JPS5792017A - Preparation of flame retardant epoxy resin - Google Patents
Preparation of flame retardant epoxy resinInfo
- Publication number
- JPS5792017A JPS5792017A JP16738780A JP16738780A JPS5792017A JP S5792017 A JPS5792017 A JP S5792017A JP 16738780 A JP16738780 A JP 16738780A JP 16738780 A JP16738780 A JP 16738780A JP S5792017 A JPS5792017 A JP S5792017A
- Authority
- JP
- Japan
- Prior art keywords
- halogenated
- epoxy resin
- polyhydric phenol
- phenol
- preparation
- 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.)
- Pending
Links
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title 1
- 239000003822 epoxy resin Substances 0.000 title 1
- 239000003063 flame retardant Substances 0.000 title 1
- 229920000647 polyepoxide Polymers 0.000 title 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 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
- MIHINWMALJZIBX-UHFFFAOYSA-N cyclohexa-2,4-dien-1-ol Chemical class OC1CC=CC=C1 MIHINWMALJZIBX-UHFFFAOYSA-N 0.000 abstract 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 2
- 239000004850 liquid epoxy resins (LERs) Substances 0.000 abstract 2
- BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 abstract 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 125000003700 epoxy group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- -1 tribromophenol Chemical class 0.000 abstract 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0313—Organic insulating material
- H05K1/032—Organic insulating material consisting of one material
- H05K1/0326—Organic insulating material consisting of one material containing O
Landscapes
- Reinforced Plastic Materials (AREA)
- Epoxy Resins (AREA)
- Organic Insulating Materials (AREA)
Abstract
PURPOSE: To obtain the titled resin, having a high halogen content and low solution viscosity, and suitable for a laminated boared used in a printed circuit, etc., by reacting a specific liquid epoxy resin with a halogenated polyhydric phenol and a halogenated monohydric phenol.
CONSTITUTION: (A) A liquid epoxy resin, e.g. diglycidyl ether of bisphenol A, which is a glycidyl ether of a polyhydric phenol having two or more epoxy groups in one molecule, is reacted with (B) a halogenated polyhydric phenol, e.g. tetrabromobisphenol A, (C) a halogenated monohydric phenol, e.g. tribromophenol, in an amount of 1W10wt% based on the total weight of the reaction raw materials and if necessary (D) a polyhydric phenol in the presence of sodium hydroxide, etc. as a catalyst under heating.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16738780A JPS5792017A (en) | 1980-11-29 | 1980-11-29 | Preparation of flame retardant epoxy resin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16738780A JPS5792017A (en) | 1980-11-29 | 1980-11-29 | Preparation of flame retardant epoxy resin |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5792017A true JPS5792017A (en) | 1982-06-08 |
Family
ID=15848754
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16738780A Pending JPS5792017A (en) | 1980-11-29 | 1980-11-29 | Preparation of flame retardant epoxy resin |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5792017A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS646018A (en) * | 1986-01-22 | 1989-01-10 | Dow Chemical Co | Vanish for epoxy resin laminate |
-
1980
- 1980-11-29 JP JP16738780A patent/JPS5792017A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS646018A (en) * | 1986-01-22 | 1989-01-10 | Dow Chemical Co | Vanish for epoxy resin laminate |
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