GB1017733A – Method of producing cured epoxy resins
– Google Patents
GB1017733A – Method of producing cured epoxy resins
– Google Patents
Method of producing cured epoxy resins
Info
Publication number
GB1017733A
GB1017733A
GB29681/62A
GB2968162A
GB1017733A
GB 1017733 A
GB1017733 A
GB 1017733A
GB 29681/62 A
GB29681/62 A
GB 29681/62A
GB 2968162 A
GB2968162 A
GB 2968162A
GB 1017733 A
GB1017733 A
GB 1017733A
Authority
GB
United Kingdom
Prior art keywords
diamine
bis
succinic anhydride
hydroxyphenyl
triethylene
Prior art date
1961-08-08
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
Application number
GB29681/62A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AT&T Corp
Original Assignee
Western Electric Co Inc
Priority date (The priority date 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 date listed.)
1961-08-08
Filing date
1962-08-02
Publication date
1966-01-19
1962-08-02
Application filed by Western Electric Co Inc
filed
Critical
Western Electric Co Inc
1966-01-19
Publication of GB1017733A
publication
Critical
patent/GB1017733A/en
Status
Expired
legal-status
Critical
Current
Links
Espacenet
Global Dossier
Discuss
239000003822
epoxy resin
Substances
0.000
title
abstract
2
229920000647
polyepoxide
Polymers
0.000
title
abstract
2
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
title
1
-1
polyethylene
Polymers
0.000
abstract
6
229920000768
polyamine
Polymers
0.000
abstract
5
WVRNUXJQQFPNMN-VAWYXSNFSA-N
3-[(e)-dodec-1-enyl]oxolane-2,5-dione
Chemical compound
CCCCCCCCCC\C=C\C1CC(=O)OC1=O
WVRNUXJQQFPNMN-VAWYXSNFSA-N
0.000
abstract
3
239000004952
Polyamide
Substances
0.000
abstract
3
229920002647
polyamide
Polymers
0.000
abstract
3
RTZKZFJDLAIYFH-UHFFFAOYSA-N
Diethyl ether
Chemical compound
CCOCC
RTZKZFJDLAIYFH-UHFFFAOYSA-N
0.000
abstract
2
ROSDSFDQCJNGOL-UHFFFAOYSA-N
Dimethylamine
Chemical compound
CNC
ROSDSFDQCJNGOL-UHFFFAOYSA-N
0.000
abstract
2
PIICEJLVQHRZGT-UHFFFAOYSA-N
Ethylenediamine
Chemical compound
NCCN
PIICEJLVQHRZGT-UHFFFAOYSA-N
0.000
abstract
2
ZRALSGWEFCBTJO-UHFFFAOYSA-N
Guanidine
Chemical compound
NC(N)=N
ZRALSGWEFCBTJO-UHFFFAOYSA-N
0.000
abstract
2
GLUUGHFHXGJENI-UHFFFAOYSA-N
Piperazine
Chemical compound
C1CNCCN1
GLUUGHFHXGJENI-UHFFFAOYSA-N
0.000
abstract
2
125000001931
aliphatic group
Chemical group
0.000
abstract
2
239000003795
chemical substances by application
Substances
0.000
abstract
2
GYZLOYUZLJXAJU-UHFFFAOYSA-N
diglycidyl ether
Chemical compound
C1OC1COCC1CO1
GYZLOYUZLJXAJU-UHFFFAOYSA-N
0.000
abstract
2
CIAMOALLBVRDDK-UHFFFAOYSA-N
1,1-diaminopropan-2-ol
Chemical compound
CC(O)C(N)N
CIAMOALLBVRDDK-UHFFFAOYSA-N
0.000
abstract
1
VILCJCGEZXAXTO-UHFFFAOYSA-N
2,2,2-tetramine
Chemical compound
NCCNCCNCCN
VILCJCGEZXAXTO-UHFFFAOYSA-N
0.000
abstract
1
FALRKNHUBBKYCC-UHFFFAOYSA-N
2-(chloromethyl)pyridine-3-carbonitrile
Chemical compound
ClCC1=NC=CC=C1C#N
FALRKNHUBBKYCC-UHFFFAOYSA-N
0.000
abstract
1
125000000022
2-aminoethyl group
Chemical group
[H]C([*])([H])C([H])([H])N([H])[H]
0.000
abstract
1
RPNUMPOLZDHAAY-UHFFFAOYSA-N
Diethylenetriamine
Chemical compound
NCCNCCN
RPNUMPOLZDHAAY-UHFFFAOYSA-N
0.000
abstract
1
OYHQOLUKZRVURQ-HZJYTTRNSA-N
Linoleic acid
Chemical compound
CCCCC\C=C/C\C=C/CCCCCCCC(O)=O
OYHQOLUKZRVURQ-HZJYTTRNSA-N
0.000
abstract
1
229920000877
Melamine resin
Polymers
0.000
abstract
1
CHJJGSNFBQVOTG-UHFFFAOYSA-N
N-methyl-guanidine
Natural products
CNC(N)=N
CHJJGSNFBQVOTG-UHFFFAOYSA-N
0.000
abstract
1
239000004698
Polyethylene
Substances
0.000
abstract
1
239000004743
Polypropylene
Substances
0.000
abstract
1
CZPWVGJYEJSRLH-UHFFFAOYSA-N
Pyrimidine
Chemical compound
C1=CN=CN=C1
CZPWVGJYEJSRLH-UHFFFAOYSA-N
0.000
abstract
1
125000004202
aminomethyl group
Chemical group
[H]N([H])C([H])([H])*
0.000
abstract
1
235000014113
dietary fatty acids
Nutrition
0.000
abstract
1
SWSQBOPZIKWTGO-UHFFFAOYSA-N
dimethylaminoamidine
Natural products
CN(C)C(N)=N
SWSQBOPZIKWTGO-UHFFFAOYSA-N
0.000
abstract
1
229930195729
fatty acid
Natural products
0.000
abstract
1
239000000194
fatty acid
Substances
0.000
abstract
1
150000004665
fatty acids
Chemical class
0.000
abstract
1
125000000623
heterocyclic group
Chemical group
0.000
abstract
1
NAQMVNRVTILPCV-UHFFFAOYSA-N
hexane-1,6-diamine
Chemical compound
NCCCCCCN
NAQMVNRVTILPCV-UHFFFAOYSA-N
0.000
abstract
1
GKQPCPXONLDCMU-CCEZHUSRSA-N
lacidipine
Chemical compound
CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C
GKQPCPXONLDCMU-CCEZHUSRSA-N
0.000
abstract
1
235000020778
linoleic acid
Nutrition
0.000
abstract
1
OYHQOLUKZRVURQ-IXWMQOLASA-N
linoleic acid
Natural products
CCCCC\C=C/C\C=C\CCCCCCCC(O)=O
OYHQOLUKZRVURQ-IXWMQOLASA-N
0.000
abstract
1
239000000203
mixture
Substances
0.000
abstract
1
KYCGURZGBKFEQB-UHFFFAOYSA-N
n’,n’-dibutylpropane-1,3-diamine
Chemical compound
CCCCN(CCCC)CCCN
KYCGURZGBKFEQB-UHFFFAOYSA-N
0.000
abstract
1
QOHMWDJIBGVPIF-UHFFFAOYSA-N
n’,n’-diethylpropane-1,3-diamine
Chemical compound
CCN(CC)CCCN
QOHMWDJIBGVPIF-UHFFFAOYSA-N
0.000
abstract
1
229920000573
polyethylene
Polymers
0.000
abstract
1
229920001155
polypropylene
Polymers
0.000
abstract
1
125000002924
primary amino group
Chemical group
[H]N([H])*
0.000
abstract
1
AOHJOMMDDJHIJH-UHFFFAOYSA-N
propylenediamine
Chemical compound
CC(N)CN
AOHJOMMDDJHIJH-UHFFFAOYSA-N
0.000
abstract
1
KIDHWZJUCRJVML-UHFFFAOYSA-N
putrescine
Chemical compound
NCCCCN
KIDHWZJUCRJVML-UHFFFAOYSA-N
0.000
abstract
1
229920005989
resin
Polymers
0.000
abstract
1
239000011347
resin
Substances
0.000
abstract
1
125000000467
secondary amino group
Chemical group
[H]N([*:1])[*:2]
0.000
abstract
1
229940014800
succinic anhydride
Drugs
0.000
abstract
1
FAGUFWYHJQFNRV-UHFFFAOYSA-N
tetraethylenepentamine
Chemical compound
NCCNCCNCCNCCN
FAGUFWYHJQFNRV-UHFFFAOYSA-N
0.000
abstract
1
229960001124
trientine
Drugs
0.000
abstract
1
Classifications
C—CHEMISTRY; METALLURGY
C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
C08G59/50—Amines
C08G59/56—Amines together with other curing agents
C08G59/58—Amines together with other curing agents with polycarboxylic acids or with anhydrides, halides, or low-molecular-weight esters thereof
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
Abstract
A method of curing an epoxide resin comprises mixing with the resin a curing agent selected from the group consisting of primary or secondary aliphatic or heterocyclic polyamines containing one primary and/or secondary amino group and polyamides derived from polymeric fatty acids and aliphatic polyamines, an accelerator consisting of dodecenyl succinic anhydride in an amount of up to 1 part by weight per 2 parts by weight of curing agent. Specified polyamines are ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, polyethylene polyamine, propylene diamine, dipropylene triamine, polypropylene polyamine, butylene diamine, pentylene diamine, hexylene diamine, octylene diamine, nonylene diamine, decylene diamine, 1:3-diamino-2-propanol, 3:3-imino-bis-(propylamine), guanidine, dimethylamine, diethylaminopropylamine, dibutylamino propylamine, piperazine, 2:4-dimethylpiperazine-melamine, 2:4 – diamino – 5 – (aminomethyl), pyrimidine, 2:4:6-triamino pyrimidine and 3:9 – bis – (aminoethyl) spirobimetadioxane. The polyamides are of conventional type. The examples disclose curable compositions comprising:-(1), (2) the diglycidyl ether of 2:2 – bis – (4 – hydroxyphenyl) propane, a triethylene diamine-ethylene oxide adduct and dodecenyl succinic anhydride; (3) the diglycidyl ether of 2:2 – bis – (4 – hydroxyphenyl) propane, a triethylene diamine-glycidyl adduct and dodecenyl succinic anhydride and (4) a polyglycidyl ether of 2:2-bis-(4-hydroxyphenyl) methane, a polyamide derived from dimerized linoleic acid and ethylene diamine, and docenyl succinic anhydride.
GB29681/62A
1961-08-08
1962-08-02
Method of producing cured epoxy resins
Expired
GB1017733A
(en)
Applications Claiming Priority (1)
Application Number
Priority Date
Filing Date
Title
US129949A
US3316191A
(en)
1961-08-08
1961-08-08
Curing epoxy resins
Publications (1)
Publication Number
Publication Date
GB1017733A
true
GB1017733A
(en)
1966-01-19
Family
ID=22442351
Family Applications (1)
Application Number
Title
Priority Date
Filing Date
GB29681/62A
Expired
GB1017733A
(en)
1961-08-08
1962-08-02
Method of producing cured epoxy resins
Country Status (2)
Country
Link
US
(1)
US3316191A
(en)
GB
(1)
GB1017733A
(en)
Cited By (1)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
CN113564745A
(en)
*
2021-08-23
2021-10-29
安徽农业大学
Polyamide fiber and preparation method thereof
Families Citing this family (5)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
NL6610758A
(en)
*
1965-08-09
1967-02-10
US3505284A
(en)
*
1967-05-15
1970-04-07
Merck & Co Inc
Catalysts for epoxy resins thickened with isocyanates
US3505283A
(en)
*
1967-05-15
1970-04-07
Merck & Co Inc
Isocyanates as thickening agents for epoxy resins
US3883342A
(en)
*
1973-04-13
1975-05-13
Akzona Inc
Plant growth regulators
US20120251830A1
(en)
*
2009-09-29
2012-10-04
Hitachi Chemical Company, Ltd
Resin composition, resin sheet, and cured resin material and method for producing the same
Family Cites Families (2)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
US2891026A
(en)
*
1955-04-15
1959-06-16
Minnesota Mining & Mfg
Composition comprising a solution of a glycidyl polyether and a glycidyl ether of a monohydric phenol
NL224266A
(en)
*
1957-01-22
1961
1961-08-08
US
US129949A
patent/US3316191A/en
not_active
Expired – Lifetime
1962
1962-08-02
GB
GB29681/62A
patent/GB1017733A/en
not_active
Expired
Cited By (1)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
CN113564745A
(en)
*
2021-08-23
2021-10-29
安徽农业大学
Polyamide fiber and preparation method thereof
Also Published As
Publication number
Publication date
US3316191A
(en)
1967-04-25
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