US3978151A
Expired / Lapsed
US
⏱️ 0.0 years remaining
High-functional polymercaptan resins in epoxy/anhydride resin compositions
Assignee: Diamond Shamrock Chemicals Co
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Filing: 1974-09-27
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Granted: 1976-08-31
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Expires: 1994-09-27
Abstract
Abstract Liquid, high-functional polymercaptan resins employed typically in sealants and adhesives, show excellent catalytic activity for preparing cured epoxy resin compositions from epoxy/anhydride systems. Blends of the epoxy resin with anhydrides and the high functional polymercaptan resins are adapted for room temperature curing into hard resinous compositions. Such compositions cured at ambient temperature show desirable hardness and achieve other characteristics such as reduced water absorption.
Inventors
- 👤 Douglas H. Strong
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-26 03:46
CPC Classifications
C; C08; C08G; C08G59/00; C08G59/18; C08G59/40; C08G59/42; C08G59/4284; C08G59/66
Claims Analysis
Total Claims: 9
Claim 1
Independent Claim
60 words
The method of preparing a cured, epoxy resin composition, wherein said epoxy resin will cure at elevated temperature with tertiary amine catalyst to a hard product, which preparation is achieved through accelerated and autogenous curing to said hard product at the situs of the application of the composition and at the ambient, non-elevated temperature of said situs, said method comprising:
Claim 2
Independent Claim
60 words
The method of preparing a cured, epoxy resin composition, wherein said epoxy resin will cure at elevated temperature with tertiary amine catalyst to a hard product, which preparation is achieved through accelerated and autogenous curing to said hard product at the situs of the application of the composition and at the ambient, non-elevated temperature of said situs, said method comprising:
Claim 3
Dependent Claim
194 words
blending together a uniform composition of continuous liquid phase and free from said amine catalyst, said composition having reactants that participate in the curing consisting essentially of: A. substance selected from the group consisting of polyglycidyl ether of a polyhydric phenol having a ratio of hydroxyl groups to 1,2-epoxy groups of not above about 2.5:2, cycloaliphatic epoxides, polyglycidyl ethers of novalac resin, and mixtures thereof; B. polycarboxylic acid anhydride in an amount sufficient to provide about 0.5-2 anhydride groups per 1,2-epoxy group, which amount of anhydride is uniformly dispersed in said continuous liquid phase; and C. liquid polymercaptan resin having an average SH functionality of greater than 2.5 and an average molecular weight between about 300-5,000, said resin being present in uniform dispersion in said liquid phase and in a catalytic amount within the range of from above about 3 to about 150 weight parts per 100 weight parts of said (A) component, with said polymercaptan resin having hydroxyl functionality in addition to said SH functionality; and 2. applying the resulting uniform composition while permitting autogenous curing of same at the ambient temperature of the situs of application to thereby prepare said hard product.
Claim 4
Dependent Claim
194 words
blending together a uniform composition of continuous liquid phase and free from said amine catalyst, said composition having reactants that participate in the curing consisting essentially of: A. substance selected from the group consisting of polyglycidyl ether of a polyhydric phenol having a ratio of hydroxyl groups to 1,2-epoxy groups of not above about 2.5:2, cycloaliphatic epoxides, polyglycidyl ethers of novalac resin, and mixtures thereof; B. polycarboxylic acid anhydride in an amount sufficient to provide about 0.5-2 anhydride groups per 1,2-epoxy group, which amount of anhydride is uniformly dispersed in said continuous liquid phase; and C. liquid polymercaptan resin having an average SH functionality of greater than 2.5 and an average molecular weight between about 300-5,000, said resin being present in uniform dispersion in said liquid phase and in a catalytic amount within the range of from above about 3 to about 150 weight parts per 100 weight parts of said (A) component, with said polymercaptan resin having hydroxyl functionality in addition to said SH functionality; and 2. applying the resulting uniform composition while permitting autogenous curing of same at the ambient temperature of the situs of application to thereby prepare said hard product.
Claim 5
Dependent Claim
35 words
The method of claim 1 wherein there is first prepared a liquid eutectic mixture of polycarboxylic acid anhydrides and the resulting liquid eutectic mixture is thereafter mixed with said part (A) and part (C) components.
Claim 6
Dependent Claim
30 words
The method of claim 1 wherein said part (B) and said part (C) components are first blended together and the resulting blend is thereafter admixed with said part (A) component.
Claim 7
Dependent Claim
13 words
A hard, cured epoxy resin composition prepared by the method of claim 1.
Claim 8
Independent Claim
251 words
The method of initiating catalytic, autogenous curing of epoxy resin composition at the situs of the application of the composition and at the ambient, non-elevated temperature of said situs, said composition having continuous liquid phase and comprising substance selected from the group consisting of polyglycidyl ether of a polyhydric phenol having a ratio of hydroxyl groups to 1,2-epoxy groups of not above about 2.5:2, cycloaliphatic epoxides, polyglycidyl ethers of novalac resin, and mixtures thereof, wherein said epoxy resin will cure at elevated temperature with tertiary amine catalyst to a hard product, and said method provides curing to a hard product of uniform blends containing said epoxy resin and free from said amine catalyst, which method comprises: admixing with said resin, at the situs of the application of said composition, reactants participating in the curing and consisting essentially of: 1. polycarboxylic acid anhydride in an amount sufficient to provide about 0.5-2 anhydride groups per 1,2-epoxy group, which amount of anhydride is uniformly dispersed in said continuous liquid phase; and 2. liquid polymercaptan resin having an average SH functionality of greater than 2.5 and and average molecular weight between about 300-5,000, said resin being present in uniform dispersion in said liquid phase and in a catalytic amount within the range of from above about 3 to about 150 weight parts per 100 weight parts of said epoxy resin, with said polymercaptan resin having hydroxyl functionality in addition to said SH functionality; and thereafter permitting autogenous curing at the ambient temperature of said situs.
Claim 9
Independent Claim
251 words
The method of initiating catalytic, autogenous curing of epoxy resin composition at the situs of the application of the composition and at the ambient, non-elevated temperature of said situs, said composition having continuous liquid phase and comprising substance selected from the group consisting of polyglycidyl ether of a polyhydric phenol having a ratio of hydroxyl groups to 1,2-epoxy groups of not above about 2.5:2, cycloaliphatic epoxides, polyglycidyl ethers of novalac resin, and mixtures thereof, wherein said epoxy resin will cure at elevated temperature with tertiary amine catalyst to a hard product, and said method provides curing to a hard product of uniform blends containing said epoxy resin and free from said amine catalyst, which method comprises: admixing with said resin, at the situs of the application of said composition, reactants participating in the curing and consisting essentially of: 1. polycarboxylic acid anhydride in an amount sufficient to provide about 0.5-2 anhydride groups per 1,2-epoxy group, which amount of anhydride is uniformly dispersed in said continuous liquid phase; and 2. liquid polymercaptan resin having an average SH functionality of greater than 2.5 and and average molecular weight between about 300-5,000, said resin being present in uniform dispersion in said liquid phase and in a catalytic amount within the range of from above about 3 to about 150 weight parts per 100 weight parts of said epoxy resin, with said polymercaptan resin having hydroxyl functionality in addition to said SH functionality; and thereafter permitting autogenous curing at the ambient temperature of said situs.
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) | 1979-08-31 | 1980-03-01 | 1980-08-31 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1983-08-31 | 1984-03-01 | 1984-08-31 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1987-08-31 | 1988-03-01 | 1988-08-31 | $7700.00 | Window Closed / Lapsed |