Patent Application
20120025692
This invention generally relates to spark plugs and other ignition devices for internal combustion engines and, in particular, to electrode materials for spark plugs.
Spark plugs can be used to initiate combustion in internal combustion engines. Spark plugs typically ignite a gas, such as an air/fuel mixture, in an engine cylinder or combustion chamber by producing a spark across a spark gap defined between two or more electrodes. Ignition of the gas by the spark causes a combustion reaction in the engine cylinder that is responsible for the power stroke of the engine. The high temperatures, high electrical voltages, rapid repetition of combustion reactions, and the presence of corrosive materials in the combustion gases can create a harsh environment in which the spark plug must function. This harsh environment can contribute to erosion and corrosion of the electrodes that can negatively affect the performance of the spark plug over time, potentially leading to a misfire or some other undesirable condition.
To reduce erosion and corrosion of the spark plug electrodes, various types of precious metals and their alloys—such as those made from platinum—have been used. These materials, however, can be costly. Thus, spark plug manufacturers sometimes attempt to minimize the amount of precious metals used with an electrode by using such materials only at a firing tip or spark portion of the electrodes where a spark jumps across a spark gap.
According to one embodiment, there is provided a spark plug comprising a metallic shell, insulator, center electrode and ground electrode. The center electrode, the ground electrode, or both includes an electrode material having: platinum (Pt) from about 50 at % to about 99.9 at %, inclusive; at least one active element from about 0.01 at % to about 30 at %, the at least one active element is selected from the group consisting of: aluminum (Al) or silicon (Si); at least one high-melting point element from about 0.01 at % to about 30 at %, inclusive, the at least one high-melting point element is selected from the group consisting of: ruthenium (Ru), iridium (Ir), tungsten (W), molybdenum (Mo), rhenium (Re), tantalum (Ta), niobium (Nb) or chromium (Cr); and a thin oxidation layer formed on or near an electrode surface after the spark plug has been exposed to sufficient heat in a combustion chamber. The thin oxidation layer minimizes a balling or bridging phenomena that can otherwise take place due to excessive evaporation and re-deposition of certain constituents of the electrode material.
According to another embodiment, there is provided an electrode material for use with a spark plug, where the electrode material is similar to that recited above.
Preferred exemplary embodiments of the invention will hereinafter be described in conjunction with the appended drawings, wherein like designations denote like elements, and wherein:
The electrode material described herein may be used in spark plugs and other ignition devices including industrial plugs, aviation igniters, glow plugs, or any other device that is used to ignite an air/fuel mixture in an engine. This includes, but is certainly not limited to, the exemplary spark plugs that are shown in
Referring to
In this particular embodiment, the first component 32 of the center electrode firing tip 20 and/or the ground electrode firing tip 30 may be made from the electrode material described herein; however, these are not the only applications for the electrode material. For instance, as shown in
Again, it should be appreciated that the non-limiting spark plug embodiments described above are only examples of some of the potential uses for the electrode material, as it may be used or employed in any firing tip, electrode, spark surface or other firing end component that is used in the ignition of an air/fuel mixture in an engine. For instance, the following components may be formed from the electrode material: center and/or ground electrodes; center and/or ground electrode firing tips that are in the shape of rivets, cylinders, bars, columns, wires, balls, mounds, cones, flat pads, disks, rings, sleeves, etc.; center and/or ground electrode firing tips that are attached directly to an electrode or indirectly to an electrode via one or more intermediate, intervening or stress-releasing layers; center and/or ground electrode firing tips that are located within a recess of an electrode, embedded into a surface of an electrode, or are located on an outside of an electrode such as a sleeve or other annular component; or spark plugs having multiple ground electrodes, multiple spark gaps or semi-creeping type spark gaps. These are but a few examples of the possible applications of the electrode material, others exist as well. As used herein, the term “electrode”—whether pertaining to a center electrode, a ground electrode, a spark plug electrode, etc.—may include a base electrode member by itself, a firing tip by itself, or a combination of a base electrode member and one or more firing tips attached thereto, to cite several possibilities.
Precious metal alloys, like platinum (Pt) based alloys, have been used for spark plug electrodes. Although Pt-based alloys can exhibit a certain degree of oxidation, corrosion and/or erosion resistance that is desirable in some applications, they can also have some drawbacks. Referring to
According to an exemplary embodiment, the electrode material is a Pt-based alloy and includes platinum (Pt), one or more active elements, and one or more high-melting point elements, where the electrode material has a thin protective oxidation layer that forms on the surface of the material during high temperature operation. The term “Pt-based alloy,” as used herein, broadly includes any alloy or other electrode material where platinum (Pt) is the single largest constituent on an atomic % basis. This may include materials having greater than 50% platinum, as well as those having less than 50% platinum, so long as the platinum is the single largest constituent. Skilled artisans will appreciate that platinum has a lower melting temperature (1768° C.) than some precious metals, like iridium (Ir), and that this can lower the erosion resistance of the electrode material. In order to compensate for this, the electrode material described herein may include one or more high-melting point elements, such as ruthenium (Ru), iridium (Ir), tungsten (W), molybdenum (Mo), rhenium (Re), tantalum (Ta), niobium (Nb), chromium (Cr), or a combination thereof. In addition, platinum-based alloys sometimes experience the balling or bridging phenomena described above. The electrode material described herein addresses this potential challenge by including one or more active elements, like aluminum (Al), silicon (Si) or a combination of both. The active elements may contribute to the formation of thin oxidation layers on the surface of the electrode material that can resist or deter the electrode material from forming balls B, as shown in
In one embodiment, the electrode material includes platinum (Pt) from about 50 at % to about 99.9 at %, inclusive, at least one active element from about 0.01 at % to about 30 at %, inclusive, and at least one high-melting point element from about 0.01 at % to about 30 at %, inclusive, where the platinum (Pt) is the single largest constituent of the electrode material on an at % basis. Aluminum (Al) and/or silicon (Si) may be the active elements referred to above, and ruthenium (Ru), iridium (Ir), tungsten (W), molybdenum (Mo), rhenium (Re), tantalum (Ta), niobium (Nb) and/or chromium (Cr) may be the high-melting point elements. Examples of suitable electrode material compositions that fall within this exemplary embodiment include those compositions having platinum (Pt) plus one active element selected from the group of aluminum (Al) and silicon (Si), plus one or more high-melting point elements selected from the group of ruthenium (Ru), iridium (Ir), tungsten (W), molybdenum (Mo), rhenium (Re), tantalum (Ta), niobium (Nb) and/or chromium (Cr), such as Pt—Al—Ru, Pt—Si—Ru, Pt—Al—Cr, Pt—Si—Cr, Pt—Al—Ir, Pt—Si—Ir, Pt—Al—W, Pt—Si—W, Pt—Al—Mo, Pt—Si—Mo, Pt—Al—Re, Pt—Si—Re, Pt—Al—Ta, Pt—Si—Ta, Pt—Al—Nb, Pt—Si—Nb, etc. These compositions may have other constituents and may include the following non-limiting examples: Pt-7Al-4Ru, Pt-7Si-4Ru, Pt-7Al-4Cr, Pt-7Si-4Cr, Pt-7Al-4Ru-4Cr, Pt-7Si-4Ru-4Cr, Pt-7Al-10Ru, Pt-7Si-10Ru, Pt-8Al-6Cr-5Ru and Pt-8Si-6Cr-5Ru; other examples are certainly possible. In one particular embodiment, the electrode material is a platinum-based alloy that includes platinum (Pt) from about 75 at % to about 95 at %, inclusive, aluminum (Al) from about 5 at % to about 10 at %, inclusive, and ruthenium (Ru) and/or chromium (Cr) from about 0.1 at % to about 10 at %, inclusive. All percentages and weights listed herein are in terms of atomic weight, which is determined by dividing the number of atoms of a certain element, per unit volume, by the number of atoms of the entire electrode material, per unit volume.
Depending on the particular embodiment, the electrode material may include platinum (Pt) from about 50 at % to about 99.9 at %, inclusive, Pt in an amount greater than 55.0 at %, Pt in an amount greater than 65.0 at %, Pt in an amount greater than 79.0 at %, Pt in an amount less than 95 at %, Pt in an amount less than 94 at %, or Pt in an amount less than 84 at %, to cite several possible examples.
The term “active element,” as used herein, includes the elements aluminum (Al) and silicon (Si). The electrode material preferably includes Al, Si or both in an amount that is sufficient to affect the oxidation performance of the electrode material. Preferably, these active element(s) are present in sufficient quantities to improve the oxidation resistance of the electrode material by assisting with the formation of thin oxidation surface layers, like those made of Al2O3 or SiO2, that prevent the excessive evaporation of platinum (Pt) from the electrode material during use of the spark plug in a combustion chamber. Depending on the particular embodiment, the electrode material may include either aluminum (Al) or silicon (Si) from about 0.01 at % to about 30 at %, inclusive; from about 5.0 at % to about 10 at %, inclusive; Al in an amount greater than 5.0 at %; Al in an amount greater than 6.2 at %; Al in an amount greater than 7.5 at %; Al in an amount less than 10.0 at %; Al in an amount less than 8.2 at %; or Al in an amount less than 6.1 at %, Si in an amount greater than 5.0 at %; Si in an amount greater than 6.1 at %; Si in an amount greater than 8.5 at %; Si in an amount less than 10.0 at %; Si in an amount less than 8.6 at %; or Si in an amount less than 7.2 at %, to cite several possible atomic percentages. Some initial testing has shown that providing an electrode material with Al or Si in amount less than 10 at % (e.g., approximately 7 at %) may be desirable because the relatively low Al content minimizes certain precipitates in the electrode material, which in turn improves the ductility and/or plasticity of the alloy. This improves the formability of the electrode material and may even enable the material to be cold extruded down to a wire diameter of about 0.4-0.7 mm, for example. The thin wire can then be cut or sheared into firing tips and attached to the center and/or ground electrodes. In addition, the relatively low Al content may improve the erosion resistance of the electrode material.
In some examples, the electrode material includes a combination of both Al and Si in a combined amount that is greater than 5.0 at % and less than 10 at %, inclusive—if the combined amount of the active elements is too small, then a sufficient protective oxidation layer may not be formed to protect the platinum (Pt) matrix during spark plug operation; if the combined amount of the active elements is too high, then it can make the oxidation rate too fast and reduce the oxidation resistance of the electrodes. Other factors regarding the adjustment of active element quantities also exist. Some exemplary embodiments of an electrode material that includes both Al and Si includes Al in an amount of greater than 1.0 at % and Si in an amount greater than 4.4 at %; Al in an amount greater than 5.1 at % and Si in an amount greater than 1.2 at %; Al in an amount greater than 2.5 at % and Si in an amount greater than 2.5 at %; Al in an amount less than 8.0 at % and Si in an amount less than 4.0 at %; Al in an amount less than 6.3 at % and Si in an amount less than 3.3 at %; and Al in an amount less than 2.1 at % and Si in an amount less than 9.1 at %, to cite several possibilities. Skilled artisans will appreciate that the precise quantities of the active elements, whether they be aluminum (Al), silicon (Si) or both, can be adjusted to meet the particular needs of the application in which the electrode material is being used. The presence and amount of Al and Si in the electrode material may be detected by a chemical analysis or by viewing an Energy Dispersive Spectra (E.D.S.) of the material. The E.D.S. may be generated by a Scanning Electron Microscopy (S.E.M.) instrument, as is understood by those skilled in the art.
The amount or quantity of active elements in the electrode material may impact or influence the oxidation performance of the material. For example, the presence and thickness of a thin oxidation layer that forms on the outer surface of electrodes or firing tips 20 and/or 30 may be influenced by the quantities of active elements in the electrode material. If the electrode material only includes aluminum (Al) as an active element then the thin oxidation layer will likely include aluminum oxide or alumina (Al2O3), and if the electrode material only includes silicon (Si) as an active element then the thin oxidation layer will likely have silicon dioxide or silica (SiO2). When the electrode material or Pt-based alloy includes a combination of Al and Si, the oxide layer may include a combination of Al and Si oxides, such as a combination of Al2O3 and SiO2. Providing Al or Si to the electrode material in the percentages disclosed above can cause a suitably thin oxidation layer to form at an electrode surface with a predetermined thickness, which in turn can provide a sufficient discharge voltage and ablation volume per spark during operation at temperatures of at least about 500° C., such as in an internal combustion engine. The predetermined thickness can vary depending on the specific composition of the electrode material and conditions within the combustion chamber. For example, the predetermined thickness of the thin oxidation layer may be about 0.10 μm to about 10.0 μm. The presence of the thin oxidation layer may be detected by heating the electrode to a temperature of at least about 500° C., and performing a chemical analysis on the electrode or by generating and viewing an Energy Dispersive Spectra (E.D.S.) with an S.E.M. instrument, as is understood by those skilled in the art.
As stated above, the thin oxidation layer or oxide layer typically forms at an outer surface of an electrode when temperatures are at least about 500° C., such as during use of spark plug 10 in an internal combustion engine. In other words, when the electrode material is heated to temperatures of 500° C. or more, a gradient structure may be formed where the bulk of the interior of the electrode material includes active elements (Al, Si or both) in an amount of about 5.0 at % to about 10.0 at % and an outer surface of the electrode (e.g., an outer surface of firing tips 20, 30) that includes the thin oxidation layer with a higher proportion of active elements. Once the thin oxidation layer is formed along the outer surface of the electrode, the thin oxidation layer will generally remain at the outer surface at all temperatures. Before the electrode material is heated to temperatures of at least 500° C., the electrode generally does not exhibit a gradient structure where active elements like Al and Si are gathered or concentrated in a thin oxidation layer along the outer surface of the electrode.
The thin oxidation layer may be present along the entire outer surface of the spark plug electrodes or firing tips 20, 30 or present only at sparking surfaces that are exposed to spark gap G. When a sparking surface comprises a planar surface, the oxide layer typically extends along the planar surface, but this is not necessary. The thin oxide layer may be dense, stable, and have a low formation free energy. The oxide layer also can limit evaporation of platinum (Pt) in the electrode material when the material is exposed to sparks and other extreme conditions of the combustion chamber. The thin oxide layer may also provide improved oxidation resistance that protects the sparking surfaces of electrodes like firing tips 20, 30 from erosion. The thin oxide layer can also help to prevent balling and bridging, which commonly occurs at the sparking surfaces of some Pt-based alloys that lack the active elements taught herein, as explained above in conjunction with
As stated above, electrode material or Pt-based alloy may also include one or more high melting point element(s) in an amount sufficient to affect or influence the melting point of the electrode material. Some examples of potentially suitable high-melting point elements include ruthenium (Ru), iridium (Ir), tungsten (W), molybdenum (Mo), rhenium (Re), tantalum (Ta), niobium (Nb), chromium (Cr), or a combination thereof. Each high-melting point element preferably has a melting temperature of at least 1700 degrees Celsius (° C.) which, when combined with platinum (Pt) and one or more active elements, should increase the melting temperature of the overall electrode material. The high-melting point elements can also strengthen the electrode material. Each of the high-melting point elements may be present in the electrode material in an amount from about 0.01 at % to about 30 at %, inclusive.
In one embodiment, the electrode material includes a high-melting point element in the form of ruthenium (Ru), which has a melting point of approximately 2310° C. That is not to say that other high-melting point elements cannot be added as well, only that Ru may be included in an amount from about 0.01 at % to about 20 at %, inclusive. The electrode material may include Ru in an amount greater than 0.1 at %; Ru in an amount greater than 5.0 at %; Ru in an amount greater than 14.6 at %; Ru in an amount less than 20.0 at %; or Ru in an amount less than 5.3 at %. Some initial testing has shown that providing an electrode material with Ru in amount from about 4 at % to about 10 at % may be desirable. The electrode material may also include one or more other high-melting point element(s), including Ir, W, Mo, Re, Ta, Nb, Cr, or combinations thereof, so that the combined high-melting point elements are present in a total amount from about 0.01 at % to about 30 at %, inclusive.
In a different embodiment, the electrode material includes a high-melting point element in the form of iridium (Ir), which has a melting point of approximately 2410° C. and is present in the electrode material in an amount from about 0.01 at % to about 30 at %, inclusive. The electrode material may include Ir in an amount greater than 0.01 at %; Ir in an amount greater than 7.2 at %; Ir in an amount greater than 20.2 at %; Ir in an amount less than 30.0 at %; Ir in an amount less than 27.6 at %; or Ir in an amount less than 12.4 at %. The electrode material may also include one or more other high-melting point element(s), including Ru, W, Mo, Re, Ta, Nb, Cr, or combinations thereof, so that the combined high-melting point elements are present in a total amount from about 0.01 at % to about 30 at %, inclusive.
The electrode material may also include a high-melting point element in the form of tungsten (W), which has a melting temperature of approximately 3407° C. and may be present in the electrode material in an amount from about 0.01 at % to about 10 at %, inclusive. Depending on the particular embodiment, the electrode material may include W in an amount that is greater than 0.01 at %; W in an amount greater than 4.1 at %; W in an amount greater than 7.3 at %; W in an amount less than 10.0 at %; W in an amount less than 7.5 at %; or W in an amount less than 4.8 at %, to cite several quantitative possibilities. The electrode material may also include one or more other high-melting point element(s), including Ru, Ir, Mo, Re, Ta, Nb, Cr, or combinations thereof, so that the combined high-melting point elements are present in a total amount from about 0.01 at % to about 30 at %, inclusive.
In yet another embodiment, the electrode material includes a high-melting point element in the form of rhenium (Re), which has a melting point of approximately 3180° C. and is present in the electrode material in an amount from about 0.01 at % to about 10 at %, inclusive. The electrode material may include Re in an amount greater than 0.01 at %; Re in an amount greater than 2.2 at %; Re in an amount greater than 7.5 at %; Re in an amount less than 10.0 at %; Re in an amount less than 6.1 at %; or Re in an amount less than 4.3 at %. The electrode material may also include one or more other high-melting point element(s), including Ru, Ir, Mo, W, Ta, Nb, Cr, or combinations thereof, so that the combined high-melting point elements are present in a total amount from about 0.01 at % to about 30 at %, inclusive.
It is also possible for the electrode material to include a high-melting point element in the form of molybdenum (Mo), which has a melting point of approximately 2617° C. and is present in the electrode material in an amount from about 0.01 at % to about 30 at %, inclusive. The electrode material may include Mo in an amount greater than 0.01 at %; Mo in an amount greater than 7.2 at %; Mo in an amount greater than 20.2 at %; Mo in an amount less than 30.0 at %; Mo in an amount less than 27.6 at %; or Mo in an amount less than 12.4 at %. The electrode material may also include one or more other high-melting point element(s), including Ru, Ir, Re, W, Ta, Nb, Cr, or combinations thereof, so that the combined high-melting point elements are present in a total amount from about 0.01 at % to about 30 at %, inclusive.
In a different embodiment, the electrode material includes a high-melting point element in the form of tantalum (Ta), which has a melting point of approximately 2996° C. and is present in the electrode material in an amount from about 0.01 at % to about 10 at %, inclusive. The electrode material may include Ta in an amount greater than 3.4 at %; Ta in an amount greater than 8.3 at %; Ta in an amount less than 10.0 at %; Ta in an amount less than 7.8 at %; or Ta in an amount less than 3.3 at %. The electrode material may also include one or more other high-melting point element(s), including Ru, Ir, Re, W, Mo, Nb, Cr, or combinations thereof, so that the combined high-melting point elements are present in a total amount from about 0.01 at % to about 30 at %, inclusive.
The electrode material may also include a high-melting point element in the form of niobium (Nb), which has a melting point of approximately 2468° C. and is present in the electrode material in an amount from about 0.01 at % to about 10 at %, inclusive. Depending on the particular embodiment, the electrode material may include Nb in an amount greater than 0.01 at %; Nb in an amount greater than 3.7 at %; Nb in an amount greater than 7.4 at %; Nb in an amount less than 10.0 at %; Nb in an amount less than 5.8 at %; or Nb in an amount less than 2.3 at %. The electrode material may also include one or more other high-melting point element(s), including Ru, Ir, Re, W, Mo, Ta, Cr, or combinations thereof, so that the combined high-melting point elements are present in a total amount from about 0.01 at % to about 30 at %, inclusive.
According to one more embodiment, the electrode material includes a high-melting point element in the form of chromium (Cr), which has a melting point of approximately 1857° C. and is present in the electrode material in an amount from about 0.01 at % to about 10 at %, inclusive. The electrode material may include Cr in an amount greater than 0.01 at %; Cr in an amount greater than 1.2 at %; Cr in an amount greater than 5.3 at %; Cr in an amount less than 10.0 at %; Cr in an amount less than 5.8 at %; or Cr in an amount less than 3.1 at %. The electrode material may also include one or more other high-melting point element(s), including Ru, Ir, Re, W, Mo, Ta, Nb, or combinations thereof, so that the combined high-melting point elements are present in a total amount from about 0.01 at % to about 30 at %, inclusive.
As mentioned above several times, it is possible for the electrode material or Pt-based alloy to have more than one high-melting point element. For example, the electrode material may include both Ru and Cr, in an amount of about 0.01 at % to 20.0 at % for the Ru and about 0.01 at % to 10.0 at % for the Cr. The Ru and Cr constituents may have the following quantities, for example: Ru and Cr in amounts greater than 0.01 at %; Ru in an amount greater than 5.0 at % and Cr in an amount greater than 0.03 at %; Ru in an amount greater than 0.05 at % and Cr in an amount greater than 6.5 at %; Ru in an amount less than 20.0 at % and Cr in an amount less than 10.0 at %; Ru in an amount less than 15.4 at % and Cr in an amount less than 3.2 at %; Ru in an amount less than 5.6 at % and Cr in an amount less than 9.5 at %. The electrode material may also include one or more other high-melting point element(s), including Ir, Re, W, Mo, Ta, Nb, or combinations thereof, so that the combined high-melting point elements are present in a total amount from about 0.01 at % to about 30 at %, inclusive. Electrode material embodiments having three, four, five or more high-melting point elements are envisioned as well.
The electrode material or Pt-based alloy may further include additives or impurities in an amount such that the thin oxide layer is formed at the outer surfaces of the electrodes or firing tips 20, 30 and provides the spark plug with the improved erosion rate. The electrode material may be a solid solution with a single homogeneous phase. The electrode material may have a ductility that allows the material to easily be cold-extruded and formed into different shapes for use in and with spark plug electrodes. In some embodiments, the electrode material is free of an intermetallic or second phase.
Table I below includes a number of exemplary embodiments of the electrode material or Pt-based alloy; other embodiments and compositions are certainly possible.
The erosion rates of a number of exemplary electrodes—some of which are formed with the electrode material described above, some of which are formed with other electrode materials—are listed in Table 2. This provides a comparison in terms of erosion rate between two examples of the present electrode material or Pt-based alloy (Pt-7Al-4Ru and Pt-7Al-4Cr) and other competitive materials (Ir-2Rh, Pt-4W, Pt-10Ni, Pt-30Ni, Ni125, Haynes 214, Inconel 600). As previously mentioned, in addition to demonstrating acceptable erosion resistance, the electrode material described herein generally has more desirable ductility attributes than some of the other materials and minimizes the balling or bridging effects sometimes experienced.
The first two entries in Table II are examples of the present electrode material (Pt-7Al-4Ru and Pt-7Al-4Cr) and respectively have melting temperatures of 1797° C. and 1769° C. and erosion rates of 0.4 μm3/spark and 0.6 μm3/spark. The next seven entries in Table II are comparative alloys and materials (Ir2Rh, Pt20Ni, Pt10Ni, Pt4W, Incone160, Haynes, and Ni125) that may also be used in the formation of spark plug electrodes. Their respective melting points and erosion rates are provided as well.
Spark plug electrodes made from the present electrode material and spark plug electrodes made from the comparative alloys were tested under conditions similar to those of an internal combustion engine. The erosion rate was tested by hot sparking at 710° C. with a spark voltage of 20 KV for 300 hours. The temperatures of the electrodes were maintained at approximately 710° C., which is a typical operating temperature of an electrode of a spark plug 10, for the entire 300 hours. The sparking frequency was 158 Hz. The erosion rate is equal to the amount of material of the sample worn away per spark applied to the sample, and it is measured in μm3/spark. The erosion rate of the sample includes rate of erosion due to sparking and rate of erosion due to oxidation. The erosion rates of electrodes formed from the electrode material or Pt-based alloy described herein and the erosion rates of electrodes made from comparative alloys are also shown in Table II.
The test results indicate that the present electrode material, complete with its thin oxide layer, exhibits an enhanced erosion resistance and prevents balling and bridging at the sparking surfaces of the electrodes, such as firing tips 20, 30. An oxide layer developed at the outer surface of the electrodes that were formed from the present electrode material during the erosion rate test; more specifically, when the material was heated to a temperature of about 710° C. These electrodes did not experience significant balling and bridging at the outer surface of the electrode. With reference to Table II, it can be seen that the two examples of the present electrode material (Pt-7Al-4Ru and Pt-7Al-4Cr) exhibit spark erosion rates that are less than the majority of the comparative alloys, and are significantly less than those of Pt30Ni, Pt10Ni, Inconcel® 600, Haynes 214 and NiSiAlY. One potential explanation for the advantageous erosion resistance is the formation of the thin oxidation layer on the surface of the electrode material, as discussed above. It should also be pointed out that because the present electrode material is a Pt-based alloy, it may exhibit superior ductility and metal forming properties than some of the other alloys, particularly the Ir-based alloys like Ir2Rh.
This application claims the benefit of U.S. Provisional Ser. No. 61/368,860 filed Jul. 29, 2010, the entire contents of which are herein incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| 61368860 | Jul 2010 | US |
