GB595366A - Synthetic resinous materials and process of making same - Google Patents
Synthetic resinous materials and process of making sameInfo
- Publication number
- GB595366A GB595366A GB23053/44A GB2305344A GB595366A GB 595366 A GB595366 A GB 595366A GB 23053/44 A GB23053/44 A GB 23053/44A GB 2305344 A GB2305344 A GB 2305344A GB 595366 A GB595366 A GB 595366A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sodium
- aldehyde
- formaldehyde
- amino
- urea
- 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
- C08G12/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J39/00—Cation exchange; Use of material as cation exchangers; Treatment of material for improving the cation exchange properties
- B01J39/08—Use of material as cation exchangers; Treatment of material for improving the cation exchange properties
- B01J39/16—Organic material
- B01J39/18—Macromolecular compounds
- B01J39/19—Macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Thermosetting resinous products containing salt-forming sulphonate groups are formed by heating at a pH of 4-10, one or more of formaldehyde, acetaldehyde, butyraldehyde, furfuraldehyde and benzaldehyde, together with a water-soluble metal salt of sulphurous acid and a carbamide, a polyaminodiazine or a polyamino triazine or mixtures thereof, at least two amino groups of which are primary, 0.5-2.0 mols. of aldehyde being used per reactive amino group and the salt yielding 0.05-0.4 mol. of bisulphite per mol. of aldehyde. The term carbamide includes urea and its derivatives, thiourea, dicyandiamide, guanidine or mixtures thereof. Amino - azines specified are 2,6-diamino - 1,3 - diazine; 5 - methyl - 2,6 - diamino - 1,3-diazine; 4-chloro-2,6-diamino-1,3-diazine; polyamino pyrimidines; melamine; melam; ammeline; thioammeline; b - b 1 - bis - thio - ammeline diethyl ether and similar compounds as described in Specification 543,256. Sulphenous acid salts of the alkali metals are particularly useful. The aldehyde and amino compound may be reacted together first and the product reacted with the sulphite, or the aldehyde and sulphite may be reacted first and the product reacted with the amino body or all three reactants may be mixed together at the outset. The preferred temperature range is from 60 DEG C. to the boiling point of the mixture. The product may be concentrated or dried, e.g. by heating with or without vacuum, drum-drying or spray-drying. Examples describe the preparation of resins from (1) urea and formaldehyde in presence of sodium metabisulphite; (2) melamine and formaldehyde in presence of sodium sulphite; (3) urea and acetaldehyde in presence of sodium metabisulphite; (4) melamine, urea and formaldehyde in presence of sodium sulphite. All the products were water-soluble. They are suitable for making films, for treating textiles, for addition to paper pulp in the beater to make paper of high wet strength, for impregnating fibrous materials such as paper, cloth or wood. They may be used as ion exchange resins, for casting or laminating, if desired in conjunction with plasticisers, pigments, fillers, starch, cereal or wood flour. The metal attached to the sulphonate group may be replaced by another metal, e.g. a heavy metal. Thus, cloth or wood may be impregnated with a solution of a resin containing a sodium sulphonate group and then treated with a solution of a salt, e.g. copper sulphate, to exchange the sodium atoms for copper (see Group VIII). Specifications 595,367, [Group VIII], and 595,368 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US595366XA | 1943-11-20 | 1943-11-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB595366A true GB595366A (en) | 1947-12-03 |
Family
ID=22023596
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23053/44A Expired GB595366A (en) | 1943-11-20 | 1944-11-20 | Synthetic resinous materials and process of making same |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE968737C (en) |
GB (1) | GB595366A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0176673A1 (en) * | 1984-08-07 | 1986-04-09 | SKW Trostberg Aktiengesellschaft | Metal compounds of acid groups containing condensation or cocondensation products of ketones and aldehydes |
WO2001023450A1 (en) * | 1999-09-29 | 2001-04-05 | Skw Polymers Gmbh | Sulfonated condensation products which are stabile in storage, method for the production thereof, and their use |
EP1693393A1 (en) | 2005-02-22 | 2006-08-23 | Lanxess Deutschland GmbH | Condensation products containing acid groups |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB259950A (en) * | 1925-10-16 | 1927-12-22 | Ig Farbenindustrie Ag | Improvements in the manufacture and production of condensation products of urea and its derivatives and formaldehyde |
US1976616A (en) * | 1933-08-31 | 1934-10-09 | Katherine J Kinnicutt | Tray insert for cooking utensils |
GB476608A (en) * | 1936-06-13 | 1937-12-13 | John Arthur Hetherington | Improvements in or relating to the manufacture of urea-formaldehyde condensation products |
DE705533C (en) * | 1938-12-15 | 1941-05-02 | Siemens Schuckertwerke Akt Ges | Electric Isolation |
DE889225C (en) * | 1942-07-15 | 1953-09-07 | Basf Ag | Process for the production of condensation products |
DE883652C (en) * | 1942-12-23 | 1953-07-20 | Basf Ag | Process for the production of condensation products |
-
1944
- 1944-11-20 GB GB23053/44A patent/GB595366A/en not_active Expired
-
1950
- 1950-03-10 DE DER5263A patent/DE968737C/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0176673A1 (en) * | 1984-08-07 | 1986-04-09 | SKW Trostberg Aktiengesellschaft | Metal compounds of acid groups containing condensation or cocondensation products of ketones and aldehydes |
US4666979A (en) * | 1984-08-07 | 1987-05-19 | Skw Trostberg Ag | Metal compounds of acid group-containing condensation products and co-condensation products of ketones and aldehydes |
WO2001023450A1 (en) * | 1999-09-29 | 2001-04-05 | Skw Polymers Gmbh | Sulfonated condensation products which are stabile in storage, method for the production thereof, and their use |
US6864344B1 (en) | 1999-09-29 | 2005-03-08 | Skw Polymers Gmbh | Sulfonated condensation products which are stabile in storage, method for the production thereof, and their use |
EP1693393A1 (en) | 2005-02-22 | 2006-08-23 | Lanxess Deutschland GmbH | Condensation products containing acid groups |
Also Published As
Publication number | Publication date |
---|---|
DE968737C (en) | 1958-03-27 |
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