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US4684538A Expired / Lapsed US ⏱️ 0.0 years remaining

Polysiloxane urethane compounds and adhesive compositions, and method of making and using the same

Assignee: Henkel Loctite Corp
•
Filing: 1986-02-21
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Granted: 1987-08-04
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Expires: 2006-02-21
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Abstract

Abstract Silicone urethane compounds, e.g., a polysiloxane urethane (meth)acrylate, obtained as a reaction product of a polysiloxane carbinol, a polyisocyanate, and a polyfunctional compound having at least one functional group which is reactive with an isocyanate group of the polyisocyanate and after reaction therewith provides an ethylenic functional group in the reaction product. The polysiloxane carbinol has a molecular weight of from about 5,000 to about 50,000 and has R'OH end groups wherein R' is linear C 4 -C 20 alkylene. Such carbinol may be obtained as a reaction product of the corresponding hydride-terminated polysiloxane and a linear C 4 -C 20 ω-alkenyl alcohol. The hydride-terminated polysiloxane in turn may be obtained as a reaction product of either (i) the corresponding silanol of molecular weight at least 10,000 and a hydridosilane having one or more hydrolyzable groups attached to the silicon atom, or (ii) a cyclosiloxane and a 1,3-dihydrido disiloxane. The disclosed compounds may be utilized in adhesive compositions for substrates including bonding surfaces such as glass, and polymers and copolymers of ethylenically unsaturated monomers. The bonding of such substrates may suitably be carried out at least partially under anoxic conditions, e.g., with elevated temperature and/or actinic radiation curing of the bonding composition in a substantially oxygen-free environment. A preferred vacuum degassing/anoxic curing process is disclosed for such bonding compositions, which is particularly advantageous for difficult to bond substrates, such as low density polyethylene.

Inventors

  • 👤 Philip T. Klemarczyk

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 16:22
CPC Classifications
C; C09; C09J; C09J175/00; C09J175/04; C09J175/14; C09J175/16; C08; C08G; C08G18/00; C08G18/06; C08G18/28; C08G18/40; C08G18/61; C08G18/67; C08G18/671; C08G18/672; C08G77/00; C08G77/04; C08G77/38; C08G77/382; C08G77/388; C08J; C08J5/00; C08J5/12; C08J5/124; C09J5/00; C09J5/06; Y; Y10; Y10T; Y10T428/00; Y10T428/31504; Y10T428/31551; Y10T428/31573; Y10T428/31587; Y10T428/31652; Y10T428/31663

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 206 words
A method of bonding a first surface formed of polyethylene, to a second surface, comprising: (1) applying to at least one of said first and second surfaces a composition comprising a polymerizable polysiloxane urethane compound formed as a reaction product of: (a) a polysiloxane carbinol having a molecular weight of from about 5,000 to about 50,000, of the formula ##STR9## wherein: each R independently is C 1 -C 8 alkyl, C 3 -C 6 cycloalkyl, or phenyl; each R' independently is linear C 4 -C 20 alkylene; and x=50-700; (b) a polyisocyanate; and (c) a polyfunctional compound having at least one functional group which is reactive with an isocyanate group of said polyisocyanate and after reaction therewith provides an ethylenic functional group in the reaction product; (2) placing the first and second surfaces in bondable relationship to one another in a curing zone; (3) establishing vacuum in said curing zone; (4) breaking said vacuum with a gas consisting essentially of nitrogen, to provide a gas environment thereof in said curing zone; and (5) exposing said composition to elevated temperature and/or actinic radiation for sufficient time to cure same in said gas environment in said curing zone, thereby bonding said first and second surfaces to one another.
Claim 2
Independent Claim 206 words
A method of bonding a first surface formed of polyethylene, to a second surface, comprising: (1) applying to at least one of said first and second surfaces a composition comprising a polymerizable polysiloxane urethane compound formed as a reaction product of: (a) a polysiloxane carbinol having a molecular weight of from about 5,000 to about 50,000, of the formula ##STR9## wherein: each R independently is C 1 -C 8 alkyl, C 3 -C 6 cycloalkyl, or phenyl; each R' independently is linear C 4 -C 20 alkylene; and x=50-700; (b) a polyisocyanate; and (c) a polyfunctional compound having at least one functional group which is reactive with an isocyanate group of said polyisocyanate and after reaction therewith provides an ethylenic functional group in the reaction product; (2) placing the first and second surfaces in bondable relationship to one another in a curing zone; (3) establishing vacuum in said curing zone; (4) breaking said vacuum with a gas consisting essentially of nitrogen, to provide a gas environment thereof in said curing zone; and (5) exposing said composition to elevated temperature and/or actinic radiation for sufficient time to cure same in said gas environment in said curing zone, thereby bonding said first and second surfaces to one another.
Claim 3
Dependent Claim 13 words
A method according to claim 1, wherein said polyethylene is low density polyethylene.
Claim 4
Dependent Claim 17 words
A method according to claim 1, wherein both the first and second surfaces are formed of polyethylene.
Claim 5
Dependent Claim 19 words
A method according to claim 1, wherein both the first and second surfaces are formed of low density polyethylene.
Claim 6
Dependent Claim 25 words
A process according to claim 1, wherein the pressure in said curing zone after establishment of vacuum therein is from about 0.1 to 10 Torr.
Claim 7
Dependent Claim 31 words
An article comprising a first surface formed of polyethylene and a second surface, wherein the first and second surfaces are bonded to one another by a method according to claim 1.

References Cited (Backward Citations)

US4130708A Cited
GB2110702A Cited
US4582885A Cited
CA1134984A Cited
US4369300A Cited
WO1984000424A1 Cited
AU2005183A Cited
EP0127321A1 Cited
US4605712A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-08-03 1991-02-02 1991-08-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-08-03 1995-02-02 1995-08-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-08-03 1999-02-02 1999-08-04 $7700.00 Window Closed / Lapsed

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