Patent classifications
C08L11/00
Heat-resistant chlorine-containing crosslinked resin formed body and method for producing the same, silane master batch, master batch mixture and formed body thereof, and heat-resistant product
A production method comprising: (a) a step of melt-mixing a base resin containing a chlorinated polyethylene; an organic peroxide, an inorganic filler, and a silane coupling agent, in specific ratios, at a temperature equal to or higher than a decomposition temperature of the organic peroxide, to prepare a silane master batch; (b) a step of mixing the silane master batch obtained in the step (a) with a silanol condensation catalyst, and then forming the resultant mixture; and conducting at least one of the melt-mixing in the step (a) and the mixing in the step (b) is performed in the coexistence of a chloroprene rubber or a polyvinyl chloride; a heat-resistant chlorine-containing crosslinked resin formed body produced by the method, a silane master batch, a mixture and formed body thereof, and a heat-resistant product.
Heat-resistant chlorine-containing crosslinked resin formed body and method for producing the same, silane master batch, master batch mixture and formed body thereof, and heat-resistant product
A production method comprising: (a) a step of melt-mixing a base resin containing a chlorinated polyethylene; an organic peroxide, an inorganic filler, and a silane coupling agent, in specific ratios, at a temperature equal to or higher than a decomposition temperature of the organic peroxide, to prepare a silane master batch; (b) a step of mixing the silane master batch obtained in the step (a) with a silanol condensation catalyst, and then forming the resultant mixture; and conducting at least one of the melt-mixing in the step (a) and the mixing in the step (b) is performed in the coexistence of a chloroprene rubber or a polyvinyl chloride; a heat-resistant chlorine-containing crosslinked resin formed body produced by the method, a silane master batch, a mixture and formed body thereof, and a heat-resistant product.
FIRE-PROOFED ANTIVIBRATOR DEVICE FOR A RAILWAY APPLICATION
The invention relates to an anti-vibration device (100), for example intended for a railroad application, comprising: a first frame (10), a second frame (20), a shock absorbing structure (30) for the vibrations, situated between the two frames (10, 20), and at least one fire barrier layer (40) at least partially covering the shock absorbing structure (30);
characterized in that said at least one fire barrier layer (40) is a polychloroprene-based elastomer including at least one fire retardance agent chosen from among alumina trihydrate or magnesium hydroxide.
FIRE-PROOFED ANTIVIBRATOR DEVICE FOR A RAILWAY APPLICATION
The invention relates to an anti-vibration device (100), for example intended for a railroad application, comprising: a first frame (10), a second frame (20), a shock absorbing structure (30) for the vibrations, situated between the two frames (10, 20), and at least one fire barrier layer (40) at least partially covering the shock absorbing structure (30);
characterized in that said at least one fire barrier layer (40) is a polychloroprene-based elastomer including at least one fire retardance agent chosen from among alumina trihydrate or magnesium hydroxide.
Thermoplastic Elastomer Composition Comprising An Elastomer And A Non-Elastomeric Polyolefin Functionalized With An Anhydride Of An Organic Carboxylic Acid
A thermoplastic elastomer composition of an elastomer and a non-elastomeric polyolefin which is functionalized with an anhydride of an organic carboxylic acid is disclosed. Furthermore, the invention also relates to the use of a mixture of an elastomer and a cross-linking agent for the elastomer for producing a thermoplastic elastomer composition. A further subject of the invention is the use of a non-elastomeric polyolefin which is functionalized with an anhydride of an organic carboxylic acid for producing a thermoplastic elastomer composition. In addition, the invention relates to the use of a thermoplastic elastomer composition for producing an article/composite material with a polyamide. The invention also relates to a process for producing a thermoplastic elastomer composition as well as a composite material made of the thermoplastic elastomer composition with a polyamide.
Thermoplastic Elastomer Composition Comprising An Elastomer And A Non-Elastomeric Polyolefin Functionalized With An Anhydride Of An Organic Carboxylic Acid
A thermoplastic elastomer composition of an elastomer and a non-elastomeric polyolefin which is functionalized with an anhydride of an organic carboxylic acid is disclosed. Furthermore, the invention also relates to the use of a mixture of an elastomer and a cross-linking agent for the elastomer for producing a thermoplastic elastomer composition. A further subject of the invention is the use of a non-elastomeric polyolefin which is functionalized with an anhydride of an organic carboxylic acid for producing a thermoplastic elastomer composition. In addition, the invention relates to the use of a thermoplastic elastomer composition for producing an article/composite material with a polyamide. The invention also relates to a process for producing a thermoplastic elastomer composition as well as a composite material made of the thermoplastic elastomer composition with a polyamide.
METHOD FOR PRODUCING PURIFIED CHLOROPRENE-BASED-POLYMER LATEX
Provided is a method for producing purified chloroprene-based-polymer latex which enables efficiently removing a residual volatile organic substance from chloroprene-based-polymer latex while suppressing foaming and the deposition of aggregates. The method for producing purified chloroprene-based-polymer latex of the present invention has at least the following steps (I) to (III):
Step (I): a step of introducing chloroprene-based-polymer latex into a container beforehand,
Step (II): a step of removing a residual volatile organic substance in the chloroprene-based-polymer latex which satisfies specific requirements (1) to (4), and
Step (III): a step of collecting the latex from the container after performing the step (II) at least once, to thereby obtain purified chloroprene-based-polymer latex.
Block copolymer and production method for block copolymer
Disclosed is a block copolymer including one or more blocks of an acrylate polymer and one or more blocks of a chloroprene polymer, wherein the number average molecular weight of the block copolymer is 110,000 or more, the number average molecular weight of the block of a chloroprene polymer is 80,000 or more in total, and the block copolymer has a functional group with a structure represented by the following chemical formula (1) or (2): ##STR00001##
wherein in the chemical formula (1), R.sup.1 represents hydrogen, chlorine, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aryl group or a substituted, or unsubstituted heterocyclyl group.
Block copolymer and production method for block copolymer
Disclosed is a block copolymer including one or more blocks of an acrylate polymer and one or more blocks of a chloroprene polymer, wherein the number average molecular weight of the block copolymer is 110,000 or more, the number average molecular weight of the block of a chloroprene polymer is 80,000 or more in total, and the block copolymer has a functional group with a structure represented by the following chemical formula (1) or (2): ##STR00001##
wherein in the chemical formula (1), R.sup.1 represents hydrogen, chlorine, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aryl group or a substituted, or unsubstituted heterocyclyl group.
CHLOROPRENE/UNSATURATED NITRILE COPOLYMER, CHLOROPRENE/UNSATURATED NITRILE COPOLYMER COMPOSITION AND VULCANIZED MOLDED ARTICLE
A chloroprene-unsaturated nitrile copolymer having 3 to 20% by mass of a structural unit derived from an unsaturated nitrile monomer, in which the chloroprene-unsaturated nitrile copolymer has a peak at 5.80 to 6.00 ppm in a 1H-NMR spectrum as measured in a deuterochloroform solvent, and a ratio (A/B) of a peak area (A) at 5.80 to 6.00 ppm and a peak area (B) at 4.05 to 6.20 ppm is 0.6/100 to 1.1/100.