Abstract: A silicone adhesive composition including an ionic silicone and useful for healthcare applications such as wound care and drug delivery.

Abstract: Anion exchange polymer electrolytes that include guanidinium functionalized polymers may be used as membranes and binders for electrocatalysts in preparation of anodes for electrochemical cells such as solid alkaline fuel cells.

Abstract: Ionomers and ionomer membranes, consisting of a non-fluorinated or partly fluorinated non-, partly or fully-aromatic main chain and a non- or partly-fluorinated side chain with ionic groups or their non-ionic precursors, have a positive impact on the proton conductivity of the ionomers. Various processes produce these polymeric proton conductors.

Abstract: Methods for producing or regenerating an iodinated anion exchange resin are presented. The methods include treating an iodide loaded anionic resin with an aqueous solution comprising an in situ formed I2 to produce the iodinated resin. The iodinated resins show reduced and stable levels of iodine elution compared to resins produced by conventional methods. Methods and systems for purifying water are also presented.

Abstract: With respect to the anionic polymer ion-exchange material used in an alkaline fuel cell, an electrodialysis apparatus, water treatment industry, catalyst industry, and the like, there are provided an anionic polymer ion-exchange material having both excellent ionic conductivity and excellent mechanical strength, as compared to the materials conventionally used, and a method for producing the same. An anionic polymer ion-exchange material having a polymer base material mainly made of an amide resin having both an aromatic structure and an aliphatic chain in the principal chain thereof, wherein the polymer base material has an anionic monomer graft-polymerized on the aliphatic chain in the principal chain of the amide resin, wherein the anionic monomer has an aromatic structure and a quaternary ammonium structure.

Abstract: The invention relates to a process for producing non-agglomerating mixed bed ion exchangers or mixed bed components.

Abstract: A method for manufacturing an anion exchange resin, in which remaining of impurities and generation of decomposition products are suppressed and leachables are reduced, the method including the following steps (1-a) to (1-e) of: (1-a) obtaining a cross-linked copolymer by copolymerizing a monovinyl aromatic monomer and a cross-linkable aromatic monomer; (1-b) specifying the content of a specific leachable compound to be 400 ?g or less relative to 1 g of the cross-linked copolymer; (1-c) haloalkylating the cross-linked copolymer so as to introduce 80 percent by mole or less of haloalkyl group relative to the monovinyl aromatic monomer; (1-d) removing a specific leachable compound from the haloalkylated cross-linked copolymer; and (1-e) subjecting the haloalkylated cross-linked copolymer to a reaction with an amine compound.

Abstract: The present invention relates to a method for improved removal of cations, preferably alkaline earth metals, in particular calcium and barium, from aqueous solutions using chelating resins having aminomethylphosphonic acid groups and iminodimethylphosphonic acid groups having high dynamic absorption capacity for cations at a low residual content of the cations and high regeneration efficiency, and a markedly lengthened loading duration of the chelating resin, to the chelating exchangers themselves, and also to uses thereof.

Abstract: An anion exchange membrane and fuel cell incorporating the anion exchange membrane are detailed in which proazaphosphatrane and azaphosphatrane cations are covalently bonded to a sulfonated fluoropolymer support along with anionic counterions. A positive charge is dispersed in the aforementioned cations which are buried in the support to reduce the cation-anion interactions and increase the mobility of hydroxide ions, for example, across the membrane. The anion exchange membrane has the ability to operate at high temperatures and in highly alkaline environments with high conductivity and low resistance.

Abstract: The present invention provides an ion-exchange resin catalyst, as a catalyst for preparing bisphenol from phenol compounds and ketone, which has a higher selectivity to bisphenol and a longer life time, as compared to a conventional ion-exchange resin, and a method for preparing the same. The present invention also provides a method for preparing bisphenol comprising reacting phenol compounds with ketone, wherein the modified acidic ion-exchange resin in which at least one kind of cationic compound selected from the following (a), (b), (c) and (d) ionically binds to an acidic functional group, is used as a catalyst: (a) a quaternary phosphonium ion, (b) a quaternary ammonium ion, (c) a bis(phosphoranylidene) ammonium ion, and (d) an N-substituted nitrogen-containing aromatic cation.

Abstract: There is provided a modified ion exchange resin catalyst which exhibits higher bisphenols selectivity than the conventional modified ion exchange resins in processes wherein bisphenols are produced by reacting a phenolic compound with ketones, and to provide such a process for producing bisphenols.

Abstract: The present invention relates to a method for improved removal of cations, preferably alkaline earth metals, in particular calcium and barium, from aqueous solutions using chelating resins having acetic acid and/or iminodiacetic acid groups having high dynamic absorption capacity for cations at a low residual content of the cations and high regeneration efficiency, to the chelating exchangers themselves, and also to uses thereof.

Abstract: A proton exchange membrane comprising modified hyper-branched polymer is disclosed. The proton exchange membrane includes 85-90 wt % of sulfonated tetrafluorethylene copolymer and 15-10 wt % of modified hyper-branched polymer. The modified hyper-branched polymer comprises the bismaleimide (BMI)-based hyper-branched polymer, and parts of the chain ends of the hyper-branched polymer are sulfonated by the sulfonic compound. Also, the modified hyper-branched polymer and sulfonated tetrafluorethylene copolymer are interpenetrated to form an interpenetrating polymer. Furthermore, the modification step could be performed before or after forming the interpenetrating polymer. For example, the sulfonation is proceeded after forming the interpenetrating polymer. Alternatively, the sulfonation of the hyper-branched polymer could be proceeded before the formation of the interpenetrating polymer.

Abstract: Oral dosage forms of benzonatate useful for anti-tussive and anti-tussive/combination applications.

Abstract: Embodiments of the invention are related to anion exchange membranes used in electrochemical metal-air cells in which the membranes function as the electrolyte material, or are used in conjunction with electrolytes such as ionic liquid electrolytes.

Abstract: A functional membrane and a production method thereof including: an ion irradiation step in which a polymer film substrate is irradiated with high energy heavy ions at 104 to 1014 ions/cm2, to generate active species in the film substrate; and a graft polymerization step in which after the ion irradiation step, the film substrate is added with one or more monomers selected from a group A consisting of monomers each having a functional group and 1 to 80 mol % of a monomer including a group B consisting of a crosslinking agent(s) for the group A monomer(s), and the film substrate and the monomer(s) are graft-polymerized. There is obtained a functional membrane having high functionality in conjunction with the gas barrier property intrinsically possessed by a polymer film substrate, in particular, a polymer electrolyte membrane optimal as a polymer electrolyte membrane for use in fuel cells, high in proton conductivity and excellent in gas barrier property.

Abstract: A modified ion exchange resin catalyst having an attached dimethyl thiazolidine promoter is disclosed. Also disclosed is a process for catalyzing condensation reactions between phenols and ketones, wherein reactants are contacted with a modified ion exchange resin catalyst having an attached dimethyl thiazolidine promoter. Also disclosed is a process for catalyzing condensation reactions between phenols and ketones that does not utilize a bulk promoter.

Abstract: The invention provides a method for producing a polymer electrolyte membrane including (A) a membrane formation step of forming a membrane-form product of an ionic group-containing polymer electrolyte on a support, (B) an acid treatment step of exchanging the ionic group into an acid type by bringing the membrane into contact with an inorganic acid-containing acidic liquid, (C) an acid removal step of removing a free acid in the acid-treated membrane, and (D) a drying step of drying the acid-removed membrane, wherein the steps (B) to (D) are carried out without separating the membrane from the support.

Abstract: A method of producing a sulfonated polyarylether block copolymer is provided. The method includes producing a sulfonated polyarylether block copolymer containing a hydrophobic segment having a structural unit represented by formula (5) and a hydrophilic segment having a structural unit having a sulfonic acid groups or derivative thereof incorporated into a structure represented by formula (6). A hydrophilic segment prepolymer having a sulfonic acid group in a potassium salt form and a hydrophobic segment prepolymer are block copolymerized. A proton conductor that includes the sulfonated polyarylether block copolymer is also provided.

Abstract: Ionomers and ionomer membranes with the ionic group on a flexible side chain have a positive impact on the proton conductivity of the ionomers. Various processes produce these polymeric proton conductors.

Abstract: The invention generally relates to amination reactions and amination reaction products, and particularly to methods for aminating vinyl aromatic polymers utilizing tertiary amines. In one embodiment, the invention includes conducting an amination reaction by combining a tertiary amine and a vinyl aromatic polymer comprising benzyl chloride groups to form a reaction mixture and maintaining the pH of the reaction mixture within a designated range. In another embodiment, the invention includes an aminated vinyl aromatic polymer. In yet another embodiment, the invention includes an ion exchange resin including quaternary ammonium functionality. The invention is useful in preparing ion exchange resins suitable for a variety of applications such as the removal of perchlorate ions from water sources and recovery of gold cyanide from mining leach solutions.

Abstract: Provided according to some embodiments of the invention are anion exchange polyelectrolytes that include an at least partially fluorinated polyaromatic polymer backbone; and at least one cationic functional group pendant therefrom. Also provided are anion exchange membranes (AEMs) formed from at least one anion exchange polyelectrolyte according to an embodiment of the invention, and fuel cells including such AEMs.

Abstract: A method of producing a scale-control resin including combining in an aqueous solution a cation-exchange resin and a weak-acid anion mineral or salt having a multivalent cation to allow ion exchange between the resin and the multivalent cation. The cation-exchange resin may a weak-acid ion exchange resin. The method may further include adding a strong-acid salt having the same multivalent cation as the weak-acid anion mineral or salt to the aqueous solution.

Abstract: There are provided ligand compositions and stationary phases comprising a polyhedral oligomeric silsequioxane moiety. Also provided are chromatographic devices comprising the stationary phases, and methods of making and using the ligands, stationary phases and chromatographic devices of the invention.

Abstract: The present invention aims at providing an optimal constitution and production method for an OH-type anion-exchange hydrocarbon-based elastomer used when manufacturing a catalyst electrode layer of a solid polymer type fuel cell, in view of a balance of stability, durability and flexibility. Also, the present invention aims to provide an ion-conductivity imparting agent comprising the OH-type anion-exchange hydrocarbon-based elastomer, wherein the elastomer is uniformly dissolved or dispersed and has appropriate viscosity even with a high concentration. The anion-exchange hydrocarbon-based elastomer of the present invention has an iodine value of 3 to 25, contains an anion-exchange group having OH?, CO32? and/or HCO3? as a counterion in its molecule and is poorly-soluble in water. The hydrocarbon-based elastomer can preferably be used as an ion-conductivity imparting agent for forming a catalyst electrode layer by mixing an organic solvent.

Abstract: A curable resin composition comprising (a) a compound having at least one ethylenically unsaturated group and at least one ion conductive group, (b) a compound having at least two ethylenically unsaturated groups, (c) an organosilicon compound having at least two SiH groups, (d) a platinum group catalyst, and (e) a solvent is dried and cured by heating into a cured film having excellent ionic conduction and serving as electrolyte membrane. The electrolyte membrane and an electrolyte membrane/electrode assembly satisfy fuel cell-related properties including ionic conduction and film strength as well as productivity.

Abstract: A proton conducting hydrocarbon-based polymer has acid groups on side chains attached to the main chain, where the acid groups are between 7 and 12 atoms away from the main chain. Another polymer includes a semi-fluorinated aromatic hydrocarbon main chain and side chains that include at least one —CF2— group and an acid group. Another polymer includes an aromatic hydrocarbon main chain and side chains that include at least one —CH2-CF2— group and an acid group. Another aromatic polymer includes acid groups attached to both the main chain and the side chains where less than about 65 weight percent of the acid groups are attached to the side chains. Another aromatic polymer includes side chains attached to the main chain that include at least one aryl ring, and acid groups attached to both the main chain and to the aryl groups. Another polymer includes an aliphatic hydrocarbon main chain, side chains that include at least one deactivating aryl ring, and acid groups attached to the deactivating aryl rings.

Abstract: There are provided a new crosslinked polymer electrolyte excellent in water resistance and solvent resistance, high in heat resistance, inexpensive and low in methanol permeability, and suitable for the proton conductive membrane of a fuel cell, by means of the crosslinked polymer electrolyte obtained by the following (1) or (2), and its production method. (1) A compound having two or three or more reactive groups is reacted with a polymer electrolyte. (2) A compound having two or three or more reactive groups is reacted with a polymer to obtain a crosslinked polymer and then an ion exchange group is introduced into the resultant polymer.

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 the field of polymer chemistry and relates to sulfonated polyarylene compounds such as can be used for example in ion exchange membranes in fuel cells, as well as a method for the production thereof and the use thereof. The object of the present invention is to disclose hydrolytically and thermally resistant sulfonated polyarylene compounds with a defined degree and position of sulfonation, from which membrane materials with an improved resistance to hydrolysis can be produced. The object is attained through sulfonated polyarylene compounds according to at least one of the general formulas (I)-(IV).

Abstract: A polyurea electrolyte includes a polyurea resin formed by a polymerization of a first compound having two or more isocyanate groups and a second compound having two or more amino groups. The first compound or the second compound contains ten or more carbon chains, and the first compound or the second compound contains a sulfonic acid group or a carboxylic acid group. A method for manufacturing the polyurea electrolyte includes neutralizing the sulfonic acid group or the carboxylic acid group in the first compound or the second compound by a neutralizing agent; after the neutralizing, polymerizing the first compound and the second compound; and after the polymerizing, removing the neutralizing agent from a polymer of the first compound and the second compound.

Abstract: An aromatic polyether sulfone block copolymer comprises hydrophilic segments which have sulfonic acid groups and hydrophobic segments which have no sulfonic acid groups, wherein the proportion by weight of hydrophilic segments is from 0.02 to 0.35.

Abstract: A process for the storage or transportation of pretreated, conditioned ion exchangers as catalysts for chemical reactions is disclosed. The preconditioned ion-exchange resin is kept as preconditioned ion-exchange resin suspension in a storage or transporting container. The container with the preconditioned ion-exchange resin suspension is transported to either a storage site for storage or to a reactor for transfer of the resin to the reactor.

Abstract: A polyarylene copolymer having a sulfonic acid group which has high proton conductivity and reduced swelling in hot water and reduced shrinkage in drying; a solid polymer electrolyte and a proton conductive membrane comprising the copolymer; and a membrane-electrode assembly using these. The polyarylene block copolymer comprises a polymer segment (A) having a sulfonic acid group, and a polymer segment (B) having substantially no sulfonic acid group, the polymer segment (B) having substantially no sulfonic acid group comprising a structural unit represented by the following formula (1).

Abstract: A polymer electrolyte membrane is made from a polymer electrolyte and a coordination polymer, and finds use in a fuel cell. The polymer electrolyte membrane may be made by dissolving a polymer electrolyte in a solvent to provide a first solution, adding a coordination polymer to the first solution to yield a second solution, and forming the second solution into a film.

Abstract: A phosphorus-adsorbing material is produced to include a polymer-based material modified with at least either of a primary and a secondary amine and a metal supported on the polymer-based material, and a phosphorus recovery system is structured by using the phosphorus-adsorbing material.

Abstract: The present invention relates generally to electrolyte materials. According to an embodiment, the present invention provides for a solid polymer electrolyte material that has high ionic conductivity and is mechanically robust. An exemplary material can be characterized by a copolymer that includes at least one structural block, such as a vinyl polymer, and at least one ionically conductive block with a siloxane backbone. In various embodiments, the electrolyte can be a diblock copolymer or a triblock copolymer. Many uses are contemplated for the solid polymer electrolyte materials. For example, the novel electrolyte material can be used in Li-based batteries to enable higher energy density, better thermal and environmental stability, lower rates of self-discharge, enhanced safety, lower manufacturing costs, and novel form factors.

Abstract: A dialysate regeneration chamber is provided. In one embodiment, the dialysate regeneration chamber may include a toxin trap configured to selectively trap toxins and repel select cations.

Abstract: The present invention relates to a poly(arylene ether) copolymer having an ion exchange group, particularly a positive ion exchange group, a method for manufacturing the same, and use thereof. In the poly(arylene ether) copolymer having the ion exchange group according to the present invention, physical characteristics, ion exchanging ability, metal ion adsorption ability and a proccessability are excellent, and thus the copolymer can be molded in various shapes and can be extensively applied to various fields such as recovering of organic metal, air purification, catalysts, water treatment, medical fields and separating of proteins.

Abstract: A non crosslinked, covalently crosslinked and/or ionically crosslinked polymer, having repeating units of the general formula (1) —K—R—??(1) In which K is a bond, oxygen, sulfur, the radical R is a divalent radical of an aromatic or heteroaromatic compound.

Abstract: Provided are poly(ferrocenyl)silane based network polymers, methods of preparing the same, and films including the poly(ferrocenyl)silane based network polymers. The network polymers have a steric network structure and are prepared by using a simplified process.

Abstract: The polymer electrolyte membrane according to the present invention comprises a polymer electrolyte having ion-exchange groups, wherein Sp and Snp satisfy a relationship expressed by the following expression (I): Sp/Snp?0.42??(I) where Sp represents the total of peak areas obtained by measurement of a 13C-solid state nuclear magnetic resonance spectrum of the polymer electrolyte membrane, the polymer electrolyte membrane having been subjected to a first immersion treatment comprising immersing the polymer electrolyte membrane in 5 mmol/L iron (II) chloride tetrahydrate aqueous solution at 25° C. for 1 hour, and thereafter drying the polymer electrolyte membrane at 25° C.

Abstract: The present invention relates to a novel proton-conducting polymer membrane based on aromatic polyazoles which contain sulfonic acid groups and in which the sulfonic acid groups are covalently bound to the aromatic ring of the polymer and which can, owing to their excellent chemical and thermal properties, be used for a variety of purposes. Such materials are particularly useful for the production of polymer electrolyte membranes (PEMs) in PEM fuel cells.

Abstract: Described herein is the synthesis of reinforced adhesive complex coacervates and their use thereof. The reinforced adhesive complex coacervates are composed of (a) at least one polycation, (b) at least one polyanion, and (c) a reinforcing component. The adhesive complex coacervates described herein can be subsequently cured to produce strong, cohesive adhesives. The reinforced adhesive complex coacervates have several desirable features when compared to conventional adhesives. The reinforced adhesive complex coacervates are effective in wet or underwater applications. The reinforced adhesive complex coacervates described herein, being phase separated from water, can be applied underwater without dissolving or dispersing into the water. The reinforced adhesive complex coacervates have numerous biological applications as bioadhesives and bioactive delivery devices.

Abstract: The preparation of aromatic sulfonimide polymers useful as membranes in electrochemical cells is described.

Abstract: A PBI compound includes imidazole nitrogens at least a portion of which are substituted with a moiety containing a carbonyl group, the substituted imidazole nitrogens being bonded to carbon of the carbonyl group. At least 85% of the nitrogens may be substituted. The carbonyl-containing moiety may include RCO—, where R is alkoxy or haloalkyl. The PBI compound may exhibit a first temperature marking an onset of weight loss corresponding to reversion of the substituted PBI that is less than a second temperature marking an onset of decomposition of an otherwise identical PBI compound without the substituted moiety. The PBI compound may be included in separatory media. A substituted PBI synthesis method may include providing a parent PBI in a less than 5 wt % solvent solution. Substituting may use more than 5 equivalents in relation to the imidazole nitrogens to be substituted.

Abstract: A polymer useful as an ion conducting membrane for fuel cell applications includes both main chain and side chain protogenic groups. Methods for preparing the polymer include addition of the side chains both before and after addition of the protogenic groups.

Abstract: This invention provides an adsorbent material capable of effectively trapping a target component in a sample solution and releasing the same, which has the satisfactory trapping capacity via hydrophobic interactions and via ion exchange reactions. The invention relates to an adsorbent material comprising a porous material of a polymer compound which is a copolymer obtained via copolymerization of a hydrophobic monomer (A), a hydrophilic monomer (B) capable of undergoing a second-order reaction, and a hydrophilic monomer (C) exhibiting a hydrogen-bonding capacity, and via introduction of an ion exchange group into a repeat unit derived from the hydrophilic monomer (B).

Abstract: This invention provides a family of functionalized polymers capable of forming membranes having exceptional OH? ionic conductivity as well as advantageous mechanical properties. The invention also provides membranes including the provided polymers and AEMFC/HEMFC fuel cells including such membranes. In a preferred embodiment, preferred function groups include a quaternary phosphonium, and in a more preferred embodiment the provided polymer is (tris(2,4,6-trimethoxyphenyl) phosphine)3 functionalized phosphonium polysulfone hydroxide.

Abstract: Silica polyamine composites (SPC) made from silanized amorphous nano-porous silica gel and poly(allylamine) (BP-1) were functionalized with phosphorus acid using the Mannich reaction, resulting in a phosphonic acid modified composite (BPAP). Zirconium (IV) was immobilized on BPAP. Arsenate anions strongly adsorbed on the ZrBPAP composite in the pH range 2 to 8, while arsenite only adsorbed well at pH 10. Regeneration of the resin was carried out successfully for As(V) and As(III) using 2M-H2SO4. Four adsorption/desorption cycles were performed for As(V) at pH 4 without significant decrease in the uptake performance. ZrBPAP capture capacity and kinetics for arsenate were tested for longevity over 1000 cycles with only a marginal loss of performance.