Disclosed is a steel for an alloy structure, the chemical elements of the steel being, in percentage by mass: 0.35-0.45% of C, 0.27-0.35% of Si, 0.6-0.8% of Mn, 0.015-0.05% of Al, 0.06-0.1% of V, 0.2-1.0% of Zr, 0.001-0.005% of Mg, 0.025% or less of P, 0.015% or less of S, 0.005% or less of N, 0.001% or less of 0, the balance being Fe and other inevitable impurities. In addition, also disclosed is a manufacturing method for the steel for an alloy structure, the method comprising steps of: (1) smelting, refining, and casting; (2) blooming and cogging; (3) secondary hot rolling to form a product; and (4) heat treatment including quenching and tempering. The steel for an alloy structure is designed by adding trace alloy elements, the steel for an alloy structure is further strengthened and toughened, and the manufacturing cost is low.

Provided are: steel for knives, having a higher hardness and better corrosion resistance than conventional steel for knives; a knife; steel for martensitic knives; and a production method for same. The steel for knives comprises a component composition containing, in mass %, 0.45%-1.00% C, 0.1%-1.5% Si, 0.1%-1.5% Mn, 7.5%-11.0% Cr, and 0.5%-3.0% of either Mo or W or a complex of both (Mo+W/2), with the remainder being Fe and unavoidable impurities. Also provided are steel for martensitic knives and a knife. A production method for steel for martensitic knives is also provided that includes a quenching temperature at quenching of 1,050-1,250° C., a processing temperature for subzero processing of no more than −50° C., and a tempering temperature at tempering of 100-400° C., and obtains steel for martensitic knives that has a hardness of at least 700 HV.

Disclosed in the present invention is complex-phase steel having high hole expansibility. The complex-phase steel has a microstructure of ferrite and bainite. The complex-phase steel having high hole expansibility comprises the following chemical elements in percentage by mass: C: 0.06-0.09%, Si: 0.05-0.5%, Al: 0.02-0.1%, Mn: 1.5-1.8%, Cr: 0.3-0.6%, Nb≤0.03%, Ti: 0.05-0.12%, and the balance of Fe and inevitable impurities. In addition, also disclosed in the present invention is a manufacturing method for the foregoing complex-phase steel having high hole expansibility. The method comprises the following steps: (1) smelting and casting; (2) heating; (3) hot-rolling; (4) phosphorous removal; (5) laminar cooling: a relaxation time period is controlled to be 0-8 s, and a laminar cooling rate is 40-70° C./s; (6) coiling; (7) leveling; and (8) pickling. The complex-phase steel having high hole expansibility can simultaneously satisfy the requirements for hole expansibility and good plasticity.

The austenitic stainless steel containing niobium according to an exemplary embodiment of the present invention includes: 16 to 26 wt. % of chromium (Cr), 8 to 22 wt. % of nickel (Ni), 0.02 to 0.1 wt. % of carbon (C), 0.2 to 1 wt. % of niobium (Nb), 0.015 to 0.025 wt. % of titanium (Ti), 0.004 to 0.01 wt. % of nitrogen (N), and 0.5 to 2 wt. % of manganese (Mn), wherein the austenitic stainless steel containing niobium has an austenitic matrix structure, a fine niobium carbide and a fine titanium nitride are precipitated in the austenitic matrix structure, and the fine niobium carbide is uniformly dispersed in the austenitic matrix structure.

The austenitic stainless steel containing niobium according to an exemplary embodiment of the present invention includes: 16 to 26 wt. % of chromium (Cr), 8 to 22 wt. % of nickel (Ni), 0.02 to 0.1 wt. % of carbon (C), 0.2 to 1 wt. % of niobium (Nb), 0.015 to 0.025 wt. % of titanium (Ti), 0.004 to 0.01 wt. % of nitrogen (N), and 0.5 to 2 wt. % of manganese (Mn), wherein the austenitic stainless steel containing niobium has an austenitic matrix structure, a fine niobium carbide and a fine titanium nitride are precipitated in the austenitic matrix structure, and the fine niobium carbide is uniformly dispersed in the austenitic matrix structure.

A precipitation-hardened stainless steel alloy is disclosed including, by weight: 14.0-16.0% Cr; 6.0-7.0% Ni; 1.25-1.75% Cu; 0.5-1.0% Mo; 0.40-0.85% Nb; 0.025-0.05% C; up to 1.0% Mn; up to 1.0% Si; up to 0.1% V; up to 0.1% Co; up to 0.1% Sn; up to 0.02% N; up to 0.025% P; up to 0.05% Al; up to 0.008% S; up to 0.005% Ag; up to 0.005% Pb; up to 0.1% As; up to 0.01% Sb; and a balance of Fe. The alloy has a ratio of Nb:(C+N) of at least 15:1.

Herein is provided a ferrous shape memory alloy (SMA) wire and processes for production of ferrous shape memory alloy wire that do not require crystallographic texturing processes to achieve superior superelastic and SMA wire properties. The shape memory alloy wire includes an elongated wire body with a longitudinal-axis length of iron alloy material and has a cross-sectional wire diameter that is less than about 1 millimeter. The iron alloy material has an oligocrystalline crystallographic morphology along the longitudinal-axis length. The iron alloy material has a ′-fcc crystallographic matrix and a volume fraction of ′-LH crystallographic precipitates in the ′-fee crystallographic matrix.

A rolled steel sheet, for press hardening is provided, having a chemical composition where Ti/N>3.42, and the carbon, manganese, chromium and silicon contents satisfy: $2.6C+\frac{\mathrm{Mn}}{5.3}+\frac{\mathrm{Cr}}{13}+\frac{\mathrm{Si}}{15}\ge 1.1\%.$
The sheet has a nickel content Ni.sub.surf at any point of the steel in the vicinity of the surface over a depth Δ, such that: Ni.sub.surf >Ni.sub.nom, Ni.sub.nom denoting the nominal nickel content of the steel, and such that, Ni.sub.max denoting the maximum nickel content within Δ: $\frac{\left({\mathrm{Ni}}_{\max }+{\mathrm{Ni}}_{\mathrm{nom}}\right)}{2}\times \left(\Delta \right)\ge 0.6,$
and such that: $\frac{\left({\mathrm{Ni}}_{\max }-{\mathrm{Ni}}_{\mathrm{nom}}\right)}{\Delta }\ge 0.01$
and the surface density of all of the particles D.sub.i and the surface density of the particles D.sub.(>2 μm) larger than 2 micrometers satisfy, at least to a depth of 100 micrometers in the vicinity of the surface of said sheet:
D.sub.i+6.75 D.sub.(>2 μm) <270
D.sub.i and D.sub.(>2 μm) being expressed as number of particles per square millimeter, and said particles denoting all the oxides, sulfides, and nitrides, either pure or combined such as oxysulfides and carbonitrides, present in the steel matrix.

A steel material showing excellent hydrogen-induced cracking resistance according to an aspect of the present invention comprises, in weight %, 0.10-0.25% of C, 0.05-0.50% of Si, 1.0-2.0% of Mn, 0.005-0.1% of Al, 0.010% or less of P, 0.0015% or less of S, 0.001-0.03% of Nb, 0.001-0.03% of V, 0.01-0.15% of Mo, 0.01-0.50% of Cu, 0.05-0.50% of Ni, and the remainder being Fe and unavoidable impurities, and has a thickness of 100-300 mm. The maximum size of pores formed inside can be 1 μm or less.

Austenitic stainless steel includes 16 to 26 wt % of chromium (Cr), 8 to 22 wt % of nickel (Ni), 0.02 to 0.1 wt % of carbon (C), 0.2 to 1 wt % of niobium (Nb), and 2 to 3.5 wt % of manganese (Mn), and has an austenite matrix, wherein a nanosized niobium carbide (NbC) is precipitated in the austenite matrix, and the nanosized niobium carbide is uniformly dispersed in the austenite matrix. The austenitic stainless steel may further include 0.5 to 1.5 wt % of molybdenum (Mo).