GB872381A - Improvements in or relating to epoxy resin compositions - Google Patents
Improvements in or relating to epoxy resin compositionsInfo
- Publication number
- GB872381A GB872381A GB3772859A GB3772859A GB872381A GB 872381 A GB872381 A GB 872381A GB 3772859 A GB3772859 A GB 3772859A GB 3772859 A GB3772859 A GB 3772859A GB 872381 A GB872381 A GB 872381A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diamine
- polyamide
- bis
- epoxy resin
- specified
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000003822 epoxy resin Substances 0.000 title abstract 4
- 239000000203 mixture Substances 0.000 title abstract 4
- 229920000647 polyepoxide Polymers 0.000 title abstract 4
- 239000004952 Polyamide Substances 0.000 abstract 4
- 229920002647 polyamide Polymers 0.000 abstract 4
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 3
- 229930195729 fatty acid Natural products 0.000 abstract 3
- 239000000194 fatty acid Substances 0.000 abstract 3
- 150000004665 fatty acids Chemical class 0.000 abstract 3
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 abstract 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 150000004984 aromatic diamines Chemical class 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 abstract 2
- 229940018564 m-phenylenediamine Drugs 0.000 abstract 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 abstract 2
- 229960001124 trientine Drugs 0.000 abstract 2
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 abstract 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 abstract 1
- -1 3-(N-isopropyl-amino) propyl Chemical group 0.000 abstract 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000004593 Epoxy Substances 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- 239000005700 Putrescine Substances 0.000 abstract 1
- RGTXVXDNHPWPHH-UHFFFAOYSA-N butane-1,3-diamine Chemical compound CC(N)CCN RGTXVXDNHPWPHH-UHFFFAOYSA-N 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 150000004985 diamines Chemical class 0.000 abstract 1
- 150000003944 halohydrins Chemical class 0.000 abstract 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N mono-n-propyl amine Natural products CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 abstract 1
- OKBVMLGZPNDWJK-UHFFFAOYSA-N naphthalene-1,4-diamine Chemical compound C1=CC=C2C(N)=CC=C(N)C2=C1 OKBVMLGZPNDWJK-UHFFFAOYSA-N 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 abstract 1
- 229960003656 ricinoleic acid Drugs 0.000 abstract 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 abstract 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
A curable composition comprises a mixture of a polyamide, a primary aromatic diamine and an epoxy resin, said polyamide being derived from a polymeric fatty acid and an aliphatic polybasic amine. Specified polymeric fatty acids are the polymerization products of oleic, linoleic, linolenic, eladic and ricinoleic acid. Specified aliphatic polybasic amines are those of the general formula: <FORM:0872381/IV (a)/1> where R is an alkylene radical and x is an integer less than 6, e.g. ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, 1, 4-diaminobutane, 1, 3-diaminobutane, hexamethylene diamine, 3-(N-isopropyl-amino) propyl amine and 3, 31-imino-bis-propylamine. Preferred aromatic primary diamines are those of the structure H2NR1NH2 where R1 is an arylene radical containing at least one and less than five aromatic nuclei, e.g. m-phenylene diamine, p, p1-methylene dianiline, p-phenylene diamine and 1, 4-diaminonaphthalene. The polyamide and the primary aromatic diamine may be blended by heating at 80 DEG -100 DEG C. Specified epoxy resins are the reaction products of polyhydric phenols, e.g. bis-phenol A with halohydrins and/or glycerol dichlorohydrin, preferably having an epoxy equivalent weight of 125 to 400. In the examples, an epoxy resin derived from bis-phenol A and epichlorohydrin is blended with a blend of polyamide made from a dimerized fatty acid and triethylene tetramine with (1) and (2) m-phenylene diamine and (3) p, p1-methylene dianiline. Specification 726,570, also U.S.A. Specifications 2,379,413, 2,450,940, 2,585,115 and 2,589,245 are referred to.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3772859A GB872381A (en) | 1959-11-06 | 1959-11-06 | Improvements in or relating to epoxy resin compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3772859A GB872381A (en) | 1959-11-06 | 1959-11-06 | Improvements in or relating to epoxy resin compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB872381A true GB872381A (en) | 1961-07-12 |
Family
ID=10398611
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3772859A Expired GB872381A (en) | 1959-11-06 | 1959-11-06 | Improvements in or relating to epoxy resin compositions |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB872381A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0240460A3 (en) * | 1986-04-02 | 1987-12-16 | Ciba-Geigy Ag | Mixture of polyfunctional aliphatic glycidyl ethers curable at room temperature |
| US8871874B2 (en) | 2012-06-13 | 2014-10-28 | E I Du Pont De Nemours And Company | Thermoplastic melt-mixed composition with epoxy-amino acid compound heat stabilizer and processes for their preparation |
| US8952107B2 (en) | 2012-06-13 | 2015-02-10 | E I Du Pont De Nemours And Company | Thermoplastic melt-mixed composition with polyetherol heat stabilizer |
| US9080034B2 (en) | 2012-06-13 | 2015-07-14 | E I Du Pont De Nemours And Company | Thermoplastic melt-mixed composition with amino acid heat stabilizer |
| CN105895290A (en) * | 2016-04-27 | 2016-08-24 | 横店集团东磁股份有限公司 | Preparation method for high-temperature-resistant magnetic powder |
-
1959
- 1959-11-06 GB GB3772859A patent/GB872381A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0240460A3 (en) * | 1986-04-02 | 1987-12-16 | Ciba-Geigy Ag | Mixture of polyfunctional aliphatic glycidyl ethers curable at room temperature |
| US8871874B2 (en) | 2012-06-13 | 2014-10-28 | E I Du Pont De Nemours And Company | Thermoplastic melt-mixed composition with epoxy-amino acid compound heat stabilizer and processes for their preparation |
| US8952107B2 (en) | 2012-06-13 | 2015-02-10 | E I Du Pont De Nemours And Company | Thermoplastic melt-mixed composition with polyetherol heat stabilizer |
| US9080034B2 (en) | 2012-06-13 | 2015-07-14 | E I Du Pont De Nemours And Company | Thermoplastic melt-mixed composition with amino acid heat stabilizer |
| CN105895290A (en) * | 2016-04-27 | 2016-08-24 | 横店集团东磁股份有限公司 | Preparation method for high-temperature-resistant magnetic powder |
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