophilicity index is 2.30 or more; and wherein the hydrophilicity index is defined by a separation coefficient of al (U/2dU), when performing a liquid chromatography measurement of a uridine (U) and a 2′-deoxyuridine (2dU) in a HILIC separation mode condition;', 'the surface-pH index is a separation coefficient of α2 (Tb/Tp), when performing a liquid chromatography measurement of a theobromine (Tb) and a theophylline (Tp) in a HILIC separation mode condition;', 'the separation coefficient α1 (U/2dU) and the separation coefficient α2 (Tb/Tp) are ratios of retention factors k of the materials, respectively;', {'sub': 0', '0', '0, 'each retention factor k is defined by k=(t-t)/t, wherein tis an elution time of toluene and, t is an elution time of each substance; and'}, 'a condition of the liquid chromatography measurement in the HILIC separation mode is shown as below:', 'a column temperature is 30° C.; and', 'a mobile phase is a mixed liquid of an acetonitrile and a water solution in a ratio (acetonitrile/water solution) of 90/10 (volume before mixing ...

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12-07-2018 дата публикации

PROCESS OF PURIFYING METHIONINE

Номер: US20180194723A1
Принадлежит:

The present invention provides a process for purifying methionine. A methionine product having a purity of up to 99% or higher is obtained by separating methionine from a salt by-product through a process comprising adsorption and desorption using a macroporous adsorption resin, where the methionine content in the salt by-product is ≤0.03%. The yield of methionine extracted with the resin is up to 98% or higher. By using the process of the present invention, the existing production process is simplified, the quality of the methionine product is improved, and the production costs for methionine are reduced. 1. A process for purifying methionine , whereinmethionine is separated from a salt by-product by using a macroporous adsorption resin, in which the methionine is adsorbed onto the macroporous adsorption resin, and then the methionine is recovered by desorbing from the resin using a desorbent; and the salt by-product is not absorbed onto the macroporous adsorption resin during the adsorption process, but enters an effluent resulting from the adsorption, the process mainly comprising the following steps:1) flowing a methionine solution, from the top to the bottom, through a macroporous adsorption resin layer, and stopping resin adsorption when the content of methionine in an effluent from the resin column is greater than or equal to 1 to 50% (w/w) of the content at an inlet, in which the effluent resulting from the resin adsorption is a salt by-product;2) resin desorption: desorbing, from the top to the bottom, the resin that has completed the adsorption in step 1) using a desorbent, and collecting the desorption solution; and3) subsequent process: subjecting the desorption solution to subsequent treatments following an existing process.2. The process for purifying methionine according to claim 1 , wherein the methionine comprises methionine and a hydroxyl derivative of methionine.3. The process for purifying methionine according to claim 1 , wherein the salt by- ...

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25-09-2014 дата публикации

COMPLEX COMPRISING CRYSTALLINE HYBRID NANOPOROUS MATERIAL POWDER

Номер: US20140287235A1

The present invention relates to a complex and a method for manufacturing same, the complex comprising: at least one crystalline hybrid nanoporous material powder, in which a metal ion, or a metal ion cluster to which oxygen is bound, and an organic ligand, or the organic ligand and a negative ion ligand are in a coordinate covalent bond; and at least one organic polymer additive, or at least one organic polymer additive and an inorganic additive, wherein the shape of the complex is spherical or pseudo-spherical, the size of the complex is 0.1 to 100 mm, a total volume of pores is 5 or more volume % based on the sum of a total volume of nanoporous material having a size of at most 10 nm and a total volume of pores having a size of at least 0.1 μm, and wherein a non-surface value per weight (m/g) of the complex as at least 83% of a non-surface value per weight (m/g) of the nanoporous material powder. 1. A composite comprising at least one crystalline hybrid nanoporous material powder , at least one organic polymeric additive and at least one optional inorganic additive; wherein said crystalline hybrid nanoporous material is prepared by coordinating at least one organic ligand and at least one optional anionic ligand to or with a metal ion or a metal ion cluster to which oxygen is bonded;{'sup': 2', '2, 'characterized by the fact that the composite has a spherical or pseudo-spherical shape and a size of 0.1˜100 mm; that the total void volume of the voids is at least 5% by volume based on the sum of the total pore volume of the nanopores having a size of 10 nm or smaller in the composite and the total void volume of the voids having a size of 0.1 μm or larger in the composite; and that the specific surface area per weight (m/g) of the composite is at least 83% based on the specific surface area per weight (m/g) of the nanoporous material powder.'}2. The opposite according to claim 1 , characterized in that the crystallinity index of the composite determined by X-ray ...

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13-07-2017 дата публикации

SELECTIVE METHODS FOR THE SEPARATION OF ONDANSETRON AND RELATED IMPURITIES

Номер: US20170197942A1
Принадлежит:

The present disclosure generally relates to methods for separating ondansetron and related impurities using CO-based chromatography. 1. A method of separating ondansetron and at least one related impurity using CO-based chromatography , comprisingapplying a sample of ondansetron and at least one related impurity to a chromatography column; and{'sub': '2', 'eluting ondansetron and at least one related impurity from the chromatography column using a mobile phase comprising CO.'}2. The method of claim 1 , wherein the mobile phase further comprises a modifier.3. The method of claim 1 , wherein the mobile phase further comprises methanol.4. The method of claim 1 , wherein the related impurities are Impurity E and Impurity F collectively.5. The method of claim 1 , wherein the related impurities are Impurity E and Impurity F collectively claim 1 , and wherein Impurity E and Impurity F have a retention time difference of greater than 10 seconds apart from one another.6. The method of claim 1 , wherein the related impurities are Impurity A claim 1 , Impurity C claim 1 , Impurity D claim 1 , Impurity E claim 1 , Impurity F claim 1 , and Impurity G collectively.7. The method of claim 1 , wherein the related impurities are Impurity A claim 1 , Impurity B claim 1 , Impurity C claim 1 , Impurity D claim 1 , Impurity E claim 1 , Impurity F claim 1 , Impurity G claim 1 , and Impurity H collectively.8. The method of claim 1 , wherein the retention time of the first related impurity eluted from the chromatography column is greater than 1.5 minutes.9. The method of claim 1 , wherein the total elution period of the ondansetron and related impurities is less than 10 minutes.10. The method of claim 1 , wherein the chromatography column comprises hybrid particles.11. The method of claim 1 , wherein the chromatography column comprises hybrid particles having an average particle size of 1.7 or 3.5 um.12. The method of claim 1 , wherein the chromatography column comprises hybrid particles ...

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30-07-2015 дата публикации

Separating agent

Номер: US20150209757A1
Автор: Takafumi Onishi
Принадлежит: Daicel Corp

Provided is a novel separating agent obtained by using core/shell particles as a support and fixing any of various ligands to the support by physical adsorption. The separating agent contains a support and a ligand fixed to the surface of the support by physical adsorption, and is characterized in that the support is core/shell particles each formed of a core constituted of a nonporous inorganic substance and a porous shell, the shell having a pore diameter of 30 nm or larger, the shell being constituted of a hydrolyzate of a polyalkoxysiloxane, and the ligand is an optically active polymer, an optically inactive polyester, a protein, or a nucleic acid.

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27-06-2019 дата публикации

Adsorbent material

Номер: US20190193050A1
Принадлежит: Hitachi Chemical Co Ltd

An object of the present invention is to provide an adsorbent material having high dispersibility and reversibility. The adsorbent material has a polymer material having a plurality of functional groups ionizable in water and exhibiting no lower limit critical solution temperature, an adsorption site capable of interacting with a target substance, and a carrier.

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18-06-2020 дата публикации

Device and method for extracting nucleic acids from biological sample materials with solvent-free reagents

Номер: US20200188910A1
Принадлежит: SIEMENS HEALTHCARE DIAGNOSTICS INC.

The present invention relates to a device comprising a container having an inner wall and at least one opening, containing a mixture containing at least one reagent, and at least one additive, a method of producing this device, and a method of extracting a substance from a sample, enriching a substance in a sample, and/or detecting a substance in a sample using the device. 1. Device , comprising a container having an inner wall and at least one opening , containing at least one reagent, and', 'at least one additive,, 'a mixture containing'}wherein the at least one reagent is fixed to at least part of the inner wall of the container with the at least one additive, wherein the at least one reagent is at least one of dispersed in the at least one additive, coated by the at least one additive, and at least partially covered by the at least one additive.2. Device according to claim 1 , wherein the at least one reagent and the at least one additive are included in the container in the form of a mixture that is essentially free of solvent.3. Device according to claim 1 , wherein no solvents are included in the device.4. Device according to claim 1 , wherein the mixture comprises amorphous and/or crystalline phases.5. Device according to claim 1 , wherein the container is a tube claim 1 , particularly a microtube claim 1 , a well plate claim 1 , or a bottle.6. Device according to claim 1 , wherein the at least one additive is in solid form at room temperature.7. Device according to claim 1 , wherein the at least one additive comprises a polymer claim 1 , preferably a water-soluble polymer claim 1 , further preferably polyethyleneglycol claim 1 , polypropyleneglycol claim 1 , polyvinylpyrrolidone and/or polyvinylalcohol claim 1 , and/or copolymers thereof.8. Device according to claim 1 , wherein the at least one reagent comprises beads claim 1 , particularly magnetic beads claim 1 , and/or at least one chaotropic agent claim 1 , particularly a chaotropic salt claim 1 , and/ ...

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29-07-2021 дата публикации

SEPARATION MEDIUM, USE FOR SEPARATION MEDIUM, STEVIOL GLYCOSIDE SEPARATION METHOD USING SEPARATION MEDIUM, AND STEVIOL GLYCOSIDE PRODUCTION METHOD USING SEPARATION METHOD

Номер: US20210229071A1
Автор: ADACHI Tadashi
Принадлежит: MITSUBISHI CHEMICAL CORPORATION

An object of the present invention is to provide a separation medium and a separation method, ensuring high selectivity and good separation efficiency for specific steviol glycosides. The present invention is related to a separation medium in which polyethyleneimine is immobilized to porous particles of a (meth)acrylic polymer having a crosslinked structure and a hydroxyl group. 18-. (canceled)9. A separation method for steviol glycosides , the method comprising a liquid chromatography step of loading a solution containing two or more types of steviol glycosides to a separation medium and flowing a solvent A through the separation medium , thereby separating at least two types of steviol glycosides included in the steviol glycosides , wherein the separation medium comprises polyethyleneimine immobilized to porous particles of a (meth)acrylic polymer having a crosslinked structure and a hydroxyl group.10. The separation method for steviol glycosides according to claim 9 , wherein the solution containing two or more types of steviol glycosides comprises rebaudioside A claim 9 , and wherein at least one fraction obtained in the liquid chromatography step is a fraction containing rebaudioside A as a main component.11. The separation method for steviol glycosides according to claim 9 , wherein the solvent A comprises alcohols freely miscible with water.12. The separation method for steviol glycosides according to claim 9 , wherein a decolorization of a pigment component in the solution containing two or more types of steviol glycosides is performed during the liquid chromatography step.13. A separation method for steviol glycosides claim 9 , the method comprising an adsorption step of bringing a solution containing two or more types of steviol glycosides and a solvent B into contact with a separation medium to form a steviol glycosides adsorbed separation medium claim 9 , and an elution step of eluting the steviol glycosides from the steviol glycosides adsorbed ...

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09-10-2014 дата публикации

DELAYED-ACTIVATION, HYDRATION MAINTENANCE APPARATUS AND METHOD

Номер: US20140298722A1
Автор: Thrash Tommy K.
Принадлежит: AQUASMART ENTERPRISES, LLC

A composite, time-delayed, polymer-coated, granulated material for maintaining hydration in plants is formulated to delay acceptance of water in order to operate in drilling, plugging, and disking equipment used for aeration, soil amendment, or both. Whether potted or outdoors, whether relying on a third-material binder or a small, hydrated portion of the polymer itself as a binder, the material may be injected or otherwise placed below the surface of soils. Water is eventually absorbed sufficiently to expose the bulk of the hydrating particles attached to each granule. Addition of the granulated material as a soil amendment resists dehydration normally occurring in plants between waterings, yet its initial delay in hydrating supports water-jet injection and soil integration by resisting premature expansion from hydration. 1. A method for treating soils , the method comprising:providing a hydrator, comprising a carrier formed as granules, an absorber disposed on a surface of the carrier, and a repellant applied to the absorber to resist absorption of water thereby for a preselected period of time;selecting a soil location;providing a cavity in the soil;positioning a quantity of the hydrator in the cavity;applying water to the soil location during the preselected period to integrate the hydrator into the soil and to close the cavity to resist escape of the hydrator upon eventual absorption of water by the absorber;penetrating by water the absorber to substantially destroy the ability of the repellant to resist absorption of water by the absorber;providing water to the soil subsequent to the preselected period to hydrate of the absorber; andmaintenance of a portion of the water by the absorber after drying of surrounding soil proximate the soil location.2. The method of claim 1 , further comprising forming the cavity by a device selected from the group comprising a drill claim 1 , a corer claim 1 , a trencher claim 1 , and a jet of fluid.3. The method of claim 1 , ...

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05-08-2021 дата публикации

PACKING MATERIAL FOR ION CHROMATOGRAPHY AND PRODUCTION METHOD THEREFOR

Номер: US20210237034A1
Принадлежит: SHOWA DENKO K.K.

A packing material for ion chromatography has a structure in which a polyethyleneimine is bonded, directly or through a spacer, to a surface of an organic porous substrate constituted of a hydroxylated crosslinked copolymer, and a functional group represented by formula (1) 2. The packing material for ion chromatography according to claim 1 , wherein R is a 2-hydroxy propylene group claim 1 , and at least one of R claim 1 , Rand Ris a C1 to C10 alkyl group having an amino group.4. The packing material for ion chromatography according to claim 1 , wherein a polyethyleneimine is bonded through a spacer to a crosslinked copolymer.5. The packing material for ion chromatography according to claim 4 , wherein a crosslinked polymer has a hydroxyl group claim 4 , and the spacer has a structure derived from a multifunctional glycidyl ether or epichlorohydrin.6. The packing material for ion chromatography according to claim 5 , wherein the spacer is a multifunctional glycidyl ether claim 5 , and the multifunctional glycidyl ether is selected from 1 claim 5 ,4-butanediol diglycidyl ether claim 5 , ethylene glycol diglycidyl ether claim 5 , polyethylene glycol diglycidyl ether claim 5 , and glycerol diglycidyl ether.7. The packing material for ion chromatography according to claim 6 , wherein the multifunctional glycidyl ether is 1 claim 6 ,4-butanediol diglycidyl ether.8. The packing material for ion chromatography according to claim 1 , wherein the crosslinked copolymer is a crosslinked polyvinyl alcohol polymer.9. A production method of the packing material for ion chromatography according to claim 1 , comprising a step of bonding claim 1 , directly or through a spacer claim 1 , a polyethyleneimine to the surface of an organic porous substrate constituted of a crosslinked copolymer (step 1) claim 1 , a step of reacting a nitrogen atom contained in the polyethyleneimine with a multifunctional glycidyl ether (step 2) claim 1 , and a step of reacting a tertiary amine with the ...

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04-07-2019 дата публикации

CYCLIC PEPTIDE, AFFINITY CHROMATOGRAPHY SUPPORT, LABELED ANTIBODY, ANTIBODY DRUG CONJUGATE, AND PHARMACEUTICAL PREPARATION

Номер: US20190202864A1
Автор: MINAMI Koichi
Принадлежит: FUJIFILM Corporation

A cyclic peptide is represented by Formula (I), 1. A cyclic peptide represented by Formula (I) ,{'br': None, 'sup': N', 'a', '1', '2', '3', 'b', 'C, 'sub': g', 'i', 'm', 'n', 'j', 'k', 'h, 'R—X—[X—X—X—X—X—X—X—X—X]—X—R\u2003\u2003(I)'}in Formula (I),{'sup': 'N', 'Rrepresents an N-terminal group;'}{'sup': 'C', 'Rrepresents a C-terminal group;'}{'sup': '1', 'Xrepresents an L-leucine residue, an L-isoleucine residue, an L-methionine residue, an L-lysine residue, or an L-arginine residue;'}{'sup': '2', 'Xrepresents an L-valine residue or an L-isoleucine residue;'}{'sup': '3', 'Xrepresents an L-tryptophan residue or an L-phenylalanine residue;'}{'sup': a', 'b', 'a', 'b, 'one of Xand Xrepresents an amino acid residue derived from an amino acid having an azide group on a side chain and the other represents an amino acid residue derived from an amino acid having an alkynyl group on a side chain, and Xand Xare bonded to each other through a triazole bond;'}{'sub': g', 'h', 'i', 'j', 'm', 'n, "X, X, X, X, X, and Xeach represent g consecutive X's, h consecutive X's, i consecutive X's, j consecutive X's, m consecutive X's, and n consecutive X's;"}X represents an amino acid residue, and in a case where there is a plurality of X's, the plurality of X's may be the same as or different from each other;g, h, i, and j each independently represent an integer equal to or greater than 0;m and n are integers satisfying 0≤m≤9, 0≤n≤9, and 3≤m+n≤9 simultaneously; and{'sup': 1', '2', '3', 'a', 'b', 'a', '1', '2', '3', 'b, 'sub': i', 'j', 'm', 'n', 'i', 'm', 'n', 'j, 'k is an integer equal to or greater than 1, and in a case where k≥2, X, X, X, X, X, X, X, X, and Xin a repeating unit [X—X—X—X—X—X—X—X—X] each may be the same or different between the repeating units.'}2. The cyclic peptide according to that is represented by Formula (IA) claim 1 ,{'br': None, 'sup': N', '4', 'a', '1', '2', '3', 'b', '5', 'C, 'sub': g', 'p2', 'r', 'p1', 'm', 'n', 'q1', 's', 'q2', 'k', 'h, 'R—X—[X—X—X—X—X—X—X—X—X— ...

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23-10-2014 дата публикации

POLYSACCHARIDE MONOLITHIC STRUCTURE AND MANUFACTURING METHOD THEREFOR

Номер: US20140311984A1
Принадлежит: JNC CORPORATION

A problem is to provide a monolithic structure that is a porous body formed of a polysaccharide being a naturally-occurring polymer, and has continuous pores having an average pore diameter suitable for biomolecule separation to allow formation into an arbitrary shape, and a manufacturing method therefor. A solution is to manufacture the polysaccharide monolithic structure by a method including a first step for dissolving a polysaccharide into a mixed solvent including a solvent into which the polysaccharide is soluble and a solvent into which the polysaccharide is insoluble, at a temperature lower than a boiling point of the mixed solvent, to give a polysaccharide solution, and a second step for cooling the polysaccharide solution to give the polysaccharide monolithic structure. The polysaccharide monolithic structure obtained is a porous body having continuous pores having an average pore diameter of 0.01 to 20 micrometers and a thickness of 100 micrometers or more. 1. A polysaccharide-containing monolithic structure , wherein the polysaccharide monolithic structure is a porous body having continuous pores having an average pore diameter of 0.01 to 20 micrometers , anda thickness of 100 micrometers or more.2. The polysaccharide monolithic structure according to claim 1 , wherein the polysaccharide is cellulose.3. The polysaccharide monolithic structure according to claim 1 , wherein at least one hydroxyl group of the polysaccharide is esterified.4. The polysaccharide monolithic structure according to claim 1 , comprising cross-linked structure.5. The polysaccharide monolithic structure according to claim 1 , wherein a ligand is introduced into at least one hydroxyl group of the polysaccharide.6. A manufacturing method for a polysaccharide monolithic structure claim 1 , comprising:a first step for dissolving a polysaccharide into a mixed solvent including a solvent into which the polysaccharide is soluble and a solvent into which the polysaccharide is insoluble, at ...

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20-08-2015 дата публикации

Rigid and contorted divinyl crosslinkers

Номер: US20150232592A1
Принадлежит: 3M Innovative Properties Co

Polymerizable compositions containing rigid and contorted divinyl crosslinkers and polymeric materials prepared from the polymerizable compositions are described. The crosslinkers have a spirobisindane-type structure and can undergo free radical polymerization reactions. Methods of preparing the polymeric materials from the polymerizable compositions are also described.

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19-08-2021 дата публикации

STATIONARY PHASE FOR CHROMATOGRAPHY

Номер: US20210252479A1
Принадлежит: Daicel Corporation

Provided is a stationary phase for chromatography, the stationary phase being made of inorganic carrier particles to which is bonded a polymer having a hydrophilic group on repeating units of a main chain thereof, and being produced by a particular production method. 111-. (canceled)13. The stationary phase for chromatography according to claim 12 , wherein the inorganic carrier particles are porous inorganic particles or non-porous inorganic particles.14. The stationary phase for chromatography according to claim 13 , wherein the inorganic carrier particles are porous inorganic particles claim 13 , and the porous inorganic particles are core-shell particles.15. The stationary phase for chromatography according to claim 12 , wherein an average particle size is from 0.1 μm to 50 μm.16. The stationary phase for chromatography according to claim 12 , which is used for supercritical fluid chromatography.17. A method for separating a target material claim 12 , the method including separating the target substance using the stationary phase described in and a mobile phase comprising a supercritical fluid.19. The stationary phase for chromatography according to claim 18 , wherein the inorganic carrier particles are porous inorganic particles or non-porous inorganic particles.20. The stationary phase for chromatography according to claim 19 , wherein the inorganic carrier particles are porous inorganic particles claim 19 , and the porous inorganic particles are core-shell particles.21. The stationary phase for chromatography according to claim 18 , wherein an average particle size is from 0.1 μm to 50 μm.22. The stationary phase for chromatography according to claim 18 , which is used for supercritical fluid chromatography.23. A method for separating a target material claim 18 , the method including separating the target substance using the stationary phase described in and a mobile phase comprising a supercritical fluid.24. A method for producing a stationary phase for ...

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19-08-2021 дата публикации

Micro Circulatory Gas Chromatography System and Method

Номер: US20210252480A1
Принадлежит:

A gas chromatography system can include a circulatory loop, a gas inlet positioned along the circulatory loop, a gas outlet positioned along the circulatory loop, a micro column positioned in line with the circulatory loop, and an in-line population sensor positioned in line with the circulatory loop. The in-line population sensor can be configured to detect changes in gas population. The gas inlet and gas outlet can be associated with a gas inlet valve and gas outlet valve, and configured to admit or withdraw gas from the circulatory loop, respectively. A gas sample can be circulated through the circulatory loop for at least one cycle, and a component of the gas sample can be detected using the in-line population sensor. 1. A gas chromatography system comprising:a recirculating loop;a gas inlet positioned along the recirculating loop and configured to admit gas into the recirculating loop;a gas inlet valve associated with the gas inlet, wherein the gas inlet valve can be switched to allow gas to flow into the recirculating loop;a gas outlet positioned along the recirculating loop and configured to withdraw gas from the recirculating loop;a gas outlet valve associated with the gas outlet, wherein the gas outlet valve can be switched to allow gas to flow out of the recirculating loop;a micro column positioned in line with the recirculating loop such that gas cycles around the recirculating loop and through the micro column multiple times; andan in-line population sensor positioned in line with the recirculating loop, the in-line population sensor configured to detect changes in gas population.2. The gas chromatography system of claim 1 , further comprising an in-line micro pump configured to recirculate gas in the recirculating loop.3. The gas chromatography system of claim 1 , further comprising an in-line blocking valve and a controller claim 1 , wherein the controller is configured to open and close the gas inlet valves claim 1 , the gas outlet valves claim 1 , ...

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18-08-2016 дата публикации

METHOD FOR PRODUCING POROUS CELLULOSE BEADS

Номер: US20160236171A1
Принадлежит: KANEKA CORPORATION

The present invention provides a method for easily and efficiently producing cellulose beads which has narrow pore size distribution and pore structure suitable for an adsorbent and of which adsorption performance is excellent without using highly toxic and highly corrosive auxiliary raw material and without industrially disadvantageous cumbersome step. The method for producing porous cellulose beads according to the present invention is characterized in comprising (a) the step of preparing a fine cellulose dispersion by mixing a low temperature alkaline aqueous solution and cellulose, (b) the step of preparing a mixed liquid by adding a water-soluble low molecular organic compound to the fine cellulose dispersion, (c) the step of preparing an emulsion by dispersing the mixed liquid in a dispersion medium, (d) the step of contacting the emulsion with a coagulating solvent. 1: A method for producing porous cellulose beads , comprising(a) the step of preparing a fine cellulose dispersion by mixing a low temperature alkaline aqueous solution and cellulose,(b) the step of preparing a mixed liquid by adding a water-soluble low molecular organic compound to the fine cellulose dispersion,(c) the step of preparing an emulsion by dispersing the mixed liquid in a dispersion medium,(d) the step of contacting the emulsion with a coagulating solvent.2: The method according to claim 1 , wherein the temperature of the alkaline aqueous solution in the step (a) is not less than 0° C. and not more than 25° C.3: The method for producing porous cellulose beads according to claim 1 , wherein the water-soluble low molecular organic compound is an amino acid.4: The method for producing porous cellulose beads according to claim 1 , wherein the water-soluble low molecular organic compound is one or more amino acids selected from the group consisting of glycine claim 1 , alanine claim 1 , serine claim 1 , threonine claim 1 , asparagine claim 1 , glutamine claim 1 , aspartic acid claim 1 , ...

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16-08-2018 дата публикации

ORGANIC GEL OR LIQUID CHROMATOGRAPHY METHOD

Номер: US20180229151A1
Автор: Parmentier Francois
Принадлежит:

The invention relates to a chromatography method in which a gaseous, liquid or supercritical mobile phase containing species to be separated is circulated through a packing, said packing comprising: —a plurality of capillary ducts extending in the packing between an upstream face through which the mobile phase enters the packing and a downstream face through which the mobile phase leaves the packing, and —a continuous medium permeable to molecular diffusion extending between said ducts, comprising a porous organic gel or an organic liquid and including at least one network of connected pores, the size of which is greater than two times the molecular diameter of at least one species to be separated and opening to the ducts, so as to give said at least one species a diffusive path between said ducts. The invention also relates to a packing for the implementation of such a method and a method for manufacturing such a packing. 1. A chromatography method wherein a gas , liquid or supercritical mobile phase containing species to be separated is circulated through a packing , said packing comprising:a plurality of capillary conduits extending in the packing between a so-called upstream face through which the mobile phase penetrates into the packing and a so-called downstream face through which the mobile phase exits the packing, anda continuous medium permeable to molecular diffusion extending between said conduits, including a porous organic gel or an organic liquid and including at least a network of connected pores for which the size is greater than twice the molecular diameter of at least one species to be separated and open on the conduits, so as to provide to said at least one species a diffusive path between said conduits.2. The method according to claim 1 , wherein the average molar flow rate of diffusion of the species to be separated between the adjacent conduits under the effect of a given concentration difference of said species between the walls of said ...

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16-08-2018 дата публикации

Porous particle made of organic polymer, method for producing porous particle made of organic polymer, and block copolymer

Номер: US20180230284A1

The present invention provides porous particles made of an organic polymer, uniform in shape, and having through holes that are not closed. The porous particles according to the present invention are porous particles having a substantially spherical shape. The porous particles are made of an organic polymer. Each of the porous particles has an interconnected pore structure in which through holes provided inside the porous particle communicate with each other, and ends of the through holes are open toward an outside of the porous particle.

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23-08-2018 дата публикации

LIQUID CHROMATOGRAPHIC COLUMN AND LIQUID CHROMATOGRAPHIC APPARATUS INCLUDING THE SAME

Номер: US20180238842A1
Принадлежит: SHOWA DENKO K.K.

A liquid chromatographic column includes: a cylindrical column body; an inflow-side filter that is disposed at an eluent inflow-side end of the column body; an outflow-side filter that is disposed at an eluent outflow-side end of the column body; and a filler that is filled between the inflow-side filter and the outflow-side filter, in which the inflow-side filter has a two-layer structure consisting of a first resin filter member and a second resin filter member which are disposed in this order from a side of the filler, and the first resin filter member has an indentation elastic modulus lower than that of the second resin filter member. 1. A liquid chromatographic column , comprising:a cylindrical column body;an inflow-side filter that is disposed at an eluent inflow-side end of the column body;an outflow-side filter that is disposed at an eluent outflow-side end of the column body; anda filler that is filled between the inflow-side filter and the outflow-side filter,wherein the inflow-side filter has a two-layer structure consisting of a first resin filter member and a second resin filter member which are disposed in this order from a side of the filler, andthe first resin filter member has an indentation elastic modulus lower than that of the second resin filter member.2. A liquid chromatographic column , comprising:a cylindrical column body;an inflow-side filter that is disposed at an eluent inflow-side end of the column body;an outflow-side filter that is disposed at an eluent outflow-side end of the column body; anda filler that is filled between the inflow-side filter and the outflow-side filter,wherein the inflow-side filter has a two-layer structure consisting of a first resin filter member and a second resin filter member which are disposed in this order from a side of the filler,the first resin filter member is made of polyethylene, polypropylene, or polytetrafluoroethylene, andthe second resin filter member is made of polyether ether ketone or a ...

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24-08-2017 дата публикации

Devices and Methods using Pore Size Modulation for Detecting Analytes in a Fluid Sample

Номер: US20170241946A1

Provided are devices that include a polymeric separation medium configured to immobilize one or more constituents of interest in the polymeric separation medium and have an increased pore size upon application of an applied stimulus. Systems including the devices, as well as methods of using the devices, are also provided. Embodiments of the present disclosure find use in a variety of different applications, including detecting whether an analyte is present in a fluid sample. 1. A device comprising:a polymeric separation medium that immobilizes one or more constituents of interest in the polymeric separation medium and has an increased pore size upon application of an applied stimulus.2. The device of claim 1 , wherein the polymeric separation medium comprises a non-labile crosslinker configured to crosslink the polymeric separation medium claim 1 , and a labile crosslinker configured to crosslink the polymeric separation medium and de-crosslink upon application of the applied stimulus.3. The device of claim 2 , wherein the labile crosslinker is selected from the group consisting of an acid cleaved crosslinker claim 2 , an alkaline cleaved crosslinker claim 2 , an oxidation cleaved crosslinker claim 2 , a reduction cleaved crosslinker claim 2 , a molecular affinity crosslinker claim 2 , a heat cleaved crosslinker claim 2 , a photo cleaved crosslinker claim 2 , a solvent cleaved crosslinker claim 2 , and an ionic crosslinker.4. The device of claim 2 , wherein the labile crosslinker comprises ethylene glycol diacrylate (EDA) claim 2 , N claim 2 ,N′-(1 claim 2 ,2-dihydroxyethylene)bisacrylamide (DHEBA) claim 2 , N—N′-diallyltartardiamide (DATD) claim 2 , N claim 2 ,N′-bis(acryloyl)cystamine (BAC) claim 2 , N claim 2 ,N′-(7 claim 2 ,7-dimethyl-3 claim 2 ,6 claim 2 ,8 claim 2 ,11-tetraoxatridecane-1 claim 2 ,13-diyl)diacrylamide (DOK) claim 2 , N claim 2 ,N′-[(1-methylethylidene)bis(oxy-2 claim 2 ,1-ethanediyl)]diacrylamide (DK) claim 2 , or alginate.5. The device of ...

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24-08-2017 дата публикации

Micro Circulatory Gas Chromatography System and Method

Номер: US20170241961A1
Принадлежит:

A gas chromatography system can include a circulatory loop, a gas inlet positioned along the circulatory loop, a gas outlet positioned along the circulatory loop, a micro column positioned in line with the circulatory loop, and an in-line population sensor positioned in line with the circulatory loop. The in-line population sensor can be configured to detect changes in gas population. The gas inlet and gas outlet can be associated with a gas inlet valve and gas outlet valve, and configured to admit or withdraw gas from the circulatory loop, respectively. A gas sample can be circulated through the circulatory loop for at least one cycle, and a component of the gas sample can be detected using the in-line population sensor. 1. A gas chromatography system comprising:a circulatory loop;a gas inlet positioned along the circulatory loop and configured to admit gas into the circulatory loop, the gas inlet associated with a gas inlet valve;a gas outlet positioned along the circulatory loop and configured to withdraw gas from the circulatory loop, the gas outlet associated with a gas outlet valve;a micro column positioned in line with the circulatory loop; andan in-line population sensor positioned in line with the circulatory loop, the in-line population sensor configured to detect changes in gas population.2. The gas chromatography system of claim 1 , further comprising an in-line micro pump configured to circulate gas in the circulatory loop.3. The gas chromatography system of claim 1 , further comprising an in-line blocking valve and a controller claim 1 , wherein the controller is configured to open and close the gas inlet valves claim 1 , the gas outlet valves claim 1 , and the in-line blocking valves in a sequence to circulate gas in the circulatory loop.4. The gas chromatography system of claim 3 , wherein the system comprises two gas inlets claim 3 , two gas outlets claim 3 , two in-line blocking valves claim 3 , and two micro columns positioned along the ...

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01-09-2016 дата публикации

PRODUCTION METHOD FOR POROUS CELLULOSE BEADS, AND ADSORBENT EMPLOYING SAME

Номер: US20160251394A1
Принадлежит: KANEKA CORPORATION

The objective of the present invention is to provide to a method for easily producing high-performance porous cellulose beads having high mechanical strength. Also, the objective of the present invention is to provide an adsorbent produced from the high-performance porous cellulose beads. According to the present invention, high-performance porous cellulose beads can be easily produced from porous cellulose beads, and an adsorbent having high strength and high adsorption amount can be easily produced from the high-performance porous cellulose beads. 1. A method for producing high-performance porous cellulose beads , comprising the step of treating crosslinked cellulose beads with a cellulolytic enzyme.2. The method for producing high-performance porous cellulose beads according to claim 1 , wherein an endo-type cellulolytic enzyme is used as the cellulolytic enzyme.3. The method for producing high-performance porous cellulose beads according to claim 2 , wherein an exo-type cellulolytic enzyme is further used as the cellulolytic enzyme.4. The method for producing high-performance porous cellulose beads according to claim 1 , wherein the crosslinked cellulose beads are treated with the cellulolytic enzyme for not less than 1 hour and not more than 10 hours.5. The method for producing high-performance porous cellulose beads according to claim 1 , wherein the crosslinked cellulose beads are crosslinked by a glycidyl ether-type compound as a crosslinking agent.6. The method for producing high-performance porous cellulose beads according to claim 1 , wherein the crosslinked cellulose beads are crosslinked using water as a reaction solvent for a crosslinking reaction.7. A method for producing an adsorbent claim 1 , comprising the step of immobilizing a ligand interacting with a target substance to be adsorbed on the high-performance porous cellulose beads produced by the method according to to obtain the adsorbent.8. An adsorbent claim 1 , comprising the high-performance ...

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17-09-2015 дата публикации

ODOR AND COLOR STABLE WATER-ABSORBING COMPOSITION

Номер: US20150258527A1
Принадлежит:

The present invention relates to a water-absorbing composition comprising at least 1. A water-absorbing composition comprising at least:i) from 89 to 99.89 wt % of at least one water-absorbing polymer;ii) from 0.1 to 10 wt % of at least one oxidizing agent; andiii) from 0.01 to 1 wt % of at least one inhibitor to inhibit free-radical polymerizations;wherein the weight quantities are each based on the overall weight of the water-absorbing composition.2. The water-absorbing composition according to wherein the water-absorbing polymer i) is particulate and at least 90 wt % of the particles of the water-absorbing polymer i) have a particle size in a range from 150 to 850 μm.3. The water-absorbing composition according to wherein the oxidizing agent ii) is a hydrogen peroxide source.4. The water-absorbing composition according to wherein the oxidizing agent ii) is a percarbonate.5. The water-absorbing composition according to wherein the inhibitor (iii) is hydroquinone or a hydroquinone derivative.6. The water-absorbing composition according to wherein the inhibitor (iii) is selected from the group consisting of hydroquinone claim 5 , hydroquinone monomethyl ether (HQME) claim 5 , 1 claim 5 ,4-dimethoxybenzene claim 5 , 4 claim 5 ,4′-oxydiphenol and a mixture of two or more thereof.7. The water-absorbing composition according to wherein the composition in addition to the components i) to iii) further comprises a bleach activator iv).8. The water-absorbing composition according to wherein the bleach activator iv) is selected from the group consisting of tetraacetylethylenediamine (TAED) claim 7 , nonanoylbenzenesulphonate (NOBS) and a mixture of two or more thereof.9. The water-absorbing composition according to wherein the composition has a measure of greyness claim 1 , ΔL claim 1 , value of at most 10.0 after the water-absorbing composition has been stored at 70° C. and a relative humidity of 75% for 10 days.10. A process for producing a water-absorbing composition ...

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08-09-2016 дата публикации

Hollow tubular oil absorbing material and preparing method thereof

Номер: US20160256849A1
Принадлежит:

A hollow tubular oil absorbing material includes: a core formed by a spring, and an outer shell formed by a flat sponge wrapped at the spring; wherein the flat sponge is fixed at both ends of the spring; the flat sponge fully covers all the spring or is sealed at a first end; a connecting tube is connected at a second end of the spring for communicating with a vacuum pump; a graphene oxide layer is coated at the outer sponge. The graphene oxide layer on the flat sponge of hollow tubular oil absorbing material is formed by immersion and coating under negative pressure. Further the reduction of graphene oxide is performed with hydrazine hydrate steam and followed by washing and drying. Finally, a hollow tubular oil absorbing material with a spring core and an outer grapheme-coated sponge structure is obtained, which can be applied to continuous oil-water separation. 1. A hollow tubular oil absorbing material , comprising: a core formed by a spring , and a outer shell formed by a flat sponge wrapped at the spring; wherein the flat sponge is fixed at both ends of the spring; the flat sponge fully covers all the spring or is sealed at a first end; a connecting tube is connected at a second end of the spring for communicating with a vacuum pump; a graphene oxide layer is coated at the outer sponge.2. A preparing method of a hollow tubular oil absorbing material , comprising steps of:1) wrapping a surface of a spring with a flat sponge, and fixing the sponge at both ends of the spring, wherein the flat sponge fully covers a top portion of the spring or is sealed at a first end; a connecting tube is connected at a second end of the spring for obtaining a hollow tubular sponge with a spring core and an outer sponge shell structure;a connecting tube is connected at the second end of the spring for obtaining a hollow tubular sponge with a spring core and an outer sponge shell structure;2) obtaining graphene oxide dispersion in water;3) connecting the connecting tube of the ...

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08-08-2019 дата публикации

Channeled Fibers in Separation of Biologically Active Nanoparticles

Номер: US20190240594A1
Принадлежит:

A relatively fast, inexpensive, and non-destructive method for separation and isolation of biologically active nanoparticles is described. Methods include the use of solid phase separation medis such as channeled fibers in a hydrophobic interaction chromatography (HIC) protocol to isolate biologically active nanoparticles from other components of a mixture. Biologically active nanoparticles can include natural nanoparticles (e.g., exosomes, lysosomes, virus particles) as well as synthetic nanoparticles (liposomes, genetically modified virus particles, etc.) 1. A method for separating biologically active nanoparticles from a mixture comprising:{'sup': '2', 'flowing a mobile phase through a fluid conduit having a first end and second end that is disposed opposite the first end, the mobile phase including a salt, the fluid conduit containing a solid phase, the solid phase defining a plurality of passages through the fluid conduit, the passages defining a cross sectional dimension of from about 1 micrometer to about 4 micrometers, the solid phase having a surface that is non-porous to nanoparticles and that has a critical surface tension of about 35 mJ/mor greater and a water contact angle of about 85° or less;'}combining a mixture with the mobile phase, the mixture comprising biologically active nanoparticles, the biologically active nanoparticles adsorbing or binding to the surface of the solid phase as the mobile phase flows through the fluid conduit.2. The method of claim 1 , further comprising following an adsorption or binding period claim 1 , modifying the mobile phase claim 1 , the biologically active nanoparticles releasing from the surface of the solid phase as the modified mobile phase flows through the fluid conduit claim 1 , the method further comprising collecting the released biologically active nanoparticles.3. The method of claim 2 , wherein at least following the adsorption or binding period claim 2 , the mobile phase comprises an organic modifier.4. ...

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30-09-2021 дата публикации

LIQUID CHROMATOGRAPHY PACKING MATERIAL, LIQUID CHROMATOGRAPHY COLUMN AND METHOD FOR ANALYZING AMINE COMPOUND

Номер: US20210299635A1
Автор: KONDO Hideyuki
Принадлежит: SHOWA DENKO K.K.

A liquid chromatography packing material which includes a polymer packing material into which 1.50 mmol or more of carboxyl groups are introduced per 1 g of the packing material, and an index indicating pH of the surface of the polymer packing material as determined by hydrophilic interaction chromatography (HILIC) is 1.30 or more and the index indicating hydrophilicity of the surface of the polymer packing material as determined by a hydrophilic interaction chromatography (HILIC) is from 1.00 to 1.30.

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22-08-2019 дата публикации

METHOD FOR DISCHARGING SUPERABSORBENT PARTICLES FROM A SILO AND FILLING THEM INTO BULK CONTAINERS

Номер: US20190255514A1
Принадлежит:

Filling process for superabsorbent polymer particles The invention relates to a filling process for superabsorbent polymer particles, comprising discharging the superabsorbent polymer particles out of a silo into bulk container for shipping, wherein the filling level of the silo during filling of the bulk container is never less than 20%, in order to avoid particle segregation. 1. A filling process for superabsorbent polymer particles , wherein the superabsorbent polymer particles are discharged out of a silo into n bulk containers , n is an integer , the sum of the filled volumes of the n bulk container corresponds to more than 80% of the effective volume of the silo and the filling level of the silo during filling of the n bulk containers is not less than 20%.2. The process according to claim 1 , wherein the sum of filled volumes of the n bulk containers corresponds to more than 85% of the effective volume of the silo and the filling level of the silo during filling of the n bulk container is not less than 30%.3. The process according to claim 1 , wherein the sum of filled volumes of the n bulk containers corresponds to more than 90% of the effective volume of the silo and the filling level of the silo during filling of the n bulk container is not less than 40%.4. The process according to claim 1 , wherein the sum of filled volumes of the n bulk containers corresponds to more than 95% of the effective volume of the silo and the filling level of the silo during filling of the n bulk containers is not less than 50%.5. The process according to claim 1 , wherein the cone angle of the silo is smaller than 30° from the vertical.6. The process according to claim 1 , wherein the effective volume of the silo is at least 100 m.7. The process according to claim 1 , wherein the effective volume of the silo is at least 300 m.8. The process according to claim 1 , wherein the effective volume of the silo is at least 500 m.9. The process according to claim 1 , wherein the silo is ...

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15-10-2015 дата публикации

POROUS POLYMER METAL COMPLEX, GAS ADSORBENT, AND GAS SEPARATION DEVICE AND GAS STORAGE DEVICE USING SAME

Номер: US20150290618A1
Принадлежит:

An object of the present invention is to provide a porous polymer metal complex which can be used as a gas adsorbent and contains two or more types of similar ligands. A porous polymer metal complex is provided expressed by [CuX](1) (in the Formula, X represents two or more types of isophthalic acid ions selected from the group consisting of isophthalic acid ions and isophthalic acid ions having a substituent at position 5, at least an amount of one type of X is 5 mol % to 95 mol % of the total number of moles of X, and n represents an assembly number of constituent units expressed by CuX and is not particularly limited). 1. A porous polymer metal complex expressed by Formula (1):{'br': None, 'sub': 'n', '[CuX]\u2003\u2003(1)'}(in the Formula, X represents two or more types of isophthalic acid ions selected from the group consisting of isophthalic acid ions and isophthalic acid ions having a substituent at position 5, at least an amount of one type of X is 5 mol % to 95 mol % of the total number of moles of X, and n represents an assembly number of constituent units expressed by CuX and is not particularly limited).2. The porous polymer metal complex according to claim 1 , expressed by Formula (2):{'br': None, 'sub': 1-m', 'm', 'n, '[CuXY]\u2003\u2003(2)'}{'sub': 1-m', 'm, '(in the Formula, each of X and Y represents isophthalic acid ions or isophthalic acid ions having a substituent at position 5, X and Y are different from each other, 0.05≦m≦0.95 is satisfied, and n represents an assembly number of constituent units expressed by CuXYand is not particularly limited).'}3. The porous polymer metal complex according to claim 1 ,wherein the porous polymer metal complex has a paddle-wheel structure having vertically coordinated two units in which a copper ion is coordinated to four carboxyl groups,the paddle-wheel structure is connected by isophthalic acid derivatives to form a Kagome structure constituted by six-membered rings and three-membered rings, andthe Kagome ...

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11-10-2018 дата публикации

POLYMER MICROCOLUMN FOR GAS OR VAPOR SEPARATION, CHROMATOGRAPHY, AND ANALYSIS

Номер: US20180292364A1

In an aspect, a method for forming a microcolumn comprises steps of: (a) providing a sacrificial fiber; (b) forming a microcolumn body around said sacrificial fiber; and (c) removing said sacrificial fiber from said microcolumn body such that a hollow channel is formed within said microcolumn body via removal of said sacrificial fiber. In any embodiment of the methods disclosed herein for forming a microcolumn, said hollow channel extends through said microcolumn body and is continuous between a first end and a second end. The first end may be an inlet and the second end may be an outlet, for example, allowing for a mobile phase to enter the hollow channel via the first end and exit via the second end. 1. A method for forming a microcolumn , the method comprising steps of:a. providing a sacrificial fiber;b. forming a microcolumn body around said sacrificial fiber; andc. removing said sacrificial fiber from said microcolumn body such that a hollow channel is formed within said microcolumn body via removal of said sacrificial fiber.2. The method of claim 1 , wherein said hollow channel extends through said microcolumn body claim 1 , and said hollow channel is continuous between a first end and a second end of said hollow channel.3. The method of claim 1 , wherein said hollow channel has a three-dimensional geometry.4. The method of claim 2 , wherein a cross-sectional shape of said hollow channel is circular between said first end and said second end of said hollow channel.5. The method of claim 4 , wherein said hollow channel has an inner diameter and an outer diameter defining a thickness of a wall of said hollow channel claim 4 , and wherein said thickness of said wall is substantially uniform between said first end and said second end of said hollow channel; and said wall comprises a stationary phase material.6. (canceled)7. The method of claim 2 , wherein an inner surface of said hollow channel is substantially smooth.8. The method of claim 1 , wherein said ...

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18-10-2018 дата публикации

Delayed-Activation, Hydration Maintenance Apparatus and Method

Номер: US20180295794A1
Автор: Thrash Tommy K.
Принадлежит:

A composite, time-delayed, polymer-coated, granulated material for maintaining hydration in plants is formulated to delay acceptance of water in order to operate in drilling, plugging, and disking equipment used for aeration, soil amendment, or both. Whether potted or outdoors, whether relying on a third-material binder or a small, hydrated portion of the polymer itself as a binder, the material may be injected or otherwise placed below the surface of soils. Water is eventually absorbed sufficiently to expose the bulk of the hydrating particles attached to each granule. Addition of the granulated material as a soil amendment resists dehydration normally occurring in plants between waterings, yet its initial delay in hydrating supports water-jet injection and soil integration by resisting premature expansion from hydration. 1. A method for treating soils , the method comprising:providing a hydrator, comprising a carrier formed as granules, an absorber disposed on a surface of the carrier, and a repellant applied to the absorber to resist absorption of water thereby for a preselected period of time;selecting a soil location;providing a cavity in the soil;positioning a quantity of the hydrator in the cavity;applying water to the soil location during the preselected period to integrate the hydrator into the soil and to close the cavity to resist escape of the hydrator upon eventual absorption of water by the absorber;penetrating by water the absorber to substantially destroy the ability of the repellant to resist absorption of water by the absorber;providing water to the soil subsequent to the preselected period to hydrate of the absorber; andmaintenance of a portion of the water by the absorber after drying of surrounding soil proximate the soil location.2. The method of claim 1 , further comprising forming the cavity by a device selected from the group comprising a drill claim 1 , a corer claim 1 , a trencher claim 1 , and a jet of fluid.3. The method of claim 1 , ...

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01-10-2020 дата публикации

Porous polymer microspheres with optical anisotropy, method of manufacturing the same and application of the same

Номер: US20200306715A1

Porous polymer microsphere having radial optical anisotropy and diverse swelling states when dispersed in different solvents, which have ability to well swell the porous microspheres. A method for preparing the porous polymer microspheres, including: forming a homogeneous liquid crystal mixture; dispersing the liquid crystal mixture into a continuous phase to form a emulsion of liquid crystal droplets; polymerizing the at least one reactive liquid crystal to form intermediate microspheres; removing the at least one non-reactive liquid crystal compound to form the porous polymer microspheres; separating, washing and dispersing or drying the porous polymer microspheres. The polymer microspheres can be used as the stationary phase in chromatograph separation, improving separation efficiency and column packing efficiency. 1. Porous polymer microspheres , having radial optical anisotropy , wherein the porous polymer microspheres have diverse swelling states when dispersed in different solvents , and wherein the solvents have ability to well swell the porous polymer microspheres.2. The porous polymer microspheres of claim 1 , wherein the average particle size of the porous polymer microspheres in ethanol is 1 μm-150 μm.3. The porous polymer microspheres of claim 1 , wherein the swelling degree of the porous polymer microspheres in tetrahydrofuran is 1.0-7.0.4. A method for preparing the porous polymer micro spheres claim 1 , comprising:(I) forming a homogeneous liquid crystal mixture, wherein the liquid crystal mixture comprises at least one reactive liquid crystal compound, at least one non-reactive liquid crystal compound and at least one polymerization initiator;(II) dispersing the liquid crystal mixture into a continuous phase containing liquid-crystal-configuration-adjusting agent through a membrane emulsification device, to form a emulsion of liquid crystal droplets, wherein the liquid-crystal-configuration-adjusting agent align liquid crystal molecules inside the ...

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17-10-2019 дата публикации

RESIN BEADS AND USE IN PROCESSING OF AQUEOUS SOLUTIONS

Номер: US20190314785A1
Принадлежит:

Provided is a resin bead comprising functional groups of structure (S1). 4. The resin bead of claim 1 , wherein the mole ratio of —Y groups to —X— groups is 0.99:1 or higher.5. A collection of the resin beads of claim 1 , wherein the collection has harmonic mean diameter of 200 μm or higher.6. The collection of resin beads of claim 5 , wherein the collection has uniformity coefficient of 1.02 or greater. A common industrial goal is the processing of aqueous solutions. A category of aqueous solutions of interest are aqueous solutions that contain one or more sugar and/or one or more sugar alcohol. It is desirable to process such an aqueous solution in a way that separates some or all of the sugars and/or sugar alcohols from each other. It is also desirable to process such an aqueous solution in a way that is capable of separating some or all of the sugars and/or sugar alcohols from other compounds that may be present in the aqueous solution. It is also desirable to be able to process aqueous solutions having pH below 6.In the past, aqueous solutions of sugars have been processed to separate the sugars by using resin beads that have sulfonic acid groups in calcium form. It has been found that, in order to effectively separate the sugars, such resin beads needed to be present in a collection of resin beads that had both a relatively small mean diameter and a relatively small uniformity coefficient. Production of such uniform collections of small resin beads is difficult and expensive. It is desired to provide resin beads that are capable separating sugars, even when the collection of resin beads has relatively large mean diameter and relatively large uniformity coefficient.J. A. Vente, et al., in “Sorption and Separation of Sugars with Adsorbents Based on Reversible Chemical Interaction,” , vol. 24, p. 171, 2006, describe a boronic acid-functionalized poly(acrylamide) resin, used at pH 6 or pH 9, that is used to separate glucose and fructose. It is desired to provide ...

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10-12-2015 дата публикации

A COLUMN FILLING MATERIAL AND A PRODUCTION METHOD THEREOF

Номер: US20150353702A1
Принадлежит: ISTANBUL TEKNIK UNIVERSITESI

The present invention relates to a column filling material which is filled inside the columns used in chromatographic analysis of aromatic hydrocarbons, alkaloids, flavonoids and pesticides and provides high adsorption by means of its porous structure, and a production method thereof essentially comprising the steps of dissolving melamine and anthraquinone in a solvent (), carrying out the reacting by refluxing the solution (), washing the material obtained after reflux (), drying the washed material by freezing (). 1. A column filling material production method , which is filled inside the columns used in chromatographic analysis and provides high adsorption by means of its porous structure , comprising the steps of:dissolving a melamine and an anthraquinone in a solvent,carrying out the reaction by refluxing the solution,washing the material obtained after reflux,drying the washed material by freezing.2. The column filling material production method according to claim 1 , further comprises the step of dissolving the melamine and the anthraquinone in the solvent wherein 3 moles of 1 claim 1 ,5-dihydroxy anthraquinone is used for 2 moles of melamine.3. The column filling material production method according to claim 1 , further comprises the step of dissolving the melamine and the anthraquinone in the solvent wherein the solvent is selected from a group consisting of dimethyl sulfoxide claim 1 , dimethyl formamide claim 1 , toluene claim 1 , 1 claim 1 ,4-dioxane claim 1 , butyl acetate and mixture thereof.4. The column filling material production method according to further comprises the step of carrying out the reaction by refluxing the solvent which is carried out for 70-90 hours at 150-180° C.5. The column filling material production method according to further comprises the step of carrying out the reaction by refluxing the solvent wherein benzoxazine synthesis takes place upon the melamine reacts with the anthraquinone.7. The column filling material production ...

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08-12-2016 дата публикации

Thermally Modified Polymeric Organosilicon Material, Method for Preparing Said Material and the Uses Thereof

Номер: US20160354758A1
Принадлежит:

Materials obtained by thermal modification of polymeric organosilicons such as polydimethylsiloxane (PDMS) or derivatives of PDMS. Methods of preparing said materials and uses of said materials. 1. A material that is a modified PDMS or derivative of PDMS prepared by thermal treatment of a column containing PDMS or a derivative of PDMS at a temperature in the range of about 400° C. to about 1000° C.2. The material according to wherein the column is a capillary column.3. The material according to wherein the capillary column has an outer tube comprising metal or fused silica claim 2 , and an inner coating of PDMS or a derivative of PDMS.4. The material according to wherein the thermal treatment takes place in the presence of oxygen.5. The material according to wherein a flow of an oxygen containing gas is passed through the column during the thermal treatment.6. The material according to wherein the modified PDMS or derivative of PDMS is in the form of nanoparticles.7. The material according to wherein the thermal treatment comprises heating the column to a temperature in the range of 400° C. to 1000° C. for 1 to 5 heating cycles of 2-15 minutes per cycle.8. The material according to wherein the thermal treatment comprises heating the column to a temperature in the range of 750° C. to 850° C. for 1 cycle of 10 minutes followed by 2 cycles of 5 minutes.9. A column containing a modified PDMS material or a modified PDMS derivative material prepared by thermal treatment of a column containing PDMS or a derivative of PDMS at a temperature in the range of about 400° C. to about 1000° C.10. The column according to wherein the column is a capillary column having an outer tube comprising metal or fused silica and an inner coating of PDMS or a derivative of PDMS.11. The column according to wherein the thermal treatment process takes place in the presence of oxygen.12. The column according to wherein a flow of an oxygen containing gas is passed through the column during thermal ...

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13-12-2018 дата публикации

SURFACE GRAFTED HIGH INTERNAL PHASE EMULSION FOAMS FOR CHEMICAL SEPARATIONS

Номер: US20180353935A1
Принадлежит:

A method of forming a high internal phase emulsion (HIPE) foam is provided. A nitroxide-containing monomer can be used in combination with other monomers that can then be used to make a high internal phase emulsion foam upon curing. The nitroxide group can subsequently be used to control the radical polymerization of many monomers, which can be grafted from the surface of the high internal phase emulsion foam. The resulting foam can be useful in performing separations of radioactive species, metals, metal ions, multi-element ions, metal complexes, halides, and organic chemical species in chemical process streams, clean-up operations, etc. 1. A method of forming a high internal phase emulsion foam , the method comprising:incorporating a functionalized co-monomer containing a nitroxide-mediated polymerization agent into a backbone of the high internal phase emulsion foam; andgrafting a monomer from a surface of the high internal phase emulsion foam, wherein the nitroxide-mediated polymerization agent controls polymerization of the monomer.2. The method of claim 1 , wherein incorporating the functionalized co-monomer into the backbone of the high internal phase emulsion foam comprises blending an oil phase with an aqueous phase to form an emulsion that is then cured claim 1 , wherein the oil phase comprises the functionalized co-monomer claim 1 , an additional monomer claim 1 , and a cross-linking agent.7. The method of claim 2 , wherein the additional monomer is selected from the following classes of monomers: styrenics claim 2 , acrylates claim 2 , methacrylates claim 2 , dienes claim 2 , acrylamides claim 2 , methacrylamides claim 2 , vinyl esters claim 2 , and vinyl pyridines.8. The method of claim 2 , wherein the cross-linking agent comprises divinyl benzene.9. The method of claim 2 , wherein the oil phase further comprises a surfactant.10. The method of claim 2 , wherein the oil phase further comprises an organic-soluble thermal initiator.11. The method of claim ...

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12-11-2020 дата публикации

METHOD AND DEVICE FOR MANUFACTURING ABSORBENT MATERIAL

Номер: US20200352793A1
Автор: Satou Hitoshi
Принадлежит:

In a method and device for manufacturing an absorbent material, the degree of freedom in design can be increased by expanding a modifiable distribution pattern of an SAP and broadening the range in which the performance of the absorbent material can be modified. Pulverized pulp is suctioned in a predetermined pattern to form a pulp layer in which the pulp is fiber-laminated. A first distribution opening through which a first distribution device discharges a first SAP and a second distribution opening through which a second distribution opening discharges a second SAP are provided facing the pulp layer, and the first and second SAPs are distributed onto the pulp layer through the first and second distribution openings while moving the pulp layer relative to the first and second distribution openings. The first and second distribution devices can control the discharge amounts of the first SAP and the second SAP, respectively. 1. An absorbent material manufacturing method comprising:a first step in which a pulp pulverized and conveyed by a duct is suctioned in a predetermined pattern to form a pulp layer in which the pulp is fiber-laminated; anda second step in which a first distribution opening through which a first distribution device discharges a first SAP and a second distribution opening through which a second distribution device discharges a second SAP are provided facing the pulp layer, and the first SAP discharged through the first distribution opening is distributed onto the pulp layer and the second SAP discharged through the second distribution opening is distributed onto the pulp layer while moving the pulp layer relative to the first distribution opening and the second distribution opening,wherein in the second step,the first distribution device can control a discharge amount of the first SAP, and the second distribution device can control a discharge amount of the second SAP.2. The absorbent material manufacturing method according to claim 1 , wherein in ...

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28-11-2019 дата публикации

SEPARATION MEDIUM, USE FOR SEPARATION MEDIUM, STEVIOL GLYCOSIDE SEPARATION METHOD USING SEPARATION MEDIUM, AND STEVIOL GLYCOSIDE PRODUCTION METHOD USING SEPARATION METHOD

Номер: US20190358610A1
Автор: ADACHI Tadashi
Принадлежит: MITSUBISHI CHEMICAL CORPORATION

An object of the present invention is to provide a separation medium and a separation method, ensuring high selectivity and good separation efficiency for specific steviol glycosides. The present invention is related to a separation medium in which polyethyleneimine is immobilized to porous particles of a (meth)acrylic polymer having a crosslinked structure and a hydroxyl group. 1. A separation medium in which polyethyleneimine is immobilized to porous particles of a (meth)acrylic polymer having a crosslinked structure and a hydroxyl group.2. The separation medium according to claim 1 , wherein a mass average molecular weight of the polyethyleneimine is 200 or more.3. The separation medium according to claim 1 , wherein a nitrogen content rate is from 0.3 to 30% by mass.4. The separation medium according to claim 1 , wherein a pore diameter of the porous particles is from 1 to 1 claim 1 ,000 nm.5. A separation medium used for separation of a steviol glycoside claim 1 , in which polyethyleneimine is immobilized to at least one porous particles selected from the group consisting of a (meth)acrylic polymer claim 1 , a vinyl acetate polymer claim 1 , polysaccharides claim 1 , silica and glass.6. The separation medium according to claim 5 , wherein the porous particles contain a (meth)acrylic polymer.7. The separation medium according to claim 5 , wherein a nitrogen content rate is from 0.3 to 30% by mass.8. Use of the separation medium according to for separation of a steviol glycoside.9. A separation method for a steviol glycoside claim 1 , comprising a liquid chromatography step of loading a solution containing two or more types of steviol glycosides to the separation medium according to and flowing a solvent A through the separation medium claim 1 , thereby separating at least two types of steviol glycosides included in the steviol glycosides.10. The separation method for steviol glycosides according to claim 9 , wherein the solution containing two or more types of ...

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19-12-2019 дата публикации

PURIFICATION COLUMN

Номер: US20190381422A1
Автор: Suzuki Hisashi
Принадлежит: Toray Industries, Inc.

The invention provides a purification column that contains an adsorbent and shows excellent adsorptivity. Specifically, this purification column is provided with an adsorbent and a case that contains the adsorbent and has a tubular housing and treatment fluid supply port and discharge port at both ends of the housing. The purification column is characterized in that: a distribution plate is disposed at least on one end face side of the adsorbent; the distribution plate has a plurality of openings that allow communication of the treatment fluid, a support body, and a protrusion extending from the supporting body to the adsorbent side; and at least part of the protrusion is inserted into the adsorbent. 1. A purification column comprising:an adsorbent;a case which contains the adsorbent and has a cylindrical housing, a supply port and a discharge port for a fluid at both ends of the housing; anda distribution plate provided at an end face side of the adsorbent,the distribution plate having:a plurality of openings capable of communicating the fluid;a supporting body; anda salient extending from the supporting body toward the adsorbent,the salient being inserted at least partially into the adsorbent.2. The purification column according to claim 1 , wherein the adsorbent is formed into a fiber bundle consisting of a plurality of fibers.3. The purification column according to claim 1 , wherein the adsorbent is formed into a plurality of beads.4. The purification column according to claim 1 , wherein the adsorbent has a packing rate defined by Formula I of 40% to 80% claim 1 ,{'br': None, 'Packing rate [%]=(Cross-section area of adsorbent at end face+Cross-section area of salient at end face of adsorbent)/(Inner cross-section area of case at end face of adsorbent)×100[%].\u2003\u2003[Formula I]'}5. The purification column according to claim 1 , wherein the salient is formed into a circular ring around the central axis of the housing.6. The purification column according to ...

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31-12-2020 дата публикации

ANALYTICAL METHOD FOR SUGAR CHAINS HAVING ACIDIC GROUPS

Номер: US20200406229A1
Принадлежит: JCR PHARMACEUTICALS CO., LTD.

A chromatography column for the use of separation of acidic sugar chains, wherein the column comprises a first column and a second column, the second column connected by a flow path downstream of an outlet of the first column, and selected from the following (1) or (2): (1) the carrier of the first column is hydrophobically modified silica having a group containing a primary amine, a secondary amine or/and a tertiary amine, and the carrier of the second column is a resin having a group containing a primary amine, a secondary amine or/and a tertiary amine; (2) the carrier of the first column is a resin having a group containing a primary amine, a secondary amine or/and a tertiary amine, and the carrier of the second column is hydrophobically modified silica having a group containing a primary amine, a secondary amine, or/and a tertiary amine. 1. A chromatography column comprising:a first column having an outlet; anda second column connected downstream of the outlet of the first column,wherein the first column and the second column satisfy either (1) or (2):(1) the first column includes a carrier 1 which is hydrophobically modified silica having a group including at least one of a primary amine, a secondary amine and a tertiary amine, and the second column includes a carrier 2 which is a resin having a group including at least one of a primary amine, a secondary amine and a tertiary amine; or(2) the first column includes the carrier 2, and the second column includes the carrier 1.2. The chromatography column according to claim 1 , wherein the first column and the second column are hydrophilic interaction chromatography columns.3. The chromatography column according to claim 1 , wherein the carrier 2 is an anion exchange resin.5. The chromatography column according to claim 1 , wherein the carrier 2 has an amino group of formula III claim 1 , {'br': None, 'sub': 2', '2', 'n, 'Y—NH(CHCHNH)H'}, 'formula III'}where Y represents a resin portion of the carrier 2, and n is ...

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21-05-2004 дата публикации

Porous inorganic/organic hybrid materials and preparation thereof

Номер: WO2004041398A2
Принадлежит: WATERS INVESTMENTS LIMITED

The present invention relates to porous inorganic/organic homogenous copolymeric hybrid material materials, including particulates and monoliths, methods for their manufacture, and uses thereof, e.g., as chromatographic separations materials.

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24-11-1998 дата публикации

Polyvinyl alcohol (PVA) based covalently bonded stable hydrophilic coating for capillary electrophoresis

Номер: US5840388A
Принадлежит: Northeastern University Boston

A coated microcapillary column for high performance electrophoresis is disclosed. A preferred microcapillary includes a fused silica capillary column, the inner surface of the column having an interconnected polymeric coating of a polyvinyl alcohol (PVA) based polymer covalently attached to the column wall by Si--O--Si bonds. The resulting coated microcapillary column has good hydrolytic and pH stability and minimizes electroosmotic flow and interactions between sample components and the capillary wall. Also disclosed are a method of forming a polymeric coating layer for any surface by polymerizing the appropriate organic compounds in an organic solvent and a method of forming a column with a hydrophilic polymeric coating by directly converting an attached hydrophobic polymeric coating material to a hydrophilic polymeric coating material.

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23-01-2018 дата публикации

Sorption material, method of its production and method of its application

Номер: RU2641924C1

FIELD: chemistry. SUBSTANCE: claimed sorption material contains a porous carrier, the functional groups on the surface of which are covalently bound to a ligand capable of forming strong complexes with bacterial endotoxins. The porous carrier is a pellet with a size of 50 to 900 microns, made of a polymer or a copolymer. The carrier is obtained on the basis of such monomers as acrylic acid, methacrylic acid, acrylamide, metakrilamid, methyl acrylate, methyl methacrylate, glicidil methacrylate, vinyl acetate, allilamin, sodium 2-metilprop-2-en-1-sulfonate, allylglycidyl ether, divinylbenzene, divinylbenzene, ethylene glycol, triethylene glycol dimetakrilat, N,N-bis (metakrilamid). The ligand for binding bacterial endotoxins is an amphiphilic organic compound containing primary and secondary amino groups and hydrophobic substituents. A method for the preparation of a new sorption material and its use for purifying an aqueous solution of protein or an aqueous saline solution or a solution of a blood plasma are proposed. EFFECT: obtaining new selective sorbents for purification of liquid media from bacterial endotoxins. 3 cl, 2 tbl, 15 ex РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2 641 924 C1 (51) МПК B01J 20/26 (2006.01) B01J 20/32 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ОПИСАНИЕ ИЗОБРЕТЕНИЯ К ПАТЕНТУ (52) СПК B01J 20/26 (2006.01); B01J 20/3208 (2006.01); B01J 20/3242 (2006.01) (21)(22) Заявка: 2016150466, 21.12.2016 (24) Дата начала отсчета срока действия патента: Дата регистрации: 23.01.2018 (45) Опубликовано: 23.01.2018 Бюл. № 3 Адрес для переписки: 105005, Москва, ул. 2-я Бауманская, 5, стр. 1, МГТУ им. Н.Э. Баумана, ЦЗИС, для Карелиной Н.В. (МИЦ КМ) 6159377 A, 12.12.2000. US 6699386 B2, 02.03.2004. US 6106723 A1, 22.08.2000. US 5547576 A1, 20.08.1996. WO 2008/063666 A3, 29.05.2008. BY 15108 C1, 30.12.2011. RU 2448897 С1, 27.04.2012. RU 2189835 С1, 27.09.2011. МОРОЗОВ А.С. и др. Сорбенты для экстрапорального удаления токсических веществ и ...

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29-12-2022 дата публикации

CHROMATOGRAPHIC COLUMN HAVING STATIONARY PHASE THICKNESS GRADIENT

Номер: US20220410122A1

A gas chromatography device for peak focusing of one or more target analytes is provided that include a chromatographic column with an inlet and an outlet. A stationary phase is deposited inside the chromatographic column and has a positive thickness gradient. The stationary phase extends from the inlet to the outlet and has a first thickness at the inlet of the chromatographic column and a second thickness at the outlet of the chromatographic column. The second thickness is at least about 10% greater than the first thickness. Methods of peak focusing in a gas chromatography device, method of verifying peak focusing in a gas chromatography device and creating a gas chromatography device having a chromatographic column with a positive thickness gradient are also provided. 1. A gas chromatography device for peak focusing of one or more target analytes , comprising:a chromatographic column with an inlet and an outlet, wherein the inlet receives a sample comprising one or more target analytes that exits the chromatographic column at the outlet; anda stationary phase deposited inside the chromatographic column and having a positive thickness gradient, wherein the stationary phase extends from the inlet to the outlet and has a first thickness at the inlet of the chromatographic column and a second thickness at the outlet of the chromatographic column, wherein the second thickness is at least about 10% greater than the first thickness.2. The gas chromatography device of claim 1 , wherein the first thickness is greater than or equal to about 10 nm to less than or equal to about 10 micrometers and the second thickness is greater than or equal to about 30 nm to less than or equal to about 30 micrometers.3. The gas chromatography device of claim 1 , wherein the second thickness is at least about 100% greater than or equal to the first thickness.4. The gas chromatography device of claim 1 , wherein the second thickness is at least about 300% greater than or equal to the first ...

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30-10-2003 дата публикации

Capillary column chromatography process and system

Номер: US20030200794A1
Автор: Carlton Paul
Принадлежит: Individual

A microfluidic system is provided for separating components of many fluid samples in a parallel fashion through an array of capillary conduits. The system includes capillary conduits for receiving fluid samples, and for effecting separation of substituents of the sample by passing the sample through a corresponding array of capillary separation conduits containing a solid separation medium. The microfluidic circuit is made of three or more substrate layers and preferably includes etched channels in different layers that are dimensioned relative to one another to provide for retaining the solid composition within the capillary separation conduits. The system also includes an array of detector flow cells in fluid communication with the capillary separation conduits, and an array of high pressure connectors for connecting discrete capillary tubes to the fluid passages in the microfluidic circuit for introducing and removing the fluid samples from the system. The connections for the capillary tubes have a small footprint, are readily reversible (allowing ease of maintenance and replacement), and can seal against high pressures.

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07-02-2006 дата публикации

Capillary column chromatography process and system

Номер: US6993958B2
Автор: Carlton H. Paul
Принадлежит: PerSeptive Biosystems Inc

A microfluidic system is provided for separating components of many fluid samples in a parallel fashion through an array of capillary conduits. The system includes capillary conduits for receiving fluid samples, and for effecting separation of substituents of the sample by passing the sample through a corresponding array of capillary separation conduits containing a solid separation medium. The microfluidic circuit is made of three or more substrate layers and preferably includes etched channels in different layers that are dimensioned relative to one another to provide for retaining the solid composition within the capillary separation conduits. The system also includes an array of detector flow cells in fluid communication with the capillary separation conduits, and an array of high pressure connectors for connecting discrete capillary tubes to the fluid passages in the microfluidic circuit for introducing and removing the fluid samples from the system. The connections for the capillary tubes have a small footprint, are readily reversible (allowing ease of maintenance and replacement), and can seal against high pressures.

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27-06-2002 дата публикации

Polymeric Support Having Novel Pore Structures

Номер: SE0202016D0
Принадлежит: Amersham Biosciences Ab

The invention is a method of producing a cross-linked polymeric support having a multimodal pore structure, which comprises providing a degradable initiator molecule; providing an organic phase comprising said initiator molecule, radically polymerizable monomers and a porogen in a solvent; providing an aqueous phase comprising a transition metal catalyst; suspension polymerization of the organic phase by adding a ligand, co-ordinating to the transition metal in the aqueous phase to produce a cross-linked polymeric support having a primary pore structure and comprising initiator molecule; and subjecting the support obtained to degrading conditions to remove the initiator molecule from within the support to produce a cross-linked polymeric support having a secondary pore structure in addition to the primary pore structure.

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16-01-2013 дата публикации

吸附材料及其制造方法

Номер: CN102883805A
Принадлежит: HITACHI LTD

本发明提供对于包括高极性溶质分子的具有广泛的色谱极性的溶质,能够抑制杂质吸附并且进行高效率且选择性优异的固相萃取的吸附材料,和固相萃取方法。本发明提供一种含杂环共聚物吸附材料,其特征在于,由包含多官能含杂环单体和能够与该单体进行共聚反应的单体的共聚物构成,所述多官能含杂环单体具有在环结构中包含至少2个以上杂原子的杂环,其中多官能杂环构成主链结构。另外,固相萃取的方法包含下述工序:使以低极性溶质分子、中极性溶质分子和高极性溶质分子中的任一种作为溶质的溶液与该含杂环共聚物吸附材料进行接触,从而选择性地吸附保持1种以上溶质。

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23-10-1995 дата публикации

Method for the preparation of a macroporous polymeric sorbent

Номер: AU6565794A
Принадлежит: ALLTECH FRANCE

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