A composition including a polysiloxane compound (A) containing a structural unit represented by formula (1) and a structural unit represented by formula (2), wherein a siloxane structural unit ratio represented by Q unit/(Q unit+T unit) in all Si structural units is 0.60 or more and less than 1.00, and the solvent (B).

[(R.sup.1).sub.b(R.sup.2).sub.m(OR.sup.3).sub.lSiO.sub.n/2]  (1)

[In the formula, R.sup.1 is a group represented by following formula.]

##STR00001##

[(R.sup.4).sub.pSiO.sub.q/2]  (2)

A thermal interface composition includes a polysiloxane component, a thermal conductive component, a curing agent, a curing accelerator, an organosilicon coupling agent, and a crosslinking agent having three or more epoxy groups. The polysiloxane component includes not lower than 50 wt % and lower than 100 wt % of a first polysiloxane and a second polysiloxane. The thermal conductive component includes not lower than 30 wt % and lower than 70 wt % of a first thermal conductive filler, not lower than 30 wt % and lower than 70 wt % of a second thermal conductive filler, and greater than 0 wt % and not greater than 40 wt % of a third thermal conductive filler. A method for preparing a thermal interface material is also disclosed.

A thermal interface composition includes a polysiloxane component, a thermal conductive component, a curing agent, a curing accelerator, an organosilicon coupling agent, and a crosslinking agent having three or more epoxy groups. The polysiloxane component includes not lower than 50 wt % and lower than 100 wt % of a first polysiloxane and a second polysiloxane. The thermal conductive component includes not lower than 30 wt % and lower than 70 wt % of a first thermal conductive filler, not lower than 30 wt % and lower than 70 wt % of a second thermal conductive filler, and greater than 0 wt % and not greater than 40 wt % of a third thermal conductive filler. A method for preparing a thermal interface material is also disclosed.

The present invention particularly relates to synthesizing photo-initiators having poly-oligo-silsesquioxane (POSS) structure and realizing photo-polymerization by using these photo-initiators and simultaneous and in-situ synthesis of Ag nano-particles in polymer matrix comprising POSS structure and obtaining wrinkled surfaces as a result of self-arranging thereof.

A high-voltage DC cable joint including a multi-wall layered construction having individual concentrically arranged layers. The joint includes, from inside to outside, an inner conductive rubber layer, a field grading rubber layer made from a predetermined tailored formulation, an insulating rubber layer and an outer conductive rubber layer. The field grading rubber layer separates and interconnects the conductive rubber layers, and wherein the rubber layers are cross-linked by a by-product-free manufacturing method. The cable joint is preferably made from platinum cured rubbers by moulding process steps. In a preferred embodiment the cable joint is made by injection moulding.

The invention comprises a butyl acetate-silicone formulation comprising (A) an organopolysiloxane containing an average of at least two silicon-bonded alkenyl groups per molecule, (B) an organosilicon compound containing an average of at least two silicon-bonded hydrogen atoms per molecule; (C) a hydrosilylation catalyst; and a coating effective amount of (D) butyl acetate. The invention also comprises related silicone formulations made by removing a portion, or all, of (D) butyl acetate therefrom, and related cured products, methods, articles and devices.

The invention comprises a butyl acetate-silicone formulation comprising (A) an organopolysiloxane containing an average of at least two silicon-bonded alkenyl groups per molecule, (B) an organosilicon compound containing an average of at least two silicon-bonded hydrogen atoms per molecule; (C) a hydrosilylation catalyst; and a coating effective amount of (D) butyl acetate. The invention also comprises related silicone formulations made by removing a portion, or all, of (D) butyl acetate therefrom, and related cured products, methods, articles and devices.

A weather resistant matte silicone coating special for EMAS, comprising: 80˜130 parts by weight of α,ω-dihydroxypolydimethylsiloxane; 0.5˜10 parts by weight of a linear polydimethylsiloxane with terminal hydroxyl group; 1˜10 parts by weight of fumed silica; 10˜50 parts by weight of precipitated silica; 1˜5 parts by weight of color masterbatch; 0.9˜5 parts by weight of organotin chelate catalyst; crosslinking agent, comprising 1.5˜7 parts by weight of methyltri(methylethylketoximino)silane, 1.5˜7 parts by weight of vinyltri(methylethylketoximino)silane, and 1˜7 parts by weight of aminopropyltriethoxysilane; 1.5˜6 parts by weight of delustering agent; and 250˜350 parts by weight of a solvent. The coating has the properties of low viscosity, high flow, relatively fast curing, moderate strength, good adhesion, good mattness, being environmentally friendly and the like.

A weather resistant matte silicone coating special for EMAS, comprising: 80˜130 parts by weight of α,ω-dihydroxypolydimethylsiloxane; 0.5˜10 parts by weight of a linear polydimethylsiloxane with terminal hydroxyl group; 1˜10 parts by weight of fumed silica; 10˜50 parts by weight of precipitated silica; 1˜5 parts by weight of color masterbatch; 0.9˜5 parts by weight of organotin chelate catalyst; crosslinking agent, comprising 1.5˜7 parts by weight of methyltri(methylethylketoximino)silane, 1.5˜7 parts by weight of vinyltri(methylethylketoximino)silane, and 1˜7 parts by weight of aminopropyltriethoxysilane; 1.5˜6 parts by weight of delustering agent; and 250˜350 parts by weight of a solvent. The coating has the properties of low viscosity, high flow, relatively fast curing, moderate strength, good adhesion, good mattness, being environmentally friendly and the like.

A gel is provided which is the condensation reaction product of the following composition: (i) at least one condensation curable silyl terminated polymer having at least one hydrolysable and/or hydroxyl functional group(s) per molecule; (ii) a cross-linker selected from the group of a silicone, an organic polymer, a silane or a disilane molecule which contains at least two hydrolysable groups per molecule; and (iii) a condensation catalyst selected from the group of titanates, zirconates or tin (II). The molar ratio of hydroxyl and/or hydrolysable groups in polymer (i) to hydrolysable groups from component (ii) is between 0.5:1 and 1:1 using a monosilane cross-linker or 0.75:1 to 3:1 using disilanes, and the molar ratio of M-OR or tin (II) functions to the hydroxyl and/or hydrolysable group(s) in polymer (i) is comprised between 0.01:1 and 0.5:1, where M is titanium or zirconium. The composition, and uses for the gel are also disclosed.