The statements in this section merely provide background information related to the present disclosure and may not constitute prior art.
The disclosure is related in general to wellsite equipment such as oilfield surface equipment, oilfield cables and the like.
As oil and gas exploration evolves, wells are drilled to increasing depths and in increasingly harsh conditions. Cables used in the oilfield industry can be subjected to repeated physical stress, high temperatures, hydrocarbon solvents, and high concentrations of hydrogen sulfide (H2S). Greater demands are being placed on electrical conductors to carry electricity to these increasing depths.
When polymer insulated or jacketed metallic members are run into and out of an oil well, there are mechanical forces acting at the interfaces between metals and polymers. There may be separation of polymer from the metallic interfaces due to the deformation of polymer when such components are bent, when the cable passes over sheaves or rollers, when the cable passes through a stuffing box or packers that are used for pressure control, when there is a coefficient of thermal expansion difference between polymer and metal, when there is gas migration between polymer and metal interface, and when any similar operations are performed. These physical stresses may cause the polymeric covering to pull away from the metal and leave air gaps. In the case of electrical conductors, these air gaps may lead to the development of coronas.
As shown in
The presence of H2S in well fluids may result in failures when standard galvanized improved plow steel (GIPS) armor wires are used as strength members. H2S in the form of a gas or a gas dissolved in liquids may attack metals by combining with them to form metallic sulfides and atomic hydrogen. The destructive process is principally hydrogen embrittlement, accompanied by chemical attack. Chemical attack is commonly referred to as sulfide stress cracking. H2S attacks metals with a wide variation in intensity. Many commonly used carbon and alloy steels are susceptible to H2S damage. High-strength steels used in armor wires, which may have high carbon content and may be highly cold-worked, may be particularly susceptible to H2S damage.
Some metals and special alloys such as, for example, the nickel-steel alloy HC265, are very resistant to H2S attack. However, these special alloys may have much lower electrical conductivity than standard GIPS armor wire. This is a drawback in wireline operations, where armor wire is typically used as an electrical return path.
It remains desirable to provide improvements in wireline cables and/or downhole assemblies.
In an embodiment, a method for manufacturing a component first includes providing at least one metallic element. A surface of the at least one metallic element is modified to facilitate bonding of the at least one metallic element to a polymeric layer. The polymeric layer is bonded to the at least one metallic element to form the component.
In an embodiment, modifying the surface of the at least one metallic element comprises heating the surface of the at least one metallic element. The heating facilitates bonding of the at least one metallic element to the polymeric layer. The heating is performed by passing the at least one metallic element adjacent a heat source, such as an infrared heat source. The at least one metallic element is thereby heated to a temperature of about 500° F. for a time sufficient to modify the surface. The at least one metallic element is also heated in a modifying fluid that modifies the surface of the at least one metallic element when heated. Bonding the at least one metallic element to the polymeric layer may further comprise extruding the polymeric layer over the at least one metallic element, whereby the polymeric layer is bonded to the at least one metallic element and forms the component.
In an embodiment, a component includes at least one metallic element having a modified surface, and a polymeric layer bonded to the at least one metallic element to form the component.
The embodiments discussed in this disclosure use a variety of metals, alloys and platings as well as polymer jacketing materials chosen for their insulating and chemical protective properties and their abilities to bond to metal.
The embodiments of the present disclosure particularly relate to polymer insulation/jackets that are chemically/mechanically bonded to the metal surface. The polymer insulation/jackets that are chemically/mechanically bonded to the metal surface are used to prevent separation of polymer from metal interface due to the dynamics of going over a sheave, through a stuffing box or packers that are used for pressure control, due to coefficient of thermal expansion difference between polymer and metal, and due to other operations in an oil well environment. The polymer insulation/jackets that are chemically/mechanically bonded to the metal surface further prevent gas migration between the polymer and metal interface.
These and other features and advantages of the present invention will be better understood by reference to the following detailed description when considered in conjunction with the accompanying drawings wherein:
The methods described herein are for making and using metallic wire oilfield cable components with continuously bonded polymeric jackets. However, it should be understood that the methods may equally be applied to other metallic components having bonded polymeric jackets, and that methods for making and using such metallic components having bonded polymeric jackets are also within the scope of the present disclosure.
Bonding to the metal surface is used to prevent separation of polymer from metal at the polymer and metal interface due to the dynamics of going over a sheave, through a stuffing box or packers that are used for pressure control, and coefficient of thermal expansion differences between polymer and metal. Bonding to the metal surface is also used to prevent gas migration between polymer and metal interface. Bonding techniques include modifying metal surfaces through exposure to heat sources, such as infrared heat sources, to facilitate bonding with polymers, and using polymers amended to facilitate bonding with those metals. By eliminating the presence of gaps between the metallic components and the polymers extruded over those components, these embodiments may greatly minimize the occurrence of coronas and eliminate potential pathways for downhole gases inside the insulation. These embodiments may be advantageously used individually as slickline cables capable of telemetry transmission for battery-operated downhole tools, for example, as part of monocable or coaxial cable embodiments, as conductor or conductor/strength member components in hepta-configuration cables, and as components in other multi-conductor wireline cable configurations, as will be appreciated by those skilled in the art.
Metallic Wires
The metallic wires used at the cores of the components described in this disclosure may comprise copper-clad steel, aluminum-clad steel, anodized aluminum-clad steel, titanium-clad steel, Carpenter alloy 20Mo6HS, GD31Mo, austenitic stainless steel, galvanized carbon steel, copper, titanium clad copper GIPS wire, combinations thereof, or other metals, as will be appreciated by those skilled in the art.
Modified Polymer
The modified polymer may comprise modified polyolefins. Where needed to facilitate bonding between materials that would not otherwise bond, the described polymers may be amended with one of several adhesion promoters such as, but not limited to, unsaturated anhydrides, (mainly maleic-anhydride, or 5-norbornene2,3-dicarboxylic anhydride), carboxylic acid, acrylic acid, or silanes. Trade names of commercially available, amended polyolefins with these adhesion promoters may include ADMER© from Mitsui Chemical, Fusabond® and Bynel® from DuPont, and Polybond® from Chemtura. Other suitable adhesion promoters may also be employed, as desired.
The modified polymer may comprise modified TPX (4-methylpentene-1 based, crystalline polyolefin). Where needed to facilitate bonding between materials that would not otherwise bond, the described polymers may be amended with one of several adhesion promoters, such as, but not limited to, unsaturated anhydrides, (mainly maleic-anhydride, or 5-norbornene-2,3-dicarboxylic anhydride), carboxylic acid, acrylic acid, or silanes. TPX™ from Mitsui Chemical is a commercially available, amended TPX (4-methylpentene-1 based, crystalline polyolefin) comprising these adhesion promoters. Other suitable adhesion promoters may also be employed, as desired.
The modified polymer may comprise modified fluoropolymers. Modified fluoropolymers containing adhesion promoters may be used where needed to facilitate bonding between materials that would not otherwise bond. As listed above, these adhesion promoters may comprise unsaturated anhydrides, (mainly maleicanhydride or 5-norbornene-2,3-dicarboxylic anhydride), carboxylic acid, acrylic acid, and silanes). Examples of commercially available fluoropolymers modified with adhesion promoters include Tefzel® from DuPont Fluoropolymers, modified ETFE resin, which may be configured to promote adhesion between polyamide and fluoropolymer; Neoflon™-modified fluoropolymer from Daikin America, Inc., which is configured to promote adhesion between polyamide and fluoropolymer; ETFE (Ethylene tetrafluoroethylene) from Daikin America, Inc., or EFEP (ethylene-fluorinated ethylene propylene) from Daikin America, Inc.
Polymer Insulation—Unmodified and Reinforced which have Low Dielectrical Coefficient.
The polymer insulation may include, for example, commercially available polyolefins. The polyolefin may be used as is or reinforced with, carbon, glass, aramid or any other suitable natural or synthetic fiber. Along with fibers in polymer matrix, any other reinforcing additives such as, but not limited to, micron sized PTFE, graphite, Ceramer™, HDPE (High Density Polyethylene), LDPE (Low Density Polyethylene), PP (Ethylene tetrafluoroethylene), PP copolymer or similar materials may also be utilized.
The polymer insulation may also include, for example, commercially available fluoropolymers. The fluoropolymer may be used as is or reinforced with carbon, glass, aramid or any other suitable natural or synthetic fiber. Along with fibers in polymer matrix, any other reinforcing additives such as, but not limited to, micron sized PTFE, graphite, Ceramer™, ETFE (Ethylene tetrafluoroethylene) from Du Pont, ETFE (Ethylene tetrafluoroethylene) from Daikin America, Inc., EFEP (ethylene-fluorinated ethylene propylene) from Daikin America, Inc. PFA (perfluoroalkoxy polymer) from Dyneon™ fluoropolymer, PFA (perfluoroalkoxy polymer) from Solvay Slexis, Inc., PFA (perfluoroalkoxy polymer) from Daikin America, Inc., PFA (perfluoroalkoxy polymer) from DuPont Fluoropolymer, Inc., may also be used.
Jacketing Materials
The jacketing materials may comprise polyamide. Polyamides may comprise Nylon 6, Nylon 66, Nylon 6/66, Nylon 6/12, Nylon 6/10, Nylon 11, or Nylon 12. Trade names of commercially available versions of these polyamide materials may comprise Orgalloy®, RILSAN® or RILSAN® from Arkema, BASF Ultramid®, Miramid® from BASF, and Zytel® DuPont Engineering Polymers.
The jacketing materials may comprise unmodified or reinforced fluoropolymers. Commercially available fluoropolymers can be used as is or reinforced with carbon, glass, aramid or any other suitable natural or synthetic fiber, for example. Along with fibers in polymer matrix, any other reinforcing additives such as micron sized PTFE, graphite, Ceramer™, ETFE (Ethylene tetrafluoroethylene) from Du Pont, ETFE (Ethylene tetrafluoroethylene) from Daikin America, Inc., EFEP (ethylene-fluorinated ethylene propylene) from Daikin America, Inc., PFA (perfluoroalkoxy polymer) from Dyneon™ fluoropolymer, PFA (perfluoroalkoxy polymer) from Solvay Slexis, Inc., PFA (perfluoroalkoxy polymer) from Daikin America, Inc., PFA (perfluoroalkoxy polymer) from DuPont Fluoropolymer, Inc., may also be used.
Material Combinations
The materials and processes described hereinabove may be used to form a number of different types of metallic wire cable components, such as wireline cable components or the like, with continuously bonded polymeric jackets. First through fifth embodiments, discussed in more detail below, disclose different combinations of materials which may be used. In each embodiment, the metallic wire used may be any of those discussed above. The specific materials for polymeric layers are also discussed above. The heating and extrusion processes used may be any of those discussed hereinbelow.
As shown in
In the method of the present disclosure, a surface 108 of the metallic element 104 is modified to facilitate a bonding between the metallic element 104 and the polymeric layer 106. The surface 108 may be modified by heating the metallic element 104 prior to extruding the polymeric layer 106 thereover to enhance the bonding. For example, the surface 108 may be heated through infrared heating, although other forms of heating are also within the scope of the present disclosure. The polymeric layer 106 forms the bonded polymer insulation of the cable component 102. The polymeric layer 106 may be modified to bond to the metallic element 104. The polymer of the polymeric layer 106 may be selected for its low dielectrical rating to offer enhanced telemetry capabilities.
In
As shown in
In
One of ordinary skill in the art should appreciate that a variety of metal combinations may be used for the metallic element 104 in first embodiment including, but not limited to, copper-clad steel, aluminum-clad steel, anodized aluminum-clad steel, titanium-clad steel, Carpenter alloy 20Mo6HS, GD31Mo, austenitic stainless steel, high strength galvanized carbon steel, copper, and titanium clad copper. Other suitable metal combinations may also be used within the scope of the present disclosure.
As depicted in
In the second embodiment, the polymeric layer 206 includes a thin tie layer 218 of polymer that is modified to bond the metallic element 204 to an outer unmodified polymer insulation 220. The unmodified polymer insulation 220 may be chosen for its dielectrical properties to enhance telemetry capabilities of the cable component 202, for example. The basic process is depicted in
As shown in
One of ordinary skill in the art should appreciate that a variety of metal combinations may be used for the metallic element 204 of the second embodiment including, but not limited, to copper-clad steel, aluminum-clad steel, anodized aluminum-clad steel, titanium-clad steel, Carpenter alloy 20Mo6HS, GD31Mo, austenitic stainless steel, high strength galvanized carbon steel, copper, and titanium clad copper. Other suitable metal combinations may also be used within the scope of the present disclosure.
As depicted in
In the third embodiment, the polymeric layer 306 includes a chemically protective virgin outer polymer jacket 322. The chemically protective virgin outer polymer jacket 322 is applied over the thin tie layer 318 of modified polymer to form or create a bond from the metallic element 304 to the chemically protective virgin outer polymer jacket 322. The unmodified polymer of the chemically protective virgin outer polymer jacket 322 is chosen for its chemically protective properties. In
As shown in
One of ordinary skill in the art should appreciate that a variety of metal combinations may be used for the metallic element 304 of the third embodiment including, but not limited to, copper-clad steel, aluminum-clad steel, anodized aluminum-clad steel, titanium-clad steel, Carpenter alloy 20Mo6HS, GD31Mo, austenitic stainless steel, high strength galvanized carbon steel, copper, and titanium clad copper. Other suitable metal combinations may also be used within the scope of the present disclosure.
As depicted in
In the fourth embodiment, the amended polymeric layer 406 is extruded directly over the metallic element 404, followed by the chemically protective polymeric outer jacket 422. In the fifth embodiment, the thin tie layer 518 bonds the metallic element 504 to the unmodified polymer insulation 520, followed by the chemically protective polymeric outer jacket 522. The metallic element 404, 504 may either be solid as shown in
In
As shown in
One of ordinary skill in the art should appreciate that a variety of metal combinations may be used for the metallic element 404 of the fourth embodiment including, but not limited to, copper-clad steel, aluminum-clad steel, anodized aluminum-clad steel, titanium-clad steel, Carpenter alloy 20Mo6HS, GD31Mo, austenitic stainless steel, high strength galvanized carbon steel, copper, and titanium clad copper). Other suitable metal combinations may also be used within the scope of the present disclosure.
The fifth embodiment of the disclosure is shown in
As shown in
One of ordinary skill in the art should appreciate that a variety of metal combinations may be used for the metallic element 504 of the fifth embodiment including, but not limited to, copper-clad steel, aluminum-clad steel, anodized aluminum-clad steel, titanium-clad steel, Carpenter alloy 20Mo6HS, GD31Mo, austenitic stainless steel, high strength galvanized carbon steel, copper, and titanium clad copper. Other suitable metal combinations may also be used within the scope of the present disclosure.
Wire and Polymer Heating
To facilitate bonding between successive layers in the various embodiments disclosed herein, the surface 108, 208, 308, 408, 508 of a current outer layer (either the inner metallic element 104, 204, 304, 404, 504 or one of the polymeric layers 106, 206, 306, 406, 506) is heated and, in the case of a polymeric layer 106, 206, 306, 406, 506, melted slightly immediately prior to the next polymer being extruded onto the cable component 102, 202, 302, 402, 502. These processes can be applied during the addition of any of the polymeric layers 106, 206, 306, 406, 506.
The process of the present disclosure may be better facilitated by adding small amounts of short carbon fibers (such as about 1% to about 10% weight) into the polymer matrices used in the polymeric layers 106, 206, 306, 406, 506. In general, carbon fibers are electromagnetically reflective. As a result, electromagnetic (EM) waves (heat) transfer more quickly and efficiently to the polymer matrix. This optimized heating of the polymer matrix may reduce polymer melting times, minimize potentially damaging heat exposure, and enables greatly increased production line speeds for armor-wire-caging and jacket-extrusion processes.
Process Heating Methods to Facilitate Bonding or Embed Metallic Elements into Polymeric Layers
A variety of heating methods may be used alone or in combination to embed metallic elements 104, 204, 304, 404, 504 into the polymeric layers 106, 206, 306, 406, 506 or facilitate bonding between the polymeric layers 106, 206, 306, 406, 506 as required in the embodiments described in this disclosure. Suitable heating methods may include, but are not limited to, infrared heaters emitting short, medium or long infrared waves; ultrasonic waves; microwaves; lasers; other suitable electromagnetic waves; conventional heating; induction heating; and combinations thereof, as will be appreciated by those skilled in the art.
The metallic element 104, 204, 304, 404, 504 is heated to a temperature sufficient to modify the surface 108, 208, 308, 408, 508 of the metallic element 104, 204, 304, 404, 504, for example, in a modifying fluid. As a nonlimiting example, the modifying fluid is ambient air and the surface 108, 208, 308, 408, 508 of the metallic element 104, 204, 304, 404, 504 is modified when heated in the air by reacting with oxygen in the air. Other modifying fluids suitable for modifying the surface 108, 208, 308, 408, 508 of the metallic element 104, 204, 304, 404, 504 when heated, and thereby facilitate a bonding of the metallic element 104, 204, 304, 404, 504 to the polymeric layers 106, 206, 306, 406, 506, may also be employed within the scope of the present disclosure.
In particular embodiments, the at least one metallic element 104, 204, 304, 404, 504 is heated to a temperature of at least about 500° F. In a most particular embodiment, the metallic element 104, 204, 304, 404, 504 is heated to a temperature between about 800° F. and about 1000° F. A skilled artisan may select other suitable temperatures to which to heat the metallic element 104, 204, 304, 404, 504 to modify the surface 108, 208, 308, 408, 508, and increase bonding with the polymeric layers 106, 206, 306, 406, 506, as desired.
Multi-Layer Extrusion Processes
Multi-pass extrusion (where a single polymeric layer 106, 206, 306, 406, 506 is applied on each extrusion line), tandem extrusion (see
With reference to
Referring now to
Whenever possible, co-extrusion of the polymeric layers 106, 206, 306, 406, 506 including the insulation layers, the jacket layers, and the tie-layers may be preferred to maximize adhesion. In particular, co-extrusion may provide longer diffusion time and chemical reaction time between the polymeric layers 106, 206, 306, 406, 506 at elevated temperatures, may keep polymer melt temperature in co-extrusion head from cooling, and may provide higher contact pressure between the polymeric layers 106, 206, 306, 406, 506 than the tandem extrusion process.
Suitable applications for the cables 102, 202, 302, 402, 502 described hereinabove may include: slickline cables or multiline cables, wherein these components may be used as single or multiple strength members or strength and power/data carriers; wireline logging cables, wherein these components may be used as strength members, or combination strength and power/data carriers—cable configurations may be mono, coaxial, hepta, quad, triad or any other configuration; and seismic and oceanographic cables, wherein these elements or components may be used as strength members or combination strength and power carriers.
The polymer-bonded metallic components 102, 202, 302, 402, 502 may be advantageously utilized as strength members, and/or power or data carriers in oilfield cables. However, it should be understood that the methods may equally be applied to other metallic components having bonded polymeric jackets, and that methods for making and using such metallic components having bonded polymeric jackets are also within the scope of the present disclosure.
The preceding description has been presented with reference to present embodiments. Persons skilled in the art and technology to which this disclosure pertains will appreciate that alterations and changes in the described structures and methods of operation can be practiced without meaningfully departing from the principle, and scope of this invention. Accordingly, the foregoing description should not be read as pertaining only to the precise structures described and shown in the accompanying drawings, but rather should be read as consistent with and as support for the following claims, which are to have their fullest and fairest scope.
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PCT/US2011/034545 | 4/29/2011 | WO | 00 | 5/10/2013 |
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WO2011/137337 | 11/3/2011 | WO | A |
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