GB484200A - Improvements in or relating to the preparation of compositions containing urea-formaldehyde condensation products - Google Patents
Improvements in or relating to the preparation of compositions containing urea-formaldehyde condensation productsInfo
- Publication number
- GB484200A GB484200A GB26307/36A GB2630736A GB484200A GB 484200 A GB484200 A GB 484200A GB 26307/36 A GB26307/36 A GB 26307/36A GB 2630736 A GB2630736 A GB 2630736A GB 484200 A GB484200 A GB 484200A
- Authority
- GB
- United Kingdom
- Prior art keywords
- urea
- formaldehyde
- soluble
- alcohol
- alcoholic solvent
- 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
-
- 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)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Reaction products of urea, thiourea and derivatives thereof with formaldehyde, which are still water-soluble, are dissolved or suspended in a primary or secondary monohydric alcoholic solvent and are heated in the presence of an acid catalyst and of an amount of formaldehyde sufficient to bring the total free and combined formaldehyde into excess of two molecular proportions to one of urea, the alcoholic solvent together with any water present or formed being simultaneously or subsequently distilled off and the heating being continued until the product is soluble in hydrocarbon solvents. The reaction may be carried out in a vessel heated by a bath maintained between 120-140 DEG C. and at atmospheric, or under increased or reduced pressure, according to the solvent. The quantity of formaldehyde used depends upon the initial condensation product and upon the quantity and strength of acid employed. Specified acids are hydrochloric, sulphuric, acetic, oxalic, lactic, phthalic and maleic. The alcoholic solvent, which may be added at once or in stages, preferably consists of an alcohol containing at least four carbon atoms and sparingly soluble in water, e.g. butyl alcohol; benzyl alcohol may be employed in conjunction with an alcohol of lower boiling point. Natural and artificial resins, soluble in the alcoholic solvent, may be added at any suitable stage. In a number of examples, dimethylol urea is worked up with paraformaldehyde in butyl alcohol. Examples 12 and 13 include further additions, respectively, of ethylene glycol mono linoleate and linoleic diglyceride. Examples 9-11 involve the use, respectively, of commercial amyl, octadecyl, and benzyl alcohols. In example 5, urea and formalin, acidified with sodium acetate and boric acid, are first heated at 50 DEG C., after which butyl alcohol and alcoholic hydrochloric acid are added and distillation effected first at 130 DEG C., and then at 140 DEG C. Specification 442,054 is referred to.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB26307/36A GB484200A (en) | 1936-09-28 | 1936-09-28 | Improvements in or relating to the preparation of compositions containing urea-formaldehyde condensation products |
GB12493/38A GB501388A (en) | 1936-09-28 | 1938-04-26 | Improvements in or relating to the preparation of compositions containing urea-formaldehyde condensation products |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB26307/36A GB484200A (en) | 1936-09-28 | 1936-09-28 | Improvements in or relating to the preparation of compositions containing urea-formaldehyde condensation products |
GB12493/38A GB501388A (en) | 1936-09-28 | 1938-04-26 | Improvements in or relating to the preparation of compositions containing urea-formaldehyde condensation products |
Publications (1)
Publication Number | Publication Date |
---|---|
GB484200A true GB484200A (en) | 1938-04-28 |
Family
ID=62527922
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB26307/36A Expired GB484200A (en) | 1936-09-28 | 1936-09-28 | Improvements in or relating to the preparation of compositions containing urea-formaldehyde condensation products |
GB12493/38A Expired GB501388A (en) | 1936-09-28 | 1938-04-26 | Improvements in or relating to the preparation of compositions containing urea-formaldehyde condensation products |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12493/38A Expired GB501388A (en) | 1936-09-28 | 1938-04-26 | Improvements in or relating to the preparation of compositions containing urea-formaldehyde condensation products |
Country Status (1)
Country | Link |
---|---|
GB (2) | GB484200A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2524472A (en) * | 1946-11-08 | 1950-10-03 | American Cyanamid Co | Process for preparing thermosetting aminoplast compositions |
US2544351A (en) * | 1946-11-08 | 1951-03-06 | American Cyanamid Co | Process for preparing thermosetting urea-formaldehyde compositions |
US2824855A (en) * | 1954-12-20 | 1958-02-25 | Freeman Chemical Corp | Preparation of epoxide resins |
CN111848894A (en) * | 2020-06-30 | 2020-10-30 | 长兴化学工业(中国)有限公司 | Urea-formaldehyde resin with high solid content and low free formaldehyde content and preparation method thereof |
-
1936
- 1936-09-28 GB GB26307/36A patent/GB484200A/en not_active Expired
-
1938
- 1938-04-26 GB GB12493/38A patent/GB501388A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2524472A (en) * | 1946-11-08 | 1950-10-03 | American Cyanamid Co | Process for preparing thermosetting aminoplast compositions |
US2544351A (en) * | 1946-11-08 | 1951-03-06 | American Cyanamid Co | Process for preparing thermosetting urea-formaldehyde compositions |
US2824855A (en) * | 1954-12-20 | 1958-02-25 | Freeman Chemical Corp | Preparation of epoxide resins |
CN111848894A (en) * | 2020-06-30 | 2020-10-30 | 长兴化学工业(中国)有限公司 | Urea-formaldehyde resin with high solid content and low free formaldehyde content and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
GB501388A (en) | 1939-02-27 |
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