Crosslinked organopolysiloxane and method for producing same, mist suppressant, and solvent-free silicone composition for release paper

Patent metadata

Field	Value
Publication number	US-10113036-B2
Application number	US-201515320386-A
Country	US
Kind code	B2
Filing date	Jun 4, 2015
Priority date	Jun 23, 2014
Publication date	Oct 30, 2018
Grant date	Oct 30, 2018

Abstract

Provided are: a crosslinked organopolysiloxane which has properties intermediate between a dimethylpolysiloxane oil and a gel-like crosslinked siloxane; and a method for producing the crosslinked organopolysiloxane. An oil-like organopolysiloxane which is produced by: adding a compound having a siloxane unit represented by formula (3) to a gel-like silicone, wherein the gel-like silicone is produced by a hydrosilylation reaction of an organopolysiloxane having an alkenyl group with an organohydrogenpolysiloxane having a hydrogen atom bonded to a silicon atom in the presence of a platinum-group metal catalyst; and then equilibrating the resultant product with an acid or alkali catalyst.

R 1 2 SiO 2/2   (3)

(R 1 represents a group selected from a monovalent hydrocarbon group having no aliphatic unsaturated bond and an alkenyl group represented by the formula: —(CH 2 ) a —CH═CH 2 (wherein a represents a numerical value of 0 to 6), and the average polymerization degree of formula (3) is 3 to 2,000.)

First claim

The invention claimed is:

1. A method of producing a crosslinked organopolysiloxane, comprising the steps of preparing a gel-like silicone by hydrosilylation of an organopolysiloxane having the structure of formula (1) below with an organohydrogenpolysiloxane having the structure of formula (2) below
M α M Vi β D γ D Vi δ T ε T Vi ζ Q η   (1)

M θ M H ι D κ D H λ T μ T H ν   (2)

(wherein M is R 3 SiO 1/2 , M Vi is R 2 PSiO 1/2 , D is R 2 SiO 2/2 , D Vi is RPSiO 2/2 , T is RSiO 3/2 , T Vi is PSiO 3/2 , M H is R 2 HSiO 1/2 , D H is RHSiO 2/2 , T H is HSiO 3/2 and Q is SiO 4/2 , each R being independently an unsubstituted or substituted monovalent hydrocarbon group of 1 to 12 carbon atoms that has no aliphatic unsaturated bonds and P being an alkenyl group represented by —(CH 2 ) a —CH═CH 2 (where “a” is 0 or an integer from 1 to 6); and α, β, γ, δ, ε, ζ, η, θ, ι, κ, λ, μ and ν are each independently 0 or a positive number, with the provisos that β, δ and ζ are not all 0, β+δ+ζ≥2, ι, λ and ν are not all 0, and ι+λ+ν≥2); and subsequently adding to the gel-like silicone a compound having siloxane units of formula (3) below
R 1 2 SiO 2/2   (3)

(wherein each R 1 is the same or a different group selected from among monovalent hydrocarbon groups of 1 to 20 carbon atoms that have no aliphatic unsaturated bonds and alkenyl groups represented by —(CH 2 ) a —CH═CH 2 (where “a” is 0 or an integer from 1 to 6; and an average degree of polymerization of the siloxane of formula (3) is from 3 to 2,000 in the compound having siloxane units of formula (3)) and carrying out equilibration so as to obtain an organopolysiloxane which contains 0.1 to 50 moles of silethylene linkages per 1,000 moles of siloxane units.

2. The method of claim 1 wherein, in formula (1), 1≤α+γ+δ+η≤1,000 and, in formula (2), 1≤θ+κ+μ≤200.

3. The method of claim 1 wherein, in formula (1), 1≤γ≤1,000 and, in formula (2), 1≤κ≤200.

4. The method of claim 1 , wherein the compound having siloxane units of formula (3) is an organosiloxane selected from among octamethyltetrasiloxane, decamethylpentasiloxane, linear siloxanes of the formula M 2 D n (M being an R 3 SiO 1/2 unit, D being an R 2 SiO 2/2 unit, each R being independently an unsubstituted or substituted monovalent hydrocarbon group of 1 to 12 carbon atoms which has no aliphatic unsaturated bonds, and n being an integer from 0 to 200) and branched siloxanes of the formula M 2+m D n T m (M, D and n being the same as above, T being an RSiO 3/2 unit, R being the same as above, and m being an integer from 1 to 10).

5. The method of claim 1 , wherein the organopolysiloxane of formula (1) has a weight-average molecular weight of 260 to 74,186 and the organohydrogenpolysiloxane of formula (2) has a weight-average molecular weight of 208 to 14,934.

Assignees

• Shinetsu Chemical Co

Inventors

• Ihara Toshiaki

Classifications

• C09D183/04 Primary

  Polysiloxanes · CPC title

• C08G77/38 Primary

  Polysiloxanes modified by chemical after-treatment · CPC title

• C08G77/12 Primary

  containing silicon bound to hydrogen · CPC title

• C08G77/20 Primary

  containing silicon bound to unsaturated aliphatic groups · CPC title

• C09D7/65

  macromolecular (C09D7/41-C09D7/48 take precedence) · CPC title