The present invention relates to a biocompatible device which comprises on its surface an adsorbed layer of a polymer P which is a copolymer of at least one macromonomer selected from an ester E of (meth)acrylic acid and polyethylene oxide or a polyethylene glycol (meth)acrylamide, at least one monomer M selected from alkyl (meth)acrylate, aryloxyalkyl (meth)acrylate, alkyl (meth)acrylamide or aryl (meth)acrylamide, and at least one cationic monomer C selected from cationic ethylenically unsaturated N-containing monomers. It further relates to a process for making a biocompatible device which comprises on its surface an adsorbed layer of the polymer P comprising the following steps: providing a biocompatible device, and applying to the surface of the biocompatible device a solution S of the polymer Pin a solvent L. It further relates to a solution S comprising the polymer P in the solvent L, where the solvent L comprises an alcohol; and to a process for cultivating cells, comprising the following steps: providing the biocompatible device and cultivating the cells in the supernatant medium above the surface of the biocompatible device.

The present invention provides a binder for a nonaqueous secondary battery electrode capable of greatly improving the peeling strength of an electrode active material layer to a current collector while suppressing the occurrence of cracks in the electrode active material layer formed on the current collector. The binder for a nonaqueous secondary battery electrode includes a copolymer (P) having a structural unit (a) derived from a monomer (A) represented by formula (1), a structural unit (b) derived from a monomer (B) which is at least one kind selected from the group consisting of a (meth)acrylic acid and a salt thereof, and a structural unit (c) derived from a monomer (C) which is an ethylenically unsaturated carboxylic acid ester of an aromatic alcohol.

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The present invention provides a binder for a nonaqueous secondary battery electrode capable of greatly improving the peeling strength of an electrode active material layer to a current collector while suppressing the occurrence of cracks in the electrode active material layer formed on the current collector. The binder for a nonaqueous secondary battery electrode includes a copolymer (P) having a structural unit (a) derived from a monomer (A) represented by formula (1), a structural unit (b) derived from a monomer (B) which is at least one kind selected from the group consisting of a (meth)acrylic acid and a salt thereof, and a structural unit (c) derived from a monomer (C) which is an ethylenically unsaturated carboxylic acid ester of an aromatic alcohol.

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A polymeric surfactant for use in chemical enhanced oil recovery, including a terpolymer of a first non-ionic monomer, a second non-ionic monomer, and an ionic monomer, the first non-ionic monomer being a hydrophilic monomer and the second non-ionic monomer being a hydrophobic monomer, the ionic monomer being in a lower proportion than the first and second non-ionic monomers. A method of preparation of polymeric surfactants.

A polymeric surfactant for use in chemical enhanced oil recovery, including a terpolymer of a first non-ionic monomer, a second non-ionic monomer, and an ionic monomer, the first non-ionic monomer being a hydrophilic monomer and the second non-ionic monomer being a hydrophobic monomer, the ionic monomer being in a lower proportion than the first and second non-ionic monomers. A method of preparation of polymeric surfactants.

The invention relates to methods of lubricating biological tissue, such as joints, bone, ocular tissue, nasal tissue, tendons, tendon capsule, and vaginal tissue, by contacting the biological tissue with an effective amount of a block copolymer lubricating composition which functions at least or better than lubricin. In particular embodiments, the method is used to treat osteoarthritis. In specific embodiments, the block copolymer has an ammonium-containing polymer block and a non-ionic hydrophilic polymer block, or the copolymer has a carboxylic acid-containing polymer block and a non-acid non-ionic hydrophilic polymer block.

The invention relates to methods of lubricating biological tissue, such as joints, bone, ocular tissue, nasal tissue, tendons, tendon capsule, and vaginal tissue, by contacting the biological tissue with an effective amount of a block copolymer lubricating composition which functions at least or better than lubricin. In particular embodiments, the method is used to treat osteoarthritis. In specific embodiments, the block copolymer has an ammonium-containing polymer block and a non-ionic hydrophilic polymer block, or the copolymer has a carboxylic acid-containing polymer block and a non-acid non-ionic hydrophilic polymer block.

Embodiments of the present application relate to polymers used as polymeric polyvalent hub for liquid phase oligonucleotide synthesis. Methods for making an oligonucleotide by liquid phase oligonucleotide synthesis using the polyvalent hub are also provided.

An inkjet ink includes a polyurethane binder particle including at least two polyurethane polymers; a pigment; and an aqueous vehicle. A first of the at least two polyurethane polymers has a first backbone chain formed from a first diisocyanate, a first hydrophobic graft diol, a first polycarbonate based diol, and a sulfonated diamine. A second of the at least two polyurethane polymer has a second backbone chain formed from a second diisocyanate, a second hydrophobic graft diol, and a second polycarbonate based diol, and includes a mono-amino substituted sulfonic acid as its capping moiety.

A polymer for an electrode protective layer including a polymer (A) including a fluorine-based polymer in which a monomer unit including poly(alkylene oxide) and a monomer unit including a curable functional group (e.g., a thermocurable functional group or a photocurable functional group) are grafted on the fluorine-based polymer, and when preparing an electrode by coating an electrode active material layer using the polymer and curing (e.g., thermally curing or photocuring) the result, excellent lithium ion conductivity is obtained since lithium ion flow is not inhibited, chemical resistance for an electrolyte liquid is high, and voltage stability of a secondary battery may be enhanced by suppressing side reactions with the electrolyte liquid occurring on an electrode active material surface due to properties of a uniform and flexible protective layer.