JPS6359409B2 - - Google Patents

Info

Publication number: JPS6359409B2
Authority: JP; Japan
Prior art keywords: epoxy resin; formula; curing; room temperature; type
Prior art date: 1981-02-04
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

JP1532281A

Other languages

English (en)

Japanese (ja)

Other versions

JPS57128719A (en

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.)

1981-02-04

Filing date

1981-02-04

Publication date

1988-11-18

1981-02-04 Application filed filed Critical

1981-02-04 Priority to JP1532281A priority Critical patent/JPS57128719A/ja

1982-08-10 Publication of JPS57128719A publication Critical patent/JPS57128719A/ja

1988-11-18 Publication of JPS6359409B2 publication Critical patent/JPS6359409B2/ja

Status Granted legal-status Critical Current

Links

239000003822 epoxy resin Substances 0.000 claims description 34
229920000647 polyepoxide Polymers 0.000 claims description 34
239000000203 mixture Substances 0.000 claims description 29
239000003795 chemical substances by application Substances 0.000 claims description 17
FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 claims description 13
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 9
229920000768 polyamine Polymers 0.000 claims description 9
KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 claims description 8
150000002989 phenols Chemical class 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 3
239000000047 product Substances 0.000 description 12
150000001875 compounds Chemical class 0.000 description 11
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 description 10
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
238000005266 casting Methods 0.000 description 8
229910052757 nitrogen Inorganic materials 0.000 description 7
229920005989 resin Polymers 0.000 description 6
239000011347 resin Substances 0.000 description 6
239000003502 gasoline Substances 0.000 description 5
238000002156 mixing Methods 0.000 description 5
239000000853 adhesive Substances 0.000 description 4
230000001070 adhesive effect Effects 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
230000000704 physical effect Effects 0.000 description 4
239000004606 Fillers/Extenders Substances 0.000 description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000003085 diluting agent Substances 0.000 description 3
239000000945 filler Substances 0.000 description 3
239000000446 fuel Substances 0.000 description 3
239000003921 oil Substances 0.000 description 3
239000003973 paint Substances 0.000 description 3
239000012779 reinforcing material Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
239000004593 Epoxy Substances 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
238000005452 bending Methods 0.000 description 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 description 2
239000006227 byproduct Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
-1 floor coatings Substances 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000000463 material Substances 0.000 description 2
238000000034 method Methods 0.000 description 2
229920003986 novolac Polymers 0.000 description 2
238000011417 postcuring Methods 0.000 description 2
239000007787 solid Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
YSUQLAYJZDEMOT-UHFFFAOYSA-N 2-(butoxymethyl)oxirane Chemical compound CCCCOCC1CO1 YSUQLAYJZDEMOT-UHFFFAOYSA-N 0.000 description 1
CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
229930040373 Paraformaldehyde Natural products 0.000 description 1
FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
239000004809 Teflon Substances 0.000 description 1
229920006362 Teflon® Polymers 0.000 description 1
XZAHJRZBUWYCBM-UHFFFAOYSA-N [1-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1(CN)CCCCC1 XZAHJRZBUWYCBM-UHFFFAOYSA-N 0.000 description 1
GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001334 alicyclic compounds Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
229930003836 cresol Natural products 0.000 description 1
239000010779 crude oil Substances 0.000 description 1
238000007872 degassing Methods 0.000 description 1
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
238000011049 filling Methods 0.000 description 1
239000008098 formaldehyde solution Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000002828 fuel tank Substances 0.000 description 1
238000001879 gelation Methods 0.000 description 1
230000020169 heat generation Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000007654 immersion Methods 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
229920002866 paraformaldehyde Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
229920002379 silicone rubber Polymers 0.000 description 1
239000004945 silicone rubber Substances 0.000 description 1
125000006850 spacer group Chemical group 0.000 description 1
238000003756 stirring Methods 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
238000005829 trimerization reaction Methods 0.000 description 1
230000002087 whitening effect Effects 0.000 description 1

Landscapes

Compositions Of Macromolecular Compounds (AREA)
Epoxy Resins (AREA)

JP1532281A 1981-02-04 1981-02-04 Epoxy resin composition Granted JPS57128719A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP1532281A JPS57128719A (en)	1981-02-04	1981-02-04	Epoxy resin composition

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP1532281A JPS57128719A (en)	1981-02-04	1981-02-04	Epoxy resin composition

Publications (2)

Publication Number	Publication Date
JPS57128719A JPS57128719A (en)	1982-08-10
JPS6359409B2 true JPS6359409B2 (fr)	1988-11-18

Family

ID=11885531

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP1532281A Granted JPS57128719A (en)	1981-02-04	1981-02-04	Epoxy resin composition

Country Status (1)

Country	Link
JP (1)	JPS57128719A (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2005185889A (ja) *	2003-12-24	2005-07-14	Mitsubishi Gas Chem Co Inc	ガソリンバリア性の優れた燃料容器、燃料系統部品および／または接合部の製造方法

1981
- 1981-02-04 JP JP1532281A patent/JPS57128719A/ja active Granted

Also Published As

Publication number	Publication date
JPS57128719A (en)	1982-08-10

Publication	Publication Date	Title
US8143331B2 (en)	2012-03-27	Alkylated polyalkyleneamines and uses thereof
US8729213B2 (en)	2014-05-20	Benzylated polyamine curing agents
US8519091B2 (en)	2013-08-27	Polyalkyleneamine adducts as curing agents for thick layer water-based epoxy systems
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EP0783010B1 (fr)	2000-05-03	Produit d'addition de méthylamine pour le durcissement de résines époxydes
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JPS62197412A (ja)	1987-09-01	エボキシおよびウレタン樹脂用硬化剤、および該硬化剤と該樹脂よりなる硬化性混合物
JPH0160165B2 (fr)	1989-12-21