The present disclosure provides a room-temperature-vulcanizing (RTV) silicone rubber foam with ablation resistance and high-efficiency heat insulation and a preparation method thereof. In the present disclosure, hydroxyl-terminated polydimethylsiloxane, vinyl-terminated polydimethylsiloxane, a catalyst, an inhibitor, a ceramifiable emulsion foaming agent, a functionalized ceramic filler, and a heat-resistant additive are placed in a planetary stirring tank, and stirred to obtain a base rubber A. The hydroxyl-terminated polydimethylsiloxane, the vinyl-terminated polydimethylsiloxane, a hydrogen-containing silicone oil, a functionalized low-melting glass powder, and functionalized hexagonal boron nitride are placed in the planetary stirring tank, and stirred to obtain a base rubber B. The base rubber B is transferred to the base rubber A, vulcanization is conducted, followed by after vulcanization in an oven to obtain a final product.

The present disclosure provides a room-temperature-vulcanizing (RTV) silicone rubber foam with ablation resistance and high-efficiency heat insulation and a preparation method thereof. In the present disclosure, hydroxyl-terminated polydimethylsiloxane, vinyl-terminated polydimethylsiloxane, a catalyst, an inhibitor, a ceramifiable emulsion foaming agent, a functionalized ceramic filler, and a heat-resistant additive are placed in a planetary stirring tank, and stirred to obtain a base rubber A. The hydroxyl-terminated polydimethylsiloxane, the vinyl-terminated polydimethylsiloxane, a hydrogen-containing silicone oil, a functionalized low-melting glass powder, and functionalized hexagonal boron nitride are placed in the planetary stirring tank, and stirred to obtain a base rubber B. The base rubber B is transferred to the base rubber A, vulcanization is conducted, followed by after vulcanization in an oven to obtain a final product.

A nitrile rubber-based composition comprising 1,000 to 2,500 parts by weight of a magnetic powder or silylated magnetic powder having a compressed density of 3.4 to 3.7 g/cm.sup.3, 0.5 to 20 parts by weight of alkoxyalkylsilane, and 8 to 40 parts by weight of a plasticizer, based on 100 parts by weight of nitrile rubber, hydrogenated nitrile rubber, or blend rubber thereof. The nitrile rubber-based composition that does not cause deterioration in roll processability and in adhesion between an adhesive applied to a metal plate and the rubber, even when a magnetic powder is added at a ratio as high as 1,000 parts by weight or more based on 100 parts by weight of nitrile rubber, hydrogenated nitrile rubber, or blend rubber thereof.

A nitrile rubber-based composition comprising 1,000 to 2,500 parts by weight of a magnetic powder or silylated magnetic powder having a compressed density of 3.4 to 3.7 g/cm.sup.3, 0.5 to 20 parts by weight of alkoxyalkylsilane, and 8 to 40 parts by weight of a plasticizer, based on 100 parts by weight of nitrile rubber, hydrogenated nitrile rubber, or blend rubber thereof. The nitrile rubber-based composition that does not cause deterioration in roll processability and in adhesion between an adhesive applied to a metal plate and the rubber, even when a magnetic powder is added at a ratio as high as 1,000 parts by weight or more based on 100 parts by weight of nitrile rubber, hydrogenated nitrile rubber, or blend rubber thereof.

An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): about 30 to about 50 phr of polybutadiene having a cis-1,4 linkage content of at least 95%; about 40 to about 70 phr of styrene/butadiene copolymer; about 0 to about 20 phr of natural rubber or polyisoprene; about 0 to about 30 phr of a processing oil; about 10 to about 30 phr of a hydrocarbon resin; about 50 to about 75 phr of a filler; a curative agent; an antioxidant; a silane coupling agent; and about 5 to about 30 phr of a butyl copolymer rubber containing about 85 to about 99.5 mol % C.sub.4-C.sub.7 isoolefin(s) and from about 0.5 to about 15 mol % C.sub.4-C.sub.14 conjugated dienes.

An elastomeric composition is disclosed. The elastomeric composition includes, per 100 parts by weight of rubber (phr): about 30 to about 50 phr of polybutadiene having a cis-1,4 linkage content of at least 95%; about 40 to about 70 phr of styrene/butadiene copolymer; about 0 to about 20 phr of natural rubber or polyisoprene; about 0 to about 30 phr of a processing oil; about 10 to about 30 phr of a hydrocarbon resin; about 50 to about 75 phr of a filler; a curative agent; an antioxidant; a silane coupling agent; and about 5 to about 30 phr of a butyl copolymer rubber containing about 85 to about 99.5 mol % C.sub.4-C.sub.7 isoolefin(s) and from about 0.5 to about 15 mol % C.sub.4-C.sub.14 conjugated dienes.

An antimicrobial coating composition is disclosed. The composition delivers several orders of magnitude improvement in the reduction of infectious materials (i.e., microbial substances, including bacteria, fungus, germs, and other pathogens). An advanced high performance antimicrobial coating composition that is able to eliminate and reduce the bacteria and germ count at a log reduction of greater than 5 within 10 minutes of exposure.

An antimicrobial coating composition is disclosed. The composition delivers several orders of magnitude improvement in the reduction of infectious materials (i.e., microbial substances, including bacteria, fungus, germs, and other pathogens). An advanced high performance antimicrobial coating composition that is able to eliminate and reduce the bacteria and germ count at a log reduction of greater than 5 within 10 minutes of exposure.

Described is a method for the production of a moisture curable composition whereby the reactive end groups of a reactive polymer are reacted with a cross-linking agent for forming a prepolymer, whereby the method is operated in batch mode and the production of the prepolymer occurs in a mixing vessel, characterized in that the reactive polymer and the cross-linking agent, as well as the additional ingredients necessary for the production step in the mixing vessel, are introduced into the closed mixing vessel and react without opening the mixing vessel, and the mixing takes place without opening the mixing vessel, and the product is removed from the mixing vessel without opening the mixing vessel.

Described is a method for the production of a moisture curable composition whereby the reactive end groups of a reactive polymer are reacted with a cross-linking agent for forming a prepolymer, whereby the method is operated in batch mode and the production of the prepolymer occurs in a mixing vessel, characterized in that the reactive polymer and the cross-linking agent, as well as the additional ingredients necessary for the production step in the mixing vessel, are introduced into the closed mixing vessel and react without opening the mixing vessel, and the mixing takes place without opening the mixing vessel, and the product is removed from the mixing vessel without opening the mixing vessel.