GB771327A - Production of heat hardenable melamine-formaldehyde condensation products - Google Patents
Production of heat hardenable melamine-formaldehyde condensation productsInfo
- Publication number
- GB771327A GB771327A GB30844/54A GB3084454A GB771327A GB 771327 A GB771327 A GB 771327A GB 30844/54 A GB30844/54 A GB 30844/54A GB 3084454 A GB3084454 A GB 3084454A GB 771327 A GB771327 A GB 771327A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenyl
- melamine
- group
- guanamine
- formaldehyde
- 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
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
- C08G12/263—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with at least two compounds covered by more than one of the groups C08G12/28 - C08G12/32
- C08G12/266—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with at least two compounds covered by more than one of the groups C08G12/28 - C08G12/32 one being melamine
Abstract
Heat-hardenable internally plasticised resins are prepared by heating together at a pH of 8-12, melamine, formaldehyde (or a polymer thereof) and a guanamine having the general formula <FORM:0771327/IV(a)/1> wherein n is an integer of 1 to 4, R1 is a phenyl, mono- or di-halophenyl, mono- or di-alkylphenyl or haloalkylphenyl group in which the alkyl group or groups have 1 to 4 carbon atoms, or a cyano or straight chain omega-cyanoalkyl group having 1 to 4 methylene groups, and each of R2, R3, R5 and R4 is a hydrogen atom or a phenyl, cresyl, xylyl, halophenyl or dihalophenyl group or an alkyl group having one to eight carbon atoms, at least one being a hydrogen atom and not more than one being a phenyl, cresyl, xylyl, halophenyl or dihalophenyl group. Many examples of such guanamines are given. The amount of formaldehyde, or polymer such as paraformaldehyde or trioxymethylene, should be from 1 to 6 equivalents per mol. of melamine, and the preferred amount of guanamine is 5 to 25 mol. per cent of melamine. The guanamine may be mixed with the other reactants before the reaction or may be added to a partially condensed melamine-formaldehyde product so long as it is allowed to condense substantially completely with the melamine and formaldehyde. The pH may be adjusted by means of sodium or potassium hydroxide, triethanolamine, benzyl trimethylammonium hydroxide or choline. Temperatures may vary from 40 DEG C. to reflux temperatures at atmospheric pressure. The resinous products, while still in the fusible state, are preferably mixed with fillers, such as glass, asbestos, paper, wood flour and cellulose, for moulding purposes, or may be dissolved in a solvent, e.g. water or wateralcohol mixtures, and used as laminating syrups. Curing is effected at temperatures of 100 DEG to 250 DEG C. with or without a catalyst. The examples describe the preparation of condensates using phenylacetoguanamine, omegacyanovaleroguanamine, 4 - N - ethyl - phenyl - valeroguanamine, omega - cyanopropioguan - amine, 4 - N - ethyl - omega - cyanovalero - guanamine, 4 - N - phenyl - cyanoacetoguana - mine, 4 - N - phenyl - phenylacetoguanamine and omega - cyanononoguanamine. Specification 642,409, [Group IV (b)], and U.S.A. Specifications 2,394,526 and 2,427,314 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US771327XA | 1953-10-26 | 1953-10-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB771327A true GB771327A (en) | 1957-03-27 |
Family
ID=22136254
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB30844/54A Expired GB771327A (en) | 1953-10-26 | 1954-10-26 | Production of heat hardenable melamine-formaldehyde condensation products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB771327A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6380194B1 (en) | 1996-10-01 | 2002-04-30 | Janssen Pharmaceutica N.V. | Substituted diamino-1,3,5-triazine derivatives |
-
1954
- 1954-10-26 GB GB30844/54A patent/GB771327A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6380194B1 (en) | 1996-10-01 | 2002-04-30 | Janssen Pharmaceutica N.V. | Substituted diamino-1,3,5-triazine derivatives |
US6858609B2 (en) | 1996-10-01 | 2005-02-22 | Janssen Pharmaceutica N.V. | Substituted diamino-1,3,5-triazine derivatives |
US6962916B2 (en) | 1996-10-01 | 2005-11-08 | Janssen Pharmaceutica N.V. | Substituted diamino-1,3,5-triazine derivatives |
US7449575B2 (en) | 1996-10-01 | 2008-11-11 | Janssen Pharmaceutica, Inc. | Substituted diamino-1,3,5-triazine derivatives |
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