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Room temperature vulcanizable organopolysiloxane compositions and method for making

Assignee: General Electric Co
•
Filing: 1984-02-24
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Granted: 1985-05-14
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Expires: 2004-02-24
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Abstract

Abstract Room temperature vulcanizable organopolysiloxane compositions are provided based on the use of a silanol or alkoxy terminated organopolysiloxane and an effective amount of a diorganotinbis(chelate) catalyst.

Inventors

  • 👤 Thomas P. Lockhart
  • 👤 Jeffrey H. Wengrovius

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 10:21
CPC Classifications
C; C08; C08K; C08K5/00; C08K5/56; C08K5/57; C08K5/04; C08K5/07; C08K5/16; C08K5/17; C08K5/54; Y; Y10; Y10S; Y10S528/00; Y10S528/901

Claims Analysis

Total Claims: 25
Claim 1
Independent Claim 174 words
Room temperature vulcanizable compositions comprising by weight, (A) 100 parts of organopolysiloxane consisting essentially of chemically combined diorganosiloxy and terminated with polyalkoxy siloxy units, (B) 0 to 10 parts of a polyalkoxy silane of the formula ##STR9## (C) 0 to 5 parts of amine accelerator, (D) an effective amount of a tin condensation catalyst of the formula ##STR10## (E) 0 to 5 parts of a β-diketone of the formula ##STR11## (F) 0 to 700 parts of filler, where R is selected from C.sub.(1-18) monovalent hydrocarbon radicals and substituted monovalent hydrocarbon radicals, and R 1 , R 2 and R 3 are the same or different monovalent radials selected from the class consisting of hydrogen, R, --Si(R) 3 , acyl and nitrile R 5 is a monovalent radical selected from C.sub.(1-13) hydrocarbon radicals and substituted C.sub.(1-13) hydrocarbon radicals, R 6 is a C.sub.(1-8) aliphatic organic radical selected from alkyl radicals, alkylether radicals, alkyl ester radicals, alkylketone radicals and alkylcyano or a C.sub.(7-13) aralkyl radical and a is a whole number equal to 0 or 1.
Claim 2
Dependent Claim 174 words
Room temperature vulcanizable compositions comprising by weight, (A) 100 parts of organopolysiloxane consisting essentially of chemically combined diorganosiloxy and terminated with polyalkoxy siloxy units, (B) 0 to 10 parts of a polyalkoxy silane of the formula ##STR9## (C) 0 to 5 parts of amine accelerator, (D) an effective amount of a tin condensation catalyst of the formula ##STR10## (E) 0 to 5 parts of a β-diketone of the formula ##STR11## (F) 0 to 700 parts of filler, where R is selected from C.sub.(1-18) monovalent hydrocarbon radicals and substituted monovalent hydrocarbon radicals, and R 1 , R 2 and R 3 are the same or different monovalent radials selected from the class consisting of hydrogen, R, --Si(R) 3 , acyl and nitrile R 5 is a monovalent radical selected from C.sub.(1-13) hydrocarbon radicals and substituted C.sub.(1-13) hydrocarbon radicals, R 6 is a C.sub.(1-8) aliphatic organic radical selected from alkyl radicals, alkylether radicals, alkyl ester radicals, alkylketone radicals and alkylcyano or a C.sub.(7-13) aralkyl radical and a is a whole number equal to 0 or 1.
Claim 3
Dependent Claim 16 words
A room temperature vulcanizable composition in accordance with claim 1, where the tin catalyst is di(n-butyl)tinbis(acetylacetonate).
Claim 4
Dependent Claim 13 words
A composition in accordance with claim 1, whwere the alkoxy silane is methyltrimethoxysilane.
Claim 5
Dependent Claim 13 words
A composition in accordance with claim 1, where the organopolysiloxane is a polydimethylsiloxane.
Claim 6
Dependent Claim 13 words
A composition in accordance with claim 1, where the amine accelerator is diisobutylamine.
Claim 7
Dependent Claim 12 words
A composition in accordance with claim 1, where the β-diketone is acetylacetone.
Claim 8
Dependent Claim 100 words
Room temperature vulcanizable compositions comprising by weight, (A) 100 parts of silanol terminated polydiorganosiloxane, (B) 0.1 to 10 parts of a polyalkoxy silane, (C) 0 to 5 parts of amine accelerator, (D) an effective amount of a tin condensation catalyst of the formula ##STR12## (E) 0 to 5 parts of a β-diketone of the formula,, ##STR13## where R is selected from C.sub.(1-18) monovalent hydrocarbon radicals and substituted monovalent hydrocarbon radicals, and R 1 , R 2 and R 3 are the same or different monovalent radicals selected from the class consisting of hydrogen, R, Si(R) 3 , acyl and nitrile.
Claim 9
Dependent Claim 100 words
Room temperature vulcanizable compositions comprising by weight, (A) 100 parts of silanol terminated polydiorganosiloxane, (B) 0.1 to 10 parts of a polyalkoxy silane, (C) 0 to 5 parts of amine accelerator, (D) an effective amount of a tin condensation catalyst of the formula ##STR12## (E) 0 to 5 parts of a β-diketone of the formula,, ##STR13## where R is selected from C.sub.(1-18) monovalent hydrocarbon radicals and substituted monovalent hydrocarbon radicals, and R 1 , R 2 and R 3 are the same or different monovalent radicals selected from the class consisting of hydrogen, R, Si(R) 3 , acyl and nitrile.
Claim 10
Dependent Claim 16 words
A room temperature vulcanizable composition in accordance with claim 7, where the tin catalyst is di(n-butyl)tinbis(acetylacetonate).
Claim 11
Dependent Claim 13 words
A composition in accordance with claim 7, where the alkoxy silane is methyltrimethoxysilane.
Claim 12
Dependent Claim 17 words
A composition in accordance with claim 7, where the silanol terminated polydiorganosiloxane is a silanol terminated polydimethylsiloxane.
Claim 13
Dependent Claim 13 words
A composition in accordance with claim 6, where the amine accelerator is diisobutylamine.
Claim 14
Dependent Claim 11 words
A composition in accordance with claim 7 where β-diketone is acetylacetone.
Claim 15
Independent Claim 124 words
A method for making room temperature vulcanizable organopolysiloxane compositions which comprises mixing together under substantially anhydrous conditions a mixture comprising by weight, (i) 100 parts of alkoxy terminated organopolysiloxane, (ii) 0 to 10 parts of polyalkoxy silane, of the formula ##STR14## (iii) 0 to 5 parts of amine accelerator, (iv) an effective amount of tin condensation catalyst of the formula ##STR15## (v) 0 to 5 parts of a β-diketone of the formula ##STR16## (vi) 0 to 700 parts of filler, where R is selected from C.sub.(1-18) monovalent hydrocarbon radicals and substituted monovalent hydrocarbon radicals, and R 1 , R 2 and R 3 are the same or different monovalent radicals selected from the class consisting of hydrogen, R, Si(R) 3 , acyl and nitrile.
Claim 16
Independent Claim 124 words
A method for making room temperature vulcanizable organopolysiloxane compositions which comprises mixing together under substantially anhydrous conditions a mixture comprising by weight, (i) 100 parts of alkoxy terminated organopolysiloxane, (ii) 0 to 10 parts of polyalkoxy silane, of the formula ##STR14## (iii) 0 to 5 parts of amine accelerator, (iv) an effective amount of tin condensation catalyst of the formula ##STR15## (v) 0 to 5 parts of a β-diketone of the formula ##STR16## (vi) 0 to 700 parts of filler, where R is selected from C.sub.(1-18) monovalent hydrocarbon radicals and substituted monovalent hydrocarbon radicals, and R 1 , R 2 and R 3 are the same or different monovalent radicals selected from the class consisting of hydrogen, R, Si(R) 3 , acyl and nitrile.
Claim 17
Independent Claim 159 words
A method for making a room temperature vulcanizable organopolysiloxane composition which comprises, (1) mixing together under substantially anhydrous conditions a mixture comprising by weight, (i) 100 parts of silanol terminated polydiorganosiloxane, (ii) 0.1 to 10 parts of polyalkoxy silane, (iii) 0 to 5 parts of amine accelerator, and (iv) 0 to 700 parts of filler, (v) 0 to 5 parts, per 100 parts of the alkoxy terminated polydiorganosiloxane, of a β-diketone of the formula ##STR17## (2) allowing the mixture of (1) to equilibrate to produce polyalkoxy terminated polydiorganosiloxane, and (3) further agitating the mixture of (2) under substantially anhydrous conditions and thereafter adding an effective amount of a tin condensation catalyst of the formula, ##STR18## where R is selected from C.sub.(1-18) monovalent hydrocarbon radicals and substituted monovalent hydrocarbon radicals, and R 1 , R 2 and R 3 are the same or different monovalent radicals selected from the class consisting of hydrogen, R, Si(R) 3 , acyl and nitrile.
Claim 18
Independent Claim 159 words
A method for making a room temperature vulcanizable organopolysiloxane composition which comprises, (1) mixing together under substantially anhydrous conditions a mixture comprising by weight, (i) 100 parts of silanol terminated polydiorganosiloxane, (ii) 0.1 to 10 parts of polyalkoxy silane, (iii) 0 to 5 parts of amine accelerator, and (iv) 0 to 700 parts of filler, (v) 0 to 5 parts, per 100 parts of the alkoxy terminated polydiorganosiloxane, of a β-diketone of the formula ##STR17## (2) allowing the mixture of (1) to equilibrate to produce polyalkoxy terminated polydiorganosiloxane, and (3) further agitating the mixture of (2) under substantially anhydrous conditions and thereafter adding an effective amount of a tin condensation catalyst of the formula, ##STR18## where R is selected from C.sub.(1-18) monovalent hydrocarbon radicals and substituted monovalent hydrocarbon radicals, and R 1 , R 2 and R 3 are the same or different monovalent radicals selected from the class consisting of hydrogen, R, Si(R) 3 , acyl and nitrile.
Claim 19
Dependent Claim 19 words
An RTV composition made in accordance with the method of claim 13 which is reinforced with a silica filler.
Claim 20
Dependent Claim 19 words
An RTV composition made in accordance with the method of claim 14 which is reinforced with a silica filler.
Claim 21
Dependent Claim 14 words
A method in accordance with claim 13, where the tin condensation catalyst is di(n-butyl)tin-bis(acetylacetonate).
Claim 22
Dependent Claim 13 words
A method in accordance with claim 13, where the alkoxy silane is methyltrimethoxysilane.
Claim 23
Dependent Claim 13 words
A method in accordance with claim 13, where the organopolysiloxane is a polydimethylsiloxane.
Claim 24
Dependent Claim 13 words
A method in accordance with claim 13, where the amine accelerator is diisobutylamine.
Claim 25
Dependent Claim 12 words
A method in accordance with claim 13, where the β-diketone is acetylacetone.

References Cited (Backward Citations)

US2607792A Cited
GB835790A Cited
US3153007A Cited
US3161614A Cited
US3664997A Cited
US3661887A Cited
US4100129A Cited
US4395526A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-05-13 1988-11-12 1989-05-14 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-05-13 1992-11-12 1993-05-14 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-05-13 1996-11-12 1997-05-14 $7700.00 Window Closed / Lapsed

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