GB413345A - Improvements in the manufacture and production of resinous condensation products - Google Patents
Improvements in the manufacture and production of resinous condensation productsInfo
- Publication number
- GB413345A GB413345A GB1219/33A GB121933A GB413345A GB 413345 A GB413345 A GB 413345A GB 1219/33 A GB1219/33 A GB 1219/33A GB 121933 A GB121933 A GB 121933A GB 413345 A GB413345 A GB 413345A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acids
- formaldehyde
- acid
- substances
- ethylene glycol
- 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
-
- 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
- C08G12/22—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paints Or Removers (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Resinous condensation products are made by heating polyamides of carboxylic acids containing more than four carbon atoms with formaldehyde substances, which include formaldehyde, its polymers such as tri- or poly-oxymethylene, para- and meta-formaldehyde and substances yielding formaldehyde such as hexamethylenetetramine and acetals. If the reaction is carried out in a weakly alkaline medium, N-methylol compounds of the polyamides are formed, which are further condensed to resinous products. Suitable polyamides are those of open chain and cycloaliphatic, aliphatic-aromatic and aromatic polycarboxylic acids, for example adipic, methyl-adipic, suberic, sebacic, phthalic, hexahydro-o-phthalic, chlorinated phthalic, phenylene di-acetic, naphthalic, citric and diphenic acids; of acids obtained by addition of hydrocyanic acid to unsaturated fatty acids with subsequent saponification of the nitrile group; of acids obtained by oxidation of substances such as waxes, e.g. paraffin wax, oils, fats, fatty acids; distillation residues from the refining of fatty acids, hydrogenated mono- or poly-nuclear aromatic hydrocarbons or their derivatives with the aid of oxygen-containing or -supplying substances, e.g. nitric acid and nitrous gases; of polybasic ether carboxylic acids such as diglycollic or dilactylic acids; of oxidation products of polyalkylene glycols; of sulphur-containing acids such as thiodiglycollic or dithiodiglycollic; or of nitrogen-substituted acids such as imino-a a <1> dipropionic and trimethylamine tricarboxylic acids. The formaldehyde substance may be used in the vapour or solid form or dissolved in water or organic solvents, especially those containing oxygen, e.g. esters such as butyl acetate, dioxane, ketones, methyl, ethyl, propyl, butyl, amyl or benzyl alcohols and ethylene glycol mono-phenyl ether. The reaction is carried out preferably at temperatures of between 120 DEG and 130 DEG C. There may be added organic liquids, especially those containing hydroxyl groups, for example ethyl, butyl or benzyl alcohol, ethylene glycol, glycerol, ethylene glycol monoethyl, monophenyl, or monocresyl ethers, ethylene glycol monoacetate, oleic acid, linoleic acid, china wood oil acid or ricinoleic acid mono- and di-glycerides, castor oil, and hydroxy-ketones. Acid or other usual condensing agents may be used. Substances capable of reacting with formaldehyde, such as urea and its derivatives and amines such as aniline may be added before, during or after the condensation. The products may be hardened by heating to temperatures above those used in the condensation, and hardening accelerators, for example acids or substances capable of splitting off acids, such as ammonium chloride or benzalchloride may be used. The resins may be added to resinous materials to reduce their brittleness and may be used in making lacquers and varnishes, artificial leather, laminated sheets and foils, pressed articles and as impregnating agents for textiles and binding agents for abrasive materials. Specifications 17414/11, [Class 2 (iii)], and 395,340 are referred to.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1219/33A GB413345A (en) | 1932-11-05 | 1933-01-13 | Improvements in the manufacture and production of resinous condensation products |
DEI47456D DE616429C (en) | 1932-11-05 | 1933-06-22 | Process for the production of condensation products |
GB28452/33A GB424076A (en) | 1932-11-05 | 1933-10-14 | Improvements in the manufacture and production of resinous condensation products |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI45687D DE608591C (en) | 1932-11-05 | 1932-11-05 | Process for the production of condensation products |
GB1219/33A GB413345A (en) | 1932-11-05 | 1933-01-13 | Improvements in the manufacture and production of resinous condensation products |
DEI47456D DE616429C (en) | 1932-11-05 | 1933-06-22 | Process for the production of condensation products |
GB28452/33A GB424076A (en) | 1932-11-05 | 1933-10-14 | Improvements in the manufacture and production of resinous condensation products |
Publications (1)
Publication Number | Publication Date |
---|---|
GB413345A true GB413345A (en) | 1934-07-13 |
Family
ID=41719129
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1219/33A Expired GB413345A (en) | 1932-11-05 | 1933-01-13 | Improvements in the manufacture and production of resinous condensation products |
GB28452/33A Expired GB424076A (en) | 1932-11-05 | 1933-10-14 | Improvements in the manufacture and production of resinous condensation products |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB28452/33A Expired GB424076A (en) | 1932-11-05 | 1933-10-14 | Improvements in the manufacture and production of resinous condensation products |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE616429C (en) |
GB (2) | GB413345A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3365471A (en) * | 1963-06-25 | 1968-01-23 | Basf Ag | Production of nitrogenous diepoxides |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2698787A (en) * | 1951-12-17 | 1955-01-04 | American Cyanamid Co | Urea-formaldehyde resins for wet strength paper and their use |
-
1933
- 1933-01-13 GB GB1219/33A patent/GB413345A/en not_active Expired
- 1933-06-22 DE DEI47456D patent/DE616429C/en not_active Expired
- 1933-10-14 GB GB28452/33A patent/GB424076A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3365471A (en) * | 1963-06-25 | 1968-01-23 | Basf Ag | Production of nitrogenous diepoxides |
Also Published As
Publication number | Publication date |
---|---|
GB424076A (en) | 1935-02-14 |
DE616429C (en) | 1935-07-30 |
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