JPS6219769B2 - - Google Patents

Info

Publication number

JPS6219769B2

JPS6219769B2 JP169680A JP169680A JPS6219769B2 JP S6219769 B2 JPS6219769 B2 JP S6219769B2 JP 169680 A JP169680 A JP 169680A JP 169680 A JP169680 A JP 169680A JP S6219769 B2 JPS6219769 B2 JP S6219769B2

Authority

JP

Japan

Prior art keywords

curing agent

epoxy resin

group

formula

alkyl group

Prior art date

1980-01-09

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

• Espacenet
• Global Dossier
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• 239000003795 chemical substances by application Substances 0.000 claims description 28
• 239000003822 epoxy resin Substances 0.000 claims description 26
• 229920000647 polyepoxide Polymers 0.000 claims description 26
• 125000000217 alkyl group Chemical group 0.000 claims description 6
• 150000001875 compounds Chemical class 0.000 claims description 5
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
• 229910052739 hydrogen Inorganic materials 0.000 claims description 4
• 239000001257 hydrogen Substances 0.000 claims description 4
• 125000005843 halogen group Chemical group 0.000 claims description 3
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
• 125000001424 substituent group Chemical group 0.000 claims description 3
• 125000003118 aryl group Chemical group 0.000 claims description 2
• 125000000623 heterocyclic group Chemical group 0.000 claims description 2
• 150000002989 phenols Chemical class 0.000 claims description 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 description 9
• 238000006243 chemical reaction Methods 0.000 description 8
• 230000000052 comparative effect Effects 0.000 description 7
• BLLFPKZTBLMEFG-UHFFFAOYSA-N 1-(4-hydroxyphenyl)pyrrole-2,5-dione Chemical compound C1=CC(O)=CC=C1N1C(=O)C=CC1=O BLLFPKZTBLMEFG-UHFFFAOYSA-N 0.000 description 6
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
• 239000000047 product Substances 0.000 description 6
• 239000000126 substance Substances 0.000 description 6
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
• 238000010521 absorption reaction Methods 0.000 description 4
• CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 3
• 230000015572 biosynthetic process Effects 0.000 description 3
• 230000008034 disappearance Effects 0.000 description 3
• 230000009477 glass transition Effects 0.000 description 3
• PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
• MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 2
• 125000003700 epoxy group Chemical group 0.000 description 2
• 238000004519 manufacturing process Methods 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• 229910052757 nitrogen Inorganic materials 0.000 description 2
• 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
• 229930185605 Bisphenol Natural products 0.000 description 1
• 239000004593 Epoxy Substances 0.000 description 1
• 239000002253 acid Substances 0.000 description 1
• 238000007259 addition reaction Methods 0.000 description 1
• 239000000654 additive Substances 0.000 description 1
• 230000000996 additive effect Effects 0.000 description 1
• 125000002723 alicyclic group Chemical group 0.000 description 1
• 150000001412 amines Chemical class 0.000 description 1
• 150000004982 aromatic amines Chemical class 0.000 description 1
• 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 1
• 150000001735 carboxylic acids Chemical class 0.000 description 1
• 150000004820 halides Chemical class 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• 238000004128 high performance liquid chromatography Methods 0.000 description 1
• 230000010354 integration Effects 0.000 description 1
• FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
• 238000005259 measurement Methods 0.000 description 1
• 239000000155 melt Substances 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 239000004570 mortar (masonry) Substances 0.000 description 1
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
• 229920003986 novolac Polymers 0.000 description 1
• 238000004806 packaging method and process Methods 0.000 description 1
• 150000008442 polyphenolic compounds Chemical class 0.000 description 1
• 235000013824 polyphenols Nutrition 0.000 description 1
• 239000002244 precipitate Substances 0.000 description 1
• 239000002994 raw material Substances 0.000 description 1
• 239000004576 sand Substances 0.000 description 1
• 239000007787 solid Substances 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1

Cited By (1)