GB1102337A - Polyamide esters and polyimides - Google Patents

Polyamide esters and polyimides

Info

Publication number
GB1102337A
GB1102337A GB3842565A GB3842565A GB1102337A GB 1102337 A GB1102337 A GB 1102337A GB 3842565 A GB3842565 A GB 3842565A GB 3842565 A GB3842565 A GB 3842565A GB 1102337 A GB1102337 A GB 1102337A
Authority
GB
United Kingdom
Prior art keywords
dicarboxylic acid
aminonaphthalene
ester
aminophthalate
substrates
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
GB3842565A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB1102337A publication Critical patent/GB1102337A/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
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/16Polyester-imides
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Laminated Bodies (AREA)

Abstract

The invention comprises polyamide-esters of inherent viscosity at least 0.04 and formula <FORM:1102337/C3/1> where R is a hydrocarbon radical having 1 or 2 aromatic rings and R1 is a C6- 10 hydrocarbon radical having 1 or 2 aromatic rings. They may be prepared by heating the diaryl ester of the corresponding amino-dicarboxylic acid at 100-200 DEG C., where the alkyl group may contain up to 5 carbon atoms. Esters specified are diphenyl 3-aminophthalate, diphenyl 4-aminophthalate, the diphenyl ester of 3-aminonaphthalene - 1,8 - dicarboxylic acid, 2-aminonaphthalene - 1,8 - dicarboxylic acid, 4-aminonaphthalene -1,8 - dicarboxylic acid and 5 - aminonaphthalene - 2,3 - dicarboxylic acid, di - p - tolyl 3 - aminophthalate, phenyl naphthyl 4 - aminophthalate, and the phenyl p-tolyl ester of 4-aminonaphthalene-1,2-dicarboxylic acid. The product which may contain some phenol as plasticizer and may have an inherent viscosity up to 5.0 may be shaped in to fibre, films, rods and tubes or used as a self-curing coating on one of many specified substrates. Fillers, e.g. pigments, electrical conducting carbon black, abrasives, metals, di-electrics, and lubricating or other polymers may be added before or after shaping and the material may be foamed by adding blowing agents or by bubbling air, CO2 or N2 through the molten polymer before shaping. The polyamide-ester may be converted to a polyimide by heating at above 175 DEG C., preferably under reduced pressure.ALSO:Substrates may be coated with polyamideesters of formula: <FORM:1102337/B1-B2/1> where R is composed of 1 or 2 aromatic rings, R\sv is composed of 1 or 2 aromatic rings and n is such that the inherent viscosity is at least 0.04. The coating may be applied by doctoring, rolling, dipping, brushing or spraying. Substrates specified are copper, brass, aluminium, steel, as sheets, fibres, wires and screening, asbestos, glass, Cellophane (R.T.M.), wood, paper, polyethylene, polypropylene, polystyrene, polyethylene terephthalate, polyamides, polyimides, polytetrafluoroethylene and copolymers of tetrafluoroethylene and hexafluoro-propylene and polyurethanes as sheets, fibres, foams, woven and non-woven fabrics and screening, and leather sheets. The substrates can be metallized before coating or treated with an adhesive. The polyamide-ester may be cured to the corresponding polyimide.
GB3842565A 1964-09-08 1965-09-08 Polyamide esters and polyimides Expired GB1102337A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US39506964A 1964-09-08 1964-09-08

Publications (1)

Publication Number Publication Date
GB1102337A true GB1102337A (en) 1968-02-07

Family

ID=23561570

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3842565A Expired GB1102337A (en) 1964-09-08 1965-09-08 Polyamide esters and polyimides

Country Status (3)

Country Link
CH (1) CH490443A (en)
DE (1) DE1595155A1 (en)
GB (1) GB1102337A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989007120A1 (en) * 1988-02-05 1989-08-10 O'connor, John, David Water dispersible polyamide ester
SG108269A1 (en) * 2001-08-15 2005-01-28 Inst Materials Research & Eng Chemical modification of polyimides

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989007120A1 (en) * 1988-02-05 1989-08-10 O'connor, John, David Water dispersible polyamide ester
SG108269A1 (en) * 2001-08-15 2005-01-28 Inst Materials Research & Eng Chemical modification of polyimides

Also Published As

Publication number Publication date
DE1595155A1 (en) 1970-03-05
CH490443A (en) 1970-05-15

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