Disclosed are a curable composition characterized by using a curable composition including an organic polymer (A1) having one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds in which the one or more silicon-containing functional groups capable of cross
Disclosed are a curable composition characterized by using a curable composition including an organic polymer (A1) having one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds in which the one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds are silicon-containing functional groups each having three or more hydrolyzable groups on one or more silicon atoms thereof; and a method for controlling the recovery properties, durability and creep resistance of the cured article. Herewith, the present invention provides a curable composition capable of giving a cured article excellent in recovery properties, durability and creep resistance, and a method for controlling the recovery properties, durability and creep resistance of the cured article.
대표청구항▼
1. A curable composition comprising: an organic polymer (A1) having one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds in which the one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds are silicon-contain
1. A curable composition comprising: an organic polymer (A1) having one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds in which the one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds are silicon-containing functional groups each having three or more hydrolyzable groups on one or more silicon atoms thereof, and a main chain skeleton of the organic polymer (A1) is a polyoxyalkylene polymer; andat least one silanol condensation catalyst selected from the group consisting of a tin carboxylate (C), an organotin catalyst (D), and a non-tin catalyst (E),wherein the tin carboxylate (C) isa divalent Sn compound represented by the general formula (17): Sn(OCOR)2 (17)where Rs each are a substituted or unsubstituted hydrocarbon group, and may include carbon-carbon double bonds, and the two RCOO— groups may be the same or different,a tetravalent Sn compound represented by the general formula (18): Sn(OCOR)4 (18)where Rs are the same as described above, and four RCOO— groups may be the same or different,a tin salt of a chain fatty acid represented by the general formula (19): where R14, R15 and R16 each are independently a substituted or unsubstituted monovalent organic group, and the group may include carboxyl groups,a tin salt of a cyclic fatty acid represented by the general formula (20): where R17 is a substituted or unsubstituted monovalent organic group, R18 is a substituted or unsubstituted divalent organic group, and these groups each may include carboxyl groups; ora tin salt of a cyclic fatty acid represented by the general formula (21): where R19 is a substituted or unsubstituted trivalent organic group, and the group may include carboxyl groups,and wherein the curable composition further comprises any one of the following features (1) and (4) to (6):(1) the curable composition further comprises an inorganic microballoon (F), andthe one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds each are a trimethoxysilyl group and/or a triethoxysilyl group;(4) the organic polymer (A1) is an organic polymer (A2) having one or more silicon-containing functional groups capable of crosslinking by forming siloxane bonds in which the one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds are represented by the general formula (2): —Si(OR1)3 (2)where three R1s each are independently a monovalent organic group having 2 to 20 carbon atoms, andthe curable composition further comprises an aminosilane coupling agent (G) having a group represented by the general formula (3): —SiR2a(OR3)3-a (3)where aR2s each are independently a monovalent organic group having 1 to 20 carbon atoms, (3−a)R3s each are independently a monovalent organic group having 2 to 20 carbon atoms, and a represents 0, 1 or 2;(5) the organic polymer (A1) is an organic polymer (A2) having one or more silicon-containing functional groups capable of crosslinking by forming siloxane bonds in which the one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds are represented by the general formula (2): —Si(OR1)3 (2)where three R1s each are independently a monovalent organic group having 2 to 20 carbon atoms, andthe curable composition further comprises an aminosilane coupling agent (H) having a group represented by the general formula (4): —SiR4b(OCH3)c(OR5)3-b-c (4)where bR4s each are independently a monovalent organic group having 1 to 20 carbon atoms, (3−b−c)R5s each are independently a monovalent organic group having 2 to 20 carbon atoms, b represents 0, 1 or 2, and c represents 1, 2 or 3; the relation, 3−b−c≧0, is to be satisfied, andthe curable composition is obtained by pre-aging; or(6) the organic polymer (A1) is a polyoxyalkylene polymer (A3) having one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds in which the one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds are represented by the general formula (2): —Si(OR1)3 (2)where three R1s each are independently a monovalent organic group having 2 to 20 carbon atoms, andthe curable composition further comprises a (meth)acrylate copolymer (A6) having one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds in which the one or more silicon-containing functional groups capable of cross-linking by forming siloxane bonds are represented by the general formula (2): —Si(OR1)3 (2)where three R1s each are independently a monovalent organic group having 2 to 20 carbon atoms. 2. The curable composition according to claim 1, wherein the silicon-containing functional groups capable of cross-linking by forming siloxane bonds in feature (1) are a trimethoxysilyl group. 3. The curable composition according to claim 1, wherein R1 of general formula (2) is an ethyl group. 4. The curable composition according to claim 1, wherein the organic polymer (A1) of feature (1) is an organic polymer obtained by an addition reaction between an organic polymer having one or more unsaturated groups introduced into the terminals thereof and a trimethoxysilane and/or a triethoxysilene. 5. The curable composition according to claim 1, wherein the organic polymer (A1) of features (4) to (6) is an organic polymer obtained by an addition reaction between an organic polymer having one or more unsaturated groups introduced into the terminals thereof and a hydrosilane compound represented by the general formula (5): H—Si(OR1)3 (5)where three R1s each are independently a monovalent organic group having 2 to 20 carbon atoms. 6. The curable composition according to claim 1, wherein the organic polymer (A1) is an organic polymer which substantially does not contain an amide segment (—NH—CO—) in the main chain skeleton thereof. 7. The curable composition according to claim 1, wherein the silanol condensation catalyst is a tin carboxylate (C), and the curable composition further comprises an amine compound. 8. The curable composition according to claim 7, which further comprises an organotin catalyst (D), wherein the organotin catalyst (D) is at least one selected from the group consisting of dialkyltin carboxylates, dialkyltin oxides, reaction products between tetravalent tin and low molecular-weight, hydrolyzable silicon group-containing silicon compounds, and compounds represented by the formula QgSn(OZ)4-g or [Q2Sn(OZ)]2O, where Q represents a monovalent hydrocarbon group having 1 to 20 carbon atoms, Z represents a monovalent hydrocarbon group having 1 to 20 carbon atoms or an organic group having therein one or more functional groups capable of forming coordination bonds with Sn, and g is any one of 1, 2, and 3. 9. The curable composition according to claim 1, wherein the tin carboxylates (C) isa tin salt of a chain fatty acid represented by the general formula (19): where R14, R15 and R16 each are independently a substituted or unsubstituted monovalent organic group, and the group may include carboxyl groups,a tin salt of a cyclic fatty acid represented by the general formula (20): where R17 is a substituted or unsubstituted monovalent organic group, R18 is a substituted or unsubstituted divalent organic group, and these groups each may include carboxyl groups; ora tin salt of a cyclic fatty acid represented by the general formula (21): where R19 is a substituted or unsubstituted trivalent organic group, and the group may include carboxyl groups. 10. The curable composition according to claim 1, wherein non-tin catalyst (E) is a carboxylic acid. 11. The curable composition according to claim 10, which further comprises an amine. 12. The curable composition according to claim 10, wherein the carboxylic acid is a carboxylic acid in which the α-carbon atom of the carboxyl group is a quaternary carbon atom. 13. The curable composition according to claim 1, wherein the group represented by the general formula (3) is a triethoxysilyl group.
Roberts Gary P. ; Vander Louw Steven J., Curable compositions comprising the hydrosilation product of olefin-containing polymers and organosiloxane hydrides, cured compositions made therefrom, and methods of making same.
Liu Junkang Jacob ; Leir Charles M. ; Moore George G. I. ; Sherman Audrey A. ; Everaerts Albert I. ; Boulos Marie A., Cure-on-demand, moisture-curable compositions having reactive silane functionality.
Hirose Toshifumi (Kobe JPX) Isayama Katsuhiko (Kobe JPX), Curing composition containing polyether having reactive silicon-containing group and a (meth)acrylate polymer.
Hagimori Shigeru,JPX ; Tsuneishi Koji,JPX ; Yamanaka Yoshimichi,JPX ; Wachi Syun,JPX ; Yonezawa Kazuya,JPX, Hydrosilylation process and polymers produced by the process.
Takago Toshio (Annaka JPX) Arai Masatoshi (Annaka JPX) Futatsumori Koji (Annaka JPX), Method for the preparation of silicone-modified polyoxyalkylene polyethers and room temperature-curable compositions the.
White Mary A. (El Cerrito CA) Hallgren John E. (Scotia NY) Lockhart Thomas P. (Schenectady NY), One package, stable, moisture curable, alkoxy-terminated organopolysiloxane compositions.
White Mary A. (Schenectady NY) Beers Melvin D. (Schenectady NY) Lucas Gary M. (Scotia NY) Smith Robert A. (Schenectady NY) Swiger Roger T. (Schenectady NY), One package, stable, moisture curable, polyalkoxy-terminated organopolysiloxane compositions and method for making.
Chromecek Richard C. (Macedon NY) Deichert William G. (Macedon NY) Falcetta Joseph J. (Pittsford NY) VanBuren Martin F. (Chelmsford MA), Polysiloxane/acrylic acid/polcyclic esters of methacrylic acid polymer contact lens.
Kudo Muneo,JPX ; Morioka Shinichi,JPX ; Asai Mitsuo,JPX, Process for producing organosilicon resin and process for producing polyurethane foam by using the organosilicon resin obtained by that process.
Lampe Warren R. (Ballston Lake NY) Mitchell Tyrone D. (Albany NY) Cella James A. (Clifton Park NY), Self-bonding one-component RTV silicone rubber compositions.
Hill Michael Philip Louis ; Tselepis Arthur James ; Wolf Andreas Thomas Franz, Silicone elastomers from aqueous silicone emulsions having improved adhesion to substrates.
Cavezzan Jacques (Villeurbanne FRX) Frances Jean-Marc (Villeurbanne FRX) Millet Claude (Saint-Priest FRX), Tin monochelate catalysis of organopolysiloxane compositions.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.