# US 10,865,308 B1 · Addition-curable liquid silicone rubber composition

> Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt

- Number: US 10,865,308 B1
- Document ID: US10865308B1
- Status: Granted
- Kind: B1
- Application number: 16/097,766
- Filed: 2017-04-07
- Published: 2020-11-26
- Granted: 2020-12-15
- Earliest claimed: 2016-06-17
- Assignees: Shin-Etsu Chemical Co., Ltd.
- Applicants: Shin-Etsu Chemical Co., Ltd.
- Inventors: Nobu Kato
- Web page: https://patentgrep.com/patent/US10865308B1

## CPC

- C08K 3/36: Silica
- C08L 83/04: Polysiloxanes
- C08L 83/06: containing silicon bound to oxygen-containing groups (C08L83/12 takes precedence)
- C08G 77/08: characterised by the catalysts used
- C08G 77/12: containing silicon bound to hydrogen
- C08G 77/20: containing silicon bound to unsaturated aliphatic groups
- C08G 77/50: by carbon linkages
- C08L 2205/025: containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
- C08L 2205/035: containing four or more polymers in a blend
- C08K: Use of inorganic or non-macromolecular organic substances as compounding ingredients (paints, inks, varnishes, dyes, polishes, adhesives C09)
- C08L: COMPOSITIONS OF MACROMOLECULAR COMPOUNDS (compositions based on polymerisable monomers C08F, C08G; artificial filaments or fibres D01F; textile treating compositions D06)
- C08G: MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS

## Abstract

Provided is an addition-curable liquid silicone rubber composition which has good curability and still provides a silicone rubber having a durometer type A hardness of 5-15 as measured after being cured and a high tear strength. The addition-curable liquid silicone rubber composition contains (A) an alkenyl group-containing organopolysiloxane having two or more silicon atom-bonded alkenyl groups per molecule, and an average polymerization degree of 1,500 or less, and is liquid at 25° C., (B) (B-1) an organohydrogenpolysiloxane containing six or more silicon atom-bonded hydrogen atoms per molecule, and not having an aromatic group, (B-2) an organohydrogenpolysiloxane containing 3-5 silicon atom-bonded hydrogen atoms per molecule, and not having an aromatic group, (B-3) an organohydrogenpolysiloxane containing 1 or 2 silicon atom-bonded hydrogen atoms per molecule, and not having an aromatic group, (C) a fumed silica having a BET specific surface area of 130 m2/g or more, and (D) an addition reaction catalyst.

## Claims

### Claim 1

An addition-curable liquid silicone rubber composition comprising the following components (A) to (D):
(A) 100 parts by weight of an alkenyl-containing organopolysiloxane having at least two silicon-bonded alkenyl groups per molecule and an average degree of polymerization of up to 1,500, the organopolysiloxane being liquid at 25° C.,
(B) an organohydrogenpolysiloxane consisting of the following components (B-1) to (B-3):
(B-1) an organohydrogenpolysiloxane containing at least 6 silicon-bonded hydrogen atoms per molecule and free of an aromatic group,
(B-2) an organohydrogenpolysiloxane containing 3 to 5 silicon-bonded hydrogen atoms per molecule and free of an aromatic group, and
(B-3) an organohydrogenpolysiloxane containing 1 or 2 silicon-bonded hydrogen atoms per molecule and free of an aromatic group,
the moles of Si—H groups in the respective components relative to the total moles (total Si—H groups) of silicon-bonded hydrogen atoms (Si—H groups) in components (B-1), (B-2) and (B-3) are such that [Si—H groups in (B-1)]]/[total Si—H groups] is 50 mol % to 80 mol %, [Si—H groups in (B-2)]]/[total Si—H groups] is 5 mol % to 40 mol %, and [Si—H groups in (B-3)]]/[total Si—H groups] is 5 mol % to 40 mol %, and a ratio of the moles of total Si—H groups to the total moles of alkenyl groups in the composition (total alkenyl groups) is such that [total Si—H groups]/[total alkenyl groups] is 1/1 to 3/1,
(C) fumed silica having a BET specific surface area of at least 130 m2/g, in an amount of 5 to 60 parts by weight per 100 parts by weight of components (A) and (B) combined, and
(D) an addition reaction catalyst in an amount of 0.5 to 1,000 ppm of platinum group metal based on the total weight of components (A) and (B).

### Claim 2 (depends on 1)

The addition-curable liquid silicone rubber composition of claim 1, further comprising (E) an organopolysiloxane having an average degree of polymerization of at least 2,000, the organopolysiloxane being gum-like at 25° C., in an amount of 1 to 200 parts by weight per 100 parts by weight of component (A).

### Claim 3 (depends on 1, 2)

The addition-curable liquid silicone rubber composition of claim 1 or 2, further comprising (F) an organopolysiloxane having an average degree of polymerization of up to 500 and free of a substituent active to addition reaction, the organopolysiloxane being liquid at 25° C., in an amount of 1 to 200 parts by weight per 100 parts by weight of component (A).

### Claim 4 (depends on 1)

The addition-curable liquid silicone rubber composition of claim 1 wherein component (B-2) is an organohydrogenpolysiloxane capped with a dimethylhydrogensiloxy group in an amount of at least 50 mol % of ends on the average.

### Claim 5 (depends on 1)

The addition-curable liquid silicone rubber composition of claim 1 wherein a molded composition after curing has a hardness of 5 to 15 on Durometer type A scale according to JIS K 6253-3:2012.

### Claim 6 (depends on 1)

The addition-curable liquid silicone rubber composition of claim 1 wherein a molded composition after curing has a tear strength of at least 10 kN/m as measured on a crescent test piece according to JIS K 6252:2007.

### Claim 7 (depends on 1)

The addition-curable liquid silicone rubber composition of claim 1 wherein in a vulcanization test using a torsional oscillating conical die type vulcanization tester according to JIS K 6300-2:2001, provided that T10 is a 10% cure time and T90 is a 90% cure time during measurement at 165° C. for 3 minutes, T10 is at least 3 seconds and T90 is up to 60 seconds.
