US4173593A
Expired / Lapsed
US
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Metal acetylacetonate latent accelerators for an epoxy-styrene resin system
Assignee: Westinghouse Electric Corp
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Filing: 1977-04-05
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Granted: 1979-11-06
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Expires: 1997-04-05
Abstract
Abstract An epoxy-styrene, solventless resin impregnating varnish, having an atmospheric catalyzed pot life at room temperature of at least 45 days, is made by mixing: (1) the product of the reaction of (a) 1 part of an epoxy resin mixture, comprising solid epoxy resin and liquid epoxy resin wherein the weight ratio of solid epoxy: liquid epoxy is between 1:1 to 1:10; with (b) between about 0.01 part to 0.06 part of maleic anhydride and (c) a catalyst under such conditions that the epoxy diester formed has an acid number of between about 0.5 to 3.0; with (2) a coreactive vinyl monomer; and between about 0.0003 part to 0.004 part of a room temperature stabilizer; (3) between about 0.3 part to 1.2 part of a polycarboxylic anhydride, which is soluble in the mixture of (1) and (2), and an amount of free radical catalyst that is effective to provide a catalytic effect on the impregnating varnish and to cure it at temperatures of over about 85 DEG C., and with (4) between 0.0005 part to 0.005 part of a metal acetylacetonate, selected from the group consisting of chromium (III) acetylacetonate, manganese (III) acetylacetonate, ferric (iron III) acetylacetonate, zinc (II) acetylacetonate, aluminum (III) acetylacetonate, sodium (I) acetylacetonate, uranyl (VI) acetylacetonate, and mixtures thereof, acting as latent accelerator.
Inventors
- 👤 James D. B. Smith
- 👤 Robert N. Kauffman
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-27 08:14
CPC Classifications
H; H01; H01B; H01B3/00; H01B3/18; H01B3/30; H01B3/40; C; C08; C08F; C08F299/00; C08F299/02; C08F299/022; C08F299/026; C08G; C08G59/00; C08G59/18; C08G59/20; C08G59/22; C08G59/226; C08G59/40; C08G59/42; C08G59/4207; C08L; C08L63/00; C08L63/10; H01B3/02; H01B3/04; H02; H02K; H02K3/00; H02K3/30; Y; Y10; Y10T; Y10T428/00; Y10T428/29; Y10T428/2913; Y10T428/2933; Y10T428/2936; Y10T428/31504; Y10T428/31511; Y10T428/31529
Claims Analysis
Total Claims: 10
Claim 1
Independent Claim
331 words
A resinous, solventless, low viscosity liquid impregnating composition having fast cure properties, comprising the admixture of: (A) an epoxy diester, formed from the reaction of: (I) 1 part of a mixture of a solid 1,2-epoxy resin having an epoxy equivalent weight of between about 390 to 2,500, and a liquid 1,2-epoxy resin having an epoxy equivalent weight of between about 100 to 385, wherein the weight ratio of solid epoxy resin:liquid epoxy resin is between about 1:1 to 1:10, with (II) between about 0.01 part to about 0.06 part of maleic anhydride and about 0.0001 part to about 0.005 part of a catalyst selected from the group consisting of piperidine, pyridine, imidazoles, and aliphatic tertiary amines, and mixtures thereof; to form an epoxy diester having an acid number between about 0.5 to 3.0; with (B) between about 0.05 part to about 3.0 parts of a vinyl monomer co-reactive with the epoxy diester; about 0.0003 part to about 0.004 part of a room temperature stabilizer selected from the group consisting of dinitrophenols, trinitrophenols, aromatic quinones, and mixtures thereof; between about 0.3 part to about 1.2 parts of a polycarboxylic anhydride which is soluble in the epoxy diester-vinyl monomer-stabilizer mixture at temperatures of between about 0° C. to 35° C.; and an amount of a free radical catalyst selected from the group consisting of azo compounds, peroxides, and mixtures thereof, that is effective to provide a catalytic curing effect on the mixture at a temperature of over about 85° C.; and (C) between 0.0005 part to 0.005 part of a metal acetylacetonate, selected from the group consisting of sodium (I) acetylacetonate, zinc (II) acetylacetonate, chromium (III) acetylacetonate, manganese (III) acetylacetonate, ferric (III) acetylacetonate, aluminum (III) acetylacetonate, uranyl (VI) acetylacetonate, and mixtures thereof, acting as the latent accelerator; to provide an epoxy-styrene solventless, liquid impregnating composition, having a viscosity of between about 5 cps to 500 cps at 25° C., and an atmospheric catalyzed pot life at 25° C. of at least 45 days.
Claim 2
Dependent Claim
331 words
A resinous, solventless, low viscosity liquid impregnating composition having fast cure properties, comprising the admixture of: (A) an epoxy diester, formed from the reaction of: (I) 1 part of a mixture of a solid 1,2-epoxy resin having an epoxy equivalent weight of between about 390 to 2,500, and a liquid 1,2-epoxy resin having an epoxy equivalent weight of between about 100 to 385, wherein the weight ratio of solid epoxy resin:liquid epoxy resin is between about 1:1 to 1:10, with (II) between about 0.01 part to about 0.06 part of maleic anhydride and about 0.0001 part to about 0.005 part of a catalyst selected from the group consisting of piperidine, pyridine, imidazoles, and aliphatic tertiary amines, and mixtures thereof; to form an epoxy diester having an acid number between about 0.5 to 3.0; with (B) between about 0.05 part to about 3.0 parts of a vinyl monomer co-reactive with the epoxy diester; about 0.0003 part to about 0.004 part of a room temperature stabilizer selected from the group consisting of dinitrophenols, trinitrophenols, aromatic quinones, and mixtures thereof; between about 0.3 part to about 1.2 parts of a polycarboxylic anhydride which is soluble in the epoxy diester-vinyl monomer-stabilizer mixture at temperatures of between about 0° C. to 35° C.; and an amount of a free radical catalyst selected from the group consisting of azo compounds, peroxides, and mixtures thereof, that is effective to provide a catalytic curing effect on the mixture at a temperature of over about 85° C.; and (C) between 0.0005 part to 0.005 part of a metal acetylacetonate, selected from the group consisting of sodium (I) acetylacetonate, zinc (II) acetylacetonate, chromium (III) acetylacetonate, manganese (III) acetylacetonate, ferric (III) acetylacetonate, aluminum (III) acetylacetonate, uranyl (VI) acetylacetonate, and mixtures thereof, acting as the latent accelerator; to provide an epoxy-styrene solventless, liquid impregnating composition, having a viscosity of between about 5 cps to 500 cps at 25° C., and an atmospheric catalyzed pot life at 25° C. of at least 45 days.
Claim 3
Dependent Claim
16 words
The solventless impregnating composition of claim 1, wherein chromium (III) acetylacetonate is used as latent accelerator.
Claim 4
Dependent Claim
31 words
The solventless impregnating composition of claim 1, wherein the epoxy resins are diglycidyl ethers of bisphenol A, and the solid epoxy resin has an epoxy equivalent weight of between about 390-800.
Claim 5
Dependent Claim
69 words
The solventless impregnating composition of claim 1, wherein the catalyst added in (A) (II) is an aliphatic tertiary amine, the vinyl monomer is selected from the group consisting of styrene, vinyl toluene, alphamethyl styrene, 2,4-dichlorostyrene, paramethyl styrene, vinyl acetate, methyl metacrylate, ethyl acrylate, methyl vinyl ketone, butyl methacrylate, and mixtures thereof, and about 0.01 to 0.001 part of free radical catalyst added in (B) is used in the reaction.
Claim 6
Dependent Claim
92 words
The solventless impregnating composition of claim 4, wherein the room temperature stabilizer is selected from the group consisting of picric acid; 2,4 dinitrophenol; 2,6 dinitrophenol; dinitroresorcinol; trinitroresorcinol; para-benzoquinone; 2,5-ditertiary butylhydroquinone; tertiary butylhydroquinone; catechol; cresylic acid, and mixtures thereof; and the polycarboxylic anhydride which is mixed with the formed epoxy diester is selected from the group consisting of NADIC methyl anhydride, a eutectic mixture of tetrahydrophthalic anhydride and hexahydrophthalic anhydride, dodecenyl succinic anhydride, trimellitic anhydride, methyl tetrahydrophthalic anhydride, chlorendic anhydride, benzophenone tetracarboxylic dianhydride, pyromellitic dianhydride, phthalic anhydride, 1-methyl hexahydrophthalic anhydride, and mixtures thereof.
Claim 7
Dependent Claim
271 words
A resinous, solventless, low viscosity liquid impregnating composition having fast cure properties, useful for impregnating insulated electrical components, comprising the product of mixing: (A) an epoxy diester, formed from the reaction of: (I) 1 part of a mixture of a solid 1,2-epoxy resin having an epoxy equivalent weight of between about 390 to 2,500 and a liquid 1,2-epoxy resin having an epoxy equivalent weight of between about 100 to 385, wherein the weight ratio of solid epoxy resin:liquid epoxy resin is between about 1:1 to 1:10, with (II) between about 0.01 part to 0.06 part of maleic anhydride and about 0.0001 part to 0.005 part of an aliphatic tertiary amine catalyst, to form an epoxy diester having an acid number between about 0.5 to 3.0; with (B) between about 0.05 part to 3.0 parts of styrene, about 0.0003 part to 0.004 part of a room temperature stabilizer selected from the group consisting of dinitrophenols, trinitrophenols, aromatic quinones, and mixtures thereof; between about 0.3 part to 1.2 parts of a polycarboxylic anhydride which is soluble in the epoxy diester-styrene-stabilizer mixture at temperatures of between about 0° C. to 35° C.; and about 0.01 part to 0.001 part of peroxide catalyst that is effective to provide a catalytic curing effect on the mixture at a temperature of over 85° C.; and (C) between 0.0005 part to 0.005 part of chromium (III) acetylacetonate, acting as the latent accelerator to provide an epoxy-styrene solventless, liquid impregnating composition, having a vicosity of between about 5 cps to 500 cps at 25° C., and an atmospheric catalyzed pot life at 25° C. of at least 45 days.
Claim 8
Dependent Claim
271 words
A resinous, solventless, low viscosity liquid impregnating composition having fast cure properties, useful for impregnating insulated electrical components, comprising the product of mixing: (A) an epoxy diester, formed from the reaction of: (I) 1 part of a mixture of a solid 1,2-epoxy resin having an epoxy equivalent weight of between about 390 to 2,500 and a liquid 1,2-epoxy resin having an epoxy equivalent weight of between about 100 to 385, wherein the weight ratio of solid epoxy resin:liquid epoxy resin is between about 1:1 to 1:10, with (II) between about 0.01 part to 0.06 part of maleic anhydride and about 0.0001 part to 0.005 part of an aliphatic tertiary amine catalyst, to form an epoxy diester having an acid number between about 0.5 to 3.0; with (B) between about 0.05 part to 3.0 parts of styrene, about 0.0003 part to 0.004 part of a room temperature stabilizer selected from the group consisting of dinitrophenols, trinitrophenols, aromatic quinones, and mixtures thereof; between about 0.3 part to 1.2 parts of a polycarboxylic anhydride which is soluble in the epoxy diester-styrene-stabilizer mixture at temperatures of between about 0° C. to 35° C.; and about 0.01 part to 0.001 part of peroxide catalyst that is effective to provide a catalytic curing effect on the mixture at a temperature of over 85° C.; and (C) between 0.0005 part to 0.005 part of chromium (III) acetylacetonate, acting as the latent accelerator to provide an epoxy-styrene solventless, liquid impregnating composition, having a vicosity of between about 5 cps to 500 cps at 25° C., and an atmospheric catalyzed pot life at 25° C. of at least 45 days.
Claim 9
Dependent Claim
17 words
The solventless impregnating composition of claim 6, wherein the epoxy resins are diglycidyl ethers of bisphenol A.
Claim 10
Dependent Claim
92 words
The solventless impregnating composition of claim 4, wherein the room temperature stabilizer is selected from the group consisting of picric acid; 2,4 dinitrophenol; 2,6 dinitrophenol; dinitroresorcinol; trinitroresorcinol; para-benzoquinone; 2,5-ditertiary butylhydroquinone; tertiary butylhydroquinone; catechol; cresylic acid, and mixtures thereof; and the polycarboxylic anhydride which is mixed with the formed epoxy diester is selected from the group consisting of NADIC methyl anhydride, a eutectic mixture of tetrahydrophthalic anhydride and hexahydrophthalic anhydride, dodecenyl succinic anhydride, trimellitic anhydride, methyl tetrahydrophthalic anhydride, chlorendic anhydride, benzophenone tetracarboxylic dianhydride, pyromellitic dianhydride, phthalic anhydride, 1-methyl hexahydrophthalic anhydride, and mixtures thereof.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1982-11-05 | 1983-05-07 | 1983-11-06 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1986-11-05 | 1987-05-07 | 1987-11-06 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1990-11-05 | 1991-05-07 | 1991-11-06 | $7700.00 | Window Closed / Lapsed |