GB420525A - Improvements in the manufacture and production of resinous condensation products - Google Patents
Improvements in the manufacture and production of resinous condensation productsInfo
- Publication number
- GB420525A GB420525A GB1514933A GB1514933A GB420525A GB 420525 A GB420525 A GB 420525A GB 1514933 A GB1514933 A GB 1514933A GB 1514933 A GB1514933 A GB 1514933A GB 420525 A GB420525 A GB 420525A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formaldehyde
- condensed
- cyanuric acid
- acid
- condensation products
- 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
- 239000007859 condensation product Substances 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 18
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 6
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 abstract 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- 239000004202 carbamide Substances 0.000 abstract 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
- 239000003085 diluting agent Substances 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- 239000000126 substance Substances 0.000 abstract 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000004982 aromatic amines Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000004090 dissolution Methods 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- ABOYDMHGKWRPFD-UHFFFAOYSA-N phenylmethanesulfonamide Chemical compound NS(=O)(=O)CC1=CC=CC=C1 ABOYDMHGKWRPFD-UHFFFAOYSA-N 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
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
- C08G4/00—Condensation polymers of aldehydes or ketones with polyalcohols; Addition polymers of heterocyclic oxygen compounds containing in the ring at least once the grouping —O—C—O—
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Resinous condensation products are prepared by heating cyanuric acid in the presence or absence of other substances capable of forming resins with formaldehyde with formaldehyde in the presence of a diluent at temperatures not exceeding 160 DEG C. until dissolution has taken place and then removing the diluent under reduced pressure. Acid condensing agents such as hydrochloric acid or acetic anhydride may be used. Other substances that may be added include urea, thiourea, aromatic amines such as aniline, toluene sulphonamide and phenol. The products are soluble in water and organic solvents such as acetone, cyclohexanone, dioxane and glycol monoalkyl or monoaryl ethers. In examples, cyanuric acid is condensed with aqueous formaldehyde under various conditions of acidity, the product, if desired, being condensed with further quantities of formaldehyde; (8) cyanuric acid is condensed with formaldehyde in the presence of dioxane; (9) cyanuric acid and formaldehyde are condensed with urea or thiourea.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1514933A GB420525A (en) | 1933-05-25 | 1933-05-25 | Improvements in the manufacture and production of resinous condensation products |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1514933A GB420525A (en) | 1933-05-25 | 1933-05-25 | Improvements in the manufacture and production of resinous condensation products |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB420525A true GB420525A (en) | 1934-11-26 |
Family
ID=10053901
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1514933A Expired GB420525A (en) | 1933-05-25 | 1933-05-25 | Improvements in the manufacture and production of resinous condensation products |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB420525A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2500489A (en) * | 1946-06-05 | 1950-03-14 | Monsanto Chemicals | Manufacture of melamine and resinous products therefrom |
| US3028264A (en) * | 1959-04-02 | 1962-04-03 | Jr John G Frick | Wrinkle resistance treatment for cellulosic textile materials |
| US3223656A (en) * | 1961-03-28 | 1965-12-14 | Allied Chem | Urea-formaldehyde molding compositions containing cyanuric acid as latent curing catalyst and method |
| US3296207A (en) * | 1961-12-29 | 1967-01-03 | Fmc Corp | Process for the production of polyformals of beta-hydroxyalkyl-isocyanurates and products thereof |
| US3296309A (en) * | 1967-01-03 | Process for stabilizino an aqueous formaldehyde solution |
-
1933
- 1933-05-25 GB GB1514933A patent/GB420525A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3296309A (en) * | 1967-01-03 | Process for stabilizino an aqueous formaldehyde solution | ||
| US2500489A (en) * | 1946-06-05 | 1950-03-14 | Monsanto Chemicals | Manufacture of melamine and resinous products therefrom |
| US3028264A (en) * | 1959-04-02 | 1962-04-03 | Jr John G Frick | Wrinkle resistance treatment for cellulosic textile materials |
| US3223656A (en) * | 1961-03-28 | 1965-12-14 | Allied Chem | Urea-formaldehyde molding compositions containing cyanuric acid as latent curing catalyst and method |
| US3296207A (en) * | 1961-12-29 | 1967-01-03 | Fmc Corp | Process for the production of polyformals of beta-hydroxyalkyl-isocyanurates and products thereof |
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