Abstract: Described herein are cationic polymers having a plurality of quaternary amino groups, methods of making such polymers, and uses of such polymers as ion exchange membranes in electrochemical devices.

Abstract: A method of synthesizing polyamide microparticles may comprise: dehydrating and shearing a mixture comprising a matrix fluid, an emulsion stabilizer at about 0.01 wt % to about 50 wt % based on the weight of the matrix fluid, a solvent at about 13 wt % to about 75 wt % based on the weight of the matrix fluid, and a cyclic amide monomer at about 20 wt % to about 90 wt % based on the weight of the matrix fluid to yield an emulsion having a water content of about 1 wt % or less based on the total weight of the emulsion; adding a deprotonating agent to the emulsion at a concentration of about 0.01 wt % to about 1 wt % based on the weight of the matrix fluid; and contacting the emulsion with a polymerization initiator under conditions effective to polymerize the cyclic amide monomer into a plurality of polyamide microparticles.

Abstract: A polymeric bead having radius R wherein the polymer comprises 0.3% to 20% by weight, based on the weight of the polymer, of polymerized units of one or more multifunctional vinyl monomer and 80% to 99.7% by weight, based on the weight of the polymer, of polymerized units of one or more monofunctional vinyl monomer, (a) wherein the polymerized units of multifunctional vinyl monomer have radial distribution factor MR of 0.9 to 1.1, and (b) wherein some of the vinyl groups in the polymerized units of multivinyl monomer are unreacted, and the unreacted vinyl groups have a radial distribution factor VR of 2.5 or higher.

Abstract: Ion exchange resin macroporous beads for the highly selective extraction of univalent anions from aqueous solutions. A specific example is the removal of dicyanoaurate and dicyanoargentate from cyanide leach solutions and tailings. The beads have a maximum number of ligands specific for the desired univalent anion, while maintaining sufficient separation to minimize binding of polyvalent ions. The beads are prepared using a functionalized monomer with the use of a specifically tuned coordinator. The beads can be used as a sensor for detecting the amount of anions captured when interrogated by an appropriate light source.

Abstract: The present invention relates to an iminodiacetic acid chelating resin, wherein the water amount in the resin is from 50 to 75% and the volume ratio of Na form/H form is from 1.4 to 1.8. Furthermore, the present invention relates to a method for producing an iminodiacetic acid chelating resin, wherein an alcohol is used as a solvent for the amination reaction of a chloromethylated styrene crosslinked copolymer with iminodiacetonitrile or sodium iodide and/or potassium iodide is used as a catalyst for the amination reaction.

Abstract: An oxygen permeable polymer has the following formula: wherein RS is a non-sulfonyl halide portion of a sulfonyl halide monomer or polymer; XP is —NH or —NHCO; A is an optionally substituted alkyl; L is 0, 1 or 2; m is 2 or 3; Z is H or CH3; and n is 5-m. The polymer can be used in air separation devices, air concentrators, and in electrodes for electrochemical devices.

Abstract: The invention relates to a process for preparing aminomethylated bead polymers using condensed formaldehydes and carboxylic anhydrides.

Abstract: The present disclosed are a high exchange-capacity anion exchange resin with dual functional-groups and method of synthesis thereof. The invention relates to the field of environmental function material synthesis and application. The resin is based on chloromethylated polystyrene-divinylbenzene polymer as matrix, and by primary amination and quaternization, yields an anion exchange resin with dual functional-groups having both a weak base anionic group and a strong base anionic group. The anion exchange resin not only has high adsorption capacity for water-born nitrate ions, but also can effectively squelch natural organic acids such as phytic acid in water, thus simultaneously removing nitrate ions and phytic acid organic matter from water. Therefore, the resin has a broad application potential in the fields of drinking water treatment, groundwater remediation, and advanced urban sewage treatment.

Abstract: The invention relates to sulfonated aminomethylated chelate resins, to a method for producing same, to the use thereof for obtaining and purifying metals, in particular rare earth metals, from aqueous solutions and organic liquids, and for producing highly pure silicon.

Abstract: Disclosed herein are methods and systems for the simultaneous production of oxo-alcohols comprising n-butanol, isobutanol, and 2-ethylhexanol. Also disclosed are methods and systems for simultaneous production of plasticizers using the disclosed oxo-alcohols.

Abstract: Described herein are modified sulfonated block copolymers which comprise at least two polymer end blocks A and at least one polymer interior block B, wherein each A block contains essentially no sulfonic acid or sulfonate functional groups and each B block comprises sulfonation susceptible monomer units and, based on the number of the sulfonation susceptible monomer units, from about 10 to about 100 mol % of a functional group of formula (I) —SO2—NR1R2??(I) or of a salt thereof, methods of making them as well as methods of using them, e.g., as membrane materials for electrically or osmotically driven applications.

Abstract: Bi-metal nanoadsorbents and methods for their preparation and use are provided. Methods of using bi-metal nanoadsorbents to remove contaminants from samples, such as water, are also provided.

Abstract: Ligand functionalized substrates, methods of making ligand functionalized substrates, and methods of using functionalized substrates are disclosed.

Abstract: The invention relates to a process to produce phthalimides by heating diammonium phthalate in the presence of aromatic solvents and to a process to produce phthalimides by heating diammonium phthalate in the presence of aromatic solvents for their recycled use during the ion exchanger production process. The diammonium phthalate is prepared by making use of the phthalic add salts solution resulted from the on exchanger production process.

Abstract: The present invention relates to a process for preparing unsaturated ketone by using an ion exchange polymer as a catalyst. The process comprises the steps of mixing an aldehyde with a ketone and passing the mixture of aldehyde and ketone through a fixed bed catalytic reactor comprising the ion exchange polymer at a temperature of at least 60 degree C. at atmospheric pressure for a retention period of 30-50 min. The unsaturated ketone obtained from the reaction is purified by distillation and 99.5% pure unsaturated ketone with a yield of not less than 80% is obtained.

Abstract: Amino-containing polymeric materials and methods of making these materials are provided. More specifically, the amino-containing polymeric materials are prepared by treating a precursor polymeric material with an amine compound. The precursor polymeric materials are formed from a polymerizable composition that contains a rigid and contorted divinyl crosslinker. The amino-containing polymeric materials can be used as anion exchange resins.

Abstract: This invention relates to the field of resin, particularly to a magnetic, acrylic strongly basic anion exchange microsphere resin and its manufacturing method. Its basic structure is as follow: wherein its matrix contains magnetic grains and A is a group containing quaternary ammonium salts; the manufacturing method is: taking acrylic compounds as the monomer and mixing it with the crosslinking agent and porogenic agent to form an oil phase; evenly mixing the oil phase with magnetic grains and then conducting suspension polymerization; aminating and alkylating the polymerized magnetic grains so as to form the quaternary ammonium salts, namely the magnetic, acrylic strongly basic anion exchange microsphere resin.

Abstract: Articles that contain a solid support with a grafted chain extending from the solid support, methods of making these articles, and various uses of the articles are described. More specifically, the grafted chain has a functional group that can react with or interact with target compound. Alternatively, the functional group on the grafted chain can react with a modifying agent to provide another group that can react with or interact with the target compound. The grafted chains are attached to the solid support through a ring-opened azlactone group. The articles can be used to purify the target compound or to separate the target compound from other molecules in a sample.

Abstract: The present invention addresses a need in the art by providing a composition comprising an aqueous dispersion of a binder and porous ion exchange resin particles that are functionalized with primary amine groups or secondary amine groups or both. The composition of the present invention provides an efficient way of removing aldehydes from or in the vicinity of a coating prepared from the composition.

Abstract: A tamper-resistant dosage form including a therapeutic agent-substrate complex embedded in a thermo-formable matrix; such that the complex includes at least one therapeutic agent bound to at least one substrate to form the therapeutic agent-substrate complex. The at least one substrate is being selected from the group consisting of a polyelectrolyte, an organic counter-ion, a pharmacologically inert organic component of a prodrug, an inclusion compound and an inorganic adsorbent; and the thermo-formable matrix includes one or more thermoplastic polymers and optionally at least one pharmaceutical additive.

Abstract: A particle comprising at least one polymer having negative or positive charges and at least one antibody bound to the polymer, wherein the antibody specifically binds to a surface marker of at least one target cell, and kit comprising same.

Abstract: A composite having ion exchange function, preparation method and use thereof are provided. The composite is formed by compounding ion exchange resin with fluorine-containing polymer porous membrane, wherein the nitrile groups in the ion exchange resin react with the nitrile groups grafted on the fluorine-contained polymer porous membrane to form triazine ring crosslinked structure. The composite has excellent mechanical property and gas impermeability, high ion exchange capacity and high electroconductivity.

Abstract: The present disclosure provides a method for melt processing a sulfonated block copolymer in which the sulfonic acid or sulfonate functional groups are partially or completely neutralized by an amine, and to articles obtained by the method. Moreover, the shaped articles which are obtained by molding a composition comprising the neutralized sulfonated block copolymer may can be converted into shaped articles which comprise the sulfonated block copolymer(s) employed in the preparation of the amine neutralized block copolymer(s). The present disclosure further provides a sulfonated block copolymer comprising which is modified by an amine of formula (Ia) wherein Het together with the nitrogen to which it is bonded represents an optionally substituted 5- or 6-membered hetero cycle.

Abstract: A method for producing a protein adsorbent comprising a substrate and a molecular chain fixed on the surface of the substrate is disclosed. The method comprises, in this order: a dry-heat treatment step of heating a pretreatment adsorbent comprising the substrate and the molecular chain fixed on the surface of the substrate, in which the molecular chain contains a weak electrolytic ion-exchange group; and a wet-heat treatment step of heating the pretreatment adsorbent in a moistened state with a liquid or steam to obtain the protein adsorbent.

Abstract: The present invention discloses a 3-[3-(dimethylamino)-1-ethyl-2-methylpropyl]phenol resin complex, preferably an amorphous 3-[3-(dimethylamino)-1-ethyl-2-methylpropyl]phenol resin complex formed by the reaction between a cation exchange resin and 3-[3-(dimethylamino)-1-ethyl-2-methylpropyl]phenol or a pharmaceutically acceptable acid addition salt thereof. It can exhibit an in-vitro release rate of 3-[3-(dimethylamino)-1-ethyl-2-methylpropyl]phenol from the 3-[3-(dimethylamino)-1-ethyl-2-methylpropyl]phenol resin complex which is in accordance with the requirements of Ph. Eur. on “conventional-release dosage forms”.

Abstract: A functionalized block copolymer polymerized using vinylbenzylamino derivative monomers for use in such applications as anionic exchange membranes.

Abstract: The present invention relates to a process for producing novel ion exchange resins which are based on crosslinked bead polymers composed of acrylic compounds having thiol groups as functional group and have a high uptake capacity for heavy metals, and also their use for removing heavy metals from liquids, preferably process water in or from the electronics industry, the electroplating industry and the mining industry.

Abstract: This invention relates to a method for manufacturing a cation exchange resin, wherein the method includes the steps of: copolymerizing a monovinyl aromatic monomer and a cross-linkable aromatic monomer to obtain a cross-linked copolymer; specifying a content of a leachable compound represented by formula (I) to be 400 ?g or less relative to 1 g of the cross-linked copolymer, wherein Z represents a hydrogen atom or an alkyl group, and l represents a natural number; and then sulfonating the cross-linked copolymer to form a sulfonylated cross-linked copolymer.

Abstract: Chromatographic media of porous media particles derivatized with allylamine or polyallylamine obtained directly or through intermolecular polymerization on the surface thereof and such media functionalized with further functionalization groups. Such media are particularly useful for separating biomolecules.

Abstract: This invention relates to certain novel anion exchange resins and methods of making them. It relates more particularly to aminated cross-linked resin bead polymers containing an inert and/or chloromethylated core, and an aminated outer shell, and to methods for preparing the same. These resins exhibit improved anion exchange properties.

Abstract: Selectively amino- or phosphino-functionalized block copolymers, and their preparation, for use as anion exchange membrane materials. The selectively functionalized block copolymers have at least two end blocks A each of which are substantially free of amino- or phosphino-functional groups, and have at least one interior block D which comprises on average at least one amino- or phosphino-functionalized polymer unit of formula (I) wherein Z is nitrogen or phosphorous; R1 is hydrogen or alkyl; R2 is hydrogen or is tertiary alkyl; R each independently, is hydrogen or is alkyl optionally substituted by a moiety -(A1-NRa)xRb; or two R groups, together with the Z to which they are bonded, form an optionally substituted ring; x is 1, 2 or 3; A1 is straight chain alkylene optionally substituted by one or more methyl and/or ethyl groups; and Ra and Rb, each independently, is hydrogen or alkyl; or a corresponding onium salt.

Abstract: This invention concerns the preparation and use of novel polymeric chromatographic media and preferably mixed mode polymeric chromatographic media. In accordance with the present invention, polymeric media is prepared using polymeric particles derivatized with polyethyleneimine, and preferably such polyethyleneimine derivatized polymeric particles further functionalized with appropriate reactants. The polymeric chromatographic media is especially useful for bioseparations.

Abstract: Disclosed are methods and compositions for purifying the non-addictive alkaloid noribogaine.

Abstract: The invention relates to a method for manufacturing an anion exchange resin, wherein the method includes the step of contacting a water soluble polymer containing an anionic dissociative group with a resin to produce an anion exchange resin. In the method, an amount of contact of the water soluble polymer is 0.01 to 10 mmol/L, in terms of an amount of the anionic dissociative group, relative to 1 liter of the anion exchange resin, and a wafer surface flatness (Rms) of the anion exchange resin is 4 ? or less, determined by a silicon wafer test.

Abstract: Articles that contain a solid support with a grafted chain extending from the solid support, methods of making these articles, and various uses of the articles are described. More specifically, the grafted chain has a functional group that can react with or interact with target compound. Alternatively, the functional group on the grafted chain can react with a modifying agent to provide another group that can react with or interact with the target compound. The grafted chains are attached to the solid support through a ring-opened azlactone group. The articles can be used to purify the target compound or to separate the target compound from other molecules in a sample.

Abstract: The present invention relates to novel polyazoles, a proton-conducting polymer membrane based on these polyazoles and its use as polymer electrolyte membrane (PEM) for producing membrane-electrode units for PEM-fuel cells, and also other shaped bodies comprising such polyazoles.

Abstract: The present invention addresses a need in the art by providing a composition comprising an aqueous dispersion of a binder and porous ion exchange resin particles that are functionalized with primary amine groups or secondary amine groups or both. The composition of the present invention provides an efficient way of removing aldehydes from or in the vicinity of a coating prepared from the composition.

Abstract: A new class of membranes for use in protective clothing. More specifically, the present invention relates to a polymer-polymer membrane with an ionic polymer located within the nanopores of a porous polymer host membrane. A method for making the polymer-polymer membranes involves filling porous polymers with ionic polymers. The porous polymers may be fabricated by a template synthesis which involves sorption. The ionic polymers may be filled in the nanopores of the porous polymer by plasma-induced graft copolymerization of the ionic polymer with the porous polymeric host membrane.

Abstract: The invention relates to a modified separating material having improved properties, to the preparation thereof, and to the use thereof for the separation of charged biopolymers from liquids.

Abstract: Treatment of anion exchange materials containing hydroxyl containing moieties in the beta position relative to the quaternary center in the hydroxide form with glycidol substantially alters the selectivity of the anion exchange material. Furthermore, sequential treatments of first a hydroxide containing solution to put the anion exchange material in the hydroxide form followed by treatment with glycidol in an alternating sequence progressively changes selectivity in a predictable manner allowing facile manipulation of selectivity. Unique to the selectivities achievable with this chemistry is the ability to reverse the elution order of sulfate and carbonate. With all other known systems, carbonate elutes ahead of sulfate and sometimes compromises the ability to quantitate sulfate. With glycidol treatment, carbonate can be moved after sulfate which eliminates interference issues for samples containing significantly more carbonate than sulfate.

Abstract: Described herein is a process to prepare crosslinkable polymers based on trifluorostyrene, and their use as polymer electrolyte membranes.

Abstract: A method for treating exhaust gas, comprising first contacting exhaust gas comprising inorganic halogenated gas discharged from sources of the exhaust gas with Fe2O3 or synthetic zeolite and then contacting with an anion exchange resin having water content of 5 w/w % or less and halogen content of 10 mg/g or less.

Abstract: Articles that contain a solid support with a grafted chain extending from the solid support, methods of making these articles, and various uses of the articles are described. More specifically, the grafted chain has a functional group that can react with or interact with target compound. Alternatively, the functional group on the grafted chain can react with a modifying agent to provide another group that can react with or interact with the target compound. The grafted chains are attached to the solid support through a ring-opened azlactone group. The articles can be used to purify the target compound or to separate the target compound from other molecules in a sample.

Abstract: A polymeric compound is provided having the general formula (A) wherein R is an alkyl chain preferably having from 1 to 6 carbon atoms in the chain which may be either saturated or unsaturated and may have substituents attached to the chain, and R? and R?, which may be the same or different from each other and preferably have from 1 to 4 carbon atoms in a chain, are selected from alkyl groups, substituted or unsubstituted, or R? and R? are linked to form a saturated or unsaturated cyclic moiety incorporating the adjacent nitrogen atom, with or without additional heteroatoms in the ring. The polymeric compound is preferably in a particulate form and most particularly in the form of nanoparticles. A method of producing the polymers is disclosed. A method of adsorbing, separating and stripping the polymers is also disclosed.

Abstract: A process for the preparation of cross-linked fluorinated polymers comprising sulfonic acid functional groups comprising the steps of: a) providing at least one fluorinated polymer (P) comprising at least one —SO3M functional group and less than 2% of —SO2F functional groups with respect to the total amount of —SO3M and —SO2F functional groups, wherein each M is selected from H and alkaline metals; and b) reacting said fluorinated polymer with at least one cross-linking agent of formula R(X)n under conditions that promote the formation of covalent bonds between the at least one functional group —SO3M of fluorinated polymer (P) and at least one functional group X of the cross-linking agent.

Abstract: The invention provides a tetrazole-containing polymer of intrinsic microporosity comprising (10) or more subunits, wherein one or more of the subunits comprise one or more tetrazolyl moieties. In one embodiment, a polymer of intrinsic microporosity (PIM-1) was modified using a “click chemistry” [2+3] cycloaddition reaction with sodium azide and zinc chloride to yield new PIMs containing tetrazole units. Polymers of the present invention are useful as high-performance materials for membrane-based gas separation, materials for ion exchange resins, materials for chelating resins, materials for superabsorbents, materials for ion conductive matrixes, materials for catalyst supports or materials for nanoparticle stabilizers.

Abstract: Articles that contain a solid support with a grafted chain extending from the solid support, methods of making these articles, and various uses of the articles are described. More specifically, the grafted chain has a functional group that can react with or interact with target compound. Alternatively, the functional group on the grafted chain can react with a modifying agent to provide another group that can react with or interact with the target compound. The grafted chains are attached to the solid support through a ring-opened azlactone group. The articles can be used to purify the target compound or to separate the target compound from other molecules in a sample.

Abstract: A proton exchange material includes perfluorinated carbon backbone chains and side chains extending off of the perfluorinated carbon backbone chains. The perfluorinated side chains include cross-link chains that have multiple sulfonimide groups, —SO2—NH—SO2—.

Abstract: Materials are provided that may be useful as ionomers or polymer ionomers, including compounds including bis sulfonyl imide groups which may be highly fluorinated and may be polymers.

Abstract: A method of producing a polymeric compound having a structural unit that is decomposed and generates acid upon exposure, including reacting a first precursor polymer having a first ammonium cation with an amine whose conjugate acid has an acid dissociation constant (pKa) larger than that of the first ammonium cation to obtain a second precursor polymer having a second ammonium cation that is a conjugate acid of the amine; and performing a salt-exchange between the second precursor polymer and a sulfonium cation or an iodonium cation, in which the second ammonium cation is less hydrophobic than the first ammonium cation, and also less hydrophobic than the sulfonium cation or the iodonium cation.