GB364304A - Improvements in and relating to resinous compositions - Google Patents
Improvements in and relating to resinous compositionsInfo
- Publication number
- GB364304A GB364304A GB37546/30A GB3754630A GB364304A GB 364304 A GB364304 A GB 364304A GB 37546/30 A GB37546/30 A GB 37546/30A GB 3754630 A GB3754630 A GB 3754630A GB 364304 A GB364304 A GB 364304A
- Authority
- GB
- United Kingdom
- Prior art keywords
- liquid
- urea
- aldehyde
- parts
- rapidly
- 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
- 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
- C08G14/08—Ureas; Thioureas
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)
- Investigating Materials By The Use Of Optical Means Adapted For Particular Applications (AREA)
Abstract
Phenol-aldehyde condensation products.--A phenolaldehyde condensation product, which is permanently liquid at ordinary temperature but which solidifies on heating, is produced by condensing a phenol and an aldehyde in presence of an ethanolamine, such as mono-, di- or triethanolamine, a dispersing agent, and urea the reaction mixture being rapidly heated and subsequently rapidly cooled. As dispersing agents are mentioned alkali iodides, bromides, chlorides, nitrates and sulphates, sodium benzoate, salicylate formate and citrate, potassium tartrate and calcium chloride. The aldehyde is preferably used in the solid form, but the commercial liquid can also be used. In an example 30 parts of cresol, 18 parts of paraformaldehyde, 2 parts of triethanolamine, 1 part of potassium bromide, 0,5 part of urea and 0,5 part of guanidine carbonate are rapidly heated to 95-100 DEG C. and then rapidly chilled to room temperature. The liquid product, to which fillers may be added, is stable, but gels at 80 DEG C. in an hour and is fully hardened at 105 DEG C. or higher in 20 hours. The liquid product may be used to impregnate an article such as an electric coil, which is warmed, dipped into the cold or warmed liquid and finally heated; the impregnation may be effected in an evacuated chamber, pressure being applied after the liquid is admitted. Specification 302,609, [Class 2 (iii), Dyes &c.], is referred to. The Specification as open to inspection under Sect. 91 (3) (a) refers to guanidine carbonate as an alternative to urea and uses the expression "a urea body." This subject-matter does not appear in the Specification as accepted.ALSO:A phenol-aldehyde condensation product which is permanently liquid at ordinary temperature but which solidifies on heating, is produced by condensing a phenol such as mono-, di- or triethanolamine and an aldehyde in presence of an ethanolamine, a dispersing agent, and urea, the reaction mixture being rapidly heated and subsequently rapidly cooled. As dispersing agents are mentioned alkali iodides, bromides, chlorides, nitrates and sulphates, sodium benzoate, salicylate, formate, and citrate potassium tartrate and calcium chloride. The aldehyde is preferably used in the solid form but the commercial liquid can also be used. In an example 30 parts of cresol, 18 parts of paraformaldehyde, 2 parts of triethanolamine, 1 part of potassium bromide, 0,5 part of urea, and 0,5 part of guanidine carbonate are rapidly heated to 95-100 DEG C. and then rapidly chilled to room temperature. The liquid product to which fillers may be added is stable, but gels at 80 DEG C. in an hour and is fully hardened at 105 DEG C. or higher in 20 hours. The liquid product may be used to impregnate an article such as an electric coil, which is warmed, dipped into the cold or warmed liquid and finally heated; the impregnation may be effected in an evacuated chamber, pressure being applied after the liquid is admitted. Specification 302,609, [Class 2 (iii), Dyes &c.], is referred to. The Specification as open to inspection under Sect. 91 (3) (a) mentions guanidine carbonate as an alternative to urea, and uses the expression "a urea body." This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US364304XA | 1929-12-13 | 1929-12-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB364304A true GB364304A (en) | 1932-01-07 |
Family
ID=21888565
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB37546/30A Expired GB364304A (en) | 1929-12-13 | 1930-12-12 | Improvements in and relating to resinous compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB364304A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0480778A2 (en) * | 1990-10-12 | 1992-04-15 | Isover Saint-Gobain | Phenolic resin, process for producing this resin, and resin composition for adhering mineral fibres |
US5270434A (en) * | 1990-10-12 | 1993-12-14 | Isover Saint-Gobain | Phenolic resin, procedure for preparation of the resin, and sizing composition for mineral fibers containing this resin |
-
1930
- 1930-12-12 GB GB37546/30A patent/GB364304A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0480778A2 (en) * | 1990-10-12 | 1992-04-15 | Isover Saint-Gobain | Phenolic resin, process for producing this resin, and resin composition for adhering mineral fibres |
FR2667865A1 (en) * | 1990-10-12 | 1992-04-17 | Saint Gobain Isover | PHENOLIC RESIN, PROCESS FOR PREPARING THE RESIN AND COMPOSITION FOR THE SIZING OF MINERAL FIBERS CONTAINING THE SAME. |
EP0480778A3 (en) * | 1990-10-12 | 1993-09-01 | Isover Saint-Gobain | Phenolic resin, process for producing this resin, and resin composition for adhering mineral fibres |
US5270434A (en) * | 1990-10-12 | 1993-12-14 | Isover Saint-Gobain | Phenolic resin, procedure for preparation of the resin, and sizing composition for mineral fibers containing this resin |
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