GB1333939A - Electrical conductors coated with polyamideimide resins prepared from the reaction of aromatic diisocyanates with mixtures of polycarboxylic acids and anhydrides - Google Patents

Electrical conductors coated with polyamideimide resins prepared from the reaction of aromatic diisocyanates with mixtures of polycarboxylic acids and anhydrides

Info

Publication number
GB1333939A
GB1333939A GB1333939DA GB1333939A GB 1333939 A GB1333939 A GB 1333939A GB 1333939D A GB1333939D A GB 1333939DA GB 1333939 A GB1333939 A GB 1333939A
Authority
GB
United Kingdom
Prior art keywords
polyamide
coats
wire
aromatic
anhydrides
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
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.)
SI Group Inc
Original Assignee
Schenectady Chemicals Inc
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 Schenectady Chemicals Inc filed Critical Schenectady Chemicals Inc
Publication of GB1333939A publication Critical patent/GB1333939A/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
    • C08G73/14Polyamide-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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/34Carboxylic acids; Esters thereof with monohydroxyl compounds
    • C08G18/343Polycarboxylic acids having at least three carboxylic acid groups
    • C08G18/346Polycarboxylic acids having at least three carboxylic acid groups having four carboxylic acid groups
    • 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
    • H01B3/303Macromolecular 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 H01B3/38 or H01B3/302
    • H01B3/306Polyimides or polyesterimides
    • 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
    • H01B3/308Wires with resins

Landscapes

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

Abstract

1333939 Polyamide-imides SCHENECTADY CHEMICALS Inc 10 Nov 1970 53446/70 Heading C3R [Also in Divisions B2 and H1] An electrical conductor has a continuous coating of a polyamide-imide resin made by reacting (A) 0À95 to 1À01 moles of an aromatic diisocyanate with each mole of (B) a mixture of carboxylic reactants consisting of (i) 5 to 40 mol. per cent of an aromatic dicarboxylic acid in which the COOH groups are not ortho, (ii) 1 to 30 mol. per cent of an aromatic dianhydride and (iii) trimellitic anhydride. Various such reactants are specified as are solvents in which they may be reacted and diluents which may be included in the resulting wire enamel. Such solutions may be applied to copper, silver, aluminium or stainless steel wire by the "free dip" or "die application" procedures described in U.S.A. Specification 3,201,276 with one or more passes to provide the desired build, e.g. at 15 to 45 feet/minute at 250‹ to 800‹ F. to a build of 0À005 to 0À001 inches. The coating may be applied directly to the conductor or over a cured polyester base coat. Various suitable polyesters are mentioned, those from terephthalic acid, ethylene glycol and tris-(2-hydroxyethyl) isocyanurate according to U.S.A. Specification 3,249,578 being preferred. In examples, polyamide-imides are prepared from (A) 4,4<SP>1</SP> - diisocyanato - diphenyl methane, (B) (i) terephthalic acid, (B) (ii) trimellitic and/or benzophenone dianhydride and (B) (iii) trimellitic anhydride in N-methyl pyrrolidone and the products diluted with various diluents and used either to provide 6 coats directly on copper wire or 2 or 3 coats on such a wire having 3 or 4 base coats of the preferred polyester blended with a cresol-formaldehyde resin. Reference is made to Specifications 1,009,956 and 1,217,041.
GB1333939D 1970-11-10 1970-11-10 Electrical conductors coated with polyamideimide resins prepared from the reaction of aromatic diisocyanates with mixtures of polycarboxylic acids and anhydrides Expired GB1333939A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB5344670 1970-11-10

Publications (1)

Publication Number Publication Date
GB1333939A true GB1333939A (en) 1973-10-17

Family

ID=10467836

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1333939D Expired GB1333939A (en) 1970-11-10 1970-11-10 Electrical conductors coated with polyamideimide resins prepared from the reaction of aromatic diisocyanates with mixtures of polycarboxylic acids and anhydrides

Country Status (1)

Country Link
GB (1) GB1333939A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4348460A (en) * 1981-10-19 1982-09-07 Essex Group, Inc. Power insertable polyamide-imide coated magnet wire
US4350738A (en) * 1981-10-13 1982-09-21 Essex Group, Inc. Power insertable polyamide-imide coated magnet wire
US4378407A (en) * 1980-01-24 1983-03-29 Sumitomo Electric Industries Ltd. Magnet wire
US4385437A (en) * 1981-10-19 1983-05-31 United Technologies Corporation Method of power inserting polyamide-imide coated magnet wire
US4385435A (en) * 1981-10-13 1983-05-31 United Technologies Corporation Method of power inserting polyamide-imide coated magnet wire
US4390590A (en) * 1981-10-19 1983-06-28 Essex Group, Inc. Power insertable polyamide-imide coated magnet wire
US4406055A (en) * 1981-10-19 1983-09-27 Essex Group, Inc. Power insertable polyamide-imide coated magnet wire
US20190016849A1 (en) * 2016-05-24 2019-01-17 Lg Chem, Ltd. Polyamide-imide, method for preparing same, and polyamide-imide film using same

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4378407A (en) * 1980-01-24 1983-03-29 Sumitomo Electric Industries Ltd. Magnet wire
US4350738A (en) * 1981-10-13 1982-09-21 Essex Group, Inc. Power insertable polyamide-imide coated magnet wire
US4385435A (en) * 1981-10-13 1983-05-31 United Technologies Corporation Method of power inserting polyamide-imide coated magnet wire
US4348460A (en) * 1981-10-19 1982-09-07 Essex Group, Inc. Power insertable polyamide-imide coated magnet wire
US4385437A (en) * 1981-10-19 1983-05-31 United Technologies Corporation Method of power inserting polyamide-imide coated magnet wire
US4390590A (en) * 1981-10-19 1983-06-28 Essex Group, Inc. Power insertable polyamide-imide coated magnet wire
US4406055A (en) * 1981-10-19 1983-09-27 Essex Group, Inc. Power insertable polyamide-imide coated magnet wire
US20190016849A1 (en) * 2016-05-24 2019-01-17 Lg Chem, Ltd. Polyamide-imide, method for preparing same, and polyamide-imide film using same

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee