A nano-silver dispersion and a preparation method thereof is disclosed. The method, includes: mixing γ-aminopropyltriethoxysilane, polyvinylpyrrolidone, sodium lauryl sulfate, silver nitrate and water, and conducting a chelation, to obtain a chelating dispersion, wherein before the mixing, the γ-aminopropyltriethoxysilane is exposed to the air for less than 5 min; and dropwise adding a sodium borohydride solution into the chelating dispersion, to obtain a mixture, and subjecting the mixture to an oxidation-reduction reaction, to obtain the nano-silver dispersion.

A nano-silver dispersion and a preparation method thereof is disclosed. The method, includes: mixing γ-aminopropyltriethoxysilane, polyvinylpyrrolidone, sodium lauryl sulfate, silver nitrate and water, and conducting a chelation, to obtain a chelating dispersion, wherein before the mixing, the γ-aminopropyltriethoxysilane is exposed to the air for less than 5 min; and dropwise adding a sodium borohydride solution into the chelating dispersion, to obtain a mixture, and subjecting the mixture to an oxidation-reduction reaction, to obtain the nano-silver dispersion.

Embodiments of the present invention provide a functionalized processing aid represented by the following Chemical Formula 1 in which a silane-based compound and a cardanol-derived structure are combined, a preparation method thereof, and a rubber composition including the same:

(R.sub.1).sub.3Si—R.sub.2—Z-(E).sub.n  [Chemical Formula 1] in Chemical Formula 1, the definitions of R.sub.1, R.sub.2, Z, E, and n are as described in the specification.

Embodiments of the present invention provide a functionalized processing aid represented by the following Chemical Formula 1 in which a silane-based compound and a cardanol-derived structure are combined, a preparation method thereof, and a rubber composition including the same:

(R.sub.1).sub.3Si—R.sub.2—Z-(E).sub.n  [Chemical Formula 1] in Chemical Formula 1, the definitions of R.sub.1, R.sub.2, Z, E, and n are as described in the specification.

It has been unexpected found that silylated triglyceride oils can be incorporated into tire tread rubber formulations that include reinforcing fillers to provide improved wet traction characteristic, rolling resistance, and tread-wear without compromising cured stiffness (dry traction) and ultimate properties (chip/chunk resistance). The level of silica coupling agent needed in such formulation can also typically reduced. The present invention more specifically discloses a rubber formulation which is comprised of (1) a rubbery polymer; (2) a reinforcing filler, such as silica or carbon black; and (3) a silylated triglyceride oil. The silylated triglyceride oil will include silyl groups of the structural formula: —(CH.sub.2).sub.n—Si(OR).sub.3, wherein n represents an integer within the range of 1 to 8, and wherein R represents an alkyl group containing from 1 to 8 carbon atoms.

It has been unexpected found that silylated triglyceride oils can be incorporated into tire tread rubber formulations that include reinforcing fillers to provide improved wet traction characteristic, rolling resistance, and tread-wear without compromising cured stiffness (dry traction) and ultimate properties (chip/chunk resistance). The level of silica coupling agent needed in such formulation can also typically reduced. The present invention more specifically discloses a rubber formulation which is comprised of (1) a rubbery polymer; (2) a reinforcing filler, such as silica or carbon black; and (3) a silylated triglyceride oil. The silylated triglyceride oil will include silyl groups of the structural formula: —(CH.sub.2).sub.n—Si(OR).sub.3, wherein n represents an integer within the range of 1 to 8, and wherein R represents an alkyl group containing from 1 to 8 carbon atoms.

A radiation-sensitive resin composition capable of forming a resin film for which development residue formation is sufficiently inhibited and that has excellent extensibility. The radiation-sensitive resin composition contains: a cycloolefin polymer (A-1) including a protonic polar group; a cycloolefin polymer (A-2) including a protonic polar group; a difunctional epoxy compound (B); and a radiation-sensitive compound (C). The cycloolefin polymer (A-1) has a weight-average molecular weight of not less than 1,000 and less than 10,000, and the cycloolefin polymer (A-2) has a weight-average molecular weight of not less than 10,000 and not more than 100,000. Content of the cycloolefin polymer (A-2) is not less than 5 mass % and not more than 55 mass % of total content of the cycloolefin polymer (A-1) and the cycloolefin polymer (A-2).

A radiation-sensitive resin composition capable of forming a resin film for which development residue formation is sufficiently inhibited and that has excellent extensibility. The radiation-sensitive resin composition contains: a cycloolefin polymer (A-1) including a protonic polar group; a cycloolefin polymer (A-2) including a protonic polar group; a difunctional epoxy compound (B); and a radiation-sensitive compound (C). The cycloolefin polymer (A-1) has a weight-average molecular weight of not less than 1,000 and less than 10,000, and the cycloolefin polymer (A-2) has a weight-average molecular weight of not less than 10,000 and not more than 100,000. Content of the cycloolefin polymer (A-2) is not less than 5 mass % and not more than 55 mass % of total content of the cycloolefin polymer (A-1) and the cycloolefin polymer (A-2).

A method for the preparation of an alkoxy-functional hydrogensiloxane oligomer includes reacting a polyorganohydrogensiloxane oligomer and an aliphatically unsaturated alkoxysilane in the presence of a hydrosilylation reaction and a promoter. The resulting crude reaction product is treated with a treating agent, and thereafter distilled to produce the alkoxy-functional organohydrogensiloxane oligomer. The alkoxy-functional hydrogensiloxane oligomer can be reacted with polyorganosiloxane having an aliphatically unsaturated monovalent hydrocarbon group to form a polyalkoxy-functional polyorganosiloxane. The polyalkoxy-functional polyorganosiloxane can be formulated in condensation reaction curable compositions.

A method for the preparation of an alkoxy-functional hydrogensiloxane oligomer includes reacting a polyorganohydrogensiloxane oligomer and an aliphatically unsaturated alkoxysilane in the presence of a hydrosilylation reaction and a promoter. The resulting crude reaction product is treated with a treating agent, and thereafter distilled to produce the alkoxy-functional organohydrogensiloxane oligomer. The alkoxy-functional hydrogensiloxane oligomer can be reacted with polyorganosiloxane having an aliphatically unsaturated monovalent hydrocarbon group to form a polyalkoxy-functional polyorganosiloxane. The polyalkoxy-functional polyorganosiloxane can be formulated in condensation reaction curable compositions.