GB542932A - Improved resinous condensation products and methods of producing same - Google Patents
Improved resinous condensation products and methods of producing sameInfo
- Publication number
- GB542932A GB542932A GB12380/40A GB1238040A GB542932A GB 542932 A GB542932 A GB 542932A GB 12380/40 A GB12380/40 A GB 12380/40A GB 1238040 A GB1238040 A GB 1238040A GB 542932 A GB542932 A GB 542932A
- Authority
- GB
- United Kingdom
- Prior art keywords
- urea
- condensation products
- parts
- aldehyde
- acylated
- 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
- C08G12/04—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C08G12/10—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with acyclic compounds having the moiety X=C(—N<)2 in which X is O, S or —N
- C08G12/12—Ureas; Thioureas
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Lubricants (AREA)
Abstract
542,932. Urea-aldehyde condensation products. BRITISH THOMSON-HOUSTON CO., Ltd. July 31, 1940, No. 12380. Convention date, Aug. 9, 1939.. [Class 2 (iii)] Self-curing resinous condensation products are produced by the condensation of a urea, an aliphatic aldehyde and an aldehyde reactable halogenated acylated urea in which at least one halogen atom is attached to an alpha or a beta carbon atom. Numerous examples of such acylated ureas are given. Specified urea compounds are urea, thiourea, acetyl-, benzoyl-, phenyl-, assymetrical diethyl-, allyl-, 2-chloro-allyl-, ethylidene-, methylol-, and methylene ureas ; guanidine, dicyandiamide, guanyl urea, guanylthiourea, biguanidine, aminoguanidine, aminotriazole, creatine, creatinine, guanoline, ethylene pseudo-sulphocarbamide derivatives, sulphohydantoin and triazine derivatives. Aldehydes specified comprise paraformaldehyde, hexamethylenetetramine, acetaldehyde, propionaldehyde, butyraldehyde, acrolein, methacrolein, crotonaldehydes or mixtures thereof. The condensation may be carried out under neutral, alkaline or acid conditions, e.g. in presence of 'alkalies, acids or amines. The mixed reactants may be condensed together. Alternatively the acylated urea may be added to a partial urea-aldehyde condensation product or the acylated urea and aldehyde may be condensed and the urea re-acted with the condensation product. In examples (1) 60 parts urea, 7.6 parts ammonia (28 per cent.), 161 parts aqueous formaldehyde and 0.04 parts sodium hydroxide are mixed and re-fluxed together for 20-30 mins.,. and one part of mono chlor acetyl urea added to the mixture. 61 parts of alpha flock and 0.4 parts zinc stearate are then added and the mixture heated to 50‹ C. and dried to form a moulding composition. (4) Similar proportions are used with chloroacetyl-ethyl-hydantoate. Up to “ mol. of the halogenated urea may be used per mol. urea. Modifying agents may be added, e.g. monohydric or polyhydric alcohols ; monoamides, e.g. formamide, acetamide, stearamide, acylic acid amides, benzamide, toluene sulphonamide or polyamides, e.g. adipic diamide, or phthalamide, or amines, e.g. ethylene diamine, aniline, phenylenediamine or aminophenols ; condensation products of aldehydes with proteins, furfural, aniline, phenol, sulphonamide ; polyhydric alcohol. polybasic acid condensation products cellulose derivatives ; natural gums and resins polyvinyl compounds ; synthetic linear condensation products known as " nylon " ; dyes, pigments, opacifiers, mould lubricants and fibrous fillers. The products may be used for making buttons, clock cases, radio cabinets, arc extinguishing tubes, liquid compositions may be employed as varnishes, lacquers, anti-creasing agents &c. Many of the acylated ureas specified in the Specification as open to inspection under Sect. 91 do not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US542932XA | 1939-08-09 | 1939-08-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB542932A true GB542932A (en) | 1942-02-03 |
Family
ID=21990053
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12380/40A Expired GB542932A (en) | 1939-08-09 | 1940-07-31 | Improved resinous condensation products and methods of producing same |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB542932A (en) |
-
1940
- 1940-07-31 GB GB12380/40A patent/GB542932A/en not_active Expired
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