Patent Application
20170011820
The invention generally relates to insulated windings and methods for making the windings. Such windings are resistant to high temperature and high voltage, and may be useful for a variety of high temperature electrical submersible pump (ESP) applications.
The global increase in demand for energy has necessitated exploration of resources such as shale, oil sand, or subsea environment to procure oil and gas using various technologies, such as steam assisted gravity drainage (SAGD). Artificial lift using ESP technology is commonly used to retrieve fluids from deep wells. The motors that drive the ESPs (ESP motors) are typically submersed in the fluid in a deep well, wherein the fluid may be a mixture of crude oil, brine, and sour gas; and the temperature of the fluid may reach up to 300° C. The ESP motor performance and its reliability may be limited by the thermal stability and chemical resistance of the currently available electrical insulation systems used in windings. Therefore, a thermally stable and chemically resistant electrical insulation system that is mechanically viable for use in an ESP motor may be desirable.
For electrical insulation of ESP motor windings, commercially available flexible ceramic coatings can be used. However, the commercially available ceramic coating is usually thin, unstable to high voltage (e.g., more than hundred volts) and unable to provide dielectric capability required by ESP motors (e.g., 5 to 8 kV breakdown voltage). Though a thicker ceramic coating can improve the breakdown voltage, it has a tendency to generate cracks during the winding manufacturing process. In contrast, the available polymeric coatings are flexible for winding. However, the thermal stability of polymeric coatings may be limited to 250° C. for long-term applications.
Thus, an electrically insulating coating system for an ESP motor that has the thermal stability and chemical resistance of ceramics, and mechanical flexibility and dielectric strength of the polymers is desirable. Further, an improved method of making an electrically insulating coating system for a winding that can meet both the thermal and mechanical requirements is also desirable.
In one embodiment, an insulated winding is provided. The insulated winding includes (a) an electrically conductive core; (b) an electrically insulating non-porous ceramic coating disposed on the conductive core; and (c) a composite silicone coating including a plurality of electrically insulating filler particles disposed on the ceramic coating.
In another embodiment, an insulated winding includes (a) an electrically conductive core; (b) an electrically insulating non-porous ceramic coating disposed on the conductive core, wherein the non-porous ceramic coating includes an aluminum magnesium phosphate, a potassium silicate, or a combination thereof; (c) a silicone coating disposed on the ceramic coating; and (d) a protective coating disposed on the silicone coating, wherein the protective coating includes glass impregnated with silazane.
In one embodiment, a method of making an insulated winding is provided. The method includes (a) disposing a pre-ceramic material on an electrically conductive core to form a green ceramic coating; (b) disposing a composite silicone coating including a plurality of electrically insulating filler particles on the green ceramic coating to form a pre-shaped winding; and (c) heating the pre-shaped winding to substantially cure the pre-ceramic material and form the insulated winding.
These and other features, aspects, and advantages of the present invention will become better understood when the following detailed description is read with reference to the accompanying drawings in which like characters represent like parts throughout the drawings, wherein:
In the following specification and the claims, reference will be made to a number of terms, which shall be defined to have the following meanings.
The singular forms “a”, “an” and “the” include plural references unless the context clearly dictates otherwise. As used herein, the term “or” is not meant to be exclusive and refers to at least one of the referenced components being present and includes instances in which a combination of the referenced components may be present, unless the context clearly dictates otherwise.
Approximating language, as used herein throughout the specification and claims, may be applied to modify any quantitative representation that could permissibly vary without resulting in a change in the basic function to which it is related. Accordingly, a value modified by a term or terms, such as “about”, and “substantially” are not to be limited to the precise value specified. In some instances, the approximating language may correspond to the precision of an instrument for measuring the value. Here and throughout the specification and claims, range limitations may be combined and/or interchanged; such ranges are identified and include all the sub-ranges contained therein unless context or language indicates otherwise.
As used herein, the term “coating” refers to a material disposed on at least a portion of an underlying surface in a continuous or discontinuous manner. Further, the term “coating” does not necessarily mean a uniform thickness of the disposed material, and the disposed material may have a uniform or a variable thickness. The term “coating” may refer to a single layer of the coating material or may refer to a plurality of layers of the coating material. The coating material may be the same or different in the plurality of layers.
The term coating is not limited by size; the coating-area can be as large as an entire device or as small as a specific functional area. Unless otherwise indicated, coating can be formed by any conventional deposition technique, including vapor deposition, liquid deposition (continuous and discontinuous techniques), and thermal transfer. Continuous deposition techniques, include but are not limited to, spin coating, gravure coating, curtain coating, dip coating, slot-die coating, spray coating, and continuous nozzle coating. Discontinuous deposition techniques include, but are not limited to, ink jet printing, gravure printing, and screen printing.
As used herein, the term “disposed on” refers to layers or coatings disposed directly in contact with each other or indirectly by having intervening layers there between, unless otherwise specifically indicated. The term “depositing on” refers to a method of laying down material in contact with an underlying or adjacent surface in a continuous or discontinuous manner. The term “adjacent” as used herein means that the two materials or coatings are disposed contiguously and are in direct contact with each other.
As used herein, the term “electrically conductive” refers to a material having an electrical conductivity greater than 106 s/m.
As used herein, the term “electrically insulating” refers to a material having an electrical resistivity greater than 1010 Ohm-m.
As used herein the term “electrically insulating filler” refers to a material, for example in a particulate form, which may be added to a binder material to improve the insulation properties of the binder.
As used herein, the term “ceramic”, refers to an inorganic solid including metal, nonmetal or metalloid atoms primarily held in ionic and covalent bonds. The crystallinity of ceramic materials ranges from highly oriented to semi-crystalline, and often completely amorphous (e.g., glasses). In contrast to ceramics, the “ceramifiable polymers” may be broadly defined as inorganic polymers or precursors thereof, which solidify at high temperatures to produce refractory ceramics.
As used herein, the term “non-porous” refers to a coating that is substantially devoid of “pores”, such that the coating can resist penetration of any undesirable material through the coating to contact the surface on which the coating is deposited. For example, a non-porous ceramic coating deposited on a conductor surface can resist oxygen permeation through the coating and protect the conductor surface from oxidizing at high temperature.
As used herein the term “aliphatic radical” refers to an organic radical having a valence of at least one consisting of a linear or branched array of atoms which is not cyclic. Aliphatic radicals are defined to include at least one carbon atom. The array of atoms including the aliphatic radical may include heteroatoms such as nitrogen, sulfur, silicon, selenium and oxygen or may be composed exclusively of carbon and hydrogen. For convenience, the term “aliphatic radical” is defined herein to encompass, as part of the “linear or branched array of atoms which is not cyclic” a wide range of functional groups such as alkyl groups, alkenyl groups, alkynyl groups, haloalkyl groups, conjugated dienyl groups, alcohol groups, ether groups, aldehyde groups, ketone groups, carboxylic acid groups, acyl groups (for example carboxylic acid derivatives such as esters and amides), amine groups, nitro groups, and the like. For example, the 4-methylpent-1-yl radical is a C6 aliphatic radical including a methyl group, the methyl group being a functional group which is an alkyl group. Similarly, the 4-nitrobut-1-yl group is a C4 aliphatic radical including a nitro group, the nitro group being a functional group. An aliphatic radical may be a haloalkyl group which includes one or more halogen atoms which may be the same or different. Halogen atoms include, for example; fluorine, chlorine, bromine, and iodine. Aliphatic radicals including one or more halogen atoms include the alkyl halides trifluoromethyl, bromodifluoromethyl, chlorodifluoromethyl, hexafluoroisopropylidene, chloromethyl, difluorovinylidene, trichloromethyl, bromodichloromethyl, bromoethyl, 2-bromotrimethylene (e.g., —CH2CHBrCH2—), and the like. Further examples of aliphatic radicals include allyl, aminocarbonyl (i.e., —CONH2), carbonyl, 2,2-dicyanoisopropylidene (i.e., —CH2C(CN)2CH2—), methyl (i.e., —CH3), methylene (i.e., —CH2—), ethyl, ethylene, formyl (i.e., —CHO), hexyl, hexamethylene, hydroxymethyl (i.e., —CH2OH), mercaptomethyl (i.e., —CH2SH), methylthio (i.e., —SCH3), methylthiomethyl (i.e., —CH2SCH3), methoxy, methoxycarbonyl (i.e., CH3OCO—), nitromethyl (i.e., —CH2NO2), thiocarbonyl, trimethylsilyl (i.e., (CH3)3Si—), t-butyldimethylsilyl, 3-trimethoxysilylpropyl (i.e., (CH3O)3SiCH2CH2CH2—), vinyl, vinylidene, and the like. By way of further example, a C1-C10 aliphatic radical contains at least one but no more than 10 carbon atoms. A methyl group (i.e., CH3—) is an example of a C1 aliphatic radical. A decyl group (i.e., CH3(CH2)9—) is an example of a C10 aliphatic radical.
As used herein, the term “aromatic radical” refers to an array of atoms having a valence of at least one including at least one aromatic group. The array of atoms having a valence of at least one including at least one aromatic group may include heteroatoms such as nitrogen, sulfur, selenium, silicon and oxygen, or may be composed exclusively of carbon and hydrogen. As used herein, the term “aromatic radical” includes but is not limited to phenyl, pyridyl, furanyl, thienyl, naphthyl, phenylene, and biphenyl radicals. As noted, the aromatic radical contains at least one aromatic group. The aromatic group is invariably a cyclic structure having 4n+2 “delocalized” electrons where “n” is an integer equal to 1 or greater, as illustrated by phenyl groups (n=1), thienyl groups (n=1), furanyl groups (n=1), naphthyl groups (n=2), azulenyl groups (n=2), anthraceneyl groups (n=3) and the like. The aromatic radical may also include nonaromatic components. For example, a benzyl group is an aromatic radical, which includes a phenyl ring (the aromatic group) and a methylene group (the nonaromatic component). Similarly a tetrahydronaphthyl radical is an aromatic radical including an aromatic group (C6H3) fused to a nonaromatic component —(CH2)4—. For convenience, the term “aromatic radical” is defined herein to encompass a wide range of functional groups such as alkyl groups, alkenyl groups, alkynyl groups, haloalkyl groups, haloaromatic groups, conjugated dienyl groups, alcohol groups, ether groups, aldehyde groups, ketone groups, carboxylic acid groups, acyl groups (for example carboxylic acid derivatives such as esters and amides), amine groups, nitro groups, and the like. For example, the 4-methylphenyl radical is a C7 aromatic radical including a methyl group, the methyl group being a functional group which is an alkyl group. Similarly, the 2-nitrophenyl group is a C6 aromatic radical including a nitro group, the nitro group being a functional group. Aromatic radicals include halogenated aromatic radicals such as 4-trifluoromethylphenyl, hexafluoroisopropylidenebis (4-phen-1-yloxy) (i.e., —OPhC(CF3)2PhO—), 4-chloromethylphen-1-yl, 3-trifluorovinyl-2-thienyl, 3-trichloromethylphen-1-yl (i.e., 3-CCl3Ph-), 4-(3-bromoprop-1-yl)phen-1-yl (i.e., 4-BrCH2CH2CH2Ph-), and the like. Further examples of aromatic radicals include 4-allyloxyphen-1-oxy, 4-aminophen-1-yl (i.e., 4-H2NPh-), 3-aminocarbonylphen-1-yl (i.e., NH2COPh-), 4-benzoylphen-1-yl, dicyanomethylidenebis(4-phen-1-yloxy) (i.e., —OPhC(CN)2PhO —), 3-methylphen-1-yl, methylenebis(4-phen-1-yloxy) (i.e., —OPhCH2PhO—), 2-ethylphen-1-yl, phenylethenyl, 3-formyl-2-thienyl, 2-hexyl-5-furanyl, hexamethylene-1,6-bis(4-phen-1-yloxy) (i.e., —OPh(CH2)6PhO—), 4-hydroxymethylphen-1-yl (i.e., 4-HOCH2Ph-), 4-mercaptomethylphen-1-yl (i.e., 4-HSCH2Ph-), 4-methylthiophen-1-yl (i.e., 4-CH3SPh-), 3-methoxyphen-1-yl, 2-methoxycarbonylphen-1-yloxy (e.g., methyl salicyl), 2-nitromethylphen-1-yl (i.e., 2-NO2CH2Ph), 3-trimethylsilylphen-1-yl, 4-t-butyldimethylsilylphenl-1-yl, 4-vinylphen-1-yl, vinylidenebis(phenyl), and the like. The term “a C3-C10 aromatic radical” includes aromatic radicals containing at least three but no more than 10 carbon atoms. The aromatic radical 1-imidazolyl (C3H2N2—) represents a C3 aromatic radical. The benzyl radical (C7H7—) represents a C7 aromatic radical.
In some embodiments an insulated winding is presented. The insulated winding includes two components: an electrically conductive core and a multilayer coating system disposed on the core. In some embodiments, the multilayer coating system is a high temperature insulation coating, which may withstand a temperature of about 350° C. or above, and may be flexible enough for windings used for various systems, such as ESP motors. The multilayer coating may reduce coefficient of thermal expansion (CTE)-mismatch by introducing intervening layers in the coating, which may function as a buffer layer, in some embodiments. The multilayer coating may also improve one or more of adhesion, thermal stress absorption, electrical breakdown voltage, and chemical resistance of the winding, in some embodiments.
In some embodiments, the insulated winding includes (a) an electrically conductive core; (b) an electrically insulating non-porous ceramic coating disposed on the conductive core; and (c) a composite silicone coating including a plurality of electrically insulating filler particles disposed on the ceramic coating. Embodiments of the structure of the insulated winding are described in greater detail hereinafter, and further illustrated in
In some other embodiments, as illustrated in
In some embodiments, the concentration of the plurality of electrically insulating filler particles in at least some of the plurality of composite silicone coatings is different. In some embodiments, the concentration of the plurality of electrically insulating filler particles in each of the plurality of composite silicone coatings is different. In some embodiments, the plurality of electrically insulating filler particles are present in the plurality of composite silicone coating in an amount in a range from about 5 weight percent to about 50 weight percent of the total weight of the respective composite silicone coating.
The insulated winding may further include a silicone coating that is substantially free of the electrically insulating filler particles. The term “substantially free” as used herein refers to a silicone coating that includes the electrically insulating filler particles in an amount less than or equal to about 0.001 weight percent of the total weight of the silicone coating. The silicone coating, which is substantially free of electrically insulating filler particles is referred to herein throughout the text as “silicone coating” to differentiate it from silicone coating including electrically insulating filler particles (referred to herein throughout the text as “composite silicone coating”).
In some embodiments, as shown in
Referring again to
In some other embodiments, a plurality of silicone coatings may be disposed between the ceramic coating 14 and the composite silicone coating 16A (not shown in figures). The plurality of silicone coatings may provide for a thicker silicone coating with improved thermal stability when compared to the stability achieved using a single silicone coating. However, a silicone coating (filler free silicone coating) having a total thickness above 30 μm may not be desirable in some embodiments, as the thicker silicone coating has lower resistance to crack formation during exposure to high temperature steam. Similarly, a plurality of composite silicone coatings may be also disposed on the silicone coating 18, which increases the thickness of the composite silicone coating.
In some other embodiments, as mentioned earlier, and illustrated in
In some embodiments, the composite silicone coating 16A is disposed between two different silicone coatings 18, 24, as shown in
In some embodiments, the insulated winding 26 further includes a protective coating 28, as shown in
As noted earlier, the insulated winding includes an electrically conductive core. The conductive core may include a metal or a metal alloy, non limiting examples of which include, copper, aluminum, nickel, zinc, brass, bronze, iron, silver, gold, platinum, or combinations thereof. In some embodiments, the conductive core includes a copper wire. In some embodiments, the conductive core includes an aluminum wire. The conductive core may be electrically insulated using one or more coatings deposited on the core.
Unlike the conventional electrically insulation systems that typically include only a ceramic layer, only a polymer layer, or only a polymer composite coating, embodiments of the present invention include a multilayered mixed coating system. In some embodiments, the multilayered coating system includes a combination of a ceramic coating and a polymer composite coating, which provide stability as well as flexibility to the insulated winding.
The ceramic coating includes a ceramic material, wherein the ceramic material may be present in an amorphous or a crystalline form, depending upon the composition and the processing temperature of the ceramic material. The ceramic material may include silica, metal silicates, metal oxides, aluminum silicates, aluminum phosphates, magnesium phosphates, or combinations thereof.
In some embodiments, the insulated winding includes a non-porous ceramic coating, wherein the electrically insulating non-porous ceramic coating includes one or more of aluminum phosphates, alkaline earth aluminum phosphates (such as aluminum-magnesium phosphate), or alkali silicates (such as potassium silicate (K2SiO3)). In some embodiments, aluminum-magnesium phosphate may be disposed on the potassium silicate (K2SiO3) coating or vice versa. The ceramic coating may be formed using solutions of phosphate salts, silicates or sol-gel solutions of K2SiO3, aluminum-magnesium phosphate, or a combination of K2SiO3 and aluminum-magnesium phosphate. In certain embodiments, the electrically insulating non-porous ceramic coating includes potassium silicate (K2SiO3). Ceramic coatings including potassium silicate (K2SiO3) may be desirable in a moisture containing environment. In some embodiments, the use of alkaline earth modified aluminum phosphate, such as magnesium aluminum phosphate is desirable for one or more of its high resistivity, low ionic mobility, low oxygen permeability, and better adhesion property.
In some embodiments, the ceramic coating may be in direct contact with the conductive core. The ceramic coating may provide improved adhesion towards the conductive core (for example, copper wire) when compared to conventional insulating coating materials. In embodiments including magnesium aluminum phosphate, the ratio of Mg/Al may vary from 1:4 to 2:1. Without being bound by any theory, it is believed that the magnesium-aluminum (Mg/Al) ratio affects the adhesion of the ceramic coating towards the conductive core, such as copper. The adhesion may increase when the magnesium-aluminum (Mg/Al) ratio is less than or equal to 0.5. Further, the ceramic coating may exhibit improved combination of Cu adhesion and bather to oxygen permeation (e.g., to prevent Cu oxidation) when the Mg/Al ratio is between 1:4 to 1:2. The ceramic coating may provide improved density, which prevents oxidation of conductive core at elevated temperature when magnesium phosphate is mixed in aluminum phosphate sol. Without being bound by any theory it is believed that for Mg/Al ratios between 1:4 and 2:1, and particularly between 1:4 and 1:2, the ceramic coating is amorphous, and hence has a higher degree of flexibility and oxygen/water impermeability, thereby protecting the underlying conductor (e.g., Cu) from oxidation at high temperatures (>300 C).
In some embodiments, the electrically insulating non-porous ceramic coating is substantially chemically unreactive to the electrically conductive core, the composite silicone coating, the silicone coating, the electrically insulating filler particles, or combinations thereof. As used herein, the term “substantially chemically unreactive” means that a degree of chemical reactivity of the non-porous ceramic coating to the conductive core or to the other coating materials is significantly low under both the coating application process and the working condition. The degree of chemical reactivity of the ceramic is significantly low such that the ceramic is non-oxidative in oxygen environment, hydrolytically stable in water environment, and the composition remains substantially unchanged in a hydrocarbon environment. In some embodiments, the non-porous ceramic coating is completely unreactive to the conductive core or to the other coating materials. The chemical inertness (or being completely unreactive) to the core metal conductor (such as Cu) pertains to the fact that the coating forms no reaction products or interfaces that may affect the conductance of the core and/or the insulation properties of the coating. Further, the coating does not react and form products that may enhance oxidation of the core resulting in cracking or spallation of the coatings in service.
The non-porous ceramic coating may form an oxygen impermeable, electrically insulating layer on the conductive core, such as copper (Cu), and prevent oxidation of Cu even at high temperature, in some embodiments. In some embodiments, the ceramic coating may include a complex phosphate composition that provides a barrier to the core for water, oxygen and hydroxyl ion penetrate.
Thickness of the ceramic coating has an impact on the winding characteristics. For example, a thick ceramic coating may improve breakdown voltage of the winding. On the other hand, a thin ceramic coating may provide a flexible winding without generating a large number of cracks. In some embodiments, the thickness of the ceramic coating is in a range from about 0.1 microns to about 10 microns. In some embodiments, the ceramic coating has a thickness in a range from about 1 micron to about 5 microns.
The ceramic coating may provide a desired flexibility for winding process and coil manufacturing in a motor assembly. The wire coated with ceramic coating may bend in a radius of 0.5″ or greater without any crack formation. In one embodiment, the wire coated with ceramic coating may bend to 0.5″ radius with no cracking of ceramic layer.
As noted earlier, the insulated winding further includes a composite silicone coating. The composite silicone coating includes a matrix with a plurality of electrically insulating particles dispersed therein. The matrix includes a silicone resin. In some embodiments, the insulated winding further includes a silicone coating. The silicone coating is substantially free of the filler particles and includes a silicone resin. The silicone resin in the composite silicone coating and the silicone coating may be the same or different.
The silicone resin may include one or more disiloxy units, one or more trisiloxy units, or combinations thereof. In some embodiments, the silicone resin may include a plurality of trisiloxy units. The silicone resin, in some embodiments, is composed of disiloxy units R2SiO2/2, trisiloxy units RSiO3/2, or combinations thereof, wherein R is independently at each occurrence a C1-C10 aliphatic radical or a C5-C30 aromatic radical. In some embodiments, R is independently at each occurrence a methyl group, an ethyl group, 3,3,3-trifluoropropyl group, a phenyl group, or combinations thereof. In one embodiment, R is independently at each occurrence a methyl group or a phenyl group such that one or both of the silicone coating and the composite silicone coating includes a dimethyl silicone, methyl, phenyl silicone, or diphenyl silicone. In one embodiment, the silicone resin includes a plurality of trisiloxy units (such as methyl trisiloxy units and phenyl trisiloxy units) in an amount greater than or equal to about 40 mole percent.
The silicone resin may further include reactive silanol end groups, which are cross linked to each other by an exposure to an elevated temperature. The condensation process is accelerated by catalysts, such as metal salts of carboxylic acids (e.g., Zinc 2-ethylhexanoate). Commercially available methyl-phenyl silicone resins, such as Xiameter RSN-805, Xiameter RSN-806, Xiameter RSN-409 or combination of these three, from Dow Corning, may be used for the coatings. Similar methyl-phenyl silicone resins are also available from Momentive Performance Materials, Wacker and other silicone suppliers. These materials are typically supplied as solutions in organic solvent, such as toluene or xylene. A recently developed Silres™ MSE 100 silicone resin, which is commercially available from Wacker, may be also used as the silicone resin. The cure chemistry of the silicone resin as well as physical properties of the resulting coatings may be controlled by a selection of silicone additives e.g. silanol stopped oligomers, adhesion promoters, type of catalyst, humidity level and temperature of the cure process.
The composite silicone coating, as described earlier, includes a plurality of electrically insulating filler particles. Without being bound by a theory, it is believed that the electrically insulating filler particles may provide improved hydrolytic stability at high temperature and high pressure. In some embodiments, the plurality of electrically insulating filler particles are present in the composite silicone coating in an amount in a range from about 2 weight percent to about 50 weight percent of the composite silicone coating. In some embodiments, the plurality of electrically insulating filler particles are present in the composite silicone coating in an amount in a range from about 10 weight percent to about 50 weight percent of the composite silicone coating.
In some embodiments, the plurality of electrically insulating filler particles includes mica, alumina, silica, titania, alkaline earth titanates, zirconates, aluminates, silicates, calcined talc, steatite, or combinations thereof. In some embodiments, the plurality of electrically insulating filler particles includes mica. Incorporation of the inorganic filler may further improve one or more of mechanical, thermal and electrical properties of the coating, in some embodiments. The high aspect ratio fillers such as mica and talc may be desirable for high voltage applications.
The electrically insulating filler particles may be of different shapes or sizes. Non limiting examples of filler shapes include spherical, elliptical, cuboidal, hemispherical, and platelet. The particle size of the filler particles is represented as “median particle size”. Median values are defined as the value where half of the population resides above this point, and half resides below this point. For particle size distributions this median is called the D50. The electrically insulating filler particles may have a median particle size in a range from about 2 μm to about 100 μm. In one embodiment, the electrically insulating filler particles have a median particle size in a range from about 25 to about 50 μm. The particle size distribution of the electrically insulating filler particles may also be represented by an aspect ratio. In some embodiments, the electrically insulating filler particles have an aspect ratio in a range from about 5 to about 100. In some other embodiments, the electrically insulating filler particles may have an aspect ratio in a range of about 60 to about 100. In certain embodiments, the electrically insulating filler particles have an aspect ratio of about 80.
In some embodiments, the filler particles are dispersed in the silicone resin to enhance the stability of the coating at a high temperature or at a high pressure. In certain embodiments, the mica fillers with median particle size of about 30 μm and an aspect ratio of about 80 may be effective at a loading level of about 10 weight percent to about 50 weight percent. In certain embodiments, the mica-filled composite silicone, with about 30 weight percent mica loading may provide the desired dielectric strength to the composite silicone coating. In certain embodiments, the composite silicone coating may provide a breakdown voltage of greater than 5 KV at a temperature up to 350° C. in the presence of chemical reagents, such as oil and water.
As mentioned earlier, the insulated winding may also include a protective coating, wherein the protective coating may include a glass, a ceramic, or a combination thereof. The protective coating may further include a silicone resin, a silazane resin, or a combination thereof. A glass fiber, glass tape or a ceramic tape impregnated with silicone resin or silazane (such as polysilazane) may be used for the protective coating of the insulated winding.
In some embodiments, the insulated winding can withstand a temperature of about 350° C. or above. Further, the insulated winding may have a breakdown voltage of about 5 kV or above in oil and water environment. Motors used for recovering oil and gas from natural reservoirs using SAGD and geothermal technology may employ insulated windings as described above. In some embodiments, an ESP motor includes a motor stator, wherein the motor stator includes an insulated winding as described herein. The ESP motor including the electrically insulated winding may improve reliability and longer operating life of the pump for SAGD application. In some embodiments, a motor stator includes the insulated winding as described herein, which may enable development of compact ESP systems with high power density for horizontal wells in various applications, such as geothermal and subsea applications.
In some embodiments, a method of making an insulated winding is also presented. In some embodiments, a method of making an insulated winding includes the steps of: (a) disposing a pre-ceramic material on an electrically conductive core to form a green ceramic coating; (b) disposing a composite silicone coating including a plurality of electrically insulating filler particles on the green ceramic coating to form a pre-shaped winding; and (c) heating the pre-shaped winding to substantially cure the pre-ceramic material and form the insulated winding.
The term “green ceramic coating”, as used herein refers to a pre-ceramic stage of a ceramic coating formed by partial reaction of the pre-ceramic material. The term “pre-ceramic” material as used herein refers to materials that are liquid at the application temperature, and can be pyrolyzed at elevated temperatures to form a ceramic material.
The step (a) of the method may include reacting the pre-ceramic material at a temperature less than or equal to 260° C. to form a solid flexible coating. The pre-ceramic coating may provide winding flexibility by disposing a pre-ceramic material on the conductor core (such as, copper wire) followed by transformation at lower temperature (equal to or less than 260° C.) in a pre-ceramic stage such that it is flexible enough for formation of coil into the required shape. In some embodiments, the ceramic coating is pre-cured at 250° C. and post cured at 350° C., instead of reacting at high temperature.
The partial curing at low temperature may allow the pre-ceramic material to maintain a balance between an optimum hardness and flexibility, which is sufficient to form a coil into a desired shape. In some embodiments, the first step (a) may also be performed at a lower temperature of 100° C. to form a flexible pre-ceramic coating having the desired mechanical and adhesion properties.
The method further includes a second step (b), wherein the step (b) includes disposing a composite silicone coating on the green pre-ceramic coating to form a pre-shaped winding. The term “pre-shaped” winding” refers to a shape of the winding which is an immature or incomplete form of the winding. The pre-shaped winding may form as a result of an intermediary step of the method of forming an insulated winding. The step (b) may be performed at a temperature equal to or greater than 200° C., which may lead to the fully cured organic-inorganic hard coating.
In some embodiments, the step (c) includes heating the pre-shaped winding at a temperature in a range from about 250° C. to about 500° C. The pre-shaped winding may be placed into slots in a motor stator for in-situ curing, followed by applying a current to the conductor core to heat the pre-shaped winding to a temperature, which may be in a range from about 250° C. to about 500° C. The pre-shaped winding may be heated to substantially cure and form the insulated winding. The term, “substantially cure” as used herein refers to a curing process such that the elastic modulus of the silicone coating is higher than 90% of the elastic modulus of completely cured silicone coating. During this curing process, greater than or equal to 90% of the pre-ceramic material may be converted to the ceramic stage.
In some embodiments, the method further includes disposing a silicone coating on the green pre-ceramic coating or on the pre-shaped winding. In some embodiments, a plurality of silicone coatings may be deposited on the green pre-ceramic coating or on the pre-shaped winding.
The method may further include encapsulating the insulated winding with a protective coating, wherein the protective coating includes glass, ceramic, or a combination thereof.
The method may involve passing the conductor core, such as the copper wire through different chemical baths and curing stations to build the desired multilayer coating system on the conductor core. The multi-step curing process may allow formation of multilayer coatings with mechanical strength sufficient to survive a wire-manufacturing and desired winding.
This written description uses examples to disclose the invention, including the best mode, and also to enable any person skilled in the art to practice the invention, including making and using any devices or systems and performing any incorporated methods. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal language of the claims.
A coating of methyl-phenyl silicone resin from Dow Corning (Xiameter 0805) was applied with a doctor blade to a piece of copper foil (copper substrate). The coated copper foil was heated to 200° C. for 2 hours to remove solvent and to cross-link the silicone resin through a condensation reaction. The resulting cross-linked silicone coating was 35 micron thick. The breakdown voltage of this coating was measured while submersing the coated copper foil in Clearco STO-50 oil and applying an AC voltage at 500 V/s. The voltage at which breakdown occurred was 5.4±0.3 kVAC. When the coated copper foil was heated to 350° C. in air to measure the AC breakdown voltage, the coated copper foil oxidized and the silicone coating delaminated from the coil.
Aluminum foil coupons (aluminum substrate) were dip coated into a methyl-phenyl silicone resin solution (Xiameter RSN-0805 from Dow Corning) and the coating was dried at 80° C. for 2 hours. A second layer of methyl-phenyl silicone coating was disposed on top of the first layer and the coating was dried at 80° C. for 2 hours. The two-layer coating was cured at 350° C. for 2 hours to remove solvent and to cross-link the silicone. The resulting coating had a thickness in a range from about 16 microns to about 29 microns, and had a breakdown voltage of 3.3±0.6 kVAC at 20° C. and 0.8±0.5 at 350° C. The lower than expected breakdown voltage at 350° C. may be explained by an observed softening of the silicone coating during the 350° C. breakdown measurement.
These results suggest that a thicker coating may be needed to achieve higher breakdown voltages, and perhaps a catalyst may also be needed to completely cure the resin and prevent softening at 350° C.
The example showed silicone coating of thickness above 30 microns on aluminum substrate induces cracking after 24 hours exposure to condensing steam at 120° C. and 14 psi. 4×8×0.016 inch Aluminum coupons (aluminum substrate) were coated with methyl-phenyl silicone resin solution (Xiameter RSN-0805 from Dow Corning) containing 1 wt % of Zinc ethyl hexanoate using 3 mil doctor blade applicator and the resulting coating was partially cured at 250° C. for 20 minutes, and referred here as a first layer. A second layer of methyl-phenyl silicone coating was applied on top of the first layer and the coating was partially cured at 250° C. for 20 minutes. The two-layer coating was completely cured at 350° C. for 2 hours. The resulting coating had a thickness in a range from 20 to 30 microns (for one layer) and from 40 to 50 microns (for two layers). These coatings were subjected to a hydrolytic stability test at 120° C. in a pressure cooker at 14 psi pressure (PCT) for 24 hours. All samples with thickness above 30 micron showed cracking. Room temperature break down voltage of RSN-0805 coating (thickness 22 microns) after PCT was only 1.42 kV AC. These results suggest that a pure RSN-0805 silicone coating with thickness above 30 micron is not resistant to crack formation and cannot achieve break down voltage above 5 kV AC.
To alleviate the issue of copper oxidation, the copper foil was coated with a thin non-porous layer of potassium silicate (K2SiO3), which provided an oxidative bather layer to prevent the oxidation of the copper foil. Copper foil coupons (copper substrate) were dip coated into a KASIL solution and the coating was dried at 95° C. for 1 hour followed by incubation at 260° C. for 1 hour. The coating was cured at 350° C. for 1 hour to network a polymer-like structure. The resulting coating had a thickness in a range from about 1 micron to about 5 microns.
A layer of methyl-phenyl silicone resin (Dow Corning, Xiameter RSN-0805) was disposed on top of the potassium silicate coating and was cured in an oven at 210° C. for 1 hour followed by a thermal conditioning at 350° C. for 2 hours. The protected surface of the copper did not show any signs of oxidation. The resulting silicone coating was 3 to 7 microns thick and had a breakdown voltage of 0.29 kVAC at room temperature and was stable when heated up to 350° C. for 2 hours. In order to achieve a higher AC breakdown voltage the silicone coating thickness was increased.
Several formulations of RSN-0805 resin with different content of mica filler (C-3000) from Imerys were formulated. The mica filler was blended with silicone resin using high shear mixer. The final formulation was degassed for 15 minutes under vacuum. The prepared formulations were applied on 4×8×0.016 inch Aluminum coupons using 7 mil doctor blade. A first layer of RSN-0805 with from 9 to 50 wt % mica was partially cured at 250° C. for 20 minutes. A second layer of RSN-0805 with from 9 to 50 wt % mica was applied on a top of the first layer and the coating was partially cured at 250° C. for 20 minutes. The two layered-coatings were cured at 350° C. for 2 hours. The properties of the resulting two layered-coatings are summarized in Table. 1. No cracking after PCT was observed in any of the studied coatings.
These results suggest that an incorporation of even small amount of mica into RSN-0805 strongly improves resistance to cracking of the final coating. Formulations with the mica content between 17 wt % and 38 wt % showed the best breakdown voltage. However, two layered-coating is not sufficient to reach break down voltage of 5 kV AC.
Formulation of RSN-0805 with 30 wt % of mica was selected for subsequent experiments. Effect of thickness of the individual layer on coating quality was also evaluated using 1 mil, 3 mil, 5 mil, 7 mil, 10 mil and 15 mil doctor blade (DB). The coatings were cured by heating at 350° C. for 2 hrs. The results are presented in Table 2. These results suggest that consistent, good quality coating of RSN-0805 with 30 wt % mica can be obtained only using doctor blade applicators with size 5 mil and below.
Four layered-coatings were applied to flat aluminum 4×8×0.016 inch panels using a procedure described in Example 3. The coating made of two layers of a methyl-phenyl silicone resin (RSN-0805, which is represented by “R” in Table 5) and two layers of the same methyl-phenyl silicone resin filled with 30% by weight mica particles (which is represented by “M” in Table 5). The RSN-0805 (R) layer was applied using 3 mil DB applicator; RSN-0805 with 30 wt % mica (M) was applied using 5 mil DB applicator. The evaluated coating configurations of RMMR (40), MRMR (42) and RMRM (44) on the aluminum substrate are depicted in the schematic in
The cured samples of the coatings on aluminum substrates were exposed to 120° C. condensing steam in a pressure cooker at 14 psi for 24 hours. After this hydrolytic aging, the samples did not show any sign of degradation, delamination or cracking, and maintained their high breakdown voltage when measured at both room temperature and 350° C. These data are listed in Table 3. The results suggest that four layered-coating systems with different configuration of layers and thickness about 120 microns showed good break down voltage performance.
Three layered-coatings of RSN-0805 with 30 wt % mica were applied to flat aluminum 4×8×0.16 inch panels using a procedure described in Example 3. The individual layers were applied using 3 mil and 5 mil DB applicators. The coating configuration with regard to use of DB applicator, such as 5-5-3 (5 mil, 5 mil, 3 mil), 5-3-5 (5 mil, 3 mil, 5 mil), and 3-5-5 (3 mil, 5 mil, 5 mil) are indicated in the Table 4. The cured samples of the coatings were exposed to 120° C. condensing steam in a pressure cooker at 14 psi for 24 hours. After this hydrolytic aging, the samples did not show any sign of degradation, delamination or cracking, and maintained their high breakdown voltage when measured at both room temperature and 350° C. These data are listed in Table 4.
The 4×8×0.016 inch flat copper coupon was coated with a thin ceramic layer, such as a layer of non-porous magnesium aluminum phosphate (represented by P in Table 5), wherein the ratio of Mg/Al was equal to 0.25. The ceramic coating on the copper substrate was generated by dip coating. The coating was partially cured by heating at 200° C. for 2 hrs. Four layered-coating system consisting of three layers of RSN-0805 with 30 wt % mica (M) and one top layer of RSN-0805 (R) was applied to the copper coupon prepared above and to 4×8×0.016 inch aluminum coupon using a procedure described in Example 3. The evaluated coating configurations of P-M-M-M-R (46) on the Cu substrate and M-M-M-R (48) on the aluminum substrate are depicted in the schematic in
While only certain features of the invention have been illustrated and described herein, many modifications and changes will occur to those skilled in the art. It is, therefore, to be understood that the appended claims are intended to cover all such modifications and changes as fall within the true spirit of the invention.
