GB1101211A - Aleohol-soluble polyamides - Google Patents

Aleohol-soluble polyamides

Info

Publication number
GB1101211A
GB1101211A GB4346263A GB4346263A GB1101211A GB 1101211 A GB1101211 A GB 1101211A GB 4346263 A GB4346263 A GB 4346263A GB 4346263 A GB4346263 A GB 4346263A GB 1101211 A GB1101211 A GB 1101211A
Authority
GB
United Kingdom
Prior art keywords
polymerized fatty
acid
terminating
anhydride
tetrahydrophthalic
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
GB4346263A
Inventor
Alec Frank Wilson
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.)
Coates Brothers and Co Ltd
Original Assignee
Coates Brothers and Co Ltd
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 Coates Brothers and Co Ltd filed Critical Coates Brothers and Co Ltd
Priority to GB4346263A priority Critical patent/GB1101211A/en
Publication of GB1101211A publication Critical patent/GB1101211A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/26Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
    • C08G69/34Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids using polymerised unsaturated fatty acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/48Polymers modified by chemical after-treatment

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Polyamides (AREA)
  • Paints Or Removers (AREA)

Abstract

Imide-terminated polyamides are prepared by reacting a polymerized fatty acid with a polyamine in the presence of a dicarboxylic acid or acid anhydride or by reacting the said anhydride with a polymer prepared from the polymerized fatty acid and the polyamine. The polymerized fatty acids may be dimers or trimers and may contain some monomer, e.g. hydrolysed stand oils. They may be hydrogenated catalytically to remove unsaturation. Polyamines specified are: ethylene, 1,3-propylene, tetramethylene, hexamethylene, phenylene and xylylene diamines and diethylene triamine. An excess of amine may be used. Terminating agents specified are phthalic, tetrahydrophthalic, methyl tetrahydrophthalic, methyl endomethylene tetrahydrophthalic, hexahydrophthalic, methyl hexahydrophthalic, succinic, tetrapropenylsuccinic, dodecyl succinic, and maleic acids. 5-50 moles of terminating agent may be used per 100 of polymerized fatty acid. When the terminating agents is an acid some diamide may be formed in addition to imide. All 3 reactants may be mixed together or the terminating anhydride may be added to the preformed polyamide. Minor amounts of other aliphatic dicarboxylic acids may be added, e.g. sebacic, pimelic and azelaic. The product is soluble in methanol, ethanol, I.M.S. and propanol. It may be used as a varnish, ink, lacquer or paint for metal, wood, glass, plastic, or rubber or as an adhesive.
GB4346263A 1963-11-04 1963-11-04 Aleohol-soluble polyamides Expired GB1101211A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4346263A GB1101211A (en) 1963-11-04 1963-11-04 Aleohol-soluble polyamides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4346263A GB1101211A (en) 1963-11-04 1963-11-04 Aleohol-soluble polyamides

Publications (1)

Publication Number Publication Date
GB1101211A true GB1101211A (en) 1968-01-31

Family

ID=10428853

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4346263A Expired GB1101211A (en) 1963-11-04 1963-11-04 Aleohol-soluble polyamides

Country Status (1)

Country Link
GB (1) GB1101211A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2374392A1 (en) * 1976-12-20 1978-07-13 Chem Plast Spa THERMAL FUSE ADHESIVE

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2374392A1 (en) * 1976-12-20 1978-07-13 Chem Plast Spa THERMAL FUSE ADHESIVE

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