Welding wires commonly used for GMAW (Gas Metal Arc Welding) and SAW (Submerged Arc Welding) typically carry a copper metal coating (cladding) to reduce friction and electrical resistance between the welding wire and the welding gun's contact tip through which the welding wire passes. In contrast, FCAW (Flux-Cored Arc Welding) welding wires typically carry a wire feeding lubricant comprising a solid lubricant such as MoS2, WS2, graphite and/or PTFE (Teflon) for this purpose. A binder such as vegetable oil, mineral oil, synthetic oil or petroleum wax is included in the wire feeding lubricant for adhesion purposes and to enhance feedability, i.e., the ease of withdrawing the wire from its supply container and feeding the wire through the contact tip without tangling. Arc stabilizers, which are typically sodium or potassium containing soaps or detergents, etc., can also be dissolved and/or dispersed in the binder. See, for example, Kokai (Japanese Published Unexamined Application) 2004-034131, Kokai 08-257788, Kokai 2002-219595, Kokai 2002-239779, U.S. Pat. No. 6,337,144 and Kokai 2003-039191, the disclosures of which are incorporated herein by reference.
In accordance with this invention, the electrical resistance between a welding wire and the welding gun's contact tip is substantially reduced by providing on the welding wire's surface a thermally stable, electrically conductive solid in fine particulate form. The result, it is believed, is that arc stability will be improved and the useful life of the contact tip will be increased.
Thus, this invention in its broader aspects provides a welding wire for use in arc welding comprising a welding wire substrate and a solid conductor on the surfaces of the welding wire substrate, the solid conductor comprising a thermally stable, electrically conductive particulate solid.
In a particular embodiment, this invention provides a welding wire comprising a welding wire substrate and a wire coating on the outside surfaces of the welding wire substrate, the wire coating comprising a solid lubricant, a solid conductor comprising a thermally stable, electrically conductive particulate solid, and a binder.
In addition, this invention also provides an improved welding wire coating comprising a solid lubricant, a solid conductor comprising a thermally stable, electrically conductive particulate solid, and a binder.
In accordance with this invention, a thermally stable, electrically conductive solid in fine particulate form is provided on the surfaces of a welding wire used for arc welding for reducing the electrical resistance between the welding wire and the welding gun's contact tip through which the welding wire passes.
Wire Substrate
This invention is applicable to any type of welding wire previously used, or that may be used in the future, in any type of arc welding process including but not limited to GMAW (Gas Metal Arc Welding), SAW (Submerged Arc Welding) and FCAW (Flux-Cored Arc Welding). Welding wire made for GMAW and SAW in accordance with this invention will most commonly be a solid core metal wire, i.e., a wire comprising a solid mass of metal of essentially uniform composition, which is both “clean,” i.e., not coated with any type of lubricant, binder or other ingredient commonly included in conventional welding wire coatings, and “unclad,” i.e., not clad or otherwise coated with copper or any other metal or metal alloy (“bare metal wire”). Such wires are most commonly made from carbon (mild) steel, although they can also be made from a variety of other metals and metal alloys such as stainless steels including austenitic, martensitic, ferritic and duplex stainless steels, low CTE alloys such as Invar and Kovar, and nickel-based superalloys such as Inconel, etc. In addition, they can also be clad with copper or any other metal, if desired, although this is generally unnecessary in accordance with the present invention. Similarly, they can also be coated with conventional feeding lubricants and other conventional ingredients as would occur, for example, if the wire substrate to which the inventive wire coating composition is applied is a typical commercially available “bare metal wire,” which normally carries some type of wire feeding lubricant.
Normally, welding wire for GMAW will have a diameter of about 1/16 inch (˜1.6 mm) or less, while welding wire for SAW will have a diameter of about 1/16 inch (˜1.6 mm) or more. SAW welding wire with diameters of at least about 2 mm, at least about 3 mm, and even at least about 4 mm, are not uncommon.
When this invention is used for making flux-cored welding wires, any type of welding flux can be included in the wire's core. Although such flux-cored welding wires will normally be unclad, they can be clad with copper or any other metal or metal alloy, as desired.
Solid Lubricant and Binder
Although the solid conductor of this invention can be used alone, it will normally be combined with other materials typically applied to the surfaces of bare metal welding wire for enhancing lubricity, feedability, arc stability and/or other properties. So, for example, in some embodiments of this invention the solid conductor can be a part of a welding wire coating including a solid particulate lubricant such as MoS2, WS2, ZnO (normally together with WS2), graphite and/or PTFE (Teflon) as well as a binder such as vegetable oil, mineral oil, synthetic oil, petroleum wax or the like. For this purpose, any solid lubricant which has previously been used, or which may be used in the future, for enhancing the lubricity between a welding wire and the equipment through which it is fed can be used in this invention. Similarly, any binder which has previously been used, or which may be used in the future, for promoting adhesion between such solid particles and the welding wire surfaces to which they adhere can be used in this invention. See the various domestic and foreign patent documents cited above for an extensive disclosure of the different types of solid lubricants and binders typically used for making conventional feeding lubricants.
In other embodiments of this invention, the solid conductor can be combined with a suitable binder, as described above, without a solid lubricant also being present.
In addition to the solid lubricants and binders discussed above, other ingredients included in conventional welding wire lubricants such as arc stabilizers and the like can also be included in the welding wire coatings of this invention.
Solid Conductor
In accordance with this invention, the electrical resistance between a welding wire used for arc welding and the welding gun's contact tip is reduced during welding by providing on the surfaces of the welding wire a solid conductor comprising a thermally stable, electrically conductive solid in fine particulate form. In this context, “thermally stable” means that the solid conductor remains solid (e.g., does not melt) and, in addition, is essentially unreactive in air at 1,200° C., as determined by TGA (Thermal Gravimetric Analysis) according to ASTM E2550-07. Solid conductors which are thermally stable at 1,350° C., 1,500° C., and even 1,600° C., are more interesting. In this regard see, for example, Shimizu et al., Wear Mechanism in Contact Tube, Science and Technology of Welding and Joining, Vol. 11, No. 1, 2006, pp 94-105, which indicates that graphite oxidizes at welding temperatures and hence is not “thermally stable” in the context of this disclosure.
In addition to being thermally stable, the solid conductors used in this invention are also electrically conductive. In this context, “electrically conductive” means that the solid conductor has an electrical conductivity, σ, of at least 10 S/cm (Siemens per centimeter) at 800° C., as determined by ASTM B193-02. Solid conductors with electrical conductivities at 800° C. of at least about 50 S/cm, at least about 75 S/cm and at least about 90 S/cm are more interesting. Solid conductors with electrical conductivities at 800° C. of at least about 200 S/cm, at least about 300 S/cm, at least about 400 S/cm, at least about 500 S/cm, and even at least about 1000 S/cm are contemplated.
As a result of providing a thermally stable, electrically conductive solid conductor on the surfaces of a welding wire in accordance with this invention, the electrical resistance between the welding wire used and the contact tip of the welding gun through which the welding wire passes during arc welding is reduced. This, in turn, results is a corresponding reduction in Joule heating of the contact tip, it is believed. This should lead to a significant decrease in the rate of contact tip wear due to excessive heating, and hence a corresponding increase in contact tip useful life. This, in turn, is a significant benefit in robotic welding where “down time” is very costly.
Any solid material which is thermally stable and electrically conductive, and which can also be provided in fine, particulate form, can be used as the solid conductor of this invention. The particle size of the solid conductor is not critical, and essentially any particle size can be used. Generally speaking, the particle size of the solid conductor should be small enough so that it will adhere to the wire substrate surface with the particular binder selected and large enough so that the cost of obtaining the solid conductor does not become prohibitively expensive. In practical terms, this means that the average particle size of the solid conductor will normally be about 40 microns or less. Average particle sizes on the order of about 20 microns or less, about 10 microns or less, about 5 microns or less or even 2 microns or less are more interesting.
Moreover, while any thermally stable solid which has an electrical conductivity, σ, of at least about 10 S/cm (Siemens per centimeter) at 800° C. can be used as the solid conductor of this invention, those exhibiting electrical conductivities, σ, of at least about 25 S/cm at 800° C. are more interesting, while those exhibiting electrical conductivities, σ, of at least about 50 S/cm, at least about 75 S/cm, or even at least about 100 S/cm, at 800° C. are even more interesting. Thermally stable solids with even higher electrical conductivities, such as at least about 200 S/cm, at least about 300 S/cm, at least about 400 S/cm, at least about 500 S/cm, at least about 700 S/cm, or even at least about 1,000 S/cm, at 800° C. are contemplated. See, Table 1 below which identifies particular thermally stable solids with electrical conductivities at these and even higher levels.
One class of solid materials which can be used for this purpose are the electrically conductive perovskites. “Perovskite” refers to a general group of crystalline mixed metal oxides whose basic chemical formulas follows the pattern ABO3. Common A-cations in perovskites are the rare earths, alkaline earths, alkalis and other large cations such as Pb+2 and Bi+3, with the following cations being more common: Na+, K+, Rb+, Ag+, Ca+2, Sr+2, Ba+2, Pb+2, La+3, Pr+3, Nd+3, Bi+3, Ce+4 and Th+4. Common B cations in perovskites include: Li+, Cu+2, Mg+2, Ti+3, V+3, Cr+3, Mn+3, Fe+3, Co+3, Ni+3, Rh+3, Ti+4, Mn+4, Ru+4, Pt+4, Nb+5, Ta+5, Mo+6 and W+6.
The crystal structure of perovskites can be regarded as a primitive cube, with larger A-cations occupying the middle of the cube, smaller B-cations occupying the corners, and the oxygen anions occupying the center of the cube's edges. The structure is stabilized by the 6 coordination of the B-cation (octahedron) and 12 of the A-cation. The packing of the ions can be thought of the A and O ions together form a cubic closed packed array, where the B ions occupy a quarter of the octahedral holes.
Although a primitive cube is the idealized structure, differences in radii between the A and B cations can alter the structure to a number of different so-called distortions, of which tilting is the most common one. With perovskite tilt the BO6 octahedron twists along one or more axes to accommodate the difference.
Complex perovskite structures may contain two or more different A-cations, two or more different B-cations, or both. This normally results in ordered and disordered variants. Such complex perovskites crystal can also exhibit a stoichiometric excess or deficiency of oxygen atoms, especially when the crystal contains multiple A-cations (or B-cations) having different valence states from one another. Thus, complex perovskites can also be viewed as corresponding to the formula A1-xA′xB1-yB′yOz, where z can vary above and below 3 so as to satisfy the valence states of the other elements present. Note, also, that sometimes complex perovskites are described with formulas such as Y1Ba2Cu3O7-δ in which the oxygen subscript varies around 6, rather than 3 as in the case of ABO3. However, this is merely semantics, as Y1Ba2Cu3O6 is equivlant to Y0.5Ba1Cu1.5O3.
For a general description of perovskites, see Tejuca, et al., Properties and Applications of Perovskite-type Oxides, © Marcel Dekker, Inc., New York, 1993; Bhyiyan, “TOPICAL REVIEW, Solution-derived Textured Oxide Thin Films-A Review,” Superconductivity Science Technology, Vol. 19, Institute of Physics Publishing, Jan. 4, 2006; H. Kamimura, Theory of Copper Oxide Superconductors, 2005, Springer-Verlag, Berlin; Pena, Chemical Structures of Pemformce of Perovskie Oxides, Chem. Rev., 101 (7), 1981-2018, 2001, 10.1021/cr980129f S0009-2665(98)001129-0, Web Release Date: May 31, 2001; and McEvoy, Materials for High-temperature Oxygen reduction in Solid Oxide Fuel Cells, Journal of Materials Science, Vol. 36, pp 1087-1091, 2001.
Being ceramics, perovskites are thermally stable. In addition, as a class they show widely varying electrical conductivities. Some are dielectric, i.e., electrically insulating, while others conduct electricity like metals. Many are semiconductors, i.e., solids whose electrical conductivities are normally in between that of a dielectric and a conductor but which can be controlled over a wide range, either permanently or dynamically.
Electrically conductive perovskites are well known and used in a number of different electrical applications where good electrical conductivity at high temperatures is required. For example, they are widely used to form the cathodes of solid oxide fuel cells (SOFC). See, for example, the above-noted McEvoy article.
An interesting class of perovskites for this purpose is described as corresponding to the formula ABOx, where A is at least one of La, Ce, Pr, Sm, Nd, Gd and Y; B is at least one of Ga, Mg, Mn, Fe, Cr, Co, Cu, Zn and Ni; and x is 2.5-3.2; wherein A may optionally be partially substituted with one or more of Sr, Ba and Ca. In this context, “partially substituted” means that up to 50 atom % of the A atoms can be replaced by the indicated substitutes, so long as the ratio of the total amount of A atoms plus substituents to the total amount of B atoms is preserved. Perovskites of this type in which A is substituted with at least 5 atom %, at least 10 atom %, or even at least 15 atom % t, of the indicated substituents are interesting.
Particular examples of electrically conductive perovskites include all of those perovskites which have been disclosed, or may be disclosed in the future, as useful in making electrodes for solid oxide fuel cells. Examples include LaMnO3, CaMnO3, LaNiO3, LaCoO3, LaCrO3, etc. LaMnO3 doped with strontium is particularly interesting. Other examples include LaAlO3, GdFeO3, SrTiO3, BaCeO3, BaxSr1-xTiO3, BaZrO3, BaSnO3, BaZr0.3Ti0.65O3, La1-xCaxMnO3, LaNiO3, (Pb,Sr)TiO3, [Pb(SC0.5Nb0.5)]xTi1-xO3, Pb1-xCaxTiO3, PbTiO3, Pb(Yb,Nb)TiO3, PbZrO3, Pb(Zr,Ti)O3 and SrRuO3. It is also well-known that these materials can be doped with a wide variety of different doping elements including, but not limited to, Y, Hg, Tl and the lanthanide elements (La through Yb). See, the Bhyiyan article cited above.
Additional specific examples of useful perovskites, including their electrical conductivities, are set forth in the following Table 1:
In addition to perovskites, other thermally stable, electrically conductive solid materials capable of being supplied in fine particulate form can be used as the solid conductors of this invention. Examples include the lanthanum nickelates such as shown in U.S. Published Application 2007/0184324 and materials exhibiting the pyrochlore structure (A2B2O7) such as La2Zr2O7, Gd2Zr2O7, Eu2Nb2O7, Gd2Nb2O7, Sm2Nb2O7, Ho2Nb2O7, Y3NbO7 and Yb3NbO7.
The amount of solid conductor on the surfaces of the wire substrate can vary widely, and essentially any amount can be used. In general, enough solid conductor should be used to provide a noticeable decrease in electrical resistance between the welding wire and the contact tip of the weld gun through which it passes during welding but not so much that handling of the welding wire becomes difficult. Thus, solid conductor loadings on the order of 0.001 to 10 gms/m2 of wire surface area, or 0.01 to 1 gm/m2, or even 0.05 to 0.5 gm/m2 can be used.
In some embodiments of this invention as indicated above, the solid conductor is combined with a liquid or solid organic binder such as vegetable oil, mineral oil, synthetic oil or petroleum wax in a suitable amount for adhesion purposes without a solid lubricant being present. In this case, the welding wire coating thereby provided can be viewed as normally containing about 1 to 50 wt. % solid conductor, more commonly about 2 to 25 wt. % solid conductor, about 5 to 15 wt. % solid conductor, or even about 7 to 13 wt. % solid conductor, based on the weight of the entire wire coating.
In other embodiments of this invention as indicated above, the welding wire coating will include both the solid conductor of this invention as well as a solid lubricant such MoS2, WS2, graphite, ZnO and/or PTFE (Teflon). In these instances, the solid conductor of this invention can be present in a weight ratio as low as 1:10 to as high as 10:1, based on the weight of the solid lubricant. Relative weight ratios of 5:1 to 1:5, 2:1 to 1:2, 1.5:1 to 1:1.5 and even about 1:1 are possible. Normally, such coatings will also include a liquid or solid organic binder such as vegetable oil, mineral oil, synthetic oil or petroleum wax in a suitable amount for adhesion purposes. In this case, the welding wire coating can be viewed as containing about 1 to 20 wt. % solid lubricant and about 1 to 20 wt. % thermally stable solid conductor. More interesting are those welding wire coatings containing about 4 to 15 wt. % solid lubricant and about 4 to 15 wt. % thermally stable solid conductor. Welding wire coatings containing about 6 to 11 wt. % solid lubricant and about 6 to 11 wt. % thermally stable solid conductor are even more interesting.
In general, such compositions (i.e., with or without solid lubricant) will normally contain about 60 to 98 wt. % binder, more commonly about 70 to 92 wt. % binder, and even about 78 to 88 wt. % binder.
In order to more thoroughly describe this invention, the following working examples were conducted.
In each example, a 0.045 inch (˜1.1 mm) diameter solid mild steel bare metal welding wire was welded in the IF position (“bead-on-plate”) to form a weld on a 0.375 inch (˜9.5 mm) thick plate of shot-blasted mild steel using a PowerWave 455 automatic welding machine available from Lincoln Electric of Cleveland, Ohio. The welding wire was fed through the machine at a speed of 450 inches per minute (˜1143 cm/min.), while the machine was operated at a constant voltage of 31 Volts and an amperage of about 340 Amps, using a constant stick-out of 0.75 inch (˜19.1 mm).
Each welding test lasted 60 seconds. Thereafter, the contact tip of the welding gun was removed from the machine and sectioned axially and radially so that the contact surface of the contact tip, i.e., the surface of the orifice in the contact tip through which the welding wire passes, at the outer end of the contact tip could be inspected visually. In addition, one of the sections was also etched with a suitable reagent so that the microstructure of the alloy forming the contact tip at this location could also be determined visually.
At least four, and sometimes five, runs were made for each example, with the most representative run for each example being selected for discussion below:
In this example, the welding wire used was a conventional copper clad mild steel welding wire coated with a conventional water-based organic feeding lubricant commonly used on copper coated welding wire (“standard copper lubricant” or “copper lube”). The results obtained are shown in the photomicrographs of
As shown in
Finally,
In this example, the welding wire used was the same mild steel welding wire used in Comparative Example A except that its copper cladding was omitted. In addition, this welding wire was coated with a non-aqueous organic feeding lubricant commonly used on bare steel (non-copper clad) welding wire comprising a mixture of commercially available synthetic oils and a commercially available arc stabilizer (“standard bare wire lubricant” or “bare wire lube”). The results obtained are shown in the photomicrographs of
As shown in
Finally,
In this example, the same welding wire used in Comparative Example B (no copper cladding but coated with standard bare wire lubricant) was overcoated with a mixture comprising 5.0 wt. % particulate WS2, 1.7 wt. % particulate ZnO and 2.5 wt. % particulate graphite dispersed in 90.8 wt. % of an organic binder comprising the standard bare wire lubricant mentioned above.
As shown in
Finally,
In this example, the same welding wire used in Comparative Example B (no copper cladding but coated with standard bare wire lubricant) was overcoated with a mixture comprising 8.4 wt. % particulate WS2 and 8.4 wt. % of an “LSM” solid conductor comprising a perovskite of the formula (La0.85Sr0.15)0.98MnO3 having an average particle size of 20 microns and an electrical conductivity at 800° C. of about 100 S/cm dispersed in 83.2 wt. % of an organic binder comprising the standard bare wire lubricant mentioned above.
As shown in
By comparing
Electrical Resistance Measurements
To further demonstrate the effect of the present invention, the voltage drop between the welding wire and the contact tip during each 60 second welding test run of the above working examples was measured and recorded at a data collection rate of 600 Hz. That is, for each test run of each example, voltage drop was automatically measured by computer 600 times per second and recorded, thereby producing 36,000 data points per 60 second test run. Then, all data points for all four or five test runs for each example were combined to provide all the data points for each example, i.e., 146,000 or 180,000 data points per example depending on whether four or five test runs were made for that example. The data was then analyzed to determine the mean voltage drop, the voltage drops at the 25th and 75th percentiles and the variance between the 25th and 75th percentiles. In addition, statistically insignificant data points were identified at voltage levels of greater than 150% of the 75th percentile level and less that 66.7% of the 25th percentile level. The generation of Joule heat for each working example was also calculated according to formula:
P=I×V, where
P=Joule Heat generated, in Watts,
I=Current, in Amps, and
V=Voltage, in Volts
The results obtained are reported in the following Table 2 and visually presented in
From Table 2 and
Table 2 and
Thus, the analytically-determined electrical resistance data discussed immediately above, when considered in combination with the visual evidence of wear reduction discussed above in connection with Example 1 and Comparative Examples A-C, demonstrates that the inventive welding wire performs at least as well as a conventional copper clad/copper lube welding wire, and significantly better than the conventional solid lubricant coated wire, in terms of reducing Joule heat generation in the contact tip, avoiding physical and microstructural damage to the contact tip, and maintaining arc stability. This, in turn, suggests that the inventive welding wire will exhibit a useful life at least as good as that of conventional copper clad welding wire and significantly better than that of welding wire coated with conventional solid feeding lubricants.
In order to show that the improved results provided by this invention are independent of the particular organic binder used, Example 1 and Comparative Example B were repeated in a series of experiments, some using as the organic binder the same standard bare wire lubricant used in the above Example 1 and Comparative Example B and others using a different bare wire lubricant as the organic binder, in particular Mobil Velocite Oil No. 10 available from Exxon Mobile Corporation of Fairfax, Va., which is a non-aqueous product believed to be severely refined base oil containing stability-enhancing additives. In addition, the following additional changes were also made:
welding was done at about 250 Amps along a 15 foot feeding path with a 180° turn midway through rather at 340 Amps along a straight 6-8 feet feeding path,
welding was done for 300 seconds at 350 ipm and 31.7V,
data was collected at 750 Hz,
the organic feeding lubricant undercoating between the bare wire substrate and the welding wire coating of this invention was omitted,
the LSM perovskite solid conductor used was obtained from a different source and had a particle size of ˜2μ instead of ˜20μ, and
the welding wire coatings of this invention were made from 1 gm LSM perovskite solid conductor dispersed in 10 milliliters of the organic binder being tested.
Meanwhile, in order to demonstrate the repeatability of these tests, two otherwise identical control experiments were conducted on different days using copper clad wires identical to those used in the above Comparative Example A (copper clad/copper lube) welded under the same conditions as used in this series of tests.
As in the case of Example 1 and Comparative Example B, the voltage drop between the welding wire and the contact tip during each welding test run was measured, recorded and analyzed to determine the mean voltage drop, the voltage drops at the 25th and 75th percentiles, the variance between the 25th and 75th percentiles, and the generation of Joule heat. The results obtained are reported in the following Tables 3-5 and visually presented in
From Tables 3-5 and
Now, by comparing the results obtained for Examples 2 and 3 as reported in Tables 3-5 and visually presented in
On the other hand, the variance between the 25th and 75th percentile voltage levels generated when Lube 2 (Mobil Velocite Oil No. 10) was used was slightly better than the voltage variance obtained when Lube 1 (standard bare wire lubricant used in above Example 1) was used. These results show that Lube 2 (Mobil Velocite Oil No. 10) is at least as good as Lube 1 (standard bare wire lubricant used in above Example 1) in terms of the advantageous results realized by this invention.
Although only a few embodiments of this invention have been described above, it should be appreciated that many modifications can be made without departing from the spirit and scope of the invention. All such modifications are intended to be included within the scope of the present invention, which is to be limited only by the following claims:
Number | Name | Date | Kind |
---|---|---|---|
3620830 | Kramer | Nov 1971 | A |
3767888 | Sullivan | Oct 1973 | A |
3783234 | Russell | Jan 1974 | A |
4197362 | Schmidberger et al. | Apr 1980 | A |
4213025 | Kuhnen | Jul 1980 | A |
4913927 | Anderson | Apr 1990 | A |
5223478 | Whitlow et al. | Jun 1993 | A |
5378875 | Hirama et al. | Jan 1995 | A |
5426094 | Hull et al. | Jun 1995 | A |
5550348 | Masaie et al. | Aug 1996 | A |
5554308 | Masaie et al. | Sep 1996 | A |
5672287 | Masaie et al. | Sep 1997 | A |
5686198 | Kuo et al. | Nov 1997 | A |
5935911 | Yamada et al. | Aug 1999 | A |
5981444 | Sawada et al. | Nov 1999 | A |
6337144 | Shimizu et al. | Jan 2002 | B1 |
6346566 | Yabe et al. | Feb 2002 | B1 |
6696170 | Kim et al. | Feb 2004 | B2 |
6699926 | Yabe et al. | Mar 2004 | B2 |
20030015511 | Kim et al. | Jan 2003 | A1 |
20050044687 | Matsuguchi et al. | Mar 2005 | A1 |
20050045699 | Konishi et al. | Mar 2005 | A1 |
20060255027 | Katiyar | Nov 2006 | A1 |
20060261054 | Katiyar | Nov 2006 | A1 |
20060278627 | Burt et al. | Dec 2006 | A1 |
20070158768 | Pilchowski et al. | Jul 2007 | A1 |
20070184324 | Lyons et al. | Aug 2007 | A1 |
Number | Date | Country |
---|---|---|
1733838 | Dec 2006 | EP |
502823 | Mar 1939 | GB |
1538973 | Jan 1979 | GB |
54-081138 | Jun 1979 | JP |
55-128395 | Oct 1980 | JP |
55128395 | Oct 1980 | JP |
02-098595 | Mar 1990 | JP |
04-300095 | Oct 1992 | JP |
05-023731 | Feb 1993 | JP |
05-171463 | Jul 1993 | JP |
05-287293 | Nov 1993 | JP |
05-329683 | Dec 1993 | JP |
06-106129 | Apr 1994 | JP |
06-262389 | Sep 1994 | JP |
06-277877 | Oct 1994 | JP |
06-277880 | Oct 1994 | JP |
06-285677 | Oct 1994 | JP |
06-285678 | Oct 1994 | JP |
06-306385 | Nov 1994 | JP |
07-032186 | Feb 1995 | JP |
07-097583 | Apr 1995 | JP |
07-136796 | May 1995 | JP |
07-136797 | May 1995 | JP |
07-241694 | Sep 1995 | JP |
07-251295 | Oct 1995 | JP |
07-276089 | Oct 1995 | JP |
08-019893 | Jan 1996 | JP |
08-057650 | Mar 1996 | JP |
08-099188 | Apr 1996 | JP |
08-150494 | Jun 1996 | JP |
08-151548 | Jun 1996 | JP |
08-155671 | Jun 1996 | JP |
08-155674 | Jun 1996 | JP |
08-157858 | Jun 1996 | JP |
08-192292 | Jul 1996 | JP |
08-197278 | Aug 1996 | JP |
08-206879 | Aug 1996 | JP |
08-229697 | Sep 1996 | JP |
08-243779 | Sep 1996 | JP |
08-252691 | Oct 1996 | JP |
08-257788 | Oct 1996 | JP |
08-267284 | Oct 1996 | JP |
08-281471 | Oct 1996 | JP |
08-281480 | Oct 1996 | JP |
08-290287 | Nov 1996 | JP |
09-001391 | Jan 1997 | JP |
09-059667 | Mar 1997 | JP |
09-070684 | Mar 1997 | JP |
09-070685 | Mar 1997 | JP |
09-070691 | Mar 1997 | JP |
09-071792 | Mar 1997 | JP |
09-076089 | Mar 1997 | JP |
09-122974 | May 1997 | JP |
09-141489 | Jun 1997 | JP |
09-141491 | Jun 1997 | JP |
09-150292 | Jun 1997 | JP |
09-206987 | Aug 1997 | JP |
09-302374 | Nov 1997 | JP |
09-323191 | Dec 1997 | JP |
10-058183 | Mar 1998 | JP |
10-146693 | Jun 1998 | JP |
10-193175 | Jul 1998 | JP |
11-005192 | Jan 1999 | JP |
11-077373 | Mar 1999 | JP |
11-104883 | Apr 1999 | JP |
11-104887 | Apr 1999 | JP |
11-147174 | Jun 1999 | JP |
11-147194 | Jun 1999 | JP |
11-147195 | Jun 1999 | JP |
11-170082 | Jun 1999 | JP |
11-197878 | Jul 1999 | JP |
11-217578 | Aug 1999 | JP |
11-254182 | Aug 1999 | JP |
11-335685 | Dec 1999 | JP |
2000-087058 | Mar 2000 | JP |
2000-094178 | Apr 2000 | JP |
2000-117486 | Apr 2000 | JP |
2000-141080 | May 2000 | JP |
2000-158185 | Jun 2000 | JP |
2000-237894 | Sep 2000 | JP |
2000-317679 | Nov 2000 | JP |
2001-113390 | Apr 2001 | JP |
2001-179481 | Jul 2001 | JP |
2001-239393 | Sep 2001 | JP |
2001-252786 | Sep 2001 | JP |
2002-219595 | Aug 2002 | JP |
2002-226880 | Aug 2002 | JP |
2002-239779 | Aug 2002 | JP |
2002-283096 | Oct 2002 | JP |
2002-346787 | Dec 2002 | JP |
2003-039191 | Feb 2003 | JP |
2003-170293 | Jun 2003 | JP |
2003-191092 | Jul 2003 | JP |
2003-225794 | Aug 2003 | JP |
2003-236694 | Aug 2003 | JP |
2003-275893 | Sep 2003 | JP |
2003-275894 | Sep 2003 | JP |
2003-305587 | Oct 2003 | JP |
2003-311475 | Nov 2003 | JP |
2003320481 | Nov 2003 | JP |
2004-001061 | Jan 2004 | JP |
2004-025200 | Jan 2004 | JP |
2004-034131 | Feb 2004 | JP |
2004-058142 | Feb 2004 | JP |
2004-098157 | Apr 2004 | JP |
2004-141908 | May 2004 | JP |
2004-195543 | Jul 2004 | JP |
2004-202572 | Jul 2004 | JP |
2004-237299 | Aug 2004 | JP |
2004-314099 | Nov 2004 | JP |
2005-074438 | Mar 2005 | JP |
2005-074490 | Mar 2005 | JP |
2005-095972 | Apr 2005 | JP |
2005-205493 | Apr 2005 | JP |
2005-246419 | Sep 2005 | JP |
2006-095551 | Apr 2006 | JP |
2006-095552 | Apr 2006 | JP |
2006-095579 | Apr 2006 | JP |
2006-102793 | Apr 2006 | JP |
2006-102794 | Apr 2006 | JP |
2006-102799 | Apr 2006 | JP |
2006-102800 | Apr 2006 | JP |
2006-175451 | Jul 2006 | JP |
2006-175452 | Jul 2006 | JP |
2006-224172 | Aug 2006 | JP |
582932 | Dec 1977 | SU |
Entry |
---|
Buhiyan, “Topical Review, Solution-derived Textured Oxide Thin Films-A Review”, Superconductivity Science Technology, vol. 19, Institute of PHysics Publishing, Jan. 4, 2006. |
Perovskite—7 pgs. from http://wikis.lib.ncsu.edu/index.php/Perovskite, printed Oct. 5, 2007. |
McEvoy, “Materials for high-temperature oxygen reduction in solid oxide fuel cells”, J. of Materials Science, 36, pp. 1087-1091, 2001. |
Melfi et al., “Causes and Prevention of Copper Cracking in Saw Pipe Seam Welds”, copyright 2004, Rio Pipeline 2005 Conference & Exposition, pp. 1-5. |
Pena et al., “Chemical Structures and Performance of Perovskite Oxides”, Chem. Rev. 101 (7), 75 pgs, 2001. |
Shimzu et al., “Wear Mechanism in Contact Tube”, Science and Technology of Welding and Joining, vol. 11, No. 1, 2006, pp. 94-105. |
Zahid et al., Electrical conductivity of perovskites in the quasi-ternary system La[0.8]Sr[0.2]MnO[3]-La[0.8]Sr[0.2]CoO [3]-La[0.8]Sr[0.2]FeO[3] for application as cathode-interconnect contact layer in SOFC, Proceedings—Electrochemical Society, vol. 7 (2), pp. 1708-1716. |
Walck et al., “Characterization of air-annealed, pulsed laser deposited ZnO-WS2 solid film lubricants by transmission electron microscopy”, Thin Solid Films, 305, pp. 130-143, 1997. |
ExxonMobil Material Safety Data Sheet, Product Name: Mobil Velocite Oil No. 10, revision Date Nov. 1, 2006, 8 pgs. |
Lubrizol Material Safety Data Sheet, 5979A, Code A678, 6 pgs. Mar. 2, 2005. |
Lubrizol Metalworking Additives, one page , http://www.lubrizol.com/products/metalworking/default.asp; printed Jan. 22, 2008. |
Mobil Velocite Oil Numbered Series, Spindle and Hydraulic Oils, two pages, printed Jan. 22, 2008, http://www.mobile.com/USA-English/Lubes/PDS/GLXXENINDMOMobil—Velocite—Oil—. . . |
Sasol North America, Material Safety Data Sheet, 154L Specialty Alkylate, A714, printed Jan. 11, 2005, 7 pgs., version 1.5. |
Sasol North America, Technical Data Sheet, V-154L Specialty Alkylate, 7 pgs., version 1.5, printed Jan. 11, 2005. |
Sasol North America, Material Safety Data Sheet, 9050 Specialty Alkylate, printed Jan. 11, 2005, 7 pgs, version 1.4. |
Sasol North America, Technical Data Sheet, V-3060L-B Specialty Alkylate, 7 pgs., version 1.3, printed Jan. 11, 2005. |
Tejuca, et al., Marcel Dekker, Inc., NY, 1993, “Properties and Applications of Perovskite-Type Oxides”, Chapter 1, pp. 1-23 by Twu et al., “Preparation of Bulk and Supported Perovskites”, Chapter 3, “by D.M. Smyth, pp. 47-72, Oxidative Nonstoichiometry in Perovskite Oxides”, and Chapter 9, pp. 195-214, by J.L.G. Fierro, “Composition and Structure of Perovskite Surfaces”. |
Perovskite—one page from Wikipedia, printed Oct. 5, 2007, http://en.wikipedia.org/wiki/Perovskite. |
International Search Report and Written Opinion from PCT/IB09/005860 dated Aug. 20, 2009. |
International Search Report from PCT/IB09/005865 dated Sep. 21, 2009. |
Written Opinion from PCT/IB09/005865 dated Sep. 21, 2009. |
Sasol North America, Technical Data Sheet, V-159L Specialty Alkylate, 7 pgs. version 1.4 dated Jan. 11, 2005. |
Office action from U.S. Appl. No. 12/141,654 dated Apr. 6, 2012. |
Office action from U.S. Appl. No. 12/141,654 dated Aug. 23, 2013. |
Office action from U.S. Appl. No. 12/141,654 dated Nov. 28, 2012. |
Office action from European Application No. 09766180.5 dated Apr. 28, 2012. |
Response from U.S. Appl. No. 12/141,64 dated Sep. 6, 2012. |
Office communication from U.S. Appl. No. 12/141,654 dated Apr. 29, 2013. |
Office action from U.S. Appl. No. 12/141,654 dated Nov. 21, 2013. |
Advisory action from U.S. Appl. No. 12/141,654 dated Dec. 2, 2013. |
Twu, et al., “Preparation of Bulk and Supported Perovskites”, Chapter 1, pp. 1-23 (1993), from Properties and Applications of Perovskite-type Oxides. |
Smyth, “Oxidative Nonstoichiometry in Perovskite Oxides”, Chapter 3, pp. 47-72 (1993), from Properties and Applications of Perovskite-type Oxides. |
Kamimura, “Theory of Copper Oxide Superconductors”, 2005, Springer Verlag, Berlin, 10 pgs., front/back cover and table of contents. |
Fierro, “Composition and Structure of Perovskite Surfaces”, Chapter 9, pp. 195-214 (1993), from Properties and Applications of Perovskite-type Oxides. |
Notice of Allowance from U.S. Appl. No. 12/141,654 dated Jul. 24, 2014. |
Number | Date | Country | |
---|---|---|---|
20090314759 A1 | Dec 2009 | US |