GB796008A - Improvements in or relating to processes for manufacturing polyesteramides - Google Patents

Improvements in or relating to processes for manufacturing polyesteramides

Info

Publication number
GB796008A
GB796008A GB33107/56A GB3310756A GB796008A GB 796008 A GB796008 A GB 796008A GB 33107/56 A GB33107/56 A GB 33107/56A GB 3310756 A GB3310756 A GB 3310756A GB 796008 A GB796008 A GB 796008A
Authority
GB
United Kingdom
Prior art keywords
dimethyl terephthalate
trimethylol propane
diamine
hexamethylene diamine
butylene
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
GB33107/56A
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.)
Beck & Co Dr GmbH
Original Assignee
Beck & Co Dr GmbH
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 Beck & Co Dr GmbH filed Critical Beck & Co Dr GmbH
Publication of GB796008A publication Critical patent/GB796008A/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
    • C08G69/44Polyester-amides
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/38Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes condensation products of aldehydes with amines or amides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Polyamides (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Organic Insulating Materials (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

Abstract

A polyesteramide containing free hydroxyl groups is made by heating together (1) dimethyl terephthalate; (2) a linear diamine (e.g. butylene or hexamethylene diamine); and (3) a polyhydric alcohol having at least three hydroxyl groups (e.g. trimethylol propane, hexane triol, glycerine or pentaerythrite). In addition the reaction mixture may include a dihydric alcohol (e.g. ethylene, 1:3-propylene or 1:4-butylene glycol) or another dicarboxylic acid (e.g. adipic or sebacic acid) which may be added as such, as the dimethyl ester or as a diamine salt. The polyesteramide may be dissolved in cresol and used as a copper wire varnish either as such or after addition of an isocyanate, preferably a blocked triisocyanate. In examples polyesteramides are made from (1) dimethyl terephthalate, hexamethylene diamine and glycerine; (2) dimethyl terephthalate, hexamethylene diamine, trimethylol propane and ethylene glycol; (3) dimethyl terephthalate, adipic acid, hexamethylene diamine, trimethylol propane and 1:4-butylene glycol; (4) dimethyl terephthalate, adipic acid/hexamethylene diamine salt and trimethylol propane; (5) dimethyl terephthalate, adipic acid, 1:4-butylene diamine, trimethylol propane and 1:4-butane diol.
GB33107/56A 1955-11-03 1956-10-30 Improvements in or relating to processes for manufacturing polyesteramides Expired GB796008A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEB56530A DE1159642B (en) 1955-11-03 1955-11-03 Process for the preparation of polyester amides containing free hydroxyl groups
DE362227X 1955-11-03

Publications (1)

Publication Number Publication Date
GB796008A true GB796008A (en) 1958-06-04

Family

ID=74184292

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33107/56A Expired GB796008A (en) 1955-11-03 1956-10-30 Improvements in or relating to processes for manufacturing polyesteramides

Country Status (6)

Country Link
BE (1) BE551917A (en)
CH (1) CH362227A (en)
DE (1) DE1159642B (en)
FR (1) FR1156746A (en)
GB (1) GB796008A (en)
NL (2) NL210965A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3161541A (en) * 1959-04-27 1964-12-15 Gen Electric Synthetic resin and conductors insulated therewith

Also Published As

Publication number Publication date
NL210965A (en)
NL100956C (en)
BE551917A (en)
DE1159642B (en) 1963-12-19
FR1156746A (en) 1958-05-20
CH362227A (en) 1962-05-31

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