WO2016068189A1 - 溶射用粉末、溶射皮膜、皮膜、及び溶融金属浴中ロール - Google Patents
溶射用粉末、溶射皮膜、皮膜、及び溶融金属浴中ロール Download PDFInfo
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- WO2016068189A1 WO2016068189A1 PCT/JP2015/080382 JP2015080382W WO2016068189A1 WO 2016068189 A1 WO2016068189 A1 WO 2016068189A1 JP 2015080382 W JP2015080382 W JP 2015080382W WO 2016068189 A1 WO2016068189 A1 WO 2016068189A1
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- Prior art keywords
- thermal spraying
- powder
- molten metal
- film
- particles
- Prior art date
Links
- 239000000843 powder Substances 0.000 title claims abstract description 104
- 229910052751 metal Inorganic materials 0.000 title claims description 74
- 239000002184 metal Substances 0.000 title claims description 74
- 239000011248 coating agent Substances 0.000 title claims description 51
- 238000000576 coating method Methods 0.000 title claims description 51
- 238000005507 spraying Methods 0.000 title claims description 25
- 239000007921 spray Substances 0.000 title abstract description 12
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 63
- 229910052742 iron Inorganic materials 0.000 claims abstract description 59
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 37
- 239000013078 crystal Substances 0.000 claims abstract description 29
- 229910052796 boron Inorganic materials 0.000 claims abstract description 26
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 26
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 24
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 23
- 238000002441 X-ray diffraction Methods 0.000 claims abstract description 21
- 238000001228 spectrum Methods 0.000 claims abstract description 21
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 20
- 239000000470 constituent Substances 0.000 claims abstract description 15
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 82
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 80
- 238000007751 thermal spraying Methods 0.000 claims description 79
- 239000011777 magnesium Substances 0.000 claims description 28
- 239000010941 cobalt Substances 0.000 claims description 18
- 229910017052 cobalt Inorganic materials 0.000 claims description 18
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 18
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 13
- 239000010937 tungsten Substances 0.000 claims description 13
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 9
- 239000011733 molybdenum Substances 0.000 claims description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- -1 and Co Inorganic materials 0.000 abstract description 2
- 239000002245 particle Substances 0.000 description 56
- 239000002923 metal particle Substances 0.000 description 17
- 239000002994 raw material Substances 0.000 description 16
- 238000009792 diffusion process Methods 0.000 description 10
- 230000035515 penetration Effects 0.000 description 10
- 230000035939 shock Effects 0.000 description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 9
- 229910052725 zinc Inorganic materials 0.000 description 9
- 239000011701 zinc Substances 0.000 description 9
- 238000005245 sintering Methods 0.000 description 8
- 239000008188 pellet Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 5
- 239000000919 ceramic Substances 0.000 description 4
- 238000010285 flame spraying Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- OFEAOSSMQHGXMM-UHFFFAOYSA-N 12007-10-2 Chemical compound [W].[W]=[B] OFEAOSSMQHGXMM-UHFFFAOYSA-N 0.000 description 3
- LGLOITKZTDVGOE-UHFFFAOYSA-N boranylidynemolybdenum Chemical compound [Mo]#B LGLOITKZTDVGOE-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 229910000952 Be alloy Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 239000011224 oxide ceramic Substances 0.000 description 2
- 229910052574 oxide ceramic Inorganic materials 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010286 high velocity air fuel Methods 0.000 description 1
- 238000007749 high velocity oxygen fuel spraying Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C13/00—Rolls, drums, discs, or the like; Bearings or mountings therefor
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/10—Alloys containing non-metals
- C22C1/1084—Alloys containing non-metals by mechanical alloying (blending, milling)
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/007—Alloys based on nickel or cobalt with a light metal (alkali metal Li, Na, K, Rb, Cs; earth alkali metal Be, Mg, Ca, Sr, Ba, Al Ga, Ge, Ti) or B, Si, Zr, Hf, Sc, Y, lanthanides, actinides, as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C19/00—Alloys based on nickel or cobalt
- C22C19/07—Alloys based on nickel or cobalt based on cobalt
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/02—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
- C22C29/06—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
- C22C29/08—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C29/00—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
- C22C29/14—Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on borides
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/003—Apparatus
- C23C2/0034—Details related to elements immersed in bath
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
- C23C4/067—Metallic material containing free particles of non-metal elements, e.g. carbon, silicon, boron, phosphorus or arsenic
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/10—Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
- C23C4/129—Flame spraying
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C2204/00—Metallic materials; Alloys
- F16C2204/40—Alloys based on refractory metals
Definitions
- the present invention relates to a coating such as a thermal spray coating suitable for being provided on the surface of a roll used in a molten metal bath.
- the present invention also relates to a thermal spraying powder suitable for forming the coating, and a roll in a molten metal bath provided with the coating on the surface.
- a continuous hot dipping method in which a steel plate is continuously guided and passed through a molten metal bath using a roll such as a sink roll or a support roll arranged in the molten metal bath is known. ing. A sprayed coating may be provided on the surface of the roll used in the molten metal bath for the purpose of improving the durability of the roll.
- a thermal spray coating used for such a purpose sprays a powder obtained by firing a mixture containing tungsten carbide particles, tungsten boride particles, and cobalt particles. Can be formed.
- the thermal spray coating obtained by thermal spraying the thermal spraying powder described in Patent Document 1 is subject to penetration and diffusion of metal components in the molten metal bath when the roll is used in the molten metal bath for a long period of time. As a result, the molten metal gradually adheres, and the thermal shock resistance is also lowered.
- an object of the present invention is to provide a coating such as a sprayed coating which is difficult for molten metal to adhere and has excellent thermal shock resistance.
- Another object of the present invention is to provide a thermal spraying powder capable of forming such a coating, and to provide a roll in a molten metal bath having such a coating provided on the surface.
- a first element selected from tungsten and molybdenum, a second element selected from cobalt, nickel and iron, and carbon and boron are selected.
- a thermal spraying powder containing a third element and a fourth element selected from aluminum and magnesium as constituent elements.
- the thermal spraying powder contains the second element in an amount of 20 mol% or more.
- the molar ratio of the fourth element to the second element in the thermal spraying powder is 0.05 or more and 0.5 or less.
- the thermal spraying powder has a crystal phase containing cobalt, nickel or iron, tungsten and carbon, or a crystal phase containing cobalt, nickel or iron, tungsten or molybdenum and boron.
- the intensity of the peak attributed to cobalt, nickel or iron on the X-ray diffraction spectrum of the thermal spraying powder is not more than 0.1 times the intensity of the peak having the maximum intensity among the peaks appearing on the same X-ray diffraction spectrum. .
- a thermal spray coating obtained by thermal spraying the thermal spray powder is provided.
- it is a roll used in a molten metal bath, Comprising: The roll by which the said sprayed coating is provided in the surface is provided.
- a film containing a fourth element selected from the above as a constituent element is provided.
- the coating contains the second element in an amount of 20 mol% or more.
- the molar ratio of the fourth element to the second element in the film is 0.05 or more and 0.5 or less.
- the film has a crystal phase containing cobalt, nickel, or iron, tungsten, and carbon, or a crystal phase containing cobalt, nickel, or iron, tungsten, molybdenum, or boron. No peak attributed to cobalt, nickel, or iron is detected on the X-ray diffraction spectrum of the film.
- a roll used in a molten metal bath having a coating film on the surface according to the fourth aspect.
- FIG. 4 is an X-ray diffraction spectrum diagram of the thermal spray powder of Example 2.
- FIG. 4 is an X-ray diffraction spectrum diagram of the thermal spray powder of Example 2.
- the thermal spraying powder includes a first element selected from tungsten (W) and molybdenum (Mo), a second element selected from cobalt (Co), nickel (Ni) and iron (Fe), and carbon (C ) And boron (B) and a fourth element selected from aluminum (Al) and magnesium (Mg) as constituent elements.
- the thermal spraying powder may contain only one of W and Mo as the first element, or may contain both.
- the thermal spraying powder may contain only one of Co, Ni, and Fe as the second element, or may contain only two, or three. It may contain all.
- the thermal spraying powder may contain only one of C and B as the third element, or may contain both.
- the thermal spraying powder may contain only one of Al and Mg as the fourth element, or may contain both.
- the amount of the first element (W, Mo) in the thermal spraying powder is preferably 50 mol% or more, more preferably 60 mol% or more.
- the amount of the first element (W, Mo) in the thermal spraying powder is also preferably 75 mol% or less, more preferably 70 mol% or less.
- the amount of the second element (Co, Ni, Fe) in the thermal spraying powder is preferably 20 mol% or more, more preferably 22 mol% or more, and further preferably 25 mol% or more. In this case, it becomes easy to obtain a thermal spray coating excellent in thermal shock resistance.
- the amount of the second element (Co, Ni, Fe) in the thermal spraying powder is preferably 50 mol% or less, more preferably 40 mol% or less, and further preferably 30 mol% or less. In this case, it becomes easy to obtain a sprayed coating on which molten metal is difficult to adhere.
- the amount of the third element (C, B) in the thermal spraying powder is preferably 3 mol% or more, more preferably 3.5 mol% or more.
- the amount of the third element (C, B) in the thermal spraying powder is also preferably 5 mol% or less, more preferably 4.5 mol% or less.
- the amount of the fourth element (Al, Mg) in the thermal spraying powder is preferably 1 mol% or more, more preferably 1.5 mol% or more. In this case, it becomes easy to obtain a sprayed coating on which the molten metal is difficult to adhere due to the difficulty of permeating and diffusing the molten metal.
- the amount of the fourth element (Al, Mg) in the thermal spraying powder is preferably 15 mol% or less, more preferably 10 mol% or less. In this case as well, it becomes easy to obtain a sprayed coating on which the molten metal is difficult to adhere by being less susceptible to the penetration and diffusion of the molten metal.
- the molar ratio of the fourth element (Al, Mg) to the second element (Co, Ni, Fe) in the thermal spraying powder is preferably 0.05 or more, more preferably 0.1 or more, and further Preferably it is 0.2 or more. In this case, it becomes easy to obtain a sprayed coating on which molten metal is difficult to adhere.
- the molar ratio of the fourth element (Al, Mg) to the second element (Co, Ni, Fe) in the thermal spraying powder is also preferably 0.5 or less, more preferably 0.4 or less. More preferably, it is 0.3 or less. Also in this case, it becomes easy to obtain a thermal spray coating to which the molten metal is difficult to adhere.
- the thermal spraying powder has a first crystal phase containing Co, Ni or Fe, W, and C. Alternatively, it has a second crystal phase containing Co, Ni or Fe, W or Mo, and B.
- the thermal spraying powder may have both a first crystal phase and a second crystal phase.
- the thermal spraying powder includes, as the second crystal phase, a crystal phase containing Co, Ni or Fe, W and B, a crystal containing Co, Ni or Fe, Mo and B. Only one of the phases may be included, or both may be included.
- the thermal spraying powder preferably contains as little free Co, Ni or Fe as possible.
- the intensity of the peak attributed to Co, Ni or Fe on the X-ray diffraction spectrum of the powder for thermal spraying is 0 of the intensity of the peak having the maximum intensity among the peaks appearing on the same X-ray diffraction spectrum. .1 or less is preferable.
- the thermal spraying powder includes, for example, carbide particles made of tungsten carbide (WC), boride particles made of tungsten boride (WB) or molybdenum boride (MoB), and a first metal made of Co, Ni, or Fe. It is manufactured by granulating and sintering raw material powder obtained by mixing particles and second metal particles made of Al or Mg.
- the boride particles may be a combination of WB particles and MoB particles.
- the first metal particles may be a combination of two of Co particles, Ni particles, and Fe particles, or may be a combination of three. Further, the first metal particles may be alloy particles containing at least one selected from Co, Ni, and Fe.
- the second metal particles may be a combination of Al particles and Mg particles.
- the thermal spraying powder is obtained by granulating raw material powder obtained by mixing carbide particles made of WC, first metal particles made of Co, Ni or Fe, and second metal particles made of Al or Mg, and It is also possible to manufacture by sintering.
- the first metal particles may be a combination of two of Co particles, Ni particles, and Fe particles, or may be a combination of three. Further, the first metal particles may be alloy particles containing at least one selected from Co, Ni, and Fe.
- the second metal particles may be a combination of Al particles and Mg particles.
- the content of carbide particles in the raw material powder is preferably 45% by mass or more, more preferably 55% by mass or more. In this case, it becomes easy to obtain a sprayed coating that is less susceptible to penetration and diffusion of the molten metal and is excellent in wear resistance.
- the content of carbide particles in the raw material powder is preferably 90% by mass or less, more preferably 75% by mass or less. In this case, it becomes easy to obtain a sprayed coating excellent in thermal shock resistance that hardly causes cracks even when used repeatedly in a molten metal bath.
- the content of boride particles in the raw material powder is preferably 10% by mass or more, and more preferably 20% by mass or more. In this case, it becomes easy to obtain a sprayed coating that is less susceptible to penetration and diffusion of molten metal.
- the content of boride particles in the raw material powder is also preferably 40% by mass or less, and more preferably 35% by mass or less. In this case as well, it becomes easy to obtain a sprayed coating that is less susceptible to penetration and diffusion of molten metal.
- the content of the first metal particles in the raw material powder is preferably 5% by mass or more, more preferably 8% by mass or more. In this case, it becomes easy to obtain a thermal spray coating excellent in thermal shock resistance by being less susceptible to penetration and diffusion of molten metal.
- the content of the first metal particles in the raw material powder is also preferably 20% by mass or less, more preferably 15% by mass or less. Also in this case, it becomes easy to obtain a thermal spray coating excellent in thermal shock resistance by being less susceptible to penetration and diffusion of molten metal.
- the content of the second metal particles in the raw material powder is preferably 0.2% by mass or more, and more preferably 0.5% by mass or more. In this case, it becomes easy to obtain a sprayed coating on which the molten metal is difficult to adhere due to the difficulty of permeating and diffusing the molten metal.
- the content of the second metal particles in the raw material powder is also preferably 5% by mass or less, and more preferably 3% by mass or less. In this case as well, it becomes easy to obtain a sprayed coating on which the molten metal is difficult to adhere by being less susceptible to the penetration and diffusion of the molten metal.
- the molar ratio of carbide particles to boride particles in the raw powder is preferably 1.5 or more, more preferably 2 or more.
- the molar ratio of carbide particles to boride particles in the raw material powder is also preferably 3.5 or less, and more preferably 3 or less.
- the average particle diameter of the raw material powder is preferably 10 ⁇ m or less.
- the reaction between the particles in the raw material powder proceeds favorably during sintering. Further, it becomes easy to obtain a thermal spraying powder having a uniform component distribution.
- the sintering after granulating the raw material powder is preferably performed at a temperature of 1000 to 1500 ° C.
- the sintering time is preferably 30 minutes to 24 hours. In this case, it is possible to obtain a thermal spraying powder with no or almost no free metal.
- the thermal spraying powder of the first embodiment contains no or almost no free metal, it can be said that the thermal spraying powder is suitable for forming a film excellent in molten metal resistance.
- the reason why the coating obtained by spraying the thermal spraying powder of the first embodiment has excellent molten metal resistance is estimated in this way, but the present invention is not construed as being limited thereto.
- a coating suitable for being provided on the surface of a roll such as a sink roll or a support roll used in a molten metal bath such as zinc is provided.
- membrane of 2nd Embodiment was provided in the surface is provided.
- the film is a first element selected from W and Mo, a second element selected from Co, Ni and Fe, a third element selected from C and B, and a fourth element selected from Al and magnesium. These elements are included as constituent elements.
- the film may contain only one of W and Mo as the first element, or may contain both.
- the film may contain only one of Co, Ni and Fe as the second element, or may contain only two, or all three. It may be contained.
- the film may contain only one of C and B as the third element, or may contain both.
- the film may contain only one of Al and Mg as the fourth element, or may contain both.
- the amount of the first element (W, Mo) in the film is preferably 50 mol% or more, more preferably 60 mol% or more.
- the amount of the first element (W, Mo) in the film is also preferably 75 mol% or less, more preferably 70 mol% or less.
- the amount of the second element (Co, Ni, Fe) in the film is preferably 20 mol% or more, more preferably 22 mol% or more, and further preferably 25 mol% or more. In this case, the thermal shock resistance of the coating is improved.
- the amount of the second element (Co, Ni, Fe) in the film is also preferably 50 mol% or less, more preferably 40 mol% or less, and further preferably 30 mol% or less. In this case, adhesion of the molten metal to the film is further suppressed.
- the amount of the third element (C, B) in the film is preferably 3 mol% or more, more preferably 3.5 mol% or more.
- the amount of the third element (C, B) in the film is also preferably 5 mol% or less, more preferably 4.5 mol% or less.
- the amount of the fourth element (Al, Mg) in the film is preferably 1 mol% or more, more preferably 1.5 mol% or more. In this case, adhesion of the molten metal to the coating is further suppressed by suppressing penetration and diffusion of the molten metal.
- the amount of the fourth element (Al, Mg) in the film is also preferably 15 mol% or less, more preferably 10 mol% or less. Also in this case, adhesion of the molten metal to the film is further suppressed by suppressing penetration and diffusion of the molten metal.
- the molar ratio of the fourth element (Al, Mg) to the second element (Co, Ni, Fe) in the film is preferably 0.05 or more, more preferably 0.1 or more, still more preferably 0.2 or more. In this case, adhesion of the molten metal to the film is further suppressed.
- the molar ratio of the fourth element (Al, Mg) to the second element (Co, Ni, Fe) in the film is also preferably 0.03 or less, more preferably 0.02 or less, and further Preferably it is 0.015 or less. Also in this case, adhesion of the molten metal to the film is further suppressed.
- the coating has a first crystal phase containing Co, Ni or Fe, W, and C. Alternatively, it has a second crystal phase containing Co, Ni or Fe, W or Mo, and B.
- the film may have both a first crystal phase and a second crystal phase.
- the coating has a crystal phase containing Co, Ni or Fe, W and B as a second crystal phase, and a crystal phase containing Co, Ni or Fe, Mo and B. One of them may be included, or both may be included.
- the coating contains as little free Co, Ni or Fe as possible.
- the intensity of the peak attributed to Co, Ni or Fe on the X-ray diffraction spectrum of the film is 0.1 of the peak intensity having the maximum intensity among the peaks appearing on the same X-ray diffraction spectrum. It is preferable that it is less than 2 times. Furthermore, it is more preferable that no peak attributed to Co, Ni or Fe is observed on the X-ray diffraction spectrum of the film. In this case, adhesion of the molten metal to the film is suppressed.
- the coating is formed, for example, by spraying the thermal spraying powder of the first embodiment.
- the method of spraying the thermal spraying powder is preferably high-speed flame spraying such as high-speed oxygen fuel spraying (HVOF) or high-speed air fuel spraying (HVAF).
- the thermal spraying powder of 1st Embodiment may be used for uses other than forming a film
- the thermal spraying powder of the first embodiment contains elements other than the first to fourth elements, that is, elements other than W, Mo, Co, Ni, Fe, C, B, Al, and Mg as constituent elements. It may be a thing.
- the film of the second embodiment contains elements other than the first to fourth elements, that is, elements other than W, Mo, Co, Ni, Fe, C, B, Al, and Mg as constituent elements. There may be.
- the surface of the coating film of the second embodiment has various non-reactivity with molten metal such as oxide ceramics and nitride ceramics by thermal spraying method, coating firing, etc. in order to further improve non-reactivity with molten metal.
- molten metal such as oxide ceramics and nitride ceramics by thermal spraying method, coating firing, etc.
- a film made of ceramics or a mixture thereof may be formed.
- the film of the second embodiment may be subjected to a sealing treatment with various ceramics excellent in non-reactivity with molten metal such as oxide ceramics and nitride ceramics, or a mixture thereof.
- the powder for thermal spraying of the comparative example 1 was prepared by mixing WC particle
- the powder for thermal spraying of Example 7 was prepared by mixing WC particle
- the “boride particles” column in Table 1 shows the types and amounts (mass% and mol%) of boride particles used at the time of preparation of each thermal spraying powder.
- the “first metal particle” column of Table 1 the type and amount (mass% and mol%) of the first metal particles (Co particles, Ni particles or Fe particles) used at the time of preparation of each thermal spraying powder. Indicates.
- the “second metal particle” column in Table 1 shows the type and amount (mass% and mol%) of the second metal particles (Al particles or Mg particles) used in preparing each thermal spraying powder.
- the “second metal / first metal” column in Table 1 the molar ratio of Al or Mg to Co, Ni, or Fe in each thermal spraying powder is shown.
- the intensity is the highest among the peaks appearing on the X-ray diffraction spectrum of each thermal spraying powder measured under the conditions described in Table 2.
- the X-ray-diffraction spectrum figure of the powder for thermal spraying of Example 2 is shown in FIG.
- the thermal spraying powder of Example 2 had a crystal phase (CoWB) containing Co, W and B.
- the thermal spraying powders of the other examples similarly have a crystal phase containing Co, Ni or Fe and W and C and a crystal phase containing Co, Ni or Fe and W or Mo and B.
- the thermal spraying powders of the other examples similarly have a crystal phase containing Co, Ni or Fe and W and C and a crystal phase containing Co, Ni or Fe and W or Mo and B.
- each thermal spray powder was subjected to high-speed flame spraying under the conditions described in Table 3 to provide a thermal spray coating on the substrate.
- the elemental composition of each thermal spray coating was the same as the thermal spraying powder used for thermal spraying.
- peaks attributable to Co, Ni or Fe were detected in the thermal spray coatings prepared from the thermal spraying powders of Examples 1 to 10. There wasn't.
- FIG. 2 shows an X-ray diffraction spectrum of the thermal spray coating produced from the thermal spray powder of Example 2.
- the thermal spray coating produced from the thermal spraying powder of Example 2 has a crystal phase (CoW 2 B 2 ) containing Co, W, and B, while belonging to Co, Ni, or Fe. No peak was detected.
- the thermal spray coatings produced from the thermal spraying powders of the other examples similarly have a crystal phase containing Co, Ni or Fe and W and C, and Co, Ni or Fe and W or Mo and B. On the other hand, no peak attributable to Co, Ni or Fe was detected.
- the adhesion of the molten metal to the sprayed coating having a thickness of about 200 ⁇ m provided on the substrate by high-speed flame spraying of each thermal spray powder under the conditions shown in Table 3 The result of having evaluated is shown. Evaluation of molten metal adhesion was performed as follows. First, after the surface of the sprayed coating was polished until the surface roughness Ra became 0.3 ⁇ m, zinc pellets having a diameter of 10 mm and a thickness of 1 mm were placed on the sprayed coating. In this state, the zinc pellets and the sprayed coating were heated to 500 ° C. in an argon gas atmosphere for 24 hours.
- thermal shock resistance the thermal shock resistance of a sprayed coating having a thickness of about 200 ⁇ m provided on a substrate by high-speed flame spraying of each thermal spraying powder under the conditions shown in Table 4 was evaluated. Results are shown.
- a series of operations were repeated in which each sprayed coating was heated together with the substrate to 700 ° C. in the air for 1 hour and then rapidly cooled in water.
- ⁇ (excellent) indicates that no cracks were visually observed on the surface of the sprayed coating even after 20 cycles of heating and cooling
- ⁇ (good)” indicates cracks.
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Abstract
Description
本発明の第3の態様では、溶融金属浴中で使用されるロールであって、前記溶射皮膜が表面に設けられているロールが提供される。
以下、本発明の第1の実施形態を説明する。第1の実施形態では、亜鉛などの溶融金属浴中で使用されるシンクロールやサポートロールなどのロールの表面に皮膜を形成する用途で例えば使用される溶射用粉末が提供される。
前記溶射用粉末は、タングステン(W)及びモリブデン(Mo)から選ばれる第1の元素と、コバルト(Co)、ニッケル(Ni)及び鉄(Fe)から選ばれる第2の元素と、炭素(C)及びホウ素(B)から選ばれる第3の元素と、アルミニウム(Al)及びマグネシウム(Mg)から選ばれる第4の元素とを構成元素として含有する。前記溶射用粉末は、第1の元素としてW及びMoのうちいずれか一方だけを含有するものであってもよいし、両方を含有するものであってもよい。前記溶射用粉末は、第2の元素としてCo、Ni及びFeのうちいずれか1つだけを含有するものであってもよいし、2つだけを含有するものであってもよいし、3つ全てを含有するものであってもよい。前記溶射用粉末は、第3の元素としてC及びBのうちいずれか一方だけを含有するものであってもよいし、両方を含有するものであってもよい。前記溶射用粉末は、第4の元素としてAl及びMgのうちいずれか一方だけを含有するものであってもよいし、両方を含有するものであってもよい。
前記溶射用粉末中の第1の元素(W、Mo)の量はまた、75モル%以下であることが好ましく、より好ましくは70モル%以下である。
前記溶射用粉末中の第3の元素(C、B)の量はまた、5モル%以下であることが好ましく、より好ましくは4.5モル%以下である。
前記溶射用粉末は、Co、Ni又はFeと、Wと、Cとを含んだ第1の結晶相を有する。あるいは、Co、Ni又はFeと、W又はMoと、Bとを含んだ第2の結晶相を有する。前記溶射用粉末は、第1の結晶相と第2の結晶相の両方を有するものであってもよい。また、前記溶射用粉末は、第2の結晶相として、Co、Ni又はFeと、Wと、Bとを含んだ結晶相と、Co、Ni又はFeと、Moと、Bとを含んだ結晶相のうちいずれか一方だけを含むものであってよいし、両方を含むものであってもよい。
前記溶射用粉末は、例えば、炭化タングステン(WC)からなる炭化物粒子と、ホウ化タングステン(WB)又はホウ化モリブデン(MoB)からなるホウ化物粒子と、Co、Ni又はFeからなる第1の金属粒子と、Al又はMgからなる第2の金属粒子とを混合して得られる原料粉末を造粒及び焼結して製造される。ホウ化物粒子は、WB粒子とMoB粒子の組み合わせであってもよい。第1の金属粒子は、Co粒子、Ni粒子及びFe粒子のうちの2つの組み合わせであってもよいし、3つの組み合わせであってもよい。また、第1の金属粒子は、Co、Ni及びFeから選ばれる少なくとも1つを含有する合金粒子であってもよい。第2の金属粒子は、Al粒子とMg粒子の組み合わせであってもよい。
原料粉末中のホウ化物粒子に対する炭化物粒子のモル比はまた、3.5以下であることが好ましく、より好ましくは3以下である。
・ 第1の実施形態の溶射用粉末中に構成元素として含まれるCo、Ni又はFeの大部分又は全部は、遊離状態ではなく、他の元素と結合して存在している。これは、前記溶射用粉末中に同じく構成元素として含まれるAl又はMgの働きによるものと推測される。溶射用粉末中の遊離の金属が、溶射用粉末を溶射して得られる皮膜中でも遊離の状態のまま残ると、皮膜の耐溶融金属性が低下するおそれがある。これは、皮膜中の遊離の金属が溶融金属浴中の金属成分と高い親和性を有することが原因と推測される。この点、第1の実施形態の溶射用粉末は遊離の金属を全く又はほとんど含まないため、耐溶融金属性に優れた皮膜の形成に適しているといえる。第1の実施形態の溶射用粉末を溶射して得られる皮膜が優れた耐溶融金属性を有する理由はこのように推定されるが、本発明はこれによって限定して解釈されるものではない。
次に、本発明の第2及び第3の実施形態を説明する。第2の実施形態では、亜鉛などの溶融金属浴中で使用されるシンクロールやサポートロールなどのロールの表面に設けられるのに適した皮膜が提供される。また、第3の実施形態では、第2の実施形態の皮膜が表面に設けられた溶融金属浴中ロールが提供される。
前記皮膜は、W及びMoから選ばれる第1の元素と、Co、Ni及びFeから選ばれる第2の元素と、C及びBから選ばれる第3の元素と、Al及びマグネシウムから選ばれる第4の元素とを構成元素として含有する。前記皮膜は、第1の元素としてW及びMoのうちいずれか一方だけを含有するものであってもよいし、両方を含有するものであってもよい。前記皮膜は、第2の元素としてCo、Ni及びFeのうちいずれか1つだけを含有するものであってもよいし、2つだけを含有するものであってもよいし、3つ全てを含有するものであってもよい。前記皮膜は、第3の元素としてC及びBのうちいずれか一方だけを含有するものであってもよいし、両方を含有するものであってもよい。前記皮膜は、第4の元素としてAl及びMgのうちいずれか一方だけを含有するものであってもよいし、両方を含有するものであってもよい。
前記皮膜中の第1の元素(W,Mo)の量はまた、75モル%以下であることが好ましく、より好ましくは70モル%以下である。
前記皮膜中の第3の元素(C,B)の量はまた、5モル%以下であることが好ましく、より好ましくは4.5モル%以下である。
前記皮膜は、Co、Ni又はFeと、Wと、Cとを含んだ第1の結晶相を有する。あるいは、Co、Ni又はFeと、W又はMoと、Bとを含んだ第2の結晶相を有する。前記皮膜は、第1の結晶相と第2の結晶相の両方を有するものであってもよい。また、前記皮膜は、第2の結晶相として、Co、Ni又はFeと、Wと、Bとを含んだ結晶相と、Co、Ni又はFeと、Moと、Bとを含んだ結晶相のうちいずれか一方だけを含むものであってよいし、両方を含むものであってもよい。
前記皮膜は、例えば、第1の実施形態の溶射用粉末を溶射することにより形成される。前記溶射用粉末を溶射する方法は、高速酸素燃料溶射(HVOF)や高速空気燃料溶射(HVAF)のような高速フレーム溶射であることが好ましい。
・ 第2の実施形態の皮膜中に構成元素として含まれるCo、Ni又はFeの大部分又は全部は、遊離状態ではなく、他の元素と結合して存在している。これは、前記皮膜中に同じく構成元素として含まれるAl又はMgの働きによるものと推測される。皮膜中に遊離の金属が存在すると、皮膜の耐溶融金属性が低下するおそれがある。これは、皮膜中の遊離の金属が溶融金属浴中の金属成分と高い親和性を有することが原因と推測される。この点、第2の実施形態の皮膜は遊離の金属を全く又はほとんど含まないため、耐溶融金属性に優れる。第2の実施形態の皮膜が優れた耐溶融金属性を有する理由はこのように推定されるが、本発明はこれによって限定して解釈されるものではない。
・ 第1実施形態の溶射用粉末は、溶融金属浴中ロールの表面に皮膜を形成する以外の用途で使用されてもよい。
次に、実施例及び比較例を挙げて本発明をさらに具体的に説明する。
WC粒子と、WB粒子と、Co粒子とを混合し、造粒及び焼結することにより、比較例1の溶射用粉末を調製した。WC粒子と、WB粒子又はMoB粒子と、Co粒子、Ni粒子又はFe粒子と、Al粒子又はMg粒子とを混合し、造粒及び焼結することにより、実施例1~6,8~10及び比較例2~8の溶射用粉末を調製した。WC粒子と、Co粒子と、Al粒子とを混合し、造粒及び焼結することにより、実施例7の溶射用粉末を調製した。各溶射用粉末の詳細を表1に示す。
表1中の“第1の金属粒子”欄には、各溶射用粉末の調製時に使用した第1の金属粒子(Co粒子、Ni粒子又はFe粒子)の種類及び量(質量%及びモル%)を示す。
表1中の“第2の金属/第1の金属”欄には、各溶射用粉末中のCo、Ni又はFeに対するAl又はMgのモル比を示す。
ことを示し、“△(可)”は、亜鉛ペレットを引き剥がした後の溶射皮膜の表面粗さRaが1.0μmよりも大きかったことを示し、“×(不良)”は、亜鉛ペレットが溶射皮膜に強く付着していて溶射皮膜から引き剥がすことができなかったことを示す。
Claims (5)
- タングステン及びモリブデンから選ばれる第1の元素と、コバルト、ニッケル及び鉄から選ばれる第2の元素と、炭素及びホウ素から選ばれる第3の元素と、アルミニウム及びマグネシウムから選ばれる第4の元素とを構成元素として含有する溶射用粉末であって、
溶射用粉末は第2の元素を20モル%以上の量で含有し、
溶射用粉末中の第2の元素に対する第4の元素のモル比は0.05以上0.5以下であり、
溶射用粉末は、コバルト、ニッケル又は鉄と、タングステンと、炭素とを含んだ結晶相、あるいは、コバルト、ニッケル又は鉄と、タングステン又はモリブデンと、ホウ素とを含んだ結晶相を有し、
溶射用粉末のX線回折スペクトル上のコバルト、ニッケル又は鉄に帰属するピークの強度は、同じX線回折スペクトル上に現れるピークのうち強度が最大であるピークの強度の0.1倍以下である、溶射用粉末。 - 請求項1に記載の溶射用粉末を溶射して得られる溶射皮膜。
- 溶融金属浴中で使用されるロールであって、請求項2に記載の溶射皮膜が表面に設けられているロール。
- タングステン及びモリブデンから選ばれる第1の元素と、コバルト、ニッケル及び鉄から選ばれる第2の元素と、炭素及びホウ素から選ばれる第3の元素と、アルミニウム及びマグネシウムから選ばれる第4の元素とを構成元素として含有する皮膜であって、
皮膜は第2の元素を20モル%以上の量で含有し 、
皮膜中の第2の元素に対する第4の元素のモル比は0.05以上0.5以下であり、
皮膜は、コバルト、ニッケル又は鉄と、タングステンと、炭素とを含んだ結晶相、あるいは、コバルト、ニッケル又は鉄と、タングステン又はモリブデンと、ホウ素とを含んだ結晶相を有し、
皮膜のX線回折スペクトル上にコバルト、ニッケル又は鉄に帰属するピークが検出されない、皮膜。 - 溶融金属浴中で使用されるロールであって、請求項4に記載の皮膜が表面に設けられているロール。
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DE112015004942.8T DE112015004942T8 (de) | 2014-10-31 | 2015-10-28 | Pulver zum thermischen Spritzen, thermische Spritzbeschichtung, Beschichtungsfilm und Walze für eine Metallschmelze |
KR1020177014432A KR102372303B1 (ko) | 2014-10-31 | 2015-10-28 | 용사용 분말, 용사피막, 피막, 및 용융 금속욕 내의 롤 |
CN201580058305.0A CN107002217B (zh) | 2014-10-31 | 2015-10-28 | 喷镀用粉末、喷镀皮膜、皮膜和熔融金属浴中辊 |
US15/522,703 US10539176B2 (en) | 2014-10-31 | 2015-10-28 | Powder for thermal spray, thermal spray coating film, coating film and roll in molten metal bath |
MX2017005438A MX2017005438A (es) | 2014-10-31 | 2015-10-28 | Polvo para rocio térmico, película de revestimiento de rocío térmico, película y rodillo de revestimiento en baño metálico fundido. |
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MX (1) | MX2017005438A (ja) |
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JP2000144366A (ja) * | 1998-11-16 | 2000-05-26 | Tocalo Co Ltd | アルミニウム・亜鉛めっき浴用部材およびその製造方法 |
JP2008303459A (ja) * | 2007-04-06 | 2008-12-18 | Sanyo Special Steel Co Ltd | 溶融亜鉛浴部材の表面被覆用材料とその製造方法並びにその部材 |
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JPH086166B2 (ja) * | 1991-07-31 | 1996-01-24 | トーカロ株式会社 | 耐溶融亜鉛性に優れる溶射用粉末材料および溶融亜鉛浴部材用溶射皮膜 |
JP2977389B2 (ja) * | 1992-09-28 | 1999-11-15 | 三菱重工業株式会社 | ガスタービン高温部品の被覆材 |
US5328763A (en) * | 1993-02-03 | 1994-07-12 | Kennametal Inc. | Spray powder for hardfacing and part with hardfacing |
JPH1180917A (ja) * | 1997-09-05 | 1999-03-26 | Nippon Steel Hardfacing Co Ltd | 耐食・耐摩耗性に優れた溶融金属浴用浸漬部材 |
EP1149931A4 (en) * | 1999-11-09 | 2008-02-13 | Jfe Steel Corp | CERMET POWDER FOR PULVERIZED COATING HAVING EXCELLENT MOUNTING RESISTOR AND ROLL WITH PULVERIZED COATING |
JP2001152308A (ja) * | 1999-11-29 | 2001-06-05 | Nippon Steel Hardfacing Co Ltd | 耐食性を有し、長期間使用に耐える複合皮膜の形成方法およびその複合皮膜を有する部材 |
JP2001207252A (ja) * | 2000-01-25 | 2001-07-31 | Ishikawajima Harima Heavy Ind Co Ltd | アーク溶射成形品及びその製造方法 |
JP4628578B2 (ja) * | 2001-04-12 | 2011-02-09 | トーカロ株式会社 | 低温溶射皮膜被覆部材およびその製造方法 |
DE102006045481B3 (de) * | 2006-09-22 | 2008-03-06 | H.C. Starck Gmbh | Metallpulver |
US8269612B2 (en) * | 2008-07-10 | 2012-09-18 | Black & Decker Inc. | Communication protocol for remotely controlled laser devices |
JP2011026666A (ja) * | 2009-07-27 | 2011-02-10 | Sumitomo Metal Mining Co Ltd | 硼化物系サーメット溶射用粉末 |
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JP2000144366A (ja) * | 1998-11-16 | 2000-05-26 | Tocalo Co Ltd | アルミニウム・亜鉛めっき浴用部材およびその製造方法 |
JP2008303459A (ja) * | 2007-04-06 | 2008-12-18 | Sanyo Special Steel Co Ltd | 溶融亜鉛浴部材の表面被覆用材料とその製造方法並びにその部材 |
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DE112015004942T8 (de) | 2017-07-27 |
CN107002217B (zh) | 2019-12-31 |
TWI683034B (zh) | 2020-01-21 |
MX2017005438A (es) | 2017-12-04 |
TW201631182A (zh) | 2016-09-01 |
KR20170089856A (ko) | 2017-08-04 |
JP6550227B2 (ja) | 2019-07-24 |
US10539176B2 (en) | 2020-01-21 |
CN107002217A (zh) | 2017-08-01 |
DE112015004942T5 (de) | 2017-07-13 |
US20170314612A1 (en) | 2017-11-02 |
KR102372303B1 (ko) | 2022-03-08 |
JP2016089207A (ja) | 2016-05-23 |
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