This disclosure includes coatings for increasing the physical and/or chemical properties of articles, for example, tubular metal articles such as those found in the oil and gas industry, as well as processes for making such coatings and articles comprising such coatings.
This disclosure describes coatings comprising nanolaminates that may be applied to articles, including steels and polymeric substrates for example, to improve their physical and/or chemical properties. Processes for making such coatings and articles comprising such coatings are also disclosed. Embodiments of this disclosure include tubular articles comprising such coatings, for example, tubular materials used in the oil and gas industry such as casings, drill pipes and the like.
Electrodeposited nanolaminate coatings are provided to improve one or more properties of materials, including tubular materials and in particular tubular materials comprising iron based alloys. Embodiments disclosed herein include the use of nanolaminate coatings comprising nickel and cobalt to improve the properties of tubular items such as those used in oil and gas drilling and production (e.g., goods, such as casings, drill pipe, and the like). Other embodiments of the coated articles comprise tubular materials made from non-metallic materials such as plastics, ceramics, polymeric composites, etc.
“Laminate” or “laminated” as used herein refers to materials that comprise a series of layers, including nanolaminated materials.
“Nanolaminate” or “nanolaminated” as used herein refers to materials or coatings that comprise a series of layers less than 1 micron.
Percentages, unless stated otherwise, are percentage by weight.
The articles that can be improved by the coatings of this disclosure include conductive metallic and non-metallic substrates, including especially conductive metallic and non-metallic tubular articles such as those used in oil and gas drilling and production, e.g., goods, casings, drill pipe, and the like, including such products made from steel and also from polymer composite materials such as m-Pipe™, a polymer-carbon fiber composite made from PEEK polymer (produced by Magma).
In embodiments, conductive articles may comprise a conductive or non-conductive polymeric composition and may comprise one or more metals or non-metallic conductive materials added to the polymers (e.g., before or after curing) that render the composition conductive or more conductive. Examples of conductive, non-metallic materials that can be added to polymers to increase conductivity are carbon black, graphene, graphite, carbon nanotubes, carbon nanofibers, or graphite fibers, which can be added to the polymers alone or in combination with conductive metallic materials.
A variety of conductive polymeric materials can thus be used to prepare articles having improved properties according to this disclosure, including tubular articles.
The composition comprising a metal that is electrodeposited onto the article may vary in its constituent metals. In some embodiments, the composition comprises one or more, two or more, three or more, or four or more different metals independently selected from Ag, Al, Au, Be, Co, Cr, Cu, Fe, Hg, In, Mg, Mn, Mo, Nb, Nd, Ni, Pd, Pt, Re, Rh, Sb, Sn, Mn, Pb, Ta, Ti, W, V, Zn and Zr, wherein each of said independently selected metals is present at greater than 0.1, 0.05, 0.01, 0.005 or 0.001% by weight. In such embodiments, compositions of two or more different metals that can be electrodeposited comprise, for example, Zn and Fe, Zn and Ni, Co and Ni, Ni and Fe, Ni and Cr, Ni and Al, Cu and Zn, or Cu and Sn.
In some embodiments, the composition electrodeposited onto the article comprises a structurally and/or compositionally modulated electrodeposited material or composition. The structurally and/or compositionally modulated composition may comprise at least one portion having a plurality of layers deposited with wavelengths between about 1 nm and about 250 nm, about 1 nm and about 25 nm, about 5 nm and about 50 nm, about 10 nm and about 75 nm, about 1 nm and about 100 nm, about 2 nm and about 200 nm, about 5 nm and about 225 nm, about 10 nm and about 250 nm.
In other embodiments, the structurally and/or compositionally modulated material has at least one portion consisting of a plurality of layers, wherein each of said layers has a thickness in a range selected independently from about 5 nm to about 250 nm, from about 5 nm to about 25 nm, from about 10 nm to about 30 nm, from about 30 nm to about 60 nm, from about 40 nm to about 80 nm, from about 75 nm to about 100 nm, from about 100 nm to about 120 nm, from about 120 nm to about 140 nm, from about 140 nm to about 180 nm, from about 180 nm to about 200 nm, from about 200 nm to about 225 nm, from about 220 nm to about 250 nm, or from about 150 nm to about 250 nm.
Multilayer nanolaminate coatings may comprise a large number of layers. The coatings may comprise two or more, three or more, four or more, six or more, eight or more, ten or more, twenty or more, forty or more, fifty or more, 100 or more, 200 or more, 500 or more, 1,000 or more, 1,500 or more, 2,000 or more, 2,500 or more, 3,000 or more, 3,500 or more, 4,000 or more, 5,000 or more, 6,000 or more, 7,000 or more, or 8,000 or more layers (e.g., first and second layers each counted separately as a layer). The number of layers may be independently selected for each nanolaminate coating present on different portions of an article (e.g., the inside and outside of a pipe may have different coatings applied). The overall number of layers in a coating may also be in a range from about 100 to about 8,000, from about 50 to about 100, from about 100 to about 1,000, from about 1,000 to about 2,000, from about 2,000 to about 4,000, from about 4,000 to about 8,000 layers, or greater than about 8,000 layers.
The overall thickness of the nanolaminate coatings may vary widely depending on the application of the coatings. In some embodiments, the coatings may have a thickness in a range selected independently from 1 micron to 5 cm, from 1 micron to 50 microns, from 50 microns to 100 microns, from 100 microns to 200 microns, from 200 microns to 500 microns, from 500 microns to 800 microns, from 800 microns to 1.2 mm, from 500 microns to 1 mm, from 1 mm to 1.5 mm, from 1.2 mm to 2 mm, from 1.8 mm to 2.5 mm, from 2 mm to 3 mm, from 2.5 mm to 5 mm, from 1 mm to 5 mm, from 5 mm to 1 cm, from 1 cm to 2 cm, or from 2 cm to 5 cm.
As described above, where the electrodeposited material comprises two or more structurally and/or compositionally different layers, the layers may have discrete or diffuse interfaces or combinations of discrete and diffuse interfaces.
In embodiments where the electrodeposited material comprises two or more structurally and/or compositionally different layers, the composition may comprise a plurality of alternating first layers and second layers. The coating of electrodeposited material may consist entirely of the alternating first and second layers, which may have discrete or diffuse interfaces between the layers or. Alternatively, one or more additional layers may be present in the coating between any first and second layer. The first and second layers may be the same throughout or may themselves change in composition and/or structure, and the interfaces (e.g., discrete or diffuse), may change from layer to layer or between groups of layers.
In embodiments described herein, nanolaminate coatings for improving the properties of articles and goods, including those used in oil and gas well drilling and production, may comprise multilayer coatings comprising nickel and cobalt. In some embodiments, a plurality of alternating first layers of nickel or an alloy comprising nickel, and second layers of an alloy comprising nickel and cobalt are combined to form a coated article. Other layers may be included in addition to the first and second layers.
In some embodiments, first layers each may comprise an amount of nickel greater than about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99%. For all such first layers, the amount of nickel in each layer is independently selected and may be varied from layer to layer or among groups of layers. In some embodiments, each first layer comprises nickel in a range selected independently from 50%-55%, 55%-60%, 60%-65%, 65%-70%, 70%-75%, 75%-80%, 80%-85%, 85%-90%, 90%-92%, 92%-93%, 93%-94%, 94%-95%, 95%-96%, 96%-97%, 97%-98% or 98%-99%, and the balance or the substantial part of the balance of the layer may comprise cobalt. In other embodiments, each first layer comprises nickel in a range selected independently from 70%-99%, 70%-75%, 75%-80%, 80%-85%, 85%-90%, 90%-92%, 92%-93%, 93%-94%, 94%-95%, 95%-96%, 96%-97%, 97%-98% or 98%-99%, and the balance or the substantial part of the balance of the layer may comprise cobalt. In still other embodiments, each first layer comprises nickel in a range selected independently from 50%-55%, 55%-60%, 60%-65%, 65%-70%, 70%-75%, 75%-80%, 80%-85% or 85%-90%, and the balance or the substantial part of the balance of the layer may comprise cobalt.
In such embodiments, second layers may each comprise an amount of cobalt in a range independently selected from 5%-35%, 5%-10%, 10%-15%, 15%-20%, 20%-25%, 25%-30% or 30%-35% cobalt. As with the first layers, the amount of cobalt in each second layer is independently selected and may be varied from layer to layer or among groups of layers. In such embodiments each second layer comprises cobalt in a range selected independently from 5%-35%, 5%-10%, 10%-15%, 15%-20%, 20%-25%, 25%-30%, or 30%-35% and the balance or the substantial part of the balance of the layer may comprise nickel. In other embodiments, each second layer comprises cobalt in a range selected independently from 20%-35%, 20%-25%, 25%-30% or 30%-35% and the balance or the substantial part of the balance of the layer may comprise nickel. In yet other embodiments each second layer comprises cobalt in a range selected independently from 5%-20%, 5%-10%, 10%-15% or 15%-20%, and the balance or the substantial part of the balance of the layer may comprise nickel.
In embodiments of this disclosure, each first and/or second layer may comprise, consist essentially of, or consist of nickel and cobalt and insubstantial amounts of other components (e.g., less than 0.1%, 0.05% or 0.01% of other component elements, taken individually). In embodiments of this disclosure, in addition to their nickel and cobalt content, each first and second layer may comprise one or more, two or more, three or more, or four or more additional elements selected independently for each first and second layer from the group consisting of Ag, Al, Au, Be, C, Cr, Cu, Fe, Hg, In, Mg, Mn, Mo, Nb, Nd, P, Pd, Pt, Re, Rh, Sb, Si, Sn, Pb, Ta, Ti, W, V, Zn and Zr. In other such embodiments, in addition to their nickel and cobalt content each first and second layer may comprise one or more, two or more, three or more, or four or more additional elements selected independently for each first and second layer from the group consisting of Ag, Al, C, Cr, Cu, Fe, Mg, Mn, Mo, Nb, P, Sb, Si, Sn, Ti, W, V, Zn and Zr; or from the group consisting of Al, C, Cr, Fe, Mg, Mn, Mo, Si, Sn, Ti, W, V, and Zn. In some embodiments, additional elements that are present will be present at greater than about 0.1% in order not to be considered an insubstantial amount of the component.
As mentioned above, the coating may comprise additional layers in addition to the first and second layers. Such additional layers may comprise any materials as disclosed herein.
In other embodiments where a plurality of first and second layers are present, the first layers may each comprise zinc in a range independently selected from 1%-5%, 5%-7%, 7%-10%, 10%-15%, 15%-20%, 20%-30%, 30%-40%, 40%-50%, 50%-55%, 55%-60%, 60%-65%, 65%-70%, 70%-75%, 75%-80%, 80%-85%, 85%-90%, 90%-92%, 92%-93%, 93%-94%, 94%-95%, 95%-96%, 96%-97%, 97%-98% or 98%-99%, the balance or substantial part of the balance of which may comprise another element such as iron. In such embodiments, each second layer may comprise iron in a range independently selected from 1%-35%, 1%-3%, 2%-5%, 5%-10%, 10%-15%, 15%-20%, 20%-25%, 25%-30%, or 30%-35%, the balance or substantial part of the balance of which comprises zinc.
In other embodiments where a plurality of first and second layers are present, the first layers each may comprise copper in a range independently selected from 1%-5%, 5%-7%, 7%-10%, 10%-15%, 15%-20%, 20%-30%, 30%-40%, 40%-50%, 50%-55%, 55%-60%, 60%-65%, 65%-70%, 70%-75%, 75%-80%, 80%-85%, 85%-90%, 90%-92%, 92%-93%, 93%-94%, 94%-95%, 95%-96%, 96%-97%, 97%-98% or 98%-99%, the balance or substantial part of the balance of which may comprise zinc and/or tin. In such embodiments, each second layer comprises zinc and/or tin in a range independently selected from 1%-35%, 1%-3%, 2%-5%, 5%-10%, 10%-15%, 15%-20%, 20%-25%, 25%-30% or 30%-35%, the balance or substantial part of the balance of which comprises copper.
In embodiments where the components of the above-mentioned electrodeposited compositions are not completely defined (that is, less than 100% of the components by weight are defined and/or required), then the balance of those layers may comprise one or more different elements. That is particularly so in embodiments of the above-mentioned binary or ternary alloy compositions comprising a plurality of layers (e.g., of first and second layers). Thus, in some embodiments, the electrodeposited compositions may comprise one or more elements selected from the group consisting of Ag, Al, Au, Be, C, Cr, Cu, Fe, Hg, In, Tr, Mg, Mn, Mo, Nb, Nd, Pd, Pt, Re, Rh, Sb, Si, Sn, Pb, Ta, Ti, W, V, Zn and Zr. In other embodiments, where the electrodeposited composition comprises one or more of said first and/or second layers, the layers may each comprise one or more, two or more, three or more, or four or more elements selected independently for each first and second layer from the group consisting of Ag, Al, Au, Be, C, Cr, Cu, Fe, Hg, In, Mg, Mn, Mo, Nb, Nd, Pd, Pt, Re, Rh, Sb, Si, Sn, Pb, Ta, Ti, W, V, Zn and Zr.
Regardless of which nanolaminate coating is employed to improve the properties of an article, the nanolaminate coating composition may be oriented so that a first layer or second layer is in contact with the substrate on which the coating is applied (e.g. the surface of a pipe). Thus in some embodiments a first layer is in contact with the surface on which the electrodeposited coating is applied, and in other embodiments the second coating is in contact with the surface of the substrate. The layer in contact with the surface of the substrate may affect the adhesion of the coating and any corrosion resistance. Because different coatings may be applied to different portions of the same article (e.g., the inside and outside of a pipe or other tube may have different coatings), it will be understood that the different coatings may be oriented differently (i.e., in one coating a first layer contacts a substrate and in a coating applied on a different part of the same article a second layer contacts a substrate).
Electrodeposited alloys applied to articles (e.g., nanolaminate coatings) can be fully or substantially fully dense, having a limited number of pores or cracks, making them useful as corrosion resistant coatings, in addition to their role as a structural component of finished parts or objects.
In embodiments where the electroplated compositions are comprised of a plurality of layers less than about 20 nm (e.g., about 15 nm, 10 nm, 8 nm, or 5 nm), the compositions display increased “Hall-Petch” hardness/toughness and strength. The observed increases in hardness results from grain confinement and increased toughness results from force reflection in the laminate regions. Such coatings tend to follow the Hall-Petch relationship, which traditionally is used to describe the increase in yield strength observed in nanocrystalline materials.
In embodiments where the electroplated compositions are comprised of a plurality of layers of hard and soft materials laminated together, the electrodeposited composition may display Koehler toughening. That form of toughening results from a deflection of a nascent crack at the layer interface due to differing modulus. Such objects can thus absorb the energy that typically causes cracking and thereby prevent or substantially diminish bulk material failure, and/or prolong the time to such bulk material failure.
In addition to mechanical and physical enhancement of article properties, compositions electrodeposited onto articles also can alter the articles' chemical attributes. In some embodiments, at least a portion of the composition electrodeposited onto a article is chemically resistant to the environment and protects the underlying article (e.g., the metal coating protects the article from solvents or UV light that may damage the article). In other embodiments, at least a portion of the composition electrodeposited on the article is more noble than the underlying article and acts as a barrier coating in corrosive environments that can damage the underlying article. In yet other embodiments, at least a portion of the composition electrodeposited on the article is less noble than the article and sacrifices itself in corrosive environments to protect the article.
Where the properties of pipes, tubes and other items having tubular elements are to be improved, the coating thickness may be in the range from less than about 5% to about 25% or more (e.g., from less than 5% to 5%, from about 5% to about 10%, from about 10% to about 15%, from about 15% to about 20%, from about 20% to about 25%, or more than 25%) of the wall thickness of those items. In such ranges, pipes, tubes, and tubular elements can exhibit a marked increase in performance. In some embodiments, pipes or tubes comprised of steel alloys, display a marked improvement their properties, including burst pressure, collapse pressure, or force displacement (crushing force).
Depending on the D/T ratio and thickness and composition of the nanolaminate coating, the burst pressure, collapse pressure and/or force displacement (crushing force) of the externally coated pipe is increased from about 5% up to 100% or more relative to an uncoated pipe having substantially the same composition and substantially the same D/T ratio as the coated pipe. Hence increases in the burst pressure, collapse pressure, or force displacement (crushing force) of about 5 to about 10%, about 10 to about 15%, about 15 to about 20%, about 20 to about 25%, about 25 to about 30%, about 30 to about 35%, about 35 to about 40%, about 40 to about 45%, about 45 to about 50%, about 50 to about 60%, about 60 to about 70%, about 70 to about 80%, about 80 to about 90%, about 90 to about 100% and over 100% can be obtained relative to an uncoated pipe having substantially the same composition and substantially the same D/T ratio as the coated pipe.
In addition to nickel and cobalt containing first and second layers, the coatings may comprise additional layers, such as a coating or nanolaminate coating of NiCr alloys to increase improve the tribological properties and/or chemical resistance of the overall coating.
Improving the properties of articles with nickel-cobalt or nickel-chromium containing nanolaminate coatings can provide the article a variety of desirable properties including, but not limited to, increased hardness, strength, wear resistance, and corrosion resistance.
In one series of embodiments, where pipes, tubes and other items having tubular elements are to be coated, the resulting article can exhibit increases in its collapse and/or burst pressure.
In embodiments where the article is a pipe or tube formed from steel, a steel alloy comprising: carbon, iron, molybdenum, or an alloy comprising carbon, iron, molybdenum and cobalt (such as American Petroleum Institute L80, C95, P110 or Q125 grade steels or American Iron and Steel Institute 4130, 4135, 4137, 4140, or 4145 steels) the nanolaminated nickel-cobalt or nickel-chromium coatings described herein can markedly improve the performance of the tubes and pipes in burst and collapse pressure tests. In embodiments where the nanolaminated nickel-cobalt coatings are applied only to the exterior surface of the pipe and they have a coating thickness from about 5% to about 25% of the wall thickness (e.g., less than 5%, from about 5% to about 10%, from about 10% to about 15%, from about 15% to about 20%, from about 20% to about 25%, or greater than 25% of the wall thickness), the performance exceeds what would be expected from the properties of the separate materials by finite element analysis (FEA) when the data are corrected for changes in the D/T ratio (i.e., the additional thickness of the pipe is included in the measurement). For pipes with typical wall thicknesses in the range of about 0.2 inches to about 0.65 inches, the coating thickness may be from about 10 thousandths to about 160 thousandths of an inch (about 0.25 mm to about 4 mm), but may be either thinner or thicker.
In such embodiments when the D/T ratio is from about 14 to about 15 the burst pressure and/or collapse pressure of the externally coated pipe is increased from about 5% to about 22%, from about 5% to about 10%, from about 10% to about 15% or from about 15% to about 22% relative to an uncoated pipe having substantially the same composition and substantially the same D/T ratio as the coated pipe.
Where the D/T ratio is from about 15 to about 21 the burst pressure and/or collapse pressure of the externally coated pipe is increased from about 10% to about 36%, from about 10% to about 15%, from about 15% to about 20%, from about 20% to about 25%, from about 25% to about 30%, or from about 30% to about 36% relative to an uncoated having substantially the same composition and substantially the same D/T ratio as the coated pipe.
Depending on the D/T ratio and thickness and composition of the nickel-cobalt or nickel-chromium nanolaminate coating, increases in the burst pressure, collapse pressures and/or force displacement (crushing force) of the externally coated pipe is increased from about 5% up to 100% or more the relative to an uncoated having substantially the same composition and substantially the same D/T ratio as the coated pipe. Hence increases in the burst pressure, collapse pressures, or force displacement (crushing force) of about 5 to about 10%, about 10 to about 15%, about 15 to about 20%, about 20 to about 25%, about 25 to about 30%, about 30 to about 35%, about 35 to about 40%, about 40 to about 45%, about 45 to about 50%, about 50 to about 60%, about 60 to about 70%, about 70 to about 80%, about 80 to about 90%, about 90 to about 100% and over 100% can be obtained relative to an uncoated having substantially the same composition and substantially the same D/T ratio as the coated pipe.
In some embodiments a steel pipe having a D/T ratio of about 15 and a nanolaminated nickel-cobalt or nickel-chromium coating on its exterior surface from about 50 to about 70 thousandths of an inch thick has a collapse pressure greater than about 13,000 psi.
In some embodiments a steel pipe having a D/T ratio of about 16 and a nanolaminated nickel-cobalt or nickel-chromium coating on its exterior surface from about 50 to about 70 thousandths of an inch thick has a collapse pressure greater than about 11,000 psi.
In some embodiments a steel pipe having a D/T ratio of about 17 and a nanolaminated nickel-cobalt or nickel-chromium coating on its exterior surface from about 50 to about 70 thousandths of an inch thick has a collapse pressure greater than about 10,500 psi.
In some embodiments a steel pipe having a D/T ratio of about 18 and a nanolaminated nickel-cobalt or nickel-chromium coating on its exterior surface from about 50 to about 70 thousandths of an inch thick has a collapse pressure greater than about 9,750 psi.
In some embodiments a steel pipe having a D/T ratio of about 19 and a nanolaminated nickel-cobalt or nickel-chromium coating on its exterior surface from about 50 to about 70 thousandths of an inch thick has a collapse pressure greater than about 9,000 psi.
The nickel-cobalt or nickel-chromium coatings may also function as corrosion barriers imparting resistance to corrosion of underlying substrates (e.g., susceptible materials such as steels) by acids, bases, H2S and the like.
In order to electrodeposit a composition comprising a metal on at least a portion of an article surface that is accessible to liquids, e.g., a tubular article, the surface must be conductive and brought in contact with a bath containing salts of the metals to be electrodeposited. To make the surface of a non-conductive article conductive, or to increase the conductivity of an article that is already conductive, typically requires subjecting the surface to electroless plating of a metal such as nickel, cadmium, gold, silver, rhodium, chrome, zinc, tin, or copper. In some embodiments, the metal applied to the article by electroless deposition is nickel. Preparation of articles for electroless plating, particularly of non-conductive plastic/polymer articles such as tubular articles, generally includes a step of etching the surface of the article. Etching is typically accomplished by using a strong oxidizing agent to create microscopic pores or holes in the surface of the plastic. The pores or holes increase the surface area and improve adhesion of subsequently applied metal layers. Some strong oxidizing solutions/suspensions used as etchants include peroxides (e.g., hydrogen peroxide), persulfates, chromic acid, acidic or basic permanganate solutions, chromium trioxide solutions or suspensions, and sulfuric acid. In embodiments, the article comprises a tube made from ABS and the etchant is chromic acid or chromium trioxide containing solution/suspension.
Following etching, at least a portion of the etched section of the article may be contacted with a composition that deposits a metallic catalyst on the etched surface of the polymeric article. The catalyst is typically palladium, which can be applied using tin as a reducing agent (e.g., Sn+2+Pd+2═Sn+4)Pd0, however, other catalysts including noble metal catalysts may be used (e.g., platinum, rhodium, iridium, nickel, copper, silver, gold). Upon contact with the electroless plating bath, the catalyst causes a layer of metal to form on the surface of the polymeric article exposed to the catalyst and then the bath.
Metals, polymers, and semiconductors can all be electroplated (electrodeposited), and in most cases the required conditions are at or near ambient temperature and pressure. Embodiments of the processes described herein include methods of electrodepositing a composition comprising a metal on an article prepared by additive manufacturing, where the process comprises:
a) optionally subjecting all or part of the article to electroless plating;
b) providing a bath including at least one electrodepositable component;
c) contacting all or part of the article with the bath; and
d) applying voltage or current to the article to deposit at least one electrodepositable component comprising a metal.
In some embodiments, the bath comprises at least two, at least three, or at least four electrodepositable components. The electrodepositable components include metal salts, from which metals may be electroplated onto the article, and where the bath comprises more than one metal salt as an electrodepositable component, alloys of varying composition may be electrodeposited on the article depending on the current and voltage applied.
In some embodiments, the method of electrodepositing comprises applying a time varying current density, wherein the time varying current density oscillates at least for two cycles to deposit a structurally and/or compositionally modulated material on the article. The structural and or compositionally modulated material may be applied such that it has a discrete interface, or a diffuse interface, where the composition changes from a first composition to a second composition over a distance from about 3 nm to about 8 nm, about 5 nm to about 10 nm, about 7 nm to about 15 nm or about 10 nm to about 20 nm. In other embodiments, a discrete interface between two layers may be considered as one in which the composition shifts between the compositions of the first layer and the second layer over a distance that is less than about 20%, about 15%, about 10%, about 8%, about 5%, about 4% or about 2% of the thickness of the thinner of the first and second layers. In other embodiments layers have diffuse interfaces where the compositions vary from that of a first composition to a second composition in a continuous manner. In some embodiments, the diffuse interface varies between the compositions of the first and second layer over a distance that is greater than about 20%, about 25%, about 30%, about 35%, about 40% or about 45% or less than or equal to 50% of the thickness of the thinner of the first and second layers.
The composition comprising a metal that is electrodeposited onto the article may vary in its constituent metals. In some embodiments, the composition comprises one or more, two or more, three or more, or four or more different metals independently selected from Ag, Al, Au, Be, Co, Cr, Cu, Fe, Hg, In, Mg, Mn, Mo, Nb, Nd, Ni, Pd, Pt, Re, Rh, Sb, Sn, Mn, Pb, Ta, Ti, W, V, Zn and Zr, wherein each of said independently selected metals is present at greater than 0.1, 0.05, 0.01, 0.005 or 0.001% by weight.
In other embodiments, the composition electrodeposited onto the article comprises two or more or three or more different metals independently selected from Ag, Al, Au, Be, Co, Cr, Cu, Fe, Hg, In, Mg, Mn, Mo, Nb, Nd, Ni, Pd, Pt, Re, Rh, Sb, Sn, Mn, Pb, Ta, Ti, W, V, Zn and Zr, wherein each of said independently selected metals is present at more than 0.1, 0.05, 0.01, 0.005, or 0.001% by weight. In such embodiments, compositions of two or more different metals that can be electrodeposited comprise, for example, Zn and Fe, Zn and Ni, Co and Ni, Ni and Fe, Ni and Cr, Ni and Al, Cu and Zn, or Cu and Sn.
In some embodiments, the composition electrodeposited onto the article comprises a structurally and/or compositionally modulated electrodeposited material or composition. The structurally and/or compositionally modulated composition may comprise at least one portion having a plurality of layers deposited with wavelengths between about 1 nm and about 250 nm, about 1 nm and about 25 nm, about 5 nm and about 50 nm, about 10 nm and about 75 nm, about 1 nm and about 100 nm, about 2 nm and about 200 nm, about 5 nm and about 225 nm or about 10 nm and about 250 nm.
In other embodiments, the structurally and/or compositionally modulated material has at least one portion consisting of a plurality of layers, wherein each of said layers has a thickness in a range selected independently from about 5 nm to about 250 nm, from about 5 nm to about 25 nm, from about 10 nm to about 30 nm, from about 30 nm to about 60 nm, from about 40 nm to about 80 nm, from about 75 nm to about 100 nm, from about 100 nm to about 120 nm, from about 120 nm to about 140 nm, from about 140 nm to about 180 nm, from about 180 nm to about 200 nm, from about 200 nm to about 225 nm, from about 220 nm to about 250 nm or from about 150 nm to about 250 nm.
As described above, where the electrodeposited material comprises two or more structurally and/or compositionally different layers, the layers may have discrete or diffuse interfaces.
In embodiments where the electrodeposited material comprises two or more structurally and/or compositionally different layers, the material may comprise a plurality of alternating first layers and second layers. The coating of electrodeposited material may consist entirely of the alternating first and second layers, which may have discrete or diffuse interfaces between the layers. Alternatively, one or more additional layers may be present in the coating between any first and second layer.
In embodiments where the electrodeposited composition applied to all or part of the article comprises a plurality of layers (e.g., first layers and second layers or alternating first and second layers), the electrodeposited composition applied to the article (e.g., as a conformal coating or partial coating) may comprise two or more, three or more, four or more, six or more, eight or more, ten or more, twenty or more, forty or more, fifty or more, 100 or more, 200 or more, 500 or more, 1,000 or more, 1,500 or more or 2,000 or more alternating first and second layers independently selected for each multilayer coating.
Coatings comprising nickel and cobalt described herein can be applied to the conductive surfaces of articles by electrodeposition as described above. In some embodiments, the electrodeposition of a coating used to improve the properties of an article is carried out in a single bath. Such processes generally comprise the steps of:
Nanolaminated nickel-cobalt coatings can also be applied to the conductive surfaces of articles by electrodeposition using serial electrodeposition in two or more baths. Such processes include electrodepositing each first and second layer in separate baths by alternately electrodepositing layers in each bath. Alternatively, nanolaminate layers may be formed by: serially electrodepositing a series of first and second layers from a first electrolyte comprising a salt of nickel, cobalt and any other species of metal to be electrodeposited by varying in time one or more of: the amplitude of the electrical current, electrolyte temperature, electrolyte additive concentration, or electrolyte agitation; followed by serially electrodepositing a series of first and second layers from a second electrolyte comprising a salt of nickel, cobalt and any other species of metal to be electrodeposited by varying in time one or more of: the amplitude of the electrical current, electrolyte temperature, electrolyte additive concentration, or electrolyte agitation.
Accordingly one process employing two different electrolytes for electrodepositing a nanolaminate nickel coating may comprise the steps of:
wherein steps (a) through (d) are repeated at least two times.
In other embodiments, a nickel-cobalt coating may be electrodeposited by a process employing two different electrolytes to deposit the nanolaminate coating layers comprising the steps of:
applying to all or part of a surface of said article one or more electrodeposited multilayered coatings comprising a plurality of alternating first layers of nickel or an alloy comprising nickel, and second layers of an alloy comprising nickel and cobalt to form a coated article;
wherein said one or more multilayer coatings comprises from about 50 to about 100, from about 100 to about 1,000, from about 1,000 to about 2,000, from about 2,000 to about 4,000, from about 4,000 to about 8,000 or greater than 8,000 alternating first and second layers independently selected for each multilayer coating;
wherein each of said first layers and each of said second layers have a thickness in a range selected independently from about 5 nm to about 200 nm, from about 5 nm to about 25 nm, from about 10 nm to about 30 nm, from about 30 nm to about 60 nm, from about 40 nm to about 80 nm, from about 75 nm to about 100 nm, from about 100 nm to about 120 nm, from about 120 nm to about 140 nm, from about 140 nm to about 180 nm, from about 180 nm to about 200 nm or from about 200 to about 250 nm; and
wherein the burst pressure and collapse pressure of said coated article are increased relative to said article or a substantially identical article having the same overall dimensions and composition but uncoated.
said method further comprising applying the multilayer coating to at least one of the interior and/or exterior surfaces to form a coated pipe;
wherein when the D/T ratio is from about 14 to about 15 the burst pressure and/or collapse pressure of the coated pipe is increased from about 5% to about 22%, from about 5% to about 10%, from about 10% to about 15% or from about 15% to about 22% relative to an uncoated pipe having said composition and substantially the same D/T ratio as the coated pipe; and
wherein when the D/T ratio is from about 15 to about 21 the burst pressure and/or collapse pressure of the coated pipe is increased from about 10% to about 36%, from about 10% to about 15%, from about 15% to about 20%, from about 20% to about 25%, from about 25% to about 30% or from about 30% to about 36% relative to an uncoated pipe having said composition and substantially the same D/T ratio as the coated pipe.
a wall comprised of a material having a composition, an interior surface, and an exterior surface;
said pipe having dimensions including a wall thickness, an inner diameter defined by said interior surface, and an exterior diameter defined by said exterior surface;
where at least one of said interior surface and said exterior surface comprises an electrodeposited multilayered coating;
said pipe having a burst pressure and a collapse pressure, wherein said burst pressure and/or collapse pressure of said pipe is greater than the collapse pressure and/or burst pressure of a pipe having substantially the same composition and dimensions in the absence of a coating on its interior or exterior surface.
This application is a continuation of U.S. application Ser. No. 14/855,088, filed Sep. 15, 2015, which is a continuation of International Application No. PCT/US2014/031096, filed Mar. 18, 2014, which claims the benefit of U.S. Provisional Patent Application No. 61/802,301, filed Mar. 15, 2013, each of which is incorporated herein by reference in its entirety.
Number | Name | Date | Kind |
---|---|---|---|
2428033 | Nachtman | Sep 1947 | A |
2436316 | Lum et al. | Feb 1948 | A |
2470775 | Jernstedt et al. | May 1949 | A |
2558090 | Jernstedt | Jun 1951 | A |
2642654 | Ahrens | Jun 1953 | A |
2678909 | Jernstedt et al. | May 1954 | A |
2694743 | Ruskin et al. | Nov 1954 | A |
2706170 | Marchese | Apr 1955 | A |
2891309 | Fenster | Jun 1959 | A |
3090733 | Brown | May 1963 | A |
3255781 | Gillespie, Jr. | Jun 1966 | A |
3282810 | Odekerken | Nov 1966 | A |
3359469 | Levy et al. | Dec 1967 | A |
3362851 | Dunster | Jan 1968 | A |
3483113 | Carter | Dec 1969 | A |
3549505 | Hanusa | Dec 1970 | A |
3616286 | Aylward et al. | Oct 1971 | A |
3633520 | Stiglich, Jr. | Jan 1972 | A |
3716464 | Kovac et al. | Feb 1973 | A |
3753664 | Klingenmaier et al. | Aug 1973 | A |
3759799 | Reinke | Sep 1973 | A |
3787244 | Schulmeister et al. | Jan 1974 | A |
3866289 | Brown et al. | Feb 1975 | A |
3941674 | Vanmunster | May 1976 | A |
3994694 | Clauss et al. | Nov 1976 | A |
3996114 | Ehrsam | Dec 1976 | A |
4053371 | Towsley | Oct 1977 | A |
4105526 | Lewellen, Jr. et al. | Aug 1978 | A |
4107003 | Anselrode | Aug 1978 | A |
4191617 | Hurley et al. | Mar 1980 | A |
4204918 | McIntyre et al. | May 1980 | A |
4216272 | Clauss | Aug 1980 | A |
4246057 | Janowski et al. | Jan 1981 | A |
4284688 | Stücheli et al. | Aug 1981 | A |
4314893 | Clauss | Feb 1982 | A |
4405427 | Byrd | Sep 1983 | A |
4422907 | Birkmaier et al. | Dec 1983 | A |
4461680 | Lashmore | Jul 1984 | A |
4464232 | Wakano et al. | Aug 1984 | A |
4510209 | Hada et al. | Apr 1985 | A |
4519878 | Hara et al. | May 1985 | A |
4540472 | Johnson et al. | Sep 1985 | A |
4543300 | Hara et al. | Sep 1985 | A |
4543803 | Keyasko | Oct 1985 | A |
4591418 | Snyder | May 1986 | A |
4592808 | Doubt | Jun 1986 | A |
4597836 | Schaer et al. | Jul 1986 | A |
4613388 | Walter et al. | Sep 1986 | A |
4620661 | Slatterly | Nov 1986 | A |
4652348 | Yahalom et al. | Mar 1987 | A |
4666567 | Loch | May 1987 | A |
4670356 | Sato et al. | Jun 1987 | A |
4678552 | Chen | Jul 1987 | A |
4678721 | den Broeder et al. | Jul 1987 | A |
4702802 | Umino et al. | Oct 1987 | A |
H543 | Chen et al. | Nov 1988 | H |
4795735 | Liu et al. | Jan 1989 | A |
4834845 | Muko et al. | May 1989 | A |
4839214 | Oda et al. | Jun 1989 | A |
4869971 | Nee et al. | Sep 1989 | A |
4885215 | Yoshioka et al. | Dec 1989 | A |
4904542 | Mroczkowski | Feb 1990 | A |
4904543 | Sakakima et al. | Feb 1990 | A |
4923574 | Cohen | May 1990 | A |
4975337 | Hyner et al. | Dec 1990 | A |
5043230 | Jagannathan et al. | Aug 1991 | A |
5045356 | Uemura et al. | Sep 1991 | A |
5056936 | Mahrus et al. | Oct 1991 | A |
5059493 | Takahata | Oct 1991 | A |
5073237 | Bacher et al. | Dec 1991 | A |
5079039 | Heraud et al. | Jan 1992 | A |
5156729 | Mahrus et al. | Oct 1992 | A |
5156899 | Kistrup et al. | Oct 1992 | A |
5158653 | Lashmore et al. | Oct 1992 | A |
5190637 | Guckel | Mar 1993 | A |
5228967 | Crites et al. | Jul 1993 | A |
5268235 | Lashmore et al. | Dec 1993 | A |
5300165 | Sugikawa | Apr 1994 | A |
5320719 | Lasbmore et al. | Jun 1994 | A |
5326454 | Engelhaupt | Jul 1994 | A |
5352266 | Erb et al. | Oct 1994 | A |
5378583 | Guckel et al. | Jan 1995 | A |
5413874 | Moysan, III et al. | May 1995 | A |
5431800 | Kirchhoff et al. | Jul 1995 | A |
5461769 | McGregor | Oct 1995 | A |
5472795 | Atita | Dec 1995 | A |
5489488 | Asai et al. | Feb 1996 | A |
5500600 | Moyes | Mar 1996 | A |
5547096 | Kleyn | Apr 1996 | A |
5527445 | Palumbo | Jun 1996 | A |
5545435 | Steffier | Aug 1996 | A |
5620800 | De Leeuw et al. | Apr 1997 | A |
5660704 | Murase | Aug 1997 | A |
5679232 | Fedor et al. | Oct 1997 | A |
5738951 | Goujard et al. | Apr 1998 | A |
5742471 | Barbee, Jr. et al. | Apr 1998 | A |
5775402 | Sachs et al. | Jul 1998 | A |
5783259 | McDonald | Jul 1998 | A |
5798033 | Uemiya et al. | Aug 1998 | A |
5800930 | Chen et al. | Sep 1998 | A |
5828526 | Kagawa et al. | Oct 1998 | A |
5912069 | Yializis et al. | Jun 1999 | A |
5930085 | Kitade et al. | Jul 1999 | A |
5942096 | Ruzicka et al. | Aug 1999 | A |
5958604 | Riabkov et al. | Sep 1999 | A |
6036832 | Knol et al. | Mar 2000 | A |
6071398 | Martin et al. | Jun 2000 | A |
6143424 | Jonte et al. | Nov 2000 | A |
6143430 | Miyasaka et al. | Nov 2000 | A |
6193858 | Hradil et al. | Feb 2001 | B1 |
6200452 | Angelini | Mar 2001 | B1 |
6203936 | Cisar et al. | Mar 2001 | B1 |
6212078 | Hunt et al. | Apr 2001 | B1 |
6214473 | Hunt et al. | Apr 2001 | B1 |
6284357 | Lackey et al. | Sep 2001 | B1 |
6312579 | Bank et al. | Nov 2001 | B1 |
6344123 | Bhatnagar | Feb 2002 | B1 |
6355153 | Uzoh et al. | Mar 2002 | B1 |
6398937 | Menini et al. | Jun 2002 | B1 |
6409907 | Braun et al. | Jun 2002 | B1 |
6415942 | Fenton et al. | Jul 2002 | B1 |
6461678 | Chen et al. | Oct 2002 | B1 |
6466417 | Gill | Oct 2002 | B1 |
6468672 | Donovan, III et al. | Oct 2002 | B1 |
6482298 | Bhatnagar | Nov 2002 | B1 |
6537683 | Staschko et al. | Mar 2003 | B1 |
6547944 | Schreiber et al. | Apr 2003 | B2 |
6592739 | Sonoda et al. | Jul 2003 | B1 |
6725916 | Gray et al. | Apr 2004 | B2 |
6739028 | Sievenpiper et al. | May 2004 | B2 |
6800121 | Shahin | Oct 2004 | B2 |
6884499 | Penich et al. | Apr 2005 | B2 |
6902827 | Kelly et al. | Jun 2005 | B2 |
6908667 | Christ et al. | Jun 2005 | B2 |
6979490 | Steffier | Dec 2005 | B2 |
7581933 | Bruce et al. | Sep 2009 | B2 |
7736753 | Deligianni et al. | Jun 2010 | B2 |
8084564 | Kano et al. | Dec 2011 | B2 |
8152985 | Macary | Apr 2012 | B2 |
8177945 | Arvin et al. | May 2012 | B2 |
8253035 | Matsumoto | Aug 2012 | B2 |
8585875 | Cummings et al. | Nov 2013 | B2 |
8814437 | Braun | Aug 2014 | B2 |
8916001 | Pryce Lewis et al. | Dec 2014 | B2 |
9005420 | Tomantschger et al. | Apr 2015 | B2 |
9056405 | Sato et al. | Jun 2015 | B2 |
9080692 | Tomomori et al. | Jul 2015 | B2 |
9108506 | Whitaker et al. | Aug 2015 | B2 |
9115439 | Whitaker | Aug 2015 | B2 |
9234294 | Whitaker et al. | Jan 2016 | B2 |
9273932 | Whitaker et al. | Mar 2016 | B2 |
9732433 | Caldwell et al. | Aug 2017 | B2 |
9758891 | Bao | Sep 2017 | B2 |
9783907 | Cai et al. | Oct 2017 | B2 |
9938629 | Whitaker et al. | Apr 2018 | B2 |
10253419 | Lomasney | Apr 2019 | B2 |
10266957 | Sugawara et al. | Apr 2019 | B2 |
10472727 | Lomasney | Nov 2019 | B2 |
10513791 | Lomasney | Dec 2019 | B2 |
10544510 | Lomasney | Jan 2020 | B2 |
10662542 | Caldwell et al. | May 2020 | B2 |
10689773 | Whitaker et al. | Jun 2020 | B2 |
10781524 | Whitaker et al. | Sep 2020 | B2 |
10808322 | Whitaker et al. | Oct 2020 | B2 |
10844504 | Sklar | Nov 2020 | B2 |
10961635 | Whitaker | Mar 2021 | B2 |
20010037944 | Sanada et al. | Nov 2001 | A1 |
20020011419 | Arao et al. | Jan 2002 | A1 |
20020100858 | Weber | Aug 2002 | A1 |
20020179449 | Domeier et al. | Dec 2002 | A1 |
20030134142 | Ivey et al. | Jul 2003 | A1 |
20030234181 | Palumbo et al. | Dec 2003 | A1 |
20030236163 | Chaturvedi et al. | Dec 2003 | A1 |
20040027715 | Hixson-Goldsmith et al. | Feb 2004 | A1 |
20040031691 | Kelly et al. | Feb 2004 | A1 |
20040067314 | Joshi et al. | Apr 2004 | A1 |
20040154925 | Podlaha et al. | Aug 2004 | A1 |
20040178076 | Stonas et al. | Sep 2004 | A1 |
20040211672 | Ishigami et al. | Oct 2004 | A1 |
20040232005 | Hubel | Nov 2004 | A1 |
20040234683 | Tanaka et al. | Nov 2004 | A1 |
20040239836 | Chase | Dec 2004 | A1 |
20050002228 | Dieny et al. | Jan 2005 | A1 |
20050109433 | Danger et al. | May 2005 | A1 |
20050205425 | Palumbo et al. | Sep 2005 | A1 |
20050279640 | Shimoyama et al. | Dec 2005 | A1 |
20060065533 | Inoue et al. | Mar 2006 | A1 |
20060135281 | Palumbo et al. | Jun 2006 | A1 |
20060135282 | Palumbo et al. | Jun 2006 | A1 |
20060201817 | Guggemos et al. | Sep 2006 | A1 |
20060243597 | Matefi-Tempfli et al. | Nov 2006 | A1 |
20060269770 | Cox et al. | Nov 2006 | A1 |
20060272949 | Detor et al. | Dec 2006 | A1 |
20060286348 | Sauer | Dec 2006 | A1 |
20070158204 | Taylor et al. | Jul 2007 | A1 |
20070269648 | Schuh et al. | Nov 2007 | A1 |
20070278105 | Ettel | Dec 2007 | A1 |
20080063866 | Allen et al. | Mar 2008 | A1 |
20080093221 | Basol | Apr 2008 | A1 |
20080102360 | Stimits et al. | May 2008 | A1 |
20080226976 | Stimits | Sep 2008 | A1 |
20080245669 | Yoshioka et al. | Oct 2008 | A1 |
20080271995 | Savastiouk et al. | Nov 2008 | A1 |
20080283236 | Akers et al. | Nov 2008 | A1 |
20090004465 | Kano et al. | Jan 2009 | A1 |
20090101511 | Lochtman et al. | Apr 2009 | A1 |
20090114530 | Noda et al. | May 2009 | A1 |
20090130424 | Tholen et al. | May 2009 | A1 |
20090130425 | Whitaker | May 2009 | A1 |
20090155617 | Kim et al. | Jun 2009 | A1 |
20090283410 | Sklar et al. | Nov 2009 | A1 |
20100078330 | Hyodo | Apr 2010 | A1 |
20100116675 | Sklar et al. | May 2010 | A1 |
20100187117 | Lingenfelter et al. | Jul 2010 | A1 |
20100304063 | McCrea et al. | Dec 2010 | A1 |
20100304179 | Facchini et al. | Dec 2010 | A1 |
20100319757 | Oetting | Dec 2010 | A1 |
20110111296 | Berdichevsky et al. | May 2011 | A1 |
20110162970 | Sato | Jul 2011 | A1 |
20110180413 | Whitaker et al. | Jul 2011 | A1 |
20110186582 | Whitaker et al. | Aug 2011 | A1 |
20110256356 | Tomantschger et al. | Oct 2011 | A1 |
20110277313 | Soracco et al. | Nov 2011 | A1 |
20120118745 | Bao | May 2012 | A1 |
20120135270 | Wilbuer et al. | May 2012 | A1 |
20120231574 | Wang | Sep 2012 | A1 |
20120282417 | Garcia et al. | Nov 2012 | A1 |
20130052343 | Dieny et al. | Feb 2013 | A1 |
20130071755 | Oguro | Mar 2013 | A1 |
20130075264 | Cummings et al. | Mar 2013 | A1 |
20130130057 | Caldwell et al. | May 2013 | A1 |
20130186852 | Dietrich et al. | Jul 2013 | A1 |
20130220831 | Vidaurre Heiremans et al. | Aug 2013 | A1 |
20130224008 | Cheung et al. | Aug 2013 | A1 |
20130323473 | Dietsch et al. | Dec 2013 | A1 |
20140163717 | Das et al. | Jun 2014 | A1 |
20140178637 | Rajagopalan et al. | Jun 2014 | A1 |
20140231266 | Sherrer et al. | Aug 2014 | A1 |
20150315716 | Whitaker | Nov 2015 | A1 |
20150322588 | Lomasney et al. | Nov 2015 | A1 |
20160002790 | Whitaker et al. | Jan 2016 | A1 |
20160002803 | Sklar | Jan 2016 | A1 |
20160002806 | Lomasney et al. | Jan 2016 | A1 |
20160002813 | Lomasney | Jan 2016 | A1 |
20160024663 | Lomasney | Jan 2016 | A1 |
20160047980 | Page et al. | Feb 2016 | A1 |
20160145850 | Cook et al. | May 2016 | A1 |
20160159488 | Roach et al. | Jun 2016 | A1 |
20160160863 | Roach et al. | Jun 2016 | A1 |
20160214283 | Schick et al. | Jul 2016 | A1 |
20170191177 | Whitaker et al. | Jul 2017 | A1 |
20170191179 | Sklar | Jul 2017 | A1 |
20170275775 | Guadarrama Calderon et al. | Sep 2017 | A1 |
20180016694 | Bao | Jan 2018 | A1 |
20180066375 | Morgan et al. | Mar 2018 | A1 |
20180071980 | Lomasney et al. | Mar 2018 | A1 |
20180245229 | Whitaker et al. | Aug 2018 | A1 |
20190309430 | Sklar | Oct 2019 | A1 |
20190360116 | Collinson et al. | Nov 2019 | A1 |
20200115998 | Lomasney | Apr 2020 | A1 |
20200131658 | Lomasney et al. | Apr 2020 | A1 |
20200173032 | Lomasney | Jun 2020 | A1 |
20200283923 | Lomasney | Sep 2020 | A1 |
20200318245 | Lomasney | Oct 2020 | A1 |
20200354846 | Whitaker et al. | Nov 2020 | A1 |
20200392642 | Lomasney | Dec 2020 | A1 |
20210054522 | Lomasney et al. | Feb 2021 | A1 |
20210071303 | Whitaker et al. | Mar 2021 | A1 |
Number | Date | Country |
---|---|---|
1236024 | Nov 1999 | CN |
1380446 | Nov 2002 | CN |
1924110 | Mar 2007 | CN |
101113527 | Jan 2008 | CN |
101195924 | Jun 2008 | CN |
102148339 | Aug 2011 | CN |
39 02 057 | Jul 1990 | DE |
10 2004 006 441 | Dec 2005 | DE |
10 2010 011 087 | Sep 2011 | DE |
1 688 518 | Aug 2006 | EP |
1 498 976 | Oct 2006 | EP |
2 189 554 | May 2010 | EP |
3 128 045 | Feb 2017 | EP |
2 324 813 | Nov 1998 | GB |
47-2005 | Feb 1972 | JP |
47-33925 | Nov 1972 | JP |
52-109439 | Sep 1977 | JP |
58-197292 | Nov 1983 | JP |
60-97774 | May 1985 | JP |
S61-99692 | May 1986 | JP |
1-132793 | May 1989 | JP |
2-214618 | Aug 1990 | JP |
5-251849 | Sep 1993 | JP |
6-196324 | Jul 1994 | JP |
7-065347 | Mar 1995 | JP |
2000-239888 | Sep 2000 | JP |
2001-152388 | Jun 2001 | JP |
2001-181893 | Jul 2001 | JP |
2006-35176 | Feb 2006 | JP |
2009-215590 | Sep 2009 | JP |
10-2015-0132043 | Nov 2015 | KR |
36121 | Apr 1934 | SU |
8302784 | Aug 1983 | WO |
9514116 | May 1995 | WO |
9700980 | Jan 1997 | WO |
0233150 | Apr 2002 | WO |
03100484 | Dec 2003 | WO |
2004001100 | Dec 2003 | WO |
2007045466 | Apr 2007 | WO |
2007136387 | Nov 2007 | WO |
2007138619 | Dec 2007 | WO |
2008057401 | May 2008 | WO |
2009045433 | Apr 2009 | WO |
2011033775 | Mar 2011 | WO |
2012145750 | Oct 2012 | WO |
2013133762 | Sep 2013 | WO |
2017097300 | Jun 2017 | WO |
Entry |
---|
“Appendix 1: Literature review (Task 1): Literature review concerning the improvement of galvanneal (GA) coating adherence during shear test of adhesively bonded GA steel sheets,” 70 pages, no date. |
“Low-temperature iron plating,” web blog article found at http://blog.sina.com.cn/s/blog_48ed0a9c0100024z.html, published Mar. 22, 2006, 3 pages. (with English translation). |
Adams et al., “Controlling strength and toughness of multilayer films: A new multiscalar approach,” J. Appl. Phys. 74(2):1015-1021, 1993. |
Aizenberg et al., “Skeleton of Euplectella sp.: Structural Hierarchy from the Nanoscale to the Macroscale,” Science 309:275-278, 2005. |
Alfantazi et al., “Synthesis of nanocrystalline Zn—Ni alloy coatings,” JMSLD5 15(15):1361-1363, 1996. |
Atanassov et al., “Electrodeposition and properties of nickel-manganese layers,” Surface and Coatings Technology 78:144-149, 1996. |
Bakonyi et al., “Electrodeposited multilayer films with giant magnetoresistance (GMR): Progress and problems,” Progress in Materials Science 55:107-245, 2010. |
Bartlett et al., “Electrochemical deposition of macroporous platinum, palladium and cobalt films using polystyrene latex sphere templates,” Chem. Commun., pp. 1671-1672, 2000. |
Beattie et al., “Comparison of Electrodeposited Copper-Zinc Alloys Prepared Individually and Combinatorially,” J. Electrochem. Soc. 150(11):C802-C806, 2003. |
Bird et al., “Giant Magnetoresistance in Electrodeposited Ni/Cu and Co/Cu Multilayers,” J. Electrochem. Soc. 142(4):L65-L66, 1995. |
Blum, “The Structure and Properties of Alternately Electrodeposited Metals,” presented at the Fortieth General Meeting of the American Electrochemical Society, Lake Placid, New York, Oct. 1, 1921, 14 pages. |
Cohen et al., “Electroplating of Cyclic Multilayered Alloy (CMA) Coatings,” J. Electrochem. Soc. 130(10):1987-1995, 1983. |
Cowles, “High cycle fatigue in aircraft gas turbines—an industry perspective,” International Journal of Fracture 80(2-3):147-163, 1996 (abstract only). |
“Designing with Metals: Dissimilar Metals and the Galvanic Series,” printed Oct. 5, 2017, 3 pages. |
Despic et al., “Electrochemical Formation of Laminar Deposits of Controlled Structure and Composition,” J. Electrochem. Soc. 136(6):1651-1657, 1989. |
Dini et al. “On the High Temperature Ductility Properties of Electrodeposited Sulfamate Nickel,” Plating and Surface Finishing 65(2):36-40, 1978. |
Etminanfar et al., “Corrosion resistance of multilayer coatings of nanolayered Cr/Ni electrodeposited from Cr(III)-Ni(II) bath,” Thin Solid Films 520:5322-5327, 2012. |
Gasser et al., “Materials Design for Acoustic Liners: an Example of Tailored Multifunctional Materials,” Advanced Engineering Materials 6(1-2):97-102, 2004. |
Georgescu et al., “Magnetic Behavior of [Ni/Co—Ni—Mg—N] x n Cylindrical Multilayers prepared by Magnetoelectrolysis,” Phys. Stat. Sol. (a) 189(3):1051-1055, 2002. |
Ghanem et al., “A double templated electrodeposition method for the fabrication of arrays of metal nanodots,” Electrochemistry Communications 6:447-453, 2004. |
Grimmett et al., “Pulsed Electrodeposition of Iron-Nickel Alloys,” J. Electrochem. Soc. 137(11):3414-3418, 1990. |
Hariyanti, “Electroplating of Cu—Sn Alloys and Compositionally Modulated Multilayers of Cu—Sn—Zn—Ni Alloys on Mild Steel Substrate,” Master of Science Thesis, University of Science, Malaysia, Penang, Malaysia, 2007. |
Harris et al., “Improved Single Crystal Superalloys, CMSX-4® (SLS)[La+Y] and CMSX-486®,” TMS (The Minerals, Metals & Materials Society), Superalloys, p. 45-52, 2004. |
Huang et al., “Hardness variation and annealing behavior of a Cr—Ni multilayer electroplated in a trivalent chromium-based bath,” Surface and Coatings Technology 203:3320-3324, 2009. |
Huang et al., “Characterization of Cr—Ni multilayers electroplated from a chromium(III)-nickel(II) bath using pulse current,” Scripta Materialia, 57:61-64, 2007. |
Igawa et al., “Fabrication of SiC fiber reinforced SiC composite by chemical vapor infiltration for excellent mechanical properties,” Journal of Physics and Chemistry of Solids 66:551-554, 2005. |
Ivanov et al., “Corrosion resistance of compositionally modulated multilayered Zn—Ni alloys deposited from a single bath,” Journal of Applied Electrochemistry 33:239-244, 2003. |
Jeong et al., “The Effect of Grain Size on the Wear Properties of Electrodeposited Nanocrystalline Nickel Coatings,” Scripta Mater. 44:493-499, 2001. |
Jia et al., “LIGA and Micromolding” Chapter 4, The MEMS Handbook, 2nd edition, CRC Press, Boca Raton, Florida, Edited by Mohamed Gad-el-Hak, 2006. |
Kalu et al., “Cyclic voltammetric studies of the effects of time and temperature on the capacitance of electrochemically deposited nickel hydroxide,” Journal of Power Sources 92:163-167, 2001. |
Kaneko et al., “Vickers hardness and deformation of Ni/Cu nano-multilayers electrodeposited on copper substrates,” Eleventh International Conference on Intergranular and Interphase Boundaries 2004, Journal of Material Science 40:3231-3236, 2005. |
Karimpoor et al., “Tensile Properties of Bulk Nanocrystalline Hexagonal Cobalt Electrodeposits”, Materials Science Forum 386-388:415-420, 2002. |
Keckes et al., “Cell-wall recovery after irreversible deformation of wood,” Nature Materials 2:810-814, 2003. |
Kirilova et al., “Corrosion behaviour of Zn—Co compositionally modulated multilayers electrodeposited from single and dual baths,” Journal of Applied Electrochemistry 29:1133-1137, 1999. |
Kockar et al., “Effect of potantiostatic waveforms on properties of electrodeposited NiFe alloy films,” Eur. Phys. J. B(42):497-501, 2004. |
Lashmore et al., “Electrodeposited Cu—Ni Textured Superlattices,” J. Electrochem. Soc. 135(5):1218-1221, 1988. |
Lashmore et al., “Electrodeposited Multilayer Metallic Coatings”, Encyclopedia of Materials Science and Engineering, Supp. vol. 1:136-140, 1988. |
Leisner et al., “Methods for electrodepositing composition-modulated alloys,” Journal of Materials Processing Technology 58:39-44, 1996. |
Leith et al., “Characterization of Flow-Induced Compositional Structure in Electrodeposited NiFe Composition-Modulated Alloys” J. Electrochem. Soc. 145(8):2827-2833, 1998. |
Lekka et al., “Corrosion and wear resistant electrodeposited composite coatings,” Electrochimica Acta 50:4551-4556, 2005. |
Lewis et al., “Stability in thin film multilayers and microlaminates: the role of free energy, structure, and orientation at interfaces and grain boundaries,” Scripta Materialia 48:1079-1085, 2003. |
Low et al., “Electrodeposition of composite coatings containing nanoparticles in a metal deposit,” Surface & Coating Technology 201:371-383, 2006. |
Malone, “New Developments in Electroformed Nickel-Based Structural Alloys,” Plating and Surface Finishing 74(1):50-56, 1987. |
Marchese, “Stress Reduction of Electrodeposited Nickel,” Journal of the Electrochemical Society 99(2):39-43, 1952. |
Meng et al., “Fractography, elastic modulus, and oxidation resistance of Novel metal-intermetallic Ni/Ni3Al multilayer films,” J. Mater. Res. 17(4):790-796, 2002. |
Naslain et al., “Synthesis of highly tailored ceramic matrix composites by pressure-pulsed CVI,” Solid State Ionics 141-142:541-548, 2001. |
Naslain, “The design of the fibre-matrix interfacial zone in ceramic matrix composites,” Composites Part A 29A:1145-1155, 1998. |
Nicholls, “Advances in Coating Design for High-Performance Gas Turbines,” MRS Bulletin, p. 659-670, 2003. |
Onoda et al., “Preparation of Amorphous/Crystalloid Soft Magnetic Multilayer Ni—Co—B Alloy Films by Electrodeposition,” Journal of Magnetism and Magnetic Materials 126(1-3):595-598, 1993. |
Parkin et al., “Oscillations in Exchange Coupling and Magnetoresistance in Metallic Superlattice Structures: Co/Ru, Co/Cr, and Fe/Cr,” Physical Review Letters 64(19):2304-2307, 1990. |
Pilone et al., “Model of Multiple Metal Electrodeposition in Porous Electrodes,” Journal of the Electrochemical Society 153(5):D85-D90, 2006. |
Podlaha et al. “Induced Codeposition: I. An Experimental Investigation of Ni—Mo Alloys,” J. Electrochem. Soc. 143(3):885-892, 1996. |
Ross, “Electrodeposited Multilayer Thin Films,” Annual Review of Materials Science 24:159-188, 1994. |
Rousseau et al., “Single-bath Electrodeposition of Chromium-Nickel Compositionally Modulated Multilayers (CMM) From a Trivalent Chromium Bath,” Plating and Surface Finishing, p. 106-110, 1999. |
Saleh et al., “Effects of electroplating on the mechanical properties of stereolithography and laser sintered parts,” Rapid Prototyping Journal 10(5)305-315, 2004. |
Sanders et al., “Mechanics of hollow sphere foams,” Materials Science and Engineering A347:70-85, 2003. |
Sartwell et al., “Replacement of Chromium Electroplating on Gas Turbine Engine Components Using Thermal Spray Coatings,” Report No. NPL/MR/6170-05-8890, Naval Research Laboratory, 2005. (207 pages). |
Schwartz, “Multiple-Layer Alloy Plating”, ASM Handbook 5: Surface Engineering, p. 274-276, 1994. |
Sherik, “Synthesis, Structure and Properties of Electrodeposited Bulk Nanocrystalline Nickel”, Master's Thesis, Queen's University, Ontario, Canada, 1993. |
Shishkovski, “Laser synthesis of functionally graded meso structures and bulk products,” FIZMATLIT, Moscow, Russia, pp. 30-38, 2009. (with English Abstract). |
Simunovich et al., “Electrochemically Layered Copper-Nickel Nanocomposites with Enhanced Hardness,” J. Electrochem. Soc. 141(1):L10-L11, 1994. |
Sperling et al., “Correlation of stress state and nanohardness via heat treatment of nickel-aluminide multilayer thin films,” J. Mater. Res. 19(11):3374-3381, 2004. |
Srivastava et al., “Corrosion resistance and microstructure of electrodeposited nickel-cobalt alloy coatings,” Surface & Coatings Technology 201:3051-3060, 2006. |
Stephenson, Jr., “Development and Utilization of a High Strength Alloy for Electroforming,” Plating 53(2): 183-192, 1966. |
Suresh, “Graded Materials for Resistance to Contact Deformation and Damage,” Science 292:2447-2451, 2001. |
Switzer et al., “Electrodeposited Ceramic Superlattices,” Science 247(4941):444-446, 1990. |
Tench et al., “Considerations in Electrodeposition of Compositionally Modulated Alloys,” J. Electrochem. Soc. 137(10):3061-3066, 1990. |
Tench et al., “Enhanced Tensile Strength for Electrodeposited Nickel-Copper Multilayer Composites,” Metallurgical Transactions A(15A):2039-2040, 1984. |
Thangaraj et al., “Corrosion behavior of composition modulated multilayer Zn—Co electrodeposits produced using a single-bath technique,” J. of Appl. Electrochem. 39:339-345, 2009. |
Thangaraj et al., “Surface Modification by Compositionally Modulated Multilayered Zn—Fe Coatings,” Chinese Journal of Chemistry 26:2285-2291, 2008. |
Tokarz et al., “Preparation, structural and mechanical properties of electrodeposited Co/Cu multilayers,” Phys. Stat. Sol.i 5(11):3526-3529, 2008. |
Touchstone Research Laboratory, Ltd., Material Safety Data Sheet, CFOAM Carbon Foams, 2008. (4 pages). |
Vill et al., “Mechanical Properties of Tough Multiscalar Microlaminates,” Acta metall. mater. 43(2):427-437, 1995. |
Voevodin et al., “Superhard, functionally gradient, nanolayered and nanocomposite diamond-like carbon coatings for wear protection,” Diamond and Related Materials 7:463-467, 1998. |
Wearmouth et al., “Electroforming with Heat-Resistant, Sulfur-Hardened Nickel,” Plating and Surface Finishing 66(10):53-57, 1979. |
Weil et al., “Pulsed Electrodeposition of Layered Brass Structures,” Metallurgical Transactions A 19A:1569-1573, 1988. |
Weil et al., “Properties of Composite Electrodeposits,” U.S. Army Research Office, Final Report, Contract No. DAALO3-87-K-0047, U.S. Army Research Office, 21 pages, 1990. |
Wikipedia, “Gold,” URL= http://en.wikipedia.org/wiki/Gold, version modified Nov. 3, 2008, 15 pages. |
Wikipedia, “Silver,” URL= http://en.wikipedia.org/wiki/Silver, version modified Nov. 3, 2008, 12 pages. |
Wilcox, “Surface Modification With Compositionally Modulated Multilayer Coatings,” The Journal of Corrosion Science and Engineering 6(Paper 52), 2004. |
Wu et al., “Preparation and characterization of superhard CNx/ZrN multilayers,” J. Vac. Sci. Technol. A 15(3):946-950, 1997. |
Yahalom et al., “Formation of composition-modulated alloys by electrodeposition,” Journal of Materials Science 22:499-503, 1987. |
Yang et al., “Effects of SiC sub-layer on mechanical properties of Tyranno-SA/SiC composites with multiple interlayers,” Ceramics International 31:525-531, 2005. |
Yang et al., “Enhanced elastic modulus in composition-modulated gold-nickel and copper-palladium foils,” Journal of Applied Physics 48(3):876-879, 1977. |
Yogesha et al., “Optimization of deposition conditions for development of high corrosion resistant Zn—Fe multilayer coatings,” Journal of Materials Processing Technology 211:1409-1415, 2011. |
Zabludovsky et al., “The Obtaining of Cobalt Multilayers by Programme-controlled Pulse Current,” Transactions of the Institute of Metal Finishing 75(5):203-204, 1997. |
Kruth et al., “Progress in Additive Manufacturing and Rapid Prototyping” CIRP Annals 47(2):525-540, 1998. |
Paz et al., “Nano-Laminated Alloys for Improved Return on Oilfield Assets,” Society of Petroleum Engineers, 2016 (14 pages). |
Number | Date | Country | |
---|---|---|---|
20200277706 A1 | Sep 2020 | US |
Number | Date | Country | |
---|---|---|---|
61802301 | Mar 2013 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 14855088 | Sep 2015 | US |
Child | 16671104 | US | |
Parent | PCT/US2014/031096 | Mar 2014 | US |
Child | 14855088 | US |