Abstract: A composition and process to make polyisocyanurate or polyurethane foam using a catalyst composition comprising at least one bismuth carboxylate catalyst and one or more co-catalysts selected from the group of alkali metal carboxylates and quaternary ammonium carboxylate salts, such that the resultant foam has improved insulation properties. The polyisocyanurate or polyurethane foams produced by this catalyst composition and method are useful for laminated boardstock, construction panels, appliance insulation, and spray-applied insulation.

Abstract: The invention relates to alkoxylation products, their preparation, compositions comprising the alkoxylation products of the invention, and the use thereof as or for producing adhesives and sealants.

Abstract: Embodiments include polymer polyol dispersions which include a polyol liquid phase and solid particle phase. Embodiments include methods of making the polymer polyol dispersions. The polymer polyol dispersions are essentially free of tin, have a solid content of between about 20 and 50 wt % based on the total weight of the polymer polyol dispersion, and have a viscosity at 20C of less than 9000 mPas. The solid particle phase has more than 90% by weight of particles in the solid particle phase having a particle diameter of less than 5 ?m.

Abstract: The present invention describes the preparation of an aqueous polyurethane dispersion which is cured by radiation, and its use as binder.

Abstract: The invention relates to siloxane polymers comprising a central polysiloxane polymer block B with organofunctional radicals bonded terminally or laterally to the polymer block and based on IPDI and UV/Vis chromophores or derivatives, in particular UV chromophores, which are covalently bonded via a hydrophobic or hydrophilic linker group Q1?, Q2?, and compositions comprising these siloxanes. Also disclosed are processes for their preparation and their use.

Abstract: The invention relates to a method for functionalizing a thermoset, crosslinked isocyanate-based polymeric solid material which is made of isocyanate and isocyanate reactive components, at least one of which comprises an anchor component which has at least one anchor group. The anchor groups on the solid material are formed by terminal alkene and/or alkyne groups. To functionalize this polymeric solid material it is brought in contact with a solution which contains at least one functional component. This functional component comprises at least one thiol group and is allowed to bind covalently to the polymeric solid material by a free-radical addition reaction between the thiol groups on the functional component and the terminal alkene and/or alkyne anchor groups on the undissolved solid material. An effective functionalization of the polymeric material can thus be achieved notwithstanding the heterogeneous reaction conditions.

Abstract: The present disclosure is directed to a sag control agent comprising a reaction product of an isocyanate and a fluorinated amine. This disclosure is further directed to a coating composition comprising the sag control agent. This disclosure is also directed to a process of forming a sag-free coating layer on a substrate.

Abstract: A method of forming an implantable article includes providing a biodegradable polymer including anti-thrombogenic groups along the length of the biodegradable polymer, biodegradable groups in the backbone of the biodegradable polymer and a plurality of functional groups adapted to react with reactive functional groups on a surface of the implantable article, and reacting at least a portion of the plurality of functional groups with the reactive functional groups on the surface of the implantable article.

Abstract: Compositions for golf balls that are formed from the reaction product of an isocyanate-containing component and an amine-terminated component having an unsaturated backbone, which is cured with a curing agent. In particular, the compositions of the invention may be formed from a prepolymer having urea linkages and at least one carbon-carbon double bond in the backbone that is cured with an amine-terminated component resulting in golf balls having weight gain comparable to ionomers and less loss of COR as compared to ionomers and conventional polyurethanes after submersion in water.

Abstract: The present technology is an epoxy resin composition containing an epoxy resin (A), a urethane resin (B) in which the terminal isocyanate of the urethane prepolymer is blocked by at least one of an ?-polycaprolactam, an oxime, or a pyrazole, and in which bisphenol A is included in the backbone of the aforementioned urethane prepolymer, and a curing agent (C).

Abstract: Disclosed are oligomeric phosphonates including oligophosphonates, random or block co-oligo(phosphonate ester)s and co-oligo(phosphonate carbonate)s produced using a condensation process terminated with hydroxyl, epoxy, vinyl, vinyl ester, isopropenyl, isocyanate groups, and the like. These materials can be used as a reactive additive to other polymers, oligomers or monomer mixtures to impart flame resistance without diminishing melt processability which is important in the fabrication of polymers for many applications.

Abstract: An aqueous crosslinkable coating composition that includes a PU polymer and a vinyl polymer bearing carbonyl groups (i.e., a carbonyl-functional vinyl polymer) and/or latex polymer. The composition also preferably includes carbonyl-reactive amine and/or hydrazine functional groups.

Abstract: Elastomeric material having a density of more than 100 kg/m3 and comprising a matrix material comprising a plurality of urethane, urea and/or isocyanurate groups and having a hardblock content of more than 50% (hereinafter called matrix A); and a polymeric material which 1) has no groups which are able to form a urethane, urea or isocyanurate group with an isocyanate group, 2) is interpenetrating said matrix A, and 3) is the reaction product of a polyisocyanate and a polymer having an average molecular weight of more than 500 and one isocyanate-reactive group at an isocyanate index of 100-250 (hereinafter called polymeric material B); and wherein the relative amount of all ingredients used to make said matrix A and of said polymeric material B, on a weight basis, ranges from 10:90 to 90:10 and process for making such materials.

Abstract: A flame retardant polyurethane elastomer composition containing an oligomeric phosphate obtained by reaction of a trialkyl phosphate with phosphorous pentoxide and an epoxides is provided. In a preferred embodiment, the polyurethane elastomer is a spandex. A method to prepare a fiber or yarn of the flame retardant elastomer and a fabric containing the fiber or yarn is also provided.

Abstract: The present invention relates to the discovery of new class of hydrolysable amino acid derivatives and absorbable polyester amides, polyamides, polyepoxides, polyureas and polyurethanes prepared therefrom. The resultant absorbable polymers are useful for drug delivery, tissue engineering, tissue adhesives, adhesion prevention, bone wax formulations, medical device coatings, stents, stent coatings, highly porous foams, reticulated foams, wound care, cardiovascular applications, orthopedic devices, surface modifying agents and other implantable medical devices. In addition, these absorbable polymers should have a controlled degradation profile.

Abstract: Polymer polyols and dispersions are prepared by polymerizing certain starting materials in a continuous phase. The continuous phase includes a polyol containing hydroxylmethyl groups, which is derived from a fatty acid. The dispersed phase may be, for example, a vinyl polymer, a polyurea or a polyurethane-urea.

Abstract: There is provided a composition for forming a resist underlayer film not only having a large selection ratio of a dry etching rate but also exhibiting desired values of the k value and of the refractive index n at a short wavelength such as a wavelength of an ArF excimer laser. A resist underlayer film forming composition for lithography comprising: a linear polymer; and a solvent, wherein a backbone of the linear polymer has a unit structure in which 2,4-dihydroxy benzoic acid is introduced through an ester bond and an ether bond.

Abstract: The present invention is a method of manufacturing an eye lens material having a process in which a phosphorylcholine group-containing chemical compound represented by the following formula (1) is reacted and covalently bonded to the surface of an eye lens material having hydroxyl groups wherein the chemical compound represented by the following formula (2) is reacted and covalently bonded through ester-bonding to the eye lens material in an organic solvent. The object of the present invention is to provide an eye lens material that prevents protein adsorption and a method of manufacturing thereof.

Abstract: A thixotropic agent comprising a first polyurea reaction product of a first polyisocyanate with a first amine and a second polyurea reaction product of a second polyisocyanate with a second amine different from the first polyurea reaction product precipitated in the presence of the colloidal particles of the first reaction product.

Abstract: A curable polyimide resin composition containing a polyimide resin obtainable from by a reaction of a reaction mixture containing a diisocyanate compound, a carbonate group-containing diol compound and an imide compound having two terminal hydroxyhydrocarbyl groups gives a cured insulation film having improved characteristics.

Abstract: The present invention relates to cure accelerators useful for anaerobic curable compositions, such as adhesives and sealants. The cure accelerators are constructed as urethane/urea/thiourethane (meth)acrylate resins from diols and include a unit embraced within structure A where X is C1-20 alkyl, C2-20 alkenyl, or C7-20 alkaryl, any of which may be interrupted by one or more hereto atoms, and which are functionalized by at least one and preferably at least two groups selected from —OH, —NH2 or —SH and z is 1-3.

Abstract: The present invention is directed to a coating composition comprising polyurea formed from a reaction mixture comprising: (a) a first component comprising isocyanate, wherein said isocyanate comprises an isocyanate functional prepolymer formed from a reaction mixture comprising isocyanate and a material comprising a phosphorus-containing polyol; and (b) a second component comprising an amine.

Abstract: Block copolymer having improved compression set comprising 40-98 wt-% soft segment, 1.9-20 wt-% hard segment, and 0.05-3 wt-% monofunctional ionic endgroups. The incorporation of ionomers into diisocyanate-based thermoplastic polyurethane materials greatly improves compression set with little impact on the overall TPU formulation. A typical formulation for making the block copolymer contains 84.2% polydimethylsiloxane, 12.9% diisocyanate, 2.9% diamine chain extender, 0.15% sodium 2-[bis(2-hydroxyethyl)amino]ethylsulfonate, and 0.05% isethionic acid. The polymeric material may be configured, for instance, as a contact lens, prosthetic spinal nucleus, orthopedic bearing surface, gasket, or sealant.

Abstract: An aluminum chelate latent curing agent is configured such that an aluminum chelating agent and a specific arylsilane compound or a hydrolysate thereof are held in a polymer obtained by subjecting the aluminum chelating agent, the arylsilane compound, and a polyfunctional isocyanate compound to an emulsifying treatment, and then subjecting the polyfunctional isocyanate to interfacial polymerization. The aluminum chelating agent does not have an alkoxy group bonded to the aluminum. The arylsilane compound is a compound represented by the formula W. (Ar)mSi(OR)n ??(A) In the formula (A), m is 2 or 3, and the sum of m and n is 4. Ar represents an optionally-substituted aryl group. R represents a hydrogen atom, a methyl group, or an ethyl group. When n is two, the two Rs may be the same or different.

Abstract: The present invention provides a water-soluble crosslinkable polyurea prepolymer. The crosslinkable polyurea prepolymer of the invention is prepared by reacting an amine- or isocyanate-capped polyurea with a multifunctional compound having at least one one ethylenically unsaturated group and a function group coreactive with the capping amine or isocyanate groups of the amine- or isocyanate-capped polyurea. The amine- or isocyanate-capped polyurea is a copolymerization production of: (a) at least one poly(oxyalkylene)diamine, (b) optionally at least one organic di- or poly-amine, (c) optionally at least one diisocyanate, and (d) at least one polyisocyanate. The crosslinkable polyurea prepolymer of the invention can find use in economically producing contact lenses which have durable, highly elastic soft contact lenses with desired physical properties. In addition, the present invention provides method for making a medical device, preferably an ophthalmic device, more preferably a contact lens.

Abstract: A pharmaceutical controlled release composition in solid dosage form is provided which comprises (I) a water-swellable linear polymer obtainable by reacting together: (a) a dried polyethylene oxide; (b) a dried C5 to C20 diol; and (c) a Bifunctional diisocyanate; and (II) a releasable pharmaceutically active agent.

Abstract: Polymers whose surfaces are modified by endgroups that include amphipathic surface-modifying moieties. An amphipathic endgroup of a polymer molecule is an endgroup that contains at least two moieties of significantly differing composition, such that the amphipathic endgroup spontaneously rearranges its positioning in a polymer body to position the moiety on the surface of the body, depending upon the composition of the medium with which the body is in contact, when that re-positioning causes a reduction in interfacial energy. An example of an amphipathic surface-modifying endgroup is one that has both a hydrophobic moiety and a hydrophilic moiety in a single endgroup. For instance, a hydrophilic poly(ethylene oxide) terminated with a hydrophilic hydroxyl group is not surface active in air when the surface-modifying endgroup is bonded to a more hydrophobic base polymer.

Abstract: Star polymers prepared by reacting a highly branched polymer and either a lactone or lactam are disclosed. These star polymers find particular application as additives for powder coating compositions, to improve various performance properties thereof. Powder coating composition comprising the described star polymers are also disclosed.

Abstract: A moisture-curable silylated resin possessing improved storage stability and short cure time is obtained by reacting a prepolymer with a silylating reactant comprising silane (i) possessing three methoxy groups, silane (ii) possessing three alkoxy groups independently containing from 2 to 4 carbon atoms, and, optionally, silane (iii) possessing two methoxy groups and one alkoxy group of from 2 to 4 carbon atoms and/or silane (iv) possessing one methoxy group and two alkoxy groups independently containing from 2 to 4 carbon atoms.

Abstract: The invention provides a flame-retardant waterborne polyurethane dispersion. The dispersion includes: 1 to 15 parts by weight of a phosphorus flame retardant containing active hydrogen; 10 to 40 parts by weight of a diisocyanate; 30 to 80 parts by weight of a polyol; and 1 to 15 parts by weight of an active hydrogen-containing compound, which is capable of forming a hydrophilic group.

Abstract: Polymers whose surfaces are modified by endgroups that include amphipathic surface-modifying moieties. An amphipathic endgroup of a polymer molecule is an endgroup that contains at least two moieties of significantly differing composition, such that the amphipathic endgroup spontaneously rearranges its positioning in a polymer body to position the moiety on the surface of the body, depending upon the composition of the medium with which the body is in contact, when that re-positioning causes a reduction in interfacial energy. An example of an amphipathic surface-modifying endgroup is one that has both a hydrophobic moiety and a hydrophilic moiety in a single endgroup. For instance, a hydrophilic poly(ethylene oxide) terminated with a hydrophilic hydroxyl group is not surface active in air when the surface-modifying endgroup is bonded to a more hydrophobic base polymer.

Abstract: The present invention pertains to aqueous polyurethane-polyurea dispersions which are prepared by the acetone process using methyl acetate instead of ketones and are chain-extended using hydrazine or derivatives thereof, these dispersions having an improved stability towards thermal yellowing and a relatively low residual hydrazine/hydrazine derivative content.

Abstract: The present invention is a photoconductive element containing an electrically conductive support, an electrical barrier layer disposed over said electrically conductive support and a charge generation layer capable of generating positive charge carriers when exposed to actinic radiation disposed over the barrier layer. The barrier layer is formed from a blocked polyisocyanate containing tetracarbonylbisimide groups. The present invention also discloses a new composition of a blocked polyisocyanate containing tetracarbonylbisimide groups.

Abstract: The present invention relates to one-component moisture-curing compositions comprising at least one isocyanate-containing polyurethane polymer P which has a mean molecular weight of at least 4000 g/mol, and at least one polyaldimine ALD of the formula (I) or (II), where the content of isocyanate groups is at most 3.5% by weight, based on the sum of the isocyanate-containing constituents present in the composition. The compositions are suitable especially as sealants and are notable for good low-temperature performance.

Abstract: Processes for preparing siloxane-modified polyisocyanates, the processes comprising: providing a polyisocyanate reactant; and reacting the polyisocyanate reactant with a hydroxyl-containing siloxane having a number-average molecular weight of 200 to 3000 g/mol and an average OH functionality of greater than or equal to 1.8, and corresponding to the general formula (I): wherein X represents an aliphatic, unbranched or branched C1 to C20 radical optionally containing ether groups; R represents a hydroxyl-functional radical; R1 represents a hydrogen or an optionally heteroatom-containing C1 to C20 hydrocarbon radical; and n is 1 to 40; siloxane-modified polyisocyanates prepared thereby, and uses therefor.

Abstract: Disclosed is a room temperature curable silicon group-containing polymer composition containing a reactive silicon group-containing polymer (A) having a group represented by the formula (1) at an end of the main chain, which is obtained through a reaction between a polyoxypropylene polyol and a ?-isocyanate propyltrialkoxysilane, a curing catalyst (B), an amino-functional organosiloxane (C), and optionally an inorganic filler (D) which is surface-treated with glycol.

Abstract: An elastomeric composition includes a reaction product of an isocyanate component and a resin component comprising a polyol and a polyetheramine in the presence of a first catalyst comprising a metal and a second catalyst comprising an amine. An elastomeric system and a method of making an elastomer are provided. The method includes providing the isocyanate component and the resin component, combining the resin component and the isocyanate component in the presence of the first and second catalysts to form an elastomeric composition, applying the elastomeric composition to a mold having a mold cavity, curing the elastomeric composition to form the elastomer, and demolding the elastomer from the mold cavity. An article including a first layer formed from the elastomeric composition emits less than 100 ?g/g of volatile organic compounds over 0.5 hour at 90° C.

Abstract: The present invention provides a cationic electrodeposition coating composition having good appearance of coated film and high throwing power, and a method for making an amine-modified epoxy resin used for the cationic electrodeposition coating composition. The present invention relates to a method for making an amine-modified epoxy resin comprised in a cationic electrodeposition coating composition comprising the steps of: providing a half blocked isocyanate by reaction of an isocyanate compound with a blocking agent, preparing a blocked prepolymer by reaction of the half blocked isocyanate with a polyol, forming an epoxy resin containing oxazolidone ring by reaction of the blocked prepolymer with a diglycidyl ether type epoxy resin, chain-extending the epoxy resin containing oxazolidone ring with at least saturated or non-saturated hydrocarbon group containing dicarboxylic acid, and modifying the chain-extended epoxy resin with an amine.

Abstract: The present invention relates to an isocyanate-terminated composition having utility in the preparation of hydrophilic polyurethanes. The isocyanate composition has an isocyanate content of less than about 15 weight percent and comprises the reaction product of an aliphatic or aromatic polyisocyanate, or mixtures thereof; with a polyol composition that contains a polyether polyol derived from a molecule containing tertiary nitrogen.

Abstract: Star polymers prepared by reacting a highly branched polymer and either a lactone or lactam are disclosed. These star polymers find particular application as additives for powder coating compositions, to improve various performance properties thereof. Powder coating composition comprising the described star polymers are also disclosed.

Abstract: The present invention provides a cleaning blade member which can be excellently produced by molding and which exhibits small variation in physical properties with temperature, and excellent wear resistance. The cleaning blade member formed of a castable polyurethane member produced through hardening and molding a polyurethane composition containing at least a polyol, a polyisocyanate, and a diamino compound, wherein the diamino compound has a melting point of 80° C. or lower, the polyisocyanate is a blend of 4,4?-diphenylmethane diisocyanate (MDI) and 3,3-dimethylphenyl-4,4-diisocyanate (TODI), and the ratio of TODI in the entirety of polyisocyanate is 30 to 100% by weight.

Abstract: A method and apparatus for the removal of free, emulsified, or dissolved water from liquids of low volatility, such as oil, is shown. The liquid of low volatility is removed by contacting the fluid stream of concern with one side of a semi-permeable membrane. The membrane divides a separation chamber into a feed side into which the stream of fluid is fed, and a permeate side from which the water is removed. The permeate side of the chamber is maintained at a low partial pressure of water through presence of vacuum, or by use of a sweep gas.

Abstract: Golf ball compositions, and components formed therefrom, including trifunctional materials, such as trifunctional isocyanates, polyols, and amines, that have improved performance and durability characteristics, e.g., improved heat resistance, improved resiliency, and dimensional stability.

Abstract: High green strength reactive hot melt adhesives are prepared using relatively low levels of reactive acrylic, and may be prepared with one or more difunctionals having cyclic or polycyclic structures.

Abstract: A polyurethane composition comprising: A) from 3 to 35% by weight of a polymeric composition comprising 1) at least one polymer and 2) at least one thermoset in amounts of from 0.5 to 50% by weight, based on the sum of A1) and A2), prepared by reaction in the polymer matrix A1) of a) at least one starting component containing NH2 groups and b) at least one starting component containing NCO groups, a) and b) having simultaneously or independently a functionality of ?2 and at least one starting component having a functionality of >2 being present in amounts of from 0.5 to 100% by weight, based on the weight of A2); B) from 15 to 45% by weight in the polymeric composition A), based thereon, of at least one amorphous and/or crystalline polyester having an OH number of from 10 to 250 mg KOH/g; C) from 7 to 25% by weight in the polymeric composition A), based thereon, of at least one curing agent based on blocked polyisocyanates, isocyanurates and/or uretdiones having a functionality of at least 1.

Abstract: This invention relates to dendritically modified polyurethane, to a process for preparing the dendritically modified polyurethane and to uses thereof.

Abstract: The invention relates to a polymeric urea-urethane obtainable by first reacting a diisocyanate with a polyol to form a doubly NCO-terminated urethane prepolymer. Further reaction is subsequently carried out with a mixture of a primary monoamine and a primary diamine. After the second reaction the polymeric urea-urethane present is substantially free of isocyanate and of the monoamine and diamine used. It can be used as an agent for controlling the rheology of liquid polymers or polymer solutions.

Abstract: A method and apparatus for the removal of free, emulsified, or dissolved water from liquids of low volatility, such as oil, is shown. The liquid of low volatility is removed by contacting the fluid stream of concern with one side of a semi-permeable membrane. The membrane divides a separation chamber into a feed side into which the stream of fluid is fed, and a permeate side from which the water is removed. The permeate side of the chamber is maintained at a low partial pressure of water through presence of vacuum, or by use of a sweep gas.

Abstract: This invention relates to the process of preparation and application of a plural component, fast cure phenolic/polyurea elastomer coating co-polymer system. The disclosed coating system is prepared from the reaction of an isocyanate component and an amine terminated resin blend component. Each of the two components may individually or both contain a phenolic resin based product as part of the active hydrogen donation for the reaction with the isocyanate. These phenolic/polyurea co-polymers are characterized as having significantly improved chemical resistance and lower moisture vapor transmission through the coating system over conventional polyurea elastomer coating systems, thus making the coatings suitable for highly corrosive environments.

Abstract: Powder coating materials based on acidic polyesters, polyureas, crosslinkers, and other customary additives for coatings having a matt appearance.