GB957409A - Synthetic waxes - Google Patents
Synthetic waxesInfo
- Publication number
- GB957409A GB957409A GB1760959A GB1760959A GB957409A GB 957409 A GB957409 A GB 957409A GB 1760959 A GB1760959 A GB 1760959A GB 1760959 A GB1760959 A GB 1760959A GB 957409 A GB957409 A GB 957409A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acids
- mixtures
- heating
- temperature until
- condensation
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Abstract
Synthetic waxes are prepared by reacting dicarboxylic acids (6-12C) with a molar excess of one or more aliphatic diamines (2-6C) by heating at an elevated temperature until evolution of water ceases, and condensing the polyamide product with one or more aliphatic monocarboxylic acids (11-25C) in an amount from 1/20 to 1/10 mole per mole of diamine used in the first condensation and less than sufficient to condense with all the terminal amine groups in the polyamide product by heating the reactants at a temperature higher than the first condensation temperature until a homogenous mass is obtained. Ethylene diamine, 1,2- and 1,3-diaminopropane and 1,6-diaminohexane, or mixtures thereof may be used, and adipic and sebacic acids are preferred acids. Mixtures of acids may be used and other dibasic acids such as succinic and phthalic acids may be included in the first stage. Lauric, oleic, palmitic, stearic or 12-hydroxystearic acids or mixtures thereof, and mixtures of long chain fatty acids derived from the hydrolysis of natural oils and fats such as linseed, castor, sunflower oils and tall oil, hardened castor oil or dehydrated castor oil fatty acids are examples of the monocarboxylic acids. The products may be used in a solvent, e.g. hot dimethylformamide, as coating compositions for the interior of steam condensers.ALSO:Synthetic waxes are prepared by reacting dicarboxylic acids (6-12C) with a molar excess, of one or more aliphatic diamines (2-6C) by heating at an elevated temperature until evolution of water ceases and condensing the polyamide product with one or more aliphatic monocarboxylic acids (11-25C) in an amount from 1/20 to 1/10 mole per mole of diamine used in the first condensation and less than sufficient to condense with all the terminal amine groups in the polyamide product, by heating the reactants at a temperature higher than the first condensation temperature until a homogenous mass is obtained. Ethylene diamine, 1,2- and 1,3- diaminopropane and 1,6-diamino hexane, or mixtures thereof may be used, and adipic and sebacic acids are the preferred acids. Mixtures of acids may be used and other dibasic acids such as succinic and phthalic may be included in the first stage. Lauric, oleic, palmitic, stearic, or 12-hydroxy stearic acids or mixtures thereof, and mixtures of long chain fatty acids derived from the hydrolysis of natural oils and fats such as linseed, castor, sunflower oils, and tall oil, hardened castor oil, or dehydrated castor oil fatty acids are examples of the monocarboxylic acids. The products may be used, in a solvent, e.g. hot dimethylformamide, as coating compositions for the interior of steam condensers.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1760959A GB957409A (en) | 1959-05-22 | 1959-05-22 | Synthetic waxes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1760959A GB957409A (en) | 1959-05-22 | 1959-05-22 | Synthetic waxes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB957409A true GB957409A (en) | 1964-05-06 |
Family
ID=10098133
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1760959A Expired GB957409A (en) | 1959-05-22 | 1959-05-22 | Synthetic waxes |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB957409A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20170369748A1 (en) * | 2016-06-22 | 2017-12-28 | Hexion Inc. | Chemical products for adhesive applications |
US20180030339A1 (en) * | 2016-06-22 | 2018-02-01 | Hexion Inc. | Chemical products for adhesive applications |
-
1959
- 1959-05-22 GB GB1760959A patent/GB957409A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20170369748A1 (en) * | 2016-06-22 | 2017-12-28 | Hexion Inc. | Chemical products for adhesive applications |
US20180030339A1 (en) * | 2016-06-22 | 2018-02-01 | Hexion Inc. | Chemical products for adhesive applications |
CN109476823A (en) * | 2016-06-22 | 2019-03-15 | 瀚森公司 | Chemical products for adhesive application |
CN109476823B (en) * | 2016-06-22 | 2021-12-14 | 瀚森公司 | Chemical products for adhesive applications |
US11492544B2 (en) * | 2016-06-22 | 2022-11-08 | Hexion Inc. | Chemical products for adhesive applications |
US11492522B2 (en) * | 2016-06-22 | 2022-11-08 | Hexion Inc. | Chemical products for adhesive applications |
US11578242B2 (en) | 2016-06-22 | 2023-02-14 | Hexion Inc. | Chemical products for adhesive applications |
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