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US4525566A Expired / Lapsed US ⏱️ 0.0 years remaining

Coating method and silicone composition for PSA release coating

Assignee: Dow Silicones Corp
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Filing: 1984-03-02
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Granted: 1985-06-25
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Expires: 2004-03-02
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Abstract

Abstract Moisture-curable silicone compositions for adhesive-release coatings comprising an alkoxysilylorganosiloxane, a titanium ester and an aminoorganosiloxane have an adhesive-release force, when cured, which is directly related to the amount and type of aminoorganosiloxane. The compositions are useful for coating a flexible sheet material, such as paper or polymeric film, to provide a surface that will release pressure sensitive adhesive with a pre-selected release force of up to 400 g/in (154 N/m). Thin coatings of the composition cure in as little as 15 seconds when exposed to moisture.

Inventors

  • 👤 Gary R. Homan
  • 👤 David L. Stickles

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 10:52
CPC Classifications
C; C08; C08L; C08L83/00; C08L83/14; C08K; C08K5/00; C08K5/04; C08K5/05; C08K5/56; C08L83/04; C08L83/08; Y; Y10; Y10S; Y10S528/00; Y10S528/901; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31652; Y10T428/31663

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 291 words
A liquid composition which cures when applied to a substrate and exposed to moisture, said liquid composition being prepared by mixing, under substantially anhydrous conditions, components comprising (A) 100 parts by weight of an organopolysiloxane fluid bearing an average of at least two silicon-bonded, alkoxysilylorganic radicals per molecule, said radicals having the formula --QSiR a 1 (OR 2 ) 3-a and said organopolysiloxane fluid having the formula ZR 2 1 SiO(Me 2 SiO) x (MeRSiO) y SiR 2 1 Z, (B) a titanium ester, or a partial hydrolyzate or partial alcoholate thereof, soluble in said liquid composition, in sufficient amount to provide from 0.5 to 4.0 parts by weight of titanium, and (C) from 0.5 to 50 parts by weight of an aminoorganosiloxane bearing an average of at least 1 silicon-bonded aminoorgano radical per molecule, said aminoorgano radical having the formula --Q(NR 3 CH 2 CH 2 ) m NHR 3 , all other silicon-bonded radicals of the aminoorganosiloxane being selected from the group consisting of siloxane oxygen atoms, R 1 radicals and OR 2 radicals; wherein, independently at each occurrence in the components, R denotes the --QSiR a 1 (OR 2 ) 3-a radical; R 1 denotes a monovalent hydrocarbon radical having from 1 to 6, inclusive, carbon atoms; R 2 denotes a methyl, ethyl, propyl or methoxyethyl radical; R 3 denotes a H atom or an R 1 radical; Q denotes an alkylene radical; Z denotes an R radical or an R 1 radical; Me denotes a methyl radical; a has a value of 0 or 1; x has an average value of from about 50 to 500; y has an average value of from 0 to (x+y)/4; and m has a value of from 0 to about 3.
Claim 2
Dependent Claim 291 words
A liquid composition which cures when applied to a substrate and exposed to moisture, said liquid composition being prepared by mixing, under substantially anhydrous conditions, components comprising (A) 100 parts by weight of an organopolysiloxane fluid bearing an average of at least two silicon-bonded, alkoxysilylorganic radicals per molecule, said radicals having the formula --QSiR a 1 (OR 2 ) 3-a and said organopolysiloxane fluid having the formula ZR 2 1 SiO(Me 2 SiO) x (MeRSiO) y SiR 2 1 Z, (B) a titanium ester, or a partial hydrolyzate or partial alcoholate thereof, soluble in said liquid composition, in sufficient amount to provide from 0.5 to 4.0 parts by weight of titanium, and (C) from 0.5 to 50 parts by weight of an aminoorganosiloxane bearing an average of at least 1 silicon-bonded aminoorgano radical per molecule, said aminoorgano radical having the formula --Q(NR 3 CH 2 CH 2 ) m NHR 3 , all other silicon-bonded radicals of the aminoorganosiloxane being selected from the group consisting of siloxane oxygen atoms, R 1 radicals and OR 2 radicals; wherein, independently at each occurrence in the components, R denotes the --QSiR a 1 (OR 2 ) 3-a radical; R 1 denotes a monovalent hydrocarbon radical having from 1 to 6, inclusive, carbon atoms; R 2 denotes a methyl, ethyl, propyl or methoxyethyl radical; R 3 denotes a H atom or an R 1 radical; Q denotes an alkylene radical; Z denotes an R radical or an R 1 radical; Me denotes a methyl radical; a has a value of 0 or 1; x has an average value of from about 50 to 500; y has an average value of from 0 to (x+y)/4; and m has a value of from 0 to about 3.
Claim 3
Dependent Claim 32 words
A liquid composition according to claim 1 wherein each R 1 radical is a methyl radical and the titanium ester is a tetraalkyl titanate or a partial hydrolyzate or partial alcoholate thereof.
Claim 4
Dependent Claim 65 words
A liquid composition according to claim 2 wherein the tetraalkyl titanate is tetraisopropyl titanate, the value of y in component (A) does not exceed the value of 3600/(x+y) for values of (x+y) exceeding 120 and the aminoorganosiloxane has the formula ##STR8## wherein p has an average value of from about 50 to 500 and q has an average value of from about 1 to p/10.
Claim 5
Dependent Claim 36 words
A liquid composition according to claim 3 wherein Z denotes Me, component (B) is a partial methanolate of tetraisopropyl titanate and the aminoorganosiloxane has the formula ##STR9## wherein n has a value of 3 or 4.
Claim 6
Dependent Claim 53 words
A liquid composition according to claim 2 wherein the tetraalkyl titanate is tetraisopropyl titanate, the value of y in component (A) does not exceed the value of 3600/(x+y) for values of (x+y) exceeding 120 and the aminoorganosiloxane has the formula ##STR10## wherein r has an average value of from about 5 to 250.
Claim 7
Dependent Claim 36 words
A liquid composition according to claim 5 wherein Z denotes Me, component (B) is a partial methanolate of tetraisopropyl titanate and the aminoorganosiloxane has the formula ##STR11## wherein n has a value of 3 or 4.

References Cited (Backward Citations)

US4191817A Cited
US4387177A Cited
US4417042A Cited
US4472551A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-06-24 1988-12-24 1989-06-25 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-06-24 1992-12-24 1993-06-25 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-06-24 1996-12-24 1997-06-25 $7700.00 Window Closed / Lapsed

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