This disclosure generally relates to coatings for use with fluid energy device components, particularly those components that come into contact with the working fluid.
In some fluid energy devices, such as hydraulic devices, the working fluid flowing through the device during operation is corrosive and/or abrasive. This fluid comes into contact with certain components of the device and can attack, degrade, or otherwise damage component surfaces over time. Hydraulic devices are often used in relatively heavy-duty applications with large and expensive equipment, making reliability important due to the time and costs typically associated with the repair of such equipment and with lost revenue associated with equipment downtime.
In accordance with one or more embodiments, a coated component for use in a fluid energy device includes a component substrate and a hardcoat layer of coating material disposed over the component substrate. The hardcoat layer of coating material has a hardness greater than the hardness of the component substrate. The coated component further includes a softcoat layer of coating material disposed over the hardcoat layer that has a hardness less than the hardness of the hardcoat layer.
In accordance with one or more embodiments, a method of making a coated component for use in a fluid energy device includes the steps of: (a) applying a hardcoat layer of material over a component substrate, the hardcoat layer being harder than the component substrate; and (b) applying a softcoat layer of material over the component substrate so that the softcoat layer interlocks with the hardcoat layer or with an interposed porous interlayer.
In accordance with one or more embodiments, a coated component for use in a fluid energy device includes a coating system coated over a component substrate. The coating system has an interlocking portion that includes a polymeric material in an interlocking arrangement with a metallic material, and the metallic material is harder than the component substrate.
Preferred exemplary embodiments of the invention will hereinafter be described in conjunction with the appended drawings, wherein like designations denote like elements, and wherein:
The coating system described below may be used on fluid energy device components such as rotors and/or stators of fluid motors or pumps. In a fluid motor, fluid pressure is converted to mechanical motion as a working fluid flows therethrough. A fluid pump works similarly, but in reverse, with mechanical motion of one or more pump components pressurizing a fluid as it flows through the pump. For purposes of this description, both are considered fluid energy devices, as each either extracts energy from or imparts energy to the fluid that flows through it. Where the fluid is a liquid, these devices may be referred to as hydraulic devices. While the following description makes reference to hydraulic devices as illustrative examples, the coating system taught herein may be employed with other fluid energy devices, particularly in applications where surface wear and/or corrosion is a concern, such as gerotor pumps, plastics extrusion screws, Archimedes screw pumps, etc. The coating system may also be useful in applications outside of fluid energy devices, such as gears, frictional devices, bearing surfaces, or other applications.
Referring to
In drilling applications, the working fluid may be the same fluid as the drilling fluid that is used to lubricate and cool the drill bit and carry the crushed or cut pieces of earth back to the surface. For example, in the drilling tool of
The hardcoat layer 52 is a layer of material that, even in the absence of layers 54 and 56, increases the wear-resistance and/or the corrosion-resistance of the underlying substrate 45 in the given application. The hardcoat layer 52 is formed from a material having a hardness that is higher than that of the underlying substrate 45. In one embodiment, the substrate 45 is formed from steel or stainless steel, and the hardcoat layer 52 is formed from a material having a hardness greater than the particular substrate steel. Suitable hardcoat layers 52 may be formed from materials that comprise a carbide component, such as tungsten carbide or chromium carbide. In one embodiment, the hardcoat layer 52 comprises a mixture or alloy of tungsten carbide, cobalt, and chromium (WC—Co—Cr). In another embodiment, the hardcoat layer 52 comprises a mixture or alloy of chromium carbide, nickel and chrome (CrC—Ni—Cr). The hardcoat layer 52 may consist essentially of WC—Co—Cr or CrC—Ni—Cr. The hardcoat layer 52 may also be formed from ceramic or other materials with hard particles dispersed within a softer metal binder material.
These illustrative hardcoat layer materials can be applied over the substrate 45 by high-velocity (HV) spraying techniques in which particles of the desired material(s) are projected toward the substrate at speeds sufficiently high to cause the particles to deform or flatten upon impact to form the coating layer. In some HV spraying processes, the particles of material are softened with heat prior to impact. Examples of suitable HV spraying processes include high-velocity oxygen fuel spraying (HVOF), high-velocity air fuel spraying (HVAF), high-velocity plasma spraying (HVP), or detonation gun spraying. The hardcoat layer 52 can be formed from other materials suitable for use in HV spraying processes, such as ceramic materials, cermets, or any of a variety of metals or metal alloys. Other coating processes, such as cold spraying, electroplating, slurry coating, arc spraying, combustion spraying, or plasma spraying processes may be used to apply certain types of hardcoat layers, so long as the hardcoat layer bonds sufficiently with the underlying material and is suitably hard to enhance the wear properties of the surface of the coated component. In fact, when combined with the overlying softcoat layer 54 to form the coating system 50, some materials that were previously disfavored as wear-resistant coating materials, due to overly-rough surface finishes, costly pre-coating processes, or other reasons, may be suitable materials for use in the hardcoat layer 52.
The bond strength between the hardcoat layer 52 and the underlying material is preferably greater than 10,000 psi, but this is not always necessary. The hardcoat layer 52 may also be characterized by a low porosity, which may be most apparent with certain spray application processes like HV spraying processes in which the porosity of the deposited coating layer may be somewhat controllable. The hardcoat layer 52 preferably has a porosity of 1% or less—i.e., the bulk volume of the hardcoat layer is preferably 99% or more solid material. The thickness of the hardcoat layer 52 may be in a range from 0.003 inches to 0.008 inches (3-8 mils). The hardcoat layer 52 can be thicker than 8 mils, provided that the bond strength formed with the underlying material is sufficiently high and/or that other application specific requirements are met. The illustrated hardcoat layer 52 is applied directly to the substrate 45, but there could be one or more interposed layers of material as well.
The softcoat layer 54 is a layer of material that is softer than the hardcoat layer 52. The softcoat layer 54 may also have a hardness that is less than or equal to the hardness of the material of the opposing surface in the given application, which is the inner surface of the stator in the examples in the figures. For example, the softcoat layer 54 may be formed from an organic material, such as a polymeric or a polymer-based material, particularly where the opposing stator surface is polymeric and/or elastomeric. In one embodiment, the softcoat layer 54 is formed from a material having a hardness of 75 or less on the Shore A scale. In another embodiment, the softcoat layer 54 is formed from a material having a hardness of 50 or less on the Shore A scale. The softcoat layer 54 may thus be considered at least partly sacrificial in nature as the first material to wear away during component operation.
The softcoat layer 54 may serve to protect the inner surface of the stator during the initial stages of operation—i.e., when the rotor 14 is first put into service. For example, with the hardcoat layer 52 alone, the outer surface of the rotor may be a very rough surface, especially when applied via an HV spraying process with no further surface treatment thereafter. Combined with the relative hardness of the hardcoat layer material, this rough outer surface can quickly damage the soft inner surface of the mating stator. It has been found that without the softcoat layer 54, the hardcoat layer requires additional post-coating treatment, such as a meticulous polishing operation, to smooth the surface enough to prevent extensive stator damage. For example, a rotor with a hardcoat layer alone may require polishing down to a surface roughness in the range of 10 rms or less to prevent damage to the mating elastomeric stator. The relative hardness of the hardcoat material and the complex contours of the rotor lobes can make such a polishing operation accordingly more difficult, expensive, and time-consuming, often requiring diamond-based polishes. The softcoat layer 54 can allow the rotor to have a hardcoat layer 52 sufficient to increase the wear performance of the rotor over time without the need for expensive and time-consuming secondary operations like polishing to smooth the hardcoat layer. The manner in which this combination of hard and soft layers functions will be subsequently described in greater detail.
Suitable softcoat layer 54 materials include nearly any thermoplastic or thermoset polymeric material. It may be preferred that the softcoat layer 54 include one or more polymeric materials with a low coefficient of friction and/or high wear-resistance. Polytetrafluoroethylene (PTFE) or other fluorinated polymers along with their copolymers and alloys are examples of suitable polymeric materials for use in the softcoat layer. Such low friction polymeric materials may be the major component of the finished softcoat layer 54, or they may be less than half of the finished softcoat layer composition with an organic binder component such as a cured or curable polymer in which the low friction material is distributed. The softcoat layer 54 material is preferably applied in liquid form so that it can penetrate any porosity present in the underlying layer(s). For example, the softcoat layer material may be applied as part of a liquid solution or suspension, either organic solvent-based or water-based, with a viscosity sufficiently low to allow penetration into the porosity of the underlying layer. The applied liquid material can form the softcoat layer 54 when the solvent or carrier liquid evaporates and/or reacts with some other component of the applied liquid or the surrounding atmosphere during a curing step. The application process may be similar to a painting process where a thin and relatively low viscosity layer of material is applied and allowed to dry and/or cure.
In one particular embodiment, the softcoat layer 54 is applied in liquid form, and the liquid material includes a friction reducer, such as a fluoropolymer (e.g., PTFE, PEF, PFA, ETFE, etc.), and a curable binder material. The applied liquid is flash dried to remove solvent, then allowed the cure or heated to cure. During the curing step, the binder material and the friction reducer may at least partly stratify or separate from one another. In other words, the friction reducer may migrate toward the outer surface 36. Where the applied material includes a fluoropolymer friction reducer, the fluoropolymer may be sintered during the curing step. The softcoat layer 54 thus may include primarily fluoropolymer at the finished outer surface 36 and primarily binder material nearest the underlying material layer(s).
Additives may be included in the softcoat layer 54 during application, such as a polymer binder, curing agent, a surfactant or wetting agent, friction reducers, high-wear additives, etc. Examples of friction reducers besides fluoropolymers include molybdenum disulfide, or any other materials commonly used in thin film lubricant applications (e.g., silver, bronze, nanoparticles, etc.). Whether the softcoat layer 54 is polymer-based or not, it is preferably corrosion-resistant, hydrophobic, and oleophobic and can be applied and cured at a temperature of 1000° F. or less, and preferably at a temperature between 500° F. and 800° F. Some polymeric materials may be formulated to cure without heat, such as reactive polymer systems, air-cure, or UV-cure materials. Other non-organic materials may be used as the softcoat layer in some instances, such as certain cermet materials and nanocoatings.
Depending on whether the interlayer 56 is included between the hardcoat and softcoat layers 52, 54, the thickness of the softcoat layer 54 is preferably in a range from 0 to 0.0015 inches (0-1.5 mils), which includes its depth of penetration into the underlying layer. For example, depending on the surface roughness of the layer over which the softcoat layer 54 is directly applied, the softcoat layer may have discontinuities where roughness peaks from the underlying layer are present, defining areas of zero thickness for the softcoat layer. The final thickness of the softcoat layer 54 may preferably be minimized so that it penetrates the pores and fills in between roughness peaks in the underlying layer of material. Thus, at the outer surface 36, the softcoat layer 54 may be a discontinuous layer. In at least this manner, the softcoat layer and the underlying hardcoat layer 52 or interlayer 56 may be mutually beneficial. For instance, the softcoat layer 54 helps reduce the otherwise harsh effect of the roughness peaks of the underlying layer, and the harder underlying layer locks the softcoat layer in place so that the softcoat layer is more than simply a continuous overlying layer in sheet form that could easily be peeled away.
The coating system 50 preferably includes the interlayer 56 between the hardcoat and softcoat layers 52, 54, as depicted in
The interlayer 56 is preferably formed from the same type of material and with the same type of application process as the hardcoat layer 52, but this is not necessary. The interlayer 56 could be the same type of material as the hardcoat layer material but applied by a different process, a different type of material applied by the same process, or a different type of material applied by a different process. The interlayer 56 material should generally meet the same criteria for bond strength and hardness as the hardcoat layer 52 material. In one embodiment, the interlayer 56 is formed from the same material as the hardcoat layer 52 using the same coating process, and the porosity of the interlayer is higher than the porosity of the hardcoat layer. For example, both the hardcoat layer 52 and the interlayer 56 may be formed from a material comprising a carbide component (e.g., WC—Co—Cr or CrC—Ni—Cr) by an HV spraying process, where the process is adjusted to increase the porosity of the applied material after the desired hardcoat layer thickness 52 is achieved. In another example, the hardcoat layer 52 is an HV-sprayed layer comprising or consisting of tungsten carbide, and the interlayer 56 is a plasma-sprayed ceramic layer. Non-HV spraying methods may be more suitable for the interlayer 56 than for the hardcoat layer 52 in some cases due to the higher porosity achieved by non-HV spraying.
The interlayer 56 may range in thickness from 0.0005 inches to 0.002 inches (0.5-2.0 mils). In one embodiment, the interlayer has a thickness that is from 5% to 25% of the thickness of the hardcoat layer. In another embodiment, the hardcoat layer 52 and the interlayer 56 are the same type of material and may be described together as a hard layer of material with the outer 5-20% of the hard layer of material being more porous than the inner 80-95%. The combined thickness of the interlayer 56 and the overlying softcoat layer 54 may range from 0.00075 inches to 0.001 inches (0.75-1 mils). Thus, where the interlayer 56 is present, the thickness of the portion of the softcoat material layer lying on top of or over the interlayer may range from 0 to 0.0005 inches (0-0.5 mils). These are of course only illustrative thickness ranges, as individual layer thicknesses may vary depending on the material type or other factors.
After application of the softcoat layer 54, the roughness parameter Ra of the coated component is preferably 50 or lower, and the roughness parameter of the surface underlying the softcoat layer is higher than 50. In one embodiment, the application of the softcoat layer reduces the roughness parameter of the coated component by 140-160. Another embodiment includes adjusting the roughness of the coating system during application of the softcoat layer 54. For example, the softcoat layer may be partially applied, then subjected to a roughness adjustment to bring the roughness parameter down into a desired range prior to finishing the application of the softcoat layer. In one particular example, a liquid polymer-based coating material is applied over the interlayer 56. The liquid coating includes additives such as PTFE, moly, or other additives that can be lightly abraded without losing integrity. The liquid coating is applied in multiple coats. One to three light coats may be applied before allowing the liquid to flash dry at a temperature of about 200-300° F. to bring the applied material to a workable state—not necessarily fully cured, but with sufficient integrity to withstand light abrasion treatment. The surface roughness may be measured at this stage of the process. If the roughness is sufficiently high that the remaining softcoat layer material will likely not bring the roughness parameter down into the desired final range, then the surface of the coated component may be lightly sanded or abraded before the remainder of the softcoat layer material is applied. For example, if the partially-coated interlayer has a roughness parameter in a range from about 80-150 higher than the desired final roughness parameter, a roughness adjustment may be performed. In one particular example, the partially-coated interlayer is abraded until it is 20-40 points higher than the desired final roughness. This step can serve to smooth the peaks of carbide or other hard interlayer particles as well as polymer particles that may be present due to dry spray. Then, an additional one to three light coats of the liquid polymer material can be applied to the desired final thickness, flash-dried, and cured. The curing step may occur at a temperature higher than the flash-drying steps.
The interlocking portion 60 of the coating system is thus characterized by a mixture of hard and soft regions that can advantageously enhance the service life of fluid energy device components like mud rotors. By way of illustration,
In this controlled-wear configuration, the wear-resistance of the coated component actually increases as coating material is worn away. In addition, the above-described coating system can allow the abrasiveness of the working fluid, such as drilling mud, to be used advantageously to polish or smooth the hard portions of the coating system during use and in a controlled manner, thereby eliminating the need to polish an applied hard coating in a way that protects the opposing device surface, such as the stator inner surface. In other words, while an abrasive working fluid could be used on a hardcoat layer alone to smooth or polish the outer surface of the rotor during use, the soft inner surface of the mating stator would be substantially damaged in the time required to sufficiently smooth the rotor surface. The more gradual exposure of the harder layers of material at the rotor surface depicted in
The softcoat layer material also fills the space in between the hard, sharp peaks of the rough surface of the harder underlying material so that the outer surface of the rotor is more continuous and the hard peaks cannot dig into the stator material. This more continuous rotor outer surface also allows for a higher quality seal between the rotor and stator, thereby providing for more efficient pump or motor operation, particularly during the initial stages of service. The softcoat layer material can also provide lubricity via polymer material composition (e.g., PTFE) or additives, providing smoother and cooler operation due to lower friction between the rotor and stator surfaces. This lower friction condition can allow for more efficient device operation that results in reduced energy loss when powering the device and/or during device start-up after an idle time. In addition, filling the porous portion of the harder underlying layers with corrosion-resistant softcoat layer material can reduce or eliminate the sub-surface corrosion sites to better protect the coating system from corrosion by the working fluid.
It is to be understood that the foregoing is a description of one or more preferred exemplary embodiments of the invention. The invention is not limited to the particular embodiment(s) disclosed herein, but rather is defined solely by the claims below. Furthermore, the statements contained in the foregoing description relate to particular embodiments and are not to be construed as limitations on the scope of the invention or on the definition of terms used in the claims, except where a term or phrase is expressly defined above. Various other embodiments and various changes and modifications to the disclosed embodiment(s) will become apparent to those skilled in the art. All such other embodiments, changes, and modifications are intended to come within the scope of the appended claims.
As used in this specification and claims, the terms “for example,” “e.g.,” “for instance,” “such as,” and “like,” and the verbs “comprising,” “having,” “including,” and their other verb forms, when used in conjunction with a listing of one or more components or other items, are each to be construed as open-ended, meaning that that the listing is not to be considered as excluding other, additional components or items. Other terms are to be construed using their broadest reasonable meaning unless they are used in a context that requires a different interpretation.
This application claims the benefit of U.S. Provisional Patent Application No. 61/692,993 filed Aug. 24, 2012, the entire contents of which are hereby incorporated by reference.
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Number | Date | Country | |
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20140054091 A1 | Feb 2014 | US |
Number | Date | Country | |
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61692993 | Aug 2012 | US |