GB785930A - Thermosetting etherified resins - Google Patents
Thermosetting etherified resinsInfo
- Publication number
- GB785930A GB785930A GB2225053A GB2225053A GB785930A GB 785930 A GB785930 A GB 785930A GB 2225053 A GB2225053 A GB 2225053A GB 2225053 A GB2225053 A GB 2225053A GB 785930 A GB785930 A GB 785930A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenol
- alkaline
- etherified
- formaldehyde
- mol
- 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
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
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/08—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols from phenol-aldehyde condensates
Abstract
An etherified thermosetting resin is produced by condensing 1 mol. of a reactive monohydric phenol with 0.5-0.75 mol. of formaldehyde at a temperature above 80 DEG C. and in the presence of 1/200 -\ba1/10 of an equivalent of alkaline condensing agent (based on the phenol) until substantially all the formaldehyde has condensed and thereafter etherifying the condensate in an alkaline medium at a temperature not above 100 DEG C. with an amount of epihalogenhydrin or dihalogenhydrin in excess of the amount equivalent to the phenolic hydroxyl groups in the reaction mixture. A list of suitable phenols is given. Phenol or m-cresol is preferred. Aqueous formalin or paraformaldehyde may be used. Preferred alkaline catalysts are alkali or alkaline earth metal or ammonium hydroxides. Etherification may be arrested by neutralization of the alkaline medium and/or by separation of the etherified product. Completely etherified products usually separate from aqueous media and may be dehydrated and purified by distillation, e.g. azeotropic at atmospheric or reduced pressure. The products which may be soluble in "Cellosolve" (Registered Trade Mark), dioxan or cyclohexanone have low viscosities and are particularly useful for glass fibre laminates. They may be cured by heating with conventional catalysts, e.g. weak acids, triethylamine, pyridine, piperidine, ethylene diamine, diethylaminoethylamine, b -dimethylaminopropionitrile dicyandiamide, or benzyldimethylamine. Detailed examples are given of the preparation of ethers from phenol-formaldehyde condensates and epichlorhydrin and of their use as casting resins, as adhesives for metal, and for preparing glass fabric laminates. Belgian Specification 503,549 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2225053A GB785930A (en) | 1953-08-12 | 1953-08-12 | Thermosetting etherified resins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2225053A GB785930A (en) | 1953-08-12 | 1953-08-12 | Thermosetting etherified resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB785930A true GB785930A (en) | 1957-11-06 |
Family
ID=10176324
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2225053A Expired GB785930A (en) | 1953-08-12 | 1953-08-12 | Thermosetting etherified resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB785930A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2128616A (en) * | 1982-08-20 | 1984-05-02 | Sumitomo Chemical Co | Glycidyl ether of novolak type substituted phenolic resin and its production |
EP0122086A1 (en) * | 1983-04-04 | 1984-10-17 | Sumitomo Chemical Company, Limited | A method for producing an encapsulated semiconductor using a curable epoxy resin composition |
-
1953
- 1953-08-12 GB GB2225053A patent/GB785930A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2128616A (en) * | 1982-08-20 | 1984-05-02 | Sumitomo Chemical Co | Glycidyl ether of novolak type substituted phenolic resin and its production |
EP0122086A1 (en) * | 1983-04-04 | 1984-10-17 | Sumitomo Chemical Company, Limited | A method for producing an encapsulated semiconductor using a curable epoxy resin composition |
US4931515A (en) * | 1983-04-04 | 1990-06-05 | Sumitomo Chemical Company, Limited | Method for producing encapsulated semiconductor from improved epoxy resins |
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