GB721150A - Polymerization of epoxy compounds and products thereof - Google Patents
Polymerization of epoxy compounds and products thereofInfo
- Publication number
- GB721150A GB721150A GB10914/51A GB1091451A GB721150A GB 721150 A GB721150 A GB 721150A GB 10914/51 A GB10914/51 A GB 10914/51A GB 1091451 A GB1091451 A GB 1091451A GB 721150 A GB721150 A GB 721150A
- Authority
- GB
- United Kingdom
- Prior art keywords
- epoxy
- sulphonated
- phenols
- phenol
- butyl
- 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
- 239000004593 Epoxy Substances 0.000 title abstract 5
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 238000006116 polymerization reaction Methods 0.000 title 1
- -1 3,4-epoxy butyl- Chemical group 0.000 abstract 6
- 150000002989 phenols Chemical class 0.000 abstract 5
- 239000003456 ion exchange resin Substances 0.000 abstract 4
- 229920003303 ion-exchange polymer Polymers 0.000 abstract 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 3
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 abstract 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- 239000004014 plasticizer Substances 0.000 abstract 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract 2
- LSWYGACWGAICNM-UHFFFAOYSA-N 2-(prop-2-enoxymethyl)oxirane Chemical compound C=CCOCC1CO1 LSWYGACWGAICNM-UHFFFAOYSA-N 0.000 abstract 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical class CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 abstract 1
- OECTYKWYRCHAKR-UHFFFAOYSA-N 4-vinylcyclohexene dioxide Chemical compound C1OC1C1CC2OC2CC1 OECTYKWYRCHAKR-UHFFFAOYSA-N 0.000 abstract 1
- 229930185605 Bisphenol Natural products 0.000 abstract 1
- GXBYFVGCMPJVJX-UHFFFAOYSA-N Epoxybutene Chemical compound C=CC1CO1 GXBYFVGCMPJVJX-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 239000010425 asbestos Substances 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- JRPRCOLKIYRSNH-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC2OC2)C=1C(=O)OCC1CO1 JRPRCOLKIYRSNH-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 239000003245 coal Substances 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- 150000001896 cresols Chemical class 0.000 abstract 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 125000003700 epoxy group Chemical group 0.000 abstract 1
- 239000003822 epoxy resin Substances 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 235000013312 flour Nutrition 0.000 abstract 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000000314 lubricant Substances 0.000 abstract 1
- 150000004780 naphthols Chemical class 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- JKXONPYJVWEAEL-UHFFFAOYSA-N oxiran-2-ylmethyl acetate Chemical compound CC(=O)OCC1CO1 JKXONPYJVWEAEL-UHFFFAOYSA-N 0.000 abstract 1
- 229920001568 phenolic resin Polymers 0.000 abstract 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 1
- 229920000647 polyepoxide Polymers 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229910052895 riebeckite Inorganic materials 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
- 150000003739 xylenols Chemical class 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
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4064—Curing agents not provided for by the groups C08G59/42 - C08G59/66 sulfur containing compounds
-
- 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
-
- 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 Compounds (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US721150XA | 1950-05-27 | 1950-05-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB721150A true GB721150A (en) | 1954-12-29 |
Family
ID=22105670
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10914/51A Expired GB721150A (en) | 1950-05-27 | 1951-05-09 | Polymerization of epoxy compounds and products thereof |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE503552A (enrdf_load_html_response) |
FR (1) | FR1066037A (enrdf_load_html_response) |
GB (1) | GB721150A (enrdf_load_html_response) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL108217C (enrdf_load_html_response) * | 1952-06-06 | |||
NL248735A (enrdf_load_html_response) * | 1959-02-25 | 1900-01-01 |
-
0
- BE BE503552D patent/BE503552A/xx unknown
-
1951
- 1951-05-09 GB GB10914/51A patent/GB721150A/en not_active Expired
- 1951-05-25 FR FR1066037D patent/FR1066037A/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR1066037A (fr) | 1954-06-01 |
BE503552A (enrdf_load_html_response) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2511913A (en) | Compositions of resinous epoxides | |
US2494295A (en) | Compositions of resinous epoxides and aromatic sulfonamide-aldehyde condensates | |
GB579698A (en) | Improvements in or relating to a process for the manufacture of thermo-setting synthetic resins by the polymerisation of alkylene oxide derivatives | |
GB681578A (en) | A composition of matter curable to give a hard resinous product, the resulting resinous product and articles made therefrom | |
GB681099A (en) | A method of producing a resinous composition containing glycidyl ethers and suitable for use as an adhesive, the resinous composition so produced and articles made therefrom | |
GB675168A (en) | Manufacture of epoxide resins | |
US2713565A (en) | Composition containing glycidyl polyether of a polyhydric phenol, a methylol substituted 2-alkenyloxybenzene, and a polyvinyl acetal | |
US2928803A (en) | Curing of polyepoxides | |
US2865887A (en) | Glycidyl ethers of reaction products of certain phenols with polymerizable aromatic substances containing at least one vinyl group | |
US2939859A (en) | Process for preparing resinified product from polyepoxy polyether and aromatic-substituted-alkene-1 and composition for production of said product | |
GB1122082A (en) | Polyglycidyl ether-containing compositions | |
GB721150A (en) | Polymerization of epoxy compounds and products thereof | |
GB675169A (en) | Improvements in synthetic resins obtained by condensation of polyhydric phenol and halogenhydrins | |
US3308094A (en) | Catalyst for curing polyepoxides | |
US3787508A (en) | Solid,curable polyepoxides modified with hydrolyzed liquid polyepoxides | |
GB791303A (en) | Process for preparing compositions containing glycidyl ethers | |
US3632555A (en) | Preparation of epoxylated phenolic resins by reacting polymers fro aralkyl ethers and phenols with epihalohydrin | |
US2965611A (en) | Polyphenol glycidyl ethers | |
US3310528A (en) | New epoxide resins, processes for their production and hardenable compositions containing such epoxide resins | |
GB941960A (en) | Hardenable phenol-aldehyde resins and process for preparing them | |
GB1098528A (en) | Polyepoxy ethers of polyhydric phenols and cured products obtained therefrom | |
US3395120A (en) | Epoxy resins containing the diphenyl oxide moiety | |
KR101778778B1 (ko) | 알파메틸스티렌네이티드 페놀의 제조방법 | |
GB753268A (en) | Process for the preparation of epoxy resins from novolac resins | |
US3352823A (en) | Process for curing epoxy resins with methyl polyborate |