US3523820A - Electrical conductor coated with high temperature insulating varnishes - Google Patents

Electrical conductor coated with high temperature insulating varnishes Download PDF

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US3523820A
US3523820A US543150A US3523820DA US3523820A US 3523820 A US3523820 A US 3523820A US 543150 A US543150 A US 543150A US 3523820D A US3523820D A US 3523820DA US 3523820 A US3523820 A US 3523820A
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oil
acid
electrical conductor
polyester
acids
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Howard E Sheffer
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SI Group Inc
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Schenectady Chemicals Inc
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    • 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
    • H01B3/42Insulators 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 polyesters; polyethers; polyacetals
    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/68Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/685Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen
    • C08G63/6854Polyesters containing atoms other than carbon, hydrogen and oxygen containing nitrogen derived from polycarboxylic acids and polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D161/00Coating compositions based on condensation polymers of aldehydes or ketones; Coating compositions based on derivatives of such polymers
    • C09D161/04Condensation polymers of aldehydes or ketones with phenols only
    • C09D161/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/08Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
    • 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/92Fire or heat protection feature
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • Y10T428/2933Coated or with bond, impregnation or core
    • Y10T428/294Coated or with bond, impregnation or core including metal or compound thereof [excluding glass, ceramic and asbestos]
    • Y10T428/2942Plural coatings
    • Y10T428/2947Synthetic resin or polymer in plural coatings, each of different type
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31721Of polyimide
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31786Of polyester [e.g., alkyd, etc.]

Definitions

  • This invention relates to oil-modified alkyd resins and insulating varnishes containing such resins as Well as to electrical conductors coated with such varnishes.
  • Another object is to prepare an insulating varnish suitable for continuous use at 180 C.
  • An additional object is to develop an improved wire having an polyester or polyimide under coat and a Dacron top coat and a protective coat of insulating varnish over the top coat.
  • a further object is to prepare an enameled wire having improved properties in the burnout test.
  • insulating varnishes containing alkyd resin from isophthalic acid, tris (Z-hydroxyethyl) isocyanurate and drying oil acids.
  • drying oil acids do not have substantially more unsaturation than soybean oil acids.
  • an oil-soluble phenol-formaldehyde resin in an amount of 10' to 80% of the total of the alkyd resin and phenolic resin.
  • terephthalic acid in the higher oil length ranges, e.g. a 55% oil length.
  • a portion of the tris (Z-hydroxyethyl) isocyanurate (THEI) can be replaced by another polyol, e.g. glycerine or pentaerythritol.
  • the THEI can be 50 to 100% of the total polyol.
  • replacing part of the THEI by another polyol will impair to some extent the improved thermal properties of the varnishes of the present invention.
  • drying oil acids there can be used soybean oil acids, cottonseed oil acids, corn oil acids, whale oil acids, safllower oil acids or sunflower oil acids, or less preferably, linseed oil acids, tung oil acids, oiticica oil acids, perilla oil acids.
  • drying or semi-drying oil acids can 3523,82 Patented Aug. 11, 1970 "ice be replaced by non-drying oil acids such as coconut oil fatty acids, oilve oil acids, castor oil acids, peanut oil acids and rapeseed oil acids.
  • the latter need not be added as such but can be added in the form of an oil, e.g. soybean oil, corn oil, linseed oil, or the like. In such case, of course, the oil supplies part or all of the oil fatty acid component.
  • an oil e.g. soybean oil, corn oil, linseed oil, or the like.
  • the oil-modified alkyd resin can include 20 to 65% of the fatty acids but preferably contains 30 to 55% of the fatty acids, e.g. soybean fatty acids.
  • an electrical conductor e.g. a wire 2 having a first (or under coat) continuous coating 4 of a polymeric ester of terephthalic acid and tris (Z-hydroxyethyl) isocyanurate, a second (or top coat) continuous coating 6 of polyethylene terephthalate and a protective coat 8 of soybean oil fatty acid modified polymeric ester of isophthalic acid and tris (Z-hydroxyethyl) isocyanurate admixed With p-t-butylphenol formaldehyde resin.
  • polyester or polyimide suitable for continuous use at C. or above.
  • the polyester employed in forming the under coat is the reaction product of a polymeric ester of terephthalic acid or isophthalic acid with THEI.
  • a portion of the THEI, up to 50% of the total polyhydric alcohol on a weight basis can be replaced by a modifying polyhydric alcohol such as ethylene glycol, butanediol-l,4, pentanediol 1,5, butene-2-diol-1,4, butyne-2-diol-l,4; 2,2,4,4- tetramethyl-1,3-cyclobutanediol, 1,4-cyclohexanedimethanol, hydroquinone di-B-hydroxyethyl ether, glycerine, trimethylolethane, 1,1,1-trimethylolpropane, pentaerythritol, dipentaerythritol, sorbitol or mannitol.
  • a portion of the terephthalic acid or isophthalic acid up to 50 equivalent percent of the acid component can be replaced by a modifying polycarboxylic acid such as o-phthalic anhydride, adipic acid, sebacic acid, hemimellitic acid, trimellitic acid, trimesic acid, succinic acid, tetrachlorophthalic anhydride or hexachloroendomethylene tetrahydrophthalic acid.
  • a modifying polycarboxylic acid such as o-phthalic anhydride, adipic acid, sebacic acid, hemimellitic acid, trimellitic acid, trimesic acid, succinic acid, tetrachlorophthalic anhydride or hexachloroendomethylene tetrahydrophthalic acid.
  • the total number of hydroxyl groups on the alcohols normally is 1 to 1.6 times the total number of carboxyl groups on the acids in the under coat.
  • the polyester can also be modified by adding an organo titanate and/or a polyisocyanate.
  • titanate there can be used tetraalkyl titanates such as tetraisopropyl titanate, tetrabutyl titanate, tetramethyl titanate, tetrahexyl titanate and tetrapropyl titanate.
  • the titanate is used in an amount of 0.001 to 4.0% titanium metal on the total solids of the under coat.
  • polyisocyanate there can be used 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, hexamethylene diisocyanate, blocked isocyanates such as the reaction product of three mols of mixed 2,4- and 2,6-tolylene diisocyanates with trimethylol propane and blocked by esterification with phenol (Mondur S), and the cyclic trimers of 2,4- and 2,6-tolylene diisocyanates having the three free isocyanate groups blocked by esterification with m-cresol (Mondur SH).
  • the polyisocyanates including the blocked isocyanates, set forth in Sheffer et al. Pat. No. 2,982,754, or in Meyer et al. Pat. No. 3,211,585.
  • I to 40% of the total solids are polyisocyanates.
  • the polyester under coat can be applied to the electrical conductor in the manner disclosed in Meyer et al. Pat. No. 3,211,585, and Meyer et al. Pat. No. 3,201,276.
  • polyester under coat there can be used any of the THEI containing terephthalates of the two Meyer et al. patents as well as the corresponding isophthalates.
  • a polyester-polyimide in which at least 20%, and preferably at least 50%, of the alcohol component of the polyester is THEI and the polybasic acid component comprises terephthalic acid, isophthalic acid or benzo phenone dicarboxylic acid.
  • the polyimide component of the molecule normally has a member of the group consisting of benzene and naphthalene rings joined to two carbon atoms of a heterocyclic imide ring having to 6 members in the ring, one of the atoms in the heterocyclic ring being nitrogen and the balance carbon.
  • polyester-polyimide The usual components of the polyester-polyimide are (1) an aromatic or aliphatic diamine, e.g. methylene dianiline, oxydianiline, benzidine, 3,3-diamin0-diphenyl, pphenylene diamine, 1,4diamino-naphthalene, a, W-nonamethylene diamine, 4,4-diaminodiphenyl ether, heptamethylene diamine, diamino-diphenyl ketone, hexamethylenc diamine, ethylene diamine, diamino-diphenyl sulfone, 4,4'-dicyclohexylmcthane diamine, (2) an anhydride having 3 to 4 carboxyl groups such as trimellitic anhydride, pyromellitic dianhydride, benzophenone 2,3-, 2',3'-tetracarboxylic dianhydride, 2,3,6,7-naphthalene dian
  • the under coat whether it is a polyester of polyesterpolyimide, also usually contains 1 to 5% based on the total solids of a melamine-formaldehyde resin or a phenolic resin such as phenol-formaldehyde, cresol-formaldehyde or xylenol-formaldehyde resin.
  • top coat there is preferably employed polyethylene tercphthalate. It is applied from a solvent solution, as set forth in Meyer et a1. Pat. No. 3,201,276.
  • the preferred solvent contains to of monochlorophenol and the balance a cresol or mixture of cresol with phenol.
  • polyimide-polyamides In place of polyethylene terephthalate there can be employed as the top coat polyimide-polyamides, polyesterpolyimidamicies, straight polyimides and other linear polymers.
  • polyimide-polyamides there can be employed the pyromellitimide available commercially as Pyre-ML as well as other polyimides such as the reaction product of 3,3'-diaminodiphenyl and pyromellitic anhydride, the reaction product of oxydianiline with pyromellitic anhydride, the reaction product of methylene dianiline with pyromellitic anhydride or the polyimides disclosed in Edwards Pat. No.
  • polyester-polyimide-polyamide from ethylene glycol, terephthalic acid, methylene dianiline and pyromellitic anhydride, etc.
  • polyesters such as polyhexamethylene glycol terephthalate and other linear polyesters.
  • the insulating varnishes of the present invention can be applied directly to electrical conductors but are preferably employed as a protective coat over the under coat and top coat formulations just described.
  • the insulating varnishes can be used to coat copper, aluminum and silver wires and to impregnate armature and field coils of motors and for both power and distribution transformers of either the oil or dry type where long life at high operating temperatures is required. While the insulating varnishes of Thielking Pat. No. 3,080,331 are indicated as being suitable only at temperatures of up to C. the insulating varnishes of the present invention are suitable for continuous use at temperatures of C. and higher.
  • the varnish also includes an oilsoluble phenol-formaldehyde resin.
  • the preferred phenols for forming these phenol-formaldehyde resins are ortho and para alkyl substituted phenols, 2,2-bis (phydroxyphenyl) propane and 4,4-bis (p-hydroxyphenyl) propane.
  • Suitable phenols for making the resin mention can be made of p-t-hutylphenol, p-tamylphenol, p-t-octylphenol, p-phenylphenol, o-t-butylphenol, and the phenols of Honel Pat. No. 1,800,296. Any of the oilsoluble phenol aldehyde resins set forth in the Thielking patent can be employed.
  • the insulating varnish contains conventional varnish solvents in addition to the resin components.
  • solvents include one or more of xylene, mineral spirits, isophorone, naphtha, toluene and benzene.
  • EXAMPLE 1 762 grams of soybean oil fatty acids (Emery 610 soy oil fatty acids), 945 grams of tris(2-hydroxyethyl) isocyanurate and 597 grams of isophthalic acid were loaded in a flask, the temperature raised in one hour to 440 F. and held in the 440-470 F. range for 3.5 hours until the acid number was 25. The batch was thinned with 2000 grams of xylene to Z7 viscosity at 50% solids to give a 41% oil length alkyd resin.
  • EXAMPLE 2 1344 grams of soybean oil fatty acids (Emery 610 soy oil fatty acids), 885 grams of THEI and 348 grams of isophthalic acid were loaded in a flask and the temperature raised to 480 F. in 3.5 hours. The batch was then heated in the 480520 F. for 4.5 hours until the acid number was 6. The batch was thinned with 1350 grams of aromatic naphtha to Z viscosity at 65% solids.
  • EXAMPLE 3 An insulating varnish was prepared similar to that of Example 1 but using an alkyd resin made from 387 grams of soybean oil fatty acids, 243 grams of coconut oil fatty acids, 597 grams of isophthalic acid and 945 grams of THEI.
  • EXAMPLE 4 A motor stator was impregnated with the insulating varnish of Example 1 in a dip tank operation. The varnish was cured by baking in an oven at 395 F. for 1 hour.
  • Isonel 200E is the mixture of (a) 86 parts of the polyester from 4400 parts of THEI, 481 parts of ethylene glycol and 5019 parts of dimcthyl terephthalate, (b) 5 parts of Mondur SH, (e) 5 parts of tetraisopropyl titanate and (d) 5 parts of m-p-cresolformaldehyde resin (made from 3440 parts of m-p-cresol and 1962 parts of 37% aqueous formaldehyde).
  • the thus coated wire was dipped twice through the in sulating varnish prepared in Example 1 with curing at 395 F. for 1 hour after each dip.
  • the wire having the three coatings was tested by AIEE No. 57 twisted pairs with the following results:
  • EXAMPLE 6 The same procedure as that of Example 5 was repeated but using the insulating varnish of Example 2 to obtain a coated wire which had a Class H rating.
  • EXAMPLE 7 It was also found that the insulating varnish of Example 2 applied to wire coated with Isonel 200E and topcoated with polyethylene terephthalate (Isonel 17) gave improved results in the burnout test.
  • the burnout test is run by twisting pairs of the enameled wire, dipping in the varnish and curing for 1 hour at 400 P. Then 33 amperes is applied for four minutes and the breakdown voltage of the system tested. The results obtained in the burnout tests were as follows, final voltages were expressed in kilovolts.
  • ester of tris (2-hydroxyethyl) isocyanurate and an aromatic dicarboxylic acid and (2) a polyester polymide wherein at least 20% of the alcohol component of the polyester is tris (Z-hydroxyethyl) isocyanurate, a second coating selected from the group consisting of (1) linear polyethylene terephthalate, (2) and linear polyimide-polyamides, and a third coating of an insulating varnish including (a) an alkyd resin selected from the group consisting of unsaturated higher fatty acid modified tris (2-hydroxyethyl) isocyanurate isophthalate and unsaturated higher fatty acid modified tris (Z-hydroxyethyl) isocyanurate terephthalate, said resin having 20 to of higher fatty acids, and (b) an oil soluble phenol-formaldehyde resin, the phenol-formaldehyde resin being present in an amount of to 15% of the total of the alkyd resin and phenolformaldehyde resin over said coating

Description

Aug 11 1970 ,H. E. 'HEFF 3,523,820
ELECTRICAL C UCTOR TED WI HIGH TEMPERATURE NSULATING vmmsnms Filed April 18, 1966 BY %%%%M ATTORNEYS United States Patent U.S. Cl. 117-218 6 Claims ABSTRACT OF THE DISCLOSURE Electrical conductors having improved properties at high temperature are produced by providing such conductors with three resinous coatings, the second coating being polyethylene terephthalate or linear polyimidepolyamides.
This invention relates to oil-modified alkyd resins and insulating varnishes containing such resins as Well as to electrical conductors coated with such varnishes.
It has previously been proposed to prepare insulating varnishes from short oil-modified glyceryl isophthalate and an oil-soluble phenol-formaldehyde resin, Thielking Pat. No. 3,080,331. Such a varnish is quite valuable but, unfortunately, cannot be employed where the final product must be classified as 180 C. (Class H) in the AIEE No. 57 heat life test.
It is an object of the present invention to prepare a novel oil-modified alkyd resin.
Another object is to prepare an insulating varnish suitable for continuous use at 180 C.
An additional object is to develop an improved wire having an polyester or polyimide under coat and a Dacron top coat and a protective coat of insulating varnish over the top coat.
A further object is to prepare an enameled wire having improved properties in the burnout test.
Still further objects and the entire scope of applicability of the present invention will become apparent from the detailed description given hereinafter; it should be understood, however, that the detailed description and specific examples, while indicating preferred embodiments of the invention, are given by Way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description.
It has now been found that these objects can be at tained by preparing insulating varnishes containing alkyd resin from isophthalic acid, tris (Z-hydroxyethyl) isocyanurate and drying oil acids. Preferably the drying oil acids do not have substantially more unsaturation than soybean oil acids. In addition to the oil-modified alkyd resin there should be present an oil-soluble phenol-formaldehyde resin in an amount of 10' to 80% of the total of the alkyd resin and phenolic resin. In place of isophthalic acid less preferably there can be used terephthalic acid in the higher oil length ranges, e.g. a 55% oil length.
A portion of the tris (Z-hydroxyethyl) isocyanurate (THEI) can be replaced by another polyol, e.g. glycerine or pentaerythritol. Thus, the THEI can be 50 to 100% of the total polyol. However, it should be realized that replacing part of the THEI by another polyol will impair to some extent the improved thermal properties of the varnishes of the present invention.
As the drying oil acids there can be used soybean oil acids, cottonseed oil acids, corn oil acids, whale oil acids, safllower oil acids or sunflower oil acids, or less preferably, linseed oil acids, tung oil acids, oiticica oil acids, perilla oil acids.
A portion of the drying or semi-drying oil acids can 3523,82 Patented Aug. 11, 1970 "ice be replaced by non-drying oil acids such as coconut oil fatty acids, oilve oil acids, castor oil acids, peanut oil acids and rapeseed oil acids.
When a portion of the THEI is replaced by glycerine the latter need not be added as such but can be added in the form of an oil, e.g. soybean oil, corn oil, linseed oil, or the like. In such case, of course, the oil supplies part or all of the oil fatty acid component.
The oil-modified alkyd resin can include 20 to 65% of the fatty acids but preferably contains 30 to 55% of the fatty acids, e.g. soybean fatty acids.
Unless otherwise indicated, all parts and percentages are by weight.
The invention will be understood best in connection with the drawings wherein the single figure is a crosssectional view of an electrical conductor having an insulating coating according to the invention.
Referring more specifically to the drawings, there is provided an electrical conductor, e.g. a wire 2 having a first (or under coat) continuous coating 4 of a polymeric ester of terephthalic acid and tris (Z-hydroxyethyl) isocyanurate, a second (or top coat) continuous coating 6 of polyethylene terephthalate and a protective coat 8 of soybean oil fatty acid modified polymeric ester of isophthalic acid and tris (Z-hydroxyethyl) isocyanurate admixed With p-t-butylphenol formaldehyde resin.
As the under coat there is employed a polyester or polyimide suitable for continuous use at C. or above.
The polyester employed in forming the under coat is the reaction product of a polymeric ester of terephthalic acid or isophthalic acid with THEI. A portion of the THEI, up to 50% of the total polyhydric alcohol on a weight basis can be replaced by a modifying polyhydric alcohol such as ethylene glycol, butanediol-l,4, pentanediol 1,5, butene-2-diol-1,4, butyne-2-diol-l,4; 2,2,4,4- tetramethyl-1,3-cyclobutanediol, 1,4-cyclohexanedimethanol, hydroquinone di-B-hydroxyethyl ether, glycerine, trimethylolethane, 1,1,1-trimethylolpropane, pentaerythritol, dipentaerythritol, sorbitol or mannitol.
A portion of the terephthalic acid or isophthalic acid up to 50 equivalent percent of the acid component can be replaced by a modifying polycarboxylic acid such as o-phthalic anhydride, adipic acid, sebacic acid, hemimellitic acid, trimellitic acid, trimesic acid, succinic acid, tetrachlorophthalic anhydride or hexachloroendomethylene tetrahydrophthalic acid.
The total number of hydroxyl groups on the alcohols normally is 1 to 1.6 times the total number of carboxyl groups on the acids in the under coat.
The polyester can also be modified by adding an organo titanate and/or a polyisocyanate.
As the titanate there can be used tetraalkyl titanates such as tetraisopropyl titanate, tetrabutyl titanate, tetramethyl titanate, tetrahexyl titanate and tetrapropyl titanate. The titanate is used in an amount of 0.001 to 4.0% titanium metal on the total solids of the under coat.
As the polyisocyanate there can be used 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, hexamethylene diisocyanate, blocked isocyanates such as the reaction product of three mols of mixed 2,4- and 2,6-tolylene diisocyanates with trimethylol propane and blocked by esterification with phenol (Mondur S), and the cyclic trimers of 2,4- and 2,6-tolylene diisocyanates having the three free isocyanate groups blocked by esterification with m-cresol (Mondur SH). There can be used any of the polyisocyanates, including the blocked isocyanates, set forth in Sheffer et al. Pat. No. 2,982,754, or in Meyer et al. Pat. No. 3,211,585. Usually I to 40% of the total solids are polyisocyanates.
The polyester under coat can be applied to the electrical conductor in the manner disclosed in Meyer et al. Pat. No. 3,211,585, and Meyer et al. Pat. No. 3,201,276. As
the polyester under coat there can be used any of the THEI containing terephthalates of the two Meyer et al. patents as well as the corresponding isophthalates.
In place of using a polyester as an under coat, there can be used a polyester-polyimide in which at least 20%, and preferably at least 50%, of the alcohol component of the polyester is THEI and the polybasic acid component comprises terephthalic acid, isophthalic acid or benzo phenone dicarboxylic acid. The polyimide component of the molecule normally has a member of the group consisting of benzene and naphthalene rings joined to two carbon atoms of a heterocyclic imide ring having to 6 members in the ring, one of the atoms in the heterocyclic ring being nitrogen and the balance carbon.
The usual components of the polyester-polyimide are (1) an aromatic or aliphatic diamine, e.g. methylene dianiline, oxydianiline, benzidine, 3,3-diamin0-diphenyl, pphenylene diamine, 1,4diamino-naphthalene, a, W-nonamethylene diamine, 4,4-diaminodiphenyl ether, heptamethylene diamine, diamino-diphenyl ketone, hexamethylenc diamine, ethylene diamine, diamino-diphenyl sulfone, 4,4'-dicyclohexylmcthane diamine, (2) an anhydride having 3 to 4 carboxyl groups such as trimellitic anhydride, pyromellitic dianhydride, benzophenone 2,3-, 2',3'-tetracarboxylic dianhydride, 2,3,6,7-naphthalene dianhydride and 3,3',4,4-diphenyl tetracarboxylic dianhydride, (3) a dibasic acid such as terephthalic acid, isophthalic acid or benzophenone dicarboxylic acid, and (4) a polyhydric alcohol containing at least THEI. The polyesterpolyimide preferably contains 5 to 50% polyimide groups based on the total of the polyester and polyimide groups.
There can be employed any of the polyester-polyimides disclosed in Meyer et al. application Ser. No. 457,474, filed May 20, 1965, now Pat. 3,426,098, and the under coat can be applied to the electrical conductor as set forth in that application. As disclosed in that Meyer et al. application, there can be employed as modifiers the same polyisocyanates in an amount of 1 to and alkyl titanates in an amount of l to 10% as mentioned in the Meyer et a1. Pat. No. 3,211,585 and Sheffer et al. Pat. No. 2,982,754.
The under coat, whether it is a polyester of polyesterpolyimide, also usually contains 1 to 5% based on the total solids of a melamine-formaldehyde resin or a phenolic resin such as phenol-formaldehyde, cresol-formaldehyde or xylenol-formaldehyde resin.
As the top coat there is preferably employed polyethylene tercphthalate. It is applied from a solvent solution, as set forth in Meyer et a1. Pat. No. 3,201,276. The preferred solvent contains to of monochlorophenol and the balance a cresol or mixture of cresol with phenol.
In place of polyethylene terephthalate there can be employed as the top coat polyimide-polyamides, polyesterpolyimidamicies, straight polyimides and other linear polymers. Thus, there can be used the pyromellitimide available commercially as Pyre-ML as well as other polyimides such as the reaction product of 3,3'-diaminodiphenyl and pyromellitic anhydride, the reaction product of oxydianiline with pyromellitic anhydride, the reaction product of methylene dianiline with pyromellitic anhydride or the polyimides disclosed in Edwards Pat. No. 3,179,634, the polyester-polyimide-polyamide from ethylene glycol, terephthalic acid, methylene dianiline and pyromellitic anhydride, etc. There can also be used polyesters such as polyhexamethylene glycol terephthalate and other linear polyesters.
The insulating varnishes of the present invention can be applied directly to electrical conductors but are preferably employed as a protective coat over the under coat and top coat formulations just described. The insulating varnishes can be used to coat copper, aluminum and silver wires and to impregnate armature and field coils of motors and for both power and distribution transformers of either the oil or dry type where long life at high operating temperatures is required. While the insulating varnishes of Thielking Pat. No. 3,080,331 are indicated as being suitable only at temperatures of up to C. the insulating varnishes of the present invention are suitable for continuous use at temperatures of C. and higher.
In addition to the higher fatty acid modified THEI polyester as indicated the varnish also includes an oilsoluble phenol-formaldehyde resin. The preferred phenols for forming these phenol-formaldehyde resins are ortho and para alkyl substituted phenols, 2,2-bis (phydroxyphenyl) propane and 4,4-bis (p-hydroxyphenyl) propane.
As examples of suitable phenols for making the resin, mention can be made of p-t-hutylphenol, p-tamylphenol, p-t-octylphenol, p-phenylphenol, o-t-butylphenol, and the phenols of Honel Pat. No. 1,800,296. Any of the oilsoluble phenol aldehyde resins set forth in the Thielking patent can be employed.
The insulating varnish contains conventional varnish solvents in addition to the resin components. Such solvents include one or more of xylene, mineral spirits, isophorone, naphtha, toluene and benzene.
EXAMPLE 1 762 grams of soybean oil fatty acids (Emery 610 soy oil fatty acids), 945 grams of tris(2-hydroxyethyl) isocyanurate and 597 grams of isophthalic acid were loaded in a flask, the temperature raised in one hour to 440 F. and held in the 440-470 F. range for 3.5 hours until the acid number was 25. The batch was thinned with 2000 grams of xylene to Z7 viscosity at 50% solids to give a 41% oil length alkyd resin.
To 575 grams of the alkyd resin was added 145 grams of p-t-butylphenol-formaldehyde resin (46B phenolic resin) at 50% solids in xylene and 80 grams of additional xylene. The final viscosity of the insulating varnish thus obtained was T (550 cps.) at 45% solids.
EXAMPLE 2 1344 grams of soybean oil fatty acids (Emery 610 soy oil fatty acids), 885 grams of THEI and 348 grams of isophthalic acid were loaded in a flask and the temperature raised to 480 F. in 3.5 hours. The batch was then heated in the 480520 F. for 4.5 hours until the acid number was 6. The batch was thinned with 1350 grams of aromatic naphtha to Z viscosity at 65% solids.
To 1158 grams of this alkyd resin were added 1500 grams of p-t-butylphenol-formaldehyde resin and 342 grams of aromatic naphtha. The final viscosity of the insulating varnish thus produced was G at 50% solids.
EXAMPLE 3 An insulating varnish was prepared similar to that of Example 1 but using an alkyd resin made from 387 grams of soybean oil fatty acids, 243 grams of coconut oil fatty acids, 597 grams of isophthalic acid and 945 grams of THEI.
EXAMPLE 4 A motor stator was impregnated with the insulating varnish of Example 1 in a dip tank operation. The varnish was cured by baking in an oven at 395 F. for 1 hour.
EXAMPLE 5 No. 18 copper wire was coated with Isonel 200E and then given a top coat of polyethylene terephthalate (Isonel 17) in conventional fashion. Isonel 200E is the mixture of (a) 86 parts of the polyester from 4400 parts of THEI, 481 parts of ethylene glycol and 5019 parts of dimcthyl terephthalate, (b) 5 parts of Mondur SH, (e) 5 parts of tetraisopropyl titanate and (d) 5 parts of m-p-cresolformaldehyde resin (made from 3440 parts of m-p-cresol and 1962 parts of 37% aqueous formaldehyde).
The thus coated wire was dipped twice through the in sulating varnish prepared in Example 1 with curing at 395 F. for 1 hour after each dip. The wire having the three coatings was tested by AIEE No. 57 twisted pairs with the following results:
Temp. C.: Hours to failure at 1000 volts 280 268 This data extrapolates to 180 C. for 20,000 hours which shows that the system of the fatty acid alkyd insulating varnish, polyethylene terephthalate top coat and Isonel 200 under coat had a Class H rating. The product had improved bonding strength and less weight loss than a conventional top coated Isonel 200 wire enamel which was not further coated with the fatty acid modified alkyd resin varnish.
EXAMPLE 6 The same procedure as that of Example 5 was repeated but using the insulating varnish of Example 2 to obtain a coated wire which had a Class H rating.
EXAMPLE 7 It was also found that the insulating varnish of Example 2 applied to wire coated with Isonel 200E and topcoated with polyethylene terephthalate (Isonel 17) gave improved results in the burnout test. The burnout test is run by twisting pairs of the enameled wire, dipping in the varnish and curing for 1 hour at 400 P. Then 33 amperes is applied for four minutes and the breakdown voltage of the system tested. The results obtained in the burnout tests were as follows, final voltages were expressed in kilovolts.
Without With varnish varnish Isonel 17 over Isonel 200 E 4. 98 8. 6 Isonel 17 over Isomid 0.77 2. 38 Isomid 0.75 1.16
ester of tris (2-hydroxyethyl) isocyanurate and an aromatic dicarboxylic acid and (2) a polyester polymide wherein at least 20% of the alcohol component of the polyester is tris (Z-hydroxyethyl) isocyanurate, a second coating selected from the group consisting of (1) linear polyethylene terephthalate, (2) and linear polyimide-polyamides, and a third coating of an insulating varnish including (a) an alkyd resin selected from the group consisting of unsaturated higher fatty acid modified tris (2-hydroxyethyl) isocyanurate isophthalate and unsaturated higher fatty acid modified tris (Z-hydroxyethyl) isocyanurate terephthalate, said resin having 20 to of higher fatty acids, and (b) an oil soluble phenol-formaldehyde resin, the phenol-formaldehyde resin being present in an amount of to 15% of the total of the alkyd resin and phenolformaldehyde resin over said coating.
2. An electrical conductor according to claim 1, wherein the second coating is polyethylene terephthalate, said conductor having said three coatings, having a heat life at C. of at least 20,000 hours.
3. An electrical conductor according to claim 2, wherein the alkyd resin is an isophthalate.
4. An electrical conductor according to claim 2, wherein the first coating is a continuous coating of a polyesterpolyimide.
5. An electrical conductor according to claim 2, wherein the first coating is a continuous coating of a polyester of an aromatic acid selected from the group consisting of terephthalic acid, isophthalic acid and benzophenone dicarboxylic acid.
6. An electrical conductor according to claim 1, Wherein the second coating is a linear polyimide-polyamide.
References Cited UNITED STATES PATENTS 3,201,276 8/1965 Meyer et al 117218 3,297,785 l/19 67 George et al 260-22 3,312,573 4/1967 Sheifer 117218 3,312,645 4/ 1967 George et a1. 260 22 3,428,486 2/1969 George 1 17-218 FOREIGN PATENTS 1,046,910 10/ 1966 Great Britain. 1,322,055 2/ 1963 France.
DONALD E. CZAJ A, Primary Examiner R. W. GRIFFIN, Assistant Examiner US. Cl. X.R.
ll7-l28.4, 161, 232; 260 -20, 22, 33.6
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US3732168A (en) * 1969-11-13 1973-05-08 Herberts & Co K Process and composition for the production of insulating solderable coatings
US4000362A (en) * 1972-03-06 1976-12-28 Sumitomo Electric Industries, Ltd. Insulated wire with a silicone releasing layer
US4129678A (en) * 1976-06-02 1978-12-12 Hitachi, Ltd. Self-bondable insulated wires comprising three coatings including a phenoxy resin outer layer
US4206098A (en) * 1978-09-15 1980-06-03 Westinghouse Electric Corp. High solids polyester-amide-imide wire enamels
US4216263A (en) * 1979-05-04 1980-08-05 Rea Magnet Wire Co., Inc. Magnet wire
US4347335A (en) * 1981-01-19 1982-08-31 Westinghouse Electric Corp. High bond strength aqueous phenol modified polyester coating composition
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
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US4508779A (en) * 1981-06-18 1985-04-02 Sumitomo Electric Industries, Ltd. Enamelled wire
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US5554443A (en) * 1990-03-20 1996-09-10 Texas Instruments Incorporated Bonding wire with heat and abrasion resistant coating layers
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FR1322055A (en) * 1962-05-17 1963-03-22 Shawinigan Resins Corp Improvements to metallic conductor coatings
US3312573A (en) * 1963-05-06 1967-04-04 Schenectady Chemical Non-linear overcoat for coated electrical conductor
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US3732168A (en) * 1969-11-13 1973-05-08 Herberts & Co K Process and composition for the production of insulating solderable coatings
US4000362A (en) * 1972-03-06 1976-12-28 Sumitomo Electric Industries, Ltd. Insulated wire with a silicone releasing layer
US4129678A (en) * 1976-06-02 1978-12-12 Hitachi, Ltd. Self-bondable insulated wires comprising three coatings including a phenoxy resin outer layer
US4206098A (en) * 1978-09-15 1980-06-03 Westinghouse Electric Corp. High solids polyester-amide-imide wire enamels
US4216263A (en) * 1979-05-04 1980-08-05 Rea Magnet Wire Co., Inc. Magnet wire
US4378407A (en) * 1980-01-24 1983-03-29 Sumitomo Electric Industries Ltd. Magnet wire
US4347335A (en) * 1981-01-19 1982-08-31 Westinghouse Electric Corp. High bond strength aqueous phenol modified polyester coating composition
US4508779A (en) * 1981-06-18 1985-04-02 Sumitomo Electric Industries, Ltd. Enamelled wire
US4385435A (en) * 1981-10-13 1983-05-31 United Technologies Corporation Method of power inserting polyamide-imide coated magnet wire
US4350738A (en) * 1981-10-13 1982-09-21 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
US4390590A (en) * 1981-10-19 1983-06-28 Essex Group, Inc. Power insertable 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
US5554443A (en) * 1990-03-20 1996-09-10 Texas Instruments Incorporated Bonding wire with heat and abrasion resistant coating layers
US5248713A (en) * 1990-06-13 1993-09-28 Raychem Corporation Stabilized polymeric compositions
WO2005075586A1 (en) * 2004-02-09 2005-08-18 Altana Electrical Insulation Gmbh Overcoat lacquer
US20080035016A1 (en) * 2004-02-09 2008-02-14 Klaus-Wilhelm Lienert Overcoat Lacquer
US7728101B2 (en) 2004-02-09 2010-06-01 Altana Electrical Insulation Gmbh Overcoat lacquer

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