The invention relates generally to a component having multiple magnetic and nonmagnetic regions, and a method of forming the same. More particularly, the invention relates to the formation of a component having multiple magnetic and nonmagnetic regions through expelling nitrogen in a controlled manner.
The need for high power density and high efficiency electrical machines (i.e., electric motors and generators) has long been prevalent for a variety of applications, particularly for hybrid and/or electric vehicle traction applications. The current trend in hybrid/electric vehicle traction motor applications is to increase rotational speeds to increase the machine's power density, and hence reduce its mass and cost. However, it is recognized that when electrical machines are used for traction applications in hybrid/electric vehicles, there is a clear tradeoff between power density, efficiency, and the machine's constant power speed range limited by rotor mechanical strength—and that this tradeoff presents numerous design challenges.
The power density of an electric machine may be increased by increasing the machine size, improving thermal management, increasing rotor speed, or by increasing the magnetic utilization. The magnetic utilization may be increased by using a combination of processing and alloying of a rotor lamination to create a dual phase magnetic material by developing localized areas of high and low permeability. The localized areas of high and low permeability generally reduce flux losses during rotor operation.
A range of ferrous based soft magnetic compositions of the rotor lamination may be austenitized by a combination of processes to form regions of low permeability. This phase transformation at selected regions in this process may be thermally driven in the presence of carbides in the alloy. Upon local heating, the carbides that are present at selected locations dissolve in the matrix and depress the martensite start temperature, thereby aiding the stabilization of austenite regions at room temperature. However, the presence of carbides in a magnetic microstructure is known to increase coercivity and to lower the magnetic saturation, as compared to traditional ferrous-based magnetic steels. A different method of stabilizing the austenite phase at room temperature in intermediate regions of the soft magnet, while starting from a substantially single phase microstructure, is desired to decrease the coercivity.
Aspects and advantages will be set forth in part in the following description, or may be obvious from the description, or may be learned through practice of the invention.
Methods are generally provided for forming a dual-phase magnetic component from an initial component comprising a non-magnetic austenite composition. In one embodiment, the method may include: forming a coating on a portion of the surface of the initial component to form a masked area while leaving an unmasked area thereon. Thereafter the initial component may be heated to a treatment temperature such that nitrogen diffuses out of the unmasked area of the initial component to transform the non-magnetic austenite composition to a magnetic phase in the unmasked area. Thereafter, the initial component may be cooled from the treatment temperature to form a dual-phase magnetic component having a magnetic region corresponding to the unmasked area and a non-magnetic region corresponding to the masked area.
These and other features, aspects and advantages will become better understood with reference to the following description and appended claims. The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and, together with the description, serve to explain certain principles of the invention.
A full and enabling disclosure of the present invention, including the best mode thereof, directed to one of ordinary skill in the art, is set forth in the specification, which makes reference to the appended FIGS., in which:
Repeat use of reference characters in the present specification and drawings is intended to represent the same or analogous features or elements of the present invention.
Reference now will be made in detail to embodiments of the invention, one or more examples of which are illustrated in the drawings. Each example is provided by way of explanation of the invention, not limitation of the invention. In fact, it will be apparent to those skilled in the art that various modifications and variations can be made in the present invention without departing from the scope of the invention. For instance, features illustrated or described as part of one embodiment can be used with another embodiment to yield a still further embodiment. Thus, it is intended that the present invention covers such modifications and variations as come within the scope of the appended claims and their equivalents.
Different embodiments of the present invention relate to a dual-phase magnetic component formed with a nonmagnetic phase and a magnetic phase and a method of forming the dual-phase magnetic component. The term “dual-phase magnetic component” as used herein may be a magnetic part of any product, such as for example, a rotor lamination or a stator lamination of a motor. The dual-phase magnetic component described herein has intermixed first and second regions, where the first region includes a magnetic phase and the second region includes a non-magnetic phase. The “intermixed first and second regions” hereby means that there are many first regions and second regions that are in the vicinity of each other.
Thus, the dual-phase magnetic component has dual magnetic regions with one set of regions having a magnetic phase, and another set having a non-magnetic phase. As used herein, the “magnetic phase” is a region where greater than 99 volume % of the region is magnetic, and in general, would act as a magnetic region. Further, a “non-magnetic phase” may be the region where greater than 90 volume % of the region is non-magnetic. The dual-phase magnetic component as used herein is usually prepared from a single material. As an example, the material may be a composite dual-phase magnetic component which is formed by providing a non-magnetic portion (e.g., an austenite portion) and a magnetic portion formed by expelling nitrogen to form a ferromagnetic portion in a controlled manner. When the dual-phase magnetic component is made using a single material, the negative effects of bonding or other joining methods a ferromagnetic portion and a non-magnetic portion are reduced by ensuring reliability, hermeticity, and the bond strength of the magnetic component, since many joining methods to join magnetic/non-magnetic materials have the disadvantage of mechanical property degradation at the joint. Further, joining method for thin laminates is time consuming, costly, and requires additional surface finish, thus less practical to be adopted for mass production. Thus, a monolithic piece of material having magnetic, non-magnetic properties at designated regions is superior to any joining methods.
The “magnetic phase” as used herein is a material in a magnetic state having a relative permeability greater than 1. In one embodiment, the relative permeability of the magnetic phase of the first region of the magnetic component is greater than 100, and a saturation magnetization is greater than 1.5 Tesla. A “non-magnetic phase” as used herein has greater than 90 volume % of the material in which the permeability is approximately 1, and the saturation magnetization is about zero.
Austenite, also known as gamma phase iron (y-Fe), is a metallic, non-magnetic allotrope of iron or a solid solution of iron. Heating the iron, iron-based metal, or steel to a temperature at which it changes crystal structure from ferrite to austenite is called austenitization. The addition of certain alloying elements, such as manganese, nickel, nitrogen, and carbon, can stabilize the austenitic structure even at room temperature. A dual phase magnetic component may be formed by stabilizing austenite at room temperature, in some regions of the magnetic component, while retaining the strongly ferromagnetic martensite or ferrite phases at some other regions of the magnetic component.
The presence of carbon is known to stabilize the non-magnetic austenite structure. Earlier efforts had been directed at dissolving formed carbides at selected regions of the magnetic component to stabilize non-magnetic phases at those regions of the magnetic component. In one embodiment of the present invention, a magnetic region of the magnetic component is formed by forming a ferrite structure (e.g., ferromagnetic martensite or ferrite phases) by the removal of nitrogen in those regions while retaining the austenite regions.
Carbides as second phases are known to be undesirable for the dual-phase magnetic component. Thus, in some embodiments of the present invention, the material forming the dual-phase magnetic component is substantially free of carbon. However, in other embodiments of the invention, the composition may contain a relatively small level of carbon, which can sometimes increase the tensile strength of the magnetic region. In these embodiments, the total amount of carbon in the magnetic and non-magnetic regions must be less than about 0.05 weight %.
Like carbon, as nitrogen dissolves into a ferrous alloy, the austenite phase is stabilized. Generally, the presence of carbides, which serve to stabilize the austenite phase upon local heat treatment and dissolution, is established by alloying the initial materials with carbon in the melt.
In one embodiment, the initial component is formed from a nonmagnetic austenite iron-based alloy, which also includes chromium, manganese, nitrogen, and/or other alloying elements. In one particular embodiment, the initial component has a composition formed from melting high nitrogen steel via high pressure-electroslag-remelting or counter-pressure-casting methods to generate high-nitrogen austenitic ingots, as nitrogen solubility in molten steel is very low in conventional melting methods without high pressure of nitrogen gas. Thus, the non-magnetic region includes nitrogen in a quantity that stabilizes the austenite phase. In one embodiment, the austenite composition of the initial component has a nitrogen concentration that is greater than 0.4% by weight (e.g., greater than 0.5% by weight). Thus, the state of the initial component 10 is nonmagnetic.
A method is generally disclosed for forming a dual-phase magnetic component. Thermodynamic and empirical calculations may be used to predict austenite alloy compositions that upon the removal of nitrogen at elevated temperatures to form the ferromagnetic phase. A dual-phase magnetic component using the designed austenite alloy composition may be formed by using the traditional methods. In one embodiment, a formed nonmagnetic component is subjected to selective expelling of nitrogen in particular regions of the near-final component, without the need to substantially alter the shape and size of the formed dual-phase magnetic component after selective expelling of nitrogen. As used herein the term “selective expelling of nitrogen” is the removal of nitrogen of some regions of the dual-phase magnetic component, without substantially altering the austenite nature of the nearby regions. The austenite nature of the nearby regions may be considered to be “substantially altered,” if the average saturation magnetization of those regions is increased by more than about 5 percent.
The selective expelling of nitrogen to form the dual-phase magnetic component may be attained by using different methods of expelling of nitrogen. A chemical, physical, or mechanical block may be provided to the regions of the initial component where the expelling of nitrogen is not desirable to prevent magnetization in those areas. For example, a chemical composition that discourages nitrogen diffusion out of the initial component may be used as the “nitrogen stop-off” material at some regions. A physical method of selectively expelling nitrogen at selected regions, while retaining the nitrogen in the other regions, may be used. A mechanical block may be able to mechanically prevent the diffusion of the nitrogen at certain regions.
In one embodiment of the present invention, elevated temperature gas expelling of nitrogen is used as the preferred method to remove nitrogen from the part. The elevated temperatures in this technique allow for fast diffusion of nitrogen out of the unmasked regions, providing a quick processing route. In order to avoid nitrogen removal in those areas which are intended to stay austenitic (and thus nonmagnetic), in one embodiment, a mechanical mask or stop-off material is applied to locations where nitrogen diffusion out of the part or significant nitrogen loss is not desirable. Thus, in this embodiment, the pre-selected regions that correspond to the regions that are supposed to remain nonmagnetic (austenitic) are masked, using a mechanical method, e.g., a nitrogen stop-off material. As used herein a “nitrogen stop-off material” is a material that is capable of substantially stopping the nitrogen from leaving from that region. It is not necessary that the stop-off material itself contain nitrogen.
The nonmagnetic component that is subjected to the selective expelling of nitrogen to form the dual-phase magnetic component may be exemplified in
For ease of understanding herein, the initial component 10 is depicted as having a rectangular shape with the top surface 12 and the bottom surface 14 in
The coating 16 may be formed of any material suitable for inhibiting and/or blocking diffusion of nitrogen from the masked area 21 without significantly impacting the other properties of the component 10 (e.g., a nitrogen stop-off material). For example, when formed of an iron alloy comprising chromium, the coating 16 may be formed from a chromium oxide, aluminum-silicate materials, aluminide silicide materials, etc., or mixtures thereof. The coating 16 may be formed to a thickness that is generally sufficient to inhibiting and/or blocking diffusion of nitrogen from the masked area 21 without being too thick as to be wasteful of excessive material. For example, the coating 16 may have a thickness of 125 μm or less (e.g., 10 μm to 125 μm, such as 10 μm to 100 μm) on the surfaces 12, 14 of the component 10.
The first region 20 (corresponding to the masked area 21) is designed to be the nonmagnetic region, and the second region 30 (corresponding to an unmasked, exposed area 31) is designed to be the magnetic region. Referring to
The nitrogen stop-off material masks formed by the coating 16 may be applied to the component 10 depending on the desired pattern of nitrogen expelling out of the component (and non-expelling) for the component 10. For example, in
Nitrogen may be diffused out of the component 10 through selective expelling of nitrogen during a heat treatment process. Generally, the diffusion of nitrogen out of the unmasked area 31 is expected to increase with a higher heat-treatment temperature and/or a reduced treatment pressure. For example, the heat treatment process may be performed at a treatment temperature that is greater than 1000° C. (e.g., 1100° C. to 1300° C.). Generally, the diffusion kinetics of nitrogen out of the unmasked area 31 is expected to increase with a higher heat-treatment temperature. However, if the treatment temperature is too low, then the interstitial nitrogen may form nitrides in the masked regions, which would increase the magnetism therein. If the treatment temperature is too high (e.g., greater than 1300° C.), there could be challenges with coating integrity.
Additionally, the diffusion of nitrogen out of the unmasked area 31 is expected to increase with a reduced treatment pressure in the treatment environment. In one embodiment, the heat treatment process is performed at a treatment pressure that is less than atmospheric pressure (i.e., a negative pressure atmosphere that is less than 1 atmosphere in pressure). For example, the treatment pressure may be less than 0.75 atmosphere (e.g., less than 0.5 atmosphere). The treatment pressure may be created by evacuating a furnace cavity and may be maintained through the continuous evacuation of nitrogen during processing. In certain embodiments, the heat treatment may be performed in an oxygen-deficient atmosphere, particularly when the component composition includes chromium, so as to inhibit the formation of oxides (e.g., chromium oxide) on the surface of the unmasked area. Such oxides may interfere with the nitrogen evacuating from those unmasked areas. In one particular embodiment, an ambient pressure of less than 1 atmosphere (e.g., less than 0.75 atmosphere) and a temperature greater than 1000° C. (e.g., 1100° C. to 1300° C.) is used for selective expelling of nitrogen.
When the initial component 10 is subjected to selective expelling of nitrogen, the nitrogen diffuses out of the component 10, through all exposed faces of the component 10, including the top surface 12, bottom surface 14, and all of the unmasked side surfaces of the component. This removal of nitrogen, in conjunction with the composition of the component 10, changes the local phase stability in those unmasked regions 31, and converts those regions from a non-magnetic austenite to magnetic ferromagnetic martensite or ferrite phases.
The nitrogen may be diffusing out of the interior of the component 10 through the non-masked surface regions, but depending on the pressure and temperature, and certain other parameters, nitrogen may also slightly expel from the surface masked regions 20, thereby diffusing out of some of the masked areas 21. Hence, the strict boundaries of the magnetic and non-magnetic regions in the surface portion may be more integral in the interior portions.
Through empirical and thermodynamic calculations, the parameters of selective expelling of nitrogen may be adjusted, and the selective expelling of nitrogen at different directions may be predicted for certain regions of the magnetic component 10, and accordingly, the mask size and shape may be altered so that the end product obtained is approximately the desired outcome of the selective expelling of nitrogen.
In one embodiment, the thickness of the component 10 is in a range from 0.1 mm to 5 mm. The desired pattern of the magnetic and non-magnetic regions of this component may be obtained by selective expelling of nitrogen through the selectively masked top surface 12 and bottom surface 14, keeping the side surfaces of the thickness completely masked. Width 24 (
Selective expelling of nitrogen from the initial component 10 at designed conditions allows the removal of a tailored amount of interstitial nitrogen from the magnetic component. In one embodiment, the unmasked region 31 includes less than 0.4% by weight of nitrogen following heat treatment, such as less than 0.1% by weight (e.g., less than 0.05% by weight). The expelling of nitrogen is not only limited to the unmasked regions of the surface, but may also occur in both the surface portion and the interior portion of the magnetic component 10. However, the concentration of nitrogen in the surface portion and the interior portion need not be uniform.
Following the heat treatment process, the initial component 10 may be cooled from the treatment temperature to form a dual-phase magnetic component having a magnetic region corresponding to the unmasked area and a non-magnetic region corresponding to the masked area. For example, the component 10 may be quenched by rapid cooling to lock in the phase change in the unmasked areas such that the magnetic ferromagnetic martensite or ferrite phases remain in the resulting dual phase magnetic component 100 (
The coating 16 may then be removed from the surfaces 12, 14 through any method, including physical methods (e.g., grit blasting), chemical methods (e.g., chemical etching), laser removal methods, etc.
Depending on the applications, the desired magnetic region and the non-magnetic region shapes and ratios may vary, and the selective expelling of nitrogen may be designed to satisfy these requirements. Accordingly, in one embodiment, a volume percent of the first region in the surface and interior portions is equal to or greater than the volume percent of the second region in the surface and interior portions. In one embodiment, at least one of the first and second regions has an interconnected geometry. The “interconnected geometry” as used herein implies that a region is connected all through the component, and is hence not isolated completely from the similar regions, being surrounded by the other regions completely.
Different topologies may be presented, having dual phase magnetic materials, by using this technology.
With continued reference to
Further aspects of the invention are provided by the subject matter of the following clauses:
1. A method of forming a dual-phase magnetic component from an initial component comprising a non-magnetic austenite composition and having a surface, the method comprising: forming a coating on a portion of the surface of the initial component to form a masked area while leaving an unmasked area thereon; thereafter, heating the initial component to a treatment temperature such that nitrogen diffuses out of the unmasked area of the initial component to transform the non-magnetic austenite composition to a magnetic phase in the unmasked area; and thereafter, cooling the initial component from the treatment temperature to form a dual-phase magnetic component having a magnetic region corresponding to the unmasked area and a non-magnetic region corresponding to the masked area.
2. The method of any preceding clause, wherein nitrogen is retained in the unmasked area of the initial component during heating the initial component to the treatment temperature such that the masked area retains the non-magnetic austenite composition.
3. The method of any preceding clause, wherein the treatment temperature is greater than 1000° C.
4. The method of any preceding clause, wherein the treatment temperature of 1100° C. to 1300° C.
5. The method of any preceding clause, wherein cooling the initial component from the treatment temperature is performed at a cooling rate sufficiently fast to retain both magnetic and non-magnetic phases formed during heating.
6. The method of any preceding clause, wherein the heating the initial component is performed at a treatment pressure of less than 1 atmosphere.
7. The method of any preceding clause, wherein the heating the initial component is performed at a treatment pressure of less than 0.5 atmosphere.
8. The method of any preceding clause, wherein the coating comprises chromium oxide.
9. The method of any preceding clause, wherein the non-magnetic austenite composition comprises an iron alloy that includes chromium, manganese, and nitrogen.
10. The method of any preceding clause, wherein heating the initial component is performed in an oxygen-deficient atmosphere to inhibit formation of chromium oxide on the unmasked area.
11. The method of any preceding clause, further comprising: after cooling the initial component from the treatment temperature, removing the coating from the dual-phase magnetic component.
12. The method of any preceding clause, wherein removing the coating comprises mechanically or chemically removing the coating from the dual-phase magnetic component.
13. The method of any preceding clause, wherein the non-magnetic austenite composition that has a nitrogen concentration that is greater than 0.4% by weight.
14. The method of any preceding clause, wherein the non-magnetic austenite composition that has a nitrogen concentration that is greater than 0.5% by weight.
15. The method of any preceding clause, wherein the magnetic region of the dual-phase magnetic component has a nitrogen concentration that is less than 0.4% by weight.
16. The method of any preceding clause, wherein the magnetic region of the dual-phase magnetic component has a nitrogen concentration that is less than 0.1% by weight.
17. A method of forming a dual-phase magnetic component from an initial component comprising a non-magnetic austenite composition, the method comprising: removing nitrogen from a portion of the non-magnetic austenite composition to form a magnetic region therein.
18. The method of any preceding clause, wherein the non-magnetic austenite composition has a nitrogen concentration that is greater 0.4% by weight.
19. The method of any preceding clause, wherein the magnetic region of the dual-phase magnetic component has a nitrogen concentration that is less than 0.4% by weight.
20. The method of any preceding clause, wherein removing nitrogen from the portion of the non-magnetic austenite composition to form the magnetic region therein, comprises: forming a coating on a portion of the surface of the initial component to form a masked area while leaving an unmasked area thereon; removing nitrogen from the unmasked area at a treatment temperature and at a treatment pressure to transform the non-magnetic austenite composition to a magnetic phase in the unmasked area, wherein the treatment temperature is greater than 1000° C. and the treatment pressure is less than 1 atmosphere; and thereafter, cooling the initial component from the treatment temperature to form a dual-phase magnetic component having a magnetic region corresponding to the unmasked area and a non-magnetic region corresponding to the masked area.
This written description uses exemplary embodiments to disclose the invention, including the best mode, and also to enable any person skilled in the art to practice the invention, including making and using any devices or systems and performing any incorporated methods. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they include structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal languages of the claims.
This invention was made with government support under DE-EE0007755 awarded by the Department of Energy. The government has certain rights in the invention.
Number | Name | Date | Kind |
---|---|---|---|
905817 | Howell | Dec 1908 | A |
1031316 | Apple | Jul 1912 | A |
1042408 | Dearborn | Oct 1912 | A |
1279643 | Brown | Sep 1918 | A |
1581876 | Samson | Apr 1926 | A |
2015554 | Fisher | Sep 1935 | A |
2452530 | Snoek | Sep 1945 | A |
2451633 | Perrigo | Oct 1948 | A |
3257572 | Ludemann et al. | Jun 1966 | A |
3334252 | Gayral | Aug 1967 | A |
3797106 | Costello | Mar 1974 | A |
3869629 | Ogawa et al. | Mar 1975 | A |
3954648 | Belcak et al. | May 1976 | A |
3979821 | Noodleman | Sep 1976 | A |
4121953 | Hull | Oct 1978 | A |
4354126 | Yates | Oct 1982 | A |
4445062 | Glaser | Apr 1984 | A |
4572792 | Muller | Feb 1986 | A |
4588914 | Heyne | May 1986 | A |
4663536 | Roesel, Jr. et al. | May 1987 | A |
4713122 | Dawes et al. | Dec 1987 | A |
4721549 | Bogenschuetz et al. | Jan 1988 | A |
4724348 | Stokes | Feb 1988 | A |
4746376 | Bessey | May 1988 | A |
4790888 | Bessey | Dec 1988 | A |
4912353 | Kondo et al. | Mar 1990 | A |
4916027 | Delmundo | Apr 1990 | A |
4918831 | Kliman | Apr 1990 | A |
5010267 | Lipo et al. | Apr 1991 | A |
5029265 | Staats | Jul 1991 | A |
5124607 | Rieber et al. | Jun 1992 | A |
5155404 | Sadarangani | Oct 1992 | A |
5214839 | Rieber et al. | Jun 1993 | A |
5221139 | Belfer | Jun 1993 | A |
5238507 | Kugimiya et al. | Aug 1993 | A |
5250867 | Gizaw | Oct 1993 | A |
5266859 | Stanley | Nov 1993 | A |
5296773 | El-Antably et al. | Mar 1994 | A |
5376188 | Tahara et al. | Dec 1994 | A |
5547770 | Meelu et al. | Aug 1996 | A |
5580800 | Zhang et al. | Dec 1996 | A |
5643474 | Sangeeta | Jul 1997 | A |
5672925 | Lipo et al. | Sep 1997 | A |
5684352 | Mita et al. | Nov 1997 | A |
5698917 | Shultz | Dec 1997 | A |
5731666 | Folker et al. | Mar 1998 | A |
5818140 | Vagati | Oct 1998 | A |
5841212 | Mita et al. | Nov 1998 | A |
5900126 | Nelson et al. | May 1999 | A |
6058596 | Jansen et al. | May 2000 | A |
6064132 | Nose | May 2000 | A |
6080245 | Uchida et al. | Jun 2000 | A |
6093984 | Shiga et al. | Jul 2000 | A |
6132520 | Schilbe et al. | Oct 2000 | A |
6146692 | Sangeeta et al. | Nov 2000 | A |
6187664 | Yu | Feb 2001 | B1 |
6191511 | Zysset | Feb 2001 | B1 |
6232692 | Kliman | May 2001 | B1 |
6245441 | Yokoyama et al. | Jun 2001 | B1 |
6255005 | Yokoyama et al. | Jul 2001 | B1 |
6261361 | Iida et al. | Jul 2001 | B1 |
6274960 | Sakai et al. | Aug 2001 | B1 |
6284388 | Blotzer et al. | Sep 2001 | B1 |
6288467 | Lange et al. | Sep 2001 | B1 |
6300703 | Kawano et al. | Oct 2001 | B1 |
6313560 | Dooley | Nov 2001 | B1 |
6345544 | Mizuno et al. | Feb 2002 | B1 |
6354310 | Farr et al. | Mar 2002 | B1 |
6468365 | Uchida et al. | Oct 2002 | B1 |
6487769 | Ketterer et al. | Dec 2002 | B2 |
6515395 | Jansen | Feb 2003 | B1 |
6531049 | Kariya et al. | Mar 2003 | B1 |
6534891 | Kliman et al. | Mar 2003 | B2 |
6574079 | Sun et al. | Jun 2003 | B2 |
6603226 | Liang et al. | Aug 2003 | B1 |
6611076 | Lindbery et al. | Aug 2003 | B2 |
6664696 | Pham et al. | Dec 2003 | B1 |
6675460 | Reiter, Jr. et al. | Jan 2004 | B2 |
6758914 | Kool et al. | Jul 2004 | B2 |
6769167 | Lee et al. | Aug 2004 | B2 |
6772503 | Fathimulla et al. | Aug 2004 | B1 |
6781184 | Solayappan et al. | Aug 2004 | B2 |
6784588 | DeCristofaro et al. | Aug 2004 | B2 |
6809442 | Kaneko et al. | Oct 2004 | B2 |
6815861 | Suzuki et al. | Nov 2004 | B2 |
6822417 | Kawaji et al. | Nov 2004 | B2 |
6849983 | Tajima et al. | Feb 2005 | B2 |
6874221 | Jansen et al. | Apr 2005 | B2 |
6878215 | Zimmerman, Jr. | Apr 2005 | B1 |
6888270 | Reiter, Jr. et al. | May 2005 | B2 |
6911756 | Chang | Jun 2005 | B1 |
6916429 | Kool et al. | Jul 2005 | B2 |
6967420 | Laurent et al. | Nov 2005 | B2 |
6998757 | Seguchi et al. | Feb 2006 | B2 |
7154191 | Jansen et al. | Dec 2006 | B2 |
7204012 | Kloepzig et al. | Apr 2007 | B2 |
7205695 | Smith | Apr 2007 | B2 |
7268450 | Takeuchi | Sep 2007 | B2 |
7279116 | Sax | Oct 2007 | B2 |
7321176 | Strothmann | Jan 2008 | B2 |
7348706 | Ionel et al. | Mar 2008 | B2 |
7377986 | Schoen et al. | May 2008 | B2 |
7471025 | Sheeran et al. | Dec 2008 | B2 |
7504755 | Yabe et al. | Mar 2009 | B2 |
7514833 | Hsu et al. | Apr 2009 | B2 |
7556082 | Welchko et al. | Jul 2009 | B2 |
7605503 | El-Rafai et al. | Oct 2009 | B2 |
7652404 | El-Refaie et al. | Jan 2010 | B2 |
7687334 | Zou et al. | Mar 2010 | B2 |
7696662 | Komuro et al. | Apr 2010 | B2 |
7709057 | Fusaro et al. | May 2010 | B2 |
7727892 | Morrow et al. | Jun 2010 | B2 |
7791237 | Shah et al. | Sep 2010 | B2 |
7846271 | Choi et al. | Dec 2010 | B2 |
7927937 | Zou et al. | Apr 2011 | B2 |
8004140 | Alexander et al. | Aug 2011 | B2 |
8018110 | Alexander et al. | Sep 2011 | B2 |
8069555 | Tang et al. | Dec 2011 | B2 |
8076811 | Zhu et al. | Dec 2011 | B2 |
8154167 | Tang | Jan 2012 | B2 |
8159103 | Rodriguez et al. | Apr 2012 | B2 |
8179009 | Saban | May 2012 | B2 |
8319388 | Yoshino et al. | Nov 2012 | B2 |
8344581 | Yabe et al. | Jan 2013 | B2 |
8410656 | Lokhandwalla et al. | Apr 2013 | B2 |
8567040 | Kubo | Oct 2013 | B2 |
8659199 | Tokoi et al. | Feb 2014 | B2 |
8729766 | Reutlinger et al. | May 2014 | B2 |
8836196 | Calley et al. | Sep 2014 | B2 |
9000642 | Moulin et al. | Apr 2015 | B2 |
9212555 | Manier et al. | Dec 2015 | B2 |
9214846 | Fubuki | Dec 2015 | B2 |
9384987 | Jung et al. | Jul 2016 | B2 |
9634549 | Dial et al. | Apr 2017 | B2 |
9803139 | Bonitatibus, Jr. et al. | Oct 2017 | B1 |
9879356 | Wittel et al. | Jan 2018 | B2 |
10020098 | Furusawa et al. | Jul 2018 | B2 |
10190206 | Dial et al. | Jan 2019 | B2 |
10229776 | Johnson et al. | Mar 2019 | B2 |
10229777 | Zou et al. | Mar 2019 | B2 |
10276667 | Atanackovic | Apr 2019 | B1 |
10396615 | Galioto et al. | Aug 2019 | B2 |
10483037 | Lambourne et al. | Nov 2019 | B2 |
10501839 | Kool | Dec 2019 | B2 |
10673288 | Kool et al. | Jun 2020 | B2 |
10748678 | Kurokawa et al. | Aug 2020 | B2 |
10749385 | Reddy et al. | Aug 2020 | B2 |
20020054462 | Sun et al. | May 2002 | A1 |
20020100493 | Kool et al. | Aug 2002 | A1 |
20030003765 | Gibson et al. | Jan 2003 | A1 |
20030062786 | Reiter, Jr. et al. | Apr 2003 | A1 |
20030062791 | Reiter, Jr. et al. | Apr 2003 | A1 |
20030201687 | Asai | Oct 2003 | A1 |
20040021396 | Ehrhart et al. | Feb 2004 | A1 |
20040074873 | Kool et al. | Apr 2004 | A1 |
20040090135 | Maslov et al. | May 2004 | A1 |
20040189108 | Dooley | Sep 2004 | A1 |
20040201358 | Kawaji et al. | Oct 2004 | A1 |
20040245869 | Dooley | Dec 2004 | A1 |
20050041432 | McCarthy et al. | Feb 2005 | A1 |
20050161438 | Kool et al. | Jul 2005 | A1 |
20050281023 | Gould et al. | Dec 2005 | A1 |
20070017601 | Miyata et al. | Jan 2007 | A1 |
20070086131 | Miller et al. | Apr 2007 | A1 |
20070203041 | Lee | Aug 2007 | A1 |
20070252465 | Sasaki et al. | Nov 2007 | A1 |
20070252471 | Holmes et al. | Nov 2007 | A1 |
20080018189 | Dooley | Jan 2008 | A1 |
20080143207 | Shah | Jun 2008 | A1 |
20080191578 | Evans | Aug 2008 | A1 |
20080238217 | Shah et al. | Oct 2008 | A1 |
20080238236 | El-Refaie | Oct 2008 | A1 |
20090002978 | Tran et al. | Jan 2009 | A1 |
20090021105 | Evans | Jan 2009 | A1 |
20090038713 | Ueda | Feb 2009 | A1 |
20090072647 | Hino et al. | Mar 2009 | A1 |
20090115361 | Nitta | May 2009 | A1 |
20090302004 | Manier et al. | Dec 2009 | A1 |
20100090557 | El-Rafaie et al. | Apr 2010 | A1 |
20100120230 | Grivna et al. | May 2010 | A1 |
20100126878 | Marjanovic et al. | May 2010 | A1 |
20100141076 | Blissenbach et al. | Jun 2010 | A1 |
20100253174 | Yabe et al. | Oct 2010 | A1 |
20100277017 | Alexander et al. | Nov 2010 | A1 |
20100277028 | Alexander et al. | Nov 2010 | A1 |
20110037338 | Leiber et al. | Feb 2011 | A1 |
20110088720 | Varanasi et al. | Apr 2011 | A1 |
20110175225 | Seddon et al. | Jul 2011 | A1 |
20110186191 | Murakami et al. | Aug 2011 | A1 |
20110266893 | El-Refaie | Nov 2011 | A1 |
20120021917 | Sakamoto et al. | Jan 2012 | A1 |
20120040840 | Okayama et al. | Feb 2012 | A1 |
20120126652 | Shah et al. | May 2012 | A1 |
20120129049 | Rayner | May 2012 | A1 |
20120288396 | Lee et al. | Nov 2012 | A1 |
20120315180 | Soderman et al. | Dec 2012 | A1 |
20120328467 | Fernandez Acevedo et al. | Dec 2012 | A1 |
20130002064 | De Bock et al. | Jan 2013 | A1 |
20130022833 | Wakade | Jan 2013 | A1 |
20130043760 | Osborne et al. | Feb 2013 | A1 |
20130106500 | Yin et al. | May 2013 | A1 |
20130119810 | Aoyama | May 2013 | A1 |
20130140932 | Reddy et al. | Jun 2013 | A1 |
20130204018 | Parvulescu et al. | Aug 2013 | A1 |
20130214620 | Kobayashi et al. | Aug 2013 | A1 |
20140001906 | Li et al. | Jan 2014 | A1 |
20140028145 | Luise et al. | Jan 2014 | A1 |
20140062247 | Dorfner et al. | Mar 2014 | A1 |
20140239763 | Raminosoa et al. | Aug 2014 | A1 |
20140246944 | Koka et al. | Sep 2014 | A1 |
20140265708 | Galito et al. | Sep 2014 | A1 |
20150031084 | Banta et al. | Jan 2015 | A1 |
20150054380 | Suzuki | Feb 2015 | A1 |
20150109080 | Fullerton | Apr 2015 | A1 |
20150115749 | Dial | Apr 2015 | A1 |
20150115757 | Reddy et al. | Apr 2015 | A1 |
20150159262 | Bremer | Jun 2015 | A1 |
20150171682 | Fujisawa et al. | Jun 2015 | A1 |
20150179917 | Greer et al. | Jun 2015 | A1 |
20150295454 | El-Refaie et al. | Oct 2015 | A1 |
20150361545 | Walker | Dec 2015 | A1 |
20160087503 | Galioto et al. | Mar 2016 | A1 |
20160102012 | Pilon et al. | Apr 2016 | A1 |
20160121421 | Uhm et al. | May 2016 | A1 |
20160203898 | Johnson et al. | Jul 2016 | A1 |
20160203899 | Zou et al. | Jul 2016 | A1 |
20160294236 | Alexander et al. | Oct 2016 | A1 |
20160359100 | Bhushan et al. | Dec 2016 | A1 |
20170183764 | Dial | Jun 2017 | A1 |
20180175678 | Papini | Jun 2018 | A1 |
20180183279 | Kool et al. | Jun 2018 | A1 |
20180337565 | Reddy et al. | Nov 2018 | A1 |
20190279795 | Zhang | Sep 2019 | A1 |
20210277506 | Shinozaki et al. | Sep 2021 | A1 |
Number | Date | Country |
---|---|---|
101467330 | Jun 2009 | CN |
101645628 | Feb 2010 | CN |
101728911 | Sep 2010 | CN |
202395537 | Aug 2012 | CN |
106346146 | Jan 2018 | CN |
102005025944 | Dec 2006 | DE |
102005046165 | Apr 2007 | DE |
102009044196 | Apr 2010 | DE |
0880216 | Nov 1998 | EP |
0959549 | Nov 1999 | EP |
1251624 | Oct 2002 | EP |
1431421 | Jun 2004 | EP |
1450462 | Aug 2004 | EP |
1777795 | Apr 2007 | EP |
2237390 | Oct 2010 | EP |
2333906 | Aug 1999 | GB |
S57189542 | Nov 1982 | JP |
S60219945 | Nov 1985 | JP |
H06113493 | Apr 1994 | JP |
H0636664 | May 1994 | JP |
H11146586 | May 1999 | JP |
H11168864 | Jun 1999 | JP |
H11206082 | Jul 1999 | JP |
2000060036 | Feb 2000 | JP |
2000069699 | Mar 2000 | JP |
2000184643 | Jun 2000 | JP |
2000312446 | Nov 2000 | JP |
2001145284 | May 2001 | JP |
2002180215 | Jun 2002 | JP |
2002199679 | Jul 2002 | JP |
2006054932 | Feb 2006 | JP |
2006271058 | Oct 2006 | JP |
2007244026 | Sep 2007 | JP |
2007336771 | Dec 2007 | JP |
2008099360 | Apr 2008 | JP |
2008136320 | Jun 2008 | JP |
2009071910 | Apr 2009 | JP |
2009278838 | Nov 2009 | JP |
2010158130 | Jul 2010 | JP |
2010178493 | Aug 2010 | JP |
2012518378 | Aug 2012 | JP |
2014050218 | Mar 2014 | JP |
2015053823 | Mar 2015 | JP |
1020130049189 | May 2013 | KR |
WO 0067360 | Nov 2000 | WO |
WO03075324 | Sep 2003 | WO |
WO2008009706 | Jan 2008 | WO |
WO2011151138 | Dec 2011 | WO |
WO2012004343 | Jan 2012 | WO |
Entry |
---|
Mosecker et al., “Nitrogen in chronium-manganese stainless steels: a review on the evaluation of stacking fault energy by computational thermodynamics”, Science and Technology of Advanced Materials, vol. 14, No. 3, Mar. 1, 2023, pp. 033001-6996. |
Calfo et al., High-Speed Generators for Power-Dense, Medium-Power, Gas Turbine Generator Sets, Naval Engineers Journal, vol. 119, Issue 2, Published on-line Nov. 14, 2007, pp. 63-81. |
Connor et al., Coating Rejuvenation: New Repair Technology for High Pressure Turbine Blades, ASME Turbo Expo 2000: Power for Land, Sea, and Air, vol. 4, Munich Germany, May 8-11, 2000, 7 Pages. (Abstract Only). |
Czerwiec et al., Fundamental and Innovations in Plasma Assisted Diffusion of Nitrogen and Carbon in Austenitic Stainless Steels and Related Alloys, Plasma Processes and Polymers, vol. 6, Issue 6-7, Jul. 18, 2009, pp. 401-409. |
El-Refaie et al., Application of Bi-State Magnetic Material to an Automotive IPM Starter/Alternator Machine, IEEE Transactions on Energy Conversion, vol. 20, Issue 1, Mar. 2005, pp. 71-79. |
El-Refaie et al., Optimal Flux Weakening in Surface PM Machines Using Fractional-Slot Concentrated Windings, IEEE Transactions on Industry Applications, vol. 41, No. 3, May/Jun. 2005, pp. 790-800. |
Ghasaei et al., Torque Ripple Reduction by Multi-Layering Technique in an Interior Permanent Magnet Motor Used in Hybrid Electric Vehicle, Power Electronics, Electrical Drives, Automation and Motion (SPEEDAM), 2014 International Symposium on Jun. 18-20, Ischia, pp. 372-377. (Abstract Only). |
Hausbrand et al., Corrosion of Zinc-Magnesium Coatings: Mechanism of Paint Delamination, Corrosion Science, vol. 51, Issue 9, Sep. 2009, pp. 2107-2114. |
IDC, Why is 02 Paramagnetic while N2 Diamagnetic, 4 Pages. Retrieved Nov. 16, 2020 from Website: http://www.idc-online.com/technical_references/pdfs/chemical_engineering/Why_is_O2_Paramagnetic_while_N2_Diamagnetic.pdf. |
Kolehmainen, Machine with a Rotor Structure Supported Only by Buried Magnets, ISEF 2007—XIII International Symposium on Electromagnetic Fields in Mechatronics, Electrical and Electronic Engineering, Prague, Sep. 2007, 6 Pages. |
Lavanya et al., Performance Analysis of Three Phase Induction Motor Using Different Magnetic Slot Wedges, Electric Energy Systems (ICEES), 2014 IEEE 2nd International Conference in Chennai, Jan. 7-9, 2014, pp. 164-167. (Abstract Only). |
Lee et al., Photoresist Removal after Plasma Etching of Metal Film using TiW as Antireflective Coating or as a Barrier Metal, ESSDERC 94: 24th European Solid-State Device Research Conference, Edinburgh Scotland, Sep. 11-15, 1994, pp. 295-298. |
Marcos et al., Stainless Steel Patterning by Combination of Micro-Patterning and Driven Strain Produced by Plasma Assisted Nitriding, Surface & Coatings Technology, vol. 205, Jan. 20, 2011, pp. S275-S279. |
Mita et al., Magnetic Screw Rod Using Dual State 0.6C—13Cr—Fe Bulk Magnetic Material, Journal of Applied Physics, vol. 91, Issue 10, May 15, 2002, 4 Pages. |
Mita et al., Study of Internal Permanent Magnet Rotor Made of 0.6C—13Cr—Fe Dual State Magnetic Material, Journal of Applied Physics, vol. 93, No. 10, May 15, 2003, 4 Pages. |
Mita et al., A Study of Retainer Ring Made of 13.5Cr—0.6C—Fe Dual State Magnetic Material, Journal of Magnetism and Magnetic Materials, vols. 254-255, Jan. 2003, pp. 272-274. |
Oh et al., New Rotor Shape Design of SRM to Reduce the Torque Ripple and Improve the Output Power, Proceedings of the Eighth International Conference on Electrical Machines and Systems, ICEMS 2005, vol. 1, Sep. 27-29, 2005, pp. 652-654. (Abstract Only). |
Putatunda et al., Mechanical and Magnetic Properties of a New Austenitic Structural Steel, Materials Science and Engineering: A, vol. 406, Issue 1-2, Oct. 15, 2005, pp. 254-260. https://doi.org/10.1016/j.msea.2005.06.056; (Abstract Only). |
Raminosoa et al., Reduced Rare-Earth Flux-Switching Machines for Traction Applications, IEEE Transactions on Industry Applications, vol. 51, Issue 4, Jul./Aug. 2015, pp. 2959-2971. (Abstract Only). |
Rawers et al., Nitrogen Concentration in Fe—Cr—Mn Alloys, Journal of Materials Engineering and Performance, ASM International, vol. 2, Oct. 1993, pp. 561-658. (Abstract Only). |
Reddy et al., Performance Testing and Analysis of Synchronous Reluctance Motor Utilizing Dual-Phase Magnetic Material, IEEE Transactions on Industry Applications, vol. 54, Issue 3, May-Jun. 2018, pp. 2193-2201. (Abstract Only) doi: 10.1109/TIA.2018.2801264. |
Rudnizki et al., Phase-Field Modeling of Austenite Formation from a Ferrite plus Pearlite Microstructure during Annealing of Cold-Rolled Dual-Phase Steel, Metallurgical & Materials Transactions, vol. 42, Issue 8, Aug. 2011, pp. 2516-2525. |
Sanada et al., Rotor Structure for Reducing Demagnetization of Magnet in a PMASynRM with Ferrite Permanent Magnet and its Characteristics, IEEE 2011, pp. 4189-4194. (Abstract Only). |
Sanada et al., Torque Ripple Improvement for Synchronous Reluctance Motor Using an Asymmetric Flux Barrier Arrangement, IEEE Transactions on Industry Applications, vol. 40, No. 4, Jul./Aug. 2004, pp. 1076-1082. |
Shah et al., Eddy Current Loss Minimization in Conducting Sleeves of High-Speed Machine Rotors by Optimal Axial Segmentation and Copper Cladding, Industry Applications Conference 2007, 42snd IAS Annual Meeting Conference Record of the 2007 IEEE, Sep. 2007, pp. 554-551. |
Shashank et al., Selective Plasma Nitridation and Contrast Reversed Etching of Silicon, Journal of Vacuum Science & Technology B, vol. 19, No. 5, Sep./Oct. 2001, 5 Pages. |
Simmons, Overview: High-Nitrogen Alloying of Stainless Steels, Materials Science and Engineering, vol. 207, Issue 2, Mar. 30, 1996, pp. 159-169. |
Tschiptschin, Predicting Microstructure Development During High Temperature Nitriding of Martensitic Stainless Steels Using Thermodynamic Modeling, Materials Research, vol. 5, No. 3, 2002, pp. 257-262. |
Tsuchiyama et al., Thermodynamics of Nitrogen Absorption into Solid Solution in Fe—Cr—Mn Ternary Alloys, Materials Science Forum, Trans Tech Publication, vols. 426-432, Aug. 15, 2003, pp. 957-962. (Abstract Only). |
Wan et al., Analysis of Magnetism in High Nitrogen Austenitic Stainless Steel and its Elimination by High Temperature Gas Nitriding, J. Mater Sci Technology, vol. 27, Issue 12, 2011, pp. 1139-1142. |
Wang et al., Fabrication and Experimental Analysis of an Axially Laminated Flux-Switching Permanent-Magnet Machine, IEEE Transactions on Industrial Electronics, vol. 64, No. 2, Feb. 2017, pp. 1081-1091. (Abstract Only). |
Werner et al., Energy-Efficient Steels for Motor Laminations, Journal of Materials Engineering and Performance, vol. 1, Issue 2, Mar. 1992, pp. 227-234. (Abstract Only). |
Weyand, What is the Difference Between Austenitic, Ferritic, and Martensitic Stainless Steel?, All America Threaded Products, Technical, 2015, 1 Page. (Abstract Only). Retrieved from https://www.aatprod.com/hrf_faq/what-is-the-difference-between-austentic-ferritic-and-martensitic-stainless/. |
Williamson et al., Calculation of the Bar Resistance and Leakage Reactance of Cage Rotors with Closed Slots, IEEE Proceedings B-Electric Power Applications, vol. 132, Issue 3, May 1985, pp. 125-132. (Abstract Only) DOI: 10.1049/ip-b.1985.0018. |
Wolbank, Evaluation of Lamination Materials in Zero-Speed Sensorless Controlled Induction Machine Drives, TENCON 2001, Proceedings of IEEE Region 10 International Conference on Electrical and Electronic Technology IEEE Explore, vol. 2, Apr. 19-22, 2001, pp. 613-619. |
Wolbank et al., Transient Magnetic Modelling of Sensorless Controlled Induction Machines, Magnetics Conference, 2002 Intermag Europe 2002, Digest of Technical Papers, 2002 IEEE International , IEEE Xplore, Amsterdam, The Netherlands, Apr. 28-May 2, 2002. (Abstract Only). |
Yadav et al., Slurry Erosive Wear Study of D-Gun Sprayed Coatings on SAE 431, 2013 International Conference on Control, Computing, Communication and Materials (ICCCCM), Allahabad, 2013, 5 Pages. (Abstract Only). |
Zeng et al., Prediction of Interstitial Diffusion Activation Energies of Nitrogen, Oxygen, Boron and Carbon in BCC, FCC, and HCP Metals Using Machine Learning, Science Direct, Computational Materials Science, vol. 144, 2018, pp. 232-247. |
ZYP Coatings Inc, For Long-Term Oxidation Protection of Metals, ZYP Coatings, Sealmet Flyer, 1 Page. Retrieved on Apr. 10, 2018 from: https://www.zypcoatings.com/wp-content/uploads/Sealmet-zyp01.pdf. |
Number | Date | Country | |
---|---|---|---|
20220340987 A1 | Oct 2022 | US |