EP3729469A1 - Formulierung zur herstellung eines isolationssystems, elektrische maschine und verfahren zur herstellung eines isolationssystems - Google Patents
Formulierung zur herstellung eines isolationssystems, elektrische maschine und verfahren zur herstellung eines isolationssystemsInfo
- Publication number
- EP3729469A1 EP3729469A1 EP19706909.9A EP19706909A EP3729469A1 EP 3729469 A1 EP3729469 A1 EP 3729469A1 EP 19706909 A EP19706909 A EP 19706909A EP 3729469 A1 EP3729469 A1 EP 3729469A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- formulation
- formulation according
- resin
- hardener
- insulation system
- 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.)
- Pending
Links
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- 238000009472 formulation Methods 0.000 title claims abstract description 38
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- 229910052799 carbon Inorganic materials 0.000 claims description 13
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- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 14
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- QYIMZXITLDTULQ-UHFFFAOYSA-N 4-(4-amino-2-methylphenyl)-3-methylaniline Chemical group CC1=CC(N)=CC=C1C1=CC=C(N)C=C1C QYIMZXITLDTULQ-UHFFFAOYSA-N 0.000 description 3
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- KWOIWTRRPFHBSI-UHFFFAOYSA-N 4-[2-[3-[2-(4-aminophenyl)propan-2-yl]phenyl]propan-2-yl]aniline Chemical compound C=1C=CC(C(C)(C)C=2C=CC(N)=CC=2)=CC=1C(C)(C)C1=CC=C(N)C=C1 KWOIWTRRPFHBSI-UHFFFAOYSA-N 0.000 description 3
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- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
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- 238000006467 substitution reaction Methods 0.000 description 3
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- NUIURNJTPRWVAP-UHFFFAOYSA-N 3,3'-Dimethylbenzidine Chemical compound C1=C(N)C(C)=CC(C=2C=C(C)C(N)=CC=2)=C1 NUIURNJTPRWVAP-UHFFFAOYSA-N 0.000 description 2
- ZBMISJGHVWNWTE-UHFFFAOYSA-N 3-(4-aminophenoxy)aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC(N)=C1 ZBMISJGHVWNWTE-UHFFFAOYSA-N 0.000 description 2
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- HESXPOICBNWMPI-UHFFFAOYSA-N 4-[2-[4-[2-(4-aminophenyl)propan-2-yl]phenyl]propan-2-yl]aniline Chemical compound C=1C=C(C(C)(C)C=2C=CC(N)=CC=2)C=CC=1C(C)(C)C1=CC=C(N)C=C1 HESXPOICBNWMPI-UHFFFAOYSA-N 0.000 description 2
- HPUJEBAZZTZOFL-UHFFFAOYSA-N 4-[3-(4-aminophenoxy)-2,2-dimethylpropoxy]aniline Chemical compound C=1C=C(N)C=CC=1OCC(C)(C)COC1=CC=C(N)C=C1 HPUJEBAZZTZOFL-UHFFFAOYSA-N 0.000 description 2
- WUPRYUDHUFLKFL-UHFFFAOYSA-N 4-[3-(4-aminophenoxy)phenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC(OC=2C=CC(N)=CC=2)=C1 WUPRYUDHUFLKFL-UHFFFAOYSA-N 0.000 description 2
- JCRRFJIVUPSNTA-UHFFFAOYSA-N 4-[4-(4-aminophenoxy)phenoxy]aniline Chemical compound C1=CC(N)=CC=C1OC(C=C1)=CC=C1OC1=CC=C(N)C=C1 JCRRFJIVUPSNTA-UHFFFAOYSA-N 0.000 description 2
- KIFDSGGWDIVQGN-UHFFFAOYSA-N 4-[9-(4-aminophenyl)fluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 KIFDSGGWDIVQGN-UHFFFAOYSA-N 0.000 description 2
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- ZHBXLZQQVCDGPA-UHFFFAOYSA-N 5-[(1,3-dioxo-2-benzofuran-5-yl)sulfonyl]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(S(=O)(=O)C=2C=C3C(=O)OC(C3=CC=2)=O)=C1 ZHBXLZQQVCDGPA-UHFFFAOYSA-N 0.000 description 2
- QHHKLPCQTTWFSS-UHFFFAOYSA-N 5-[2-(1,3-dioxo-2-benzofuran-5-yl)-1,1,1,3,3,3-hexafluoropropan-2-yl]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)(C(F)(F)F)C(F)(F)F)=C1 QHHKLPCQTTWFSS-UHFFFAOYSA-N 0.000 description 2
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- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- DJUWPHRCMMMSCV-UHFFFAOYSA-N bis(7-oxabicyclo[4.1.0]heptan-4-ylmethyl) hexanedioate Chemical compound C1CC2OC2CC1COC(=O)CCCCC(=O)OCC1CC2OC2CC1 DJUWPHRCMMMSCV-UHFFFAOYSA-N 0.000 description 1
- XFUOBHWPTSIEOV-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) cyclohexane-1,2-dicarboxylate Chemical compound C1CCCC(C(=O)OCC2OC2)C1C(=O)OCC1CO1 XFUOBHWPTSIEOV-UHFFFAOYSA-N 0.000 description 1
- WKDNYTOXBCRNPV-UHFFFAOYSA-N bpda Chemical compound C1=C2C(=O)OC(=O)C2=CC(C=2C=C3C(=O)OC(C3=CC=2)=O)=C1 WKDNYTOXBCRNPV-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000011353 cycloaliphatic epoxy resin Substances 0.000 description 1
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000007590 electrostatic spraying Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 150000004693 imidazolium salts Chemical class 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical compound [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000004382 potting Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 125000006158 tetracarboxylic acid group Chemical group 0.000 description 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000012876 topography Methods 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- 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
- H01B3/46—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 silicones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/03—Powdery paints
-
- 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
- H01B3/40—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 epoxy resins
-
- 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
- H01B3/44—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 vinyl resins; acrylic resins
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02K—DYNAMO-ELECTRIC MACHINES
- H02K3/00—Details of windings
- H02K3/30—Windings characterised by the insulating material
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02K—DYNAMO-ELECTRIC MACHINES
- H02K3/00—Details of windings
- H02K3/32—Windings characterised by the shape, form or construction of the insulation
- H02K3/40—Windings characterised by the shape, form or construction of the insulation for high voltage, e.g. affording protection against corona discharges
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2150/00—Compositions for coatings
- C08G2150/20—Compositions for powder coatings
-
- 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
- H01B3/302—Polyurethanes or polythiourethanes; Polyurea or polythiourea
Definitions
- the invention relates to a formulation for producing an insulating system for an electrical machine, in particular a rotating electrical machine of high voltage or medium voltage range such as a generator and / or motor, the higher rated voltages at operating voltages, so for example from 1 kV or more exposed are, as well as such an electrical machine with an insulation system that can be produced at least in part from the formulation.
- the inven tion relates to a method for at least partially automated production of an insulation system for such an electric machine.
- a high-performance generator such as a Turbogenera gate, in particular has a stator or stator with a stator core and a plurality of generator grooves in which the generator insulation system, usually in the form of a winding, is located.
- the main insulation of generators based on epoxide resin-impregnated mica tapes, provides shielding of the high-voltage conductors, in particular Kupferlei ter against the grounded stator. It has a high partial discharge insertion voltage, which allows it to permanently degrade, for example, 3.5kV per millimeter.
- the conductors in particular copper conductors, so the electric coil, the so-called verröbelten bars are pressed together, if appropriate, applied on the bars mecanicpotentialsteue tion, IPS, the main insulation and then the outer corona, AGS and possibly an end corona.
- End corona protection applied to control the electrical potential, for example, to raise the potential across the EGS length.
- All these components of the Isolationsssys system, so IPS, main insulation, AGS and EGS, are so far usually wound as bands on the sub-conductor, where parts of it, such as the EGS, are applied completely by hand. Also, the other parts can not be applied automatically, because either the number of automation does not make the Sieren economic and / or the risk of trapped air in the folds does not guarantee the quality that is required in the winding.
- the tapes which are wound, usually consist of glued mica platelets, the nen in the insulation, the erosion path in the insulation system to extend, ie the direct path from the high voltage side, ie the Lei tern, to grounded laminated core, creating a significantly longer life of an insulation system results.
- Object of the present invention is therefore to overcome the Häei le of the prior art, in particular the cost of producing an insulation system for a ro animal electrical machine of high voltage or medium voltage range such as a generator and / or motor, the higher rated voltages at Railspannun gene, so for example, from 1 kV or more, is exposed to minimize.
- the subject of the present invention ei ne sprayable formulation for an insulation system of an electrical machine, in particular a rotating electric machine of the high voltage or Mittelwoodsbe range such as a generator and / or a motor, the higher rated voltages at operating voltages, so for example from 1 kV or more exposed, wherein the formulation comprises a sprayable resin mixture, the ben ben of a monomeric and / or oligomeric, at least one diepoxidische carbon-based resin component nor a monomeric and / or oligomeric resin component on methyl / phenyl polysiloxane-based having at least Diglycidylester- and / or Diglycidyletherfunktionalität and / or still one or more, usable as a hardener compounds on anhydride and / or (poly) amine-based and / or amino and / or alkoxyfunktionale methyl / phenyl-polysiloxane-based comprises.
- mer platelets can be dispensed with the use of glued to the band large Glim and formulated the insulating material in the form of a sprayable solution and produced.
- Partial discharge resistant resins and resin blends are at play as those in which the polymeric component is a component having a - [SiR 2 _ 0-] n - backbone as a minor component of the resin mixture and / or resin-hardener mixture, ie less than 50 mol %, in particular less than 40 mol%, and more preferably less than 30 mol% of polymerisierba ren resin mixture and / or resin-hardener mixture is present.
- resin mixtures and / or resin-hardener mixtures for electrical insulation and in particular as impregnating resins for winding tape insulation preferably epoxy resins based on carbon used in liquid form on a carbon-based - [- CH2-] n _ backbone all These are reacted with hardener to a thermosetting plastic material, which forms a potting and / or, for example, the impregnation of Wickelbandisoltechnik possible functional groups, for example.
- thermosetting resin mixture and / or resin-hardener mixture for the insulation system is a siloxane-containing compound which has a - [SiR 2 -O] n backbone in the duromer forms.
- R stands for all types of organic radicals which are suitable for curing and / or crosslinking to an insulating material which is suitable for an isolation system, in particular R is -aryl, -alkyl, -heterocycles, nitrogen, oxygen and / or sulfur-substituted Aryls and / or alkyls.
- R may be the same or different and represent the following groups:
- Alkyl for example methyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, isopentyl, cyclopentyl and all other analogs up to dodecyl, ie the homolog with 12 carbon atoms;
- Aryl for example: benzyl, benzoyl, biphenyl,
- Toluyl-, xylenes and similar aromatics in particular, for example, all aryl radicals, with one or more ren rings whose structure corresponds to the definition of Hückel for the aromaticity,
- Heterocycles in particular sulfur-containing heterocycles such as thiophene, tetrahydrothiophene, 1,4-thioxane and homologues and / or derivatives thereof,
- Oxygen-containing heterocycles e.g. Dioxane
- Nitrogen-containing heterocycles e.g. those with -CN, -CNO, -CNS, -N3 (azide) substituents on the ring or on the rings and
- Sulfur-substituted aryls and / or alkyls e.g. Thiophene, but also thiols.
- the Hückel Rule for Aromatic Compounds refers to the connexion that planar, cyclic-conjugated molecules comprising a number of P-electrons, which can be represented in the form of 4n + 2, possess particular stability, also known as Aromaticity is called.
- Aromaticity is called.
- the resin mixture and / or resin-hardener mixture in addition to the polymerization functionalized monomer and / or oligomeric component having a - [SiR 2 -0] n- backbone, at least one for the polymerization functionalized monomeric or oligomeric resin component with a carbon - ie - [-CR1R2-] n-units comprising backbone.
- R is -hydrogen, -aryl, -alkyl, -heterocycles,
- Nitrogen, oxygen and / or sulfur-substituted aryls and / or alkyls are particularly suitable.
- epoxide-functionalized components such as bisphenol F diglycidyl ether (BFDGE) or bisphenol A diglycidyl ether (BADGE), polyurethane and mixtures thereof.
- BFDGE bisphenol F diglycidyl ether
- BADGE bisphenol A diglycidyl ether
- BFDGE bisphenol A diglycidyl ether
- BADGE bisphenol A diglycidyl ether
- the monomer or oligomeric component functionalized for the polymerization which has a - [SiR 2 _ 0] n - backbone with one or more, - [- CRiR 2] n _ backbone-containing components selected from the group of the following compounds to the resin Mixture and / or resin-hardener mixture combined:
- glycidyl-based and / or epoxy-terminated aryl and / or alkyl siloxanes are particularly suitable glycidoxy-terminated siloxanes.
- a siloxane such as the 1,3-bis (3-glycidyl-oxypropyl) tetramethyldisiloxane, the DGTMS, and / or the glycidoxy-terminated phenyl-dimethylsiloxane and / or phenylmethyl-siloxane in monomeric and / or oligomeric is suitable Form, as well as in any mixtures and / or in the form of Deriva th.
- the 4 methyl substituents on the silicon in the DGTMS may be different, identical or different any alkyl and / or aryl substituents.
- One of these already tested components is commercially available as "Silres® HP® 1250®. It has been shown that at least two-functionalized siloxanes which can be used for the production of thermosets are suitable here.
- Suitable hardeners are cationic and anionic Härtungska catalysts, such as organic salts, such as organic cal ammonium, sulphonium, iodonium, phosphonium and / or imidazolium salts and amines, such as tertiary amines, pyrazoles and / or imidazole compounds.
- organic salts such as organic cal ammonium, sulphonium, iodonium, phosphonium and / or imidazolium salts and amines, such as tertiary amines, pyrazoles and / or imidazole compounds.
- organic salts such as organic cal ammonium, sulphonium, iodonium, phosphonium and / or imidazolium salts and amines, such as tertiary amines, pyrazoles and / or imidazole compounds.
- amines such as tertiary amines, pyrazoles and
- oxirane group-containing compounds such as
- Glycidyl ether can be used as a hardener.
- the hardener can alternatively or additionally by a compound with - [-S1R2-O-] n- backbone, here called siloxane-based compound, partially or completely he sets.
- high polymers solid di- or trianhydrides may be useful as curing agents at room temperature, e.g. 3, 3 ', 4, 4' - benzophenone tetracarboxylic dianhydride (BTDA, CAS No. 2421-28-5).
- BTDA CAS No. 2421-28-5
- a PHthal Acidanhydridderivat and / or a polyamine, and / or a product of Wacker AG the alkyl and / or aryl and / or alkoxy-substituted Wacker HP 2000 or HP 2020 will be.
- the carbon-based hardener is also partially or completely replaced by siloxane-based hardeners with the same funcionalities.
- the siloxane-containing component is therefore present in an amount of 10 to 50 mol% in the resin mixture and / or resin-hardener mixture of the formulation. It is particularly preferred if the amount of siloxane-containing component in the base resin is not more than 20 mol%, in particular not more than 18 mol% and especially preferably not more than 15 mol%.
- the partial discharge resistance of the insulating material is virtually increased by the presence of a certain amount of - [SiR 2 _ 0 -] n -forming monomers or oligomers in the base resin.
- filler is added to the formulation.
- filler fractions such as small mica powder and / or other metal oxide Ke ceramics, such as alumina, silica, but also Alumi niumnitrites used as fillers.
- the fillers are used for example in particle size fractions 1-150 ym, in particular from 10 to 120ym, preferably in the range of 30 to 100 ym, because it increases the partial discharge resistance and, above all, the heat conductivity of the insulating system.
- nanoparticulate filler in particular those based on quartz, Si0 2, for example.
- an additive in particular a sintering additive, for example based on an organic Phos phortagen added according to an advantageous embodiment of the For formulation additionally.
- the organic phosphorus compound catalyzes the fusing and / or sintering of simultaneously present Si0 2 nanoparticles to vitreous regions in the resin. For example, this creates a vitreous region as a barrier layer in the insulation system.
- the formulation preferably contains a combination of the sintering additive and the nanoparticulate filler, since in the presence of an electrical discharge, glazed regions form in the finished duromer, which form a particularly good insulating effect.
- Latest storage of such fully cured insulation materials show a lifetime increase by a factor of 8.
- a formulation could be applied by spraying to produce the insulation system as follows:
- organic phosphorus compound which may also be present as a mixture of several phosphorus compounds.
- organic phosphorus compound which may also be present as a mixture of several phosphorus compounds.
- mica in pulverized form which may be present in various particle sizes and / or particle shapes,
- quartz nanoparticles 4 to 10% by weight of quartz nanoparticles, which may also be present in different fractions,
- hardener which may be anhydride-free or anhydride-containing
- a Formu lation for forming a producible by spraying insulation system comprises:
- polymerisable carbon-based resin that is to say a polymer having a - [-CH 2 -] backbone and 2.5 to 6% by weight of a polymerisable resin
- a concrete example of such a formulation is: 0.5% by weight of organic phosphorus compound,
- MHHPA methylhexahydrophthalic anhydride
- epoxidized siloxane e.g. Silres HP1250.
- the epoxy resin fraction was successively stoichiometricized by various siloxane-containing components [1], [2] and [3]. replaced.
- the resulting isolation systems samples 2,3 and 4 were targeted for test purposes and exposed to electrical discharges.
- pattern 1 a conventional isolation system without - [SiR 2 _ 0 -] n backbone in the resin was compared with these patterns 2 to 4.
- the eroded volumes were scanned by a laser and thus the eroded volume - or the eroded Tie fe of the insulation system - evaluated.
- FIG. 1 shows the results of the tests, ie the reduction of the erosion volume, visualized by measuring the surface topography by means of laser triangulation.
- the aging parameters were at room temperature, in air, duration 100 hours, atmosphere air 50% RH and voltage 10kV AC. It has been shown that even with a small sub-position of 20% of the CH 2 -based resin component, shown by the example of the epoxide-containing base resin DGEBA achieved by a - [SiR 2 -0] n- containing monomer, a significant increase in the partial discharge resistance which results in a significantly reduced eroded volume.
- the pattern 1 shows the prior art. To know he is in the middle of a circle 8, representing the contact surface of metalli's conductor. Following this, a red circle 3, indicating an erosion depth of -40 ym to -80 ym, as the legend on the right edge of Figure 1 shows. The surrounding a flat yellow circle 4, indicating an erosion depth of -30 to -10 ym. The flat yellow circle 4 closes a white circle 5 indicating zero erosion.
- the circle 5 has a radius which surrounds the entire test surface of the pattern 1 inside and touches the edges 7 of the pattern 1. With 6 the areas are marked, in which no erosion took place.
- FIG. 1 shows the patterns 2
- Figures 3 and 4 show exemplary embodiments of the invention which were tested under the identical conditions simultaneously with Sample 1 above.
- the samples relate to three embodiments of the invention in which a portion, 20mol%, of the epoxy resin and / or
- FIG. 1 shows an average reduction of the erosion volumes by partial - in this case 20% - replacement of the conventional epoxy resin by a component which has a - [SiR 2 _ 0] n backbone by about a factor of 9, which is simply sensational.
- siloxane-containing compo nent which is solid at room temperature
- formulations which are solid at room temperature and can be sprayed as powder coating, can then be applied, for example, by means of fluidized-bed spraying and / or electrostatic spraying.
- HHPA Hexahydrophthalic anhydride "HHPA” CAS No. 85-42-7; - tetrahydrophthalic anhydrides isomers of THPA, CAS no. 2426-02-0 and CAS no. 935-79-5;
- Amine derivatives as a curing agent is that by previous, in particular unique, melting with a solid at room tempera ture and / or normal pressure and / or normal conditions solid epoxy resin and / or Siloxanepoxidharz a homogeneously solid de melt is present.
- a solidified melt thus obtained can be pulverized again immediately or after storage, is stoichiometrically easy to mix and best possible mixed preserved.
- the powder produced, for example, from the solidified melt melts again and begins to crosslink immediately.
- the aforementioned amine derivatives then no longer require long-lasting oven curing periods, but only short-segment post-curing phases at significantly lower temperatures.
- the spray as a powder coating can also be a liquid paint, so the resin-hardener system in liq siger form or dissolved in a solvent sprayed who the.
- This spraying can be carried out using compressed air or without compressed air.
- the obvious advantage of spraying with solvent is that the viscosity of the resin-hardener mixture increases significantly as the solvent evaporates. This means that if the resin-hardener mixture is based on a The metal surface was sprayed, the viscosity of which rises so that it can no longer run.
- the sprayed-on paint is finally subjected to a post-curing to complete it, which can take place thermally and / or by irradiation.
- a sprayed layer of the insulation system has a thickness in the range of 50 microns to 150 microns, preferably 50 microns to 130 microns, and most preferably from 70 microns to 120 microns.
- insulation thickness Be in the range of 700ym up to about 6mm insulation thickness required, so that the sprayed insulation systems are always applied in multiple layers.
- the sprayable formulation at least one poly merisierbare component comprising a resin-hardener system, and one or more fillers.
- the polymerizable component is a mixture of at least one of a - [SiR 2 -0-] n -containing backbone and a - [-CH 2] n _ containing backbone-containing compound to verstan.
- the polymerisable component is selected from thermosets and / or thermoplastics.
- 2-butanone, acetone and / or 1-butanol may be present as solvent in the sprayable liquid formulation.
- fine mica as filler results in the advantage that the particles formed therefrom have a relatively low abrasiveness and therefore they can be simply sprayed on a conductor in the form of a particle-paint suspension with a nozzle to an insulation system to obtain.
- a sprayed formulation either as a powder coating or as a liquid formulation with or without solvents, in particular for the production of the main insulation, allows a partially or fully automated production of Isolationsssys system also individually adapted to the respective machine th insulation systems.
- the spray technology allows an increase in the power density of electrically rotating machines, assuming that the sprayed insulation system has the same electrical life as a conventional insulation system with corona protection tape, tape adhesive, Bandbe faster, possibly applied by hand Umwicke- followed by resin impregnation, optionally in vacuo and final resin curing.
- Figure 2 shows the state of the art with mica tape insulation wound around the conductor
- Figure 3 shows the spray insulation applied as a sprayable formulation.
- FIG. 2 shows the state of the art, which conventionally inserted wound insulation system 11 around the square profile of the conductor 13, for example a copper conductor, in the sheet metal package 12.
- the winding thickness 15 is less than the winding 15 'on the flat side. This is a simple consequence of the winding
- a winding thickness 15 of 2.2 mm is measured at the edge 14, whereas at the flat side 16, a winding thickness 15 of 2.7 mm can be measured.
- Figure 3 shows in contrast to the sprayed insulation system according to an embodiment of the invention. To know he is again the square profile 13 of the head of all recently no longer the wound, but sprayed in accordance with the inven tion insulation system 11 in the laminated core 12th
- the conductor 13 has a maximum width 18 of 12 mm whereas, according to the invention, as shown in FIG. 3, it may have up to one mm more width, that is to say a width 18 of 13 mm.
- the sprayable insulation in particular also also transport other quantities of electricity.
- the invention discloses for the first time a sprayable formulation for producing an insulation system for an electric machine, particularly a rotary electric machine of the high voltage or medium voltage range such as a generator and / or motor, the higher measurement voltages at operating voltages, that is, for example, from 1 kV or more are exposed, as well as the her synthe isolation system.
- the method for producing the insulation system comprises spraying and can thereby be automated.
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- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Power Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Insulation, Fastening Of Motor, Generator Windings (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102018202058.2A DE102018202058A1 (de) | 2018-02-09 | 2018-02-09 | Formulierung zur Herstellung eines Isolationssystems, elektrische Maschine und Verfahren zur Herstellung eines Isolationssystems |
PCT/EP2019/053048 WO2019154932A1 (de) | 2018-02-09 | 2019-02-07 | Formulierung zur herstellung eines isolationssystems, elektrische maschine und verfahren zur herstellung eines isolationssystems |
Publications (1)
Publication Number | Publication Date |
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EP3729469A1 true EP3729469A1 (de) | 2020-10-28 |
Family
ID=65520231
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP19706909.9A Pending EP3729469A1 (de) | 2018-02-09 | 2019-02-07 | Formulierung zur herstellung eines isolationssystems, elektrische maschine und verfahren zur herstellung eines isolationssystems |
Country Status (6)
Country | Link |
---|---|
US (1) | US20210035705A1 (zh) |
EP (1) | EP3729469A1 (zh) |
CN (1) | CN111684545B (zh) |
DE (1) | DE102018202058A1 (zh) |
RU (1) | RU2756232C1 (zh) |
WO (1) | WO2019154932A1 (zh) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
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DE102020117995A1 (de) | 2020-07-08 | 2022-01-13 | Bayerische Motoren Werke Aktiengesellschaft | Elektrische Maschine für ein Kraftfahrzeug, Verwendung einer solchen elektrischen Maschine sowie Kraftfahrzeug |
EP4046773A1 (de) * | 2021-02-22 | 2022-08-24 | Siemens Aktiengesellschaft | Isolationssystem für elektrische rotierende maschinen, herstellungsverfahren dazu sowie pulverlackbeschichtung |
DE102021201666A1 (de) | 2021-02-22 | 2022-08-25 | Siemens Aktiengesellschaft | Nutisolationssystem für eine elektrische rotierende Maschine, Verfahren zur Herstellung eines Nutisolationssystems |
US20240318032A1 (en) * | 2021-02-22 | 2024-09-26 | Siemens Aktiengesellschaft | Insulation System for Electrically Rotating MachinesAnd Method for the Production Thereof |
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CH500248A (de) * | 1968-06-19 | 1970-12-15 | Ciba Geigy Ag | Verfahren zur Herstellung von neuen epoxidgruppenhaltigen Addukten aus Polyepoxidverbindungen und sauren Polyestern aliphatisch-cycloaliphatischer Dicarbonsäuren und ihre Anwendung |
KR20000011132A (ko) * | 1996-05-15 | 2000-02-25 | 칼 하인쯔 호르닝어 | 전기 컨덕터, 전기 컨덕터 장치 및 대형 전기기계의전기 컨덕터를 절연하는 방법 |
HU217112B (hu) * | 1997-01-21 | 1999-11-29 | Furukawa Electric Institute Of Technology | Epoxi-szilikon hibrid gyanta alapú villamos szigetelőkompozíciók |
DE19963492A1 (de) * | 1999-12-28 | 2001-07-05 | Alstom Power Schweiz Ag Baden | Verfahren zur Herstellung einer hochwertigen Isolierung von elektrischen Leitern oder Leiterbündeln rotierender elektrischer Maschinen mittels thermischen Spritzens |
US6778053B1 (en) * | 2000-04-19 | 2004-08-17 | General Electric Company | Powder coated generator field coils and related method |
EP1354916A1 (de) * | 2002-04-17 | 2003-10-22 | Abb Research Ltd. | Selbstheilende Epoxidharze für die Herstellung von elektrischen Isolierungen |
US7157143B2 (en) * | 2003-03-24 | 2007-01-02 | Dow Global Technologies Inc. | Two-component epoxy adhesive formulation for high elongation with low modulus |
US7834121B2 (en) * | 2004-09-15 | 2010-11-16 | Ppg Industries Ohio, Inc. | Silicone resin containing coating compositions, related coated substrates and methods |
US20060124693A1 (en) * | 2004-12-15 | 2006-06-15 | Meloni Paul A | Thermally conductive polyimide film composites having high mechanical elongation useful as a heat conducting portion of an electronic device |
JP2010254966A (ja) * | 2009-03-31 | 2010-11-11 | Jsr Corp | 電線被覆用放射線硬化性樹脂組成物 |
WO2011095208A1 (en) * | 2010-02-03 | 2011-08-11 | Abb Research Ltd | Electrical insulation system |
DE102011083228A1 (de) * | 2011-09-22 | 2013-03-28 | Siemens Aktiengesellschaft | Isoliersysteme mit verbesserter Teilentladungsbeständigkeit, Verfahren zur Herstellung dazu |
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DE102012205563A1 (de) * | 2012-04-04 | 2013-10-10 | Siemens Aktiengesellschaft | Isoliersystem mit Endenglimmschutz und Verfahren zur Herstellung des Endenglimmschutzes |
DE102013216781A1 (de) * | 2013-08-23 | 2015-02-26 | Evonik Industries Ag | Beschichtungsmassen |
GB201402053D0 (en) * | 2014-02-06 | 2014-03-26 | Hexcel Composites Ltd | Amino benzoates or benzamides as curing agents for epoxy resins |
DE102014219765A1 (de) * | 2014-09-30 | 2016-03-31 | Siemens Aktiengesellschaft | Formulierung für ein Isoliersystem und Isoliersystem |
JP6779476B2 (ja) * | 2015-03-19 | 2020-11-04 | ナガセケムテックス株式会社 | 屋外電気絶縁用エポキシ樹脂組成物及び屋外電気絶縁用部材 |
US10683441B2 (en) * | 2016-03-02 | 2020-06-16 | 3M Innovative Properties Company | Composition including epoxy adhesive and aluminum flakes and method for using the same |
CN106009527B (zh) * | 2016-07-27 | 2019-01-15 | 苏州巨峰电气绝缘系统股份有限公司 | 一种耐低温电机用绝缘树脂及其制备方法 |
EP3460959A1 (de) * | 2017-09-20 | 2019-03-27 | Siemens Aktiengesellschaft | Elektrisches isolationsmaterial und/oder imprägnierharz für die wickelbandisolierung einer mittel- und/oder hochspannungsmaschine sowie ein isolationssystem daraus |
-
2018
- 2018-02-09 DE DE102018202058.2A patent/DE102018202058A1/de active Pending
-
2019
- 2019-02-07 WO PCT/EP2019/053048 patent/WO2019154932A1/de unknown
- 2019-02-07 EP EP19706909.9A patent/EP3729469A1/de active Pending
- 2019-02-07 US US16/968,055 patent/US20210035705A1/en active Pending
- 2019-02-07 CN CN201980012041.3A patent/CN111684545B/zh active Active
- 2019-02-07 RU RU2020128157A patent/RU2756232C1/ru active
Also Published As
Publication number | Publication date |
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CN111684545A (zh) | 2020-09-18 |
RU2756232C1 (ru) | 2021-09-28 |
DE102018202058A1 (de) | 2019-08-14 |
CN111684545B (zh) | 2023-05-26 |
WO2019154932A1 (de) | 2019-08-15 |
US20210035705A1 (en) | 2021-02-04 |
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