US4518631A
Expired / Lapsed
US
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Thixotropic curable coating compositions
Assignee: Dow Silicones Corp
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Filing: 1983-11-14
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Granted: 1985-05-21
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Expires: 2003-11-14
Abstract
Abstract The degree of thixotropic character exhibited by curable compositions comprising specified epoxide reactants, organosilicon reactants and fillers can be varied by varying the weight ratio of epoxide reactant to organosilicon reactant between values represented by r1 and r2 wherein said values are within the range of from 1:1 to 8:1. The compositions are particularly useful as extrudable coatings for solid state electronic devices.
Inventors
- 👤 Robert C. Antonen
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-31 21:55
CPC Classifications
H; H01; H01B; H01B3/00; H01B3/18; H01B3/30; H01B3/46; C; C08; C08G; C08G59/00; C08G59/18; C08G59/40; C08G59/4007; C08G59/4085; C08L; C08L83/00; C08L83/04; C09; C09D; C09D5/00; C09D5/04; H01B3/40; C08G77/00; C08G77/04; C08G77/14; C08G77/16; C08G77/18; C08G77/20; C08G77/22; C08G77/24; C08G77/70; H10; H10W; H10W72/00; H10W72/01; H10W72/015; H10W72/01515; H10W72/071; H10W72/075; H10W74/00
Claims Analysis
Total Claims: 29
Claim 1
Independent Claim
198 words
A curable liquid coating composition comprising a homogeneous mixture of (A) a polyfunctional liquid or solubilized epoxide reactant selected from the group consisting of cycloaliphatic epoxide compounds, glycidyl ethers of polyhydric phenols, epoxidized novolak resins and mixtures thereof; (B) a polyfunctional liquid or solubilized organosilicon reactant selected from the group consisting of silanes and polyorganosiloxanes, wherein each molecule of said organosilicon reactant contains at least two silicon-bonded groups selected from the group consisting of hydroxyl and alkoxy containing from 1 to 4 carbon atoms; (C) an amount of filler sufficient to impart a viscosity of from 50 to 1000 Pa·s, measured at 25° C., to said composition; and (D) a curing catalyst in an amount sufficient to promote curing of said composition; wherein the degree of thixotropic character exhibited by said composition is a function of the weight ratio of said epoxide reactant to said organosilicon reactant, and exhibits a gradual variation from a maximum degree of thixotropic character at weight ratio value r 1 to a minimum degree of thixotropic character at weight ratio value r 2 , the values represented by r 1 and r 2 being within the range of from 1:1 to 8:1, inclusive.
Claim 2
Dependent Claim
198 words
A curable liquid coating composition comprising a homogeneous mixture of (A) a polyfunctional liquid or solubilized epoxide reactant selected from the group consisting of cycloaliphatic epoxide compounds, glycidyl ethers of polyhydric phenols, epoxidized novolak resins and mixtures thereof; (B) a polyfunctional liquid or solubilized organosilicon reactant selected from the group consisting of silanes and polyorganosiloxanes, wherein each molecule of said organosilicon reactant contains at least two silicon-bonded groups selected from the group consisting of hydroxyl and alkoxy containing from 1 to 4 carbon atoms; (C) an amount of filler sufficient to impart a viscosity of from 50 to 1000 Pa·s, measured at 25° C., to said composition; and (D) a curing catalyst in an amount sufficient to promote curing of said composition; wherein the degree of thixotropic character exhibited by said composition is a function of the weight ratio of said epoxide reactant to said organosilicon reactant, and exhibits a gradual variation from a maximum degree of thixotropic character at weight ratio value r 1 to a minimum degree of thixotropic character at weight ratio value r 2 , the values represented by r 1 and r 2 being within the range of from 1:1 to 8:1, inclusive.
Claim 3
Dependent Claim
18 words
A composition according to claim 1 where the epoxide reactant is a diglycidyl ether of a dihydric phenol.
Claim 4
Dependent Claim
13 words
A composition according to claim 2 where the dihydric phenol is bisphenol A.
Claim 5
Dependent Claim
23 words
A composition according to claim 2 where the diglycidyl ether of a dihydric phenol is present in combination with an epoxidized novolak resin.
Claim 6
Dependent Claim
18 words
A composition according to claim 1 where the epoxide reactant is a cycloaliphatic epoxide of the formula ##STR3##
Claim 7
Dependent Claim
22 words
A composition according to claim 5 where said cycloaliphatic epoxide resin is present in combination with a diglycidyl ether of bisphenol A.
Claim 8
Dependent Claim
40 words
A composition according to claim 1 where the organosilicon reactant is a polyorganosiloxane containing repeating units of the general formula ##EQU2## where R" is a hydrocarbyl or halohydrocarbyl radical and the value of n is from 1 to 2, inclusive.
Claim 9
Dependent Claim
17 words
A composition according to claim 7 where R" is methyl, phenyl, vinyl, 3,3,3-trifluoropropyl or a combination thereof.
Claim 10
Dependent Claim
16 words
A composition according to claim 8 where at least 50% of the R" radicals are phenyl.
Claim 11
Dependent Claim
13 words
A composition according to claim 8 where the organosilicon reactant is a polymethylphenylsiloxane.
Claim 12
Dependent Claim
34 words
A composition according to claim 7 where the organosilicon reactant is a polyorganosiloxane resin containing φSiO 3/2 , φ 2 SiO, CH 3 100 SiO and CH 3 SiO 3/2 units, where φrepresents phenyl.
Claim 13
Dependent Claim
38 words
A composition according to claim 1 where said composition includes from 0.005 to 0.5%, based on the combined weight of epoxide and organosilicon reactants of a silane or siloxane containing at least one silicon-bonded hydrogen atom per molecule.
Claim 14
Dependent Claim
48 words
A composition according to claim 1 where the epoxide reactant is a diglycidyl ether of bisphenol A or ##STR4## the organosilicon reactant is a hydroxyl endblocked polymethylphenylsiloxane and the weight ratios of epoxide to organosilicon reactant represented by r 1 and r 2 are 1:1 and 3:1, respectively.
Claim 15
Dependent Claim
43 words
A composition according to claim 11 where the epoxide reactant is a diglycidyl ether of bisphenol A in combination with ##STR5## and the weight ratio of epoxide reactant to organosilicon reactant represented by r 1 and r 2 are 5:1 and 8:1, respectively.
Claim 16
Dependent Claim
53 words
A composition according to claim 1 where the epoxide reactant is a cycloaliphatic epoxide compound and the composition contains from 0.01 to about 1%, based on the weight of said composition, of a viscosity stabilizer comprising an alkaline earth metal salt of an aliphatic carboxylic acid containing from 10 to 20 carbon atoms.
Claim 17
Dependent Claim
12 words
A composition according to claim 15 where said salt is calcium stearate.
Claim 18
Dependent Claim
32 words
A composition according to claim 1 where said filler is a ground fused silica and is present at a concentration of from 50 to 75%, based on the weight of said composition.
Claim 19
Dependent Claim
45 words
A composition according to claim 1 where the curing catalyst is an aluminum compound selected from the group consisting of alkoxides, carboxylates, and reaction products of (1) said alkoxides or carboxylates with (2) compounds containing silicon-bonded hydroxyl groups, silicon-bonded alkoxy groups or silicon-bonded halogen atoms.
Claim 20
Dependent Claim
14 words
A composition according to claim 18 where said curing catalyst is an aluminum carboxylate.
Claim 21
Dependent Claim
13 words
A composition according to claim 19 where said aluminum carboxylate is aluminum benzoate.
Claim 22
Dependent Claim
28 words
A composition according to claim 18 where the concentration of curing catalyst is from 0.05 to 5%, based on the combined weight of epoxide reactant and organosilicon reactant.
Claim 23
Dependent Claim
24 words
A composition according to claim 1 where said composition contains up to 20% by weight of a monofunctional epoxide compound as a reactive diluent.
Claim 24
Dependent Claim
19 words
A composition according to claim 1 where said composition contains up to 20% by weight of a nonreactive solvent.
Claim 25
Dependent Claim
20 words
A composition according to claim 1 where the composition is cured at a temperature of from ambient to 200° C.
Claim 26
Dependent Claim
203 words
A curable liquid coating composition, said composition being a homogeneous product obtained by mixing together (A) a polyfunctional liquid or solubilized epoxide reactant selected from the group consisting of cycloaliphatic epoxide compounds, glycidyl ethers of polyhydric phenols, epoxidized novolak resins and mixtures thereof; (B) a polyfunctional liquid or solubilized organosilicon reactant selected from the group consisting of silanes and polyorganosiloxanes, wherein each molecule of said organosilicon reactant contains at least two silicon-bonded groups selected from the group consisting of hydroxyl and alkoxy containing from 1 to 4 carbon atoms; (C) an amount of filler sufficient to impart a viscosity of from 50 to 1000 Pa·s, measured at 25° C., to said composition; and (D) a curing catalyst in an amount sufficient to promote curing of said composition; wherein the degree of thixotropic character exhibited by said composition is a function of the weight ratio of said epoxide reactant to said organosilicon reactant, and exhibits a gradual variation from a maximum degree of thixotropic character at weight ratio value r 1 to a minimum degree of thixotropic character at weight ratio value r 2 , the values represented by r 1 and r 2 being within the range of from 1:1 to 8:1, inclusive.
Claim 27
Dependent Claim
203 words
A curable liquid coating composition, said composition being a homogeneous product obtained by mixing together (A) a polyfunctional liquid or solubilized epoxide reactant selected from the group consisting of cycloaliphatic epoxide compounds, glycidyl ethers of polyhydric phenols, epoxidized novolak resins and mixtures thereof; (B) a polyfunctional liquid or solubilized organosilicon reactant selected from the group consisting of silanes and polyorganosiloxanes, wherein each molecule of said organosilicon reactant contains at least two silicon-bonded groups selected from the group consisting of hydroxyl and alkoxy containing from 1 to 4 carbon atoms; (C) an amount of filler sufficient to impart a viscosity of from 50 to 1000 Pa·s, measured at 25° C., to said composition; and (D) a curing catalyst in an amount sufficient to promote curing of said composition; wherein the degree of thixotropic character exhibited by said composition is a function of the weight ratio of said epoxide reactant to said organosilicon reactant, and exhibits a gradual variation from a maximum degree of thixotropic character at weight ratio value r 1 to a minimum degree of thixotropic character at weight ratio value r 2 , the values represented by r 1 and r 2 being within the range of from 1:1 to 8:1, inclusive.
Claim 28
Independent Claim
232 words
A method for coating an electronic device that is bonded to a printed circuit board, said method consisting essentially of (I) applying over the exposed surfaces of said device a curable, thixotropic composition comprising (A) a polyfunctional liquid or solubilized epoxide reactant selected from the group consisting of cycloaliphatic epoxide compounds, glycidyl ethers of polyhydric phenols, epoxidized novolak resins and mixtures thereof; (B) a polyfunctional liquid or solubilized organosilicon reactant selected from the group consisting of silanes and polyorganosiloxanes, wherein each molecule of said organosilicon reactant contains at least two silicon-bonded groups selected from the group consisting of hydroxyl and alkoxy containing from 1 to 4 carbon atoms; (C) an amount of filler sufficient to impart a viscosity of from 50 to 1000 Pa·s, measured at 25° C., to said composition; and (D) a curing catalyst in an amount sufficient to promote curing of said composition; wherein the degree of thixotropic character exhibited by said composition is a function of the weight ratio of said epoxide reactant to said organosilicon reactant, and exhibits a gradual variation from a maximum degree of thixotropic character at weight ratio value r 1 to a minimum degree of thixotropic character at weight ratio value r 2 , the values represented by r 1 and r 2 being within the range of from 1:1 to 8:1, inclusive; and (II) curing said composition to form a solid material.
Claim 29
Independent Claim
232 words
A method for coating an electronic device that is bonded to a printed circuit board, said method consisting essentially of (I) applying over the exposed surfaces of said device a curable, thixotropic composition comprising (A) a polyfunctional liquid or solubilized epoxide reactant selected from the group consisting of cycloaliphatic epoxide compounds, glycidyl ethers of polyhydric phenols, epoxidized novolak resins and mixtures thereof; (B) a polyfunctional liquid or solubilized organosilicon reactant selected from the group consisting of silanes and polyorganosiloxanes, wherein each molecule of said organosilicon reactant contains at least two silicon-bonded groups selected from the group consisting of hydroxyl and alkoxy containing from 1 to 4 carbon atoms; (C) an amount of filler sufficient to impart a viscosity of from 50 to 1000 Pa·s, measured at 25° C., to said composition; and (D) a curing catalyst in an amount sufficient to promote curing of said composition; wherein the degree of thixotropic character exhibited by said composition is a function of the weight ratio of said epoxide reactant to said organosilicon reactant, and exhibits a gradual variation from a maximum degree of thixotropic character at weight ratio value r 1 to a minimum degree of thixotropic character at weight ratio value r 2 , the values represented by r 1 and r 2 being within the range of from 1:1 to 8:1, inclusive; and (II) curing said composition to form a solid material.
References Cited (Backward Citations)
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| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1988-05-20 | 1988-11-19 | 1989-05-21 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1992-05-20 | 1992-11-19 | 1993-05-21 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1996-05-20 | 1996-11-19 | 1997-05-21 | $7700.00 | Window Closed / Lapsed |