US20050013723A1 - Formation of metallic thermal barrier alloys - Google Patents

Formation of metallic thermal barrier alloys Download PDF

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US20050013723A1
US20050013723A1 US10/776,473 US77647304A US2005013723A1 US 20050013723 A1 US20050013723 A1 US 20050013723A1 US 77647304 A US77647304 A US 77647304A US 2005013723 A1 US2005013723 A1 US 2005013723A1
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alloying element
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Daniel Branagan
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    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C33/00—Making ferrous alloys
    • C22C33/02—Making ferrous alloys by powder metallurgy
    • C22C33/0257—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements
    • C22C33/0278—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5%
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00—Making metallic powder or suspensions thereof
    • B22F9/02—Making metallic powder or suspensions thereof using physical processes
    • B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
    • B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
    • B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00—Making metallic powder or suspensions thereof
    • B22F9/02—Making metallic powder or suspensions thereof using physical processes
    • B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
    • B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
    • B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
    • B22F2009/088—Fluid nozzles, e.g. angle, distance
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31678—Of metal

Definitions

  • This invention is directed at metallic alloys, and more particularly at unique metallic alloys having low electrical and thermal conductivity. In coating form, when applied, such alloys present the ability to provide thermal barrier characteristics to a selected substrate.
  • Metals and metallic alloys have metallic bonds consisting of metal ion cores surrounded by a sea of electrons. These free electrons which arise from an unfilled outer energy band allow the metal to have high electrical and thermal conductivity which makes this class of materials conductors. Due to the nature of the metallic bonds, metals and metallic alloys may exhibit a characteristic range of properties such as electrical and thermal conductivity. Typical metallic materials may exhibit values of electrical resistivity that generally fall in a range of between about 1.5 to 145 10 ⁇ 8 ⁇ m, with iron having an electrical resistivity of about 8.6 10 ⁇ 8 ⁇ m. Typical values of thermal conductivity for metallic materials may be in a range of between about 0.2 to 4.3 watts/cm° C., with iron exhibiting a thermal conductivity of about 0.8 watts/cm° C.
  • ceramics are a class of materials which typically contain positive ions and negative ions resulting from electron transfer from a cation atom to an anion atom. All of the electron density in ceramics is strongly bonded resulting in a filled outer energy band. Ceramic alloys, due to the nature of their ionic bonding, will exhibit a different characteristic range of properties such as electrical and thermal conductivity. Because of the lack of free electrons, ceramics generally have poor electrical and thermal conductivity and are considered insulators. Thus, ceramics may be suitable for use in applications such as thermal barrier coatings while metals are not.
  • a metal alloy comprising an alloy metal and greater than about 4 atomic % of at least one P-group alloying element.
  • a method of reducing the thermal and/or electrical conductivity of a metal alloy composition comprising supplying a base metal with a free electron density, supplying a P-group alloying element and combining said P-group alloying element with said base metal and decreasing the free electron density of the base metal.
  • a metallic alloy which exhibits relatively low thermal conductivity and a low electrical conductivity.
  • the alloy may include primary alloying metals, such as iron, nickel, cobalt, aluminum, copper, zinc, titanium, zirconium, niobium, molybdenum, tantalum, vanadium, hafnium, tungsten, manganese, and combinations thereof, and increased fractions of P-Group elemental additions in the alloy composition.
  • P-group elements are the non-metal and semi-metal constituents of groups IIIA, IVA, VA, VIA, and VIIA found in the periodic table, including but not limited to phosphorous, carbon, boron, silicon, sulfur, and nitrogen.
  • the metallic alloy exhibiting relatively low thermal conductivity and electrical conductivity may be provided as a coating suitable for thermal and/or electrical barrier applications on a variety of substrates.
  • metallic alloys are provided that exhibit relatively low thermal and electrical conductivity.
  • the alloys according to the present invention may include relatively high fractions of P-group elemental alloying additions in admixture with a metal.
  • the added P-group elements may include, but are not limited to, carbon, nitrogen, phosphorus, silicon, sulfur and boron.
  • the P-group elements may be alloyed with the metal according to such methods as by the addition of the P-group elements to the metal in a melt state.
  • an alloy according to the present invention may include P-group alloying constituents. Such constituents are preferably present at a level of at least 4 at % (atomic percent) of the alloy. Desirably, the alloy consistent with the present invention may include more than one alloying component selected from P-group elements, such that the collective content of all of the P-group elements is between about 4 at % to 50 at %.
  • the alloy may include relatively large fractions of silicon in the alloy composition.
  • an iron/silicon coating alloy can be prepared according to the present invention which coating may be applied, e.g., to any given substrate.
  • the metal alloy may be applied as coating using a thermal spray process.
  • the resulting coating maybe employed to provide a thermal and/or electrical barrier coating.
  • the coating provides thermal and/or electrical barrier properties exhibited similar to a ceramic material, however without the associated brittleness of conventional ceramic coatings.
  • the alloy of the present invention may also be processed by any know means to process a liquid melt including conventional casting (permanent mold, die, injection, sand, continuous casting, etc.) or higher cooling rate, i.e. rapid solidification, processes including melt spinning, atomization (centrifugal, gas,. water, explosive), or splat quenching.
  • a liquid melt including conventional casting (permanent mold, die, injection, sand, continuous casting, etc.) or higher cooling rate, i.e. rapid solidification, processes including melt spinning, atomization (centrifugal, gas,. water, explosive), or splat quenching.
  • melt spinning centrifugal, gas,. water, explosive
  • splat quenching atomization to produce powder in the target size range for various thermal spray coating application devices.
  • the present invention provides a metal alloy that behaves similar to a ceramic with respect to electrical and thermal conductivity.
  • An exemplary alloy consistent with the present invention was prepared containing a combination of several alloying elements present at a total level of 25.0 atomic % P-group alloying elements in combination with, e.g. iron.
  • the experimental alloy was produced by combining multiple P group elements according to the following distribution: 16.0 atomic % boron, 4.0 atomic % carbon, and 5.0 atomic % silicon with 54.5 atomic % iron, 15.0 atomic % chromium, 2.0 atomic % manganese, 2.0 atomic % molybdenum, and 1.5 atomic % tungsten.
  • the experimental alloy was prepared by mixing the alloying elements at the disclosed ratios and then melting the alloying ingredients using radio frequency induction in a ceramic crucible. The alloy was then process into a powder form by first aspirating molten alloy to initiate flow, and then supplying high pressure argon gas to the melt stream in a close coupled gas atomization nozzle. The power which was produced exhibited a Gaussian size distribution with a mean particle size of 30 microns. The atomized powder was further air classified to yield preferred powder sized either in the range of 10-45 microns or 22-53 microns. These preferred size feed stock powders were then sprayed onto selected metal substrates using high velocity oxy-fuel thermal spray systems to provide a coating on the selected substrates.
  • conventional metals and metallic alloys typically cool rapidly from a melt state on a conventional water cooled copper arc-melter, and can be safely handled in a matter of a few minutes.
  • the experimental alloy prepared as described above required in excess of 30 minutes to cool from a melt state down to a safe handling temperature after being melted on a water cooled copper hearth arc-melter.
  • the experimental alloy powder does not transfer heat sufficiently using conventional operating parameters due to its relatively low conductivity and inability to absorb heat.
  • conventional alloys can be sprayed with equivalence ratios (kerosene fuel/oxygen fuel flow rate) equal to 0.8. Because of the low thermal conductivity of the modified experimental alloys, much higher equivalence ratios, in the range of 0.9-1.2, are necessary in order to provide sufficient heating of the power.
  • the very thin deposit (225 ⁇ m thick weld) took excessive time before another layer can be deposited since it glows red hot for an extended time.
  • alloy compositions of the following are to be noted, with the numbers reflecting atomic %: SHS717 Powder, with an alloy composition of Fe (52.3), Cr (19.0), Mo (2.5), W (1.7), B (16.0), C (4.0), Si (2.5) and Mn (2.0); SHS717 wire, with an alloy composition of Fe (55.9), Cr (22.0), Mo (0.6), W (0.4), B (15.6), C (3.5), Si (1.2) and Mn (0.9).
  • the thermal conductivity data for the SHS717 coatings was measured by a Laser Flash method and the results are given in Table 1. Note that the wire-arc conductivity is generally lower than the HVOF due to the higher porosity in the wire-arc coating. Note that the conductivity of the coatings is lower than that of titanium which is the lowest thermal conductivity metal and at room temperature are even lower than alumina ceramic (see Table 2).

Abstract

Metal alloys having low electrical and thermal conductivity including relatively large fractions of P-Group element additions. The P-Group elements may be selected from the group including phosphorous, carbon, boron, and silicon. The resultant alloys do not exhibit significantly increased brittleness, and are applied as a coating that provides a metallic thermal barrier coating.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application claims priority to U.S. Provisional Application No. 60/446,610 filed Feb. 11, 2003.
    • FIELD OF THE INVENTION
  • This invention is directed at metallic alloys, and more particularly at unique metallic alloys having low electrical and thermal conductivity. In coating form, when applied, such alloys present the ability to provide thermal barrier characteristics to a selected substrate.
    • BACKGROUND OF THE INVENTION
  • Metals and metallic alloys have metallic bonds consisting of metal ion cores surrounded by a sea of electrons. These free electrons which arise from an unfilled outer energy band allow the metal to have high electrical and thermal conductivity which makes this class of materials conductors. Due to the nature of the metallic bonds, metals and metallic alloys may exhibit a characteristic range of properties such as electrical and thermal conductivity. Typical metallic materials may exhibit values of electrical resistivity that generally fall in a range of between about 1.5 to 145 10−8 Ωm, with iron having an electrical resistivity of about 8.6 10−8 Ωm. Typical values of thermal conductivity for metallic materials may be in a range of between about 0.2 to 4.3 watts/cm° C., with iron exhibiting a thermal conductivity of about 0.8 watts/cm° C.
  • By contrast, ceramics are a class of materials which typically contain positive ions and negative ions resulting from electron transfer from a cation atom to an anion atom. All of the electron density in ceramics is strongly bonded resulting in a filled outer energy band. Ceramic alloys, due to the nature of their ionic bonding, will exhibit a different characteristic range of properties such as electrical and thermal conductivity. Because of the lack of free electrons, ceramics generally have poor electrical and thermal conductivity and are considered insulators. Thus, ceramics may be suitable for use in applications such as thermal barrier coatings while metals are not.
  • Designing a metal alloy to exhibit ceramic like electrical and thermal conductivities is unique. The only area where this has been utilized in material science is in the design of soft magnetic materials for transformer core applications. In such applications, extra silicon is added to iron in order to specifically reduce the electrical conductivity to minimize eddy current losses. However, iron-silicon alloys utilized for transformer cores typically contain a maximum of 2.5 at % (atomic percent) silicon because any additional silicon embrittles the alloy. Additionally, attempts to reduce electrical conductivity of iron transformer cores have not addressed reduced thermal conductivity.
    • SUMMARY OF THE INVENTION
  • A metal alloy comprising an alloy metal and greater than about 4 atomic % of at least one P-group alloying element. In method form, a method of reducing the thermal and/or electrical conductivity of a metal alloy composition comprising supplying a base metal with a free electron density, supplying a P-group alloying element and combining said P-group alloying element with said base metal and decreasing the free electron density of the base metal.
    • DESCRIPTION OF THE PREFERRED EMBODIMENT OF THE INVENTION
  • A metallic alloy is provided which exhibits relatively low thermal conductivity and a low electrical conductivity. The alloy may include primary alloying metals, such as iron, nickel, cobalt, aluminum, copper, zinc, titanium, zirconium, niobium, molybdenum, tantalum, vanadium, hafnium, tungsten, manganese, and combinations thereof, and increased fractions of P-Group elemental additions in the alloy composition. P-group elements are the non-metal and semi-metal constituents of groups IIIA, IVA, VA, VIA, and VIIA found in the periodic table, including but not limited to phosphorous, carbon, boron, silicon, sulfur, and nitrogen. The metallic alloy exhibiting relatively low thermal conductivity and electrical conductivity may be provided as a coating suitable for thermal and/or electrical barrier applications on a variety of substrates.
  • Consistent with the present invention, metallic alloys are provided that exhibit relatively low thermal and electrical conductivity. The alloys according to the present invention may include relatively high fractions of P-group elemental alloying additions in admixture with a metal. The added P-group elements may include, but are not limited to, carbon, nitrogen, phosphorus, silicon, sulfur and boron. The P-group elements may be alloyed with the metal according to such methods as by the addition of the P-group elements to the metal in a melt state.
  • Preferably, an alloy according to the present invention may include P-group alloying constituents. Such constituents are preferably present at a level of at least 4 at % (atomic percent) of the alloy. Desirably, the alloy consistent with the present invention may include more than one alloying component selected from P-group elements, such that the collective content of all of the P-group elements is between about 4 at % to 50 at %.
  • Consistent with the present invention, the alloy may include relatively large fractions of silicon in the alloy composition. For example, an iron/silicon coating alloy can be prepared according to the present invention which coating may be applied, e.g., to any given substrate. For example, it has been found that 5.0 atomic % of silicon, and greater, may be incorporated into the alloy without any measurable loss of toughness when employed in a coating application.
  • As alluded to above, consistent with the present invention, the metal alloy may be applied as coating using a thermal spray process. The resulting coating maybe employed to provide a thermal and/or electrical barrier coating. The coating provides thermal and/or electrical barrier properties exhibited similar to a ceramic material, however without the associated brittleness of conventional ceramic coatings.
  • In addition to the use as a coating, the alloy of the present invention may also be processed by any know means to process a liquid melt including conventional casting (permanent mold, die, injection, sand, continuous casting, etc.) or higher cooling rate, i.e. rapid solidification, processes including melt spinning, atomization (centrifugal, gas,. water, explosive), or splat quenching. One especially preferred method is to utilize atomization to produce powder in the target size range for various thermal spray coating application devices.
  • While not limiting the invention to any particular theory, it is believed at the time of filing that by alloying metals with P-group elements, including but not limited to carbon, nitrogen, phosphorus, and silicon, covalent bonds may be formed between the electrons in the P-group alloying element and the free electrons in the base metal, which base metal, as noted, may include iron. The interaction of the free electrons in the base metal in covalent bonds with the P-group alloying elements apparently act to reduce the free electron density of the base metal, and the outer electron energy band of the base metal is progressively filled. Accordingly, by adding significant quantities of P-group elements, the free electron density of the base metal can be continually reduced and the outer electron energy band can be progressively filled. Because the relatively high thermal conductively and electrical conductivity arise from the free electrons in the unfilled outer energy bands of the metal, as the free electron density is reduced, so are the electrical conductivity and the thermal conductivity. Therefore, the present invention provides a metal alloy that behaves similar to a ceramic with respect to electrical and thermal conductivity.
    • Experimental Observations
  • An exemplary alloy consistent with the present invention was prepared containing a combination of several alloying elements present at a total level of 25.0 atomic % P-group alloying elements in combination with, e.g. iron. The experimental alloy was produced by combining multiple P group elements according to the following distribution: 16.0 atomic % boron, 4.0 atomic % carbon, and 5.0 atomic % silicon with 54.5 atomic % iron, 15.0 atomic % chromium, 2.0 atomic % manganese, 2.0 atomic % molybdenum, and 1.5 atomic % tungsten.
  • The experimental alloy was prepared by mixing the alloying elements at the disclosed ratios and then melting the alloying ingredients using radio frequency induction in a ceramic crucible. The alloy was then process into a powder form by first aspirating molten alloy to initiate flow, and then supplying high pressure argon gas to the melt stream in a close coupled gas atomization nozzle. The power which was produced exhibited a Gaussian size distribution with a mean particle size of 30 microns. The atomized powder was further air classified to yield preferred powder sized either in the range of 10-45 microns or 22-53 microns. These preferred size feed stock powders were then sprayed onto selected metal substrates using high velocity oxy-fuel thermal spray systems to provide a coating on the selected substrates.
  • Reduced thermal behavior was observed for the exemplary alloy in a variety of experiments. Specifically, a small 5 gram ingot of the exemplary alloy was arc-melted on a water cooled copper hearth. It was observed that the alloy ingots took longer time for cooling back to room temperature, relative to other alloys which did not contain the P-group composition noted herein. More specifically, the increased time for cooling was on the order of about 20 times longer.
  • Additionally, while conventional metals and alloys that have been heated to high temperatures cool below their red hot radiance level in a few seconds, it was observed that when the exemplary alloy herein was heated to a temperature above the red hot radiance level of the alloy, the red hot radiance persisted for several minutes after removal of the heat source.
  • Similarly, conventional metals and metallic alloys typically cool rapidly from a melt state on a conventional water cooled copper arc-melter, and can be safely handled in a matter of a few minutes. The experimental alloy prepared as described above required in excess of 30 minutes to cool from a melt state down to a safe handling temperature after being melted on a water cooled copper hearth arc-melter.
  • Finally, when thermally sprayed the experimental alloy powder does not transfer heat sufficiently using conventional operating parameters due to its relatively low conductivity and inability to absorb heat. When using high velocity oxy-fuel thermal spray system, conventional alloys can be sprayed with equivalence ratios (kerosene fuel/oxygen fuel flow rate) equal to 0.8. Because of the low thermal conductivity of the modified experimental alloys, much higher equivalence ratios, in the range of 0.9-1.2, are necessary in order to provide sufficient heating of the power. Additionally, when deposited via the LENS (Laser Engineered Net Shape) process, in which a high powered laser is used to melt metal powder supplied to the focus of the laser by a deposition head, the very thin deposit (225 μm thick weld) took excessive time before another layer can be deposited since it glows red hot for an extended time.
  • In the broad context of the present invention alloy compositions of the following are to be noted, with the numbers reflecting atomic %: SHS717 Powder, with an alloy composition of Fe (52.3), Cr (19.0), Mo (2.5), W (1.7), B (16.0), C (4.0), Si (2.5) and Mn (2.0); SHS717 wire, with an alloy composition of Fe (55.9), Cr (22.0), Mo (0.6), W (0.4), B (15.6), C (3.5), Si (1.2) and Mn (0.9).
  • The thermal conductivity data for the SHS717 coatings was measured by a Laser Flash method and the results are given in Table 1. Note that the wire-arc conductivity is generally lower than the HVOF due to the higher porosity in the wire-arc coating. Note that the conductivity of the coatings is lower than that of titanium which is the lowest thermal conductivity metal and at room temperature are even lower than alumina ceramic (see Table 2).
    TABLE 1
    Thermal Conductivity Data for SHS717 Coatings
    Temperature Conductivity
    Coating Type (° C.) (W/m-K)
    HVOF 25 5.07
    HVOF 200 6.93
    HVOF 400 10.0
    HVOF 600 14.2
    Wire-Arc 25 4.14
    Wire-Arc 200 4.78
    Wire-Arc 400 5.48
    Wire-Arc 600 6.94
  • TABLE 2
    Comparative Thermal Conductivity Data
    600° C.
    25° C. (298 K) 400° C. (673 K) (873 K)
    Alloy W/m-K W/m-K W/m-K
    Al 239 227.5  213.5 
    Au 311 270.5  258*  
    Cu 383 367*   352*  
    Fe 79.1  49.11 39.8
    Ni 74.9 63.0 72* 
    Ti 22.0* 14.0 13.3
    .31 wt % 69.5* 26.5 20.0
    Carbon Steel
    .65 wt % 64.7* 23.8 18.7
    Carbon Steel
    .88 wt % 59.0* 22.6 18.5
    Carbon Steel
    British Steel #7 49.6* 38.1 29.9
    White Cast Iron 12.8* 21.8 19.8
    Grey Cast Iron 29.5* 34.1 23.8
    717HV 5.07  10.00  14.20
    717WA 4.14  5.48  6.94
    302 Stainless Steel 12.3 18.6 22.1
    303 Stainless Steel 14.4* 19.7 23.0
    310 Stainless Steel 13.3* 20.1 25.1
    430 Stainless Steel 22.0* 23.3 24.0
    446 Stainless Steel 17.6* 19.8 21.0
    Alumina Ceramic 24.5*  8.2  6.69

    *Approximated Value

Claims (10)

1. A metal alloy comprising an alloy metal and greater than about 4 atomic % of at least one P-group alloying element.
2. A metal alloy of claim 1 wherein the P-group alloying element is present at a level of 4 atomic % to 50 atomic %.
3. The metal alloy of claim 1 wherein said P-group alloying element is selected from the group consisting of carbon, nitrogen, phosphorous, silicon, boron, and mixtures thereof.
4. A metal alloy according to claim 1, wherein said at least one P-group alloying element comprises 16.0 atomic % B, 4.0 atomic % C, and 5.0 atomic % Si.
5. A metal alloy according to claim 1 wherein the alloy metal is selected from the group consisting of iron, chrome, molybdenum, tungsten, manganese, cobalt, nickel, copper, and mixtures thereof.
6. A method for reducing the thermal and/or electrical conductivity of a metal alloy composition comprising:
(a) supplying a metal alloy composition; and
(b) supplying a P-group alloying element;
(c) mixing said metal alloy composition and said P-group alloying element wherein said P-group alloying element is present at a level to reduce the thermal/and or electrical conductivity of said metal alloy composition.
7. A method of reducing the thermal and/or electrical conductivity of a metal alloy composition comprising:
(a) supplying a base metal with a free electron density
(b) supplying a P-group alloying element
(c) combining said P-group alloying element with said base metal and decreasing the free electron density of the base metal.
8. The method of claim 7 wherein the free electron density of the base metal is reduced from its base metal value, and wherein said free electron density is generally representative of a fully filled outer shell after combination with said P-group alloying element.
9. The method of claim 7 wherein said P-group alloying element is selected from the group consisting of carbon, nitrogen, phosphorous, silicon, boron, and mixtures thereof.
10. The method of claim 7 wherein the base metal is selected from the group consisting of iron, nickel, cobalt, aluminum, copper, zinc. titanium, zirconium, niobium, molybdenum, tantalum, vanadium, hafnium, tungsten, manganese, and combinations thereof.
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US20100084052A1 (en) * 2005-11-14 2010-04-08 The Regents Of The University Of California Compositions of corrosion-resistant Fe-based amorphous metals suitable for producing thermal spray coatings
US20110014353A1 (en) * 2005-11-14 2011-01-20 Jor-Shan Choi Corrosion resistant neutron absorbing coatings
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US20220028589A1 (en) * 2018-10-16 2022-01-27 Magneto B.V. Magnetocaloric effect of Mn-Fe-P-Si-B-V alloy and use thereof

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US20060110278A1 (en) 2006-05-25

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