Abstract: Provided are a sulfur-modified chloroprene rubber with reduced exothermicity, a molding thereof, and a production method therefor. A sulfur-modified chloroprene rubber modified at the polymer terminals with at least one compound selected from tetramethylthiuram disulfide, tetraalkylthiuram disulfides with alkyl groups having a carbon number of 2 to 7 and dialkyldithiocarbamic acid salts with alkyl groups having a carbon number of 1 to 7, wherein there are peak tops at 3.55 to 3.61 ppm and at 3.41 to 3.47 ppm in 1H-NMR spectrum, as determined in deuterochloroform solvent, wherein the ratio (A/B) of the peak area (A) at 3.55 to 3.61 ppm to the peak area (B) at 4.2 to 6.5 ppm is 0.05/100 to 0.50/100, and the extract with ethanol/toluene azeotropic mixture, as specified by JIS K 6229, is 3.0 to 9.0 mass %.

Abstract: Provided are a sulfur-modified chloroprene rubber superior in adhesiveness to cable core and fibrous reinforcement material, a method for producing the same, and a molded body prepared from the same. A sulfur-modified chloroprene rubber is prepared in a polymerization step of mixing 100 parts by mass of 2-chloro-1,3-butadiene and 0.1 to 2.0 parts by mass of sulfur and emulsion-polymerizing the mixture to a monomer conversion rate in the range of 60 to 90% and in a plasticizing step of modifying the terminal of the polymer by adding an aqueous medium dispersion containing tetramethylthiuram disulfide in an amount of 10 to 70 mass % to the reaction solution after polymerization. The 1H-NMR spectrum of the sulfur-modified chloroprene rubber, as determined in deuterochloroform solvent, has two peak tops at 3.55 to 3.61 ppm and at 3.41 to 3.47 ppm, and the ratio (A/B) of peak area (A) at 3.55 to 3.61 ppm to peak area (B) at 4.2 to 6.5 ppm is 0.05/100 to 0.70/100.

Abstract: Provided are a sulfur-modified chloroprene rubber with reduced exothermicity, a molding thereof, and a production method therefor. A sulfur-modified chloroprene rubber modified at the polymer terminals with at least one compound selected from tetramethylthiuram disulfide, tetraalkylthiuram disulfides with alkyl groups having a carbon number of 2 to 7 and dialkyldithiocarbamic acid salts with alkyl groups having a carbon number of 1 to 7, wherein there are peak tops at 3.55 to 3.61 ppm and at 3.41 to 3.47 ppm in 1H-NMR spectrum, as determined in deuterochloroform solvent, wherein the ratio (A/B) of the peak area (A) at 3.55 to 3.61 ppm to the peak area (B) at 4.2 to 6.5 ppm is 0.05/100 to 0.50/100, and the extract with ethanol/toluene azeotropic mixture, as specified by JIS K 6229, is 3.0 to 9.0 mass %.

Abstract: A polychloroprene latex composition which has a low viscosity and which can be made to have a high solid content, obtained by emulsion polymerization of chloroprene alone or chloroprene and a monomer copolymerizable with chloroprene in the presence of a polyvinyl alcohol and a nonionic emulsifier, such as polyoxyethylene alkyl ether.

Abstract: A nonionic polychloroprene latex composition employing a polyvinyl alcohol as an emulsifier/dispersant has favorable chemical and mechanical stability but has a high viscosity, and therefore it has such drawbacks that its coating method is limited, and it is hardly made to have a high solid content. A polychloroprene latex composition which has a low viscosity and which can be made to have a high solid content, can be obtained by emulsion polymerization of chloroprene alone or chloroprene and a monomer copolymerizable with chloroprene in the presence of a polyvinyl alcohol and a nonionic emulsifier.

Abstract: A polychloroprene latex is provided with excellent adhesive strength, particularly for an EVA material, by dissolving an ethylene/vinyl acetate copolymer in a chloroprene monomer alone or in a mixture of a chloroprene monomer and a monomer copolymerizable with chloroprene to prepare a monomer solution, which is emulsified and dispersed in an aqueous solution containing an emulsifier and/or a dispersant, followed by polymerization to produce a polychloroprene latex. The obtained polychloroprene latex can provide improved adhesive strength particularly for an EVA material.

Abstract: A nonionic polychloroprene latex composition employing a polyvinyl alcohol as an emulsifier/dispersant has favorable chemical and mechanical stability but has a high viscosity, and therefore it has such drawbacks that its coating method is limited, and it is hardly made to have a high solid content. A polychloroprene latex composition which has a low viscosity and which can be made to have a high solid content, can be obtained by emulsion polymerization of chloroprene alone or chloroprene and a monomer copolymerizable with chloroprene in the presence of a polyvinyl alcohol and a nonionic emulsifier.

Abstract: To provide a polychloroprene latex providing excellent adhesive strength particularly for an EVA material, when used as a material for an aqueous adhesive. An ethylene/vinyl acetate copolymer is dissolved in a chloroprene monomer alone or in a mixture of a chloroprene monomer and a monomer copolymerizable with chloroprene to prepare a monomer solution, which is emulsified and dispersed in an aqueous solution containing an emulsifier and/or a dispersant, followed by polymerization to produce a polychloroprene latex. The obtained polychloroprene latex can provide improved adhesive strength particularly for an EVA material.