The present disclosure generally relates to position measurement systems and methods of forming position measurement systems.
Offshore drilling rigs often include direct-acting tensioners to compensate for wave-induced motion. More specifically, the direct-acting tensioners may include one or more massive hydraulic cylinders having a piston rod. The hydraulic cylinders continuously dampen wave-induced motion and thereby balance the drilling rig and/or stabilize the drill string. As such, dampening may be optimized by measuring, monitoring, and adjusting a position of the piston rod within the hydraulic cylinder. Moreover, the hydraulic cylinders are generally mounted below a deck of the drilling rig, i.e., in a splash zone, and are therefore often exposed to an extremely corrosive and wear-inducing environment from airborne salt spray, sea water, ice, moving cables, and/or debris. Consequently, the piston rods of such hydraulic cylinders must exhibit excellent corrosion-resistance and wear-resistance, and must remain crack-free over a service life.
Other types of piston rods and hydraulic cylinders may actuate large gate valves for applications including canals, locks, hydrodynamic power plants, foundries, and metal processing facilities. Actuation of the gate valves may be controlled by measuring and adjusting a position or displacement of the piston rods within the hydraulic cylinders. Further, the piston rods may undergo thousands of wear-inducing displacements and/or may experience impacts from moving machinery, components, and seals during operation of the hydraulic cylinders.
A method of forming a position measurement system includes melting a surface of a substrate formed from a first material, wherein the surface defines at least one groove therein and wherein the surface is melted within the at least one groove. The method also includes, concurrent to melting, depositing a second material into the at least one groove to form a mixture of the first material and the second material. In addition, the method includes solidifying the mixture to form an indicator material that is distinguishable from and metallurgically bonded to the first material. The method also includes depositing an alloy onto the substrate to form a corrosion-resistant cladding that covers the indicator material and the surface to thereby form the position measurement system.
In one embodiment, the method includes machining a surface of a substrate to define a plurality of grooves therein. The substrate is formed from a first magnetic material and is a cylindrical rod having a longitudinal axis. Each of the plurality of grooves is spaced apart from an adjacent one of the plurality of grooves along the longitudinal axis, and the method includes melting the surface within each of the plurality of grooves to thereby distribute the plurality of grooves evenly along the longitudinal axis. Further, the method includes, concurrent to melting, depositing a second non-magnetic material within each of the plurality of grooves to thereby form a plurality of respective mixtures of the first magnetic material and the second non-magnetic material. The method also includes solidifying each of the plurality of respective mixtures to form a non-magnetic indicator material that is distinguishable from and metallurgically bonded to the first magnetic material. In addition, the method includes depositing a non-magnetic alloy onto the substrate to form a corrosion-resistant cladding that covers and is metallurgically bonded to each of the non-magnetic indicator material and the surface to thereby form the position measurement system.
A position measurement system includes a substrate formed from a first material and having a surface defining at least one groove therein. The position measurement system further includes an indicator material disposed within the at least one groove. The indicator material is formed from a mixture of the first material and the second material, and is distinguishable from and metallurgically bonded to the first material. In addition, the position measurement system includes a corrosion-resistant cladding formed from an alloy and disposed on the substrate so as to cover the indicator material and the surface.
The above features and other features and advantages of the present disclosure are readily apparent from the following detailed description of the best modes for carrying out the disclosure when taken in connection with the accompanying drawings.
Referring to the Figures, wherein like reference numerals refer to like elements, a method of forming a position measurement system 10 is described herein. The position measurement system 10 may be useful for detecting a position of a substrate 12 that operates in a corrosive environment. That is, the position measurement system 10 exhibits excellent corrosion-resistance, and the position measurement system 10 may be useful for determining a position or displacement of a substrate 12 with respect to a reference position. As such, the position measurement system 10 may be useful for marine applications, such as offshore drilling rigs, for indicating a position of the substrate 12, e.g., a piston rod, within a hydraulic cylinder. However, the position measurement system 10 may also be useful for non-marine applications requiring position measurement and corrosion-resistance including, but not limited to, canals, locks, hydrodynamic power plants, foundries, and metal processing facilities.
Referring to
The first material may be a metal. In addition, the first material may be ferrous. Therefore, the first material may be magnetic, and may have a first magnetic permeability. The first material may be selected from materials such as, but not limited to, steel, carbon steel, alloy steel, stainless steel, tool steel, cast iron, and combinations thereof. In one non-limiting example, the first material may be a heat-treated, low alloy, high strength steel such as SAE (Society of Automotive Engineers) 4130 steel or SAE 4340 steel. In another non-limiting example, the first material may be a plain carbon steel, such as SAE 1045 steel.
Referring now to
With continued reference to
Referring again to
More specifically, the second material may be a filler metal for a laser welding operation, as set forth in more detail below. Therefore, the second material may be non-magnetic and may be provided as a powder or wire for injection and melting by a laser (not shown). As such, the indicator material 42 may also be non-magnetic. In another non-limiting variation, the second material may be magnetic. For this variation, the indicator material 42 may also be magnetic and may have a second magnetic permeability that is different from the first magnetic permeability of the first material set forth above.
For embodiments where the first material is low alloy, high strength steel or plain carbon steel, the second material may be an alloy including an element selected from the group of nickel, cobalt, and combinations thereof. Nickel and/or cobalt may be present in the second material to provide corrosion-resistance to the indicator material 42. More specifically, nickel and/or cobalt may be present in the second material in an amount of from about 1 part to about 90 parts by weight based on 100 parts by weight of the second material. For example, a suitable second material for providing the indicator material 42 with excellent corrosion-resistance may include about 65 parts by weight nickel, about 20 parts by weight chromium, about 8 parts by weight molybdenum, about 3.5 parts by weight of a combination of niobium and tantalum, and about 4.5 parts by weight of iron based on 100 parts by weight of the metal alloy, and may be commercially available under the trade name INCONEL® 625 from Special Metals Corporation of New Hartford, N.Y. Likewise, a suitable second material may include about 54 parts by weight cobalt, about 26 parts by weight chromium, about 9 parts by weight nickel, about 5 parts by weight molybdenum, about 3 parts by weight iron, about 2 parts by weight tungsten, and about 1 part by weight of a combination of manganese, silicon, nitrogen, and carbon, and may be commercially available under the trade name ULTIMET® from Haynes International, Inc. of Kokomo, Ind. Further, other suitable non-limiting examples of second materials may include alloys commercially available under the trade names Micro-Melt® CCW alloy from Carpenter Technology Corporation of Reading, Pa., Stellite® 21 from Stellite Coatings of Goshen, Ind., and Eatonite™ ABC-L1 from Eaton Corporation of Cleveland, Ohio.
Alternatively, the second material may be a stainless steel. Suitable stainless steels include, but are not limited to, 308-, 316-, 321-, and 347-grade austenitic stainless steels. For some applications requiring excellent corrosion-resistance over a comparatively shorter service life, e.g., less than about 15 years, or under comparatively less-corrosive operating environments, e.g., brackish water, suitable second materials may alternatively include martensitic stainless steels, ferritic stainless steels, super ferritic stainless steels, duplex stainless steels, super duplex stainless steels, and combinations thereof.
Referring again to
The indicator material 42 is also metallurgically bonded to the first material. For example, the indicator material 42 may be weld bonded to the first material. That is, since the indicator material 42 is formed from a mixture of the first material and the second material, e.g., after melting, the indicator material 42 is metallurgically bonded to the first material, as set forth in more detail below.
With continued reference to
The alloy of the corrosion-resistant cladding 44 may be a metal alloy for a laser cladding operation. Therefore, the alloy may be provided as a powder or wire for injection and melting by a laser (not shown). In addition, the alloy and the corrosion-resistant cladding 44 may be non-magnetic. Alternatively, the alloy and the corrosion-resistant cladding 44 may be magnetic, but may have a magnetic permeability that is different from the first magnetic permeability of the first material set forth above.
The alloy of the corrosion-resistant cladding 44 may be similar to the second material. For example, for applications where the second material is INCONEL® 625, the alloy of the corrosion-resistant cladding 44 may also be INCONEL® 625. Likewise, for applications where the second material is 316-grade stainless steel, the alloy of the corrosion-resistant cladding 44 may also be 316-grade stainless steel. Alternatively, the second material and the alloy of the corrosion-resistant cladding 44 may be dissimilar. For example, according to cost or weight considerations, the second material may be 316-grade stainless steel, and the alloy of the corrosion-resistant cladding 44 may be INCONEL® 625.
For embodiments where the first material is low alloy, high strength steel or plain carbon steel, the alloy of the corrosion-resistant cladding 44 may include an element selected from the group of nickel, cobalt, and combinations thereof. Nickel and/or cobalt may be present in the alloy to provide corrosion-resistance to the position measurement system 10. More specifically, nickel and/or cobalt may be present in the alloy in an amount of from about 1 part to about 90 parts by weight based on 100 parts by weight of the alloy. For example, a suitable alloy of the corrosion-resistant cladding 44 may include about 65 parts by weight nickel, about 20 parts by weight chromium, about 8 parts by weight molybdenum, about 3.5 parts by weight of a combination of niobium and tantalum, and about 4.5 parts by weight of iron based on 100 parts by weight of the alloy, and may be commercially available under the trade name INCONEL® 625 from Special Metals Corporation of New Hartford, N.Y. Likewise, a suitable alloy of the corrosion-resistant cladding 44 may include about 54 parts by weight cobalt, about 26 parts by weight chromium, about 9 parts by weight nickel, about 5 parts by weight molybdenum, about 3 parts by weight iron, about 2 parts by weight tungsten, and about 1 part by weight of a combination of manganese, silicon, nitrogen, and carbon, and may be commercially available under the trade name ULTIMET® from Haynes International, Inc. of Kokomo, Ind. Further, other suitable non-limiting examples of alloys may be commercially available under the trade names Micro-Melt® CCW alloy from Carpenter Technology Corporation of Reading, Pa., Stellite® 21 from Stellite Coatings of Goshen, Ind., and Eatonite™ ABC-L1 from Eaton Corporation of Cleveland, Ohio.
Alternatively, the alloy of the corrosion-resistant cladding 44 may be a stainless steel. Suitable stainless steels include, but are not limited to, 308-, 316-, 321-, and 347-grade austenitic stainless steels. For some applications, suitable alloys may alternatively include martensitic stainless steels, ferritic stainless steels, super ferritic stainless steels, duplex stainless steels, super duplex stainless steels, and combinations thereof.
Since the alloy of the corrosion-resistant cladding 44 may include nickel and/or cobalt, the corrosion-resistant cladding 44 exhibits excellent corrosion-resistance. More specifically, the corrosion-resistant cladding 44 may be substantially resistant to corrosion from sea water at an ambient temperature of from about −40° C. to about 50° C. Stated differently, the corrosion-resistant cladding 44 minimizes oxidation of the surface 20 of the substrate 12 in air after exposure to sea water. As used herein, in contrast to fresh water, the terminology “sea water” refers to water having a salinity of from about 31 parts by volume to about 40 parts by volume based on 1 trillion parts by volume of sea water, i.e., about 31 ppt to about 40 ppt (about 3.1% to about 4%), and a density of about 1.025 g/ml at 4° C. Further, sea water includes dissolved salts of one or more ions selected from the group including chloride, sodium, sulfate, magnesium, calcium, potassium, bicarbonate, bromide, borate, strontium, fluoride, and combinations thereof. Sea water may include brackish, saline water, and brine.
Additionally, the corrosion-resistant cladding 44 may exhibit a free corrosion potential, Ecorr, of less than or equal to −0.200. As used herein, the terminology “free corrosion potential” refers to an absence of net electrical current flowing to or from the substrate 12 in sea water relative to a reference electrode. Further, the corrosion-resistant cladding 44 may exhibit a corrosion rate of less than or equal to about 0.000254 mm per year. As used herein, the terminology “corrosion rate” refers to a change in the substrate 12 and/or corrosion-resistant cladding 44 caused by corrosion per unit of time and is expressed as an increase in corrosion depth per year. Therefore, the corrosion-resistant cladding 44 may exhibit minimized susceptibility to localized corrosion from, for example, pitting and/or crack propagation.
As shown in
Comparatively rougher surfaces generally exhibit less wear-resistance and wear more quickly as compared to relatively smoother surfaces, since irregularities such as peaks and valleys in surfaces may form initiation sites for cracks, stress zones, and/or corrosion. Therefore, since the external surface 48 is substantially smooth, the corrosion-resistant cladding 44 exhibits excellent smoothness and resulting wear- and corrosion-resistance.
Referring again to
Referring now to the method, the method of forming the position measurement system 10 is described with general reference to
Therefore, prior to melting, the method may include machining the surface 20 to define the plurality of grooves 22 therein, wherein each of the plurality of grooves 22 is disposed substantially perpendicular to the longitudinal axis 14 (
Referring again to
Laser welding, i.e., melting the surface 20 of the at least one groove 22 and concurrently depositing the second material into the at least one groove 22, may be carried out by a laser welding device (not shown) including a laser emitted from a welding head. The laser welding device may also include a laser-structured light seam tracker apparatus attached to the welding head to enable accurate, automatic positioning of the welding head over the plurality of grooves 22. Such an apparatus may minimize machining and positioning errors during machining.
The shape of the at least one groove 22 may minimize shrinkage cracking and porosity of the mixture. As used herein, the terminology porosity refers to an amount of void space within a material and is expressed as a percentage of the total material. In addition, the at least one groove 22 minimizes an amount of the first material that melts during laser welding, which in turn minimizes an amount of iron in the resulting mixture of the first material and the second material. Such minimized iron content of the mixture increases the corrosion-resistance of the position measurement system 10.
Referring again to
With continued reference to
Laser cladding, i.e., depositing the alloy onto the substrate to form the corrosion-resistant cladding 44, may be carried out by a laser cladding system (not shown) including a laser emitted from a welding head. The corrosion-resistant cladding 44 may be deposited onto the surface 20 and the indicator material 42 in a tightly spiraling path along the longitudinal axis 14. For example, the substrate 12 may be rotated while the laser cladding system deposits the corrosion-resistant cladding 44 onto the surface 20 and the indicator material 42 in the tightly spiraling path.
The corrosion-resistant cladding 44 may be deposited directly onto the indicator material 42 so as to cover the indicator material 42. Therefore, the method does not require intermediate grinding or machining of the indicator material 42 before deposition of the alloy to form the corrosion-resistant cladding 44. The alloy may be deposited so that the corrosion-resistant cladding 44 is a single layer having a preliminary thickness (not shown) of from about 1.7 mm to about 2.0 mm, e.g., about 1.8 mm to about 1.9 mm. Subsequently, the corrosion-resistant cladding 44 may be ground to the thickness 46 (
It is to be appreciated that the alloy may be deposited onto the substrate 12 after melting, concurrently depositing the second material, and solidifying the mixture as set forth above. Alternatively, the method may include concurrently melting, depositing the second material, and depositing the alloy. That is, melting, depositing the second material, and depositing the alloy may be concurrent. More specifically, the second material and the alloy may be of the same composition, i.e., may be the same material, so that the second material may be deposited into the at least one groove 22 as the alloy is deposited onto the substrate 12 to form the corrosion-resistant cladding 44.
The method may further include finishing the corrosion-resistant cladding 44 to define the external surface 48 that is substantially smooth. For example, the corrosion-resistant cladding 44 may be machined, ground, and/or polished so that the external surface 48 has the surface roughness, Ra, of from about 0.1 microns to about 0.15 microns.
The method may also include increasing the bond strength between the corrosion-resistant cladding 44 and each of the indicator material 42 and the first material. That is, since the corrosion-resistant cladding 44 is formed from the alloy deposited via laser cladding, the corrosion-resistant cladding 44 exhibits excellent bond strength as set forth above.
In another embodiment, as described with reference to
For this embodiment, the method also includes melting the surface 20 within each of the plurality of grooves 22 to thereby distribute the plurality of grooves 22 evenly along the longitudinal axis 14. That is, the surface 20 of each of the plurality of grooves 22 may melt and thereby expand from the machined width 50 to the groove width 34 to space each groove 22 apart from an adjacent groove 22 and define the gap 36 therebetween. Therefore, melting may distribute the plurality of grooves 22 evenly along the longitudinal axis 14 so that the ratio of the groove width 34 to the gap width 38 is about 1:1.
Concurrent to melting, the method includes depositing the second non-magnetic material within each of the plurality of grooves 22 to thereby form the plurality of respective mixtures of the first magnetic material and the second non-magnetic material. The method also includes solidifying the plurality of respective mixtures to form the non-magnetic indicator material 42 that is distinguishable from and metallurgically bonded to the first magnetic material. The method additionally includes depositing the non-metallic alloy onto the substrate 12 to form the corrosion-resistant cladding 44 that covers and is metallurgically bonded to each of the non-magnetic indicator material 42 and the surface 20 to thereby form the position measurement system 10. It is to be appreciated that melting, depositing the second non-magnetic material, and depositing the non-magnetic alloy may be concurrent. The method may further include increasing the bond strength between the corrosion-resistant cladding 44 and each of the non-magnetic indicator material 42 and the first magnetic material.
In operation, the position measurement system 10 may interact with one or more sensors (not shown), e.g., one or more Hall effect sensors or magneto-resistance sensors, to indicate the position of the substrate 12 with respect to a reference position. For example, the sensors may continuously interrogate the position measurement system 10 and detect the indicator material 42 disposed beneath the corrosion-resistant cladding 44. In particular, as the position measurement system 10 translates past the sensors, e.g., extends or retracts within a hydraulic cylinder, the sensors may detect a change in the magnetic field due to the presence of the alternating magnetic first material and non-magnetic indicator material 42, and a displacement of the position measurement system 10 with respect to a reference position may be calculated. As the position measurement system 10 changes position, the sensors may detect a position of the substrate 12 to an accuracy of about 1 mm. If desired, the sensors may also include a pulse multiplier transducer (not shown) to increase the sensitivity of the sensors. For example, in combination, the sensors and the pulse multiplier transducer may detect a position of the substrate 12 to an accuracy of about 0.1 mm. For redundancy during operation, the position measurement system 10 may interact with at least two sensors and two pulse multiplier transducers.
The aforementioned position measurement system 10 formed by the method as described herein exhibits excellent corrosion-resistance as compared to other systems (not shown) that include electroplated coatings such as nickel-chromium coatings; thermally-sprayed ceramic coatings such as chromia-titania coatings and alumina-titania coatings; high velocity oxy-fuel gas (HVOF) thermally-sprayed ceramic coatings including hard particles such as tungsten carbide, chromium carbide, oxides, and combinations thereof disposed in a cobalt, nickel-chromium, or nickel binder phase; and plasma-sprayed coatings. Therefore, the position measurement system 10 may be especially suitable for applications requiring continuous corrosion-resistance over an extended service life, e.g., about 15 years or more, such as piston rods for hydraulic cylinders in service within a saltwater splash zone of an offshore drilling rig.
In addition, the corrosion-resistant cladding 44 and indicator material 42 each exhibit minimized porosity. For example, the corrosion-resistant cladding 44 may have a porosity of about 0.03 percent, which may contribute to reduced cracking and increase corrosion-resistance. That is, the aforementioned porosity minimizes formation of interconnected paths within the corrosion-resistant cladding 44. Such interconnected paths may allow ingress of corrosive elements and compromise the corrosion-resistance of the position measurement system 10. In contrast, HVOF coatings may have a porosity of from about 0.5 percent to about 2.0 percent, and plasma sprayed ceramic coatings may have a porosity of from about 3.0 percent to about 10 percent, and may therefore exhibit reduced corrosion-resistance and spalling.
Further, the corrosion-resistant cladding 44 of the position measurement system 10 may be ductile. Therefore, the corrosion-resistant cladding 44 may remain crack-free upon comparatively high-energy impacts. In contrast, HVOF coatings and plasma sprayed coatings are generally brittle and may crack severely upon comparatively low-energy impacts.
The position measurement systems 10 and related methods provide corrosion-resistant claddings 44 having excellent hardness and corrosion-resistance. Therefore, the position measurement systems 10 are suitable for exposure to sea water, e.g., for applications requiring coated metal substrates 12 for operation within a splash-zone of an offshore drilling rig. The corrosion-resistant claddings 44 are smooth and exhibit excellent compressive residual stress. Therefore, the position measurement systems 10 exhibit improved fatigue life and resistance to tensile stress, and reduced infiltration and propagation of fatigue cracks, shrink cracks, and other flaws. Further, the methods are cost-effective, and minimize discontinuities in the corrosion-resistant claddings 44 and indicator material 42 such as cracks and/or pores.
While the best modes for carrying out the disclosure have been described in detail, those familiar with the art to which this disclosure relates will recognize various alternative designs and embodiments for practicing the disclosure within the scope of the appended claims.
This application claims the benefit of U.S. Provisional Patent Application No. 61/314,248, filed on Mar. 16, 2010, which is hereby incorporated by reference in its entirety.
Number | Date | Country | |
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61314248 | Mar 2010 | US |