GB572245A - Improvements in or relating to the production of moulding powders - Google Patents
Improvements in or relating to the production of moulding powdersInfo
- Publication number
- GB572245A GB572245A GB17251/43A GB1725143A GB572245A GB 572245 A GB572245 A GB 572245A GB 17251/43 A GB17251/43 A GB 17251/43A GB 1725143 A GB1725143 A GB 1725143A GB 572245 A GB572245 A GB 572245A
- Authority
- GB
- United Kingdom
- Prior art keywords
- urea
- mixture
- formaldehyde
- salt
- articles
- 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
- C08G12/046—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 one being urea or thiourea
Abstract
A moulding composition is obtained by reacting a urea, an aldehyde, and at least 5 per cent (based on the weight of resin produced) of a diamine-dicarboxylic acid salt, in the presence of at least 15 per cent of water based on the weight of the mixture. Some suitable diaminedicarboxylic acid salts are described in Specification 474,999. Others are listed in the Specification. The term "urea" is defined as meaning urea, thiourea or derivatives thereof which will react with aldehydes. Mono-sesqui- or di-methylol ureas may replace the mixture of urea and formaldehyde. The preferred aldehyde is formaldehyde. A list of other suitable aldehydes is given in the Specification. The ratio of formaldehyde to urea is 1.5-1.0 : 1. The reaction temperature may vary from 0 DEG to 100 DEG C., preferably it is between 50 DEG and 100 DEG C. Reaction is usually carried on until gelation is incipient, as shown by the viscosity of the mixture. Fillers may be added to the reaction mixture or incorporated latex or clear unfilled products may be produced. Acidic or basic catalysts, e.g. ammonium sulphate, formic acid, sodium hydroxide, or trisodium phosphate may be used in the reaction. The products of the mixture can be moulded at 60-200 DEG C. and 500-20,000 lbs./ sq. in. pressure. Moulding catalysts, e.g. b -brom-hydrocinnamic acid, ammonium sulphate, ammonium chloride, benzoic acid or dibromstyrene may be added. Opacifiers, fillers, pigments, lubricants, or other resins such as phenol-formaldehyde, nylon or cellulose acetate may be incorporated either with the resin syrup before drying or with the dry resin powder. Unfilled articles are clear and water-white. The products have good shock-resistance. Examples describe: (1) and (7) the reaction of urea, formaldehyde and hexamethylene diammonium adipate under reflux until gelation occurs, and drying and powdering of the gel. Articles moulded from the gel are clear, water-white and tough; (2) as in (1) a -cellulose being added as a filler to the partially reacted mixture; (3) as in (1) with hexamethylene diammonium sebacate as the salt; (4) as in (1) with decamethylene diammonium adipate as the salt; (5) as in (1) with ethylenediammonium adipate as the salt; (6) as in (1) with ethylene diammonium sebacate as the salt. The powders are especially useful for forming unfilled, clear or translucent articles or opaque articles with fillers, such as asbestos, cellulose or lignin. A list of articles for which the powders may be used is given. Specification 562,091 also is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US572245XA | 1942-10-21 | 1942-10-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB572245A true GB572245A (en) | 1945-09-28 |
Family
ID=22009260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB17251/43A Expired GB572245A (en) | 1942-10-21 | 1943-10-20 | Improvements in or relating to the production of moulding powders |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB572245A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2668155A (en) * | 1950-04-07 | 1954-02-02 | Du Pont | Urea-formaldehyde primary alkylene diamine condensation products |
US2711961A (en) * | 1950-04-07 | 1955-06-28 | Du Pont | Making paper using a modified ureaformaldehyde resin |
DE1167022B (en) * | 1958-07-25 | 1964-04-02 | Henkel & Cie Gmbh | Process for the production of modified melamine resin precondensates |
-
1943
- 1943-10-20 GB GB17251/43A patent/GB572245A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2668155A (en) * | 1950-04-07 | 1954-02-02 | Du Pont | Urea-formaldehyde primary alkylene diamine condensation products |
US2711961A (en) * | 1950-04-07 | 1955-06-28 | Du Pont | Making paper using a modified ureaformaldehyde resin |
DE1167022B (en) * | 1958-07-25 | 1964-04-02 | Henkel & Cie Gmbh | Process for the production of modified melamine resin precondensates |
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