Patent classifications
C08C19/38
Recyclable cross-linked diene elastomers comprising furanyl groups and precursors thereof
The present invention concerns new precursors of recyclable cross-linked diene elastomers comprising at least one furanyl group along the chain and comprising chain-end units with furanyl groups, their use in the preparation of said recyclable elastomers and their process of preparation. The invention also concerns new recyclable cross-linked diene elastomers, their preparation process and their uses.
Recyclable cross-linked diene elastomers comprising furanyl groups and precursors thereof
The present invention concerns new precursors of recyclable cross-linked diene elastomers comprising at least one furanyl group along the chain and comprising chain-end units with furanyl groups, their use in the preparation of said recyclable elastomers and their process of preparation. The invention also concerns new recyclable cross-linked diene elastomers, their preparation process and their uses.
Farnesene-based polymers and liquid optically clear adhesive compositions incorporating the same
A low viscosity polymer having a linear or branched backbone derived from farnesene monomers and at least one terminal-end functionalized with a hydroxyl group. This polymer may be further hydrogenated to reduce unsaturation and acrylated, such that it may be incorporated into a LOCA composition. The LOCA composition may be used in a laminated screen assembly, such as a touch screen, for electronic devices by adhering the LOCA composition between an optically transparent layer, such as a cover glass, and a display. The cured LOCA composition has a refractive index similar to the optically transparent layer. A method of making the low viscosity polymer for the LOCA composition includes anionically polymerizing farnesene monomers, quenching a living end of the polymer to provide the hydroxyl-terminated polymer; hydrogenating the hydroxyl-terminated polymer; and reacting the at least partially saturated hydroxyl-terminated polymer with at least one reagent to provide an acrylate terminated hydrogenated polymer.
Farnesene-based polymers and liquid optically clear adhesive compositions incorporating the same
A low viscosity polymer having a linear or branched backbone derived from farnesene monomers and at least one terminal-end functionalized with a hydroxyl group. This polymer may be further hydrogenated to reduce unsaturation and acrylated, such that it may be incorporated into a LOCA composition. The LOCA composition may be used in a laminated screen assembly, such as a touch screen, for electronic devices by adhering the LOCA composition between an optically transparent layer, such as a cover glass, and a display. The cured LOCA composition has a refractive index similar to the optically transparent layer. A method of making the low viscosity polymer for the LOCA composition includes anionically polymerizing farnesene monomers, quenching a living end of the polymer to provide the hydroxyl-terminated polymer; hydrogenating the hydroxyl-terminated polymer; and reacting the at least partially saturated hydroxyl-terminated polymer with at least one reagent to provide an acrylate terminated hydrogenated polymer.
Rubber Composition for Tires and Pneumatic Tire
A rubber composition for tires of the present technology contains a diene rubber, silica, and a predetermined alkyltrialkoxysilane; the diene rubber containing a butadiene rubber and a particular conjugated diene rubber, a content of the butadiene rubber in the diene rubber being 20 mass % or greater and a content of the particular conjugated diene rubber in the diene rubber being from 30 to 80 mass %; an average glass transition temperature of the diene rubber being from −65 to −45° C.; the particular conjugated diene rubber being a conjugated diene rubber produced by a particular production method and having predetermined ranges of aromatic vinyl unit content, vinyl bond content, and weight average molecular weight.
Rubber Composition for Tires and Pneumatic Tire
A rubber composition for tires of the present technology contains a diene rubber, silica, and a predetermined alkyltrialkoxysilane; the diene rubber containing a butadiene rubber and a particular conjugated diene rubber, a content of the butadiene rubber in the diene rubber being 20 mass % or greater and a content of the particular conjugated diene rubber in the diene rubber being from 30 to 80 mass %; an average glass transition temperature of the diene rubber being from −65 to −45° C.; the particular conjugated diene rubber being a conjugated diene rubber produced by a particular production method and having predetermined ranges of aromatic vinyl unit content, vinyl bond content, and weight average molecular weight.
Rubber Composition for Tires and Pneumatic Tire
A rubber composition for tires of the present technology contains a diene rubber, silica, a silane coupling agent, a fatty acid metal salt, and a predetermined alkyltrialkoxysilane; the diene rubber containing 60 mass % or greater of a modified conjugated diene rubber and 30 mass % or greater of a particular conjugated diene rubber which corresponds to a part or all of the modified conjugated diene rubber; an average glass transition temperature of the diene rubber being from −45 to −20° C.; the particular conjugated diene rubber being a conjugated diene rubber produced by a particular production method and having predetermined ranges of aromatic vinyl unit content, vinyl bond content, and weight average molecular weight.
Rubber Composition for Tires and Pneumatic Tire
A rubber composition for tires of the present technology contains a diene rubber, silica, a silane coupling agent, a fatty acid metal salt, and a predetermined alkyltrialkoxysilane; the diene rubber containing 60 mass % or greater of a modified conjugated diene rubber and 30 mass % or greater of a particular conjugated diene rubber which corresponds to a part or all of the modified conjugated diene rubber; an average glass transition temperature of the diene rubber being from −45 to −20° C.; the particular conjugated diene rubber being a conjugated diene rubber produced by a particular production method and having predetermined ranges of aromatic vinyl unit content, vinyl bond content, and weight average molecular weight.
SILANE MODIFIED STYRENE BUTADIENE COPOLYMER FOR HIGH PERFORMANCE IN DRY ADHERENCE, WET ADHERENCE AND ROLLING RESISTANCE
A curable rubber composition is provided which includes a high molecular weight diene elastomer; an optional carbon black composition; a silica composition; and a silane terminated copolymer different from the high molecular weight diene elastomer including conjugated dienes and vinyl aromatics as polymerized monomers. The silane terminated copolymer has at least one terminal end modified with at least one silane group and the silane terminated copolymer has a number average molecular weight of from 1,000 g/mol to 40,000 g/mol. A method for producing a rubber composition for use in a tire is provided. The method includes forming a composition by mixing the silane terminated copolymer modified with at least one silane group, a silica composition, a high molecular weight diene elastomer different from the silane terminated copolymer, and optionally a carbon black composition; and curing the composition.
Method for producing end-modified polybutadiene or end-modified hydrogenated polybutadiene and composition containing same
It is an object of the present invention to provide a method for producing a terminal-modified polybutadiene or terminal-modified hydrogenated polybutadiene that does not become colored or white and turbid, without using an organotin compound. The production method of the present invention includes reacting an acrylate or methacrylate represented by formula (I), a diisocyanate compound represented by formula (II), and a polybutadiene or hydrogenated polybutadiene having a hydroxyl group at a polymer terminal, represented by formula (III), in the presence of at least one selected from an organoaluminum compound and an organozinc compound (with the proviso that zinc naphthenate is excluded). ##STR00001##