GB543096A - Improved resinous condensation products and methods of producing same - Google Patents
Improved resinous condensation products and methods of producing sameInfo
- Publication number
- GB543096A GB543096A GB12632/40A GB1263240A GB543096A GB 543096 A GB543096 A GB 543096A GB 12632/40 A GB12632/40 A GB 12632/40A GB 1263240 A GB1263240 A GB 1263240A GB 543096 A GB543096 A GB 543096A
- Authority
- GB
- United Kingdom
- Prior art keywords
- condensation products
- aldehyde
- products
- resins
- condensation
- 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
- C08G12/043—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with at least two compounds covered by more than one of the groups C08G12/06 - C08G12/24
-
- 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
- C08G12/22—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with carboxylic acid amides
-
- 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)
- Chemical And Physical Treatments For Wood And The Like (AREA)
Abstract
543,096. Resinous condensation products ; proofing permeable materials. BRITISH THOMSON-HOUSTON CO., Ltd. Aug. 6, 1940, No. 12632. Convention date, Aug. 10, 1939. [Class 2 (iii)] [Also in Group VIII] Resinous condensation products are prepared by heating together an aliphatic aldehyde and a diamide of an unsaturated dicarboxylic acid containing a CH 2 =C # grouping and in which the carboxyl groups are attached to different carbon atoms. Specified diamides are itaconic diamide, methyl itaconic diamide and glutaric diamide, and the condensation may be carried out under acid, alkaline or neutral conditions. Inter-condensates may be produced by adding other aliphatic-aldehyde-reactable organic compounds capable of forming a methylol derivative as an intermediate during the resin formation, e.g. urea, phenols or acetone. The products may be used alone, or mixed with fillers, pigments, dyes or lubricants, as moulding compositions. The liquid condensates may be used in the production of paints, varnishes, lacquers or enamels, and as adhesives. The products may also be used as fire-retardants and water-repellents when applied to wood or to fabrics. Examples are given of the preparation of resinous condensates from itaconic diamide and formaldehyde, with or without phenol or urea. Curing catalysts may be incorporated with the condensates, or self-curing characteristics may be imparted to the resins by inter-condensing into the initial condensation products such substances as chloroacetamide, mono-chloroacetyl urea, chloroacetonitrile, chloral hydrate, chloroacetone, nitrourea, sodium nitrourea, methylene diamino monohydrochloride, aminoacetamide hydrochloride and diethanolamine hydrochloride. The resins of this invention may be modified by introducing before, during or after condensation, partially hydrolysed wood products, lignin, proteins, protein-aldehyde condensation products, phenol-aldehyde condensation products, aniline-aldehyde condensation products, furfural condensation products, alkyd resins, sulphonamide-aldehyde resins, water-soluble cellulose derivatives, natural gums and resins such as copal, shellac or rosin, polyvinyl compounds and super-polyamides. Specified optional additions to the condensation products are alpha cellulose flock, barium sulphate, zinc sulphide, titanium oxides, flaked aluminium or copper, stearates or palmitates of tin and zinc, and waxes such as carnauba and paraffin wax. An example is given of the preparation of a laminated article by dipping paper sheets into an acidified condensation syrup, drying at 80‹ C., superposing the sheets, and beating under pressure. Specifications 519,349 and 542,513 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US543096XA | 1939-08-10 | 1939-08-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB543096A true GB543096A (en) | 1942-02-10 |
Family
ID=21990173
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12632/40A Expired GB543096A (en) | 1939-08-10 | 1940-08-06 | Improved resinous condensation products and methods of producing same |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB543096A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4429075A (en) | 1982-05-17 | 1984-01-31 | Chem-Nuclear Systems, Inc. | Cross-linked urea-formaldehyde polymer matrix compositions containing cyclic intermediate structures |
US4499200A (en) * | 1982-05-17 | 1985-02-12 | Chem-Nuclear Systems, Inc. | Compound catalyst system usable for the polymerization or curing of urea-formaldehyde polymeric condensation systems |
-
1940
- 1940-08-06 GB GB12632/40A patent/GB543096A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4429075A (en) | 1982-05-17 | 1984-01-31 | Chem-Nuclear Systems, Inc. | Cross-linked urea-formaldehyde polymer matrix compositions containing cyclic intermediate structures |
US4499200A (en) * | 1982-05-17 | 1985-02-12 | Chem-Nuclear Systems, Inc. | Compound catalyst system usable for the polymerization or curing of urea-formaldehyde polymeric condensation systems |
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