Room temperature curable organopolysiloxane compositions
Abstract
A room temperature curable organopolysiloxane composition comprising (A) an organopolysiloxane of HO(SiR 1 2 O) n H and/or (R 2 O) 3−m R 1 m SiO(SiOR 1 2 O) n SiR 1 m (OR 2 ) 3−m wherein R 1 is a monovalent C1-10 hydrocarbon radical, R 2 is a monovalent C1-6 hydrocarbon radical, n is an integer of at least 10, and m is 0 or 1, (B) a silane compound having at least two hydrolyzable radicals, the remaining radicals being methyl, ethyl, propyl, vinyl or phenyl, and/or a partial hydrolyzate thereof, and (C) an organosilicon compound of (RO) p R 1 3−p SiR 3 —NH—R 4 —NH 2 wherein R 1 and R 2 are as defined above, R 3 is a divalent C1-10 hydrocarbon radical, R 4 is a divalent aromatic ring-bearing C7-10 hydrocarbon radical, and p is 1, 2 or 3, at least one of the NH and NH 2 radicals being not directly attached to the aromatic ring in R 4 , cures into silicone rubber which has improved adherence even upon exposure to hot steam.
Claims
exact text as granted — not AI-modified1 . A room temperature curable organopolysiloxane composition comprising
(A) 100 parts by weight of an organopolysiloxane of the following general formula (1): HO(SiR 1 2 O) n H (1) wherein R 1 is a substituted or unsubstituted monovalent hydrocarbon radical of 1 to 10 carbon atoms, and n is an integer of at least 10, or an organopolysiloxane of the following general formula (2): wherein R 1 and n are as defined above, R 2 is a substituted or unsubstituted monovalent hydrocarbon radical of 1 to 6 carbon atoms, and m is independently an integer of 0 or 1, or both, (B) 0.1 to 30 parts by weight of a silane compound having at least two hydrolyzable radicals each attached to a silicon atom in a molecule, the remaining radicals attached to silicon atoms being selected from the group consisting of methyl, ethyl, propyl, vinyl and phenyl, or a partial hydrolyzate thereof or both, and (C) 0.1 to 10 parts by weight of an organosilicon compound of the following general formula (3): wherein R 1 and R 2 are as defined above, R 3 is a divalent hydrocarbon radical of 1 to 10 carbon atoms, R 4 is a divalent aromatic ring-bearing hydrocarbon radical of 7 to 10 carbon atoms, and p is an integer of 1 to 3, at least one of the NH and NH 2 radicals being not directly attached to the aromatic ring in R 4 .
2 . The composition of claim 1 wherein the hydrolyzable radicals in component (B) are selected from among ketoxime, alkoxy, and isopropenoxy radicals.
3 . The composition of claim 1 wherein in formula (3), R 2 is methyl or ethyl, and R 3 is methylene, ethylene or propylene.
4 . The composition of claim 1 wherein in formula (3), R 4 is selected from the following structures:
-CH 2 -C 6 H 4 -
(4),
-CH 2 -C 6 H 4 -CH 2 -
(5),
-CH 2 -C 6 H 4 -CH 2 -CH 2 -
(6),
-CH 2 -C 6 H 4 -CH 2 -CH 2 -CH 2 -
(7),
-CH 2 -CH 2 -C 6 H 4 -
(8),
-CH 2 -CH 2 -C 6 H 4 -CH 2 -
(9),
-CH 2 -CH 2 -C 6 H 4 -CH 2 -CH 2 -
(10),
-CH 2 -CH 2 -CH 2 -C 6 H 4 -
(11) and
-CH 2 -CH 2 -CH 2 -C 6 H 4 -CH 2 -
(12).
5 . The composition of claim 1 which further comprises a filler.
6 . The composition of claim 5 wherein the filler is silica and/or carbon black.
7 . The composition of claim 1 which further comprises a condensation reaction catalyst.Join the waitlist — get patent alerts
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