A method of forming a fuel cell interconnect includes depositing a Cr alloy powder, sintering the Cr alloy powder, and repeating the depositing and the sintering to form the fuel cell interconnect. The Cr alloy powder may include a pre-alloyed powder containing from about 4 wt. % to about 6 wt. % Fe, and from about 94 wt. % to about 96 wt. % Cr.

A method of producing an atomized powder includes: an atomizing step of forming magnetic alloy particles from a molten metal by an atomizing method, to obtain a slurry in which the magnetic alloy particles are dispersed in an aqueous dispersion medium; a slurry concentration step of causing magnetic separation means to separate the magnetic alloy particles from the slurry to form a concentrated slurry having the magnetic alloy particles of more than 80% by mass, the magnetic separation means using a rotary drum including a magnetic circuit part fixedly disposed at a position where at least a part of the magnetic circuit part is immersed in the slurry and an outer sleeve capable of rotating outside the magnetic circuit part; and a drying step of causing drying means using an air flow dryer to dry the concentrated slurry to form a magnetic alloy powder.

A method for producing a powder-metallurgical product may include providing a powder mixture, forming the powder mixture into a green body, and sintering the green body to form a resulting powder-metallurgical product. The powder mixture may include a first hard phase, a second hard phase, 0 to 1.8% by weight of graphite, 0 to 5% by weight each of cobalt, tri-iron phosphide, copper, bronze, phosphorous, sulphur, calcium fluoride and molybdenum, 0.1 to 1.8% by weight of a pressing aid and a flow improver, and a remaining proportion that is an iron-base powder. The first hard phase may include 52 to 78% by weight of molybdenum, 0 to 2% by weight of silicon, 0 to 1.5% by weight of copper, and a remaining weight proportion of iron and production-related contaminations. The second hard phase may include 0 to 0.8% by weight of manganese and less than 0.1% by weight of carbon.

A multi-scale and multi-phase dispersion strengthened iron-based alloy, and preparation and characterization methods thereof are provided. The alloy contains a matrix and a strengthening phase. The strengthening phase includes at least two types of the strengthening phase particles with different sizes. A volume of the two types of the strengthening phase particles with different sizes having a particle size less than or equal to 50 nm accounts for 85-95% of a total volume of all the strengthening phase particles. The matrix is a Fe—Cr—W—Ti alloy. The strengthening phases include crystalline Y.sub.2O.sub.3 phase, Y—Ti—O phase, Y—Cr—O phase, and Y—W—O phase. The characterization method comprises electrolytically separating the strengthening phases in the alloy, and then characterizing by using an electron microscope. The tensile strength of the prepared alloy is more than 1600 MPa at room temperature, and is more than 600 MPa at 700° C.

Provided is alloyed steel powder having excellent fluidity, formability, and compressibility without containing Ni, Cr, or Si. The alloyed steel powder includes iron-based alloy containing Mo, in which Mo content is 0.4 mass % to 1.8 mass %, a weight-based median size D50 is 40 μm or more, and among particles contained in the alloyed steel powder, those particles having an equivalent circular diameter of 50 μm to 200 μm have a number average of solidity of 0.70 to 0.86, the solidity being defined as (particle cross-sectional area/envelope-inside area).

A metal matrix composite material includes 60-90 wt. % of aluminum alloy powders and 10-40 wt. % Fe-based amorphous alloy powders. The aluminum alloy powders are used as the matrix of the metal matrix composite material, and the Fe-based amorphous alloy powders include Fe.sub.aCr.sub.bMo.sub.cSi.sub.dB.sub.eY.sub.f, wherein 48 at. %≤a≤50 at. %, 21 at. %≤b≤23 at. %, 18 at. %≤c≤20 at. %, 3 at. %≤D≤5 at. %, 2 at. %≤c≤4 at. %, and 2 at. %≤f≤4 at. %.

The production method of a rare earth magnet of the present disclosure includes a coated magnetic powder preparation step, a mixed powder preparation step, and a pressure sintering step. In the coated magnetic preparation step, a zinc-containing coating 12 is formed on the particle surface of a samarium-iron-nitrogen-based magnetic powder to obtain a coated magnetic powder 14. In the mixed powder preparation step, a binder powder 20 having a melting point not higher than the melting point of the coating 12 and the coated magnetic powder 14 are mixed to obtain a mixed powder. In the pressure sintering step, denoting as T.sub.1° C. the temperature at which the peak disappears in an X-ray diffraction pattern of the binder powder 20 and as T.sub.2° C. the temperature at which the magnetic phase in the samarium-iron-nitrogen-based magnetic powder 10 decomposes, the mixed powder is pressure-sintered at T.sub.1° C. or more and (T.sub.2−50)° C. or less.

An amorphous soft magnetic alloy of the formula (Fe.sub.1-αTM.sub.α).sub.100-w-x-y-zP.sub.wB.sub.xL.sub.ySi.sub.z Ti.sub.pC.sub.qMn.sub.rCu.sub.s, wherein TM is Co or Ni; L is Al, Cr, Zr, Mo or Nb; 0≤α≤0.3, 2≤w≤18 at %, 2≤x≤18 at %, 15≤w+x≤23 at %, 1<y≤5 at %, 0≤z≤4 at %; p, q, r, and s represents an addition ratio such that the total mass of Fe, TM, P, B, L and Si is 100, and 0≤p≤0.3, 0≤q≤0.5, 0≤r≤2, 0≤s≤1 and r+s>0; the composition fulfills one of the following conditions: L is Cr, Zr, Mo or Nb; or L is a combination of Al and Cr, Zr, Mo or Nb, wherein 0<Al≤5 at %, 1≤Cr≤4 at %, 0<Zr≤5 at %, 2≤Mo≤5 at %, and 2≤Nb≤5 at %; the alloy has a crystallization start temperature (Tx) which is 550° C. or less, a glass transition temperature (Tg) which is 520° C. or less, and a supercooled liquid region represented by ΔTx=Tx−Tg, which is 20° C. or more.

An oxide dispersion-strengthened (ODS) iron-based alloy powder and a characterization method thereof are provided. The alloy powder comprises a matrix and strengthening phases. The strengthening phases include at least two types of strengthening phase particles with different sizes, wherein a volume of the particles with a particle size of less than or equal to 50 nm accounts for 85-95% of a total volume of all the strengthening phase particles. The matrix is a Fe—Cr—W—Ti alloy. The characterization method of the ODS iron-based alloy powder comprises separating the strengthening phases from the powder matrix through electrolysis, and analyzing and characterizing the strengthening phases using an electron microscope.

An oxide dispersion-strengthened (ODS) iron-based alloy powder and a characterization method thereof are provided. The alloy powder comprises a matrix and strengthening phases. The strengthening phases include at least two types of strengthening phase particles with different sizes, wherein a volume of the particles with a particle size of less than or equal to 50 nm accounts for 85-95% of a total volume of all the strengthening phase particles. The matrix is a Fe—Cr—W—Ti alloy. The characterization method of the ODS iron-based alloy powder comprises separating the strengthening phases from the powder matrix through electrolysis, and analyzing and characterizing the strengthening phases using an electron microscope.