GB785930A - Thermosetting etherified resins - Google Patents

Thermosetting etherified resins

Info

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
Application number
GB2225053A
Inventor
John Edward Seager Whitney
Basil William Brook
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
British Resin Products Ltd
Original Assignee
British Resin Products Ltd
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.)
Filing date
Publication date
Application filed by British Resin Products Ltd filed Critical British Resin Products Ltd
Priority to GB2225053A priority Critical patent/GB785930A/en
Publication of GB785930A publication Critical patent/GB785930A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00Polycondensates 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
    • C08G59/02Polycondensates containing more than one epoxy group per molecule
    • C08G59/04Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
    • C08G59/06Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
    • C08G59/08Polycondensates 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.
GB2225053A 1953-08-12 1953-08-12 Thermosetting etherified resins Expired GB785930A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (3)

* Cited by examiner, † Cited by third party
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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