GB771327A - Production of heat hardenable melamine-formaldehyde condensation products - Google Patents

Production of heat hardenable melamine-formaldehyde condensation products

Info

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
Application number
GB30844/54A
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.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
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 Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB771327A publication Critical patent/GB771327A/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
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/26Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08G12/263Condensation 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
    • C08G12/266Condensation 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.
GB30844/54A 1953-10-26 1954-10-26 Production of heat hardenable melamine-formaldehyde condensation products Expired GB771327A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (4)

* Cited by examiner, † Cited by third party
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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