Many articles used in industry are exposed to harsh environments. For example, tools used in a wellbore or other downhole environment in the drilling industry are often exposed to corrosive fluids, which may cause hard scales of inorganic or organic compounds such as CaCO3, BaSO4, CaSO4, SrSO4, and asphaltene to build up on the surfaces of the articles. These compounds may, for example, exist in the form of colloidal dispersions stabilized by other components in the subsurface fluid. They will often precipitate upon pressure, temperature, and compositional changes in the oil resulting from blending or other mechanical or physicochemical processing. Such precipitation occurs in pipelines, separators, and other equipment. Once deposited, scales can interfere with the normal function of the articles and cause disruption to the system and/or process in which the articles are used and may necessitate repairs or replacements. Exploration and production companies presently use remediation tools, such as abrasive jets and mechanical tools, to remove the scales. However, the techniques require costly well intervention, add up to non-productive time, and are sometimes not feasible. Accordingly, an alternative method of preventing scale-related fouling or lengthening equipment uptime through scale minimization is continuously sought.
Disclosed herein is a scale-inhibiting coating a coating applied to a substrate. The coating comprises a diamond-like carbon structure doped with a dopant. The coating includes the dopant at a concentration of between about 10 and about 40 atomic percent.
Also disclosed herein is a scale-inhibiting coating deposited on one or more surfaces of the article. The coating comprises a diamond-like carbon structure doped with a dopant. The coating includes the dopant at a concentration of between about 10 and about 40 atomic percent.
The following descriptions should not be considered limiting in any way. With reference to the accompanying drawings, like elements are numbered alike:
A detailed description of one or more embodiments of the disclosed apparatus and method are presented herein by way of exemplification and not limitation with reference to the Figures. It is to be understood that other embodiments may be utilized and changes may be made without departing from the scope of the present disclosure. In particular, the disclosure provides various examples related to a subsurface safety valve, whereas the advantages of the present disclosure as applied to other devices or to devices in a related field would be apparent to one having ordinary skill in the art and are considered to be within the scope of the present invention.
Referring to
The coating 100 of the present disclosure inhibits scaling that typically results from prolonged exposure to circulating fluids, including hydrocarbons and other subsurface fluids, such as water or a brine obtained from a well. As used herein, the term “scaling” shall be inclusive all forms of deposits that accumulate on the surface 105 of an article 110 due to compounds contained in the subsurface fluid, including those deposits which could potentially restrict the flow of fluid across the associated surface 105.
The coating 100 comprises an outer surface 115, opposite the substrate, that is hydrophobic. The coating 100 may exhibit other advantageous qualities. In some embodiments, this includes treating the outer surface 115 of the coating 100 to be oleophobic as well as hydrophobic. The coating 100 of the present disclosure is also resistant to abrasion and very durable in the presence of subsurface fluids. These qualities of abrasion-resistance and durability ensure that the article will continue to perform over the intended lifespan of the article. The coating 100 of the present disclosure inhibits scaling that typically results from prolonged exposure to circulating fluids, including hydrocarbons and other subsurface fluids, such as water or a brine obtained from a well.
The coating 100 of the present disclosure comprises a diamond-like carbon structure 120 that is doped with a dopant. Diamond-like carbon, also known as amorphous carbon, is termed “diamond-like carbon” because it exhibits many of the properties of diamond, including tribological properties. The diamond-like carbon structure 120 of the present disclosure is formed having an amorphous crystalline structure. For example, the diamond-like carbon structure 120 contains both sp2 bonds, (similar to the planar bonds found in graphite), and sp3 bonds, (similar to the tetrahedral bonds found in diamond). In some embodiments, the diamond-like carbon structure 120 contains between about 60 percent and about 90 percent of sp2 bonded carbon.
The inclusion of the dopant in the diamond-like carbon structure 120 enhances the properties of the diamond-like structure in inhibiting scaling. For example, the inclusion of fluorine or silicon as a dopant significantly increases the hydrophobicity of the coating 100. Other dopants can be included which enable the coating 100 to bond to the surface 105 of the article 110. For example, the dopant may be selected to include a material to match the resulting thermal expansion of the coating 100 to the thermal expansion of the article 110 over a selected temperature range. In various embodiments the dopant may comprise a metal or metalloid element, such as silicon, titanium, chromium, fluorine, oxygen, or a mixture of these. The dopant may further include other metals to improve the adhesion and/or the performance of the coating 100. The diamond-like carbon structure 120 may contain the dopant at a concentration of between about 10 to about 40 atomic percent. In one embodiment, the dopant comprises about 30 atomic percent of the coating 100. The distribution of the dopant within the diamond-like carbon structure 120 may further enhance the properties of the coating 100. Applicants have found that a coating comprising an amorphous diamond like carbon doped with 10 to 40 atomic percent of Si (silicon), O (oxygen), F (fluorine), or a combination comprising at least one of the foregoing can significantly increase the hydrophobicity and oleophobicity of a surface. For example, the coating increased the hydrophobicity of a steel surface by about 33% (from 70 degrees to 93 degrees).
Moreover, unlike other available hydrophobic/oleophobic coatings such as fluoropolymer, fluoropolymer containing composites and graphite-MoS2, the coating comprising an amorphous diamond like carbon doped with 10 to 40 atomic percent of Si, O (oxygen), F, or a combination comprising at least one of the foregoing has good corrosion resistance. For example, in a laboratory test the coating's chemical and mechanical properties remain intact after the aging is conducted at 300° F./1000 psi in 3% KCl brine, whereas those of fluoropolymer noticeably degraded.
In addition to a doped diamond-like carbon structure 120, a low surface energy material can also be coated on a textured surface described herein. Low surface energy materials include fluoropolymers, silicones, ceramic, fluoropolymer containing composites, or combinations comprising at least one of the foregoing. Exemplary low surface energy materials include polytetrafluoroethylene with or without reinforcements, polydimethylsiloxane, graphite/MoS2 type ceramic materials, and metal-PTFE composites. The low surface energy material can be applied to the textured surface by any method known in the art, for example, by spray coating, dip-coating, thermal evaporation coating or electrolytic or electroless coating techniques. Fluoropolymer are materials containing multiple carbon-fluorine bonds. Typical examples of commercial fluoropolymer are polytetrafluoroethylene, fluorinated ethylene propylene, and perfluoroalkoxy.
The diamond-like carbon structure 120 may be applied directly to the surface 105 of the article 110. Alternatively, a bonding layer 125 may be formed beneath the diamond-like carbon structure 120, adjacent to the surface 105 of the article to reduce the internal stresses on the diamond-like carbon structure 120. The bonding layer 125 may comprise, for example, pure chromium, a silicon-metal, or another substance or mixture of elements that is advantageous for a particular application. The thickness of the bonding layer 125 may be between about 0.05 microns and about 0.5 microns. The bonding layer 125 may be applied using physical vapor deposition (PVD), chemical vapor deposition (CVD), plasma-enhanced chemical vapor deposition, cold spray, or another technique known in the art.
The surface 105 of the article 110 or the surface of the bonding layer 125 may further be formed into a textured surface 130 to enhance the bonding with the diamond-like carbon structure 120. The coating can be applied to a textured surface 130 having micro-meter size structures or micro and nano-meter size structures. Applicants have found that when the coating is applied to a surface having certain textures, the hydrophobicity and the oleophobicity of the coating can be greatly increased. For example, surface textures can increase the hydrophobicity of the coating by greater than 30%, greater than 40%, or even greater than 50%, as determined by comparing the contact angle of water with the coating on a surface without any texture and the contact angle of water with the same coating on a surface having textures. Further, the water and oil roll-off angles of the coating on the textured surface can also be lower as compared to the same coating applied on a surface without texture.
The textured surface 130 may comprise a micro texture, a micro-nano texture, or a combination of a micro texture and a micro-nano texture. As used herein, a “micro texture” refers to a texture having micro-meter size structural features. A “micro-nano texture” refers to a texture having nano-meter size structural features superimposed on micro-meter size structural features. The micro and micro-nano texturing is provided in the form of periodic and/or non-periodic arrays of micro- and nano-meter size protrusions, holes, particles, pits, grooves, trenches, pillars, peaks, craters, cones, bumps, or other surface features. The textured surface 130 may be formed, for example, by chemical etching, laser ablation, sand-blasting, or another method as desired. Alternatively, the textured surface 130 may be formed by sputtering a material or nanostructure onto the textured surface 130.
The coating 100 may be formed using a variety of processes. These include, for example, physical vapor deposition (PVD), chemical vapor deposition (CVD), plasma-enhanced chemical vapor deposition, primary ion beam deposition of carbon ions (IBD), closed field unbalanced magnetron sputtering, and other methods known in the art and currently being developed.
In some embodiments, depositing the diamond-like carbon structure 120 comprises vapor deposition. A “vapor deposition” process refers to a process of depositing materials on a substrate through the vapor phase. Vapor deposition processes include physical vapor deposition and chemical vapor deposition. Different variations of physical deposition and chemical deposition can be used. Exemplary deposition processes can include plasma assisted chemical vapor deposition, sputtering, ion beam deposition, laser ablation, or thermal evaporation. In an embodiment, the doped amorphous carbon is deposited by plasma ion immersion implantation and deposition. The gaseous medium for the vapor deposition can be 100% hexamethyldisiloxane or a mixture of tetramethylsilane and C2H2 gases for Si or a combination of Si and O (oxygen) doped amorphous diamond like carbon. For fluorine doped amorphous diamond like carbon, the gaseous medium is a mixture of C2H2 and C2F4 gases. Alternatively, the dopant is supplied in a compound, such as an oxide, a nitride, or a chloride compound.
The coating 100 may be applied with the diamond-like carbon and the dopant supplied in the same stream. Alternatively, the dopant may be applied intermittently during the process. Where necessary, such as where the material is provided in aggregate form, the diamond-like carbon and dopant will need to be mixed in order to ensure a largely homogenous structure. Different byproducts formed depend upon the constituents used to supply the carbon and the dopant. Some other elements may also be incorporated into the structure. For example, the diamond-like carbon structure 120 of the present disclosure may contain hydrogen. Hydrogen may be included in the structure at a concentration of between about 10% and about 25% by atom.
The diamond-like carbon structure 120 may also be manipulated using heat and/or pressure during and/or after the application process. The application of high pressures and heat is used to further enhance the properties of the coating 100 by influencing the ratio of sp2 and sp3 bonds. Typically, the application of pressure increases the number of sp3 bonds. The presence of silicon may also increase the number of sp3 bonds. Diamond-like carbon structures with a high ratio of sp3 bonds are known to have a lower surface energy. Other properties, however, including hydrophobicity, hardness, smoothness, and contact angle hysteresis also significantly influence the ability of the coating 100 to inhibit scaling. For example, in some embodiments, the resulting coating 100 has a contact angle hysteresis of less than or equal to about 10°. This property is affected by the composition of the dopant, the crystallization structure, (the ratio of sp2 and sp3 bonds), and may be negatively affected by roughness on the outer surface 115.
In one embodiment of the present disclosure, the coating 100 is formed with a silicon dopant at a concentration by atom of about 30%. The coating 100 also contains some hydrogen. The diamond-like carbon structure 120 is processed using heat and pressure to contain between about 60% and about 90% sp2 bonded carbon. The structure contains between about 10% and about 40% sp3 bonded carbon. The resulting coating 100 is durable and abrasion-resistant. The coating 100 of this embodiment is also successful at inhibiting the formation of scales in the presence of subsurface fluids, such as hydrocarbons.
In some embodiments, the coating 100 is formed having a thickness of about 15 microns or less, or of about 10 microns or less. Larger thicknesses are also possible, but may in some instances require the reconfiguration of the article 110 to account for the thickness of the coating 100.
The coating 100 can be applied selectively to a surface of an article, to an entire article, or to a plurality of articles forming an apparatus or system. In the production of hydrocarbons this may include, for example, a subsurface safety valve, a flow control valve, a production tubing, a biasing member, or a sleeve. The coating can be applied to internal, external, or both the internal and the external surfaces of articles such as the inner wall tube, pipe, safety valve, or flow control valves as an anti-scale, anti-deposition, low-friction, and/or anti-corrosion coating. In an embodiment, a coated article comprises the doped amorphous diamond like carbon disposed on an un-textured or textured surface of the article.
The flow tube 205, or a mandrel connected to the flow tube 205, may form a chamber 220 against an inside of the housing 210. A force-transmitting member 225, which may be a radially extending flange or an extension of the mandrel, divides the chamber 220. A biasing member 230, such as a spring, resides in the chamber 220 between the force-transmitting member 225 and the housing 210.
Various components used in the production of subsurface fluids, including the various components of the subsurface safety valve 200 of
The advantages of the coating described herein further provide advantages in functionality. Various components of the subsurface safety valve 200 are subject to scaling. For example, scaling may occur in the chamber 220 and on the biasing member 230, interfering with the fail-safe function of these components. These components are exemplary of many others used in the production of subsurface fluids in that the chamber 220 and the biasing member 230 would be difficult to access even during intervention. Thus, the application of the coating described above to one or more of the surfaces of these components preserves the functionality of the subsurface safety valve 200. The coating may further be applied to additional surfaces of the subsurface safety valve 200 as well as any other component where scaling may occur.
While the invention has been described with reference to an exemplary embodiment or embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from the essential scope thereof. Also, in the drawings and the description, there have been disclosed exemplary embodiments of the invention and, although specific terms may have been employed, they are unless otherwise stated used in a generic and descriptive sense only and not for purposes of limitation, the scope of the invention therefore not being so limited. Moreover, the use of the terms first, second, etc., do not denote any order or importance, but rather the terms first, second, etc. are used to distinguish one element from another. Furthermore, the use of the terms a, an, etc. do not denote a limitation of quantity, but rather denote the presence of at least one of the referenced item.
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Number | Date | Country | |
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20150147495 A1 | May 2015 | US |