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US4980413A Expired / Lapsed US ⏱️ 0.0 years remaining

Curable organopolysiloxane composition exhibiting improved adhesion in the cured form

Assignee: DuPont Toray Specialty Materials KK
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Filing: 1990-01-29
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Granted: 1990-12-25
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Expires: 2010-01-29
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Abstract

Abstract Organopolysiloxane compositions curable by a hydrosilylation reaction contain a novel adhesion promoter consisting essentially of (1) a carboxylic acid ester containing an acryloyloxy or methacryloyloxy group and an alcoholic functional group and (2) an organosilicon compound containing a silicon-bonded vinyloxy or substituted vinyloxy group. The compositions exhibit excellent adhesion to both organic and inorganic substrates that are in contact with the compositions during curing. The adhesion on plastics is especially good.

Inventors

  • 👤 Akira Kasuya

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 15:56
CPC Classifications
C; C08; C08K; C08K5/00; C08K5/54; C08K5/541; C08K5/5425; C08F; C08F283/00; C08F283/12; C08F283/128; C08K5/04; C08K5/10; C08L; C08L83/00; C08L83/04; C09; C09D; C09D4/00; C09D4/06; C08G; C08G77/00; C08G77/04; C08G77/12; C08G77/20; C08G77/42; C08G77/44

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 193 words
In an improved curable organopolysiloxane composition comprising: A. an organopolysiloxane containing two or more alkenyl radicals bonded to silicon atoms in a molecule; B. an organohydrogenpolysiloxane containing at least two silicon-bonded hydrogen atoms per molecule in an amount equivalent to a molar ratio of silicon-bonded hydrogen atoms to alkenyl radicals in said organopolysiloxane of from 0.5:1 to 5:1; C. an amount of a hydrosilylation reaction catalyst sufficient to promote curing of said composition; and an amount of an adhesion promoter sufficient to achieve adhesion of the cured composition to a substrate with which said composition is in contact during curing the improvement comprises the presence as said adhesion promoter of either (1) a mixture consisting essentially of D. from 0.01 to 5 weight percent, based on the combined weights of components A and B, of a carboxylic acid ester containing an acryloyloxy or methacryloyloxy group and a hydroxyalkyl group; and E. from 0.01 to 10 weight percent, based on the combined weights of components A and B, of an organosilicon compound containing a silicon-bonded vinyloxy or substituted vinyloxy group, or (2) a reaction product of said carboxylic acid ester and said organosilicon compound.
Claim 2
Dependent Claim 193 words
In an improved curable organopolysiloxane composition comprising: A. an organopolysiloxane containing two or more alkenyl radicals bonded to silicon atoms in a molecule; B. an organohydrogenpolysiloxane containing at least two silicon-bonded hydrogen atoms per molecule in an amount equivalent to a molar ratio of silicon-bonded hydrogen atoms to alkenyl radicals in said organopolysiloxane of from 0.5:1 to 5:1; C. an amount of a hydrosilylation reaction catalyst sufficient to promote curing of said composition; and an amount of an adhesion promoter sufficient to achieve adhesion of the cured composition to a substrate with which said composition is in contact during curing the improvement comprises the presence as said adhesion promoter of either (1) a mixture consisting essentially of D. from 0.01 to 5 weight percent, based on the combined weights of components A and B, of a carboxylic acid ester containing an acryloyloxy or methacryloyloxy group and a hydroxyalkyl group; and E. from 0.01 to 10 weight percent, based on the combined weights of components A and B, of an organosilicon compound containing a silicon-bonded vinyloxy or substituted vinyloxy group, or (2) a reaction product of said carboxylic acid ester and said organosilicon compound.
Claim 3
Dependent Claim 136 words
A curable composition according to claim 1, where the organopolysiloxane is a dimethylpolysiloxane containing vinyl radicals at the terminal positions, the organohydrogenpolysiloxane is a dimethylsiloxane/methylhydrogensiloxane copolymer, the ratio of silicon-bonded hydrogen atoms to vinyl radicals in the dimethylpolysiloxane is from 0.8:1 to 3:1, the hydrosilylation reaction catalyst is platinum metal or a platinum compound and is present at a concentration of from 0.1 to 100 ppm, calculated as platinum, based on the combined weight of said organopolysiloxane and said organohydrogenpolysiloxane, the carboxylic acid ester is selected from the group consisting of 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2,3-dihydroxypropyl acrylate and 2,3-dihydroxypropyl methacrylate and the organosilicon compound is selected from the group consisting of 3-glycidoxypropyltris(1-methylvinyloxy)silane, 1,2-bis[tris(1-methylvinyloxy)silyl]ethane, tetrakis(1-methylvinyloxy)silane, partial hydrolyzates of said organosilicon compound, mixtures of said organosilicon compound with organopolysiloxanes, and mixtures of said organosilicon compound with polyhydroxylated alcohols.
Claim 4
Dependent Claim 63 words
A curable composition according to claim 2 where said carboxylic acid ester is 2-hydroxyethyl acrylate, said organosilicon compound is tetrakis(1-methylvinyloxy)silane or 1,2-bis[tris(1-methylvinyloxy)silyl]ethane, the composition contains silica as a filler and an inhibitor for said catalyst, the concentration of said carboxylic acid ester is from 0.1 to 2 weight percent, and the concentration of said organosilicon compound is from 0.1 to 5 weight percent.
Claim 5
Dependent Claim 32 words
A curable composition according to claim 1 where said carboxylic acid ester and said organosilicon compound are reacted and the resultant reaction product is blended with the other ingredients of said composition.
Claim 6
Dependent Claim 26 words
A curable composition according to claim 4 where said reaction product is prepared by heating a mixture of said carboxylic acid ester and said organosilicon compound.

References Cited (Backward Citations)

US3892707A Cited
JPS5028309A Cited
US4082726A Cited
US4087585A Cited
US4742103A Cited
US4786701A Cited
US4737562A Cited
US4788311A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1993-12-24 1994-06-25 1994-12-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1997-12-24 1998-06-25 1998-12-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2001-12-24 2002-06-25 2002-12-25 $7700.00 Window Closed / Lapsed

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