Patent classifications
C08F2810/30
Heavy-duty tire rubber compositions and tires
The invention provides a heavy-duty tire rubber composition excellent in wet grip performance and steering stability, and a tire tread, a bead filler, a tire belt and a heavy-duty tire which each partially include the composition. The heavy-duty tire rubber composition includes 100 parts by mass of a solid rubber (A), 0.1 to 50 parts by mass of a modified liquid diene rubber (B) having a functional group derived from a silane compound with a specific structure, and 20 to 200 parts by mass of a filler (C), the modified liquid diene rubber (B) satisfying the following (i) and (ii): (i) the weight average molecular weight (Mw) is not less than 1,000 and not more than 120,000, and (ii) the vinyl content is not less than 30 mol % and less than 70 mol %.
Radiopaque polymers
A hydrophilic polymer comprising pendent groups of the formula I: Wherein: W is independently selected from —OH, —COOH, —SO.sub.3H, —OPO.sub.3H, —O—(C.sub.1-4alkyl), —O—(C.sub.1-4alkyl)OH, —O—(C.sub.1-4alkyl)R.sup.2, —O—(C.sub.2H.sub.5O).sub.qR.sup.1—(C═O)—O—C.sub.1-4alkyl and —O—(C═O)C.sub.1-4alkyl; or a group —BZ; wherein —OH, COOH, O—PO.sub.3H and SO.sub.3H maybe in the form of a pharmaceutically acceptable salt; wherein: B is a bond, or a straight branched alkanediyl, oxyalkylene, alkylene oxaalkylene, or alkylene (oligooxalkylene) group, optionally containing one or more fluorine substituents; and Z is an ammonium, phosphonium, or sulphonium phosphate or phosphonate ester zwitterionic group; X is either a bond or a linking group having 1 to 8 carbons and optionally 1 to 4 heteroatoms selected from O, N and S; G is a coupling group through which the group of the formula I is coupled to the polymer and is selected from ether, ester, amide, carbonate, carbamate, 1,3 dioxolone, and 1,3 dioxane; R.sup.1 is H or C.sub.1-4 alkyl; R.sup.2 is —COOH, —SO.sub.3H, or —OPO.sub.3H.sub.2 q is an integer from 1 to 4; n is an integer from 1 to 4; p is an integer from 1 to 3; and n+p is from 2 to 5; and wherein —COOH, —OPO.sub.3H.sub.2 and —SO.sub.3H as well as phenolic —OH maybe in the form of a pharmaceutically acceptable salt.
PHOTOPOLYMERIZABLE BLOCK POLYMERS AND METHODS OF PRODUCING AND USING THE SAME
Provided herein are curable compositions for use in a high temperature lithography-based photopolymerization process, and telechelic block polymers and methods of using such polymers in curable compositions to produce medical devices such as orthodontic appliances comprising the polymeric compositions comprising the telechelic block polymers.
Method for the production of functionalized partially hydrolyzed polyvinyl acetate
A method for the production of functionalized partially hydrolyzed polyvinyl acetate comprising vinyl alcohol, vinylacetate and functionalized vinyl alcohol units by reacting in a melt a partially hydrolyzed polyvinyl acetate as component A with a reactive compound carrying at least one ethylenically unsaturated group and at least one reactive group reactive with hydroxyl or acetate groups as component B, in the presence of at least one stabilizer as component C and in the presence of at least one catalyst selected from the group consisting of tertiary amines and nitrogen-containing heterocycles as component D, the method comprising the steps: feeding the components into a mixing device capable of heating, melting and mixing components A, B, C and D, heating, melting and mixing components A, B, C and D in the device to give a melt and reacting components A and B in the melt.
Poly(vinyl alcohol)-based resin, dispersing agent and dispersing agent for suspension
An object of the present invention is to provide a PVA-based resin having a small distribution in degree of heat treatment in which the degree of heat treatment does not depend on a particle diameter. The polyvinyl alcohol-based resin of the present invention has an absorbance at 280 nm of 0.3 or more when being made to a 0.1 wt % aqueous solution and satisfies the following Formula (1): 0.9≤X.sub.1/Y.sub.1≤1.2 (in Formula (1), X.sub.1 represents an absorbance at 320 nm of a 0.1 wt % aqueous solution of a polyvinyl alcohol-based resin having a particle diameter larger than 1000 μm and 1680 μm or less, and Y.sub.1 represents an absorbance at 320 nm of a 0.1 wt % aqueous solution of a polyvinyl alcohol-based resin having a particle diameter larger than 212 μm and 500 μm or less).
Dual-cure method and system for fabrication of 3D polymeric structures cross-reference to earlier applications
A dual-cure method for forming a solid polymeric structure is provided. An end-capped, imide-terminated prepolymer is combined with at least one photopolymerisable olefinic monomer, at least one photoinitiator, and a diamine, to form a curable resin composition, which, in a first step, is irradiated under conditions effective to polymerize the at least one olefinic monomer, thus forming a scaffold composed of the prepolymer and the polyolefin with the diamine trapped therein. The irradiated composition is then thermally treated at a temperature effective to cause a transimidization reaction to occur between the prepolymer and the diamine, thereby releasing the end caps of the prepolymer and providing the solid polymeric structure. A curable resin composition comprising an end-capped, imide-terminated prepolymer, at least one photopolymerisable olefinic monomer, at least one photoinitiator, and a diamine, is also provided, as are related methods of use.
Post-Polymerization Functionalization of Pendant Functional Groups
Modification of functional groups along a polymer backbone to render the groups activatable upon exposure to actinic radiation is described. The polymers are typically controlled architecture polymers. Also described are adhesives containing the modified architectured polymers and related methods of use.
Recycle feedstocks for on-demand article manufacturing
A method of recycling a polymer structure includes converting a first polymer structure into feedstock. The first polymer structure comprises particles that are bonded to one another by chemical click bonds to form a first shape. The first polymer structure is converted into feedstock particles by breaking the click bonds. The feedstock particles are formed into a second shape, and the feedstock particles are chemically click-bonded together to form a second polymer structure having a second shape. Breaking the click bonds may include heating the particles. The structures may be formed by causing first particles having dienes to chemically bond to dienophiles of second particles.
Dual-cure method and system for fabrication of 3D polymeric structures cross-reference to earlier applications
A dual-cure method for forming a solid polymeric structure is provided. An end-capped, imide-terminated prepolymer is combined with at least one photopolymerisable olefinic monomer, at least one photoinitiator, and a diamine, to form a curable resin composition, which, in a first step, is irradiated under conditions effective to polymerize the at least one olefinic monomer, thus forming a scaffold composed of the prepolymer and the polyolefin with the diamine trapped therein. The irradiated composition is then thermally treated at a temperature effective to cause a transimidization reaction to occur between the prepolymer and the diamine, thereby releasing the end caps of the prepolymer and providing the solid polymeric structure. A curable resin composition comprising an end-capped, imide-terminated prepolymer, at least one photopolymerisable olefinic monomer, at least one photoinitiator, and a diamine, is also provided, as are related methods of use.
PROCESS FOR PREPARING A DENTAL RESIN-MODIFIED GLASS IONOMER COMPOSITION
The present invention relates to a process for the preparation of a dental resin-modified glass ionomer composition comprising a polymerizable polyacidic polymer, wherein the process comprises the following steps as further defined in claim 1.