Abstract: Grafted polymers which are the reaction products of: (a) (Meth)acrylic acid and (b) Non-symmetric maleates according to general formula (I), in which R1 stands for a linear or branched alk(en)yl radical having 1 to 22 carbon atoms and 0 or 1 double bond, while n and m independently represent integers between 0 and 200, on condition that the sum (n+m) is different from 0 are disclosed. Methods of making and using the grafted polymers are also disclosed.

Abstract: An ester-based polymer to be used in the present invention has at least a repeating unit represented with the general formula (I). A and B are substituents substituted on a stilbene group. R1 is a hydrogen atom, a linear or branched alkyl group having 1 to 10 carbon atoms, or a substituted or unsubstituted aryl group. R2 is a linear or branched alkyl group having 2 to 10 carbon atoms. R3 to R6 each independently represents a hydrogen atom, a halogen atom, a linear or branched alkyl group having 1 to 6 carbon atoms, or a substituted or unsubstituted aryl group. n is an integer of 2 or more.

Abstract: Disclosed are soft, high refractive index, methacrylic device materials. The materials contain an ethoxylate monomer to reduce glistenings and a long-chain alkyl methacrylate monomer for softening.

Abstract: A curable restorative composition is disclosed, comprising a polymerizable mono(meth)acrylate resin having a vapor pressure of 1 mm Hg or less at 20° C., a plasticizer; and a curing system for the mono(meth)acrylate resin. The composition is particularly useful for making temporary restorations. Methods of used and kits comprising the composition are also disclosed.

Abstract: The present invention relates to a process for chemically modifying, within its thickness, a polymer matrix chosen from matrices made of fluoropolymers and matrices made of aliphatic polymers, said process comprising at least one step consisting in irradiating said matrix with UV light having a wavelength of less than 300 nm in order to generate, within the thickness of said matrix, zones that have short polymer chains, formed by scission of the existing chains during the passage of the UV radiation and that have free radicals denoted hereinbelow as “activated zones”. The present invention also relates to the polymer matrix capable of being chemically modified by such a process.

Abstract: A method of making a polymerisable ethylenically unsaturated macromonomer comprising the steps of: i) providing a chosen unsaturated non-mineral oil or a mixture of unsaturated non-mineral oils having a first blend of triglycerides, ii) treating the mixture of oils with a transesterification catalyst to produce a second blend of triglycerides different to the first, iii) reacting the second blend of triglycerides with an enophile having an acid, ester or anhydride moiety to form an adduct, iv) reacting the adduct with an ethylencially unsaturated monomer having a moiety reactive with the acid, ester or anhydride moiety of the enophile to form an intermediate, v) reacting the intermediate of step (iv) with a chain extender having at least two moieties reactive with the acid, ester or anhydride moiety of the enophile to form the ethylenically unsaturated macromonomer.

Abstract: The present invention relates to a liquid-crystal (LC) display of the PS (polymer stabilised) or PSA (polymer sustained alignment) type, and to polymerisable compounds and LC media for use in PS (polymer stabilised) and PSA displays.

Abstract: A photocurable and thermosetting coating composition which is solventless and liquid at room temperature is provided. This coating composition provides scratch resistance, crack resistance, smudge resistance, and removability of oil-base felted markers by wiping with the underlying substrate, and this coating composition contains a silicone resin represented by: (R1R2R3SiO1/2)a(R4R5SiO2/2)b(R6SiO3/2)c(SiO4/2)d(O1/2X)e??(1) wherein X is hydrogen atom or an alkyl group; R1 to R6 are respectively at least one monovalent organic group which is a monovalent aliphatic hydrocarbon group or a monovalent aromatic hydrocarbon group optionally substituted with a substituent such as a poly(hexafluoropropylene oxide) structure-containing group; a, b, d, and e are 0 or a positive number; c is a positive number; and a+b+c+d is 1. The silicone resin contains at least one group represented by: CH2?C(R7)COOCH2—??(2) wherein R7 is hydrogen atom or methyl group.

Abstract: Described herein are nitric oxide (NO)-donating poly(tetrafluoroethylene) (PTFE) polymers and polymer surfaces and methods of making and using the same. The NO-donating PTFE polymers can be used to fabricate at least a portion of an implantable medical device, coat at least a portion of an implantable medical device or form at least a portion of an implantable medical device. The NO-donating PTFE polymers provide controlled release of NO once implanted at or within the target site.

Abstract: Disclosed are soft, high refractive index, acrylic device materials. The materials comprise di-block or tri-block macromers containing a hydrophilic block in the polymer backbone. The materials have improved glistening resistance.

Abstract: A sorbent polymer is provided that interacts or reacts with aqueous urea to aid the regeneration of a dialysate liquid. The sorbent polymer may include one or more specific functional groups bonded thereto. Such specific functional groups are selected from carboxylic acids, carboxylic acid esters, carboxylates, amides, dicarboxylic acids, dicarboxylic acid esters, and dicer boxylates to produce the desired urea sorbent.

Abstract: The object of the present invention is to provide an adsorbent having an excellent AGEs adsorption ability. The present invention provides an adsorbent for advanced glycation end products consists of a copolymer resin having hydrophilic methacrylate, wherein the constituent unit of said copolymer resin consists of a particular methacrylate compounds and vinyl compounds. Preferably, the copolymer resin having hydrophilic methacrylate has one or more basic ion-exchange groups.

Abstract: The present invention relates to polymeric compositions useful in the manufacture of biocompatible medical devices. More particularly, the present invention relates to certain cationic monomers capable of polymerization to form polymeric compositions having desirable physical characteristics useful in the manufacture of ophthalmic devices. Such properties include the ability to extract the polymerized medical devices with water. This avoids the use of organic solvents as is typical in the art. The polymer compositions comprise polymerized silicon-containing monomers end-capped with polymerizable cationic hydrophilic groups.

Abstract: A polymer composition is typically obtainable by reacting: a) 40-90 pphwm of vinyl acetate; b) 30-5 pphwm of cycloalkyl esters of a butenedioic acid; and optionally c) 30-5 pphwm of vinyl esters of ?-monosubstituted fatty acids; and/or d) 20-5 pphwm of an ?-olefin monomer; and/or e) 20-0.1 pphwm of a functional monomer unit such as as self-crosslinking monomer.

Abstract: Disclosed is an acid etching resistance material comprising a compound having a repeating unit represented by the following general formula (1): (in the general formula (1), R1 is a hydrogen atom or methyl group; R3 is a cyclic group selected from an alicyclic group and an aromatic group; R4 is a polar group; R2 is a group represented by the following general formula (2); and j is 0 or 1): (in the general formula (2), R5 is a hydrogen atom or methyl group).

Abstract: A copolymer which can be used in power transmission fluids to provide improved viscometric properties is disclosed. The copolymer includes a mixture of alcohols having side chains with an average number of carbons ranging from greater than 8 to less than 12 defined by the following formula: C n = ? i = j i = z ? X i ? Cn i ? i = j i = z ? X i where Xi is the mole fraction of alcohol (i); Cni represents the number of carbon atoms in alcohol (i); j is the lowest number of carbons in an alcohol in the copolymer and must be at least 6; and z is the highest number of carbons in an alcohol.

Abstract: An allyl type crosslinking agent for use in production of a super water-absorbent polymer comprising a polymerizable compound having a carbon-carbon double bond or a salt thereof. The crosslinking agent comprises a linear hydroxypolyallyl ether having at least one hydroxyl group and at least two allyl groups obtained by allyletherification of hydroxyl groups in a linear polyol compound selected from the group consisting of erythritol, xylitol and sorbitol. This allyl type crosslinking agent is highly soluble in an aqueous solvent, and can give an excellent super water-absorbent polymer, which cannot be obtained in the prior arts, having high levels of both of water absorptivity under atmospheric pressure and water absorptivity under pressurized conditions.

Abstract: To provide a polyolefin polymer having a polar group represented by Formula (i) produced by modifying, with a high modification ratio, a double bond in a polymer having the double bond at one terminal, both terminals, or at the inside of a polymer chain thereof that is obtained by a known method; a method for producing the polyolefin polymer; and a water dispersion material and a mold release agent composition each containing the polyolefin polymer, wherein in Formula (i), PO represents a polyolefin polymer obtained by polymerizing a monomer including ethylene or including an olefin having 3 to 20 carbon atoms, and a group shown in the brackets is the polar group of the polyolefin polymer; A and B each independently represent R1, a cyano group, C(O)OR1, or C(O)NR1R2, and A and B may be combined to form a cyclic structure; M represents a metal cation or an onium cation; j is an integer of 0 to 4 representing the number of the metal cation or the onium cation; i is an integer of 0 to 4 representing the nu

Abstract: The present invention relates to new cure accelerators for anaerobic curable compositions. These anaerobic cure accelerators are generally sulfonimide derivatives and sulfonamide derivatives.

Abstract: The polyethylene naphthalate fiber for industrial material having a low fatigue in a composite is a polyethylene naphthalate fiber for industrial material containing an ethylene-2,6-naphthalate unit in 80% or more, characterize by having a strength of 6 cN/dtex or more and a secondary yield point elongation degree of 8% or less. The production method thereof is a method for producing a fiber in which a fiber having been obtained by melt-spinning a polyethylene naphthalate is subjected to stretching, characterized in that prestretch satisfying such conditions as the fiber temperature of from 80° C. to 120° C. and from 0.05 to 0.3 N/dtex is performed, a first stretch satisfying such conditions as the fiber temperature of from 130° C. to 180° C. and stretch tensile force of not more than the prestretch tensile force is performed, the total stretch magnification including subsequent stretches is set to 5 or more, and finally heat-treatment under tension with a stretch ratio of from 0 to 2% is performed.

Abstract: A fluorinated polyoxyalkylene glycol diester surfactant of formula 1 B—X—COCH2O—[—CpH2pO—]n—CH2CO—X—Ra ??(1) wherein B is M or Ra, M is an ionizable hydrogen, ammonium, alkali metal, or alkaline earth metal, p is from about 2 to about 4, n is from about 5 to about 43, X is O, S, or SCH2CH2O, Ra is Rf(CH2CF2)d—(CgH2g)—; Rf[OCF2CF2]r(CgH2g)—; Rf(CH2)h[(CF2CF2)i(CH2CH2)j]k—; or RfOY—; Y is CFHCF2O(CH2CH2O)v—(CgH2g)—; CFHCF2O(CwH2w)—; or CF(CF3)CONH—(CgH2g)—; each Rf is independently CcF(2c+1) wherein c is 1 to about 6; d is 1 to about 3; g is 1 to about 4; s is 0 or 1; r is 1 to about 4; h is 1 to about 6; i, j, and k are each independently 1, 2, or 3, or a mixture thereof; provided that the total number of carbon atoms in Rf(CH2)h[(CF2CF2)i(CH2CH2)j]k—is from about 8 to about 22; v is 1 to about 4; and w is from about 2 to about 12.

Abstract: The purpose the invention is to provide a polymerizable liquid crystal compound which has an excellent solubility with other compounds, a high homeotropic property, and a spirobiindan-backbone, and a liquid crystal composition comprising this compound. The purpose is attained with a polymerizable liquid crystal compound represented by Formula (1). A polymer which is excellent in many characteristics can be obtained from this compound and a formed body having optical anisotropy, produced from this polymer can be obtained. In Formula (1), G is a single bond or oxygen; R is hydrogen, methyl (Me) or a group represented by Formula (a), wherein at least two of R are groups represented by Formula (a); P is a polymerizable group represented by any of Formula (P1) to Formula (P8). In Formula (a), a desirable A is 1,4-cyclohexylene or 1,4-phenylene; Z is a bonding group; m is an integer of 0 to 3; X0 is a single bond or alkylene; Z0 is a single bond, —O—, —OCO—, or —OCOO—; X is a single bond or alkylene.

Abstract: The present invention is directed to a polymer comprising the reaction product of (i) a monomer comprising at least two ethylenically unsaturated double bonds; (ii) a monomer comprising a carbon atom that is connected to four moieties wherein one of said moieties comprises a hydrogen atom and the remainder of said moieties comprises an alkyl group, wherein one of the alkyl group containing moieties comprises an ethylenically unsaturated double bond, and wherein none of the alkyl group containing moieties form a cycloaliphatic ring; (iii) at least one monomer that is reactive with (i) and/or (ii); wherein the reaction product is not further reacted with any other monomer comprising an ethylenically unsaturated double bond; and wherein said reaction product comprises a reactive functional group.

Abstract: One aspect of the present invention provides a method for production of a polyester resin film comprising melt extruding a polyester resin into a sheet shape, cooling and solidifying the polyester resin sheet on a casting drum, then longitudinally stretching the polyester resin sheet in a longitudinal direction, and then passing the longitudinally stretched polyester resin film through a transverse stretching apparatus to transversely stretch the longitudinally stretched polyester resin film in a transverse direction, wherein Xc, Tc, Ts and Te satisfy the formulas of: Tc?(Ts+Te)/2+2.66Xc?Tc+60??(1) and 2?Xc?30??(2), in which Xc (%) indicates a crystallinity of the film after the longitudinal stretching, Tc (° C.) indicates a crystallization temperature of the film after the longitudinal stretching, Ts (° C.) indicates a film surface temperature at an entrance of a stretching zone of the transverse stretching apparatus, and Te (° C.

Abstract: Compounds of the general formula I (variables defined herein) and processes for making compounds including 2,6 -naphthyl radicals are provided. Polymerizable or nonpolymerizable liquid-crystalline compositions including one or more compounds including 2,6 -naphthyl radicals, and products and processes employing such compositions, are also provided.

Abstract: A polymer comprising recurring units (2) obtained through polymerization of an ester compound of formula (1) is used to form a resist composition. R1 is F or C1-C6 fluoroalkyl, R2 is H or C1-C8 alkyl, R3 is O or C1-C6 alkylene, R4 and R5 each are H or C1-C10 alkyl or fluoroalkyl, and R6 is H or an acid labile group. The resist composition, when processed by ArF lithography, has advantages including improved resolution, transparency, minimal line edge roughness, and etch resistance. The resist composition exhibits better performance when processed by ArF immersion lithography with liquid interposed between a projection lens and a wafer.

Abstract: A film for insert molding comprising a base material film and a hard coat layer provided on at least one surface of the base material film, wherein the hard coat layer is formed from an ionizing radiation curable resin containing a reactive monomer having a cyclo ring structure containing at least one kind of element selected from carbon, nitrogen, oxygen, and silicon. The hard coat layer of this film for insert molding has sufficient surface hardness, and can prevent cracks which are likely to be generated at the time of molding (it has superior anti-cracking property).

Abstract: A biocompatible material having excellent biocompatibility such as small interaction with a component of a living body such as a protein or blood cell. A biocompatible material comprising a polymer obtained by polymerizing a monomer composition comprising an amino acid-type betaine monomer represented by the formula (I): wherein R1 is a hydrogen atom or a methyl group; R2 is an alkylene group having 1 to 6 carbon atoms; each of R3 and R4 is independently an alkyl group having 1 to 4 carbon atoms; R5 is an alkylene group having 1 to 4 carbon atoms; and Z is an oxygen atom or an —NH group; and a polymerizable monomer represented by the formula (II): wherein R1 is as defined above; and R6 is a monovalent organic group, in a weight ratio, i.e. amino acid-type betaine monomer/polymerizable monomer, of from 1/99 to 100/1. The biocompatible material can be suitably used, for example, in food, a food additive, a medicament, a quasi-drug, a medical device, cosmetics, a toiletry article, or the like.

Abstract: A polymerizable compound represented by general formula (1) of the invention has good solvent solubility and excellent alignment control properties and optical characteristics. In formula (1), M1 and M2 are each hydrogen or methyl; X1 and are each a single bond, or an optionally branched C1-10 alkylene, alkyleneoxy or alkyleneoxycarbonyloxy; X3 is optionally branched C1-10 alkylene; Y1 and Y2 are each an ester linkage, etc.; and rings A, B, C, and D are each a cyclic structure, such as 2,6-naphthlene.

Abstract: An insulation element is provided for installation in a gap of thickness G provided between two objects. The insulation element includes a body made from a thermoplastic polymer material. The body has a first face, a second face and a thickness defined between the first and second faces. The body is characterized by a semi permanently pre-installation thickness T1 where T1 is less than G. The body swells upon heating to a thickness T2 where T2 is greater than or equal to G so that the insulation element bridges the gap, engages the two objects and provides a spring rate of between 4.0 and 275.0 grams per square inch.

Abstract: The present invention relates to superabsorbent polymer particles having functionalizers covalently bound to the surface of precursor superabsorbent polymer particles. The functionalizers of the present invention comprise a grafting unit with a radiation activatable group and a functional unit covalently bound to the grafting unit. The grafting unit is bound to an aliphatic C—H group comprised at the surface of the precursor superabsorbent polymer particle. The functional unit comprises chemical structures which are not present in the precursor superabsorbent polymer particle. These functional units add an additional function to the precursor suberabsorbent polymer particle or modifying an existing function of the precursor superabsorbent polymer particle. Moreover, the invention relates to a process for making these superabsorbent polymer particles.

Abstract: Disclosed are soft, high refractive index device materials having improved strength. The materials contain a monofunctional or difunctional, acrylate or methacrylate terminated aromatic functional methacrylic or acrylic macromer.

Abstract: An object of the present invention is to provide a novel method for producing a vinyl polymer (P) having a polar functional group (X) and having in its main chain a branched structure. The object can be achieved by the present invention providing a method for producing a vinyl polymer (P) having a polar functional group (X) and having in its main chain a branched structure, wherein while and/or after polymerization of a vinyl polymer (I) having a protecting group (Y) and having at its molecular terminal a group (A) containing carbon-carbon double bond, the protecting group (Y) is converted to the polar functional group (X).

Abstract: The invention relates to a method for radical polymerization of one or several ethylenically unsaturated compounds, characterized in that it consists in providing at least 80.8 percent by weight ethylenically unsaturated compounds in relation to the total weight of the ethylenically unsaturated compounds, adding at least one polymerization initiator for radical polymerization in at least two steps, wherein more polymerization initiator is added in the second step than in the first.

Abstract: Composition comprising at least one ethylenically unsaturated monomer to which a photochemically isomerizable or dimerizable molecule is covalently bonded, and at least one ethylenically unsaturated monomer to which a sensitizer is covalently bonded, are outstandingly suitable for producing polymeric alignment layers for liquid crystals.

Abstract: The present invention relates to polymeric compositions useful in the manufacture of biocompatible medical devices. More particularly, the present invention relates to certain carboxylic monomers capable of polymerization to form polymeric compositions having desirable physical characteristics useful in the manufacture of ophthalmic devices. The polymeric compositions comprise polymerized carboxylic hydrophilic siloxanyl monomers.

Abstract: A polyolefin polymer comprising one or more terminal polymerizable methacryloyl groups (i.e. tethered to the main body of the polymer) and a novel process for preparing same are herein disclosed. A hyperbranched polyethylene polymer and a process for preparing same are also disclosed. The polymer is prepared by a novel one-pot copolymerization reaction of an olefin, such as ethylene, and a heterobifunctional comonomer comprising a methacryloyl group, catalyzed by a late transition metal ?-diimine catalyst which is selectively non-reactive towards methacryloyl groups. The process allows for preparation of polymers with various chain topologies, including linear, branched, and hyperbranched topologies. The terminal methacryloyl groups within the polymer are reactive in further polymerization reactions. Thus, the polymer may be used in materials and applications which require cross-linking or further polymerization, for example, UV/thermal/radical curable crosslinkers for use in thermoset applications.

Abstract: A process for recycling a coloured thermoplastic material comprising an absorbed disperse dye comprises contacting the optionally comminuted coloured thermoplastic material with a caustic wash and recovering an at least partly colour-modified thermoplastic composition from the caustic wash.

Abstract: The invention relates to highly biocompatible or biophilic un-cross-linked or cross-linked polymers comprising one or more side-chain active acrylic amino acids of formula I wherein: X is —NH(CH2)4—, —O—C6H4—CH2—, —OCH2—, —O—CH(CH3)—, —S—CH2—, —O-proline, and R is H or CH3; and wherein the polymer further includes a free radical initiator and, optionally, a cross-linking agent having a plurality of polymerizable ethylenically unsaturated groups. The invention further concerns various highly biocompatible, cross-linked co-polymers comprising one or more monomers of formula I, and one or more other polymerizable monomers. Uses of such polymers and co-polymers for the production of contact lenses, intraocular lenses, implants, wound healing slabs, additives for food and cosmetics, conductive plastics, spinnable fibers, and the like are disclosed.

Abstract: Disclosed are soft, high refractive index, acrylic materials. These materials, especially useful as intraocular lens materials, contain an aryl acrylic hydrophobic monomer as the single principal device-forming monomer and a tack-reducing macromer additive. In addition to their use as intraocular lens materials, the present materials are also suitable for use in other ophthalmic or otorhinolaryngological devices, such as contact lenses, keratoprostheses, corneal inlays or rings; otological ventilation tubes and nasal implants.

Abstract: A flow improver comprising a plurality of core-shell particles that can be formed by emulsion polymerization. The core of the core-shell particles can include a drag reducing polymer, while the shell of the particles can include repeat units of a hydrophobic compound and an amphiphilic compound. The flow improver can demonstrate increased pumping stability over conventionally prepared latex flow improvers.

Abstract: Nanostructured chemicals such as polyhedral oligomeric silsesquioxanes, polyhedral oligomeric silicates, and polyhedral oligomeric metallasesquioxanes are attached to living and nonliving systems as biomaterials to provide a nanoscopic topology that favors biomimetic function and cellular modulation. The resulting surface is nanoscopically thin, nanoscopically dispersed, provides systematic chemistry, surface area, surface volume, surface topology, and is essentially free of impurities, and has controllable properties through selection of composition, R groups, nanostructure size and topology. Highly shape specific and chemically tailorable nanostructured molecules are sized to biological material dimensions and are compatible with all sterilization methods.

Abstract: The invention provides a method of preparing a crosslinked polymer, which method comprises polymerising branched polyunsaturated monomers by a metathesis polymerisation reaction, wherein the branched polyunsaturated monomers contain acyclic ethylenically unsaturated groups that are capable of undergoing polymerization by a metathesis reaction such that the metathesis polymerisation produces a crosslinked polymer and substantially no non-volatile ethylenically unsaturated by-products.

Abstract: A high molecular weight, water-soluble polymer comprising pendant salicylic acid groups and having a weight average molecular weight of at least about 2,000,000 daltons and use of the polymer for clarifying red mud-containing liquors generated in the Bayer process for the recovery of alumina from bauxite.

Abstract: Polymerizable compositions comprising nanopartilces particularly useful for brightness enhancing films.

Abstract: The object of the present invention is to provide an adsorbent having an excellent AGEs adsorption ability. The present invention provides an adsorbent for advanced glycation end products consists of a copolymer resin having hydrophilic methacrylate, wherein the constituent unit of said copolymer resin consists of a particular methacrylate compounds and vinyl compounds. Preferably, the copolymer resin having hydrophilic methacrylate has one or more basic ion-exchange groups.

Abstract: A Chelating agent comprising a polymer backbone. The polymer backbone has a plurality of carbon atoms. There are two carboxylate groups or carboxylic acid groups per repeating unit being coupled to separate carbon atoms of the backbone.

Abstract: A method of applying a biocidal polymer to a surface including applying a solution of the biocidal polymer to the surface, wherein the biocidal polymer includes biocidal groups and the biocidal polymer is insoluble in water. The biocidal groups can be selected from the group consisting of quaternary salt groups or haloamino groups.

Abstract: A method for the cationic polymerization of unsaturated biological oils (e.g., vegetable oils and animal oils) based on the cationic reaction of double bonds initiated by superacids is provided. The process occurs under very mild reaction conditions (about 70-110° C. and atmospheric pressure) and with short reaction times. The polymerized oils have a viscosity about 10 to 200 times higher than the initial oil and relatively high unsaturation (only about 10-30% lower than that of initial oils).

Abstract: A pattern forming method which uses a positive resist composition comprises: (A) a silicon-free resin capable of increasing its solubility in an alkaline developer under action of an acid; (B) a compound capable of generating an acid upon irradiation with an actinic ray or radiation; (C) a silicon-containing resin having at least one group selected from the group of consisting (X) an alkali-soluble group, (XI) a group capable of decomposing under action of an alkaline developer and increasing solubility of the resin (C) in an alkaline developer, and (XII) a group capable of decomposing under action of an acid and increasing solubility of the resin (C) in an alkaline developer, and (D) a solvent, the method comprising: (i) a step of applying the positive resist composition to a substrate to form a resist coating, (ii) a step of exposing the resist coating to light via an immersion liquid, (iii) a step of removing the immersion liquid remaining on the resist coating, (iv) a step of heating the resist coating, a