GB494700A - Improvements in or relating to the production of urea-aldehyde synthetic resins - Google Patents
Improvements in or relating to the production of urea-aldehyde synthetic resinsInfo
- Publication number
- GB494700A GB494700A GB12432/37A GB1243237A GB494700A GB 494700 A GB494700 A GB 494700A GB 12432/37 A GB12432/37 A GB 12432/37A GB 1243237 A GB1243237 A GB 1243237A GB 494700 A GB494700 A GB 494700A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethylene glycol
- urea
- propionaldehyde
- monoethyl ether
- heptaldehyde
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/34—Condensation polymers of aldehydes or ketones with monomers covered by at least two of the groups C08L61/04, C08L61/18 and C08L61/20
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Paints Or Removers (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Urea and a saturated non-hydroxylated aliphatic aldehyde other than formaldehyde are condensed in the presence of a monohydric alcohol, in the absence of strongly acidic or basic catalysts or added water, and at a temperature above 50 DEG C. but insufficient to cause any substantial insolubilization of the product. The term urea includes substituted ureas such as compounds of the general type <FORM:0494700/IV/1> wherein R1 and R3 may be hydrogen; alkyl, e.g., methyl, propyl or dodecyl; aralkyl, e.g. benzyl; aryl, e.g. phenyl or naphthyl; cycloalkyl, e.g. cyclohexyl; and wherein R2 may be oxygen or sulphur. Suitable aldehydes include acetaldehyde, propionaldehyde, isobutyraldehyde, heptaldehyde, butyraldehyde and nonaldehyde; suitable alcohols include ethanol, propanol, dodecanol, di-isopropyl alcohol, cyclohexanol, butanol, ethylene glycol monomethyl or monoethyl ether. The products may be blended with polyhydric alcohol-polybasic acid condensation products, cellulose derivatives, fatty oils, waxes, pigments, fillers or dyes and used as coatings for textiles, paper, cloth, fabrics, wood, leather, metals, stone, brick or concrete. In examples, urea is condensed with (1) propionaldehyde in the presence of butanol; (2) propionaldehyde in the presence of ethylene glycol monomethyl ether; (3) isobutyraldehyde in the presence of ethylene glycol monoethyl ether; (4) heptaldehyde in the presence of ethylene glycol monoethyl ether. The product of example 1 may be blended with toluene solutions of a castor or linseed oil modified polyhydric alcohol - polybasic acid resin.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US494700XA | 1936-05-01 | 1936-05-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB494700A true GB494700A (en) | 1938-10-31 |
Family
ID=21959990
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12432/37A Expired GB494700A (en) | 1936-05-01 | 1937-04-30 | Improvements in or relating to the production of urea-aldehyde synthetic resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB494700A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2588640A (en) * | 1948-04-26 | 1952-03-11 | Bozel Maletra Prod Chimiques | Hydrofugation of textile materials |
US2595492A (en) * | 1948-08-09 | 1952-05-06 | Libbey Owens Ford Glass Co | Production of furfuryl urea-formaldehyde thermosetting resins |
WO2004094497A1 (en) * | 2003-03-31 | 2004-11-04 | Cytec Technology Corp. | Crosslinking composition |
US7442325B2 (en) * | 2004-09-29 | 2008-10-28 | Cytec Technology Corp. | Stabilized crosslinking composition |
-
1937
- 1937-04-30 GB GB12432/37A patent/GB494700A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2588640A (en) * | 1948-04-26 | 1952-03-11 | Bozel Maletra Prod Chimiques | Hydrofugation of textile materials |
US2595492A (en) * | 1948-08-09 | 1952-05-06 | Libbey Owens Ford Glass Co | Production of furfuryl urea-formaldehyde thermosetting resins |
WO2004094497A1 (en) * | 2003-03-31 | 2004-11-04 | Cytec Technology Corp. | Crosslinking composition |
US7381347B2 (en) | 2003-03-31 | 2008-06-03 | Cytec Technology Corp. | Crosslinking composition |
US7442325B2 (en) * | 2004-09-29 | 2008-10-28 | Cytec Technology Corp. | Stabilized crosslinking composition |
US8043526B2 (en) | 2004-09-29 | 2011-10-25 | Cytec Technology Corp. | Stabilized crosslinking composition |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB781267A (en) | Process for producing water-repellent dressings employing derivatives of aminotriazine-formaldehyde condensation products | |
GB494700A (en) | Improvements in or relating to the production of urea-aldehyde synthetic resins | |
GB533998A (en) | Method of preparing resins suitable for plastic and coating compositions | |
DE956990C (en) | Process for the preparation of salts from new, hardenable, basic, tertiary condensation products | |
GB486577A (en) | Manufacture of condensation products from aminotriazines | |
US2321451A (en) | Water-soluble condensation product | |
US2290128A (en) | Esters of glycolic acid | |
GB809662A (en) | Stable solutions of water-soluble amino-aldehyde resins | |
DE908793C (en) | Process for the production of aqueous plastic dispersions | |
US2508875A (en) | Modified melamine resins | |
US2466744A (en) | Curing catalysts for aminoplasts | |
DE1595391A1 (en) | Process for the production of water-soluble, surface-active condensation products | |
GB919808A (en) | Production of aqueous modified melamine-formaldehyde resinous compositions | |
Doughty et al. | Reactions of Ethyleneimine with Aldehydes and Ketones1 | |
US3714124A (en) | Dimethylol propionic acid-urea-aldehyde resins | |
US2497315A (en) | Oxygenated organic polymers | |
GB475072A (en) | The manufacture of new condensation products | |
GB527414A (en) | Improvements in or relating to the production of amide condensation resins | |
US2915503A (en) | Process for the manufacture of cast resins of urea-formaldehyde and the like, and resins so produced | |
US2890242A (en) | Amine modified acetals | |
EP0029907B1 (en) | Formaldehyde condensates, their preparation, their use as firing agent for basic dyestuffs, and fixing agents containing them | |
GB812505A (en) | Titanate ester compositions and processes for imparting water-repellency | |
GB486519A (en) | Manufacture of condensation products from aminotriazines | |
GB506507A (en) | The manufacture of condensation products | |
DE1569023B2 (en) | BINDERS FOR THE HOT BOX PROCESS |