EP1250195A2 - Verfahren zur herstellung von isolierungen elektrischer leiter mittels pulverbeschichtung - Google Patents
Verfahren zur herstellung von isolierungen elektrischer leiter mittels pulverbeschichtungInfo
- Publication number
- EP1250195A2 EP1250195A2 EP00982814A EP00982814A EP1250195A2 EP 1250195 A2 EP1250195 A2 EP 1250195A2 EP 00982814 A EP00982814 A EP 00982814A EP 00982814 A EP00982814 A EP 00982814A EP 1250195 A2 EP1250195 A2 EP 1250195A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- powder
- filler
- insulation
- individual layers
- powder according
- 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.)
- Granted
Links
- 239000000843 powder Substances 0.000 title claims abstract description 78
- 238000009413 insulation Methods 0.000 title claims abstract description 58
- 239000004020 conductor Substances 0.000 title claims abstract description 26
- 238000000576 coating method Methods 0.000 title claims abstract description 16
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- 239000011248 coating agent Substances 0.000 title claims abstract description 13
- 239000000945 filler Substances 0.000 claims abstract description 75
- 238000000034 method Methods 0.000 claims abstract description 27
- 239000003822 epoxy resin Substances 0.000 claims abstract description 11
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims description 14
- 239000000126 substance Substances 0.000 claims description 13
- 239000004848 polyfunctional curative Substances 0.000 claims description 12
- 230000008569 process Effects 0.000 claims description 12
- 229920001187 thermosetting polymer Polymers 0.000 claims description 12
- 230000008018 melting Effects 0.000 claims description 11
- 238000002844 melting Methods 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 10
- 230000009477 glass transition Effects 0.000 claims description 9
- 239000011256 inorganic filler Substances 0.000 claims description 8
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 8
- 229910010413 TiO 2 Inorganic materials 0.000 claims description 6
- 238000005245 sintering Methods 0.000 claims description 3
- 239000007921 spray Substances 0.000 claims description 3
- 239000000454 talc Substances 0.000 claims description 3
- 229910052623 talc Inorganic materials 0.000 claims description 3
- 239000010456 wollastonite Substances 0.000 claims description 3
- 229910052882 wollastonite Inorganic materials 0.000 claims description 3
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 2
- 238000010292 electrical insulation Methods 0.000 claims description 2
- 238000001879 gelation Methods 0.000 claims description 2
- 238000001029 thermal curing Methods 0.000 claims description 2
- 238000007751 thermal spraying Methods 0.000 claims description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 2
- 229920005989 resin Polymers 0.000 abstract description 12
- 239000011347 resin Substances 0.000 abstract description 12
- 238000012360 testing method Methods 0.000 abstract description 11
- 230000032683 aging Effects 0.000 abstract description 9
- 239000010445 mica Substances 0.000 abstract description 3
- 229910052618 mica group Inorganic materials 0.000 abstract description 3
- 239000010410 layer Substances 0.000 description 44
- 239000011810 insulating material Substances 0.000 description 13
- 230000000694 effects Effects 0.000 description 7
- 230000005684 electric field Effects 0.000 description 7
- 208000035874 Excoriation Diseases 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 230000004913 activation Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
- 239000003082 abrasive agent Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000005524 ceramic coating Methods 0.000 description 2
- 238000010382 chemical cross-linking Methods 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 229920002732 Polyanhydride Polymers 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000004870 electrical engineering Methods 0.000 description 1
- 238000007590 electrostatic spraying Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000013528 metallic particle Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000000049 pigment Substances 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
- 239000011148 porous material Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000004886 process control Methods 0.000 description 1
- 239000013587 production medium Substances 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000012031 short term test Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000001960 triggered effect Effects 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
-
- 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
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
Definitions
- the invention relates to the insulation of electrical conductors of devices in the low to medium voltage range (i.e. up to about 50 kV) by means of powder coating. Insulation in the high-voltage range is also possible, provided that the conductors are not subjected to the full potential drop.
- the invention relates in particular to insulation of electrical conductors which are subject to high thermal and electrical loads, such as insulation of electrical conductors or conductor bundles of rotating electrical machines. Switchgear and transformers are further examples of possible applications.
- E is the electric field in kV / mm
- E 0 is the electric field at the lifetime t 0
- t is the time in h
- t 0 1 h
- n is the lifetime coefficient.
- the life coefficient n can be described as characteristic of the type of insulation.
- rotating machines n 7 to 9
- high-voltage cables n ⁇ 35 which are usually insulated in the extrusion process
- the extrusion process used for the production of cable insulation is a continuous process, which is particularly suitable for the production of quasi-infinite, geometrically simple structures.
- neither the production process nor the materials used - mostly unfilled, pure polyethylene - can be used in a wide range Complex and small structures, such as motor coils or connections in switchgear, cannot be produced using this method.
- the use of polyethylene is also unsuitable for many possible applications, because such PE insulation can only be used up to approx. 90 ° C
- Powder coating is known as a largely geometry-independent insulation process. In contrast to extrusion, this insulation process is suitable even for very complex conductor structures. In theory, a large number of medium-voltage devices could be isolated effectively and inexpensively, for which the extrusion process is out of the question contrary to the fact that with the known powder coating methods and with the available coating materials no qualitatively adequate insulation can be achieved
- busbars Because there is no counter electrode on the surface of the insulation, the insulation in busbars is also only weakly or not at all. The electrical potential of the busbar is thus almost completely reduced in the air space above the layer. As a result, voids in the epoxy layer interfere far less than in the present application. Tests with a powder used for busbar coating accordingly showed an extreme content of holes.
- This layer primarily has the task of protecting against corrosion and is not or hardly loaded electrically.
- Powders are commercially available which meet the thermal requirements, but which are electrically unsuitable. Such powders are mostly used for corrosion protection in the field of chemical plant construction. The process for the production of such powders by hot mixing, melting, cooling and grinding corresponds to the general state of the art, as is described, for example, in US 4040993.
- the invention tries to avoid all these disadvantages. It is the object of the invention to provide a method for producing insulation of electrical conductors by means of powder coating, which has an aging behavior that is improved compared to glass-mica or cast resin insulation. Likewise, a powder that is suitable for such a method is to be specified.
- the powder is applied several times in succession up to a total insulation thickness of ⁇ 10 mm in the form of successive individual layers and each of the individual layers is thermally applied before the next individual layer is applied is intermediate hardened. During the intermediate hardening of each individual layer, a hardening time is observed which corresponds to 2-10 times the gel time of the powder used. Finally, the entire insulation is cured.
- a powder which contains at least one meltable and hardenable resin-hardener-auxiliary system as well as at least one inorganic filler.
- the inorganic filler content is 5 to 50 percent by weight, based on a closed density of the filler of up to 4 g / cm 3 .
- At least 3 percent by weight of the total mixture of the powder consist of fine fillers with an average grain size d 50 ⁇ 3 ⁇ m.
- the rest of the filler consists of coarse filler with an average grain size d 50 ⁇ 30 ⁇ m.
- the flow of the powder melting into a closed film is at least 25 mm and the gel time of the melted powder is at least 40 s.
- the composition of the powder in particular the proportion of fine filler according to the invention, also contributes to increasing the service life of the insulation.
- Suitable coating methods for applying the powder to the electrical conductors to be coated are spray or vortex sintering or thermal spraying of powder in the molten state.
- a selection of resin-hardener auxiliary material systems with a glass transition temperature of the thermosetting plastic of at least 130 ° C. can ensure that the insulation can be used for all applications in the medium-voltage range.
- the individual layers are applied with the smallest possible layer thickness of ⁇ 0.5 mm to an optimal layer thickness of 0.2 mm. In this way, a complete, high-quality coating of even complex surfaces and a layer thickness suitable for thermally and electrically highly stressed conductors can be achieved.
- either only individual layers with a uniform layer thickness or individual layers of different layer thickness can be applied to the electrical conductors to be insulated in any order.
- Powders of different compositions can also be used to apply individual layers. This makes it possible to use insulation to deliver, which meets the expected requirements according to the conditions of use of the insulated electrical conductors
- the most important requirements for the finished insulation are the following: 1
- Tl temperature index
- T 0p operating temperature
- the insulation should be in continuous operation be able to withstand high electrical loads, ie with E> 3 kV / mm, in particular E> 5 kV / mm
- the single figure shows the result of an electrical endurance test of various test specimens, insulated with epoxy resin powder containing filler applied in accordance with the invention, the lifespan in hours being shown horizontally, the field strength in kV / mm being shown vertically
- the polymer-based powder according to the invention contains at least one non-crosslinked system consisting of resin hard and auxiliary substances and electrically insulating inorganic fillers.
- the auxiliary substances influence, for example, the hard time or the process, whereby auxiliary substances known from the prior art can be used.
- Electrically insulating inorganic fillers are contained in amounts of about 5 to about 50 percent by weight based on fillers with a closed density of up to 4 g / cm 3.
- the filler is either entirely as a fine filler with an average grain size d 50 ⁇ 3 ⁇ m, in particular d 50 ⁇ 1 ⁇ m, especially preferred with d 50 between 0 01 and 0 3 ⁇ m, or as a mixture of fine filler and coarse filler with d 50 ⁇ 30 ⁇ m, in particular between 3 and 20 ⁇ m, before.
- the proportion of fine filler in the total mixture of the powder should be at least 3%, in particular at least 5%, and the polymer to be formed from resin and hardener is a Du be plastic that has a glass transition temperature of at least 130 ° C in the cross-linked state
- Preferred fine fillers have an average diameter d 50 of approx. 0 2 ⁇ m, whereby finer fillers can also be used, which has a positive effect on the corona resistance but has a negative effect on the flow properties (thixotropy) of the melted insulating material
- the total filler content is preferably about 40%. If the filler has an average closed density of more than 4 g / cm 3 , the limit and preferred values given above and below can be higher.
- the fine filler and the coarse filler can be different materials which have different hardness. It is also within the scope of the present invention that the fine filler or the coarse filler or the fine filler and the coarse filler are mixtures of fillers of the same or different hardness.
- the coarse filler In order to prevent abrasion during the production of the insulating material or its processing for insulation, which is essential, in particular when steel or hard metal devices are used today in the compounding and grinding of the insulating material, the coarse filler must have a Mohs hardness, which is preferred at least one hardness unit is lower than that of steel and hard metal (Mohs hardness of approx. 6).
- Mohs hardness eg quartz powder (hardness grade 7)
- the processing leads to metallic abrasion, preferably in the form of chips in the sub-mm range. These are built into the insulation and, due to their needle-like geometry, lead to locations with a locally very greatly increased electrical field strength, from which experience has shown that an electrical breakdown can be triggered. Microscopic examinations showed a surface density of such metallic particles of 1-3 / 100 mm 2 when using SiO 2 as coarse filler.
- Abrasion is avoided by using "soft" fillers (Mohs' hardness ⁇ 4) such as chalk powder and / or by using finer fillers with d 50 «1 ⁇ m.
- Such fine fillers also have the advantage that they themselves in the presence of imperfections such as cavities or metallic inclusions, can prevent or at least greatly delay the electrical breakthrough (see US 4760296, DE 40 37 972 A1).
- the coarse filler should have a hardness that is at least about a Mohs hardness level below that of the production medium or container, ie one Ceramic coating of a hardness of usually about 8 with a maximum Mohs hardness of about 7
- the electrically insulating inorganic fillers are preferably selected from carbonates, silicates and metal oxides, which may also be in the form of minced minerals.
- examples of such fillers are, for example, T ⁇ O 2 , CaCO 3 , ZnO, wollastonite, clay and talc, T ⁇ O 2 , ZnO and Clay especially as a fine filler and CaCO 3 , wollastonite and talc with grain sizes around 10 ⁇ m (medium
- 2C lere grain size d 50 are especially suitable as coarse fillers
- Fillers with the desired grain size can be obtained in various ways, for example by special falling processes, combustion processes, etc. but also by mechanical comminution, all of which can optionally be coupled with a fractionation or sieving process
- the presence of at least 5 percent by weight of filler and at least 3 percent by weight, preferably at least 5 percent by weight, of fine filler is not sent ch, because the filler has an electrically insulating effect, increases mechanical strength, improves thermal conductivity, lowers the coefficient of thermal expansion, increases UV resistance and contributes to viscosity adjustment.
- the fine filler is also essential for increasing corona resistance, while the coarse filler An increase in the filler content with a lower viscosity increase is permitted than would be the case with fine filler.
- Filler contents above 50% by weight based on fillers with a closed density of up to 4 g / cm 3 and maximum grain size of 20 ⁇ m as well as excessive fine filler contents are critical, since Set problems due to excessive viscosity both in the manufacture of the insulating material and in the processing thereof
- thermosets for the matrix of the insulating materials of the present invention have a glass transition temperature of 130 ° C. to 200 ° C., preferably 150 ° C. to 180 ° C., in the hardened state
- the resin-hard auxiliary system of the thermoset should be such that it cures without the release of volatile substances
- the resin-hardener auxiliary system has a gel time that at most allows adsorbed water or other volatile substances in it or on the surface to be coated to emerge from the insulating layer before the latter has solidified too much so that any pores or blisters that may have formed during this discharge can eat themselves
- the mixture of resin, hardener and organic auxiliaries should have a melting point of at most 200 ° C, whereby it is essential that the melting point is below the activation temperature of the hardening reaction, or that the hardening reaction takes place very slowly at the melting temperature, and at Cooling can essentially be stopped. This is necessary in order to prevent extensive curing during the manufacture of the insulating material. prevent.
- the hardening properties can be adjusted by adding suitable substances, taking care that such substances are not volatile or completely outgas within the gel time.
- the mixture of resin, hardener and organic auxiliaries preferably has a melting point of at least 5 ° C., in particular from 70 ° C. to 120 ° C. In exceptional cases, the
- the melting point of resin and / or hardener is up to about 200 ° C. Such a high melting point is problematic because of the activation of the hardening reaction, which is usually in a similar, if not lower, range. Hardening is usually carried out in a temperature range from 70 ° C. to 120 ° C., preferably in a range from 130 ° C. to 200 ° C.
- thermoset In order to be able to meet the high demands placed on the glass transition point of the thermoset, it is preferred that the thermoset is strongly cross-linked or has a high cross-linking density.
- a preferred thermoset is an epoxy resin. Epoxy resin is among others preferred because both the carboxylic acid
- epoxy resin is usually crosslinking and the crosslinking density can be increased by using di- or polyanhydrides or polyamines as hardener and / or multifunctional, branched-chain epoxy resins as resin.
- Resins and / or hardeners containing aromatic groups are preferred and to increase the glass transition point.
- the insulating material according to the invention can contain additives or auxiliary substances, such as activators, accelerators, pigments, etc., such substances preferably being non-volatile.
- the glass transition temperature (T g ) should be in this temperature range, preferably between 130 ° C and 200 ° C. Glass transition temperatures significantly higher than 200 ° C are difficult on the one hand
- the filler content is also important, which should be> 10 percent by volume with such high requirements, which is about 23 percent by weight with a closed density of 4 g / cm 3 corresponds.
- Insulation for the medium-voltage and lower high-voltage range of thermally and electrically highly stressed electrical conductors is preferably produced by at least partially covering the electrical conductors to be coated with an insulating material according to the invention, whereupon the insulating material is brought to a temperature above the melting and activation temperature for the Hardening of the resin-hardener-auxiliary system of the thermoset brought and held there until gelation.
- the powder can be applied in various ways, e.g. by spraying with and without electrostatic charge or in a fluidized bed.
- the freedom from bubbles mentioned above is determined both by the choice of process control and by different material properties. It is important that the insulating material in the liquid state has a sufficiently low viscosity to run well and that the gel time is long enough so that all bubble-forming additives (eg adsorbed water) can evaporate.
- This demand for long gel times is contrary to the trend of powder coating companies, which set the gel times by adding accelerators to achieve long throughput times in thin-film painting (typically 15 seconds (s)).
- accelerators typically 15 seconds (s)
- the proportion of accelerator By reducing the proportion of accelerator, however, the gel times of commercially available powders can easily be brought to times of> 60s, preferably 80-160s, which are sufficiently long for the present application.
- the viscosity of spray powders is usually not measured and specified as a separate size; instead, the so-called process, which results from viscosity and gel time, is specified.
- Bubble-free layers are achieved when the drain is> 25 mm, preferably 30 - 50 mm.
- the thickness a single layer is 0.05-0.3 mm, preferably 0.2 mm.
- the application of the individual layers is repeated up to the desired layer thickness.
- the system consisting of resin, hardener, auxiliary materials and fillers is annealed for approx. 60 - 300 s according to its gel time, which causes melting, water release and partial hardening.
- the insulation can be optimally adapted to the surface to be coated.
- the powder was not optimized for slow gel times and therefore contained bubbles with diameters up to 0.3 mm. Electrodes with a diameter of 80 mm were applied to the plates.
- the samples were then aged at 16 kV / mm under oil. Due to the bubbles, the samples were partially discharged (TE) active during the test. After 2600 hours (h) the tests were stopped without a breakdown being observed.
- Example 4 is The test specimens produced in 2 and 3 were subjected to an electrical life test. The result of the test is shown in the single figure. There is no significant difference between the two types of filler. The majority of the data points shown correspond to samples that have not yet penetrated; the final lifetime curve is therefore even flatter
- Example 5 30 With epoxy resin powders containing 40% TiO 2 fine filler, insulation of 10 mm total thickness was produced in 56 layers.
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Organic Insulating Materials (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Insulating Bodies (AREA)
- Inorganic Insulating Materials (AREA)
- Manufacture Of Motors, Generators (AREA)
- Processes Specially Adapted For Manufacturing Cables (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19963378 | 1999-12-28 | ||
DE19963378A DE19963378A1 (de) | 1999-12-28 | 1999-12-28 | Verfahren zur Herstellung von Isolierungen elektrischer Leiter mittels Pulverbeschichtung |
PCT/CH2000/000683 WO2001048763A2 (de) | 1999-12-28 | 2000-12-21 | Verfahren zur herstellung von isolierungen elektrischer leiter mittels pulverbeschichtung |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1250195A2 true EP1250195A2 (de) | 2002-10-23 |
EP1250195B1 EP1250195B1 (de) | 2005-09-07 |
Family
ID=7934749
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP00982814A Expired - Lifetime EP1250195B1 (de) | 1999-12-28 | 2000-12-21 | Verfahren zur herstellung von isolierungen elektrischer leiter mittels pulverbeschichtung |
Country Status (11)
Country | Link |
---|---|
US (1) | US6942900B2 (de) |
EP (1) | EP1250195B1 (de) |
JP (1) | JP2003520664A (de) |
KR (1) | KR20020075387A (de) |
CN (1) | CN1321749C (de) |
AT (1) | ATE303871T1 (de) |
AU (1) | AU1980301A (de) |
CZ (1) | CZ20022253A3 (de) |
DE (2) | DE19963378A1 (de) |
RU (1) | RU2002120489A (de) |
WO (1) | WO2001048763A2 (de) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10113299A1 (de) * | 2001-03-16 | 2002-09-19 | Alstom Switzerland Ltd | Verfahren zum Herstellen eines Leiterstabes |
WO2004034409A1 (en) * | 2002-10-04 | 2004-04-22 | Rensselaer Polytechnic Institute | Nanometric composites as improved dielectric structures |
EP1519389A1 (de) * | 2003-09-18 | 2005-03-30 | Rohm And Haas Company | Elektrisch isolerende Pulverbeschichtungen und Zusammensetzungen und Verfahren zu deren Herstellung |
EP1769511B1 (de) * | 2004-07-13 | 2011-02-02 | Areva T&D Sas | Verfahren zur herstellung eines isolators für hochspannungsanwendungen |
US7579397B2 (en) | 2005-01-27 | 2009-08-25 | Rensselaer Polytechnic Institute | Nanostructured dielectric composite materials |
US7964236B2 (en) * | 2005-10-18 | 2011-06-21 | Elantas Pdg, Inc. | Use of nanomaterials in secondary electrical insulation coatings |
JP5109449B2 (ja) * | 2007-04-04 | 2012-12-26 | 株式会社明電舎 | 絶縁処理方法,電圧機器 |
JP2009099332A (ja) * | 2007-10-16 | 2009-05-07 | Meidensha Corp | 絶縁処理された電圧機器 |
KR20110103416A (ko) * | 2008-12-18 | 2011-09-20 | 메르크 파텐트 게엠베하 | 저 에너지를 갖는 입자들에 의해 절연층을 형성하는 프로세스 |
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1999
- 1999-12-28 DE DE19963378A patent/DE19963378A1/de not_active Ceased
-
2000
- 2000-12-21 KR KR1020027008519A patent/KR20020075387A/ko not_active Application Discontinuation
- 2000-12-21 JP JP2001548397A patent/JP2003520664A/ja active Pending
- 2000-12-21 CN CNB008192332A patent/CN1321749C/zh not_active Expired - Fee Related
- 2000-12-21 RU RU2002120489/09A patent/RU2002120489A/ru not_active Application Discontinuation
- 2000-12-21 AU AU19803/01A patent/AU1980301A/en not_active Abandoned
- 2000-12-21 US US10/168,625 patent/US6942900B2/en not_active Expired - Fee Related
- 2000-12-21 AT AT00982814T patent/ATE303871T1/de active
- 2000-12-21 CZ CZ20022253A patent/CZ20022253A3/cs unknown
- 2000-12-21 WO PCT/CH2000/000683 patent/WO2001048763A2/de not_active Application Discontinuation
- 2000-12-21 DE DE50011136T patent/DE50011136D1/de not_active Expired - Lifetime
- 2000-12-21 EP EP00982814A patent/EP1250195B1/de not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
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See references of WO0148763A2 * |
Also Published As
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CN1437512A (zh) | 2003-08-20 |
AU1980301A (en) | 2001-07-09 |
DE19963378A1 (de) | 2001-07-12 |
CN1321749C (zh) | 2007-06-20 |
KR20020075387A (ko) | 2002-10-04 |
CZ20022253A3 (cs) | 2003-03-12 |
WO2001048763A3 (de) | 2001-12-20 |
RU2002120489A (ru) | 2004-02-20 |
EP1250195B1 (de) | 2005-09-07 |
US6942900B2 (en) | 2005-09-13 |
JP2003520664A (ja) | 2003-07-08 |
WO2001048763A2 (de) | 2001-07-05 |
DE50011136D1 (de) | 2005-10-13 |
ATE303871T1 (de) | 2005-09-15 |
US20030113539A1 (en) | 2003-06-19 |
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