GB957409A - Synthetic waxes - Google Patents

Synthetic waxes

Info

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
Application number
GB1760959A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JOHN RICHARD HICKMAN
Original Assignee
JOHN RICHARD HICKMAN
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by JOHN RICHARD HICKMAN filed Critical JOHN RICHARD HICKMAN
Priority to GB1760959A priority Critical patent/GB957409A/en
Publication of GB957409A publication Critical patent/GB957409A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic 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.
GB1760959A 1959-05-22 1959-05-22 Synthetic waxes Expired GB957409A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (7)

* Cited by examiner, † Cited by third party
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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