EP2382256A1 - Système de résine imprégnée pour matériaux isolants dans des installations électriques - Google Patents

Système de résine imprégnée pour matériaux isolants dans des installations électriques

Info

Publication number
EP2382256A1
EP2382256A1 EP10704111A EP10704111A EP2382256A1 EP 2382256 A1 EP2382256 A1 EP 2382256A1 EP 10704111 A EP10704111 A EP 10704111A EP 10704111 A EP10704111 A EP 10704111A EP 2382256 A1 EP2382256 A1 EP 2382256A1
Authority
EP
European Patent Office
Prior art keywords
alkyl
insulating resin
aryl
groups
insulating
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.)
Withdrawn
Application number
EP10704111A
Other languages
German (de)
English (en)
Inventor
Gernot Swiatkowski
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.)
Siemens AG
Original Assignee
Siemens AG
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 Siemens AG filed Critical Siemens AG
Publication of EP2382256A1 publication Critical patent/EP2382256A1/fr
Withdrawn legal-status Critical Current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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/40Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
    • C08G59/42Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
    • C08G59/4215Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof cycloaliphatic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L63/00Compositions of epoxy resins; Compositions of derivatives of epoxy resins
    • 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
    • H01B3/40Insulators 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 epoxy resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/15Heterocyclic compounds having oxygen in the ring
    • C08K5/151Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
    • C08K5/1535Five-membered rings
    • C08K5/1539Cyclic anhydrides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3442Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
    • C08K5/3445Five-membered rings
    • 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
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2861Coated or impregnated synthetic organic fiber fabric

Definitions

  • the present invention relates to the field of insulation resins for switchgear.
  • the insulating material plays an important role, particularly in the case of a compact design.
  • resins are used, e.g. used as impregnating resins for suitable semi-finished products, for example based on epoxy resin impregnated nonwovens.
  • a glycidyl ester-based insulating resin is proposed for insulating materials in switchgear assemblies based on the starting materials comprising a) a material containing methylnadic anhydride and / or hydrogenated methylnadic anhydride b) a material containing an imidazole of the following structure:
  • R1 is selected from the group consisting of alkyl, long chain alkyl, alkenyl, cycloalkyl, haloalkyl, aryl;
  • R, R, R 4 are independently selected from the group consisting of hydrogen, alkyl, long-chain alkyl, alkenyl, cycloalkyl, haloalkyl, aryl
  • Alkyl linear and branched C 1 -C 8 -alkyls
  • long-chain alkyls linear and branched C5-C20 alkyls
  • Alkenyl C2-C6 alkenyl
  • cycloalkyl C3-C8-cycloalkyl
  • Alkylene selected from the group containing methylenes; 1,1-ethylene; 1,2-ethylene; 1, 1-propylidenes; 1,2-propylene; 1,3-propylene; 2, 2-propylidenes; butan-2-ol-1,4-diyl; propan-2-ol-1,3-diyl; 1, 4-butylenes; cyclohexane-1, 1-diyl; cyclohexane-1,2-diyl; cyclohexane-1,3-diyl; cyclohexane-1, 4-diyl; cyclopentane-1, 1-diyl; cyclopentane-1,2-diyl; and cyclopentane-1,3-diyl, vinyl, cyanoethyl, undecyl, hydroxymethyl
  • Aryl selected from aromatics with a molecular weight below 300Da
  • Haloalkyl selected from the group consisting of mono-, di-, tri-, poly- and perhalogenated linear and branched C1-C8-alkyl
  • Alkyl linear and branched C 1 -C 6 -alkyl, in particular methyl, ethyl, propyl, isopropyl;
  • Aryl selected from the group comprising: phenyl; biphenyl; Naphthalenyl; anthracenyl; Phenanthrenyl, benzyl.
  • the term "insulating resin” includes and / or comprises in particular a (preferably low-viscosity) impregnating resin system based on epoxy resin and anhydride component with controlled reactivity.
  • circuit installations includes and / or includes in particular installations for the low, medium and high voltage.
  • glycol ester base includes and / or encompasses in particular that glycidyl ester resin is used as one starting component, in particular main component, all resins known in the art being used.
  • the term "built up on the starting component (s)" means and / or comprises, in particular, that the insulating resin is produced from this component (s).
  • methylnadic anhydride means and / or comprises in particular the following compound:
  • the ratio of material a) to material b) (in w / w) is from> 50: 1 to ⁇ 300: 1. This has changed in the
  • the ratio of the material a) to the material b) (in w / w) is preferably from ⁇ 100: 1 to ⁇ 250: 1, more preferably 150 150: 1 to ⁇ 220: 1.
  • the proportion of material a) in the resin is from ⁇ 0.8: 1 to ⁇ 1: 1. Again, this has often proved advantageous for increasing the glass transition temperature.
  • the ratio of the material a) to the material a) in the resin is preferably from ⁇ 0.85: 1 to ⁇ 0.98: 1, more preferably> 0.92 to ⁇ 0.97: 1.
  • the proportion of material b) in the resin is from ⁇ 0.01: 1 to ⁇ 0.1: 1, more preferably ⁇ 0.02: 1 to ⁇ 0.09: 1, and most preferably 0.04 : 1 to ⁇ 0.07: l
  • component b) is selected from the group consisting of 1-methylimidazole, 1-ethylimidazole, 1-propylimidazole, 1-isopropylimidazole, 1,2-dimethylimidazole, 2-ethyl-4-ethylimidazole, imidazole, 1-benzyl -2-phenylimidazole, 1-
  • the insulating resin is produced in a curing process comprising a curing step at ⁇ 140 ° C, preferably ⁇ 150 ° C and a curing time of ⁇ 12 h, preferably ⁇ 14 h, and most preferably ⁇ 16 h.
  • the present invention also relates to an insulating member containing an insulating resin according to the present invention.
  • the term "insulating part” includes and / or encompasses in particular a composite material comprising an insulating resin and / or nonwoven / fabric based on polyester, glass or aramid.
  • the insulating resin is embedded in a polyester fleece.
  • polyester nonwoven in particular includes and / or includes substances based on PETP or PBT.
  • the term "embedded” includes and / or includes, in particular, that the nonwoven is impregnated with the resin. For dielectric reasons, vacuum impregnation is preferred.
  • the present invention also relates to the use of a glycidyl ester based resin system based on the starting components
  • R1 is selected from the group consisting of alkyl, long chain alkyl, alkenyl, cycloalkyl, haloalkyl, aryl;
  • R 2 , R 3 , R 4 are independently selected from the group consisting of hydrogen, alkyl, long-chain alkyl, alkenyl, cycloalkyl, haloalkyl, aryl
  • the resin was cured at 80 0 C, then 2 hours at 100 0 C, followed by Ih at 130 ° C and finally 16 hours at 150 0 C for 2 h.
  • Comparative Example II 99 ° C It can thus be seen the significantly increased glass transition temperature of the inventive example.
  • polyester fleece was impregnated with the resin according to Example I.
  • a commercially available random fleece based on PETP with a basis weight of 150 g / m 2 was used
  • the plate also has the following electrical properties:
  • the material is characterized by a very high compressive strength. Creep tests at elevated temperatures show little creep. This is especially relevant for pressurized parts. In addition, the material has an excellent tracking behavior. In a thermal aging test (20000h at 155 ° C), the plate was included in the thermal class F.

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)
  • Organic Insulating Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)

Abstract

L'invention concerne une résine d'isolation destinée à des installations électriques, à base d'ester de glycidyle, contenant de l'anhydride méthyl-nadique/anhydride méthyl-nadique hydrogéné en tant que durcisseur, et un imidazole à substitution N en tant qu'accélérateur. La résine présente une température de transition vitreuse sensiblement supérieure et un haut niveau mécanique, ainsi qu'une très bonne résistance au cheminement.
EP10704111A 2009-01-29 2010-01-14 Système de résine imprégnée pour matériaux isolants dans des installations électriques Withdrawn EP2382256A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE200910007392 DE102009007392A1 (de) 2009-01-29 2009-01-29 Tränkharzsystem für Isolierstoffe in Schaltanlagen
PCT/EP2010/050372 WO2010086228A1 (fr) 2009-01-29 2010-01-14 Système de résine imprégnée pour matériaux isolants dans des installations électriques

Publications (1)

Publication Number Publication Date
EP2382256A1 true EP2382256A1 (fr) 2011-11-02

Family

ID=42026141

Family Applications (1)

Application Number Title Priority Date Filing Date
EP10704111A Withdrawn EP2382256A1 (fr) 2009-01-29 2010-01-14 Système de résine imprégnée pour matériaux isolants dans des installations électriques

Country Status (10)

Country Link
US (1) US20110287679A1 (fr)
EP (1) EP2382256A1 (fr)
CN (1) CN102300900A (fr)
BR (1) BRPI1007511A2 (fr)
CA (1) CA2750970A1 (fr)
DE (1) DE102009007392A1 (fr)
MX (1) MX2011007956A (fr)
RU (1) RU2499006C2 (fr)
UA (1) UA105511C2 (fr)
WO (1) WO2010086228A1 (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX357409B (es) * 2012-03-29 2018-07-09 Dow Global Technologies Llc Composiciones curables.
EP2763142A1 (fr) * 2013-02-04 2014-08-06 Siemens Aktiengesellschaft Résine d'imprégnation pour un corps d'isolation électrique, corps d'isolation électrique et procédé de fabrication du corps d'isolation électrique
DE102013226705A1 (de) * 2013-12-19 2015-06-25 Siemens Aktiengesellschaft Durchschlag- und überschlagsichere Gießharzzusammensetzung
DE102015214872A1 (de) * 2015-02-05 2016-08-11 Siemens Aktiengesellschaft Isolierband für eine Spule und Wickelband-Isoliersystem für elektrische Maschinen
DE102016203867A1 (de) 2016-03-09 2017-09-14 Siemens Aktiengesellschaft Fester Isolationswerkstoff, Verwendung dazu und damit hergestelltes Isolationssystem

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4552907A (en) * 1983-07-29 1985-11-12 Kabushiki Kaisha Toyota Chuo Kenkyusho Epoxy resin composition
US4560716A (en) * 1983-08-30 1985-12-24 Kabushiki Kaisha Toyota Chuo Kenkyusho Rust preventing epoxy resin compositions
US4559272A (en) * 1984-05-09 1985-12-17 Hughes Aircraft Company Heat curable polyglycidyl aromatic amine encapsulants
DE4434279A1 (de) * 1994-09-26 1996-03-28 Hoechst Ag Härtbare, pulverförmige Mischungen
JPH09208805A (ja) * 1994-11-09 1997-08-12 Nitto Denko Corp 光半導体素子封止用エポキシ樹脂組成物
RU2078093C1 (ru) * 1995-02-14 1997-04-27 Товарищество с ограниченной ответственностью - Научно-производственная фирма "Мелада ЛТД" Эпоксидная композиция
DE19523897C2 (de) * 1995-06-30 2002-10-24 Bosch Gmbh Robert Verwendung von Silicon-modifizierten Epoxidharzen als Vergußmassen für elektrotechnische oder elektronische Bauteile
US6194490B1 (en) * 1998-02-27 2001-02-27 Vantico, Inc. Curable composition comprising epoxidized natural oils
EP1081205B1 (fr) * 1999-02-08 2004-11-17 The Yokohama Rubber Co., Ltd. Compositions resineuses
JP3489025B2 (ja) * 2000-01-14 2004-01-19 大塚化学ホールディングス株式会社 エポキシ樹脂組成物及びそれを用いた電子部品
DE60312143T2 (de) * 2003-06-16 2007-11-29 Abb Technology Ltd. Epoxyharzzusammensetzungen und Verfahren zur Herstellung von geformten Gegenständen daraus

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2010086228A1 *

Also Published As

Publication number Publication date
BRPI1007511A2 (pt) 2016-02-23
RU2499006C2 (ru) 2013-11-20
CA2750970A1 (fr) 2010-08-05
MX2011007956A (es) 2011-08-15
RU2011135756A (ru) 2013-03-10
DE102009007392A1 (de) 2010-08-05
US20110287679A1 (en) 2011-11-24
CN102300900A (zh) 2011-12-28
WO2010086228A1 (fr) 2010-08-05
UA105511C2 (uk) 2014-05-26

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