Method for making an enoxy stabilized room temperature vulcanizable organopolysiloxane composition which resists color change upon aging

Claim 1

A method of making a room temperature vulcanizable organopolysiloxane composition utilizing a cure rate accelerator and a material having an enoxy functional group as a scavenger for chemically combined hydroxy radicals, which RTV organopolysiloxane composition is substantially colorless and exhibits an ability to resist a substantial change in color over an extended shelf period under moisture free conditions at ambient temperatures, which comprises, (1)agitating under substantially anhydrous conditions at a temperature in the range of from 0° C. to 180° C., a mixture of ingredients comprising by weight, (A) an alkoxy terminated polydiorganosiloxane of the formula, ##STR7## (B) an effective amount of a condensation catalyst,

Claim 2

A method of making a room temperature vulcanizable organopolysiloxane composition utilizing a cure rate accelerator and a material having an enoxy functional group as a scavenger for chemically combined hydroxy radicals, which RTV organopolysiloxane composition is substantially colorless and exhibits an ability to resist a substantial change in color over an extended shelf period under moisture free conditions at ambient temperatures, which comprises, (1)agitating under substantially anhydrous conditions at a temperature in the range of from 0° C. to 180° C., a mixture of ingredients comprising by weight, (A) an alkoxy terminated polydiorganosiloxane of the formula, ##STR7## (B) an effective amount of a condensation catalyst,

Claim 13

A method for making a room temperature vulcanizable composition which resists color change upon aging comprising, (1) agitating under substantially anhydrous conditions at a temperature in the range of from 0°C. to 180° C., a mixture of ingredients comprising by weight (A) a silanol terminated polydiorganosiloxane (B) an effective amount of a condensation catalyst (C) 0.001 to 0.1 part per part of the silanol terminated polydiorganosiloxane of a cross-linking polyalkoxysilane (D) an effective amount of a cure accelerator selected from the class consisting of a diorganosulfoxide and a nitrogen base free of reactive ═NH functional groups selected from the class consisting of sterically hindered secondary amines, imidazoles, aminopyridines and tertiary amines and (E) an effective amount of a scavenger having enoxy functionality selected from the class consisting of organo silanes and alkenyl carboxylates, (2) allowing the resulting mixture of ingredients of (1) to age at ambient conditions over an extended period of time.

Claim 14

A method for making a room temperature vulcanizable composition which resists color change upon aging comprising, (1) agitating under substantially anhydrous conditions at a temperature in the range of from 0°C. to 180° C., a mixture of ingredients comprising by weight (A) a silanol terminated polydiorganosiloxane (B) an effective amount of a condensation catalyst (C) 0.001 to 0.1 part per part of the silanol terminated polydiorganosiloxane of a cross-linking polyalkoxysilane (D) an effective amount of a cure accelerator selected from the class consisting of a diorganosulfoxide and a nitrogen base free of reactive ═NH functional groups selected from the class consisting of sterically hindered secondary amines, imidazoles, aminopyridines and tertiary amines and (E) an effective amount of a scavenger having enoxy functionality selected from the class consisting of organo silanes and alkenyl carboxylates, (2) allowing the resulting mixture of ingredients of (1) to age at ambient conditions over an extended period of time.

Claim 15

A method for making a room temperature vulcanizable composition which resists color change upon aging comprising, (1) agitating under substantially anhydrous conditions at a temperature in the range of from 0° C. to 180° C., a mixture of ingredients comprising by weight (A) a silanol terminated polydiorganosiloxane (B) an effective amount of a condensation catalyst (C) an effective amount of a cure accelerator selected from the class consisting of a diorganosulfoxide and a nitrogen base free of reactive ═NH functional groups selected from the class consisting of sterically hindered secondary amines, imidazoles, aminopyridines and tertiary amines and (D) an effective amount of a scavenger having the formula, ##STR10## (2) allowing the resulting mixture of ingredients of (1) to age at ambient conditions over an extended period of time, where X is an enoxy functional group of the formula, ##STR11## R is a C.sub.(1-13) monovalent substituted or unsubstituted hydrocarbon radical, R 1 , R 2 and R 3 can be the same or different monovalent radicals selected from hydrogen, C .sub.(1-8) alkyl, alkenyl, and alkoxy or C.sub.(6-13) aryl and aryloxy, R 4 is a C.sub.(1-8) aliphatic organic radical selected from alkyl radicals, alkylether radicals, alkylester radicals, alkylketone radicals and alkylcyano or a C.sub.(7-13) aralkyl radical, c is equal to 0 to 3 inclusive, d is 0 or 1, and c+d is equal to 0 to 3 inclusive.

Claim 16

A method for making a room temperature vulcanizable composition which resists color change upon aging comprising, (1) agitating under substantially anhydrous conditions at a temperature in the range of from 0° C. to 180° C., a mixture of ingredients comprising by weight (A) a silanol terminated polydiorganosiloxane (B) an effective amount of a condensation catalyst (C) an effective amount of a cure accelerator selected from the class consisting of a diorganosulfoxide and a nitrogen base free of reactive ═NH functional groups selected from the class consisting of sterically hindered secondary amines, imidazoles, aminopyridines and tertiary amines and (D) an effective amount of a scavenger having the formula, ##STR10## (2) allowing the resulting mixture of ingredients of (1) to age at ambient conditions over an extended period of time, where X is an enoxy functional group of the formula, ##STR11## R is a C.sub.(1-13) monovalent substituted or unsubstituted hydrocarbon radical, R 1 , R 2 and R 3 can be the same or different monovalent radicals selected from hydrogen, C .sub.(1-8) alkyl, alkenyl, and alkoxy or C.sub.(6-13) aryl and aryloxy, R 4 is a C.sub.(1-8) aliphatic organic radical selected from alkyl radicals, alkylether radicals, alkylester radicals, alkylketone radicals and alkylcyano or a C.sub.(7-13) aralkyl radical, c is equal to 0 to 3 inclusive, d is 0 or 1, and c+d is equal to 0 to 3 inclusive.