C22C38/002

Soft magnetic powder, powder magnetic core, magnetic element, and electronic device

A soft magnetic powder of the invention has a composition represented by Fe.sub.100-a-b-c-d-e-fCu.sub.aSi.sub.bB.sub.cM.sub.dM′.sub.eX.sub.f (at %) [wherein M is Nb, W, Ta, Zr, Hf, Ti, or Mo, M′ is V, Cr, Mn, Al, a platinum group element, Sc, Y, Au, Zn, Sn, or Re, X is C, P, Ge, Ga, Sb, In, Be, or As, and a, b, c, d, e, and f are numbers that satisfy the following formulae: 0.1≤a≤3, 0<b≤30, 0<c≤25, 5≤b+c≤30, 0.1≤d≤30, 0≤e≤10, and 0≤f≤10], wherein a crystalline structure having a particle diameter of 1 nm or more and 30 nm or less is contained in an amount of 40 vol % or more, and the difference in the coercive force of the powder after classification satisfies predetermined conditions.

Crystalline Fe-based alloy powder and method for producing same

A crystalline Fe-based alloy powder composed of Fe-based alloy particles containing, within a structure thereof, nanocrystal grains having an average grain size of 30 nm or less, and in which d50, which is a particle diameter corresponding to a cumulative frequency of 50% by volume, is from 3.5 μm to 35.0 μm in a cumulative distribution curve that is obtained by laser diffractometry and that shows the relationship between the particle diameter and the cumulative frequency from the small particle diameter side, and a ratio of Fe-based alloy particles having a particle diameter of 2 μm or less to the total of the Fe-based alloy particles, which is determined by laser diffractometry, is from 0% by volume to 8% by volume.

SEAMLESS STEEL PIPE HAVING DESIRABLE SULFURIC ACID DEW-POINT CORROSION RESISTANCE, AND METHOD FOR MANUFACTURING SAME

A seamless steel pipe of the present invention is a seamless steel pipe having a composition that includes, in mass %, C: 0.02 to 0.12%, Si: 0.010 to 1.00%, Mn: 0.10 to 2.00%, P: 0.050% or less, S: 0.004% or less, Al: 0.010 to 0.100%, Cu: 0.03 to 0.80%, Ni: 0.02 to 0.50%, Cr: 0.55 to 1.00%, Sb: 0.005 to 0.20%, and the balance Fe and incidental impurities, and satisfying the following formula (1),


1.7×Cu*+11×Cr*+3.8×Sb*≥13.5   (1), where Cu*, Cr*, and Sb* represent average concentrations of Cu, Cr, and Sb, respectively, in mass %, as measured in a region 0.5 to 2.0 mm away from an outer surface of the steel pipe, the seamless steel pipe having a yield strength of 230 MPa or more, and a tensile strength of 380 MPa or more.

ALLOY MATERIAL AND OIL-WELL SEAMLESS PIPE
20220411906 · 2022-12-29 ·

An alloy material is provided that has a chemical composition consisting of, in mass %, C: 0.030% or less, Si: 0.01 to 1.0%, Mn: 0.01 to 2.0%, P: 0.030% or less, S: 0.0050% or less, Cr: 28.0 to 40.0%, Ni: 32.0 to 55.0%, sol. Al: 0.010 to 0.30%, N: more than 0.30% and not more than 0.000214×Ni.sup.2−0.03012×Ni+0.00215×Cr.sup.2−0.08567×Cr+1.927, O: 0.010% or less, Mo: 0 to 6.0%, W: 0 to 12.0%, Ca: 0 to 0.010%, Mg: 0 to 0.010%, V: 0 to 0.50%, Ti: 0 to 0.50%, Nb: 0 to 0.50%, Co: 0 to 2.0%, Cu: 0 to 2.0%, REM: 0 to 0.10%, and the balance: Fe and impurities, and in which Fn1=Mo+(½)W is 1.0 to 6.0, and a yield strength at a 0.2% proof stress is 1103 MPa or more.

RARE EARTH SINTERED MAGNET

The present invention provides a rare earth sintered magnet which contains R (R represents one or more rare earth elements essentially including Nd), T (T represents one or more iron group elements essentially including Fe), B, M.sup.1 (M.sup.1 represents one or more elements selected from among Al, Si, Cr, Mn, Cu, Zn, Ga, Ge, Mo, Sn, W, Pb and Bi) and M.sup.2 (M.sup.2 represents one or more elements selected from among Ti, V, Zr, Nb, Hf and Ta), while comprising an R.sub.2T.sub.14B phase as the main phase. This rare earth sintered magnet is characterized in that: the M.sup.1 is in an amount of from 0.5% by atom to 2% by atom; if (R), (T), (M.sup.2) and (B) are the respective atomic percentages of the above-described R, T, M.sup.2 and B, the relational expression (1) ((T)/14)+(M.sup.2)≤(B)≤((R)/2)+((M.sup.2)/2) is satisfied; and from 0.1% by volume to 10% by volume of all grain boundary phases in the magnet is composed of an R.sub.6T.sub.13M.sup.1 phase. This rare earth sintered magnet is able to achieve excellent magnetic characteristics including a good balance between high Br and high H.sub.cJ.

AUSTENITIC STAINLESS STEEL MATERIAL

An austenitic stainless steel material is provided that has high creep strength even when used at an average operation temperature of more than 600 to 750° C. after welding with higher heat input, and furthermore, has excellent stress relaxation cracking resistance even after use for a long time period at the average operation temperature after welding with higher heat input. The steel material has a chemical composition which consists of, in mass %, C: 0.030% or less, Si: 1.50% or less, Mn: 2.00% or less, P: 0.045% or less, S: 0.0300% or less, Cr: 15.00 to 25.00%, Ni: 8.00 to 20.00%, N: 0.050 to 0.250%, Nb: 0.10 to 1.00%, Mo: 0.05 to 5.00%, and B: 0.0005 to 0.0100%, with the balance being Fe and impurities, and a ratio of the dissolved N amount (mass %) with respect to the content of N (mass %) in the steel material is 0.40 to 0.90.

IRON-BASED RARE EARTH BORON-BASED ISOTROPIC MAGNET ALLOY
20220415548 · 2022-12-29 ·

An iron-based rare earth boron-based isotropic magnet alloy, which has an alloy composition represented by T.sub.100-x-y-z(B.sub.1-nC.sub.n).sub.xRE.sub.yM.sub.z (where T is a transition metal element containing at least Fe, RE contains at least Nd, and M is one or more metal elements selected from the group consisting of Al, Si, V, Cr, Ti, Mn, Cu, Zn, Ga, Zr, Nb, Mo, Ag, Hf, Ta, W, Pt, Au, and Pb), 4.2 atom %≤x≤5.6 atom %, 11.5 atom %≤y≤13.0 atom %, 0.0 atom %≤z≤5.0 atom %, and 0.0≤n≤0.5, and the iron-based rare earth boron-based isotropic magnet alloy has an average crystal grain size of 10 nm to less than 70 nm as a main phase.

Alloy Powders and Methods for Producing the Same
20220415550 · 2022-12-29 ·

The present invention relates to an alloy with formula of RE-M-B—Fe as defined herein and oxygen content less than 0.9 wt %, wherein said RE is in the range of 29.0 weight % to 33.0 weight %; M is in the range of 0.25 weight % to 1.0 weight %; B is in the range of 0.8 weight % to 1.1 weight %; and Fe makes up the balance. The present invention also relates to a method for preparing a RE-M-Fe—B magnetic powder, as defined herein comprising the steps of: (a) melt spinning a RE-M-Fe—B alloy composition to obtain a melt-spun powder; (b) pressing the melt-spun powder of step (a) to obtain a compact body; (c) hot deforming the compact body of step (b) to obtain a die-upset magnet; (d) crushing the die-upset magnet of step (c) to obtain a powder; (e) milling and sieving the powder of step (d); and (f) passivating the powder of step (e) to obtain a magnetic powder; wherein: each of steps (d) to (f) is performed under a low oxygen environment and transfer between each of steps (d) to (f) is a sealed transfer; and wherein the oxygen content of the low oxygen environment and during each sealed transfer is below 0.5 weight %.

Hot rolled steel plate for electric resistance welded steel pipe having excellent weldability, and manufacturing method thereof
11535907 · 2022-12-27 · ·

Provided is a steel used for chassis parts, etc. of an automobile and, more specifically, to a hot rolled steel plate for an electric resistance welded steel pipe, which shows an excellent weldability in electric resistance welding, and a manufacturing method thereof.

Stainless steel material, constituting component, cell, and fuel cell stack

A stainless steel material including a base material made of ferritic stainless steel, a Cr oxide layer formed on a surface of the base material, and a spinel oxide layer formed on a surface of the Cr oxide layer, wherein a chemical composition of the base material satisfies [16.0≤Cr+3×Mo−2.5×B−17×C−3−Si≤35.0], a thickness of the Cr oxide layer (T.sub.Cr) and a thickness of the spinel oxide layer (T.sub.S) satisfy [0.55≤T.sub.Cr/T.sub.S≤6.7], the base material contains precipitate including one or more kinds selected from a M.sub.23C.sub.6, a M.sub.2B, a complex precipitate in which M.sub.2B acts as a precipitation nucleus, and M.sub.23C.sub.6 precipitates on a surface of the M.sub.2B, and a complex precipitate in which NbC acts as a precipitation nucleus, and M.sub.23C.sub.6 precipitates on a surface of the NbC, and a part of the precipitate protrude from the surface of the Cr oxide layer.