GB641703A - Manufacture of unpolymerized urea-formaldehyde reaction products - Google Patents
Manufacture of unpolymerized urea-formaldehyde reaction productsInfo
- Publication number
- GB641703A GB641703A GB6870/48A GB687048A GB641703A GB 641703 A GB641703 A GB 641703A GB 6870/48 A GB6870/48 A GB 6870/48A GB 687048 A GB687048 A GB 687048A GB 641703 A GB641703 A GB 641703A
- Authority
- GB
- United Kingdom
- Prior art keywords
- urea
- formaldehyde
- temperature
- liquid
- proportion
- 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
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)
Abstract
Liquid urea-formaldehyde compositions are made by admixing a liquid mixture of formaldehyde and water containing from 50-70 per cent of formaldehyde by weight, the temperature of said liquid having been maintained above 45 DEG C. since its preparation, with urea at a pH of 7-9, in the proportion of one molecule of urea per 3.9-10 molecules of formaldehyde and maintaining the temperature of the resulting liquid at least momentarily at from 70-90 DEG C. The proportion of formaldehyde to urea is preferably from 4.5 : 1 to 7.0 : 1, and most preferred at 6.0 : 1. Additional amounts of urea may be added subsequently to reduce the formaldehyde-urea ratio to not less than 3.9 : 1, the temperature being preferably lowered below 50 DEG C. prior to the second addition of urea. The formaldehyde solution may be prepared by liquefying a gaseous formaldehyde-watervapour mixture of corresponding composition having a temperature above 90 by cooling to 60-90 DEG C. The compositions obtained may be used for impregnating lignocellulosic and cellulosic materials, e.g. wood, and in the manufacture of lacquers, moulded products and finishes. Further additions of urea may be made immediately before such use. The pH is preferably adjusted by the use of buffer mixtures, e.g. phosphoric acid or boric acid and sodium hydroxide. Examples are given, giving details of procedures carried out in accordance with the above.ALSO:Liquid urea-formaldehyde compositions are made by admixing a liquid mixture of formaldehyde and water containing from 50-70 per cent of formaldehyde by weight, the temperature of said liquid having been maintained above 45 DEG C. since its preparation, with urea at a pH of 7-9, in the proportion of one molecule of urea per 3.9-10 molecules of formaldehyde and maintaining the temperature of the resulting liquid at least momentarily at from 70-90 DEG C. The proportion of formaldehyde to urea is preferably from 4.5 : 1 to 7.0 : 1, and most preferred at 6.0 : 1. Additional amounts of urea may be added subsequently to reduce the formaldehyde-urea ratio to not less than 3.9 : 1, the temperature being preferably lowered below 50 DEG C. prior to the second addition of urea. The formaldehyde solution may be prepared by liquefying a gaseous formaldehyde-water-vapour mixture of corresponding composition having a temperature above 90 by cooling to 60-90 DEG C. The compositions obtained may be used for impregnating lignocellulosic and cellulosic materials, e.g. wood, and in the manufacture of lacquers, moulded products, and finishes. Further additions of urea may be made immediately before such use. The pH is preferably adjusted by the use of buffer mixtures, e.g. phosphoric acid or boric acid and sodium hydroxide. Examples are given, giving details of procedures carried out in accordance with the above.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US641703XA | 1947-03-06 | 1947-03-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB641703A true GB641703A (en) | 1950-08-16 |
Family
ID=22054037
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6870/48A Expired GB641703A (en) | 1947-03-06 | 1948-03-05 | Manufacture of unpolymerized urea-formaldehyde reaction products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB641703A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1239290B (en) * | 1957-10-30 | 1967-04-27 | Montedison Spa | Continuous process for the production of concentrated permanent aqueous solutions of urea, formaldehyde and urea-formaldehyde condensation products |
-
1948
- 1948-03-05 GB GB6870/48A patent/GB641703A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1239290B (en) * | 1957-10-30 | 1967-04-27 | Montedison Spa | Continuous process for the production of concentrated permanent aqueous solutions of urea, formaldehyde and urea-formaldehyde condensation products |
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