GB483399A - Improvements in or relating to resinous condensation products - Google Patents
Improvements in or relating to resinous condensation productsInfo
- Publication number
- GB483399A GB483399A GB545/37A GB54537A GB483399A GB 483399 A GB483399 A GB 483399A GB 545/37 A GB545/37 A GB 545/37A GB 54537 A GB54537 A GB 54537A GB 483399 A GB483399 A GB 483399A
- Authority
- GB
- United Kingdom
- Prior art keywords
- urea
- acid
- water
- alcohol
- butyl
- 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
- C08G12/40—Chemically modified polycondensates
- C08G12/42—Chemically modified polycondensates by etherifying
- C08G12/421—Chemically modified polycondensates by etherifying of polycondensates based on acyclic or carbocyclic compounds
- C08G12/422—Chemically modified polycondensates by etherifying of polycondensates based on acyclic or carbocyclic compounds based on urea or thiourea
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Urea (including alkyl-, acyl- and aryl-ureas, thiourea, guanidine and substituted guanidine), formaldehyde and more than one molecular proportion of a primary aliphatic four-carbon alcohol (such as butyl and iso-butyl alcohol) for each molecular proportion of urea are condensed, the water formed in the reaction being removed by distillation until substantially two molecules of water for each molecule of urea are eliminated. Catalysts such as phthalic anhydride, maleic acid, adipic acid, citric acid, rosin, alkyd resins, hydrochloric acid, sulphuric acid, phosphoric acid, mercuric chloride, aluminium chloride or stannic chloride, iodine, bromine or benzoylperoxide may be used. Distillate other than water, separation of which may be facilitated by an entraining agent, is returned to the reaction. In examples: (1) a mixture of N-butyl alcohol, paraformaldehyde and caustic soda is warmed, mixed with phthalic anhydride, urea and toluene and the mixture heated and distilled, the distillate, less the water contained in it, being returned to yield a resin solution; (2) a mixture of aqueous formaldehyde, sodium acid phosphate and sufficient sodium hydroxide to yield a pH of 7,6 is mixed with urea and allowed to stand to obtain a crystalline methylol compound which is then mixed with isobutyl alcohol, toluene and phthalic anhydride and heated and distilled to yield a resin solution. The products may be blended with other materials such as alkyd resins, oleo-resinous varnishes, cellulose derivative lacquers, oils, waxes, natural resins (congo, copal and Damar), plasticizers (dibutyl or dicyclohexyl phthalate, tricresyl or triphenyl phosphate, camphor, ethyl or butyl tartrate or lactate), pigments, dyes or fillers. The products may be used as coating-compositions for metal, wood, glass, rubber, moulded plastic or synthetic resin products; to coat or impregnate fabric, woven fabrics of cotton, wool, silk and rayon, paper, leather, cellulose sheet (in the manufacture of shower curtains, glazed chintzes, raincoats and capes, tobacco pouches, glazed cambric for insulation, water-and greaseproof wrapping material, floor coverings and diaphragms); to impregnate and insulate electric coils; as an adhesive; and as a stiffening agent for felt or straw. The Specification as open to inspection under Sect. 91 refers in general to the polymerization of a urea, an aldehyde and an alcohol. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US483399XA | 1936-01-07 | 1936-01-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB483399A true GB483399A (en) | 1938-04-20 |
Family
ID=21954039
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB545/37A Expired GB483399A (en) | 1936-01-07 | 1937-01-07 | Improvements in or relating to resinous condensation products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB483399A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE969364C (en) * | 1941-09-04 | 1958-05-22 | Reichhold Chemie Ag | Process for the production of soft resin-like, non-hardenable condensation products from urea and formaldehyde |
-
1937
- 1937-01-07 GB GB545/37A patent/GB483399A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE969364C (en) * | 1941-09-04 | 1958-05-22 | Reichhold Chemie Ag | Process for the production of soft resin-like, non-hardenable condensation products from urea and formaldehyde |
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