Patent classifications
C08G18/44
Transparent conducting film laminate and processing method thereof
Provided are a transparent conducting film laminate to which a curl generated during a heating step and after the heating step can be controlled, and a method for processing the same. A transparent conducting film laminate comprises a transparent conducting film 20 and a carrier film 10 stacked thereon, wherein the transparent conducting film 20 comprises a transparent resin film 3, transparent conducting layer 4, and an overcoat layer 5 stacked in this order, the transparent resin film 3 having a thickness T.sub.1 of 5 to 25 μm and being made of an amorphous cycloolefin-based resin, the carrier film 10 is releasably stacked on the other main face, the face opposite to the face having the transparent conducting layer 4, of the transparent resin film 3 with an adhesive agent layer 2 therebetween, and a protection film 1 has a thickness T.sub.2 which is 5 times or more of the thickness T.sub.1 of the transparent resin film 3 and is 150 μm or less, and is made of polyester having an aromatic ring in its molecular backbone.
Synthetic leather and method for producing the same
A synthetic leather comprising a substrate, a skin layer that is disposed on one main surface of the substrate, and an anti-stain layer that is disposed to cover the skin layer. The anti-stain layer contains a base resin that comprises silicon and a unit derived from a compound that has a urethane bond. In the anti-stain layer, a fluorine atom/silicon atom atomic ratio, which is a proportion of a fluorine atom to the silicon atom, is 0.01 or less. A first color difference ΔE1* between before and after a stain adhesion test performed on the synthetic leather rubbed under a specific condition is 5 or less.
HIGH DIELECTRIC BREAKDOWN STRENGTH RESINS
A method to prepare an oligomer which includes a plurality of pendent alkenyl groups, where the method reacts a copolymer formed by copolymerizing styrene and allyl alcohol comprising a polyhydroxy oligomer wherein n is between about 3 and about 50, and having a structure:
##STR00001##
with an isocyanate having a structure:
##STR00002##
to give a urethane-modified copolymer having a structure:
##STR00003##
Photopolymerizable compositions including a polyurethane methacrylate polymer prepared using a polycarbonate diol, articles, and methods
The present disclosure provides a photopolymerizable composition. The photopolymerizable composition includes a) 40-60 parts by weight of a monofunctional (meth)acrylate monomer, per 100 parts of the total photopolymerizable composition; b) a photoinitiator; and c) a polymerization reaction product of components. A cured homopolymer of the monofunctional (meth)acrylate monomer has a glass transition temperature of 125 degrees Celsius or greater. The polymerization reaction product of components includes i) a diisocyanate; ii) a hydroxy functional methacrylate; iii) a polycarbonate diol; and iv) a catalyst. The polymerization reaction product includes a polyurethane methacrylate polymer. Often, the polyurethane methacrylate polymer has a weight average molecular weight of 8,000 g/mol or greater. The present disclosure further provides an article and methods thereof.
Photopolymerizable compositions including a polyurethane methacrylate polymer prepared using a polycarbonate diol, articles, and methods
The present disclosure provides a photopolymerizable composition. The photopolymerizable composition includes a) 40-60 parts by weight of a monofunctional (meth)acrylate monomer, per 100 parts of the total photopolymerizable composition; b) a photoinitiator; and c) a polymerization reaction product of components. A cured homopolymer of the monofunctional (meth)acrylate monomer has a glass transition temperature of 125 degrees Celsius or greater. The polymerization reaction product of components includes i) a diisocyanate; ii) a hydroxy functional methacrylate; iii) a polycarbonate diol; and iv) a catalyst. The polymerization reaction product includes a polyurethane methacrylate polymer. Often, the polyurethane methacrylate polymer has a weight average molecular weight of 8,000 g/mol or greater. The present disclosure further provides an article and methods thereof.
Chafe layer for a fluid conduit, fluid conduit, method for producing a fluid conduit and use of a polyurethane as a chafe layer and use of an ethylene copolymer as an additive
A chafe layer for a fluid conduit, wherein the chafe layer consists of thermoplastic polyurethane which contains a polyol, in particular a short-chained, diol as a chain extender and isocyanate. The polyol is a polycarbonate. A fluid conduit, a method for producing a fluid conduit as well as the use of a polyurethane and the use of an ethylene copolymer as an additive.
Chafe layer for a fluid conduit, fluid conduit, method for producing a fluid conduit and use of a polyurethane as a chafe layer and use of an ethylene copolymer as an additive
A chafe layer for a fluid conduit, wherein the chafe layer consists of thermoplastic polyurethane which contains a polyol, in particular a short-chained, diol as a chain extender and isocyanate. The polyol is a polycarbonate. A fluid conduit, a method for producing a fluid conduit as well as the use of a polyurethane and the use of an ethylene copolymer as an additive.
BIOCOMPATIBLE ADHESIVES AND METHODS OF MANUFACTURE THEREOF
A biocompatible adhesive is provided comprising one or more water insoluble compounds of structure (1) wherein B is an oligomer derived from a polyester, polyether, polyalkylene glycol, polysilicone or polycarbonate with a MW<10,000 g/mol, Linker L is a urethane, urea bond, or amide bond; Linker L′ is a urethane or urea bond, A is a chain extender of Mw≤3000 g/mol comprising substituted or unsubstituted alkyl, cycloalkyl and/or aromatic groups, W is a terminal adhesive benzene-1,2-diol derivative or a terminal adhesive benzene-1,2,3-diol derivative, m is 0 or 1; and n is 0, 1, 2, 3 or 4; or a cross-linked polymer formed from said compounds. The compound(s) have a Tg lower than 25° C. The biocompatible adhesive is suitable for use without solvent.
AQUEOUS POLYURETHANE DISPERSIONS
The present invention relates to an aqueous polyurethane dispersion, a method for the preparation thereof, a product comprising the same, and use thereof for a coating composition, an impregnating composition, an adhesive or a sealant. The aqueous polyurethane dispersion comprises a polyurethane obtained by reacting a system comprising the following components: A1) at least one polyisocyanate having an isocyanate functionality of not less than 2; A2) at least two different polytetramethylene ether glycols A2a) and A2b), the A2a) having a number average molecular weight of not more than 1500 g/mol, the A2b) having a number average molecular weight of more than 1500 g/mol; and A3) at least one anionic or potentially anionic hydrophilic agent having a number average molecular weight of 32 g/mol to 400 g/mol and containing hydroxyl and carboxyl functions; B) at least one amino-functional anionic or potentially anionic hydrophilic agent; and C) at least one amino-functional compound having a number average molecular weight of 32 g/mol to 400 g/mol and containing no hydrophilic group; wherein the ratio of the number average molecular weight of the A2a) to the number average molecular weight of the A2b) is 1:9 to less than 1:1, and the weight of the A3) amounts to 20% to 70% of the weight of the hydrophilic agents of the system, wherein the hydrophilic agents of the system are components A3 and B.
Organic-inorganic hybrid material, fabrication process of the same and its starting material
An organic-inorganic hybrid material is disclosure. The organic-inorganic hybrid material contains 5˜50 wt % of inorganic compounds and has a characteristic peak at 1050±50 cm.sup.−1 in FTIR spectrum. Furthermore, the invention also provides a fabricating process of the organic-inorganic hybrid material as well as its starting material “isocyanates”. In particular, the isocyanates are prepared from carbonate containing compounds and amines.