GB703426A - Improvements in or relating to urea-melamine-formaldehyde resins - Google Patents
Improvements in or relating to urea-melamine-formaldehyde resinsInfo
- Publication number
- GB703426A GB703426A GB6504/51A GB650451A GB703426A GB 703426 A GB703426 A GB 703426A GB 6504/51 A GB6504/51 A GB 6504/51A GB 650451 A GB650451 A GB 650451A GB 703426 A GB703426 A GB 703426A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alcohol
- water
- syrup
- melamine
- urea
- 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
- C08G12/34—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds and acyclic or carbocyclic compounds
- C08G12/36—Ureas; Thioureas
- C08G12/38—Ureas; Thioureas and melamines
Abstract
Resin syrups are made by condensing a mixture of melamine and urea, the urea being present in an amount from 5 to 35 per cent. by weight of melamine, with aqueous formaldehyde at pH 3 to 10 and in an amount to provide 0.9 to 2 mols. of formaldehyde for each amino and amido group, until the condensate has a water tolerance of not less than 1:1 at 20 DEG C.; the reaction being performed in presence of methyl or ethyl alcohol and the weight ratio of water/alcohol before reaction being 5:1 to 1:2. The formaldehyde may be formalin and/or aqueous paraformaldehyde. After condensation water and alcohol may be distilled off, preferably under vacuum at less than 50 DEG C. and at a pH greater than 7, and additional methyl or ethyl alcohol added to the syrup. Unspecified curing catalysts, fillers and plasticizers may be added to the syrup. The Provisional Specification refers also to the use of propyl, butyl and amyl alcohols. In example (1) a mixture of formalin (pH-8.9), melamine, and urea in m.w. ratio 13.2/3/1 dissolved in methylated spirits was reacted at reflux temperatures until the syrup formed had a water tolerance of 6:1. After cooling to 50 DEG C. water and alcohol were distilled off under reduced pressure to reduce the water content to 27.5 per cent. of the syrup. Further alcohol was then added to make the resin/alcohol (free and combined)/water ratio 45/27.5/27.5. The syrup had a stoved solids content of 48 per cent., a viscosity of 40.3 cs. at 25 DEG C. and a shelf life of four months. Specification 683,630 is referred to.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB6504/51A GB703426A (en) | 1951-03-19 | 1951-03-19 | Improvements in or relating to urea-melamine-formaldehyde resins |
BE509948A BE509948A (en) | 1951-03-19 | 1952-03-14 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB6504/51A GB703426A (en) | 1951-03-19 | 1951-03-19 | Improvements in or relating to urea-melamine-formaldehyde resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB703426A true GB703426A (en) | 1954-02-03 |
Family
ID=9815712
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6504/51A Expired GB703426A (en) | 1951-03-19 | 1951-03-19 | Improvements in or relating to urea-melamine-formaldehyde resins |
Country Status (2)
Country | Link |
---|---|
BE (1) | BE509948A (en) |
GB (1) | GB703426A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2808389A (en) * | 1953-08-29 | 1957-10-01 | Reichhold Chemicals Inc | Process for the production of fusible alcohol-modified melamine resins, and resulting product |
EP0185205A1 (en) * | 1984-11-22 | 1986-06-25 | BASF Aktiengesellschaft | Process for the preparation of melamine-urea-formaldehyde condensates |
-
1951
- 1951-03-19 GB GB6504/51A patent/GB703426A/en not_active Expired
-
1952
- 1952-03-14 BE BE509948A patent/BE509948A/fr unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2808389A (en) * | 1953-08-29 | 1957-10-01 | Reichhold Chemicals Inc | Process for the production of fusible alcohol-modified melamine resins, and resulting product |
EP0185205A1 (en) * | 1984-11-22 | 1986-06-25 | BASF Aktiengesellschaft | Process for the preparation of melamine-urea-formaldehyde condensates |
Also Published As
Publication number | Publication date |
---|---|
BE509948A (en) | 1952-09-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2614096A (en) | Condensation products of phenol, formaldehyde, and unsubstituted mononuclear dihydric phenols | |
US2629703A (en) | Resinous composition comprising phenol-aldehyde and ketone-aldehyde condensation products | |
GB703426A (en) | Improvements in or relating to urea-melamine-formaldehyde resins | |
GB597285A (en) | Process for the preparation of synthetic resin-modified n-alkoxymethyl polyamide compositions | |
US2538883A (en) | Phenol-modified acetone resins | |
GB475072A (en) | The manufacture of new condensation products | |
GB627167A (en) | Improvements in and relating to the production of resinous compositions of matter, and the products resulting therefrom | |
GB723884A (en) | Improvements in or relating to synthetic resin adhesives | |
GB622675A (en) | Manufacture of new synthetic resinous condensation products | |
GB790083A (en) | Improvements in or relating to hardening agents for epoxide resins | |
GB738033A (en) | Improvements in or relating to the preparation of melamine-formaldehyde syrups | |
GB597144A (en) | Improvements in or relating to synthetic resinous adhesive compositions | |
GB683630A (en) | Improvements in or relating to urea-melamine-formaldehyde resins | |
GB620412A (en) | Improvements in urea formaldehyde resinous materials | |
GB1001663A (en) | Compositions containing polyvinyl mixed acetals | |
GB690180A (en) | Improvements in or relating to the production of melamine-formaldehyde condensation products | |
GB724972A (en) | Improvements in or relating to the manufacture of etherified melamine-formaldehyde resins | |
GB861045A (en) | Beta-amino lower-alkyl carbamates | |
GB1130481A (en) | A process for preparing etherified synthetic resins for the lacquer industry | |
GB337357A (en) | An improved process for the production of urea aldehyde resins | |
SU110384A1 (en) | The method of producing cold curing adhesives | |
GB753268A (en) | Process for the preparation of epoxy resins from novolac resins | |
GB963786A (en) | Improved method of making phenol modified amino condensation resins | |
SU37338A1 (en) | The method of preparation of the composite condensation product | |
GB581702A (en) | Improvements in or relating to thermo-setting resins |