GB636496A - Method of producing a composite synthetic resin and product thereof - Google Patents
Method of producing a composite synthetic resin and product thereofInfo
- Publication number
- GB636496A GB636496A GB21361/47A GB2136147A GB636496A GB 636496 A GB636496 A GB 636496A GB 21361/47 A GB21361/47 A GB 21361/47A GB 2136147 A GB2136147 A GB 2136147A GB 636496 A GB636496 A GB 636496A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aldehyde
- resin
- resorcinol
- methylol
- solution
- 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
- C08G14/00—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
- C08G14/02—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
- C08G14/04—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
- C08G14/06—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
A composite two-stage resin is produced by condensing a resin-forming primary aryl amine or a secondary di-aryl amine with an aldehyde and forming a thermoplastic aromatic amine-aldehyde resin constituting 5 to 8 per cent of the composite resin, mixing therewith a solution of unreacted aldehyde and unreacted polyhydroxy benzene, a derivative, or a substitution product thereof, the molar ratio of aldehyde to polyhydroxy benzene, homologue, or derivative being less than 1 : 1, and reacting the solution by heating in the presence of the pre-condensed aromatic amine-aldehyde resin. The products are suitable as moulding materials, adhesives for laminates of wood, cloth, leather, natural or synthetic rubber, asbestos or glass fibres. Other fillers include wood flour, dye, calcium carbonate, kieselguhr or cellulose. Specified are aldehydes: formaldehyde, acetaldehyde, paraldehyde, propionaldehyde, butyraldehyde, furfuraldehyde, glyoxal; polyhydroxy benzenes: resorcinol, alkyl resorcinols, ethers including monomethyl resorcyl ether, esters including resorcinol disulphonic acid esters, pyrogallol, phloroglucinol and their homologues. Hardening agents include hexamethylene tetramine or methylol compounds such as dimethylol para cresol, polymethylol phenols or their salts, methylol resorcinol, methylol xylenols, dimethylol urea, dimethylol thiourea and methylol melamine. A suitable polymethylol phenol is prepared by reacting phenol and formaldehyde with an NaOH catalyst at 20 DEG to 25 DEG C. In examples: (1) ortho amino diphenyl and formaldehyde are reacted until combination is complete and a solution of resorcinol in formalin is then added and the mixture refluxed; (2) the general procedure of (1) is followed using aniline in place of the ortho amino diphenyl; (3) a solution of diphenylamine replaces the aniline of (2). The low curing temperature of the products makes them suitable for forming large laminated articles, e.g. furniture, sections of aeroplanes and hulls of dinghys. The Specification as open to inspection under Sect. 91 comprises also the preparation of one stage resins by employing a ratio of aldehyde to dihydroxy benzene of more than 1 : 1, preferably 1 : 1 to 2 : 1. The use of tertiary amines and the reaction of an aromatic amine with an aldehyde in the presence of a partially or completely condensed polyhydroxy benzene-aldehyde reaction mixture are also referred to. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US636496XA | 1942-12-03 | 1942-12-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB636496A true GB636496A (en) | 1950-05-03 |
Family
ID=22050591
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB21361/47A Expired GB636496A (en) | 1942-12-03 | 1947-08-06 | Method of producing a composite synthetic resin and product thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB636496A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2203747A (en) * | 1987-04-24 | 1988-10-26 | Bridgestone Corp | Aniline-resorcin-formaldehyde copolycondensation product |
-
1947
- 1947-08-06 GB GB21361/47A patent/GB636496A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2203747A (en) * | 1987-04-24 | 1988-10-26 | Bridgestone Corp | Aniline-resorcin-formaldehyde copolycondensation product |
GB2203747B (en) * | 1987-04-24 | 1990-12-12 | Bridgestone Corp | Adhesive composition including aniline-resorcin-formaldehyde copolycondensation product |
US5039777A (en) * | 1987-04-24 | 1991-08-13 | Bridgestone Corporation | Aniline-resorcin-formaldehyde copolycondensation product |
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