WO2009062873A1 - Système d'isolation électrique - Google Patents
Système d'isolation électrique Download PDFInfo
- Publication number
- WO2009062873A1 WO2009062873A1 PCT/EP2008/064998 EP2008064998W WO2009062873A1 WO 2009062873 A1 WO2009062873 A1 WO 2009062873A1 EP 2008064998 W EP2008064998 W EP 2008064998W WO 2009062873 A1 WO2009062873 A1 WO 2009062873A1
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- fibers
- insulation system
- fiber
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
- C08J5/046—Reinforcing macromolecular compounds with loose or coherent fibrous material with synthetic macromolecular fibrous material
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators 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
- H01B3/47—Insulators 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 fibre-reinforced plastics, e.g. glass-reinforced plastics
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B17/00—Insulators or insulating bodies characterised by their form
- H01B17/32—Single insulators consisting of two or more dissimilar insulating bodies
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B17/00—Insulators or insulating bodies characterised by their form
- H01B17/36—Insulators having evacuated or gas-filled spaces
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
Definitions
- the present invention refers to an electrical insulation system being a flber-remforced composite system which is suitable to be used in gas-insulated switchgear applications, preferably in gas-insulated metal enclosed switchgear applications, said electrical insulation system having improved mechanical properties and method of producing said electrical insulation system.
- Cylindrical insulating parts in gas-insulated switchgears are commonly made from flber-remforced materials.
- the material used is preferably a cured epoxy resin system reinforced with polyethylene tere- phthalate (PET) fibers or with aramide (Kevlar®, Twaron®) fibers or combinations thereof. These fibers have severe limitations.
- Polyethylene terephthalate fibers for example have comparatively weak mechanical properties.
- Aramide fibers have a low adhesion between fibers and the epoxy matrix as well as a high moisture uptake. Therefore, there is a need for an electrical insulation system with improved properties, especially for the use as electrical insulator to be used m gas-msulated electrical applications, for example in pressurized gas-insulated switchgear stations (GIS) .
- GIS pressurized gas-insulated switchgear stations
- a fiber-reinforced composite system comprising a thermoplastic or duroplastic polymer composition, preferably a duroplastic polymer composition, preferably a hardened epoxy resin composition, and a reinforcing fiber selected from polyethylene naphthalate (PEN) fibers, poly- butylene naphthalate (PBN) fibers, from fibers being a copoly- ester of bisphenol A and/or bisphenol F with naphthalene dicarbonic acid, from fibers being a copolyester of hydroxy-benzoic acid and hydroxy-naphthoic acid preferably a copolyester of p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid, or from a mixture of these fibers, yields an electrical insulation system with improved mechanical properties, which is especially useful as electrical insulator for the production of electrical gas- insulated switchgear applications, preferably gas-insulated metal enclosed electrical applications such as pressurized gas- msulated switchge
- PEN poly
- the present invention refers to an electrical insulation system which is suitable to be used in electrical gas-insulated switchgear applications, preferably in gas-insulated metal enclosed switchgear applications, said electrical insulation system comprising a solidified polymer composition, preferably a cured epoxy resin composition, and a reinforcing fiber, characterized m that said reinforcing fiber is selected from polyethylene naphthalate (PEN) fibers, polybutylene naphthalate (PBN) fibers, from fibers being a copolyester of bisphenol A and/or bisphenol F with naphthalene dicarbonic acid, from fibers being a copolyester of hydroxy-benzoic acid and hydroxy-naphthoic acid preferably a copolyester of p-hydroxybenzoic acid and 6-hydroxy- 2-naphthoic acid, or from a mixture of these fibers, wherein said fiber-reinforced composite system optionally may contain further additives.
- PEN polyethylene naphthalate
- the present invention further refers to a method of producing said electrical insulation system which is suitable to be used m said electrical gas-insulated switchgear applications, preferably gas-msulated metal enclosed electrical applications such as pressurized gas-insulated switchgear stations (GIS) .
- the present invention further refers to the use of said electrical insulation system m the production of said electrical gas- insulated switchgear applications, preferably gas-insulated metal enclosed electrical applications such as pressurized gas- insulated switchgear stations (GIS) or spacer insulators and related applications.
- the present invention further refers to said electrical gas-insulated switchgear applications, preferably gas-insulated metal enclosed electrical applications comprising an electrical insulation system according to the present invention.
- Polyethylene naphthalate is an ester of ethylene glycol with naphthalene dicarbonic acid and substantially contains the following chemical units:
- Polybutylene naphthalate is an ester of butylene glycol with naphthalene dicarbonic acid and substantially contains the following chemical units:
- copolyester of bisphenol A and/or bisphenol F with naphthalene dicarbonic acid substantially contains the following chemical units:
- copolyester of p-hydroxybenzoic acid and 6-hydroxy-2- naphthoic acid substantially contains the following chemical units :
- Said fibers to be used in the present invention have preferably a fiber diameter as used in roving cloths and fabrics made from said fibers.
- the diameter is within the range of about 0.4-200 micron ( ⁇ ra) , preferably within the range of about 1-100 micron and preferably within the range of about 5-50 micron.
- the diameter generally is not critical. It is within the knowledge of the expert in the art to optimize the diameter if required.
- the reinforcing fiber may be present in form of chopped fibers having an average length preferably within the range of 0.5 mm to 15 mm, preferably within the range of 1.0 mm to 8 mm.
- the use according to the present invention is that the fibers preferably are used in a non-chopped form, i.e. as a dry continuous non-woven filament, or as a fiber roving or as a woven fabric resp. cloth.
- the dry-body is preferably either produced by dry winding of a fiber roving or by dry winding of a fabric.
- one or more of such fiber rovings or cloths may be arranged within the hardened resin system in any required order, preferably by dry winding of the roving or cloth (e.g. around a mandrel) , or m a parallel and/or rectangular order.
- the system may contain also a combination of chopped fibers and/or continuous fibers and/or one or more fiber rovings or cloths.
- the reinforcing fiber selected from the fibers to be used according to the present invention and as specified herein above is preferably present in an amount within the range of 20% to 70% by weight of the total weight of the fiber-remforced composite system, preferably within the range of 30% to 60% by weight, and preferably within the range of 35% to 55% by weight of the total weight of the fiber-reinforced composite system.
- the polymers as used in the present invention are preferably selected from the group comprising epoxy resin systems, poly- urethanes, polyesters, polyamides, polybutylene terephthalate and polydicyclopentadiene.
- the polymer preferably is a duro- plastic polymer selected from epoxy resin systems and poly- urethanes and most preferably is a cured epoxy resin system.
- the fiber-reinforced composite system may further comprise components selected from filler materials, wettmg/dispersmg agents, plasticizers, antioxidants, light absorbers, silicones, and from further additives generally used m electrical applications.
- the total amount of reinforcing fiber, filler and the optional further additives may be up to 80% by weight and preferably up to 70% by weight of the total weight of the fiber-reinforced composite system.
- the fiber- reinforced composite system of the present invention may optionally contain a mineral filler material of a micro size or nano size grain size distribution or a mixture of such filler materials.
- the mineral filler has preferably an average grain size distribution within the range of 1 ⁇ m-500 ⁇ m, preferably within the range of 5 ⁇ m-100 ⁇ m.
- Preferably at least 70% of the particles, preferably at least 80% of the particles, and preferably at least 90% of the particles have a particle size within the range indicated.
- the mineral filler is preferably selected from conventional filler materials as are generally used as fillers in electrical gas-insulated switchgear applications. Such filler materials e.g. are stable against degradation products of sulfur hexa- fluo ⁇ de (SF 6 ) such as aluminum oxide and are known per se.
- SF 6 sulfur hexa- fluo ⁇ de
- the electrical isolation system according to the present invention does not contain a filler material.
- Epoxy resin systems, polyesters, polyamides, polybutylene tere- phthalate, polyurethanes and polydicyclopentadiene have been described m the literature.
- said fiber component (s) together with the optional additives may be incorporated into the respective monomeric starting material of the polymer in an analogous manner as described in the literature generally for filler materials and other additives. Subsequently the starting material is hardened or cured. This is within the knowledge of the expert in the art.
- the reinforcing fiber material is incorporated into the monomeric starting materials of the respective polymer by known methods so as to be uniformly dispersed therein.
- the non- hardened composition thus obtained e.g. the non-hardened epoxy resin composition
- APG automated pressure gelation
- the dispersion is formed into the desired shape using known methods, optionally with the help of a molding tool, and then hardened out or cured, optionally using post-curing.
- the present invention also refers to a method of producing an electrical insulation system which is suitable to be used in electrical gas-insulated switchgear applications, preferably gas-insulated metal enclosed electrical applications, characterized in that a chopped reinforcing fiber selected from polyethylene naphthalate (PEN) fibers, polybutylene naphthalate (PBN) fibers, from fibers being a copolyester of bisphenol A and/or bisphenol F with naphthalene dicarbonic acid, from fibers being a copolyester of hydroxy-benzoic acid and hydroxy- naphthoic acid preferably a copolyester of p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid, or from a mixture of these fibers, and optionally further additives as defined herein above, is incorporated into the monomeric starting material of the respective polymer as defined herein above, preferably an epoxy resin composition, so as to be uniformly dispersed therein, the dispersion is then formed into the desired shape,
- the fiber-reinforced composite system according to the present invention being suitable for the use as an electrical insulation system, preferably contains the reinforcing fiber in the form of a continuous non-woven filament, or as a fiber roving or as a woven fabric or as a non-crimp fabric.
- the dry- body is preferably either produced by dry winding of a fiber roving or by dry winding of a woven fabric or by dry winding of a non-crimp fabric.
- one or more of such fiber rovings or fabrics may be arranged within the hardened resin system m any required order, preferably by dry winding of the roving or fabric (e.g. around a mandrel) , or in a parallel and/or rectangular order.
- the system may contain also a combination of chopped fibers and/or continuous fibers and/or one or more fiber rovings or fabrics.
- the present invention refers therefore also to a process for producing an electrical insulation system which is suitable to be used m electrical gas-insulated switchgear applications, preferably gas-insulated metal enclosed electrical applications, said process being characterized by the following steps: (i) providing a mold for the product comprising at least one dry layer of reinforcing material, said reinforcing material comprising a continuous non-woven filament and/or at least one fiber roving and/or at least one woven fabric and/or at least one non-crimp fabric within the mold as defined herein above; (ii) casting an unhardened monomer composition, prefe- rably a monomeric epoxy resin mixture, into the mold so that the mold becomes filled and the at least one layer of reinforcing material becomes fully impregnated; (in) hardening and/or curing the monomer composition within the mold at the appropriate temperature for a time long enough to get hardened resp. cured; and (iv) optionally post-curing the fiber- reinforced composite system obtained.
- At least one dry layer of dry reinforcing material comprising a continuous non-woven filament and/or at least one fiber roving and/or at least one woven fabric and/or at least one non-crimp fabric is also named "drybody” .
- drybody the fibers, rovings or fabrics, as mentioned, are wound around a cylinder (the so called mandrel) .
- Polyester fleece layers may be used to stabilize the drybody. Subsequently the mandrel is put into another cylinder (outer mould) and afterwards the fibers are impregnated.
- thermosetting resins used within the context of the present invention are epoxy resins made from aromatic and/or cycloaliphatic compounds. These compounds are known per se. Epoxy resins are reactive glycidyl compounds containing at least two 1,2-epoxy groups per molecule. Preferably a mixture of poly- glycidyl compounds is used such as a mixture of diglycidyl- and triglycidyl compounds.
- Epoxy compounds useful for the present invention comprise unsub- stituted glycidyl groups and/or glycidyl groups substituted with methyl groups. These glycidyl compounds preferably have a molecular weight between 200 and 1200, especially between 200 und 1000 and may be solid or liquid.
- the epoxy value (equiv./lOO g) is preferably at least three, preferably at least four and especially at about five, preferably about 4.9 to 5.1 or higher.
- Preferred are glycidyl compounds which have glycidyl ether- and/or glycidyl ester groups. Such a compound may also contain both kinds of glycidyl groups, e.g.
- polyglycidyl esters with 1 to 4 glycidyl ester groups, especially diglycidyl ester and/or triglycidyl esters.
- Preferred glycidyl esters may be derived from aromatic, araliphatic, cycloaliphatic, heterocyclic, heterocyc- lic-aliphatic or heterocyclic-aromatic dicarbonic acids with 6 to 20, preferably 6 to 12 ring carbon atoms or from aliphatic dicarbonic acids with 2 to 10 carbon atoms.
- Examples are glycidyl ethers derived from Bisphenol A or Bis- phenol F as well as glycidyl ethers derived from Phenol-Novolak- resms or cresol-Novolak-resms .
- Cycloaliphatic epoxy resins are for example hexahydro-o-phthalic acid-bis-glycidyl ester, hexahydro-m-phthalic acid-bis-glycidyl ester or hexahydro-p-phthalic acid-bis-glycidyl ester.
- aliphatic epoxy resins for example 1 , 4-butane-diol diglycidyl- ether, may be used as a component for the composition of the present invention.
- Preferred within the present invention are also aromatic and/or cycloaliphatic epoxy resins which contain at least one, preferably at least two, ammoglycidyl group in the molecule.
- epoxy resins are known and for example described in WO 99/67315.
- Pre-- ferred compounds are those of formula (VI) :
- Hardeners are known to be used in epoxy resins. Hardeners are for example hydroxyl and/or carboxyl containing polymers such as carboxyl terminated polyester and/or carboxyl containing acrylate- and/or methacrylate polymers and/or carboxylic acid anhydrides. Useful hardeners are further cyclic anhydrides of aromatic, aliphatic, cycloaliphatic and heterocyclic poly- carbonic acids. Preferred anhydrides of aromatic polycarbonic acids are phthalic acid anhydride and substituted de ⁇ vates thereof, benzene-1, 2, 4, 5-tetracarbonic acid dianhydride and substituted de ⁇ vates thereof. Numerous further hardeners are from the literature.
- the optional hardener can be used m concentrations within the range of 0.2 to 1.2, equivalents of hardening groups present, e.g. one anhydride group per 1 epoxide equivalent. However, often a concentration within the range of 0.2 to 0.4, equiva- lents of hardening groups is preferred.
- the composition may comprise further at least a curing agent (accelerant) for enhancing the polymerization of the epoxy resin with the hardener, at least one wetting/dispersing agent, plasticizers, antioxidants, light absorbers, as well as further additives used in electrical applications .
- a curing agent for enhancing the polymerization of the epoxy resin with the hardener
- at least one wetting/dispersing agent for enhancing the polymerization of the epoxy resin with the hardener
- plasticizers plasticizers, antioxidants, light absorbers
- light absorbers as well as further additives used in electrical applications.
- Curing agents for enhancing the polymerization of the epoxy resin with the hardener are for example tertiary amines, such as benzyldimethylamine or amine-complexes such as complexes of tertiary amines with boron trichloride or boron trifluo ⁇ de; urea derivatives, such as N-4-chlorophenyl-N' ,N ' -dimethylurea (Monu- ron) ; optionally substituted imidazoles such as imidazole or 2- phenyl-imidazole.
- tertiary amines such as benzyldimethylamine or amine-complexes such as complexes of tertiary amines with boron trichloride or boron trifluo ⁇ de
- urea derivatives such as N-4-chlorophenyl-N' ,N ' -dimethylurea (Monu- ron)
- curing catalyst such as transition metal complexes of cobalt (III), copper, manganese, (II), zinc in acetylacetonate may also be used, e.g. cobalt acetylacetonate (III) .
- the amount of catalyst used is a concentration of about 50-1000 ppm by weight, calcu- lated to the composition to be cured.
- wetting/dispersing agents are known per se for example m the form of surface activators; or reactive diluents, preferably epoxy-containing or hydroxyl-contaming reactive diluents; thixotropic agents or resinous modifiers.
- reactive diluents for example are cresylglycidylether, diepoxyethyl-1, 2- benzene, bisphenol A, bisphenol F and the diglycidylethers thereof, diepoxydes of glycols and of polyglycols, such as neo- pentylglycol-diglycidylether or t ⁇ methylolpropane-diglycidyl- ether .
- Preferred commercially available wettmg/dispersmg agents are for example organic copolymers containing acidic groups, e.g. Byk® W-9010 having an acid value of 129 mg KOH/g) .
- Such wetting/ dispersing agents are preferably used m amounts of 0.5% to 1.0% based on the filler weight.
- Plasticizers, antioxidants, light absorbers, as well as further additives used in electrical applications are known in the art and are not critical.
- the insulating composition made from epoxy resin is made simply by mixing all components, optionally under vacuum, in any desired sequence and curing the mixture by heating. If a fiber- remforced composite system comprising at least one layer of reinforcing fiber roving cloth is to be manufactured, the insulating composition made from epoxy resin is made simply by mixing all components, optionally under vacuum, m any desired sequence and then adding it to the at least one layer of reinforcing fiber roving cloth.
- the hardener and the curing agent are separately added before curing.
- the curing temperature is preferably within the range of 50 0 C to 280 0 C, preferably within the range of 100°C to 200°C. Curing generally is possible also at lower temperatures, whereby at lower temperatures complete curing may last up to several days, depending also on catalyst present and its concentration.
- the casting of the unhardened monomer composition into the mold so that the mold becomes filled and the at least one layer of reinforcing material in the mold becomes fully impregnated is preferably done by using vacuum techniques, preferably m combination with the application of pressure. Vibration methods may also be applied in order to improve impregnation and minimizing air bubbles.
- the non-hardened insulating resin composition specifically is preferably applied by using vacuum casting or automated pressure gelation (APG) manufacturing processes optionally under the application of vacuum or resin transfer molding or vacuum assisted resin transfer molding, also to remove all moisture and air bubbles from the insulating composition.
- APG automated pressure gelation
- the encapsulating composition may then be cured by any method known in the art by heating the composition to the desired curing temperature.
- the electrical insulation system according to the present invention is useful for the production of electrical gas- insulated applications, especially electrical gas-insulated switchgear applications, preferably gas-insulated metal enclosed electrical applications such as pressurized gas-insulated switchgear stations (GIS) , or life-tank breakers, dead-tank breaker and related applications.
- electrical gas-insulated switchgear applications especially electrical gas-insulated switchgear applications, preferably gas-insulated metal enclosed electrical applications such as pressurized gas-insulated switchgear stations (GIS) , or life-tank breakers, dead-tank breaker and related applications.
- GIS pressurized gas-insulated switchgear stations
- the electrical insulation system according to the present invention may also be used for example m the production of transformers, high-voltage insulations for indoor and outdoor use, especially for outdoor insulators associated with high-voltage lines, as long-rod, composite and cap-type insulators.
- the following example illustrates the invention.
- Example 1 The epoxy resin compositions Formulation A and Formulation B are made from the components as given m Table 1.
- the compositions are prepared by thoroughly mixing the epoxy resin, the hardener and the accelerator at a temperature of 8O 0 C. Then the mixture is outgassed under vacuum at 80 0 C. The mixture is then transferred into a mold using vacuum impregnation to produce insulating rods and operating rods by adding the uncured epoxy composition to the mould comprising a dry winding of a roving (each time made from PEN-fiber, or PET-fiber) . The composition is then cured for ten hours at 140 0 C.
- PET-fiber type T711 from Performance Fibers GmbH
- Test results show that the mechanical properties of PEN-fiber reinforced components made from Formulation A are superior compared to the mechanical properties of PET-fiber reinforced components made from Formulation B.
- Tensile tests carried out on PET and PEN reinforced epoxy rods show that there is a significant increase in stiffness and load to failure (Figure 1) .
- the epoxy resin compositions Formulation C and Formulation D are made from the components as given m Table 2.
- the compositions are prepared by thoroughly mixing the epoxy resin, the hardener and the accelerator at a temperature of 80 0 C. Then the mixture is outgassed under vacuum at 80°C. The mixture is then transferred into a mold using vacuum impregnation to produce insula- ting rods and operating rods by adding the uncured epoxy composition to the mould comprising a dry winding of a roving (each time made from Vectran®, or Kevlar fibres) . The composition is then cured for ten hours at 14O 0 C. Definition of raw materials: CY 228 bisphenol A epoxy resin
- Vectran® a copolyester from p-hydroxybenzoic acid and 6-hydroxy-2- naphthoic acid in the form of a fiber roving from Kuraray
- Vectran® Comparison between Vectran® and Kevlar reinforced rods
- the moisture uptake of Vectran is significantly lower compared to Kevlar.
- a drying step prior to impregnation of the reinforcing fibres is only required in the case of Kevlar.
- the substitution of Kevlar with Vectran® makes the production of insulators more efficient and the product more suited for electrical insulation application, due to a lower moisture content .
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Abstract
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08850789.2A EP2209841B1 (fr) | 2007-11-13 | 2008-11-05 | Système d'isolation électrique |
CN200880116594A CN101855278A (zh) | 2007-11-13 | 2008-11-05 | 电绝缘体系 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/EP2007/062272 WO2009062543A1 (fr) | 2007-11-13 | 2007-11-13 | Système composite renforcé par une fibre comme isolation électrique |
EPPCT/EP2007/062272 | 2007-11-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2009062873A1 true WO2009062873A1 (fr) | 2009-05-22 |
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Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2007/062272 WO2009062543A1 (fr) | 2007-11-13 | 2007-11-13 | Système composite renforcé par une fibre comme isolation électrique |
PCT/EP2008/064998 WO2009062873A1 (fr) | 2007-11-13 | 2008-11-05 | Système d'isolation électrique |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/EP2007/062272 WO2009062543A1 (fr) | 2007-11-13 | 2007-11-13 | Système composite renforcé par une fibre comme isolation électrique |
Country Status (3)
Country | Link |
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KR (1) | KR20100099681A (fr) |
CN (1) | CN101855278A (fr) |
WO (2) | WO2009062543A1 (fr) |
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DE102009035097A1 (de) * | 2009-07-29 | 2011-02-03 | Siemens Aktiengesellschaft | Flächenisolierfolie und Anwendung dazu |
US20120202059A1 (en) * | 2011-02-09 | 2012-08-09 | Waukesha Electric Systems, Inc. | Dry type electrical insulation |
US9054504B2 (en) | 2009-10-23 | 2015-06-09 | Neptco, Inc. | Metallic wire tracer element including woven protective tube and methods of making same |
CN114437539A (zh) * | 2020-10-30 | 2022-05-06 | 中国石油化工股份有限公司 | 一种增强尼龙材料及其制备方法和应用 |
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DE102009052432A1 (de) * | 2009-11-10 | 2011-06-09 | Siemens Aktiengesellschaft | Beschichtete Isolationsfolien für elektrische Maschinen und Herstellungsverfahren dazu |
CN101834042B (zh) * | 2010-05-21 | 2011-11-30 | 成都盛帮密封件股份有限公司 | 一种中压电器用绝缘帽的加工工艺 |
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JP6824179B2 (ja) * | 2015-03-26 | 2021-02-03 | ハンツマン・アドヴァンスト・マテリアルズ・ライセンシング・(スイッツランド)・ゲーエムベーハー | 屋外用製品を製造するための熱硬化性エポキシ樹脂組成物、およびそれから得られる屋外用製品 |
JP6683721B2 (ja) * | 2015-03-26 | 2020-04-22 | ハンツマン・アドヴァンスト・マテリアルズ・ライセンシング・(スイッツランド)・ゲーエムベーハー | 電気工学用絶縁システムの製造方法、それから得られる製品、およびそれらの使用 |
CN104945854B (zh) * | 2015-07-23 | 2017-05-24 | 北京化工大学 | 短切碳纤维层间增强纤维复合材料的制备方法 |
CN105390180A (zh) * | 2015-10-30 | 2016-03-09 | 太仓市天合新材料科技有限公司 | 一种绝缘新材料 |
DE102017004481A1 (de) * | 2017-05-11 | 2018-11-15 | Carl Freudenberg Kg | Textiles Flächengebilde für die Elektroisolation |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995017755A1 (fr) | 1993-12-22 | 1995-06-29 | Abb Patent Gmbh | Procede permettant de realiser un systeme d'isolation |
JPH10182857A (ja) * | 1996-12-24 | 1998-07-07 | Matsushita Electric Works Ltd | プリプレグ及び積層板 |
JP2004002653A (ja) * | 2002-04-22 | 2004-01-08 | Shin Kobe Electric Mach Co Ltd | プリント基板用プリプレグ及びその製造法とプリント基板 |
EP1387368A1 (fr) | 2002-08-02 | 2004-02-04 | Abb Research Ltd. | Isolateur solide et procédé de fabrication d'un isolateur solide |
US20040039127A1 (en) * | 2002-08-26 | 2004-02-26 | Satoru Amou | Electronic device using low dielectric loss tangent insulators for high frequency signals |
WO2004097858A1 (fr) * | 2003-04-30 | 2004-11-11 | Abb Technology Ltd | Suppresseur de transitoires |
JP2004352845A (ja) * | 2003-05-29 | 2004-12-16 | Kyocera Chemical Corp | ハロゲンフリーのプリプレグ、金属箔張積層板およびビルドアップ型多層プリント配線板 |
JP2005015616A (ja) * | 2003-06-26 | 2005-01-20 | Kyocera Chemical Corp | 積層板用樹脂組成物、有機基材プリプレグ、金属箔張り積層板及びプリント配線板 |
JP2005179838A (ja) * | 2003-12-22 | 2005-07-07 | Shin Kobe Electric Mach Co Ltd | 電気絶縁用不織布及びその製造法、プリプレグ、積層板及びプリント配線板 |
JP2005306897A (ja) * | 2004-04-16 | 2005-11-04 | Tomoegawa Paper Co Ltd | 電気絶縁用基材とその製造方法、それを用いたプリプレグおよびプリント配線板 |
JP2006022433A (ja) * | 2004-07-08 | 2006-01-26 | Tomoegawa Paper Co Ltd | 電気絶縁用基材とその製造方法、および同基材を用いたプリプレグとプリント配線用基板 |
JP2006037280A (ja) * | 2004-07-28 | 2006-02-09 | Shin Kobe Electric Mach Co Ltd | 電気絶縁用不織布及びその製造法、プリプレグ、積層板及びプリント配線板 |
WO2007085414A1 (fr) * | 2006-01-27 | 2007-08-02 | Michelin Recherche Et Technique S.A. | Procede de fabrication d’un anneau composite |
-
2007
- 2007-11-13 WO PCT/EP2007/062272 patent/WO2009062543A1/fr active Application Filing
-
2008
- 2008-11-05 WO PCT/EP2008/064998 patent/WO2009062873A1/fr active Application Filing
- 2008-11-05 CN CN200880116594A patent/CN101855278A/zh active Pending
- 2008-11-05 KR KR1020107010272A patent/KR20100099681A/ko not_active Application Discontinuation
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995017755A1 (fr) | 1993-12-22 | 1995-06-29 | Abb Patent Gmbh | Procede permettant de realiser un systeme d'isolation |
JPH10182857A (ja) * | 1996-12-24 | 1998-07-07 | Matsushita Electric Works Ltd | プリプレグ及び積層板 |
JP2004002653A (ja) * | 2002-04-22 | 2004-01-08 | Shin Kobe Electric Mach Co Ltd | プリント基板用プリプレグ及びその製造法とプリント基板 |
EP1387368A1 (fr) | 2002-08-02 | 2004-02-04 | Abb Research Ltd. | Isolateur solide et procédé de fabrication d'un isolateur solide |
US20040039127A1 (en) * | 2002-08-26 | 2004-02-26 | Satoru Amou | Electronic device using low dielectric loss tangent insulators for high frequency signals |
WO2004097858A1 (fr) * | 2003-04-30 | 2004-11-11 | Abb Technology Ltd | Suppresseur de transitoires |
JP2004352845A (ja) * | 2003-05-29 | 2004-12-16 | Kyocera Chemical Corp | ハロゲンフリーのプリプレグ、金属箔張積層板およびビルドアップ型多層プリント配線板 |
JP2005015616A (ja) * | 2003-06-26 | 2005-01-20 | Kyocera Chemical Corp | 積層板用樹脂組成物、有機基材プリプレグ、金属箔張り積層板及びプリント配線板 |
JP2005179838A (ja) * | 2003-12-22 | 2005-07-07 | Shin Kobe Electric Mach Co Ltd | 電気絶縁用不織布及びその製造法、プリプレグ、積層板及びプリント配線板 |
JP2005306897A (ja) * | 2004-04-16 | 2005-11-04 | Tomoegawa Paper Co Ltd | 電気絶縁用基材とその製造方法、それを用いたプリプレグおよびプリント配線板 |
JP2006022433A (ja) * | 2004-07-08 | 2006-01-26 | Tomoegawa Paper Co Ltd | 電気絶縁用基材とその製造方法、および同基材を用いたプリプレグとプリント配線用基板 |
JP2006037280A (ja) * | 2004-07-28 | 2006-02-09 | Shin Kobe Electric Mach Co Ltd | 電気絶縁用不織布及びその製造法、プリプレグ、積層板及びプリント配線板 |
WO2007085414A1 (fr) * | 2006-01-27 | 2007-08-02 | Michelin Recherche Et Technique S.A. | Procede de fabrication d’un anneau composite |
Non-Patent Citations (8)
Title |
---|
DATABASE WPI Week 199837, Derwent World Patents Index; AN 1998-434008, XP002482150 * |
DATABASE WPI Week 200430, Derwent World Patents Index; AN 2004-319863, XP002482146 * |
DATABASE WPI Week 200504, Derwent World Patents Index; AN 2005-034953, XP002482149 * |
DATABASE WPI Week 200515, Derwent World Patents Index; AN 2005-134785, XP002482148 * |
DATABASE WPI Week 200551, Derwent World Patents Index; AN 2005-501008, XP002482145 * |
DATABASE WPI Week 200581, Derwent World Patents Index; AN 2005-789579, XP002482143 * |
DATABASE WPI Week 200614, Derwent World Patents Index; AN 2006-128433, XP002482144 * |
DATABASE WPI Week 200618, Derwent World Patents Index; AN 2006-167621, XP002482147 * |
Cited By (7)
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DE102009035097A1 (de) * | 2009-07-29 | 2011-02-03 | Siemens Aktiengesellschaft | Flächenisolierfolie und Anwendung dazu |
US9054504B2 (en) | 2009-10-23 | 2015-06-09 | Neptco, Inc. | Metallic wire tracer element including woven protective tube and methods of making same |
CN101794647A (zh) * | 2010-03-12 | 2010-08-04 | 西安航天复合材料研究所 | 一种绝缘支撑杆的制造方法 |
US20120202059A1 (en) * | 2011-02-09 | 2012-08-09 | Waukesha Electric Systems, Inc. | Dry type electrical insulation |
US9281098B2 (en) * | 2011-02-09 | 2016-03-08 | Waukesha Electric Systems, Inc. | Dry type electrical insulation |
CN114437539A (zh) * | 2020-10-30 | 2022-05-06 | 中国石油化工股份有限公司 | 一种增强尼龙材料及其制备方法和应用 |
CN114437539B (zh) * | 2020-10-30 | 2024-02-13 | 中国石油化工股份有限公司 | 一种增强尼龙材料及其制备方法和应用 |
Also Published As
Publication number | Publication date |
---|---|
CN101855278A (zh) | 2010-10-06 |
WO2009062543A1 (fr) | 2009-05-22 |
KR20100099681A (ko) | 2010-09-13 |
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