СПОСОБ ТЕРМООКИСЛИТЕЛЬНОЙ ДЕСТРУКЦИИ ГОМО(СО)ПОЛИМЕРОВ ДИЕНОВ ИЛИ СОПОЛИМЕРОВ ДИЕНОВ И ВИНИЛАРОМАТИЧЕСКИХ МОНОМЕРОВ

... 1. Способ термоокислительной деструкции гомо(со)полимеров диенов или сополимеров диенов и винилароматических мономеров в среде углеводородного растворителя при нагревании, под воздействием кислородсодержащего газа, в присутствии катализатора, отличающийся тем, что в качестве катализатора используют аддукт азодиизобутиронитрила с гетероциклическим карбосодержащим соединением в соотношении соответственно 1:2-3, при содержании аддукта в углеводородном растворителе 0,5-0,75 мас.%, процесс деструкции ведут при температуре 40≤t<60°C. ! 2. Способ по п.1, отличающийся тем, что в качестве гетероциклического карбосодержащего соединения используют γ-бутиролактон, или α-пирролидон, или N-метилпирролидон, или капролактам.

Polyazine-basierende Ladungstransportverbindungen

POLYMERE CARRIER WITH VOID STRUCTURES

PROCEDURE FOR THE PRODUCTION OF PARTICLES AND PARTICLE WITH THE HELP OF OF THIS PROCEDURE MANUFACTURED ABILITY

Polynucleotide separations on nonporous polymer beads

A method of manufacturing particles, and particles that can be produced in accordance with the method

RESINS HAVING IMPROVED EXCHANGE KINETICS

Disclosed are novel ion-exchange and chelateexchange resins having improved exchange kinetics for separating chemical species from liquids. The resins are prepared from copolymer beads consisting of a monovinyl aromatic monomer and a cross linking monomer. The copolymer beads are functionalized such that weakbase exchange moieties are substituted at haloalkylated sites which are most accessible to diffusion into the beads, while hydrophilic, strong-base exchange moieties are substituted at haloalkylated sites which are least accessible to diffusion. The resins have improved exchange kinetics due to shortened diffusion path lengths for the chemical species being separated and improved diffusion into the resin beads due to the hydrophilic, strong-base exchange moieties. 37,506-F ...

METHOD FOR PURIFICATION OF PHYSIOLOGICAL LIQUIDS OF ORGANISM, POLYMER ADSORBENT FOR ITS REALIZATION AND METHOD FOR PRODUCTION OF POLYMER ADSORBENT

METHOD AND MATERIAL FOR CLEANING PHYSIOLOGICAL LIQUID POSTS ORGANISM AND METHOD OF MANUFACTURING MATERIAL

Method for producing hollow particles, and hollow particles

Provided is a method for producing hollow particles with which it is possible to obtain hollow particles having excellent electrical insulation characteristics and solvent resistance by reducing the amount of residual hydrophobic solvent. The method for producing hollow particles according to the present invention is a method for producing hollow particles having a porosity of 50% or more, the hollow particles having a shell containing a resin and a hollow portion surrounded by the shell, the method for producing hollow particles comprises: a step for preparing a liquid mixture containing a polymerizable monomer, a hydrophobic solvent, a polymerization initiator, a dispersion stabilizer, and an aqueous medium; a step for preparing a suspension in which droplets of the monomer composition are dispersed in an aqueous medium by suspending the mixed solution; and a step in which the suspension is supplied to the polymerization reaction to prepare a precursor composition containing precursor ...

PROCESS FOR FUNCTIONALIZING A BIOCOMPATIBLE POLYMERIC BEAD, THE FUNCTIONALIZED BEADS, AND THE BEADS PRODUCED THEREBY

The invention involves functionalizing polymeric beads, such as DVB beads, to add an epoxide or aldehyde group. The resulting beads are useful In various applications.

A METHOD OF MANUFACTURING PARTICLES, AND PARTICLES THAT CAN BE PRODUCED IN ACCORDANCE WITH THE METHOD

A method of producing open porous spherical particles by polymerizing monovinyl monomers and divinyl monomers and/or polyvinyl monomers (cross-linkers) in an emulsion with the aid of an initiator. The method is characterized by the steps of (i) preparing a w/o/w emulsion which comprises an aqueous phase having emulsified therein droplets which contain a water-in-oil emulsion, wherein the oil phase in the droplets includes vinyl monomers and an emulsifier which provides an inverse emulsion and the droplets have a diameter smaller than 2,000 'mu'm, and wherein the total amount of water is between 75-99 % (w/w); and (ii) thereafter initiating polymerization and isolating the particles, optionally after sieving, from the reaction mixture after the polymerization process. A population of open spherical porous polymer particles which have a diameter within the range of 50 'mu'm-2,000 'mu'm and include a pore system comprising (a) spherical hollows whose diameters are < 1/9 of the particle diameter ...

Method of producing material for purification of physiological liquids of organism

A method of producing a material for purification of physiological liquids of organism has the steps of providing a polymer which has a size, a shape, and a structure selected so as to remove toxic compounds from the physiological liquids, chemically modifying a surface of the polymer so as to provide hydrophilicity and biocompatibility, and performing the modification in a medium with a content of organic substance which is efficient for preventing endotoxins contamination of the polymer.

Komplexbildende Polymere.

ADSORBENT MATERIAL FOR BLOOD, BLUTPLASMAUND ALBUMIN CLEANING METHOD

MATERIAL FOR PURIFICATION OF PHYSIOLOGICAL LIQUIDS OF ORGANISM, AND METHOD OF PRODUCING THE MATERIAL

Purification of physiological liquids of organism is performed by passing a physiological liquid with toxicants removed from a patient through a material which has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30000 Dalton from the physiological liquid and which is composed of a porous hydrophobic divinylbenzene copolymer which initially has surface exposed vinyl groups in which thereafter the vinyl groups are chemically modified so as to form different surface exposed functional groups with a greater hydrophilicity and greater biocompatibility than those of the vinyl groups.

Component addition polymerization

Redox polymerizable composition with photolabile transition metal complexes

Polymeric support having novel pore structures

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 polymerisable monomers and a porogen in a solvent; providing an aqueous phase comprising a transition metal catalyst; suspension polymerisation 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.

MATERIAL USED FOR RAPID SEPARATION OF OIL AND WATER AND PREPARATION METHOD AND APPLICATION THEREOF

The present invention discloses a material used for rapid separation of oil and water and preparation method and application thereof, the mesh material is placed into monomer solution, reacting with the presence of initiator to prepare material used for rapid separation of oil and water. The monomer is divinylbenzene or 2-(dimethylamino) ethyl methacrylate, and the mesh material is stainless steel mesh. The present invention modifies the functional small molecules and polymers to the surface of the materials, thereby preparing multifunctional composite materials, effectively separating oil-water emulsion, so as to achieve the purpose of oil-water separation.

CURABLE COMPOSITION FOR DENTISTRY

A dental curable composition includes: a radically polymerizable monomer; a polymerization initiator; and a hyperbranched polymer, in which the hyperbranched polymer includes a unit structure represented by the general formula (I) and unit structures represented by the general formula (IIA) and/or the general formula (IIB) (in the general formula (I), A represents a single bond for bonding C and R1, >C=O, -O-, or -COO-, R1 represents a divalent saturated aliphatic hydrocarbon group or a divalent aromatic hydrocarbon group, and R2 represents a hydrogen atom or a methyl group; and in the general formula (IIA) and the general formula (IIB), R3, R4, and R5 each represent a hydrogen atom, an alkyl group, an alkoxycarbonyl group, an aryl group, or a cyano group, and R6 represents an alkylene group).

Self-supported elastomeric film having self-healing properties made from a polymer latex

The present invention relates to self-supported elastomeric film made from a composition comprising polymer latex particles bearing ethylenically unsaturated groups pending from the polymeric backbone of the latex particles wherein the ethylenic unsaturation is separated from the polymeric backbone by at least 3 chemical bonds. Preferably the particles are core-shell particles with the ethylenic unsaturated in the shell component, and said unsaturation is provided by including in the polymer allyl methacrylate. It is envisaged that the unsaturation can be introduced after preparation of the polymer by substitution of a different group with an ethylenically unsaturated group.

POLYMERIC SUPPORT HAVING NOVEL PORE STRUCTURES

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 polymerisable monomers and a porogen in a solvent; providing an aqueous phase comprising a transition metal catalyst; suspension polymerisation 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.

COMPLEX-FORMING POLYMERS

COMPLEX-FORMING POLYMERS Novel complex-forming polymers are provided having at least one aryl group carrying a complex-forming moiety of general formula which can be prepared by contacting a compound of general formula IV with a metalating agent, followed by reaction of the metalated compound with either A.1. at least one vinylbenzyl halide, and subsequently 2. polymerizing the reaction product of A.1. or B. a halomethylated polystyrene polymer; wherein each R individually is H, or both R's together form a group -CH-CH-; R1 is H or an alkyl, R2 is H, an alkyl, a vinylbenzyl group or a group R1 and R2 together form a group -(CH2)n- wherein n is an integer in the range of from 2 up to and including 6; R is an alkyl, alkoxy, phenyl, phenoxy, alkylthio or phenylthio group; R4 is an alkyl group, or a cycloaliphatic group having from 3 to 7 carbon atoms having at least one hydrogen on the .alpha.-carbon atom; p and q are integers from O up to and including 2 and from O up to ...

PREPARATION OF RADIOLABELLED HALOAROMATICS VIA POLYMER-BOUND INTERMEDIATES

According to a first aspect of the invention, a process is disclosed for the preparation of radiolabelled haloaromatic compounds. According to a second aspect of the invention, intermediate precursor insoluble polymer compounds used in the preparation of the radiolabelled haloaromatics are disclosed, as well as processes for the preparation of the intermediate precursor insoluble polymer compounds.

Particles, connecting material and connection structure

Branched polymers

PHOTONIC CRYSTALS WHICH ARE PRODUCED FROM UNCHARGED POLYMER PARTICLES

The invention relates to the use of polymer particles for the production of photonic crystals, characterized in that the polymer particles have a weight average particle size of more than 600 nm and an ion group content of less than 0.001, preferably of less than 0.0001 mol/1 g of polymer particles and the polymer particles form the lattice structure of the photonic crystal without being embedded in a liquid or solid matrix.

SPHERICAL POLYMER FINE PARTICLES AND PROCESS FOR PRODUCTION THEREOF

Spherical polymer fine particles which exhibit, when the compression/elastic deformation characteristic of one particle at X% deflection of particle diameter, Kx, is defined by the formula [1]: KX=(3/√2)(SX -3/2)(R-1/2)FX [1] [wherein Fx is load (N) necessary to X% deflection of fine particle; Sx is compressive deformation (mm) at X% deflection of fine particle; and R is particle radius (mm)], a compression/elastic deformation characteristic at 60% deflection of particle diameter, K60, of 1000 to 12000N/mm2 at 20˚C and a recovery of particle diameter at 60% deflection of particle diameter of 20% or above at 20˚C. The polymer fine particles are freed from troubles due to imperfect contact, scratching and breakage occurring in using too hard polymer fine particles and troubles due to low recovery of compressive deformation occurring in using too soft polymer fine particles, thus having both proper hardness and proper elasticity.

Complex-forming polymers

Novel complex-forming polymers are provided having at least one aryl group carrying a complex-forming moiety of general formula which can be prepared by contacting a compound of general formula with a metalating agent, followed by reaction of the metalated compound with either A.1. at least one vinylbenzyl halide, and subsequently 2. polymerizing the reaction product of A.1. or B. a halomethylated polystyrene polymer; wherein each R individually is H, or both R's together form a group -CH=CH-; R1 is H or an alkyl, R² is H, an alkyl, a vinylbenzyl group or a group R1 and R² together form a group -(CH2)n- wherein n is an integer in the range of from 2 up to and including 6; R3 is an alkyl, alkoxy, phenyl, phenoxy, alkylthio or phenylthio group; R4 is an alkyl group, or a cycloaliphatic group having from 3 to 7 carbon atoms having at least one hydrogen on the -carbon atom; p and q are integers from 0 up to and including 2 and from 0 up to and including 3, respectively; ...

PRODUCTION OF POROUS POLYMER PARTICLE FOR ADSORBING BILIRUBIN

PURPOSE: To obtain the titled polymer particles excellent in adsorbability by subjecting a mixed monomer consisting of 35W100wt.% divinylbenzene and 0W65wt.% glycidyl methacrylate to suspension polymerization in an aqueous medium while using 5W12C monovalent alcohol as a precipitant. CONSTITUTION: A mixed monomer consisting of 35W100wt.% divinylbenzene and 0W65wt.% glycidyl methacrylate is subjected to suspension polymerization in an aqueous medium by using monovalent alcohol wherein the atomic number of carbon is 5W12 and the solubility for water is 7 and below (e.g. 3,5,5- trimethylhexanol or the like) as a precipitant. Porous polymer particles are obtained for example by firstly washing the produced polymer with water and then washing it with methanol and furthermore subjecting it to Soxhlet extraction until it shows constant weight. The polymer particles can be preferably used as an adsorbent of bilirubin. Further as the amount of the precipitant, 80W150pts.wt. is used especially preferably ...

VERFAHREN ZUR HERSTELLUNG VON TEILCHEN UND TEILCHEN DIE MIT HILFE DIESES VERFAHRENS HERGESTELLT WERDEN KÖNNEN

GEL-WELL-BEHAVED CHELATIERENDE RESINS AND PROCEDURES FOR THE DISTANCE OF MULTI-VALUED ONE, EARTHALKALINE OR HEAVYMETALLIC CATIONS FROM SOLUTIONS.

MORE VINYLMONOMER, CARRIER MATRIX AND YOUR PRODUCTION

POLYMER ABSORBENT, AND MANUFACTURING PROCESS AND USE

PROCEDURE FOR THE PRODUCTION OF INTERLACED SPHERICAL PARTICLES

PROCEDURE FOR THE PRODUCTION OF POLYMER-COATED FERROUSMAGNETIC PARTICLE AND POLYMER-COATED FERROUSMAGNETIC PARTICLE

LINEAR POLYDIVINYLBENZENE AND DERIVATIVE THEREOF

A linear polyvinylbenzene having recurring units of Formula (A), (A) and a number average molecular weight of about 500 to about 1,000,000; a linear copolymer having at least about 1 % by weight of recurring units of Formula (A) as described above and at most about 99 % by weight of recurring units of at least one of Formulae (B) and (C), and (B) (C) wherein R1 and R2 may be the same or different and each represents a hydrogen atom, a C1-20 alkyl group, a C3-10 cycloalkyl group, a C7-12 arylalkyl group, a C3-8 alkenyl group, a C6-15 aryl group, a H2N?CH2?? group wherein n is an integer of 1 to 15 or a H?NH - CH2 - CH2? group wherein m is an integer of 2 to 8; and R3 represents a hydrogen atom, a C1-12 alkyl group, a C3-10 cycloalkyl group, a C7-12 arylalkyl group or a C3-8 alkenyl group; and X is an acid radical, based on the total weight of the recurring units of Formulae (A) and (B) and/or (C), and a number average molecular weight of about 500 to about 1,000,000: and ...

POLYNUCLEOTIDE SEPARATIONS ON NONPOROUS POLYMER BEADS

The present invention describes a chromatographic method for separating polynucleotides with improved separation and efficiency. The method uses nonporous polymeric beads having a non-reactive, non-polar surface, and made from a variety of different polymerizable monomers.

AEROGEL CONTAINING A POLYMER OR COPOLYMER CARBOHYDRATE AND THEIR PROCESS DEPREPARATION

PROCESS FOR THE PREPARATION OF COMPOSITE PARTICLES, THE COMPOSITE PARTICLES OBTAINED AND THEIR USE IN DIAGNOSTIC TESTING

Resin particles and method for producing resin particles

Resin particles which contain a vinyl polymer that contains divinyl benzene as a constituent, and which have a number average particle diameter of from 2.5 [mu]m to 10.0 [mu]m (inclusive), a variation coefficient (CV value) of particle diameters of 20% or less on a number basis, and a circularity of 0.990 or more.

RESIN PARTICLES AND METHOD FOR PRODUCING RESIN PARTICLES

Resin particles which contain a vinyl polymer that contains divinyl benzene as a constituent, and which have a number average particle diameter of from 2.5 μm to 10.0 μm (inclusive), a variation coefficient (CV value) of particle diameters of 20% or less on a number basis, and a circularity of 0.990 or more.

VINYL MONOMER, SUPPORT MATRIX AND ITS PREPARATION

VINYL MONOMER, SUPPORT MATRIX AND ITS PREPARATION

A vinyl monomer of the structure R-B-Ar(-CH=CH2)n (1) in which Ar is an aromatic ring (arylene group); n is an integer > 0, in particular one or two; B is a bridge structure; R is a (C2-30)-hydrocarbon group carrying two or more protected or unprotected hydroxy groups. The monomer is characterized in that B comprises a chain of atoms linking R to Ar and consisting of 1-10 atoms selected from carbons and the heteroatoms ether oxygen, thioether sulphur or amino nitrogen, with the proviso that the terminal atom in B which is attached to R is one of the heteroatoms. A method for producing a polymer support matrix in which the vinylmonomer is one of the monomeric units. The support matrix as such is also claimed. The preferred method for producing the support matrices involves suspension polymerisation, the preferred form of matrix is beads. The matrix is cross-linked.

METHOD FOR PRDUCING HOLLOW PARTICLES, AND HOLLOW PARTICLES

A method for producing hollow particles which have a void ratio of 50% or more, the method comprising: preparing a mixture liquid containing a polymerizable monomer, a hydrophobic solvent, an aqueous medium, etc., suspending the mixture liquid to prepare a suspension in which droplets of a monomer composition containing the polymerizable monomer, the hydrophobic solvent, etc., are dispersed in the aqueous medium, and subjecting the suspension to a polymerization reaction to prepare a precursor composition containing precursor particles having a hollow portion surrounded by a shell and filled with the hydrophobic solvent, wherein the polymerizable monomer is a hydrocarbon monomer, and in 100% by mass of the polymerizable monomer, a content of a crosslinkable monomer containing two or more ethylenically unsaturated double bonds is 70% by mass or more, and wherein the hydrophobic solvent is a hydrocarbon solvent containing 5 to 8 carbon atoms.

OPTICALLY ACTIVE PHOSPHINE DERIVATIVE BEARING TWO VINYL GROUPS, POLYMER THEREFROM AND THEIR TRANSITION METAL COMPLEX

PROBLEM TO BE SOLVED: To obtain the subject novel derivative that comprises a specific optically active phosphine derivative bearing several vinyl groups and is useful as a polymer carrier ligand for an asymmetric reaction as asymmetric hydroformylation excellent in catalytic activity and asymmetric yield. SOLUTION: This novel compound is represented by formula I [Ar is a (substituted) phenyl, a (substituted) naphthyl; R1 and R2 are each, H, a lower, a lower alkoxy, halogen; R2 and R3 may incorporate to form a hydrocarbon ring], typically 2'-diarylposphino-1,1-biphenylene-2-yloxy(6,6'-divinyl-1,1'- binaphthalene-2,2'-diyl-oxy)phosphine derivative, and is useful as a polymer carrier ligand for a catalyst for an asymmetrical synthesis reaction. This compound is prepared by reaction of a dioxychlorophosphine of formula II derived from bi-naphthol with a hydroxyphosphine of formula III (Ph is phenyl). COPYRIGHT: (C)1998,JPO ...

Способ получения карбоцепных полимеров

HYBRID COPOLYMERS AND ION EXCHANGE RESINS

composiÇço de secagem, composiÇço seca, e, mÉtodo

CHELATE RESINS

The present application relates to novel chelate resins which contain, as a functional group, quaternary nitrogen atoms in structures of the general formula (I) in which at least one of the radicals R1 to R3 represents an optionally substituted radical of the series consisting of picolyl, methylquinoline or methylpiperidine, m represents an integer from 1 to 4 and M represents the polymer matrix and X represents a counterion of the series consisting of hydroxide OH−, halide, preferably Cl−, Br−, or sulphate SO42−, a process for their preparation and the use thereof, in particular the use of the novel chelate resins in hydrometallurgy and electroplating.

Inorganic nanoparticle-coated hollow particles, method for producing the same, and aqueous dispersion containing the hollow particles

Provided are hollow particles which are more excellent in heat resistance and dispersibility than ever before and which are lightweight. The hollow particles containing hollow resin particles having a surface covered with inorganic fine particles, wherein a volume average particle diameter of the hollow particles is from 0.1 μm to 9.0 μm, and a void ratio thereof is from 55% to 95%; wherein a repeating unit constituting the resin of the hollow resin particles contains a crosslinkable monomer unit, and a content of the crosslinkable monomer unit is from 25 to 100 parts by mass, with respect to 100 parts by mass of the resin; wherein a primary particle diameter of the inorganic fine particles is from 10 nm to 120 nm; and wherein the inorganic fine particles are contained at from 5 to 180 parts by mass, with respect to 100 parts by mass of the hollow resin particles.

СПОСОБ ПОЛУЧЕНИЯ МАКРОПОРИСТЫХ НЕИОНОГЕННЫХ СОРБЕНТОВ

Изобретение относится к получению полимерных макропористых неионогенных сорбентов, используемых для очистки сточных вод, и предназначено для сорбционного извлечения многокомпонентных органических соединений из водных растворов в условиях переработки больших объемов сточных вод. Для получения сорбентов с широким распределением пор по размерам, небольшим набуханием в режимах сорбции - десорбции для очистки многокомпонентных стоков, преимущественно больших объемов, с высокими воспроизводимыми сорбционными свойствами проводят суспензионную полимеризацию чистого или технического дивинилбензола в присутствии инициатора радикального типа и порообразователя при нагревании, причем в качестве порообразователя используют азеотропные смеси алифатических и ароматических соединений, имеющих общую температуру кипения не ниже 80oС.

POLYMERER TRÄGER MIT PORENSTRUKTUREN

Polymerabsorbens, und Herstellungsverfahren und Verwendung

다공성 구조체 및 그 제조 방법

... 다공성 구조체 및 그 제조 방법에 관해 개시되어 있다. 3차원 네트워크 구조 내에 기공들이 분포된 다공성 구조체(porous structure)로서, 상기 3차원 네트워크 구조는 스티렌(styrene)과 디비닐벤젠(divinylbenzene)의 공중합체(copolymer)를 포함하는 제 1 고분자 사슬 및 상기 제 1 고분자 사슬에 결합된 2-에틸헥실 메타크릴레이트 및 2-에틸헥실 아크릴레이트 중 적어도 어느 하나의 제 2 고분자 사슬을 포함한다.

POLYNUCLEOTIDE SEPARATIONS ON NONPOROUS POLYMER BEADS

The present invention describes a chromatographic method for separating polynucleotides with improved separation and efficiency. The method uses nonporous polymeric beads having a non-reactive, non-polar surface, and made from a variety of different polymerizable monomers.

Method of producing material for purification of physiological liquids of organism

A method for producing a material for purification of physiological fluids of organism by chemical modification of surface exposed vinyl groups of porous hydrophobic divinylbenzene copolymer to form different surface exposed functional groups which are hydrophilous and biocompatible, without effecting a porous structure and hydrophobic interior of the initial divinylbenzene copolymer.

Redox polymerizable composition with photolabile transition metal complexes

Polymerizable compositions comprising a redox initiator system is disclosed. The redox initiator system comprises a photolabile transition metal complex that photolyzes and initiates the redox cycle. Dental compositions comprising dental resins and the photolabile redox initiator system are also described.

Material used for rapid separation of oil and water and preparation method and application thereof

The present invention discloses a material used for rapid separation of oil and water and preparation method and application thereof, the mesh material is placed into monomer solution, reacting with the presence of initiator to prepare material used for rapid separation of oil and water. The monomer is divinylbenzene or 2-(dimethylamino) ethyl methacrylate, and the mesh material is stainless steel mesh. The present invention modifies the functional small molecules and polymers to the surface of the materials, thereby preparing multifunctional composite materials, effectively separating oil-water emulsion, so as to achieve the purpose of oil-water separation.

Particles, connecting material and connection structure

Particles that can suppress the occurrence of cracking during a stress load in a connection part that connects two members to be connected are provided. The particles according to the present invention are particles used to obtain a connecting material for forming the connection part that connects two members to be connected, and the particles are used for forming the connection part such that thickness of the connection part after connection exceeds twice the average particle diameter of the particles before connection, or the particles have an average particle diameter of 0.1 μm or more and 15 μm or less, the particles have a 10% K value of exceeding 3000 N/mm2 and 20000 K/mm2 or less, and the particles have a particle diameter CV value of 50% or less.

Gel-type chelating resins and a process for removal of multivalent, alkaline earth or heavy metal cations from solutions

COMPLEX-FORMING POLYMERS

LINEAR POLYDIVINYLBENZENE AND DERIVATIVE THEREOF

PARTICLES, CONNECTING MATERIAL AND CONNECTION STRUCTURE

Particles are provided which, in a connection portion that connects two members to be connected, can suppress the occurrence of cracking and peeling during a hot-cold cycle, can further suppress thickness variation in the connection portion, and can improve connection strength. These particles are particles used to obtain a connecting material for forming the connection portion that connects two members to be connected. The particles are used in order to form a connection portion such that the thickness of the connection portion after connection is less than or equal to twice the average particle diameter of the particles before connection, or, the particles have an average particle diameter of 1-300μm, the particles have a 10% K value of 30-3000 N/mm2 and the particles have a particle diameter CV value of 10% or less.

CAPPED BISPHENOL POLYINDANE OLIGOMER AND COMPOSITION, METHOD OF MANUFACTURE, AND ARTICLES MADE THEREFROM

A capped polyindane oligomer of formula (1): wherein R1, R2, and R3 are each independently hydrogen, halogen, C1-12 hydrocarbyl provided that the hydrocarbyl group is not tertiary hydrocarbyl, C1-12 hydrocarbylthio, C1-12 hydrocarbyloxy, or C2-12 halohydrocarbyloxy wherein at least two carbon atoms separate the halogen and oxygen atoms; and Rx and Ry are as provided herein.

VERFAHREN ZUR PERLPOLYMERISATION

POLYURETHANES AND VINYL POLYMERS

MATERIAL FOR PURIFICATION OF PHYSIOLOGICAL LIQUIDS OF ORGANISM, AND METHOD OF PRODUCING THE MATERIAL

Purification of physiological liquids of organism is performed by passing a physiological liquid with toxicants removed from a patient through a material which has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30000 Dalton from the physiological liquid and which is composed of a porous hydrophobic divinylbenzene copolymer which initially has surface exposed vinyl groups in which thereafter the vinyl groups are chemically modified so as to form different surface exposed functional groups with a greater hydrophilicity and greater biocompatibility than those of the vinyl groups.

Optically active phosphine derivative having at least two vinyl groups, polymer produced using the same as monomer, and transition metal complexes of these

A 2'-diarylphosphino-1,1'-biphenylen-2-yloxy(6,6'-divinyl-1,1'-binaphthalene-2,2'-diyloxy)phosphine derivative is disclosed, which is represented by general formula (I):wherein Ar is an optionally substituted phenyl or naphthyl; R1 and R2 each independently is a hydrogen atom, a lower alkyl, a lower alkoxy, etc.; and R3 is a lower alkyl, a lower alkoxy, etc.; provided that R2 and R3 may be bonded to each other to form a hydrocarbon ring, which may have one or more substituents selected from lower alkyl groups, halogen atoms, vinyl, etc. Also disclosed are a polymer having structural units derived from the phosphine derivative and a transition metal complex obtained by causing a transition metal compound to act on the phosphine derivative.

Vinyl monomer, support matrix and its preparation

A vinyl monomer of the structure R-B-Ar(-CH-CH₂)_n (1) in which Ar is an aromatic ring (arylene group); n is an integer >0, in particular one or two; B is a bridge structure; R is a (C_2-30)-hydrocarbon group carrying two or more protected or unprotected hydroxy groups. The monomer is characterized in that B comprises a chain of atoms linking R to Ar and consisting of 1-10 atoms selected from carbons and the heteroatoms ether oxygen, thioether sulphur or amino nitrogen, with the proviso that the terminal atom in B which is attached to R is one of the heteroatoms. A method for producing a polymer support matrix in which the vinylmonomer is one of the monomeric units. The support matrix as such is also claimed. The preferred method for producing the support matrices involves suspension polymerisation, the preferred form of matrix is beads. The matrix is cross-linked ...

Retarder composition

The invention relates to a retarder composition for the control of unwanted polymerization reactions during the production and processing of ethylenically unsaturated compounds, the composition comprising at least one di-substituted quinone compound and at least one hydroxylamine compound. Optionally, the composition also comprises at least one stable free radical nitroxyl compound and one or more formulation adjuvants. The invention also envisages a process stream comprising at least one ethylenically unsaturated compound, and a method for the prevention of unwanted polymerization reactions during the production and processing of ethylenically unsaturated compounds. The composition has been found to be far more effective than expected, given that the individual components show little or no efficacy when used alone, and poses much less hazard to humans than the compositions of the prior art.

MACROMOLECULAR COMPOSITIONS COMPRISING INDENE-DERIVATIVES, PREPARATION THEREOF, AND USE THEREOF

Polymer latex and elastomeric film made therefrom having self-healing properties

An aqueous dispersion comprising core-shell polymer latex particles wherein the shell of the core-shell bears ethylenically unsaturated groups pending from the polymeric backbone and the unsaturation is separated from the backbone by at least 3 chemical bonds and wherein the shell is cross-linked and the core is not cross-linked. Producing the aqueous dispersion comprises aqueous emulsion polymerization of the core polymer followed by a second step polymerization of the shell copolymer. The shell copolymer may derive from monomers i) including one which has two non-conjugated double bonds or ii) a monomer which is readily converted to having a pendant double bond after polymerization. A self-supporting elastomeric film made from the aqueous dispersion. The material has self-healing and shape memory properties.

POLYURETHANE/VINYL COMPOSITES

POLYNUCLEOTIDE SEPARATIONS ON NONPOROUS POLYMER BEADS

The present invention describes a chromatographic method for separating polynucleotides with improved separation and efficiency. The method uses nonporous polymeric beads having a non-reactive, non-polar surface, and made from a variety of different polymerizable monomers.

METHOD OF PREPARATION OF COMPOSITE PARTICLES, PARTICLES COMPOSITE OBTENUESET THEIR USE IN A TEST DIAGNOSIS

L'invention a pour objet un procédé de préparation de particules composites par encapsulation par polymérisation d'émulsion appauvrie en phase organique, ladite émulsion consistant en des gouttelettes d'émulsion inorganique comprenant une phase organique et des nanoparticules inorganiques distribuées dans ladite phase organique, caractérisé en ce que la polymérisation est mise en oeuvre en utilisant, à titre de monomère de polymérisation, de 60 à 100% d'au moins un agent de réticulation et de 0 à 40% d'au moins un monomère hydrophobe, étant entendu qu'au moins 95% du ou des agents de réticulation sont hydrophobes. Elle a également pour objet les particules ainsi obtenues et leur utilisation en diagnostic.

PROCEDE D'OBTENTION DES ECHANGEURS D'IONS DELECTIFS POUR BORE

SUPPORTED QUENCHER FOR OBTAINING HIGH PURITY CYCLIC OLEFIN POLYMERS AND SYNTHESIS METHOD THEREOF

The present invention relates to a synthesis method of high purity cyclic olefin polymers and a supported quencher for the same, wherein a synthesis method of high purity cyclic olefin polymers as one embodiment of the invention comprises: a ring opening metathesis polymerization (ROMP) step for performing ROMP of cyclic olefin monomers in the presence of Grubbs catalysts; a cross-metathesis step for reacting the reactants of the ROMP step with the supported quencher; and a filtration step for separating and filtering insoluble contents from the reactants of the cross-metathesis step.

Polymerabsorbens und Herstellungsverfahren und Verwendung

Preparation method of non-porous or porous polymer microsphere of surface function

This invention relates to a preparation method of surface functional, imperforation or multihole polymer microsphere, belongs to functional polymer material technosphere. The steps: remove polymerization inhibitor in alkene monomer; add mono-olefin monomer to continuous phase solvent, form reaction system, inlet nitrogen, takes reaction under homothermal condition to obtain seed polymer microsphere; mix seed polymer microsphere solution and activator, form first-order swelling reaction solution; then add mono-olefin monomer, monomer with functional group and cross-linking agent, and make them swell to seed microballoon sphere, form second grade swelling reaction solution; finally add water-solubility polymerization inhibitor, form blending reaction solution, isothermal reaction, ultimately separate to obtain imperforation polymer microsphere with functional surface; or use organic solvent to extract to obtain multihole polymer microsphere with functional surface.

Method for producing highly branched polymer

BRANCHED POLYMERS

Responsive or degradable branched polymers may be prepared by the free radical polymerisation of a multivinyl monomer in the presence of a chain transfer agent, using a source of radicals, wherein the extent of propagation is controlled relative to the extent of chain transfer to prevent gelation of the polymer. The multivinyl monomer may comprise a cleavable group, for example an ester, or a multiplicity of such groups, between two vinyl groups. Said monomer may be a macromonomer containing multiple cleavage sites.

Selected chelate resins and their use to remove multivalent metal impurities from resist components

A chemically modified chelate resin comprising the reaction product of a cross-linked polymer bead chelate resin containing amine reaction sites with an aromatic aldehyde selected from the group consisting of 4-Formyl-benzo-15-Crown-5; 4-Formyl-benzo-18-Crown-6; 3,4-dihydroxybenzaldehyde; 3-ethoxy salicylaldehyde; salicylaldehyde; 2-pyridine carboxaldehyde, 3-pyridine carboxaldehyde; 4-pyridine carboxaldehyde; and pyrrole-2-carboxaldehyde.

Complex-forming polymers and processes to prepare them

The invention is a complex-forming polymer comprising at least one aryl group having a 2,2'-bipyridine complex-forming moiety or a 1,10-phenanthroline complex-forming moiety. The complex-forming polymers are prepared by contacting a substituted 2,2'-bipyridine or a substituted 1,10-phenanthroline compound with a metalating agent, and then reacting the metalated compound with an halomethylated polystyrene polymer, or alternatively, reacting the metalated compound with at least one vinylbenzyl halide and subsequently polymerizing the reaction product. The complex-forming polymers are hydrolytically stable and may be used as polymeric ligands as such or complexed with selected metal compounds.

RETARDER COMPOSITION

MACROMOLECULAR COMPOSITIONS COMPRISING INDENE-DERIVATIVES

VERFAHREN ZUR HERSTELLUNG VON TEILCHEN UND TEILCHEN DIE MIT HILFE DIESES VERFAHRENS HERGESTELLT WERDEN KÖNNEN

POLY(AZINE)-BASED CHARGE TRANSPORTING MATERIAL FOR ORGANIC PHOTOCONDUCTOR HAVING EXCELLENT ELECTROSTATIC PROPERTIES

PURPOSE: Provided is a poly(azine)-based charge transporting material, which imparts excellent electrostatic properties including high Vacc and low Vdis to an organic photoconductor, and is removed in a small amount by the extraction with a liquid carrier. CONSTITUTION: The organic photoconductor comprises a conductive substrate and a photoconductive element disposed on the conductive substrate, wherein the photoconductive element comprises: (a) a charge transporting material comprising a polymer represented by the following formula 1, and (b) a charge generating compound. In the formula 1, each of X1 and X2 independently represents a linking group; Ar includes an aromatic functional group; each of R1, R2 and R3 independently represents H, an alkyl, alkenyl, alkynyl, aromatic group or a heterocyclic group; and n represents a distribution of integers ranging from 1 to 100,000, wherein n has an average value of 1 or more. © KIPO 2006 ...

펜플루펜 중합체 입자

... 본 발명은 펜플루펜-함유 중합체 입자, 상기 중합체 입자를 함유하는 펜플루펜-함유 제제, 그의 제조 방법, 그리고 기술적 재료들, 특히 목재, 목재 제품 및 목재-플라스틱 복합재를 보호하기 위한 그의 용도에 관한 것이다.

Gel-type chelating resins and a process for removal of multi-valent, alkaline earth or heavy metal cations from solutions

PROCESS FOR PRODUCING POLYMER-COATED FERROMAGNETIC PARTICLE, AND POLYMER-COATED FERROMAGNETIC PARTICLE

A METHOD OF MANUFACTURING PARTICLES, AND PARTICLES THAT CAN BE PRODUCED IN ACCORDANCE WITH THE METHOD

A method of producing open porous spherical particles by polymerizing monovinyl monomers and divinyl monomers and/or polyvinyl monomers (cross-linkers) in an emulsion with the aid of an initiator. The method is characterized by the steps of (i) preparing a w/o/w emulsion which comprises an aqueous phase having emulsified therein droplets which contain a water-in-oil emulsion, wherein the oil phase in the droplets includes vinyl monomers and an emulsifier which provides an inverse emulsion and the droplets have a diameter smaller than 2,000 'mu'm, and wherein the total amount of water is between 75-99 % (w/w); and (ii) thereafter initiating polymerization and isolating the particles, optionally after sieving, from the reaction mixture after the polymerization process. A population of open spherical porous polymer particles which have a diameter within the range of 50 'mu'm-2,000 'mu'm and include a pore system comprising (a) spherical hollows whose diameters are < 1/9 of the particle diameter ...

Method of producing material for purification of physiological liquids of organism, and method of producing the material

SYNTHESIS OF STRENE-DIVINYLBENZENE COPOLYMERS BY USING POLYGLUTARALDEHIDE AND THE APPLICATIONS

METHOD OF PRODUCING MATERIAL FOR PURIFICATION OF PHYSIOLOGICAL LIQUIDS OF ORGANISM, AND METHOD OF PRODUCING THE MATERIAL

Purification of physiological liquids of organism is performed by passing a physiological liquid with toxicants removed from a patient through a material which has a size, a shape, and a structure selected so as to remove toxic compounds in the molecular range of 300 to 30000 Dalton from the physiological liquid and which is composed of a porous hydrophobic divinylbenzene copolymer which initially has surface exposed vinyl groups in which thereafter the vinyl groups are chemically modified so as to form different surface exposed functional groups with a greater hydrophilicity and greater biocompatibility than those of the vinyl groups.

Polyazine-basierende Ladungstransportverbindungen

GELARTIGE CHELATIERENDE HARZE UND VERFAHREN ZUR ENTFERNUNG VON MEHRWERTIGEN, ERDALKALISCHEN ODER SCHWERMETALLISCHEN KATIONEN AUS LOESUNGEN.

Polynucleotide separations on nonporous polymer beads

SOLID PHASE EXTRACTION MEDIA

Described herein is a low back-pressure, solid phase extraction media for removing dissolved metals in a liquid. The solid phase extraction media comprises particles entrapped in a porous polymeric fiber matrix. The particles comprise at least one of a thiol-containing moiety or a thiourea-containing moiety, and the porous polymeric fiber matrix comprises a plurality of fibers and a polymeric binder. 1. A low back-pressure , solid phase extraction media for removing dissolved metals in a liquid comprising:a porous polymeric fiber matrix, comprising a plurality of fibers and a polymeric binder, and a particle comprising at least one of a thiol-containing moiety or a thiourea-containing moiety, wherein the particle is entrapped in the porous polymeric fiber matrix.2. The low back-pressure claim 1 , solid phase extraction media according to claim 1 , wherein the polymeric binder does not substantially adhere to the particle.3. The low back-pressure claim 1 , solid phase extraction media according to claim 1 , wherein the particle comprises a silica particle having the following thiol-containing moiety has the general formula:{'br': None, '—RSH'}wherein R is an alkyl, alkenyl, aryl, or alkaryl group optionally comprising heteroatoms and/or other functional groups.4. (canceled)5. The low back-pressure claim 1 , solid phase extraction media according to claim 1 , wherein the low back-pressure solid phase extraction media has a differential back pressure of 1.5 psi (10.3 kPa) at a flowrate of 3 ml/cm.6. The low back-pressure claim 1 , solid phase extraction media according to claim 1 , wherein the particle is mechanically entrapped in the porous polymeric fiber matrix.7. The low back-pressure claim 1 , solid phase extraction media according to claim 1 , wherein the particle is at least 20% by weight relative to the weight of the solid phase extraction media.8. (canceled)9. The low back-pressure claim 1 , solid phase extraction media according to claim 1 , wherein the ...

Recycling Superabsorbent Polymer Fines

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% ...

SUPERABSORBENT POLYMER HAVING A CAPACITY INCREASE

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 , ...

Impregnated nonwoven for degreasing food

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 , ...

DISPENSABLE POLYMERIC PRECURSOR COMPOSITION FOR TRANSPARENT COMPOSITE SORBER MATERIALS

A moisture sorbing acrylic-based composition comprising an ethylene glycol dimethacrylate as main liquid component, and a metal perchlorate therein dissolved is described. Use of the composition in order to obtain a moisture sorber material is also described, to be inserted for example in electronic or optoelectronic devices. 2. The moisture sorbing composition according to claim 1 , wherein the ethylene glycol dimethacrylate is selected from the group consisting of: diethylene glycol dimethacrylate claim 1 , triethylene glycol dimethacrylate claim 1 , tetraethylene glycol dimethacrylate claim 1 , polyethylene glycol dimethacrylate and mixtures thereof.3. The moisture sorbing composition according to wherein the polyethylene glycol dimethacrylate has a molecular weight comprised between 330 and 780 gr*mol.4. The moisture sorbing composition according to wherein the metal perchlorate is selected between an alkaline or alkaline-earth metal perchlorate.5. The moisture sorbing composition according to wherein the alkaline-earth metal perchlorate is magnesium perchlorate.6. The moisture sorbing composition according to wherein the polymerization initiator is a photoinitiator or a thermal initiator.7. The moisture sorbing composition according to wherein the photoinitiator is a difunctional-α-ketone in a concentration between 0.1 and 2.0 weight percent with respect the total weight of the composition.8. The moisture sorbing composition according to wherein the thermal initiator is a 2 claim 1 ,2′-azobisisobutyronitrile in a concentration between 0.5 and 1.0 weight percent with respect the total weight of the composition.9. The moisture sorbing composition according to wherein the composition further contains a crosslinking agent in an amount comprised between 0.5 and 5 weight percent with respect the total weight of the composition.10. The moisture sorbing composition according to wherein the crosslinking agent is a trimethacrylate.11. The moisture sorbing composition ...

ADSORBENT OF VOLATILE ORGANIC COMPOUNDS AND ADSORPTION METHOD USING THEREOF

The present invention relates to an adsorbent of volatile organic compounds (VOCs) comprising a novel mesoporous polymer, that shows improved adsorption property, and adsorption method of VOCs using thereof. 2. The adsorbent of VOCs of claim 1 , wherein the acrylamide-based polymer includes a plurality of pores having a diameter of 2.0 to 10.0 nm.3. The adsorbent of VOCs of claim 1 , wherein the acrylamide-based polymer has a number-average molecular weight of 5 claim 1 ,000 to 500 claim 1 ,000.4. The adsorbent of VOCs of claim 1 , wherein the material comprises a porous electrospun fiber comprising the acrylamide-based polymer.5. The adsorbent of VOCs of claim 1 , wherein the porous electrospun fiber includes a plurality of pores having a diameter of 20 to 500 nm on surface.6. The adsorbent of VOCs of claim 1 , wherein the porous electrospun fiber has a diameter of 200 nm to 10 μm.7. The adsorbent of VOCs of claim 1 , wherein the adsorbent is used for removal of at least one VOC selected from the group consisting of benzene claim 1 , toluene claim 1 , nitrobenzene claim 1 , chlorobenzene claim 1 , chloroform claim 1 , 1 claim 1 ,2-dichloroethane claim 1 , hexane claim 1 , heptane claim 1 , octane claim 1 , nonane claim 1 , decane claim 1 , dodecane claim 1 , tetradecane claim 1 , diesel claim 1 , kerosene claim 1 , acetone claim 1 , ethylacetate claim 1 , dimethyl formamide claim 1 , dimethyl sulfone claim 1 , formaldehyde claim 1 , tetrahydrofuran (THF) and their derivatives.8. The adsorbent of VOCs of claim 1 , wherein the adsorbent adsorbs 15 g or more of the VOCs per 1.0 g of the acrylamide-based polymer.9. An adsorption method of VOCs comprising the step of contacting and adsorbing VOCs onto the adsorbent of . The present invention relates to an adsorbent of volatile organic compound and adsorbent method. More particularly, the present invention relates to an adsorbent of volatile organic compounds (VOCs) comprising a novel mesoporous polymer, that shows ...

METHOD FOR PRODUCING WATER-ABSORBENT RESIN PARTICLES AND WATER-ABSORBENT RESIN PARTICLES

The present invention provides a method for producing water-absorbent resin particles which show an excellent water absorption rate and high equilibrium swelling capacity and which have an appropriate particle size to be excellent in handleability, and water-absorbent resin particles obtained by the method. The present invention is a method for producing water-absorbent resin particles by reversed phase suspension polymerization of a water-soluble ethylenically unsaturated monomer, the method including the steps of: (A) first reversed phase suspension polymerization of a water-soluble ethylenically unsaturated monomer in a petroleum hydrocarbon dispersion medium using a water-soluble radical polymerization initiator, in the absence of an internal crosslinking agent and in the presence of a surfactant having an HLB of 8 to 12; (B) intermediate crosslinking reaction by adding an intermediate crosslinking agent; (C) second reversed phase suspension polymerization of a water-soluble ethylenically unsaturated monomer added to the petroleum hydrocarbon dispersion medium containing the surfactant dissolved therein using a water-soluble radical polymerization initiator in the absence of an internal crosslinking agent, thereby producing a water-absorbent resin precursor; and (D) post crosslinking reaction of the water-absorbent resin precursor preliminary adjusted to have a moisture content of 30 to 100% by mass relative to a water-soluble ethylenically unsaturated monomer component in the water-absorbent resin precursor. 1. A method for producing water-absorbent resin particles by reversed phase suspension polymerization of a water-soluble ethylenically unsaturated monomer , the method comprising the steps of:(A) first reversed phase suspension polymerization of a water-soluble ethylenically unsaturated monomer in a petroleum hydrocarbon dispersion medium using a water-soluble radical polymerization initiator, in the absence of an internal crosslinking agent and in the ...

POLYACRYLIC ACID (SALT)-BASED WATER ABSORBENT RESIN, AND METHOD FOR PRODUCTION THEREOF

Provided is a method for producing a polyacrylic acid (salt)-based water absorbent resin, which is a convenient production method for a water absorbent resin for an absorbent suitable for practical use, the water absorbent resin having a reduced amount of residual monomers. Disclosed is a method for producing a polyacrylic acid (salt)-based water absorbent resin, the method comprising a polymerization step of polymerizing an aqueous monomer solution containing acrylic acid (salt) as a main component; a drying step of drying a water-containing gel-like crosslinked polymer obtained in the polymerization step; a surface crosslinking step of surface crosslinking the water absorbent resin under drying or the water absorbent resin which has been dried; and a packaging step of packaging the surface crosslinked water absorbent resin, wherein an iron content in the aqueous monomer solution in the polymerization step is 2 ppm (relative to the monomer(s)) or less, a moisture content of the water absorbent resin in the packaging step is 1% by weight or more, and the method further comprises, after the packaging step, a storage step of storing the packaged water absorbent resin for 3 days or longer. 121-. (canceled)22. A method for producing a polyacrylic acid (salt)-based water absorbent resin , the method comprising:a polymerization step of polymerizing an aqueous monomer solution containing acrylic acid (salt) as a main component;a drying step of drying a water-containing gel-like crosslinked polymer obtained in the polymerization step;a surface crosslinking step of surface crosslinking the water absorbent resin under drying or the water absorbent resin which has been dried; anda packaging step of packaging the surface crosslinked water absorbent resin,wherein an iron content in the aqueous monomer solution in the polymerization step is 2 ppm (relative to the monomer(s)) or less, a moisture content of the water absorbent resin in the packaging step is 1% by weight or more, ...

METHOD FOR PRODUCING WATER-ABSORBENT RESIN

A method for producing a water-absorbent resin by a reversed-phase suspension polymerization method, includes step 1 of dispersing a first aqueous solution containing a partially neutralized product (A) of a water-soluble ethylenically unsaturated monomer having acid groups in the molecule in a petroleum-type hydrocarbon dispersion medium in the presence of a dispersing agent, and then polymerizing the resulting dispersion to obtain a slurry containing primary particles of a polymer, and step 2 of adding a second aqueous solution containing a partially neutralized product (B) of a water-soluble ethylenically unsaturated monomer having acid groups in the molecule to the slurry obtained in step 1, and then polymerizing the mixture to obtain a slurry in which the primary particles are agglomerated. In the method, a molar neutralization degree X of the partially neutralized product (A) is set larger than a molar neutralization degree Y of the partially neutralized product (B), and also a difference between the molar neutralization degree X and the molar neutralization degree Y is set to 5% or more. The dispersing agent usable herein is at least one member among those of a surfactant and a polymer-type dispersing agent. The water-absorbent resin produced by this method suppresses odor originating from a dispersion medium and odor generated with the lapse of time after absorption of a body fluid or the like. 1. A method for producing a water-absorbent resin by a reversed-phase suspension polymerization method , the method comprising:step 1 of dispersing a first aqueous solution containing a partially neutralized product (A) of a water-soluble ethylenically unsaturated monomer having acid groups in the molecule in a petroleum-type hydrocarbon dispersion medium in the presence of a dispersing agent, and then polymerizing the resulting dispersion to obtain a slurry containing primary particles of a polymer, andstep 2 of adding a second aqueous solution containing a partially ...

WATER-ABSORBING RESIN COMPOSITION AND LAMINATE PRODUCED USING SAME

Provided are: a water-absorbing resin composition and a laminate using the resin composition. The resin composition is capable of giving a transparent anti-fog coating excellent in properties such as appearance, coatability, anti-fog properties, water resistance, and heat resistance. Specifically, a resin composition includes a specific (meth)acrylamide copolymer (A) in combination with at least one bifunctional or higher (meth)acrylate compound (B), in which the (meth)acrylamide copolymer (A) is copolymerized from a (meth)acrylamide monomer with another monomer. This resin composition provides an active-energy-ray-curable water-absorbing resin composition and a laminate using the resin composition, each having excellent anti-fog properties. 2. The water-absorbing resin composition of claim 1 , wherein the (meth)acrylamide monomer (A-1) partially or wholly comprises N claim 1 ,N-dimethylacrylamide; and the monomer (A-2) partially or wholly comprises methyl methacrylate.3. The water-absorbing resin composition of claim 1 , wherein the (meth)acrylamide copolymer (A) has a weight-average molecular weight of 500 to 200 claim 1 ,000 in terms of polyethylene oxide.5. An anti-fog coating resin composition comprising the water-absorbing resin composition of .6. A cured article cured from the water-absorbing resin composition of .7. A laminate comprising a substrate; and a layer present on the substrate claim 5 , the layer formed by applying the anti-fog coating resin composition of to the substrate and curing the applied resin composition.8. The water-absorbing resin composition of one of claim 2 , wherein the (meth)acrylamide copolymer (A) has a weight-average molecular weight of 500 to 200 claim 2 ,000 in terms of polyethylene oxide.11. An anti-fog coating resin composition comprising the water-absorbing resin composition of .12. An anti-fog coating resin composition comprising the water-absorbing resin composition of .13. An anti-fog coating resin composition comprising ...

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

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 ...

PROCESSES AND SORBENTS FOR SEPARATION OF GASES BY CYCLIC ADSORPTION

A sorbent medium for a cyclic adsorption process comprises at least one self-supporting porous body produced by sintering a mixture of a powdered adsorbent and polyethylene particles having a molecular weight of at least 4×10g/mol as determined by ASTM-D 4020. 1. A sorbent medium for a cyclic adsorption process , the sorbent medium comprising at least one self-supporting porous body produced by sintering a mixture of a powdered adsorbent and polyethylene particles having a molecular weight of at least 4×10g/mol as determined by ASTM-D 4020.2. The sorbent medium of claim 1 , wherein the polyethylene particles have a molecular weight from 4×10g/mol to 8×10g/mol as determined by ASTM-D 4020.3. The sorbent medium of claim 1 , wherein the polyethylene particles have an average particle size claim 1 , d claim 1 , from 5 to 500 μm.4. The sorbent medium of claim 3 , wherein the polyethylene particles have an average particle size claim 3 , d claim 3 , from 30 to 350 μm.5. The sorbent medium of claim 1 , wherein the polyethylene particles have a bulk density between 0.1 and 0.5 g/ml.6. The sorbent medium of claim 1 , wherein the weight ratio of powdered adsorbent to polyethylene binder in the sintered mixture is in the range from 90:10 to 50:50.7. The sorbent medium of claim 6 , wherein the weight ratio of powdered adsorbent to polyethylene binder in the sintered mixture is in the range from 80:20 to 60:40.8. The sorbent medium of claim 1 , wherein the powdered adsorbent comprises at least one of activated carbon claim 1 , carbon molecular sieve claim 1 , diatomaceous earth claim 1 , silica claim 1 , zeolite claim 1 , alumina claim 1 , an ion exchange resin claim 1 , titanium silicates claim 1 , titanium oxides claim 1 , and metal oxides and hydroxides.9. The sorbent medium of claim 1 , wherein the powdered adsorbent comprises carbon molecular sieve having a bulk density of from 0.3 to 0.8 g/ml.10. The sorbent medium of claim 1 , wherein the powdered adsorbent comprises ...

METHOD FOR PRODUCING WATER-ABSORBENT RESIN

A method for producing a water-absorbent resin includes a polymerization step of polymerizing a polymerizable component containing a water-soluble ethylenically unsaturated monomer dissolved in water using a water-soluble azo-type radical polymerization initiator to obtain a reaction system including a water-absorbent resin precursor, and a dehydration step of removing water from the reaction system by heating. In the dehydration step, a water-soluble radical polymerization initiator is added to the reaction system at any first dehydration stage when the residual water rate calculated by the formula (1) is 50% or more, and a reducing substance is added to the reaction system at any second dehydration stage when the residual water rate decreases from that at the first dehydration stage by 10% or more. According to this production method, a water-absorbent resin having satisfactory water-absorption capacity can be produced while suppressing the content of residual monomers. 2. The method for producing a water-absorbent resin according to claim 1 , wherein the polymerizable component is polymerized by a reversed-phase suspension polymerization method in the polymerization step.3. The method for producing a water-absorbent resin according to claim 2 , wherein the polymerizable component is further added to be polymerized to a slurry obtained by progress of the polymerization of the polymerizable component.4. The method for producing a water-absorbent resin according to claim 3 , wherein the addition of the polymerizable component to the slurry and the polymerization are repeated.5. The method for producing a water-absorbent resin according to claim 1 , wherein the water-soluble azo-type radical polymerization initiator is at least one selected from the group consisting of 2 claim 1 ,2′-azobis(2-amidinopropane)dihydrochloride claim 1 , 2 claim 1 ,2′-azobis[2-[1-(2-hydroxyethyl)-2-imidazolin-2-yl]propane]dihydrochloride claim 1 , and 2 claim 1 ,2′-azobis[N-(2-carboxyethyl ...

METAL OXIDE FOAM, AMINE FUNCTIONAL SOLID SORBENT, METHODS AND APPLICATIONS

Amine functional solid sorbents for carbon dioxide capture and sequestration may be prepared from metal oxide foam solid sorbent supports by treating an appropriate metal oxide foam solid sorbent support with an amine material. Desirable are metal oxide foam solid sorbent supports with a foam structure and morphology at least substantially absent hollow sphere, layered sphere, wormlike and amorphous structure and morphology components. The amine materials may be sorbed into the metal oxide foam solid sorbent support, or alternatively chemically bonded, such as but not limited to covalently bonded, to the metal oxide foam solid sorbent support. 1. A sorbent support comprising a metal oxide material having a foam like structure and morphology substantially absent hollow sphere , layered sphere , wormlike and amorphous structure and morphology components.2. The sorbent support of wherein the metal oxide material comprises a silica material.3. The sorbent support of wherein the metal oxide material is selected from the group consisting of silica claim 1 , titania claim 1 , hafnia and zirconia materials claim 1 , mixtures thereof claim 1 , composites thereof and alloys thereof.4. The sorbent support of wherein the sorbent support has a unit cell size from about 20 to about 200 nanometers and a window opening with a pore size from about 10 to about 40 nm.5. A method for synthesizing a sorbent support comprising reacting in aqueous solution a soluble silica source material claim 1 , a catalyst material and a surfactant material while optimizing a concentration of the surfactant material and the catalyst material with respect to the soluble silica source material to provide a silica material having a foam like structure and morphology substantially absent hollow sphere claim 1 , layered sphere claim 1 , wormlike and amorphous structure and morphology components.6. The method of wherein:the silica source material comprises sodium silicate;the surfactant material comprises an ...

NOVEL ADSORBENT COMPOSITIONS

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 ...

METHOD FOR PRODUCING WATER-ABSORBING RESIN

The invention provides a novel method for producing a water-absorbent resin comprising: subjecting at least one water-soluble ethylenic unsaturated monomer to reversed-phase suspension polymerization in a petroleum hydrocarbon dispersion medium, the reversed-phase suspension polymerization being conducted using a 0.00005 to 0.00016 mol of water-soluble azo initiator for radical polymerization per mol of the water-soluble ethylenic unsaturated monomer in the presence of 0.000015 to 0.00015 mol of hypophosphorous compound per mol of the water-soluble ethylenic unsaturated monomer. 1. A method for producing a water-absorbent resin comprising:subjecting at least one water-soluble ethylenic unsaturated monomer to reversed-phase suspension polymerization in a petroleum hydrocarbon dispersion medium,the reversed-phase suspension polymerization being conducted using 0.00005 to 0.00016 mol of water-soluble azo initiator for radical polymerization per mol of the water-soluble ethylenic unsaturated monomer to be used in the presence of 0.000015 to 0.00015 mol of hypophosphorous compound per mol of the water-soluble ethylenic unsaturated monomer to be used.2. The method for producing a water-absorbent resin according to claim 1 , wherein the water-soluble azo initiator for radical polymerization is at least one member selected from the group consisting of 2 claim 1 ,2′-azobis(2-amidinopropane)dihydrochloride claim 1 , 2 claim 1 ,2′-azobis{2-[1-(2-hydroxyethyl)-2-imidazolin-2-yl]propane}dihydrochloride claim 1 , and 2 claim 1 ,2′-azobis[N-(2-carboxyethyl)-2-methylpropioneamidine]tetrahydrate.3. The method for producing a water-absorbent resin according to claim 1 , wherein the hypophosphorous compound is at least one member selected from the group consisting of hypophosphorous acid and sodium hypophosphite.4. The method for producing a water-absorbent resin according to claim 1 , wherein the water-soluble ethylenic unsaturated monomer is at least one member selected from the ...

STABILIZATION OF ONE-POT METHAMPHETAMINE SYNTHESIS SYSTEMS

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 ...

METHOD FOR PRODUCING WATER-ABSORBING POLYMER PARTICLES BY POLYMERIZING DROPLETS OF A MONOMER SOLUTION

A process for producing water-absorbing polymer particles by polymerizing droplets of a monomer solution in a surrounding gas phase in a reaction chamber, wherein the monomer solution is metered into the reaction chamber via at least one bore, and the diameter is from 210 to 290 μm per bore and the metering rate is from 0.9 to 5 kg/h per bore. 110.-. (canceled)11. Water-absorbing polymer particles obtainable by polymerizing droplets of a monomer solution comprising ,a) at least one ethylenically unsaturated monomer which bears acid groups and may be at least partly neutralized,b) at least one crosslinker,d) at least one initiator ande) water,{'sup': '3', 'in a surrounding gas phase in a reaction chamber, the monomer solution being metered into the reaction chamber via at least one bore, wherein the diameter is from 210 to 290 μm per bore and the metering rate is from 0.9 to 5 kg/h per bore and wherein the water-absorbing polymer particles have a density of at least 0.55 g/cm, a mean particle diameter of from 300 to 450 μm and a moisture content of at least 10% by weight.'}12. Water-absorbing polymer particles according to claim 11 , wherein the water-absorbing polymer particles have a density of at least 0.6 g/cm.13. Water-absorbing polymer particles according to claim 11 , wherein the water-absorbing polymer particles a mean particle diameter of from 340 to 400 μm.14. Water-absorbing polymer particles according to claim 11 , wherein the water-absorbing polymer particles have a moisture content of at least 15% by weight.15. Water-absorbing polymer particles according to claim 11 , wherein the water-absorbing polymer particles have a mean sphericity of at least 0.84.16. Water-absorbing polymer particles according to claim 11 , wherein the water-absorbing polymer particles have a mean sphericity of at least 0.9.17. Water-absorbing polymer particles according to claim 11 , wherein the water-absorbing polymer particles have a centrifuge retention capacity of at least 15 ...

Oil Absorbing Material and Processes of Recycling Absorbent Articles to Produce the Same

An oil absorbing material is generally provided. The oil absorbing material can includes sorbent particles having an average aspect ratio of about 5 to about 500 and a mean average particle diameter of about 10 μm to about 1 millimeter. The oil absorbing material comprises polypropylene, polyethylene, inorganic filler particles, and absorbent core material. In one embodiment, the sorbent particles can have an average specific surface area of about 0.25 to about 5.0 m/g and can have a bulk density that is about 0.01 g/cmto about 0.8 g/cm. Processes of making the oil absorbing material are also provided via a solid-state shear pulverization recycling process transforming absorbent article waste into the oil absorbing material. The process can include pulverizing the absorbent article waste to form sorbent particles while cooling the absorbent article waste in an amount sufficient to maintain the absorbent article waste in a solid state. 1. An oil absorbing material comprising sorbent particles , wherein the sorbent particles have an average aspect ratio of about 5 to about 500 and a mean average particle diameter of about 10 μm to about 1 millimeter;wherein the oil absorbing material comprises a thermoplastic polyolefin material, inorganic filler particles, and absorbent core material.2. The oil absorbing material as in claim 1 , wherein the mean average particle diameter is about 100 μm to about 500 μm.3. The oil absorbing material as in claim 1 , wherein the aspect ratio is about 10 to about 400.4. The oil absorbing material of claim 1 , wherein the sorbent particles have an average specific surface area of about 0.25 to about 5.0 m/g.5. The oil absorbing material of claim 1 , wherein the sorbent particles have an average specific surface area of about 0.3 to about 2.0 m/g.6. The oil absorbing material of claim 1 , wherein the sorbent particles have a bulk density that is about 0.01 g/cmto about 0.8 g/cm.7. The oil absorbing material of claim 1 , wherein the sorbent ...

Fibers of Polymer-Wax Compositions

Disposable article that include fibers formed from compositions comprising thermoplastic polymers and waxes are disclosed, where the wax is dispersed throughout the thermoplastic polymer. 1. A disposable article comprising: (a) a thermoplastic polymer; and', '(b) a wax having a melting point greater than 25° C., 'fibers that are produced by melt spinning a composition comprising an intimate admixture of'}2. The disposable article of claim 1 , wherein the thermoplastic polymer comprises a polyolefin claim 1 , a polyester claim 1 , a polyamide claim 1 , copolymers thereof claim 1 , or combinations thereof.3. The disposable article of claim 2 , wherein the thermoplastic polymer is selected from the group consisting of polypropylene claim 2 , polyethylene claim 2 , polypropylene co-polymer claim 2 , polyethylene co-polymer claim 2 , polyethylene terephthalate claim 2 , polybutylene terephthalate claim 2 , polylactic acid claim 2 , polyhydroxyalkanoates claim 2 , polyamide-6 claim 2 , polyamide-6 claim 2 ,6 claim 2 , and combinations thereof.4. The disposable article of claim 1 , wherein the thermoplastic polymer comprises polypropylene.5. The disposable article of claim 4 , wherein the polypropylene has a weight average molecular weight of about 20 kDa to about 400 kDa.6. The disposable article of claim 4 , wherein the polypropylene has a melt flow index of greater than 5 g/10 min.7. The disposable article of claim 6 , wherein the polypropylene has a melt flow index of greater than 10 g/10 min.8. The disposable article of claim 1 , comprising about 5 wt % to about 40 wt % of the wax claim 1 , based upon the total weight of the composition.9. The disposable article of claim 8 , comprising about 10 wt % to about 20 wt % of the wax claim 8 , based upon the total weight of the composition.10. The disposable article of claim 1 , wherein the wax comprises a lipid.11. The disposable article of claim 10 , wherein the lipid comprises a monoglyceride claim 10 , diglyceride claim ...

ABSORBENT STRUCTURE

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 ...

POROUS BODY AND METHOD FOR PRODUCING THE SAME, INK JET PRINTING METHOD AND INK JET PRINTING APPARATUS

The present invention provides a porous body for the absorption of a liquid component contained in an ink image on an ink receiving medium, the porous body including a fiber having a pore structure in the inside, wherein the pore structure satisfies the following requirements (a) and (b), and an inter-fiber void ratio which indicates the volume ratio of a void formed between the each fibers is 40% or more to 80% or less: (a) average pore size/average fiber diameter is 0.2 or less; and (b) an intra-fiber void ratio is 5% or more to 40% or less. 1. A porous body for the absorption of a liquid component contained in an ink image on an ink receiving medium ,the porous body comprising a fiber having a pore structure in the inside, whereinthe pore structure satisfies the following requirements (a) and (b), andan inter-fiber void ratio which indicates the volume ratio of a void formed between the each fibers is 40% or more to 80% or less:(a) average pore size/average fiber diameter is 0.2 or less; and(b) an intra-fiber void ratio is 5% or more to 40% or less.2. The porous body according to claim 1 , wherein the average fiber diameter is 0.1 μm or more to 5.0 μm or less.3. The porous body according to claim 1 , wherein the fiber comprises a thermoplastic resin.4. The porous body according to claim 1 , wherein the fiber comprises a fluorine-containing resin.5. The porous body according to claim 1 , whereinthe porous body comprises a first fiber comprising a first material and a second fiber comprising a second material, andat least one of the first fiber and the second fiber has the pore structure.6. The porous body according to claim 1 , wherein the ink image contains a reaction solution that is rendered highly viscous upon contact with the ink.7. The porous body according to claim 1 , wherein the porous body absorbs the liquid component by contact with the ink image.8. A method for producing a porous body for the absorption of a liquid component contained in an ink image ...

Absorbent Polymer Reinforcing Fiber

A reinforced absorbent polymer is provided for improving mechanical properties without degrading their absorption performance. The reinforced polymer includes an absorbent polymer; and at least one fiber for reinforcement disposed in the polymer.

ALIPHATIC AMINE BASED NANOCARBONS FOR THE ABSORPTION OF CARBON DIOXIDE

A composition of matter, and method to make same, for a nano-based material including a nanocarbon support to which is attached an aliphatic amine. In particular, the composition of matter is an aliphatic amine-nanocarbon material that includes a nanocarbon (NC) support, such as C, nano-graphite, graphene, nanocarbon ribbons, graphite intercalation compounds, graphite oxide, nano-coal, nanohorns, and combinations thereof, and further includes an aliphatic amine, such as polyethyleneimine (PEI). 137-. (canceled)38. A composition comprising:{'sub': '60', 'a nanocarbon support, wherein the nanocarbon support is selected from the group consisting of C, nano-graphite, graphene, nanocarbon ribbons, graphite intercalation compounds, graphite oxide, nano-coal, nanohorns, and combinations thereof;'}an aliphatic amine attached to the nanocarbon support to form an aliphatic amine-nanocarbon material.39. The composition of claim 38 , wherein the aliphatic amine-nanocarbon material has a COabsorption capacity at ambient pressure and temperature of at least about 10 wt % of the aliphatic amine-nanocarbon material.40. The composition of claim 38 , wherein{'sub': '60', 'the nanocarbon support is C; and'}{'sub': '60', 'the aliphatic amine-nanocarbon material is an aliphatic amine-Cmaterial.'}41. The composition of claim 38 , whereinthe aliphatic amine is polyethyleneimine; andthe aliphatic amine-nanocarbon material is a polyethyleneimine-nanocarbon material.42. The composition of claim 41 , wherein the polyethyleneimine-nanocarbon material has a COabsorption capacity at ambient pressure and temperature of at least about 10 wt % of the polyethyleneimine-nanocarbon material.43. The composition of claim 41 , wherein the polyethyleneimine-nanocarbon material has a COabsorption capacity at ambient pressure and temperature of at least about 15 wt % of the polyethyleneimine-nanocarbon material.44. The composition of claim 41 , wherein the polyethyleneimine-nanocarbon material has a ...

REGENERATIVE PURIFICATION OF A PRETREATED BIOMASS STREAM

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 ...

METHOD FOR REMOVING BACTERIA FROM BLOOD USING HIGH FLOW RATE

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 ...

METHOD FOR PRODUCING POLYACRYLIC ACID (SALT)-BASED WATER-ABSORBENT RESIN

A method for producing polyacrylic acid (salt)-based water-absorbing resin includes a step of polymerizing an acrylic acid (salt)-based aqueous monomer solution, the polymerization step involving use of a polymerization reaction apparatus including a polymerization reaction unit covered with a casing, the polymerization step involving a polymerization reaction under internal pressure of the polymerization reaction unit, the internal pressure being slightly reduced and having a pressure reduction level of more than 0 kPa and not more than 10 kPa relative to the ambient pressure at the periphery of the polymerization reaction unit. 1. A method for producing polyacrylic acid (salt)-based water-absorbing resin comprising a step of polymerizing an acrylic acid (salt)-based aqueous monomer solution ,wherein a polymerization reaction apparatus used in said polymerization step has a polymerization reaction unit covered with a casing, andwherein, in said polymerization step, a polymerization reaction is carried out under conditions that internal pressure of said polymerization reaction unit is reduced by a range of more than 0 kPa and not more than 10 kPa relative to ambient pressure at the periphery of said polymerization reaction unit.2. The method according to claim 1 , wherein the internal pressure of said polymerization reaction unit is measured inside discharge piping connected to a discharge outlet installed at said polymerization reaction unit.3. The method according to claim 2 , wherein a plurality of said discharge outlets are installed.4. The method according to claim 1 , wherein a gas is supplied from outside to inside of said polymerization reaction unit.5. The method according to claim 4 , wherein said gas is air or a mixed gas containing air as a main component.6. The method according to claim 4 , wherein a temperature of said gas is lower than 50° C.7. The method according to claim 4 , wherein a range of temperature change for said gas is 5° C. to 40° C. by ...

METHOD OF MANUFACTURING WATER-ABSORBENT RESIN COMPOSITION

The invention provides a method of manufacturing a water-absorbent resin composition containing water-absorbent resin particles and additive particles, by which it is possible to obtain a water-absorbent resin composition that sufficiently exhibits additional functions, such as an anti-blocking property under moisture absorption, of the additive particles while maintaining an excellent water absorption property. A method of manufacturing a water-absorbent resin composition includes a resin particle preparation step and a mixing step. In the mixing step, water-absorbent resin particles which are prepared in the resin particle preparation step are mixed with additive particles in multiple stages by using a plurality of mixing apparatuses to obtain a water-absorbent resin composition. 1. A method of manufacturing a water-absorbent resin composition containing water-absorbent resin particles and additive particles , the method comprising:a resin particle preparation step of preparing the water-absorbent resin particles; anda mixing step of mixing the water-absorbent resin particles which are prepared in the resin particle preparation step, with additive particles in multiple stages by using a plurality of mixing apparatuses and obtaining a water-absorbent resin composition.2. The method of manufacturing a water-absorbent resin composition according to claim 1 , a primary mixing stage of carrying out primary mixing of the water-absorbent resin particles with the additive particles by using a first mixing apparatus, and', 'a secondary mixing stage of carrying out secondary mixing of a primary mixture which is obtained in the primary mixing stage, by using a second mixing apparatus until the additive particles are uniformly dispersed., 'wherein the mixing step includes'}3. The method of manufacturing a water-absorbent resin composition according to claim 2 ,wherein the primary mixing stage includes a plurality of mixing stages.4. The method of manufacturing a water- ...

Recycling of Superabsorbent Polymer Via UV Irradiation In Flow System

Poly(acrylic acid)-based superabsorbent polymer (SAP) in a feed stream is converted with UV irradiation into poly(acrylic acid) (PAA) in a flow system. The UV total energy used to convert SAP into PAA is less than about 50 MJ/kg SAP. 1. A method for degrading a superabsorbent polymer (SAP) to poly(acrylic acid) (PAA) comprising flowing a feed stream comprising said SAP into a UV irradiation zone , irradiating said feed stream with UV , and producing a product stream comprising said PAA at the end of said irradiation zone; wherein said feed stream comprises said SAP at a concentration greater than about 1 wt %; wherein said feed stream has a residence time in said UV irradiation zone of less than about 120 s; and wherein said UV used to convert SAP to PAA requires a UV total energy of less than about 50 MJ/kg SAP.2. The method of claim 1 , wherein said residence time is less than about 60 s.3. The method of claim 1 , wherein said UV total energy is less than about 16 MJ/kg SAP.4. The method of claim 1 , wherein said feed stream comprises SAP and water.5. The method of claim 1 , wherein said feed stream comprises SAP and hydrogen peroxide.6. The method of claim 1 , wherein said SAP has degree of neutralization (DN) greater than about 50%.7. The method of claim 1 , wherein said SAP has DN between about 65% and about 75%.8. The method of claim 1 , wherein said feed stream has a viscosity; wherein said product stream has a viscosity; wherein the ratio of the viscosity of the product stream to the viscosity of the feed stream is the viscosity ratio; and wherein the negative logarithm of said viscosity ratio is less than about 6.9. The method of claim 1 , wherein said feed stream has a viscosity; wherein said product stream has a viscosity; wherein the ratio of the viscosity of the product stream to the viscosity of the feed stream is the viscosity ratio; and wherein the negative logarithm of said viscosity ratio is less than about 4.10. The method of claim 1 , wherein ...

WATER ABSORBING RESIN PARTICLES, METHOD FOR MANUFACTURING WATER ABSORBING RESIN PARTICLES, ABSORPTION BODY, ABSORPTIVE ARTICLE, AND WATER-SEALING MATERIAL

Disclosed is a water-absorbent resin particle in which the water-absorption rate of physiological saline is 1 second to 15 seconds, the median particle size is 100 μm to 600 μm, and the residual volatile component content is 1.5% by weight or less. 1. A water-absorbent resin particle in which a water-absorption rate of physiological saline is 1 second to 15 seconds , a median particle size is 100 μm to 600 μm , and a residual volatile component content is 1.5% by weight or less.2. The water-absorbent resin particle according to claim 1 , wherein a specific surface area is 0.08 m/g or more.3. The water-absorbent resin particle according to claim 1 , wherein a water-absorption capacity of the physiological saline is 30 g/g to 90 g/g.4. A method of producing a water-absorbent resin particle claim 1 , comprising in the following order:a first polymerization step including obtaining a suspension containing a water-containing gelated polymer by polymerizing a water-soluble ethylenically unsaturated monomer in a suspension containing an oily liquid containing a hydrocarbon dispersion medium, a first aqueous liquid containing an aqueous solvent, the water-soluble ethylenically unsaturated monomer and a radical polymerization initiator, and a surfactant having an HLB value of 6 or higher, the first aqueous liquid being dispersed in the oily liquid; anda second polymerization step including mixing the suspension containing the water-containing gelated polymer at 45° C. or higher with a second aqueous liquid containing an aqueous solvent, a water-soluble ethylenically unsaturated monomer and a radical polymerization initiator, and polymerizing the water-soluble ethylenically unsaturated monomer in a suspension in which the second aqueous liquid is further dispersed.5. The method according to claim 4 , wherein in the second polymerization step claim 4 , a temperature of the suspension in which the second aqueous liquid has been further dispersed at the time of completion of ...

Systems and Methods for Purifying Solvents

The present disclosure is directed to methods and systems of purifying solvents. The purified solvents can be used for cleaning a semiconductor substrate in a multistep semiconductor manufacturing process. 1. A method of purifying an organic solvent , comprising:passing the organic solvent through a first filter unit and a second filter unit downstream of the first filter unit to obtain a purified organic solvent,wherein the first filter unit comprises a first housing and at least one first filter in the first housing, and the first filter comprises a filtration medium having a first average pore size;wherein the second filter unit comprises a second housing and at least two second filters in the second housing, the at least two second filters are arranged in the second housing in parallel, and each of the second filters independently comprises a filtration medium having a second average pore size; andwherein the number of the first filter in the first filter unit is smaller than the number of the second filters in the second filter unit, and the first average pore size is larger than the second average pore size.2. The method of claim 1 , wherein the first filter unit comprises one first filter.3. The method of claim 1 , wherein the filtration medium in the first filter comprises polypropylene claim 1 , high density polyethylene claim 1 , ultra high molecular weight polyethylene claim 1 , nylon claim 1 , polytetrafluoroethylene claim 1 , or a perfluoroalkoxy alkane polymer.4. The method of claim 1 , wherein the first average pore size is from about 50 nm to about 200 nm.5. The method of claim 1 , wherein the second filter unit comprises two or three second filters.6. The method of claim 1 , wherein the filtration medium in the second filter comprises polypropylene claim 1 , high density polyethylene claim 1 , ultra high molecular weight polyethylene claim 1 , nylon claim 1 , polytetrafluoroethylene claim 1 , or a perfluoroalkoxy alkane polymer.7. The method of ...

ADSORBENT CONTAINING CHELATING POLYMER

A metal adsorbent which can adsorb a wide variety of metals, can conform to various uses, and adsorbs metals in large amounts. Metal adsorbents in various forms, which have the property of highly efficiently adsorbing metals, are produced by (a) a method in which a polyamine polymer is chemically bonded and immobilized to a porous support, (b) a method in which a polyamine polymer is blended into a solution of a raw material for fibers and the mixture is formed into fibers by wet-spinning or dry spinning, and (c) a method in which a polyamine polymer is blended into a solution of a film-forming polymer and the mixture is formed into a film by a method of film formation from solution. The present invention relates to a metal adsorbent used for removal/collection of a wide variety of heavy metals in treated solutions such as industrial wastewater, service water and environmental water.Chelating resins are used as adsorbents/collectors of heavy metal elements in a solution containing a high-concentration salt, which are difficult to adsorb and collect with ion exchange resins. As the ability of forming a complex with metal elements varies depending on the structure of functional groups, chelating resins having various functional groups such as an iminodiasetic acid (IDA) group, a low-molecular polyamine group, aminophosphoric acid group, an isothionium group, a dithiocarbamic acid group and a glucamine group are commercially available. Among them, chelating resins introducing an IDA group are mainly used, but chelating resins introducing a low-molecular polyamine group are used for removing metals from a solution containing a large amount of alkali metals and alkali earth metals. These chelating resins form a complex with many metals, but the stability constant of a complex formed is significantly low as compared to ethylenediamine tetraacetic acid (EDTA), a typical chelating agent, and there arises a disadvantage that metal removal and collection rates are subject to ...

Absorbent Fibrous Structures Comprising a Polymeric Fluid Comprising a Soil Adsorbing Agent

Absorbent fibrous structure containing a polymeric fluid containing a polymer, including for example a copolymer and/or terpolymer, soil adsorbing agent, and absorbent fibrous structures containing such polymer soil adsorbing agents, and methods for making same. 1. An absorbent fibrous structure comprising a polymeric fluid comprising a polymer soil adsorbing agent comprising two or more different monomeric units , wherein the polymer soil adsorbing agent exhibits a weight average molecular weight of from about 50 ,000 g/mol to about 6 ,000 ,000 g/mol as measured according to the Molecular Weight Test Method and a charge density of greater than 0 meq/g as measured according to the Charge Density Test Method.2. The absorbent fibrous structure according to wherein the absorbent fibrous structure exhibits an average Soil Adsorption Value of about 90 mg soil/g absorbent fibrous structure or greater as measured according to the Soil Adsorption Test Method.3. The absorbent fibrous structure according to wherein the absorbent fibrous structure comprises a plurality of pulp fibers.3. orbent fibrous structure according to wherein the absorbent fibrous structure comprises a sanitary tissue product.54. The absorbent fibrous structure according to claim wherein the sanitary tissue product comprises a paper towel.6. The absorbent fibrous structure according to wherein the absorbent fibrous structure comprises a cleaning pad.7. The absorbent fibrous structure according to wherein the absorbent fibrous structure exhibits a moisture level of less than 30% as measured according to the Moisture Content Test Method.8. The absorbent fibrous structure according to wherein the absorbent fibrous structure exhibits an average Mirror Cleaning Densitometer Value of −0.5 or greater as measured according to the Mirror Cleaning Test Method.9. The absorbent fibrous structure according to wherein at least one of the monomeric units is derived from an acrylamide compound.10. The absorbent fibrous ...

SIMPLE SINGLE-STEP POROUS POLYMER MONOLITH FOR DNA EXTRACTION

A method and microfluidic device with a porous polymer monolith in a channel of the device with capture affinity element (such as an oligonucleotide complementary to a DNA target from the KPC antibiotic resistance gene) on the monolith surface. 1. A method for creating a monolith in a void space of a microfluidic device , comprising:filling the internal void spaces of the monolith with a polymerization mixture comprising one or more photopolymerizable monomers, a photo initiator, and a capture affinity element;masking microfluidic device to prevent light from reaching the internal void spaces with the exception of a gap to allow light to reach a preselected portion of the void spaces;exposing the microfluidic device to light to polymerize polymerization solution in the preselected portion to form in the preselected portion a porous polymer monolith with capture affinity element on a polymer monolith surface, and with the polymer monolith anchored on a device surface within the preselected portion;rinsing unpolymerized polymerization solution from the internal void spaces.2. The method of wherein the capture affinity element is a capture oligonucleotide.3. The method of wherein the polymerizable mixture comprises one or more photopolymerizable acrylate monomers.4. The method of wherein the microfluidic device is exposed to ultra-violet light.5. The method of wherein the filling claim 1 , masking claim 1 , exposing claim 1 , and rinsing steps are conducted once in a single step.6. The method of wherein the acrylate monomers are one or more from the group of PEGDA and EDMA.7. The method of wherein the capture oligonucleotide is complementary to a target DNA sequence.8. The method of wherein the capture oligonucleotide is complementary to a target from a gene from a microorganism.9. The method of wherein the capture oligonucleotide is complementary to a target from a gene from DNA of a bacterium.10. The method of wherein the capture oligonucleotide is complementary to a ...

PROCESS FOR MANUFACTURING A COMPOSITE SORBENT MATERIAL FOR CHROMATOGRAPHICAL SEPARATION OF BIOPOLYMERS

The present invention relates to a sorbent material for separation and purification of biopolymers, particularly nucleic acids, having a solid support substantially modified with a copolymer coating comprising aromatic monomers and crosslinking compounds and unsaturated esters or ethers preferably attached to the support via a vinylchlorsilane. The use of these materials for separation of nucleic acids, particularly a one-step isolation of DNA from lysates of different biological sources, is an object of the invention as well as a chromatographic column or cartridge at least partially filled with the sorbent material of the invention, a membrane-like device comprising the sorbent material of the invention, and a kit comprising the sorbent material of the invention in bulk or packed in chromatographic devices as well as other devices necessary for performing sample preparations. 122-. (canceled)24. The process of wherein the support is a porous inorganic material comprising inorganic metal oxide.25. The process of wherein the porous inorganic metal oxides show a bidisperse distribution of pore sizes.26. The process of wherein the support has an average pore size of 2-200 nm.27. The process of wherein the polymer coating has a thickness of about 10 to 250 Angstrom.28. The process of wherein the inorganic metal oxide is selected from the group consisting of oxides of aluminum claim 24 , titanium claim 24 , zirconium claim 24 , silicon oxides claim 24 , iron oxides claim 24 , controlled pore glass (CPG) claim 24 , diatomaceous earth and combinations thereof.29. The process of wherein the porous inorganic metal oxide shows a bidisperse distribution with mean pore diameters in the range of 20-100 nm for the larger pore size.30. The process of wherein the porous inorganic metal oxide has a mean pore diameter in the range of 2-15 nm for the smaller pore size.31. The process of wherein the ratio of the mean diameter of the large pore size distribution and the lower pore size ...

Polymer compositions containing zeolite for enhanced water adsorption

This invention relates generally to zeolites and polymer compositions with zeolites having enhanced adsorption capacity for adsorption of water, ammonia and other similar compounds. The invention is directed particularly to aluminosilicate zeolites, and methods for preparing zeolite entrained polymer compositions having enhanced water adsorption properties. This invention relates also to improved packaging materials with enhanced water adsorption properties incorporating the polymer compositions containing zeolites.

SUBSTRATES AND ASSOCIATED METHODS FOR ELUTION OF NUCLEIC ACIDS

A solid substrate for biological sample storage under dry-state and elution of biomolecules is provided. The dry, solid substrate is coated with saccharides, such as monosaccharides, oligosaccharides, polysaccharides or combinations thereof, and the substrate is comprised of one or more protein denaturing agents impregnated therein under a substantially dry state. A method for elution of biomolecules from biological samples is also provided. The compositions disclosed herein provide for enhanced elution and recovery of biomolecules, such as nucleic acids, from the sample. The sample is disposed on a substrate, dried to a substantially dry state; eluted from the biological sample dried on the substrate by rehydrating the substrate in an elution buffer. 1. A solid substrate for eluting biomolecules from a biological sample , comprising:one or more monosaccharides, oligosaccharides, polysaccharides or combinations thereof, andone or more protein denaturing agents impregnated therein under a substantially dry state.2. The substrate of claim 1 , wherein the substrate is selected from the group consisting of a nitrocellulose membrane claim 1 , a cellulose membrane claim 1 , a cellulose acetate membrane claim 1 , a regenerated cellulose membrane claim 1 , a nitrocellulose mixed ester membranes claim 1 , a polyethersulfone membrane claim 1 , a nylon membrane claim 1 , a polyolefin membrane claim 1 , a polyester membrane claim 1 , a polycarbonate membrane claim 1 , a polypropylene membrane claim 1 , a polyvinylidene difluoride membrane claim 1 , a polyethylene membrane claim 1 , a polystyrene membrane claim 1 , a polyurethane membrane claim 1 , a polyphenylene oxide membrane claim 1 , a poly(tetrafluoroethylene-co-hexafluoropropylene membrane claim 1 , and any combination of two or more of the above membranes.3. The substrate of claim 1 , wherein the substrate comprises cellulose.4. The substrate of claim 1 , wherein the substrate is a porous cellulose membrane.5. The ...

SANDBAG AND METHOD FOR PRODUCING SAME

Provided is a sandbag which is unlikely to break down even when using water-absorbing resin particles therein. A sandbag having a water-permeable bag and water-absorbing resin particles stored in the bag, wherein the pure-water absorption factor of the water-absorbing resin particles is at least a factor of 1,000, and the compression-breaking stress of the water-absorbing resin particles when swollen with pure water is at least 0.1N. 1. A sandbag comprising:a water-permeable bag; anda water-absorbing resin particle encased in the water-permeable bag, wherein a pure-water absorption factor of the water-absorbing resin particle is 1,000 times or more, and a compression-breaking stress of the water-absorbing resin particle in a state of being swollen with pure water is 0.1 N or more.2. The sandbag according to claim 1 , wherein the water-absorbing resin particle has a structure in which a second polymer is infiltrated into a first polymer particle.3. The sandbag according to claim 1 , wherein:the first polymer particle includes a polymer of a first monomer component including at least one of a monomer A or a salt of the monomer A,the second polymer includes a polymer of a second monomer component including at least one of a monomer B or a salt of the monomer B, andthe monomer A has an acid dissociation index smaller than an acid dissociation index of the monomer B.4. The sandbag according to claim 3 , wherein a difference between the acid dissociation index of the monomer B and the acid dissociation index of the monomer A (ΔpKa) is 1.5 or more.5. The sandbag according to claim 4 , wherein:the monomer A is an unsaturated sulfonic acid-based monomer, andthe monomer B is a water-soluble ethylenically unsaturated monomer.6. The sandbag according to claim 1 , wherein the water-absorbing resin particle has a granular shape claim 1 , a substantially spherical shape claim 1 , or a shape in which substantially spherical particles are aggregated.7. The sandbag according to claim ...

WATER ABSORBING MATERIAL AND MANUFACTURING METHOD THEREOF

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 ...

BEADS FOR BLOOD PROCESSING

Provided are beads for blood processing having porous beads and a polymer carried on the surface of the porous beads, wherein: the porous beads are configured from at least one resin selected from the group consisting of acrylic resins, styrene resins, and cellulose resins; and the polymer includes a specific monomer defined in the description as a monomer unit. 2. The beads for blood processing according to claim 1 , wherein the proportion of nitrogen atoms on the surfaces of the beads for blood processing is 0.2% to 0.7% claim 1 , as the percentage of atoms based on the total number of atoms with atomic numbers of 3 to 92.3. The beads for blood processing according to claim 1 , wherein q is 1 or 2 and m is 0 to 11.4. (canceled)5. The beads for blood processing according to claim 1 , wherein the polymer further includes a charged monomer as a monomer unit.6. The beads for blood processing according to claim 5 , wherein the charged monomer is a monomer with at least one group selected from the group consisting of amino claim 5 , carboxyl claim 5 , phosphate claim 5 , sulfonate and zwitterionic groups.7. The beads for blood processing according to claim 5 , wherein the charged monomer is at least one selected from the group consisting of 2-aminoethyl methacrylate (AEMA) claim 5 , dimethylaminoethyl methacrylate (DMAEMA) claim 5 , diethylaminoethyl methacrylate (DEAEMA) claim 5 , [2-(methacryloyloxy)ethyl]trimethylammonium claim 5 , acrylic acid (AAc) claim 5 , methacrylic acid (MAc) claim 5 , N-methacryloyloxyethyl-N claim 5 ,N-dimethylammonium-α-N-methylcarboxybetaine (CMB) and 2-(methacryloyloxy)ethyl 2-(trimethylammonio)ethyl phosphate (MPC).8. The beads for blood processing according to claim 34 , wherein the content of the charged monomer is 10 mol % to 60 mol % with respect to the total monomers composing the polymer.9. The beads for blood processing according to claim 34 , wherein the content of the charged monomer is 15 mol % to 40 mol % with respect to the ...

RESIN PARTICLES AND METHOD FOR PRODUCING RESIN PARTICLES

Provided are resin particles, including: a vinyl polymer containing divinyl benzene as a constituent, wherein a number average particle diameter of the resin particles is 2.5 micrometers or greater but 10.0 micrometers or less, wherein a coefficient of variation (CV value) of a number-based particle diameter of the resin particles is 20% or lower, and wherein a circularity of the resin particles is 0.990 or greater. 1. Resin particles , comprising:a vinyl polymer containing divinyl benzene as a constituent,wherein a number average particle diameter of the resin particles is 2.5 micrometers or greater but 10.0 micrometers or less,wherein a coefficient of variation (CV value) of a number-based particle diameter of the resin particles is 20% or lower, andwherein a circularity of the resin particles is 0.990 or greater.2. The resin particles according to claim 1 ,wherein the vinyl polymer contains a monomer containing one polymerizable double bond as a constituent.3141. The resin particles according to claim claim 1 ,wherein the resin particles are porous,wherein a pore diameter of the resin particles is 10 angstroms or greater but 950 angstroms or less, and{'sup': 2', '2, 'wherein a specific surface area of the resin particles is 10 m/g or greater but 600 m/g or less.'}4. The resin particles according to claim 3 ,{'sup': 3', '3, 'wherein a pore volume of the resin particles is 0.1 cm/g or greater but 2.0 cm/g or less.'}5. A method for producing resin particles claim 3 , the method comprising:sending a mixture liquid containing: a monomer including divinyl benzene; and a polymerization initiator into a continuous phase through a microchannel, to produce an emulsion in which dispersed phases formed of the mixture liquid are dispersed in the continuous phase; andheating the emulsion to polymerize the monomer, to obtain resin particles, which are a vinyl polymer,wherein the resin particles comprises a vinyl polymer containing divinyl benzene as a constituent,wherein a ...

MOLDED ARTICLE FOR HYDROCARBON ADSORPTION

Provided is a molded article for hydrocarbon adsorption, in which a porous metal complex, the structure of which may vary with adsorption and desorption of gases, can exhibit to a sufficient degree the adsorption and desorption capabilities inherent to the complex. This molded article for hydrocarbon adsorption is characterized by including (A) a metal complex constituted by metal ions, and organic ligands capable of bonding to the metal ions, and (B) a polymer binder component containing within its molecules a total of 0.3 mmol/g to 8.0 mmol/g, inclusive, of at least one functional group selected from group consisting of the carboxyl group, the hydroxyl group, amino groups, the mercapto group, epoxy groups, and the sulfo group. 1. A molded article for hydrocarbon adsorption comprising a metal complex (A) , composed of metal ions and organic ligands capable of bonding with the metal ions; and a polymer binder component (B) , which contains at least one functional group selected from the group consisting of a carboxyl group , hydroxyl group , amino group , mercapto group , epoxy group and sulfo group at a total of 0.3 mmol/g to 8.0 mmol/g in a molecule thereof.2. The molded article for hydrocarbon adsorption according to claim 1 , wherein a functional group of the polymer binder component (B) is a hydroxyl group or carboxyl group.3. The molded article for hydrocarbon adsorption according to claim 1 , wherein the polymer binder component (B) is an ethylenic hydrocarbon polymer claim 1 , polyester claim 1 , polyamide or polyether.4. The molded article for hydrocarbon adsorption according to claim 1 , wherein the polymer binder component (B) is a copolymer of a (meth)acrylic acid ester having 1 to 10 carbon atoms and (meth)acrylic acid.5. The molded article for hydrocarbon adsorption according to claim 1 , which contains 50% by weight to 97% by weight of the metal complex (A).6. The molded article for hydrocarbon adsorption according to claim 1 , wherein the organic ...

PORTION OF AN ELECTRONIC VAPING DEVICE FORMED OF AN OXYGEN SEQUESTERING AGENT

An electronic vaping device includes a housing extending in a longitudinal direction, a reservoir in the housing, the reservoir configured to store a pre-vapor formulation, a heater in the housing, the heater configured to heat the pre-vapor formulation, at least one portion formed of a material including at least one polymer and at least one oxygen sequestering agent, and a power supply. 1. An electronic vaping device comprising:a housing extending in a longitudinal direction;a reservoir in the housing, the reservoir configured to store a pre-vapor formulation;a heater in the housing, the heater configured to heat the pre-vapor formulation;at least one portion formed of a material including at least one polymer and at least one oxygen sequestering agent, the at least one oxygen sequestering agent configured to absorb atmospheric oxygen; anda power supply configured to selectively supply power to the heater.2. The electronic vaping device of claim 1 , wherein the at least one portion includes at least a portion of at least one of the housing claim 1 , a portion of the reservoir claim 1 , a mouth-end insert claim 1 , a gasket claim 1 , a connector claim 1 , a label claim 1 , and an end cap.3. The electronic vaping device of claim 1 , wherein the at least one polymer is a natural polymer or a synthetic polymer claim 1 , and wherein the at least one polymer includes at least one of low density polyethylene claim 1 , high density polyethylene claim 1 , low density polypropylene claim 1 , high density polypropylene claim 1 , and poly(dimethylsiloxane).4. The electronic vaping device of claim 1 , wherein the oxygen sequestering agent is an ultraviolet (UV) activated oxygen sequestering agent.5. The electronic vaping device of claim 1 , wherein the oxygen sequestering agent includes at least one of 1 claim 1 ,2 polybutadiene claim 1 , an anthroquinone system claim 1 , and a three phase blend including a reactive double bond claim 1 , a photoinitiator claim 1 , and a ...

Adsorbent For Use As A Window Desiccant

The present application provides an adsorbent strip that prevents window fogging, the strip including no more than 25 weight percent of polymer binder; and at least 75 weight percent of adsorbent particles. Also provided is a window spacer comprising the adsorbent strip and a partial window assembly, including a first pane of glass, a second pane of glass; and a window spacer comprising the adsorbent strip. 1. A window spacer , comprising:an adsorbent strip, comprising:i. no more than 25 weight percent of polymer binder; andii. at least 75 weight percent of adsorbent particles;the adsorbent strip having an aspect ratio of length to maximum cross-section dimension of at least 5, wherein the adsorbent strip prevents window fogging.2. The window spacer of claim 1 , wherein the adsorbent strip is formed using thermally induced phase separation.3. The window spacer of claim 2 , wherein the adsorbent strip comprises no more than 10% by weight of polymer binder and greater than 90% by weight of adsorbent particles.4. The window spacer of claim 2 , wherein the adsorbent strip comprises no more than 5% by weight of polymer binder and greater than 95% by weight of adsorbent particles.5. The window spacer of claim 2 , wherein the adsorbent strip comprises no more than 2% by weight of polymer binder and greater than 98% by weight of adsorbent particles.6. The window spacer of claim 2 , wherein the polymer binder is ultra-high molecular weight polyethylene.7. The window spacer of claim 2 , wherein the adsorbent particles are molecular sieves.8. The window spacer of claim 2 , wherein the adsorbent particles are interconnected by the polymer binder to form a self-supporting porous adsorbent.9. The window spacer of claim 2 , wherein the window spacer further comprises a foam contacting the top surface of the adsorbent strip.10. The window spacer of claim 2 , wherein the window spacer further comprises a non-permeable layer surrounding the bottom surface of the strip claim 2 , a ...

OXYGEN-ABSORBING RESIN COMPOSITION

An oxygen-absorbing composition of the present invention contains: a gas barrier resin (A) having an oxygen transmission rate of 500 mL·20 μm/(m·day·atm) or less as measured at 20° C. and 65% RH; a thermoplastic resin (B) including repeating units represented by General Formula (I) below 4: The oxygen-absorbing resin composition of claim 3 , wherein the thermoplastic resin (B) is a resin obtained through ring-opening metathesis polymerization of dicyclopentadiene in the presence of a tungsten compound.5: The oxygen-absorbing resin composition of claim 1 , wherein a ratio of the bifunctional processing stabilizer (D) is 500 to 20000 ppm based on a mass of the thermoplastic resin (B).7: The oxygen-absorbing resin composition of claim 1 , wherein a ratio of the metal salt (C) is 50 to 1000 ppm in terms of metal atoms based on a total mass of the gas barrier resin (A) and the thermoplastic resin (B).8: The oxygen-absorbing resin composition of claim 1 , wherein the gas barrier resin (A) is an ethylene-vinyl alcohol copolymer at least having an ethylene unit content of 5 to 60 mol % claim 1 , and having a saponification degree of 90 mol % or more.9: The oxygen-absorbing resin composition of claim 1 , further comprising a phenolic primary antioxidant (E).10: The oxygen-absorbing resin composition of claim 9 , wherein a ratio of the phenolic primary antioxidant (E) is 50 to 2000 ppm based on a mass of the thermoplastic resin (B).11: A multilayer structure claim 1 , comprising a layer made of the oxygen-absorbing resin composition of .12: A molded product made of a multilayer structure comprising a layer made of the oxygen-absorbing resin composition of . The present invention relates to an oxygen-absorbing resin composition having excellent oxygen-absorbing properties, a multilayer structure including a layer made of the resin composition, and a molded product made of the multilayer structure.Gas barrier resins, for example, ethylene-vinyl alcohol copolymers (hereinafter, ...

DISPERSIONS OF SUPERABSORBENT POLYMERS, PROCESSING THEREOF AND ARTICLES FORMED FROM THE DISPERSIONS

Dispersions of superabsorbent polymers are described comprising blends of polyols and super absorbent polymer. Products comprising deposits formed from such dispersions are also described. Suitable polyols can include, for example, polyethylene glycol. The dispersions can be flowed onto an absorbent sheet to form a deposit (sheeted SAP), which in some embodiments can be along a fraction of the sheet surface. Generally, the deposits are dried through a wicking process in which the polyol is wicked away from the superabsorbent polymer. The sheeted SAP can be incorporated into a final product with the deposit secured within the product. The dispersion allows for selective placement of superabsorbent polymer onto an absorbent sheet and/or in a final product. Embodiments based on coated yarns and the like are also presented. 1. A blend comprising: superabsorbent polymer (SAP) and at least about 15 weight percent polyol that is liquid at or above 65° C. , wherein the SAP is dispersed in a matrix of the polyol and wherein the blend comprises at least about 85 weight percent of SAP and polyethylene glycol (PEG) combined.2. The blend of wherein the polyol is a liquid at room temperature and wherein the blend is a room temperature flowable composition.3. The blend of wherein the blend is a solid at room temperature and has a melting point of no more than about 65° C.4. The blend of wherein the SAP comprises salts of polyacrylic acid and wherein the polyol is polyethylene glycol.5. The blend of comprising from about 5 weight percent SAP to about 85 weight percent SAP.6. The blend of where in the polyethylene glycol has an average molecular weight of no more than about 800 g/mol.7. The blend of comprising at least about 45 weight percent polyether polyol and superabsorbent polymers with prior to dispersion an average particle size from about 10 microns to about 250 microns and an absorption of at least about 8 weight percent of aqueous (0.9 weight % sodium chloride) solution.8. ...

DELAYED-ACTIVATION, HYDRATION MAINTENANCE APPARATUS AND METHOD

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 , ...

IMMUNOSUPPRESSIVE LEUKOCYTE ADSORPTION MATERIAL AND ADSORPTION COLUMN

An objective of the present disclosure is to provide an adsorption material that can selectively adsorb immunosuppressive leukocyte. The present disclosure provides an adsorption material for immunosuppressive leukocyte. The adsorption material includes a water-insoluble carrier to which at least one nitrogen-containing compound selected from a polyamine represented by a predetermined formula and aliphatic amines represented by predetermined formulae are bound. A form of the water-insoluble carrier is a fiber or a particle, a diameter of the fiber or the particle is 15 to 50 μm, and an arithmetic mean roughness of a surface of the water-insoluble carrier is 0.1 to 3.0 μm. 1. An adsorption material for immunosuppressive leukocyte , the adsorption material comprising:a water-insoluble carrier to which at least one nitrogen-containing compound is bound, the nitrogen-containing compound being selected from a polyamine represented by the following Formula (1), a primary aliphatic amine represented by the following Formula (2), and a secondary aliphatic amine represented by the following Formula (3), {'br': None, 'sup': 1', '2', '3', '4, 'RRN—X—NRR\u2003\u2003Formula (1)'}, 'wherein the water-insoluble carrier has a form of fiber or particle, the fiber or the particle has a diameter of 15 to 50 μm, and the water-insoluble carrier has a surface with an arithmetic mean roughness of 0.1 to 3.0 μm{'sup': 1', '4, 'claim-text': {'br': None, 'sub': '2', 'sup': '5', 'NHR\u2003\u2003Formula (2)'}, 'wherein in Formula (1), X is a saturated or unsaturated aliphatic hydrocarbon group having 2 to 20 carbon atoms, or a heteroatom-containing carbon chain in which 1 to 5 carbon atoms of a saturated or unsaturated aliphatic hydrocarbon group having 3 to 20 carbon atoms are replaced with a nitrogen atom, a hydrogen atom that bonds to the nitrogen atom may be replaced with an alkyl group that may have an amino group, and Rto Rare each independently a hydrogen atom or an alkyl group;'}{'sup ...

Water Treatment and Monitoring

The present invention relates to the provision of polymers that are selected to have either; surface properties that allow protozoa, in particular and to bind to the polymer; or have surface properties that are repellent to the binding of these protozoa. Methods for identifying suitable polymers are provided. Products comprising, consisting of or coated with the polymers of the present invention are also provided, as well as methods of treating or monitoring water employing polymers of the present invention. 130-. (canceled)31. A method for identifying polymers which are capable of binding to protozoa , or are poorly binding and hence may be considered as non-binding to protozoa , comprising:providing a library of polymer samples;exposing the polymer samples to a target protozoa andobserving binding or non-binding of the target protozoa species to the polymer samples.32CryptosporidiumGiardia. The method according to wherein method is for identifying a polymer which is able to bind or repel and/or .species.33. A method for the treatment or monitoring of water claim 31 , so that protozoa may be removed or isolated from a sample of water claim 31 , the method comprising contacting the sample of water with a polymer identified by the method according to .34. An article comprising claim 31 , consisting of claim 31 , consisting essentially of claim 31 , or coated with a protozoa binding polymer identified by the method according to .35. A coating for a substrate claim 31 , the coating comprising claim 31 , consisting of or consisting essentially of a protozoan binding polymer or a protozoan non-binding polymer identified by the method according to .36. The article according to wherein the binding occurs under one defined condition (e.g. at a particular pH) and the protozoa are released by changing the condition from the condition used for binding (e.g. altering the pH).37. An article claim 34 , or coating comprising claim 34 , consisting of claim 34 , or essentially ...

SPECIFIC CELL FRACTIONATING AND CAPTURING METHODS

Provided are specific cell-fractionating and -capturing methods which can fractionate and capture, respectively, specific cells (e.g., many types of cancer cells, including cancer cells not expressing EpCAM, or peripheral blood stem cells). Included is a method for fractionating specific cells present in blood or biological fluid, the method including fractionating the blood or biological fluid by centrifugation to collect the specific cells in the blood or biological fluid, the centrifugation being carried out using a container having a low protein adsorbing layer at least partially formed on the inner surface thereof. 1. A method for fractionating specific cells present in blood or biological fluid , the method comprisingfractionating the blood or biological fluid by centrifugation to collect the specific cells in the blood or biological fluid,the centrifugation being carried out using a container having a low protein adsorbing layer at least partially formed on an inner surface thereof.2. The method according to claim 1 ,wherein the method comprises collecting a fraction layer and upper and lower layers respectively above and below the fraction layer formed by the fractionation by centrifugation, andthe upper and lower layers to be collected each have a thickness that is not more than 2.0 times a thickness of the fraction layer.3. The method according to claim 1 ,wherein the method comprises collecting a fraction line or layer and upper and lower layers respectively above and below the fraction line or layer formed by the fractionation by centrifugation, andthe upper and lower layers to be collected each have a thickness of 5.0 mm or less.4. The method according to claim 1 ,wherein a separation liquid is used in the fractionation by centrifugation.5. The method according to claim 4 ,wherein the separation liquid has a density of 1.060 to 1.115 g/mL.6. The method according to claim 4 ,wherein the separation liquid has a density of 1.060 to 1.085 g/mL.7. The method ...

FUEL STABILIZER

A device for stabilizing fuel in a fuel tank comprises activated carbon. The activated carbon is configured to be inserted into or installed inside a fuel tank, so that it is in contact with the fuel. The device allows the activated carbon to be in contact with the fuel, but does not allow it to be dispersed in the fuel. A method for stabilizing fuel in a fuel tank comprises adding the device to the fuel tank so that it is in contact with the fuel. 1. A device for stabilizing fuel in a fuel tank , comprising activated carbon , wherein the activated carbon is configured to be inserted into or installed inside a fuel tank , so that it is in contact with the fuel , but is not dispersed in the fuel.2. The device of claim 1 , wherein the device comprises a container claim 1 , wherein the activated carbon is retained in the container.3. The device of claim 1 , wherein the device comprises a binder claim 1 , and the activated carbon and binder are compressed to form a solid mass.4. The device of claim 2 , wherein the container is a tube made of polyester felt claim 2 , wherein both ends of the tube are closed.5. The device of claim 4 , wherein the polyester fabric is from about 2.0 osy to about 5.0 osy in weight.6. The device of claim 4 , wherein the polyester fabric has dimensional stability between about −30° F. and about 400° F.7. The device of claim 1 , wherein the activated carbon is acid washed and has an iodine value above 1000.8. The device of claim 1 , wherein the device improves stability of gasoline by at least 250 minutes in the ASTM D525 test.9. The device of claim 1 , wherein a leash is connected to the device to allow it to be removed from the fuel tank.10. The device of claim 1 , wherein the activated carbon is doped with iodide.11. A method for stabilizing fuel in a fuel tank comprising adding a device to the fuel tank so that it is in contact with the fuel claim 1 , wherein the device comprises activated carbon claim 1 , wherein the activated carbon is ...

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

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 ...

RESIN COMPOSITION, DRY-ETCHING RESIST MASK, AND PATTERNING METHOD

Provided is a curable resin composition for a dry-etching resist, the curable resin composition containing a polymer (A) having, in a side chain, a particular structure including an aromatic group having a vinyl group. The polymer (A) includes 80 to 100 wt % of the particular structure. In addition, provided are a dry-etching resist mask obtained by curing the curable composition for a dry-etching resist, and the dry-etching resist mask having a pattern formed by a nanoimprint method. 4. The curable resin composition according to claim 1 , wherein the polymer (A) has a molecular weight of 300 to 100 claim 1 ,000.5. The curable resin composition for a dry-etching resist according to claim 1 , wherein a milliequivalent of the vinyl group per gram of the polymer (A) (meq/g) is 1.8 to 12.8 meq/g.6. The curable resin composition for a dry-etching resist according to claim 1 , the composition further comprising a polymerizable monomer (B).7. The curable resin composition for a dry-etching resist according to claim 1 , wherein the resin composition has an Ohnishi parameter of 3.2 or less claim 1 ,{'sub': C', 'O', 'C', 'O, 'the Ohnishi parameter here is represented by N/(N−N) where N is the total number of atoms, Nis the total number of carbon atoms, and Nis the total number of oxygen atoms in a solid content of the curable resin composition for a dry-etching resist.'}8. A dry-etching resist mask obtained by curing the curable resin composition for a dry-etching resist according to .9. The dry-etching resist mask according to having a pattern formed by a nanoimprint method.10. A pattern transfer method comprising:{'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'a step of pressing a mold against the curable resin composition for a dry-etching resist according to ;'}a step of providing a cured product having a pattern by curing the curable resin composition for a dry-etching resist to form the pattern; anda step of transferring the pattern to a workpiece by performing dry ...

PRESERVATIVE REMOVAL FROM EYE DROPS CONTAINING HYDROPHILIC DRUGS

A particulate plug for removing a preservative from a solution, suspension, or emulsion comprising a drug is presented. The plug comprises microparticles of a homopolymer comprising a hydrophilic repeating unit or of a copolymer comprising at least one hydrophilic repeating unit and at least one hydrophobic repeating unit. The microparticles are irregular-shaped rigid aggregates and are sized and packed to yield a hydraulic permeability greater than 0.01 Da. The homopolymers have absorbed portions of a preservative to be removed and/or a drug for delivery in solution, as can the copolymer. 128.-. (canceled)29. A preservative removing device , comprisingmicroparticles of a copolymer comprising a least one hydrophilic repeating unit and at least one hydrophobic repeating unit, wherein the microparticles are irregular-shaped rigid aggregates,wherein the microparticles form a particulate plug having a hydraulic permeability greater than 0.01 Da,wherein the plug fits an outlet of a container for a solution, emulsion, or suspension comprising a preservative and a therapeutic agent,wherein the copolymer further comprises absorbed portions of the preservative to be removed and the therapeutic agent for delivery, and wherein the particulate plug rapidly and selectively removes the preservative from the solution, emulsion, or suspension.30. The preservative removing device of claim 29 , further comprising a hydrophilic cross-linker and wherein the hydrophilic cross linker comprises diethylene glycol dimethacrylate (DEGDMA).31. The preservative removing device of claim 29 , further comprising a hydrophobic cross-linker and wherein the hydrophobic cross-linker comprises SR9035 or ethylene glycol dimethacrylate (EDGMA).32. The preservative removing device of claim 29 , wherein the hydrophilic repeating unit comprises one or more of hydroxyethyl methacrylate (HEMA) claim 29 , methacrylic acid (MAA) claim 29 , N-vinyl-pyrrolidone (NVP) claim 29 , or dimethylacrylamide (DMA).33. ...

METHOD FOR PREPARING MONOLITHIC COATED SURFACES

A carrier for adsorption a compound, comprising a support; and a shrink-fitted monolithic body attached to and surrounding at least a portion of the support. The monolithic body can be porous and configured to bind compounds in a solution either for the isolation or depletion of the compounds from the solution. 1. A carrier for adsorption a compound , comprising:a support; anda shrink-fitted monolithic body attached to and surrounding at least a portion of the support.2. The carrier of wherein the shrink-fitted monolithic body is porous.3. The carrier of wherein the support is a rod.4. The carrier of wherein the support is a magnet or polymer coated magnet.5. The carrier of wherein the shrink-fitted monolithic body has an average thickness of not less than about 0.5 millimeters.6. The carrier of wherein the shrink-fitted monolithic body has an average thickness of not less than about 0.75 mm.7. The carrier of wherein the shrink-fitted monolithic body has an average thickness of not less than about 1.0 millimeters.8. The carrier of wherein the shrink-fitted monolithic body has an average thickness of not greater than about 100 millimeters.9. The carrier of wherein the shrink-fitted monolithic body is polymerized divinylbenzene.10. The carrier of wherein the at least a portion of the support is partially flattened.11. A system for testing a sample for the presence of a compound claim 1 , comprising: a support; and', 'a shrink-fitted monolithic body attached to and surrounding at least a portion of the support; and, 'a carrier includinga container including a cavity for holding a sample, wherein the shrink-fitted monolithic body sized to fit within the cavity and to be in contact with the sample.12. The system of wherein the support is a rod.13. The system of wherein the support is a magnet or polymer coated magnet.14. The system of wherein the shrink-fitted monolithic body has an average thickness of not less than about 0.5 millimeters.15. (canceled)16. (canceled)17. ...

Ion absorption/desorption device and a method thereof as well as a ph adjustor

The present invention provides an ion absorption/desorption device and a corresponding method. The ion absorption device may comprise: an electrode pair ( 12, 14 ), at least one electrode of the electrode pair ( 12, 14 ) being covered by ions-permeable gel ( 16 a ) with functional groups, the gel ( 16 a ) absorbing ions in a liquid ( 26 a ) when a voltage is applied on the electrode pair ( 12, 14 ). Covering the electrode with ions-permeable gel with functional groups may facilitate chelation of the cations and/or anions in the liquid with the functional groups in the gel, thereby, immobilizing these ions in the gel so as to improve absorption efficiency.

COMPONENT ADDITION POLYMERIZATION

Provided is a collection of polymeric beads, wherein the beads comprise 1. A collection of polymeric beads , wherein the beads comprise(i) 75 to 99% by weight, based on the weight of the bead, polymerized units of monofunctional vinyl monomer, and wherein, within each bead, the average concentration of moles of polymerized units of multifunctional vinyl monomer per cubic micrometer is MVAV;', 'wherein, within each bead, T1000 is a sequence of 1,000 unique connected polymerized monomer units;', 'wherein, within each T1000, MVSEQ is the weight percent polymerized units of multifunctional vinyl monomer, based on the weight of T1000;', 'wherein MVRATIO=MVSEQ/MVAV;', 'and', 'wherein 90% or more of the beads by volume are uniform beads, wherein a uniform bead is a bead in which 90% or more of all T1000 sequences has MVRATIO of 1.5 or less., '(ii) 1 to 25% by weight, based on the weight of the bead, polymerized units of multifunctional vinyl monomer;'}2. The collection of polymeric beads of claim 1 , wherein claim 1 , in 90% or more of the beads by volume claim 1 , 90% or more of all T1000 sequences has MVRATIO of 1.25 or less.3. The collection of polymeric beads of claim 1 , wherein the monofunctional monomer comprises styrene.4. The collection of polymeric beads of claim 1 , wherein the multifunctional monomer comprises divinylbenzene.5. The collection of polymeric beads of claim 1 , wherein 35% or less of the T1000 sequences have MVRATIO of 0.5 or less. A useful method of producing polymeric beads is suspension polymerization, which is a process in which monomer droplets are suspended in an aqueous medium and then the monomer in the droplets is polymerized to form polymeric beads. When a mixture of monomers is present in the monomer droplet, it is known that the monomers usually react at different rates, thus forming an inhomogeneous polymeric bead. For example, it is contemplated that one or more regions within the droplet may form copolymer that has a proportion of ...

RELEASE RESISTANT MOISTURE ABSORBENT FOR AUTOMOBILE LAMP, AND MOISTURE ABSORBENT PRODUCT COMPRISING THE SAME

Provided are a release resistant moisture absorbent being environment-friendly and having excellent moisture absorbency and release resistance, and a moisture absorbent product comprising the same. The release resistant moisture absorbent of the present invention has an excellent moisture absorption rate, and also excellent release resistance in a high temperature and low humidity condition which is a driving environment of an automobile lamp, and thus, may be usefully used for an automobile lamp. 1. A release resistant moisture absorbent comprising:(A) a moisture absorbent material comprising at least one selected from the group consisting of magnesium chloride, calcium chloride, and sodium carbonate;(B) a curable inorganic material comprising at least one selected from the group consisting of calcium oxide, magnesium oxide having a particle size of 20 to 80 mesh, and magnesium oxide having a particle size of 200 to 500 mesh; and(C) an additive comprising at least one polymer wax selected from the group consisting of polyethylene wax, polypropylene wax, polyamide wax, carnauba wax, paraffin wax, and polytetrafluoroethylene wax.2. The release resistant moisture absorbent of claim 1 , wherein 10 wt % to 40 wt % of (A) the moisture absorbent material; 10 wt % to 60 wt % of (B) the curable inorganic material; and 3 wt % to 70 wt % of (C) the additive are comprised.3. The release resistant moisture absorbent of claim 1 , wherein the release resistant moisture absorbent is for an automobile lamp.4. The release resistant moisture absorbent of claim 1 , wherein (C) the additive further comprises at least one material selected from the group consisting of a low-density polyethylene resin and metal stearate.5. The release resistant moisture absorbent of claim 4 , wherein the low-density polyethylene resin has a melt index according to ASTM D1238 of 5 to 30 g/10 min.6. The release resistant moisture absorbent of claim 4 , wherein the metal stearate is at least one selected ...

METHOD AND DEVICE FOR MANUFACTURING ABSORBENT MATERIAL

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 ...

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

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 ...

一种高效大孔吸附树脂的制备方法

本发明涉及一种高效大孔吸附树脂的制备方法。采用的技术方案是，取一定量的分散剂溶于少量的去离子水中，加热至50～60℃，搅拌溶解，然后依次加入单体、交联剂、偶氮二异丁腈、助分散剂和致孔剂，升温至80℃开始反应，在80℃～95℃反应4～8h，得吸附树脂；将得到的吸附树脂放入加热装置中，加入适量的NaOH溶液，水浴加热搅拌，升温至80～120℃，反应3～5h，反应结束后，过滤，微球用盐酸浸泡4～5小时，得到目标产物。本发明制备的目标产物粒径在50～200微米之间，刚性强，纯化分离效果好。

一种锂离子印迹交联壳聚糖多孔微球的制备方法

本发明公开了一种锂离子印迹交联壳聚糖多孔微球的制备方法，该方法包括：以乙酸和壳聚糖粉末形成的水溶胶为分散相，氢氧化钠溶液为连续相，经过物理交联形成壳聚糖凝胶珠；以壳聚糖凝胶珠为载体，锂离子作为模板离子，以对叔丁基苯酚为功能单体进行接枝改性，以环氧氯丙烷为交联剂，通过盐酸洗脱锂离子，制备锂离子印迹交联壳聚糖多孔微球。本发明制备的多孔微球对锂离子具有较高的吸附能力和识别能力，且吸附再生性能良好，操作简单易行。

Dendritic polymer functionalized magnetic mesoporous solid for adsorption of metallic ions and method for preparation thereof

본 발명은 (S1) 페라이트 전구체와 다이아민(di-amine)을 반응시켜, 표면에 아미노기(-NH 2 )가 형성된 메조기공성(mesoporous) 페라이트 집합체를 제조하는 단계; 및 (S2) 상기 메조기공성 페라이트 집합체 표면의 아미노기와 덴드리틱 고분자의 단량체를 반응시켜 상기 메조기공성 페라이트 집합체 표면에 덴드리틱 고분자를 중합시키는 단계를 포함하는 덴드리틱 고분자가 표면에 중합된 자성 메조기공체의 제조방법, 메조기공성 페라이트 집합체 표면에 형성된 아미노기에 덴드리틱 고분자가 결합된 덴드리틱 고분자가 표면에 중합된 자성 메조기공체, 및 이를 이용한 금속성 이온 흡착 방법에 관한 것이다. 본 발명에 따르면, 저비용으로 단시간 내에 금속성 이온 흡수용 조성물을 제조할 수 있으며, 자기력 하에서 용이하게 수중 중금속을 제거할 수 있을 뿐만 아니라, 덴드리틱 고분자가 표면에 중합된 자성 메조기공체의 재사용이 가능하므로, 수중 중금속 포집 등 수중 유해물질 제거기술 등으로 유용하게 활용할 수 있을 것으로 기대된다. The present invention provides a method for preparing a mesoporous ferrite aggregate in which an amino group (-NH 2 ) is formed on a surface by reacting a (S1) ferrite precursor with a di-amine; And (S2) polymerizing a dendritic polymer on the surface of the mesoporous ferrite aggregate by reacting an amino group with a monomer of a dendritic polymer on the surface of the mesoporous ferrite aggregate. The present invention relates to a method for producing a magnetic mesoporous body, a magnetic mesoporous body in which a dendritic polymer in which an amino group is bonded to an amino group formed on the surface of a mesoporous ferrite aggregate is polymerized on a surface thereof, and a method for adsorbing metallic ions using the same. . According to the present invention, it is possible to prepare a composition for absorbing metallic ions in a short time at a low cost, not only can easily remove heavy metals in water under magnetic force, but also reuse of magnetic mesopores polymerized on the surface of the dendritic polymer Since it is possible, it is expected that it can be usefully used as a technology for removing harmful substances in water such as the collection of heavy metals in water.

一种可再生的纳米碳材料涂覆纤维吸附剂及其制备方法

本发明公开一种可再生的纳米碳材料涂覆纤维吸附剂及其制备方法。本发明材料包括聚多巴胺类表面接枝的纤维基层和纳米碳材料层，其中纳米碳材料层为氧化石墨烯或酸化碳纳米管的一种或两种的混合物。纳米碳材料涂覆纤维在经过10次的吸附‑解吸附处理后，吸附量仍达到原来的80％。本发明在纤维表面形成多巴胺类物质表面接枝层，该表面接枝层使得纤维表面含有氨基，利用氨基在酸性条件下带正电荷这一原理实现其与含有负电荷的纳米碳材料的电荷吸附，最终得到纳米碳材料涂覆纤维，该纤维具有良好的吸附染料废水的能力。

The manufacture method of water absorbency resin composition

本发明提供一种制造方法，其为包含吸水性树脂粒子和添加剂粒子的吸水性树脂组合物的制造方法，所述制造方法能够得到在维持优异的吸水特性的基础上、耐吸湿粘连性等添加剂粒子所具有的附加功能得到充分发挥的吸水性树脂组合物。吸水性树脂组合物的制造方法包括树脂粒子制备工序(s1)和混合工序(s2)。在混合工序(s2)中，使用多个混合装置以多阶段将在树脂粒子制备工序(s1)中制备的吸水性树脂粒子和添加剂粒子进行混合，得到吸水性树脂组合物。

一种载mof树脂复合吸附剂及其制备方法和应用

本发明公开了一种载MOF树脂复合吸附剂及其制备方法和应用。本发明所述复合吸附剂包括树脂以及MOF颗粒；所述树脂为含有氨基基团的树脂，所述MOF颗粒通过配体与吸附树脂结合。本发明采用MOF原位生成法，在水溶液中加入有机配体及大孔树脂得到固定有机配体的树脂材料，滤出后与金属盐化合物加入到水中，得到载MOF树脂复合吸附剂。本发明将树脂本身的离子交换和吸附性能同负载在树脂孔道内的MOF材料结合在一起，具有稳定性高、低浓度除磷效果好、不受干扰离子影响和易于从水体中分离等优点，并能有效地重复使用。

Method for preparing cobalt (II) ion imprinting composite membrane by using N-pyrrolidinylacrylamide

本发明公开一种用N‑吡咯烷基丙烯酰胺制备钴(II)离子印迹复合膜的方法，属于膜材料科学技术领域。该方法将金属离子印迹技术和膜分离技术相结合，无需研磨或过筛等复杂操作，可对特异性识别位点进行保护。克服了现行钴离子印迹聚合物制备过程繁琐，洗脱时间长等缺点。本发明所述方法基于金属离子与含N、O等杂原子的化合物之间能产生较好螯合作用的原理，以N‑吡咯烷基丙烯酰胺为功能单体，钴(II)为模板离子，商品膜为载体，制备得到的钴(II)离子印迹复合膜Co(II)‑MICM具有性能稳定，吸附量大等特点。

Separation of porphyrin and resin adsorbent therefor

(57)【要約】本公報は電子出願前の出願データであるた め要約のデータは記録されません。

Water-absorbent resin composition production method

본 발명은 흡수성 수지 입자와 첨가제 입자를 포함하는 흡수성 수지 조성물의 제조 방법에 있어서, 우수한 흡수성이 유지되면서 내흡습블로킹성 등의 첨가제 입자가 갖는 부가 기능이 충분히 발휘된 흡수성 수지 조성물을 얻을 수 있는 제조 방법이다. 흡수성 수지 조성물의 제조 방법은 수지 입자 조제 공정(s1)과 혼합 공정(s2)을 포함한다. 혼합 공정(s2)에서는 수지 입자 조제 공정(s1)에 있어서 조제된 흡수성 수지 입자와 첨가제 입자를 복수의 혼합 장치를 이용하여 다단계로 혼합하여 흡수성 수지 조성물을 얻는다.

High-molecular modified adsorbent and preparation method and application thereof

本发明公开了一种高分子改性吸附剂的制备方法，步骤为：(1)将钙盐、铝盐和镧盐溶于去离子水中，形成混合盐溶液；(2)将聚乙烯亚胺水溶液添加到混合盐溶液中，形成亚胺盐混合溶液，将Na 2 CO 3 溶液滴加到亚胺盐混合溶液内，直到混合溶液pH值稳定在8～9，获得中间反应溶液；(3)保持对中间反应溶液的搅拌，对中间反应液进行陈化，然后过滤，收集沉淀物；(4)对沉淀物进行洗涤、干燥和研磨后，制得。本申请还公开了采用上述制备方法所生产的高分子改性吸附剂及其用途。采用本申请所制作的吸附剂具有吸附速度快，吸附容量大、可循环使用等特点。

A kind of water treatment absorbent based on coal gasification lime-ash and preparation method thereof

本发明一种基于煤气化灰渣的水处理吸附剂及其制备方法，实施简便，成本低廉，实现对煤气化灰渣的综合利用，达到工程应用的标准，提高煤炭资源的综合利用效率。所述方法包括如下步骤，步骤1，将煤气化灰渣与浓度为0.1‑0.5％的聚丙烯酰胺溶液混合搅拌均匀得到混合物；聚丙烯酰胺溶液与煤气化灰渣的混合比例按每10ml聚丙烯酰胺溶液混合煤气化灰渣100‑10000克；步骤2，在混合物中加入浓度为30％‑60％聚四氟乙烯乳液，继续搅拌，掺入适量的水，使混合物成浆状的料浆；聚四氟乙烯乳液与聚丙烯酰胺溶液的体积比为3：1至1：3；步骤3，将料浆通过挤压剪切成型，再烘干后得到呈切块状的基于煤气化灰渣的水处理吸附剂。

Multiple organic decoration magnetic composite and preparation method thereof and application in the treatment of waste water

本发明公开了一种多重有机修饰磁性复合物，其由修饰有氨基的磁性材料再次进行氨基和羧基的增强修饰制得，所述修饰有氨基的磁性材料优选为修饰氨基的磁性Fe 3 O 4 ，具体方法为采用硅烷偶联剂在磁性Fe 3 O 4 表面接枝氨基，得到氨基修饰的磁性Fe 3 O 4 ，再利用丙烯酰胺和丙烯酸在修饰有氨基的磁性颗粒表面自组装聚合为聚丙烯酰胺和聚丙烯酸，从而制得多重有机修饰磁性复合物。本发明采用的制备材料易得，过程简单，易于磁分离，对单一和混合重金属离子的吸附容量高，且再生回收率高，在废水重金属去除领域中应用前景广阔。

Oil-water separation material with antifouling, sterilizing and dye adsorbing functions and preparation method thereof

本发明公开了一种具有防污杀菌和染料吸附功能的油水分离材料及其制备方法。是采用浸涂法，将基体材料浸渍于一种共聚物水溶液中，超声分散一定时间后取出，自然晾干、洗涤、二次干燥，即得具有防污杀菌和染料吸附功能的油水分离材料。本发明所述的油水分离材料制备方法简单，绿色环保，同时具备防污杀菌、染料吸附和油水分离等多种功能，可用于油水混合物分离和含染料油污水处理等领域。

The preparation method of adsorbent of precious metals

본 발명은 귀금속 흡착제로 사용가능한 폴리메틸렌 모노설파이드((-CH 2 S) n )의 제조방법에 관한 것으로, 황화나트륨, 포름알데히드 및 물을 1:6:40의 몰비로 반응시키는 것을 특징으로 한다. The present invention relates to a method for preparing polymethylene monosulfide ((-CH 2 S) n ) usable as a noble metal adsorbent, characterized in that sodium sulfide, formaldehyde and water are reacted in a molar ratio of 1: 6: 40. . 귀금속, 흡착제 Precious Metals, Adsorbents

A kind of modified polyacrylonitrile and preparation method thereof handling stibium-containing wastewater

本发明公开了一种处理含锑废水的改性聚丙烯腈及其制备方法，涉及吸附剂领域，包括以下步骤：S1)将聚丙烯腈基材浸入盐酸羟胺水溶液，加入无水碳酸钠搅拌；S2)待无水碳酸钠完全溶解，水浴加热步骤S1)中的混合溶液开始反应，将所述聚丙烯腈基材原位偕胺肟化；S3)步骤S2)的反应进行4～12小时，将产物取出用去离子水浸泡洗涤，之后将洗涤后的产物置于烘箱干燥，再将干燥后的产物真空脱水；S4)研磨步骤S3)所得到的产物。本发明所制备的改性聚丙烯腈颗粒吸附剂具有如下优点：原料可来源于废弃的PAN纤维丝和碎布；制备方法简单且工艺温和；对锑的吸附能力强，最大吸附量大；解吸附效果好，可多次回收利用。

Lead-cadmium ion double-template magnetic molecularly imprinted polymer and preparation method thereof

本发明提供一种铅镉离子双模板磁性分子印迹聚合物及其制备方法，以Pb 2+ 、Cd 2+ 为双模板、木瓜蛋白酶作为功能单体、碳二亚胺作为脱水剂和偶联剂制备了一种磁性分子印迹聚合物。所述磁性分子印迹聚合物可以高吸附量地、高选择性地同时吸附Pb 2+ 、Cd 2+ 两种重金属离子，更具有应用的广泛性，在生物样品、环境样品、食品中、农产品的Pb 2+ 、Cd 2+ 快速磁分离、富集和分析中有广泛的应用前景。

Magnetic mesoporous carbon of Polyaniline-modified and its preparation method and application

本发明公开了一种聚苯胺修饰的磁性介孔碳及其制备方法和应用，其中聚苯胺修饰的磁性介孔碳通过苯胺的氧化聚合作用使聚苯胺吸附在磁性介孔硅的表面，磁性介孔硅包括介孔碳和磁性复合物。其制备方法具体包括以下步骤：将苯胺加入到盐酸中，通过机械搅拌缓慢地加入磁性介孔碳得到磁性介孔碳复合物；将磁性介孔碳复合物加入到过硫酸铵与苯胺的混合溶液中，在冰浴的条件下持续搅拌10～12 h得到聚苯胺修饰的磁性介孔碳。该聚苯胺修饰的磁性介孔碳可用于吸附溶液中重金属离子，吸附完成后可用磁铁分离。本发明的聚苯胺修饰的磁性介孔碳制备工艺简单，吸附剂磁性能稳定，具有环保、吸附容量大、平衡时间短且适用范围广等优点。

Magnetic polymer microsphere, preparation method thereof and dye adsorbent

本申请提供一种磁性聚合物微球，所述磁性聚合物微球包括多孔树脂微球、分散于所述多孔树脂微球的内部的磁性粒子以及吸附在所述多孔树脂微球表面的重氮树脂，所述多孔树脂微球与所述重氮树脂通过‑SO 3 ‑相连，所述重氮树脂中具有氨基或者亚氨基。

Method of red mud attregation for removing contaminants

A red mud-aggregating method for release of pollutants is provided to mix the red mud seawater-neutralization-processed at a constant rate with an anionic organic polymer, to measure an organic polymer adsorption capacity and an appropriate concentration(CMC) of the red mud, to have a property that the red mud is easily precipitated and to be utilized as environment materials. A red mud in which an alkaline is neutralization-processed by utilizing the seawater is mixed with an organic polymer solution at a constant rate. An appropriate concentration(CMC) of an organic polymer is determined by observing a turbidity degree of the mixed red mud organic polymer. A solution of the red mud organic polymer is collected and a concentration of the organic polymer remaining in the solution is measured. A maximum adsorption quantity of the organic polymer of the red mud is calculated by using a Langmuir equation. A sedimentation degree is grasped in the water by comparing the red mud organic polymer with the seawater-neutralization-processed red mud.

A kind of preparation method of polystyrene microsphere fiber type element base weight metal absorbent

本发明公开了一种聚苯乙烯微球型纤维素基重金属吸附剂的制备方法，该方法以纤维素为骨架，先对纤维素材料进行丝光化超声活化处理，在活化剂作用下与酸酐发生酯化改性，再与多胺类物质进行胺化改性，所得纤维素改性产物再通过乳液聚合方法与苯乙烯生产杂化微球。本发明方法通过采用多胺类物质的高零点电位的强正电性和大量胺基对金属离子的吸附性能，改善了重金属吸附剂的pH适应性，酸酐的离子交换机制提高了吸附剂的吸附效率和吸附能力，苯乙烯杂化微粒的优异物理性能改善了纤维素基吸附剂的物理强度，再生利用饱和氯化盐再生溶液很好的保护了纤维素结构和吸附活性位点，提高了再生吸附能力。

Preparation method of hydrogel microspheres capable of adsorbing dye ions

本发明公开了一种吸附染料离子的水凝胶微球的制备方法。所述微球包含聚乙烯醇（PVA）、单宁酸（TA）、海藻酸钠（SA）。该微球制备步骤如下：先将聚乙烯醇和海藻酸钠完全混合溶解在水中，再加入一定量的单宁酸使其反应并混合均匀，最后用注射器将混合液滴入氯化钙‑硼酸饱和溶液中制成水凝胶微球。本发明制备的水凝胶微球稳定性好，不会发生团聚现象，制备工艺简单、操作性强、重复性好、成本低廉、性能稳定，可循环利用并无二次污染，在染料污水处理领域中得到广泛应用。

Biodegradable sorbent for collecting oil and oil products and a method for production thereof

FIELD: ecology.SUBSTANCE: invention relates to cleaning of environment. Disclosed is a biodegradable sorbent material for collecting oil and oil products, which is a nonwoven polymer fibrous web made of one or more layers of biopolymer fibers: polyhydroxybutyrate, polylactide or mixtures thereof, obtained by electrostatic molding on a substrate. Diameter of monofibres is 0.5–5 mcm, thickness of one layer of fibers is from 10 to 300 mcm and bulk density of web is 0.12–0.22 g/cm. Method of producing the material is also disclosed. Proposed material has high efficiency – oil absorption within 14–48 g/g. Material undergoes complete biodecomposition for 2–6 months.EFFECT: disclosed is a biodegradable sorbent material for collecting oil and oil products and a method for production thereof.8 cl, 1 tbl, 8 ex РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2 714 079 C1 (51) МПК B01J 20/26 (2006.01) B01J 20/30 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ОПИСАНИЕ ИЗОБРЕТЕНИЯ К ПАТЕНТУ (52) СПК B01J 20/26 (2019.08); B01J 20/30 (2019.08) (21)(22) Заявка: 2019109658, 02.04.2019 (24) Дата начала отсчета срока действия патента: Дата регистрации: 11.02.2020 (45) Опубликовано: 11.02.2020 Бюл. № 5 2 7 1 4 0 7 9 R U (56) Список документов, цитированных в отчете о поиске: Haitao Zhu et al., Evaluation of Electrospun Polyvinyl Cloride/Polystyrene Fibers as Sorbent Materials for Oil Spill Cleanup, Environmental Sci. & Technology, 2011, v. 45, 10, p. 4527-45-31. RU 113675 U1, 27.02.2012. RU 2311228 С1, 27.11.2007. RU 2366487 С1, 10.09.2009. RU 2681319 С1, 06.03.2019. RU 2543377 С2, 27.02.2015. Т.А. Байбурдов, С.Л. (см. прод.) (54) Биодеградируемый сорбирующий материал для сбора нефти и нефтепродуктов и способ его получения (57) Реферат: Изобретение относится к области очистки Диаметр моноволокон составляет 0,5-5 мкм, окружающей среды. Предложен толщина одного слоя волокон составляет от 10 биодеградируемый сорбирующий материал для до 300 мкм и объемная плотность полотна сбора ...

Waterborne polyurethane/hydroxyapatite/textile sorbent for heavy metal ions and a method for manufacturing the same

The present invention relates to a mixed absorbent of water-dispersed polyurethane/hydroxyapatite/textile and a manufacturing method thereof, wherein the mixed absorbent can effectively absorb and remove industrial waste water or heavy metals in foods, by impregnating a woven fabric or a nonwoven fabric in a mixed solution including water-dispersed polyurethane and hydroxyapatite.

A kind of responsive to temperature type chelating absorption resin and preparation method thereof and the method for handling waste water using it

本发明公开一种温度敏感型螯合吸附树脂及其制备方法和利用其处理废水的方法。包括如下步骤：1)将含有悬挂双键的多孔白球与溶胀剂、温度敏感型单体、类多巴胺单体、引发剂混合并溶胀；2)步骤1)所述混合体系在惰性气体环境中加热，引发温度敏感型单体、类多巴胺单体与含有悬挂双键的多孔白球中的双键聚合，同时类多巴胺单体在引发剂作用下自交联形成聚多巴胺，得到温度敏感型螯合吸附树脂。本发明的树脂特别适用于处理同时含有重金属离子和高毒性、难生物降解的萘类物质的印染废水。对废水中的重金属离子和萘类物质的吸附、回收，处理后的废水达标排，为含有重金属离子和萘类物质的工业废水零排放提供了一种可行的解决方案。

Novel low-density lipoprotein adsorption medium

本发明公开了一种新型低密度脂蛋白吸附介质。所述介质由大孔树脂、吸附性基团和选择性基团组成。其中大孔树脂是聚苯乙烯‑二乙烯苯、葡聚糖、纤维素和聚乙烯醇中的一种或几种；吸附性基团为磺酸基团；选择性基团选自亮氨酸、异亮氨酸、缬氨酸和甲硫氨酸中的一种、几种，或者由这四种氨基酸任意组成的二肽或三肽。本发明中的吸附介质可以有效选择性吸附人血浆中的低密度脂蛋白，可以用来制造用于去除人体LDL的设备或仪器。

Gas-liquid device

본 발명은 기액장치에 관한 것으로, 본 발명에 따른 기액장치(100)는 하우징(110), 하우징(110)의 내부에 구비된 회전축(120), 상단에서 하단으로 갈수록 직경이 감소하는 관형으로 형성되고, 하단이 회전축(120)에 설치되어, 회전축(120)을 중심으로 회전하는 회전 콘(130), 회전 콘(130)의 외주면 상단으로부터 하측으로 연장되고, 상단에서 하단으로 갈수록 폭이 증가하는 핀(140), 및 회전 콘(130)과 이격되도록 하우징(110)에 고정되고, 상단에서 하단으로 갈수록 직경이 감소하는 관형으로 형성된 고정 콘(150)을 포함한다. [0001] The present invention relates to a gas-liquid supply apparatus, and a gas-liquid supply apparatus according to the present invention comprises a housing 110, a rotation shaft 120 provided inside the housing 110, a tubular shape whose diameter decreases from the upper end to the lower end, The rotating cone 130 rotates around the rotating shaft 120. The rotating cone 130 extends downward from the upper end of the outer circumferential surface of the rotating cone 130 and increases in width from the upper end to the lower end. A pin 140 and a fixed cone 150 fixed to the housing 110 so as to be spaced apart from the rotary cone 130 and formed in a tubular shape whose diameter decreases from the upper end to the lower end.

Adsorbent for removing heavy metals and application thereof

本发明关于去除重金属离子领域，特别是关于一种用于去除重金属的吸附剂及其应用，包括：二硫代羧化聚丙烯酰胺、酵母菌表面活性剂、柠檬酸铁；以干物质计，所述吸附剂中的二硫代羧化聚丙烯酰胺、酵母菌表面活性剂与柠檬酸铁的质量比是100:1.5～2.0:5～10。所述吸附剂具有二硫代羧化聚丙烯酰胺吸附酵母菌表面活性剂和柠檬酸铁形成的三元结构，对流体中的重金属离子如Cd(Ⅱ)、Cu(Ⅱ)、Gr(Ⅵ)、Ni(Ⅱ)与As(Ⅴ)等的吸附去除率均可达95％以上，而且具有良好的再吸附性能，延长吸附剂的使用寿命。

Magnetic sorbent for oil and oil products collection

Изобретение может быть использовано для удаления нефти, масел и нефтепродуктов с поверхности воды и поверхностного слоя почвы или грунта. Сорбент выполнен гранулированным. Диаметр гранул составляет 1-3 мм. В состав сорбента входят магнитный наполнитель в виде металлического порошка из оксидов Fe 3 O 4 с размером частиц 5-10 мкм, в количестве 8-12%, низинный торф в количестве 75-80% и атактический полипропилен в количестве 8-17%. Низинный торф предварительно перед смешиванием высушен при температурах 105, 120 и 150°С в течение двух, одного и получаса соответственно. Сорбент обладает магнитными свойствами, высокой поглощающей способностью и плавучестью. 1 з.п. ф-лы, 2 табл., 3 пр. РОССИЙСКАЯ ФЕДЕРАЦИЯ (19) RU (11) (13) 2 646 084 C1 (51) МПК B01J 20/24 (2006.01) B01J 20/26 (2006.01) B01J 20/06 (2006.01) ФЕДЕРАЛЬНАЯ СЛУЖБА ПО ИНТЕЛЛЕКТУАЛЬНОЙ СОБСТВЕННОСТИ (12) ОПИСАНИЕ ИЗОБРЕТЕНИЯ К ПАТЕНТУ (52) СПК B01J 20/0229 (2006.01); B01J 20/24 (2006.01); B01J 20/261 (2006.01) (21)(22) Заявка: 2016145018, 16.11.2016 (24) Дата начала отсчета срока действия патента: Дата регистрации: 01.03.2018 (45) Опубликовано: 01.03.2018 Бюл. № 7 (73) Патентообладатель(и): Федеральное государственное бюджетное образовательное учреждение высшего образования "Томский государственный архитектурно-строительный университет" (ТГАСУ) (RU) Адрес для переписки: 634003, г. Томск, 3, пл. Соляная, 2, ТГАСУ, патентный отдел 2 6 4 6 0 8 4 C 1 (56) Список документов, цитированных в отчете о поиске: RU 2462303 C2, 27.09.2012. RU 2054315 C1, 20.02.1996. RU 2061541 C1, 10.06.1996. RU 2116128 C1, 27.07.1998. RU 2552449 C1, 10.06.2015. (54) Магнитный сорбент для сбора нефти, масел и нефтепродуктов (57) Реферат: Изобретение может быть использовано для низинный торф в количестве 75-80% и удаления нефти, масел и нефтепродуктов с атактический полипропилен в количестве 8-17%. поверхности воды и поверхностного слоя почвы Низинный торф предварительно перед или грунта. Сорбент выполнен гранулированным. смешиванием высушен ...

Silver ion adsorption material and preparation method and application thereof

本发明提供了一种银离子吸附材料的制备方法，先在氮气或惰性气体保护的条件下，将罗丹宁衍生物单体、N,N'‑亚甲基双丙烯酰胺、热引发剂和极性有机溶剂混合，得到原料混合物；所述罗丹宁衍生物单体为3‑烯丙基罗丹宁或3‑丁烯基罗丹宁；然后，维持氮气或惰性气体保护的氛围，进行热聚合反应，得到银离子吸附材料。本发明提供的制备方法所得银离子吸附材料可用于处理pH值为0.18的强酸性废水，且在银离子初始浓度为420mg/L时，银离子吸附材料的吸附容量可达389.4mg/g，即在强酸条件下，仍然保持了较高的吸附性。

A kind of gradable recovery Pb2+With the preparation method of the adsorbent of 4 NP

本发明公开一种可分级回收Pb 2+ 和4‑NP的吸附剂的制备方法，其制备方法在于：将N‑异丙基丙烯酰胺和甲叉又丙烯酰胺溶于去离子水中，溶解完全后加入4‑NP，再加入过硫酸铵（APS），搅拌下加入GO，最后加入四甲基乙二胺（TEMED），室温下聚合反应完成后，再用甲醇和氨水的混合液去除作为模板的4‑NP即得。所述材料制备方法简单，成本低，操作简便，适用于大规模含Pb 2+ 和4‑NP废水的处理。

Method of adsorbing transforming growth factor ß

An adsorbent for immunosuppressive substance, which can adsorb an excessive immunosuppressive substance directly from a body fluid, can carry out extracorporeal perfusion safely and can be utilized in treatment of cancer. The excessive immunosuppressive substance may be involved in growth of cancer cells. The adsorbent for immunosuppressive substance includes a water-insoluble carrier and a hydrophilic amino group immobilized to the water-insoluble carrier. An extracorporeal perfusion column contains the adsorbent of the invention. A method for treating cancer carries out extracorporeal perfusion using the extracorporeal perfusion column. A method of adsorbing the transforming growth factor β which is combined with another protein, includes adsorbing the transforming growth factor β and protein on an adsorbent containing a water-insoluble carrier to which quaternary ammonium groups each having 3 to 18 carbon atoms per one nitrogen atom are attached, and having a specific surface area of 0.1 m 2 or more per gram.

Preparation method of efficient macroporous adsorptive resin

本发明涉及一种高效大孔吸附树脂的制备方法。采用的技术方案是，取一定量的分散剂溶于少量的去离子水中，加热至50～60℃，搅拌溶解，然后依次加入单体、交联剂、偶氮二异丁腈、助分散剂和致孔剂，升温至80℃开始反应，在80℃～95℃反应4～8h，得吸附树脂；将得到的吸附树脂放入加热装置中，加入适量的NaOH溶液，水浴加热搅拌，升温至80～120℃，反应3～5h，反应结束后，过滤，微球用盐酸浸泡4～5小时，得到目标产物。本发明制备的目标产物粒径在50～200微米之间，刚性强，纯化分离效果好。

Immunosuppressive substance adsorbent, extracorporeal circulation column and method of treating cancer

본 발명은, 체액 중에서 직접 암 세포의 증식에 관련되는 것으로 생각되는 과잉의 면역 억제 물질을 높은 효율로 선택적으로 흡착하면서, 안전하게 체외 순환할 수 있는 면역 억제 물질 흡착재를 제공하고, 나아가서는 암의 치료에 유용하게 하는 것을 목적으로 한다. The present invention provides an immunosuppressive substance adsorbent capable of safely circulating in vitro while selectively adsorbing an excess immunosuppressive substance that is thought to be directly involved in the proliferation of cancer cells in body fluids at high efficiency, and furthermore, to treat cancer. The purpose is to make it useful. 즉, 본 발명은 수불용성 담체에 친수성 아미노기를 고정하여 이루어지는 것을 특징으로 하는 면역 억제 물질 흡착재이다. That is, this invention is an immunosuppressive substance adsorption material characterized by fixing a hydrophilic amino group to a water-insoluble carrier. 또한, 본 발명은 본 발명의 흡착재를 충전한 것을 특징으로 하는 체외 순환 컬럼이다. Moreover, this invention is an extracorporeal circulating column characterized by filling the adsorption material of this invention. 또한, 본 발명은 본 발명의 체외 순환 컬럼을 이용하여 체외 순환을 행하는 것을 특징으로 하는 암의 치료 방법이다. In addition, the present invention is a method for treating cancer, wherein the extracorporeal circulation is performed using the extracorporeal circulation column of the present invention. 면역 억제 물질 흡착재, 친수성 아미노기, 체외 순환 칼럼, 암의 치료 방법 Immunosuppressant Absorbent, Hydrophilic Amino Group, In Vitro Circulation Column, Cancer Treatment Method

Method for discharging superabsorbent particles from a silo and filling them into bulk containers

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.

Water-absorbing agent, method for the production thereof and use of the same

The invention relates to a water-absorbing agent in particulate form, comprising particles of a water-absorbing polymer and between 0.1 and 4 wt. %, (relative to the particulate polymer), of a fine-particle natural fibre.

Method for coating water-absorbing polymer particles

The invention relates to a method for producing water-absorbing polymer particles, wherein in a mixer water-absorbing polymer particles are coated with a particulate solid matter, the particulate solid matter is dispersed by means of a gas flow, and the supply of the dispersed particulate solid matter ends in the mixer beneath the product bed surface.

BINDING AGENT FOR LIQUIDS

Method for coating water-absorbing polymer particles

The invention relates to a method for producing water-absorbing polymer particles, wherein in a mixer water-absorbing polymer particles are coated with a particulate solid matter, the particulate solid matter is dispersed by means of a gas flow, and the supply of the dispersed particulate solid matter ends in the mixer beneath the product bed surface.

Method for coating water-absorbing polymer particles

A process for preparing water-absorbing polymer particles by coating water-absorbing polymer particles with a particulate solid in a mixer, wherein the particulate solid is dispersed by means of a gas stream and the supply of the dispersed particulate solid in the mixer ends below the product bed surface.

Method of manufacturing water-absorbent resin composition

The invention provides a method of manufacturing a water-absorbent resin composition containing water-absorbent resin particles and additive particles, by which it is possible to obtain a water-absorbent resin composition that sufficiently exhibits additional functions, such as an anti-blocking property under moisture absorption, of the additive particles while maintaining an excellent water absorption property. A method of manufacturing a water-absorbent resin composition includes a resin particle preparation step and a mixing step. In the mixing step, water-absorbent resin particles which are prepared in the resin particle preparation step are mixed with additive particles in multiple stages by using a plurality of mixing apparatuses to obtain a water-absorbent resin composition.