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WO2013018628A1 - Method for producing austenitic stainless steel - Google Patents

Method for producing austenitic stainless steel Download PDF

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Publication number
WO2013018628A1
WO2013018628A1 PCT/JP2012/068905 JP2012068905W WO2013018628A1 WO 2013018628 A1 WO2013018628 A1 WO 2013018628A1 JP 2012068905 W JP2012068905 W JP 2012068905W WO 2013018628 A1 WO2013018628 A1 WO 2013018628A1
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temperature
stainless steel
hot rolling
content
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PCT/JP2012/068905
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French (fr)
Japanese (ja)
Inventor
勇人 喜多
渋谷 将行
修二 吉田
朋之 須川
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Nippon Steel Corp
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Nippon Steel and Sumitomo Metal Corp
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Publication date
Application filed by Nippon Steel and Sumitomo Metal Corp filed Critical Nippon Steel and Sumitomo Metal Corp
Priority to KR1020147005051A priority Critical patent/KR101495483B1/en
Priority to CN201280046368.0A priority patent/CN103826766B/en
Priority to US14/235,849 priority patent/US20140261917A1/en
Priority to JP2013526850A priority patent/JP5418734B2/en
Priority to SI201230842A priority patent/SI2737961T1/en
Priority to EP12819669.8A priority patent/EP2737961B1/en
Publication of WO2013018628A1 publication Critical patent/WO2013018628A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21BROLLING OF METAL
    • B21B1/00Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations
    • B21B1/02Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations for rolling heavy work, e.g. ingots, slabs, blooms, or billets, in which the cross-sectional form is unimportant ; Rolling combined with forging or pressing
    • B21B1/026Rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/004Heat treatment of ferrous alloys containing Cr and Ni
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/008Heat treatment of ferrous alloys containing Si
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226Hot rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/001Ferrous alloys, e.g. steel alloys containing N
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/26Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/28Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/34Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of silicon
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21BROLLING OF METAL
    • B21B1/00Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations
    • B21B1/02Metal-rolling methods or mills for making semi-finished products of solid or profiled cross-section; Sequence of operations in milling trains; Layout of rolling-mill plant, e.g. grouping of stands; Succession of passes or of sectional pass alternations for rolling heavy work, e.g. ingots, slabs, blooms, or billets, in which the cross-sectional form is unimportant ; Rolling combined with forging or pressing
    • B21B2001/028Slabs
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/001Austenite
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/004Dispersions; Precipitations

Definitions

  • the present invention relates to a method for producing austenitic stainless steel exhibiting corrosion resistance against concentrated nitric acid. More specifically, the present invention relates to a method for producing a high Si-containing austenitic stainless steel that can be used in a high-temperature, high-concentration nitric acid environment.
  • the main components of the nitric acid production plant are exposed to a high temperature and high concentration nitric acid environment.
  • stainless steel is used as a corrosion resistant material for plants.
  • Stainless steel forms a stable passive film in nitric acid and exhibits excellent corrosion resistance.
  • high-temperature, high-concentration nitric acid is extremely oxidative, and general stainless steel causes transpassive corrosion.
  • the passive state corrosion the whole surface corrosion accompanied by elution of Cr 2 O 3 forming the passive state film and the intergranular corrosion occur near the grain boundary where sensitization (sensitivity of intergranular corrosion increases).
  • High Si austenitic stainless steels such as 17Cr-14Ni-4Si (Patent Document 1) and 11Cr-17Ni-6Si (Patent Document 2) are known as materials having corrosion resistance even in such an environment. These high-Si stainless steels exhibit excellent nitric acid corrosion resistance by re-oxidizing Si eluted by corrosion in the passive state region to form a silicate film.
  • One or more of Nb, Ta, Ti, and Zr are added to these high Si stainless steels.
  • These additive elements have an effect of fixing C in steel and suppressing sensitization. In particular, it is effective in suppressing sensitization of the weld heat affected zone, and has a remarkable effect in improving the intergranular corrosion resistance in high-concentration nitric acid.
  • the heating temperature of the slab in hot working is advantageously as high as possible from the viewpoint of productivity.
  • high Si stainless steel has a problem that cracking of the slab occurs during hot working when heated to a temperature higher than a predetermined temperature during hot working. This is because Si has a lower solid solubility in the austenite phase, and the higher the amount of Si, the more embrittled phases such as intermetallic compounds and ⁇ ferrite are generated at high temperatures, resulting in deterioration of high temperature ductility. Therefore, in order to stably produce high-Si stainless steel on an industrial scale, it is necessary to appropriately manage the heating temperature in hot working.
  • Patent Document 3 discloses an ingot of high Si stainless steel containing 5 to 8% Si (in this specification, “%” means “% by mass” unless otherwise specified) unless otherwise specified). Disclosed is a method of hot rolling or hot forging in a temperature range of 900 ° C. or higher after soaking in a temperature range satisfying 1100 ° C. and T (° C.) ⁇ 1470-35 ⁇ Si-5 ⁇ Ni (%). ing. As the Si content increases, a low-melting intermetallic compound is formed in the cast solidified structure, and when the soaking temperature rises, the intermetallic compound partially melts, so that cracking occurs during hot working. The soaking temperature is specified to prevent this cracking.
  • Non-Patent Document 1 describes the relationship between intermetallic compounds and hot workability in high-Si stainless steel (6.5Si-17Cr-22Ni-0.01Pd).
  • Si-- Ni-rich intermetallic compound crystallizes, and if it is present in a large amount, the hot workability is lowered, and
  • the high-Si stainless steel of Non-Patent Document 1 resulted in fracture due to partial melting of a low melting point Ni—Si intermetallic compound exceeding 1100 ° C. and crack propagation along the grain boundary. It is presumed that the heating temperature in the hot working is defined as 1100 ° C. or lower.
  • Patent Document 4 a high Si stainless steel slab containing 4 to 10% of Si and having S and O regulated to 30 ppm or less is soaked at 1100 ° C. to 1250 ° C. for 2 hours or more and hot-rolled. A method is disclosed in which hot rolling is terminated at 950 ° C. or higher and solution heat treatment is performed at 1000 ° C. or higher and 1200 ° C. or lower.
  • factors affecting the high-temperature ductility of high-Si austenitic stainless steel are (1) impurity elements of S and O, and (2) intermetallic compounds that precipitate during cooling of the slab, and It is disclosed that hot workability is improved by eliminating intermetallic compounds by reducing S and O and soaking slabs. Although the component of this intermetallic compound is not specified, it is presumed that it is a Ni—Si intermetallic compound having a low melting point as in Non-Patent Document 1.
  • the hot workability is improved by setting the heating temperature to be equal to or lower than the melting temperature of the Ni—Si intermetallic compound.
  • the heating temperature is set to be equal to or lower than the melting temperature of the Ni—Si intermetallic compound.
  • the solid solubility of C tends to be lowered and sensitized. Intergranular corrosion resistance was poor.
  • the high-Si stainless steels disclosed in Patent Documents 1 and 2 contain Nb, Ta, Ti, and Zr, thereby suppressing sensitization and greatly improving nitric acid corrosion resistance. There was a new problem that surface defects called wrinkles were likely to occur.
  • the object of the present invention is to reliably produce high-Si austenitic stainless steel with corrosion resistance suitable for use in a high-temperature, high-concentration nitric acid environment without generating lashes during the hot rolling process. It is to be.
  • the present inventors have developed a high Si-containing austenitic stainless steel suitable for use in a high-temperature, high-concentration nitric acid environment (hereinafter austenitic stainless steel).
  • austenitic stainless steel As a result of investigating conditions for reliably producing (sometimes simply referred to as stainless steel), the following items (i) to (iii) were clarified.
  • Ni—Si—X Nb, Ti, Zr
  • the melting point is approximately in the range of 1150 to 1200 ° C., and for example, Ni—Si—Nb is about 1160 ° C. from the results of the phase diagram calculation.
  • the present invention has a C: 0.04% or less, Cr: 7-20%, Ni: 10-22%, Si: 2.5-7%, Mn: 10% or less, sol. Al: 0.03% or less, P: 0.03% or less, S: 0.03% or less, N: 0.035% or less, a total of one or more of Nb, Ti, Ta, and Zr: 0.0
  • the method according to the present invention comprises heat-treating the austenitic stainless steel subjected to the hot rolling in a temperature range of 1100 to 1160 ° C., and then cooling at a cooling rate of 100 ° C./min or more.
  • a temperature range of 1100 to 1160 ° C. a temperature range of 1100 to 1160 ° C.
  • cooling at a cooling rate of 100 ° C./min or more.
  • a high Si content austenitic stainless steel suitable for use in a high-temperature, high-concentration nitric acid environment can be reliably produced without generating lashes during the hot rolling process.
  • FIG. 1 is a graph showing the results of a torsion test of the test steel 1.
  • FIG. 2 is a graph showing the relationship between ⁇ T of the test steel 1 and the rate of occurrence of whipping.
  • FIG. 3 is a graph showing the relationship between the heat treatment temperature of the test steel 1 after rolling, 0.2% proof stress, and elongation.
  • % related to the chemical composition of steel is “% by mass”. Moreover, the balance of the chemical composition of steel is Fe and impurities.
  • C [Chemical composition of steel] [C: 0.04% or less]
  • C is an element that increases the strength of steel, it is an element that deteriorates corrosion resistance, for example, forms Cr carbide at the grain boundary in the heat-affected zone of the weld and causes sensitization. Therefore, the C content is set to 0.04% or less.
  • the C content is preferably 0.03% or less, and more preferably 0.02% or less.
  • Cr 7-20%
  • Cr is a basic element for ensuring the corrosion resistance of stainless steel, and its content is 7% or more and 20% or less. If the Cr content is less than 7%, sufficient corrosion resistance cannot be obtained. On the other hand, if the Cr content is excessive, a co-existence of Si and Nb results in a two-phase structure in which a large amount of ferrite is precipitated, resulting in a decrease in workability and impact resistance. Therefore, the upper limit of the Cr content is 20%. To do.
  • the lower limit of the Cr content is preferably 10%, and more preferably 11%.
  • the upper limit of the Cr content is preferably 19%, and more preferably 18%.
  • Ni is a stabilizing element of the austenite phase and also has an effect of increasing the zero ductility temperature. Ni is contained in an amount of 10% to 22%. If the Ni content is less than 10%, the desired corrosion resistance and toughness cannot be obtained. If the Ni content exceeds 22%, the cost increases significantly.
  • the lower limit of the Ni content is preferably 12%, and more preferably 13%. Further, the upper limit of the Ni content is preferably 20%, and more preferably 16%.
  • Si is contained in an amount of 2.5% or more and 7% or less in order to enhance the corrosion resistance in concentrated nitric acid.
  • Si is contained in an amount of 2.5% or more.
  • the upper limit of the Si content is set to 7%.
  • the lower limit of the Si content is preferably 3.0%, and more preferably 3.5%.
  • the upper limit of the Si content is preferably 6%, and more preferably 5%.
  • Mn is a stabilizing element of the austenite phase and is also contained as a deoxidizing agent. If the Mn content exceeds 10%, the corrosion resistance decreases, hot cracking during welding, and further the workability decreases.
  • the upper limit of the Mn content is preferably 6%, and more preferably 4%. Moreover, in order to acquire the said effect of Mn reliably, it is preferable that Mn content is 0.5% or more, and it is further more preferable that it is 1.0% or more.
  • sol.Al 0.03% or less
  • Al is contained in the steel as a deoxidizing agent. However, since excessive inclusion of Al generates harmful inclusions, the content of sol.Al is set to 0.03% or less.
  • P and S are both elements harmful to corrosion resistance and weldability, and the lower the content of each, the better. Therefore, the P content is 0.03% or less, and the S content is 0.03% or less.
  • N 0.035% or less
  • N has a high affinity with Nb, Ti, Ta, and Zr, and inhibits the fixation of C by these elements. Therefore, the N content is preferably as low as possible. Therefore, the N content is set to 0.035% or less.
  • Nb, Ti, Ta and Zr all have an effect of fixing C and suppressing the decrease in intergranular corrosion resistance due to sensitization, and are particularly effective elements for improving the corrosion resistance of the weld heat affected zone. If the total content of these elements is less than 0.05%, the effect of improving the intergranular corrosion resistance cannot be obtained, and hot working cracks due to the formation of a low melting point Ni—Si intermetallic compound become large. On the other hand, if the total content of these elements exceeds 0.7%, workability is obtained. Therefore, the content of these elements is 0.05% or more and 0.7% or less in total of one or more kinds.
  • a hot rolling step of performing hot rolling 9Cr + 40Ni- ⁇ T ⁇ T in is heated to a heating temperature T h at 30 ° C. or higher, after heat treatment at preferably a temperature range of more 1100 ⁇ 1160 °C, 100 °C / min It consists of a heat treatment step (annealing step) for cooling at the above cooling rate.
  • Hot rolling process In order to clarify the optimum heating temperature range for hot rolling, the relationship between chemical composition and high temperature deformability was investigated by high temperature torsion test. Thereby, the zero ductility in hot rolling can be investigated.
  • one of the test pieces having a parallel part diameter of 8 mm and a length of 30 mm is fixed and held at a predetermined temperature, with a rotational speed of 300 rpm (strain speed of 4.2 sec ⁇ 1 ) and an axial force of 0 kgf in one direction.
  • the number of rotations until twisting was applied and breaking was taken as the number of twists.
  • FIG. 1 shows the relationship between the heating temperature and the number of twists as a result of conducting a high temperature return test using a test piece of high Si stainless steel having the chemical composition shown in Table 1 as test steel 1.
  • the number of twists showed a maximum at around 1100 ° C., and the number of twists decreased significantly at a temperature higher than that, and at 1275 ° C., it started to twist and broke at the same time. That is, it can be seen that the temperature at which the ductility of the high Si stainless steel shown as the test steel 1 in Table 1 becomes zero (hereinafter referred to as “zero ductility temperature”) is approximately 1275 ° C.
  • the high-temperature torsion test was conducted on high-Si stainless steels having various chemical compositions containing one or more of Nb, Ta, Ti, and Zr, and the zero ductility temperature was examined.
  • T 0 the zero ductility temperature
  • T 0 1135-90Si-2.9Cr + 40Ni (2)
  • the thickness was 4 mm by hot rolling. Thereafter, the scale was removed by pickling, and then the rate of occurrence of baldness was investigated by the following method.
  • the steel plate surface was divided into 100 mm unit meshes, and the ratio of the number of meshes with scabs in the total number of meshes investigated was defined as the scab generation rate (%). If the rate of occurrence of lashes is 5% or less, it is possible to proceed to the next step with a simple rework.
  • FIG. 2 shows the relationship between ⁇ T of the test steel 1 (Table 1) and the rate of occurrence of lashes.
  • [Delta] T is 30 ° C. or more, preferably such that 60 ° C. or higher may be set the heating temperature T h of the hot rolling.
  • the holding time to this heating temperature is not particularly limited.
  • the heating temperature is set in order to prevent the occurrence of baldness after rolling, so that the surface temperature of the slab may be a predetermined temperature.
  • the heating time required for this depends on the size of the slab, but in general, the heating time is preferably 60 minutes or more.
  • hot rolling can be performed if the hot rolling end temperature is 700 ° C. or higher. Desirably, the end temperature is set to 950 ° C. or higher.
  • Hot rolling can be performed in one or more stages. In the case of multi-stage rolling, if necessary, it can be heated between rolling stands.
  • the heating temperature at this time is not particularly required to be a temperature at which ⁇ T is 30 ° C. or higher, but is preferably a temperature at which ⁇ T is 30 ° C. or higher.
  • pickling is generally performed by a conventional method to remove oxide scale on the surface of the rolled material.
  • Heat treatment process Since the stainless steel plate obtained by hot rolling can adjust mechanical characteristics (elongation, yield strength) by performing a heat treatment for annealing, it is preferable to perform the heat treatment after the hot rolling.
  • the heat treatment temperature is increased, the proof stress is reduced although the elongation is increased.
  • the cooling rate after the heat treatment is slow, chromium carbide precipitates, and the corrosion resistance deteriorates. Therefore, it is necessary to set the heat treatment temperature and the subsequent cooling rate so as to achieve both elongation and yield strength and prevent sensitization.
  • FIG. 3 shows the relationship between the heat treatment temperature of the test steel 1, the 0.2% proof stress and the elongation.
  • the circle plot in the graph of FIG. 3 shows 0.2% yield strength (MPa), and the square plot shows elongation (%).
  • a high Si content austenitic stainless steel suitable for use in a high-temperature, high-concentration nitric acid environment can be reliably produced without generating lashes in the hot rolling process. can do.

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Abstract

It is possible to reliably produce an austenitic stainless steel, which has a high Si content and exhibits corrosion resistance high enough that the steel can be used in a high temperature environment having a high concentration of nitric acid without the occurrence of scabbing, by subjecting a stainless steel slab having a chemical composition that contains 0.04% or less of C, 7 to 20% of Cr, 10 to 22% of Ni, 2.5 to 7% of Si, 10% or less of Mn, 0.03% or less of sol.Al, 0.03% or less of P, 0.03% or less of S, 0.035% or less of N and 0.05 to 0.7% of the total of one or more elements selected from among Nb, Ti, Ta and Zr, with the remainder comprising Fe and impurities, to hot rolling by heating the steel slab to a heating temperature Th, wherein the heating temperature during hot rolling is Th and ΔT in formula (1) (Th = 1135 - 90Si - 2.9Cr + 40Ni - ΔT) is 30°C or higher, and then subjecting the steel slab to heat treatment by heating to a temperature of 1100 to 1160°C and then cooling at a cooling rate of 100°C/minute or higher.

Description

オーステナイト系ステンレス鋼の製造方法Method for producing austenitic stainless steel

 本発明は、濃硝酸に対して耐食性を示すオーステナイト系ステンレス鋼の製造方法に関する。より具体的には、高温、高濃度の硝酸環境中で使用することができる高Si含有オーステナイト系ステンレス鋼の製造方法に関する。 The present invention relates to a method for producing austenitic stainless steel exhibiting corrosion resistance against concentrated nitric acid. More specifically, the present invention relates to a method for producing a high Si-containing austenitic stainless steel that can be used in a high-temperature, high-concentration nitric acid environment.

 硝酸製造プラントの主要構成材料は、高温、高濃度の硝酸環境に曝される。一般にプラント用の耐食性材料としてステンレス鋼が使用される。ステンレス鋼は、硝酸中で安定な不働態皮膜を形成し、優れた耐食性を発揮する。しかし、高温、高濃度の硝酸は極めて酸化性が強く、一般のステンレス鋼では過不働態腐食を生じる。過不働態腐食では、不働態皮膜を形成するCr23の溶出に伴う全面腐食、および鋭敏化(粒界腐食の感受性が増大)した結晶粒界近傍で粒界腐食が起きる。 The main components of the nitric acid production plant are exposed to a high temperature and high concentration nitric acid environment. In general, stainless steel is used as a corrosion resistant material for plants. Stainless steel forms a stable passive film in nitric acid and exhibits excellent corrosion resistance. However, high-temperature, high-concentration nitric acid is extremely oxidative, and general stainless steel causes transpassive corrosion. In the passive state corrosion, the whole surface corrosion accompanied by elution of Cr 2 O 3 forming the passive state film and the intergranular corrosion occur near the grain boundary where sensitization (sensitivity of intergranular corrosion increases).

 このような環境下でも耐食性を有する材料として、17Cr-14Ni-4Si(特許文献1)、11Cr-17Ni-6Si(特許文献2)などの高Siオーステナイト系ステンレス鋼が知られている。これらの高Siステンレス鋼は、過不働態領域で腐食により溶出したSiが再酸化されてシリケート皮膜を生成することによって、優れた硝酸耐食性を示す。これらの高Siステンレス鋼には、Nb、Ta、Ti、Zrの1種又は2種以上が添加される。これらの添加元素は、鋼中Cを固定し、鋭敏化を抑制する効果がある。特に溶接熱影響部の鋭敏化抑制に有効で、高濃度硝酸中での粒界耐食性の改善に顕著な効果がある。 High Si austenitic stainless steels such as 17Cr-14Ni-4Si (Patent Document 1) and 11Cr-17Ni-6Si (Patent Document 2) are known as materials having corrosion resistance even in such an environment. These high-Si stainless steels exhibit excellent nitric acid corrosion resistance by re-oxidizing Si eluted by corrosion in the passive state region to form a silicate film. One or more of Nb, Ta, Ti, and Zr are added to these high Si stainless steels. These additive elements have an effect of fixing C in steel and suppressing sensitization. In particular, it is effective in suppressing sensitization of the weld heat affected zone, and has a remarkable effect in improving the intergranular corrosion resistance in high-concentration nitric acid.

 熱間加工におけるスラブの加熱温度は、生産性の観点からはできるだけ高温にするのが有利である。しかし、高Siステンレス鋼は、熱間加工時に所定温度より高温に加熱されると、熱間加工の途中でスラブの割れが生じるという問題がある。Siは、オーステナイト相に対する固溶度が低く、Siを多量に含有するほど、高温で金属間化合物やδフェライト等の脆化相が生成して高温延性が劣化するためである。従って、高Siステンレス鋼を工業規模で安定的に製造するには、熱間加工における加熱温度を適正に管理する必要がある。 The heating temperature of the slab in hot working is advantageously as high as possible from the viewpoint of productivity. However, high Si stainless steel has a problem that cracking of the slab occurs during hot working when heated to a temperature higher than a predetermined temperature during hot working. This is because Si has a lower solid solubility in the austenite phase, and the higher the amount of Si, the more embrittled phases such as intermetallic compounds and δ ferrite are generated at high temperatures, resulting in deterioration of high temperature ductility. Therefore, in order to stably produce high-Si stainless steel on an industrial scale, it is necessary to appropriately manage the heating temperature in hot working.

 特許文献3には、Siを5~8%(本明細書では特に断りがない限り化学組成に関する「%」は「質量%」を意味する)含有する高Siステンレス鋼の鋳塊を、1050~1100℃、かつT(℃)<1470-35×Si-5×Ni(%)を満足する温度域での均熱後に900℃以上の温度域で熱間圧延または熱間鍛造する方法が開示されている。Si含有量の増加に伴い鋳造凝固組織中に低融点の金属間化合物が形成され、均熱温度が高くなるとこの金属間化合物が部分溶融するため、熱間加工中に割れが起こる。この割れを防止するように均熱温度が特定されている。 Patent Document 3 discloses an ingot of high Si stainless steel containing 5 to 8% Si (in this specification, “%” means “% by mass” unless otherwise specified) unless otherwise specified). Disclosed is a method of hot rolling or hot forging in a temperature range of 900 ° C. or higher after soaking in a temperature range satisfying 1100 ° C. and T (° C.) <1470-35 × Si-5 × Ni (%). ing. As the Si content increases, a low-melting intermetallic compound is formed in the cast solidified structure, and when the soaking temperature rises, the intermetallic compound partially melts, so that cracking occurs during hot working. The soaking temperature is specified to prevent this cracking.

 非特許文献1には、高Siステンレス鋼(6.5Si-17Cr-22Ni-0.01Pd)における金属間化合物と熱間加工性の関係について、(a)鋳造組織の樹枝状間にはSi-Niリッチな金属間化合物が晶出し、それが多量に存在すると熱間加工性が低くなること、および(b)金属間化合物が晶出したインゴットを1000~1150℃でソーキングした場合、1150℃では金属間化合物が部分溶解して割れを生じるが、1100℃では金属間化合物の溶融はみられず、固溶させることによって熱間加工での割れが生じなくなることが報告されている。 Non-Patent Document 1 describes the relationship between intermetallic compounds and hot workability in high-Si stainless steel (6.5Si-17Cr-22Ni-0.01Pd). (A) Si-- Ni-rich intermetallic compound crystallizes, and if it is present in a large amount, the hot workability is lowered, and (b) when the ingot crystallized with the intermetallic compound is soaked at 1000 to 1150 ° C., at 1150 ° C. It is reported that the intermetallic compound partially dissolves and causes cracking, but no melting of the intermetallic compound is observed at 1100 ° C., and cracking during hot working does not occur when dissolved.

 すなわち、非特許文献1の高Siステンレス鋼は、1100℃を超えると低融点のNi-Si系金属間化合物が部分溶解して、粒界に沿って割れが伝播することによって破壊に至ったものと推定され、実質的には熱間加工における加熱温度を1100℃以下に規定したものである。 In other words, the high-Si stainless steel of Non-Patent Document 1 resulted in fracture due to partial melting of a low melting point Ni—Si intermetallic compound exceeding 1100 ° C. and crack propagation along the grain boundary. It is presumed that the heating temperature in the hot working is defined as 1100 ° C. or lower.

 特許文献4には、Siを4~10%含有し、SとOを30ppm以下に規制した高Siステンレス鋼のスラブを1100℃以上1250℃以下で2時間以上ソーキング処理して熱間圧延し、熱間圧延を950℃以上で終了し、溶体化熱処理を1000℃以上1200℃以下で行う方法が開示されている。特許文献4には、高Siオーステナイト系ステンレス鋼の高温延性に影響する因子は、(1)S、Oの不純物元素および(2)鋳片の冷却中に析出する金属間化合物であること、ならびにSとOの低減および鋳片のソーキングによって金属間化合物を消滅させることによって熱間加工性が改善されることが開示されている。この金属間化合物の成分は明示されていないが、非特許文献1と同様に、低融点のNi-Si系金属間化合物であると推定される。 In Patent Document 4, a high Si stainless steel slab containing 4 to 10% of Si and having S and O regulated to 30 ppm or less is soaked at 1100 ° C. to 1250 ° C. for 2 hours or more and hot-rolled. A method is disclosed in which hot rolling is terminated at 950 ° C. or higher and solution heat treatment is performed at 1000 ° C. or higher and 1200 ° C. or lower. In Patent Document 4, factors affecting the high-temperature ductility of high-Si austenitic stainless steel are (1) impurity elements of S and O, and (2) intermetallic compounds that precipitate during cooling of the slab, and It is disclosed that hot workability is improved by eliminating intermetallic compounds by reducing S and O and soaking slabs. Although the component of this intermetallic compound is not specified, it is presumed that it is a Ni—Si intermetallic compound having a low melting point as in Non-Patent Document 1.

 特許文献3、4に開示された技術では、加熱温度をNi-Si金属間化合物の溶融温度以下とすることで熱間加工性を改善する。しかし、高温、高濃度硝酸環境中で使用される高Si含有オーステナイト系ステンレス鋼では、多量のSiを含有することによりCの固溶度が低下して鋭敏化し易くなるため、高濃度硝酸中における耐粒界腐食性は不芳であった。 In the techniques disclosed in Patent Documents 3 and 4, the hot workability is improved by setting the heating temperature to be equal to or lower than the melting temperature of the Ni—Si intermetallic compound. However, in a high Si content austenitic stainless steel used in a high temperature and high concentration nitric acid environment, since it contains a large amount of Si, the solid solubility of C tends to be lowered and sensitized. Intergranular corrosion resistance was poor.

 特許文献1,2に開示された高Siステンレス鋼は、Nb、Ta、Ti、Zrを含有することによって鋭敏化を抑制し、硝酸耐食性を大幅に改善するが、熱間圧延の過程でヘゲ疵とよばれる表面欠陥が生じ易いという新たな課題があった。 The high-Si stainless steels disclosed in Patent Documents 1 and 2 contain Nb, Ta, Ti, and Zr, thereby suppressing sensitization and greatly improving nitric acid corrosion resistance. There was a new problem that surface defects called wrinkles were likely to occur.

 この原因は明らかではなく、スラブ加熱温度を低くすれば軽減する傾向にあったが、鋼の化学組成によっては十分な軽減効果が得られ難い場合があり、必要以上に低温で加熱するかまたは熱間圧延後のヘゲ疵除去のための研削等の手入れを行うことを余儀なくされ、大幅なコストアップの要因となっていた。 The cause of this is not clear, and there was a tendency to reduce it by lowering the slab heating temperature.However, depending on the chemical composition of the steel, it may be difficult to obtain a sufficient reduction effect. It was forced to carry out grinding and the like for removing the wrinkles after hot rolling, which caused a significant cost increase.

特許3237132号明細書Japanese Patent No. 3237132 specification 特許1119398号明細書Japanese Patent No. 1119398 特開平6-93389号公報JP-A-6-93389 特開平5-51633号明細書Japanese Patent Laid-Open No. 5-51633

NKK技報、No.154、1996、14-19頁NKK Technical Report, No.154, 1996, p.14-19

 本発明の目的は、熱間圧延の過程でヘゲ疵を発生することなく、高温、高濃度硝酸環境中で使用するのに好適な耐食性を備えた高Si含有オーステナイト系ステンレス鋼を確実に製造することである。 The object of the present invention is to reliably produce high-Si austenitic stainless steel with corrosion resistance suitable for use in a high-temperature, high-concentration nitric acid environment without generating lashes during the hot rolling process. It is to be.

 本発明者らは、熱間圧延の過程でヘゲ疵を発生することなく、高温、高濃度硝酸環境中で使用するのに好適な高Si含有オーステナイト系ステンレス鋼(以下ではオーステナイト系ステンレス鋼を単にステンレス鋼ということがある)を確実に製造するための条件を検討した結果、以下の事項(i)~(iii)が明らかになった。 The present inventors have developed a high Si-containing austenitic stainless steel suitable for use in a high-temperature, high-concentration nitric acid environment (hereinafter austenitic stainless steel). As a result of investigating conditions for reliably producing (sometimes simply referred to as stainless steel), the following items (i) to (iii) were clarified.

 (i)Siを多量に含有するステンレス鋼では、Ni-Si金属間化合物が生成する。その融点は、非引用文献1により開示されるように1100~1150℃の範囲にあると推定され、この金属間化合物の生成のために熱間圧延が困難となるような大きなスラブ割れが起こる。 (I) In a stainless steel containing a large amount of Si, an Ni—Si intermetallic compound is formed. The melting point is estimated to be in the range of 1100 to 1150 ° C. as disclosed in Non-Patent Document 1, and a large slab crack occurs that makes hot rolling difficult due to the formation of this intermetallic compound.

 (ii)Siを多量に含有するステンレス鋼がNb、Ta、Ti、Zr等を含有すると、金属間化合物としてNi-Si-X(X=Nb、Ti、Zr)が生成する。その融点はおおよそ1150~1200℃の範囲であり、例えばNi-Si-Nbでは状態図計算の結果から1160℃程度となる。このNi-Si-X三元系(X=Nb、Ta、Ti、Zr)金属間化合物は、Nb、Ta、Ti、Zr等が鋼中で偏析を生じ難い元素であるために、細かく分散して存在する。Ni-Si-X金属間化合物は、このように高融点で微細に分散するため、圧延が困難となるような大きなスラブ割れの発生を引き起こさない。 (Ii) When the stainless steel containing a large amount of Si contains Nb, Ta, Ti, Zr, etc., Ni—Si—X (X = Nb, Ti, Zr) is generated as an intermetallic compound. The melting point is approximately in the range of 1150 to 1200 ° C., and for example, Ni—Si—Nb is about 1160 ° C. from the results of the phase diagram calculation. This Ni—Si—X ternary system (X = Nb, Ta, Ti, Zr) intermetallic compound is finely dispersed because Nb, Ta, Ti, Zr, etc. are elements that do not easily segregate in steel. Exist. Since the Ni—Si—X intermetallic compound is thus finely dispersed with a high melting point, it does not cause the occurrence of large slab cracks that make rolling difficult.

 (iii)ところが、スラブ表面近傍ではNi-Si-Xの金属間化合物を起点とした割れが発生すると、表面まで割れが伝播し、割れの内部が酸化されることによって、ヘゲ疵が多発する。このヘゲ疵は、Ni-Si-Xの金属間化合物が細かく分散しているために量的に極めて多く、大量のヘゲ疵となる。 (Iii) However, when cracks originating from the Ni—Si—X intermetallic compound occur in the vicinity of the slab surface, the cracks propagate to the surface and the inside of the cracks are oxidized, resulting in frequent occurrence of baldness. . This beard is extremely large in quantity because the intermetallic compound of Ni—Si—X is finely dispersed, and becomes a large amount of beard.

 以上の結果から、熱間圧延の過程におけるヘゲ疵の発生は、上記Ni-Si-X三元系金属間化合物を起点とし、割れが表面まで伝播することによって生じることが判明した。濃硝酸環境での腐食防止の観点からSiおよびX元素の含有は必須であるので、上記の表面近傍での割れの伝播を抑制する手段について検討した。 From the above results, it has been found that the occurrence of whipping in the hot rolling process is caused by the propagation of cracks to the surface starting from the Ni—Si—X ternary intermetallic compound. Since it is essential to contain Si and X elements from the viewpoint of preventing corrosion in a concentrated nitric acid environment, a means for suppressing the propagation of cracks in the vicinity of the surface was examined.

 一般に、高温になり延性が低下すると、割れが伝播し易くなるので、鋼中の成分と延性との関係を検討した。その結果、以下の知見が得られた。 In general, cracks tend to propagate when the ductility decreases at high temperatures, so the relationship between the components in steel and ductility was examined. As a result, the following knowledge was obtained.

 (A)熱間圧延時の加熱温度を、鋼組成中のSi、Cr、Ni含有量との関係で規定することにより、製品表面の欠陥(ヘゲ疵)を防止することができる。 (A) By defining the heating temperature during hot rolling in relation to the contents of Si, Cr, and Ni in the steel composition, defects on the product surface can be prevented.

 (B)圧延後の仕上げ焼鈍の温度範囲と冷却方法を規定することにより、伸びと耐力を確保しつつ、鋭敏化を抑制することができる。 (B) By defining the temperature range and cooling method of finish annealing after rolling, it is possible to suppress sensitization while ensuring elongation and proof stress.

 以上の知見に基づく本発明は、C:0.04%以下、Cr:7~20%、Ni:10~22%、Si:2.5~7%、Mn:10%以下、sol.Al:0.03%以下、P:0.03%以下、S:0.03%以下、N:0.035%以下、Nb、Ti、Ta、Zrのうち1種または2種以上の合計:0.05~0.7%を含有し、残部がFeおよび不純物からなる化学組成を有するステンレス鋼のスラブを、熱間圧延時の加熱温度をThとし、(1)式:Th=1135-90Si-2.9Cr+40Ni-ΔT中のΔTが30℃以上である加熱温度Thに加熱して熱間圧延を行うことを特徴とするオーステナイト系ステンレス鋼の製造方法である。 Based on the above findings, the present invention has a C: 0.04% or less, Cr: 7-20%, Ni: 10-22%, Si: 2.5-7%, Mn: 10% or less, sol. Al: 0.03% or less, P: 0.03% or less, S: 0.03% or less, N: 0.035% or less, a total of one or more of Nb, Ti, Ta, and Zr: 0.0 A stainless steel slab containing 05-0.7% and having the chemical composition consisting of Fe and impurities in the balance, the heating temperature at the time of hot rolling is T h, and the formula (1): T h = 1135-90Si -2.9Cr + 40Ni-ΔT ΔT in is a manufacturing method of austenitic stainless steel which is characterized in that the heated hot rolling the heating temperature T h at 30 ° C. or higher.

 好適態様において、本発明に係る方法は、前記熱間圧延が施されたオーステナイト系ステンレス鋼を1100~1160℃の温度範囲で熱処理し、次いで100℃/分以上の冷却速度で冷却を行うことをさらに含む。 In a preferred embodiment, the method according to the present invention comprises heat-treating the austenitic stainless steel subjected to the hot rolling in a temperature range of 1100 to 1160 ° C., and then cooling at a cooling rate of 100 ° C./min or more. In addition.

 本発明により、熱間圧延の過程でヘゲ疵を発生することなく、高温、高濃度硝酸環境中で使用するのに好適な高Si含有オーステナイト系ステンレス鋼を確実に製造することができる。 According to the present invention, a high Si content austenitic stainless steel suitable for use in a high-temperature, high-concentration nitric acid environment can be reliably produced without generating lashes during the hot rolling process.

図1は、供試鋼1の捩り試験結果を示すグラフである。FIG. 1 is a graph showing the results of a torsion test of the test steel 1. 図2は、供試鋼1のΔTとヘゲ疵発生率との関係を示すグラフである。FIG. 2 is a graph showing the relationship between ΔT of the test steel 1 and the rate of occurrence of whipping. 図3は、供試鋼1の圧延後の熱処理温度と0.2%耐力、伸びとの関係を示すグラフである。FIG. 3 is a graph showing the relationship between the heat treatment temperature of the test steel 1 after rolling, 0.2% proof stress, and elongation.

 以下、本発明に係るオーステナイト系ステンレス鋼の製造方法について、添付図面も参照しながらより詳しく説明する。前述の通り、鋼の化学組成に関する%は質量%である。また、鋼の化学組成の残部は、Feおよび不純物である。 Hereinafter, the method for producing austenitic stainless steel according to the present invention will be described in more detail with reference to the accompanying drawings. As described above, “%” related to the chemical composition of steel is “% by mass”. Moreover, the balance of the chemical composition of steel is Fe and impurities.

 [鋼の化学組成]
 [C:0.04%以下]
 Cは,鋼の強度を高める元素ではあるが、溶接部の熱影響部において粒界にCr炭化物を生成し、鋭敏化の原因となるなど、耐食性を劣化させる元素である。したがって、C含有量は0.04%以下とする。C含有量は、好ましくは0.03%以下であり、さらに好ましくは0.02%以下である。
[Chemical composition of steel]
[C: 0.04% or less]
Although C is an element that increases the strength of steel, it is an element that deteriorates corrosion resistance, for example, forms Cr carbide at the grain boundary in the heat-affected zone of the weld and causes sensitization. Therefore, the C content is set to 0.04% or less. The C content is preferably 0.03% or less, and more preferably 0.02% or less.

 [Cr:7~20%]
 Crは、ステンレス鋼の耐食性を確保するための基本元素であり、その含有量は7%以上20%以下とする。Cr含有量が7%未満では十分な耐食性を得られない。一方、Cr含有量が過剰になると、SiとNbの共存により多量のフェライトが析出した二相組織となって、加工性、耐衝撃性の低下を招くので、Cr含有量の上限を20%とする。Cr含有量の下限は10%であることが好ましく、11%であることがさらに好ましい。一方、Cr含有量の上限は19%であることが好ましく、18%であることがさらに好ましい。
[Cr: 7-20%]
Cr is a basic element for ensuring the corrosion resistance of stainless steel, and its content is 7% or more and 20% or less. If the Cr content is less than 7%, sufficient corrosion resistance cannot be obtained. On the other hand, if the Cr content is excessive, a co-existence of Si and Nb results in a two-phase structure in which a large amount of ferrite is precipitated, resulting in a decrease in workability and impact resistance. Therefore, the upper limit of the Cr content is 20%. To do. The lower limit of the Cr content is preferably 10%, and more preferably 11%. On the other hand, the upper limit of the Cr content is preferably 19%, and more preferably 18%.

 [Ni:10~22%]
 Niはオーステナイト相の安定化元素であり、また、ゼロ延性温度を高める効果もある。Niは10%以上22%以下の量で含有させる。Ni含有量が10%未満では目的とする耐食性と靱性が得られない。Ni含有量が22%を超えるとコスト高が著しくなる。Ni含有量の下限は12%であることが好ましく、13%であることがさらに好ましい。また、Ni含有量の上限は20%であることが好ましく、16%であることがさらに好ましい。
[Ni: 10-22%]
Ni is a stabilizing element of the austenite phase and also has an effect of increasing the zero ductility temperature. Ni is contained in an amount of 10% to 22%. If the Ni content is less than 10%, the desired corrosion resistance and toughness cannot be obtained. If the Ni content exceeds 22%, the cost increases significantly. The lower limit of the Ni content is preferably 12%, and more preferably 13%. Further, the upper limit of the Ni content is preferably 20%, and more preferably 16%.

 [Si:2.5~7%]
 Siは、濃硝酸中での耐食性を高めるために2.5%以上7%以下の量で含有させる。硝酸中での耐食性を確保するシリケート皮膜を形成するためにSiを2.5%以上含有する。一方、Siを過剰に含有するとゼロ延性温度が低下する。さらにコストアップになるだけでなく、溶接性の低下を招くため、Si含有量の上限を7%とする。Si含有量の下限は3.0%であることが好ましく、3.5%であることがさらに好ましい。Si含有量の上限は6%であることが好ましく、5%であることがさらに好ましい。
[Si: 2.5-7%]
Si is contained in an amount of 2.5% or more and 7% or less in order to enhance the corrosion resistance in concentrated nitric acid. In order to form a silicate film that ensures corrosion resistance in nitric acid, Si is contained in an amount of 2.5% or more. On the other hand, when Si is contained excessively, the zero ductility temperature is lowered. Further, not only the cost is increased, but also the weldability is lowered, so the upper limit of the Si content is set to 7%. The lower limit of the Si content is preferably 3.0%, and more preferably 3.5%. The upper limit of the Si content is preferably 6%, and more preferably 5%.

 [Mn:10%以下]
 Mnは、オーステナイト相の安定化元素であり、脱酸剤としても含有するので、10%以下の量で含有させる。Mn含有量が10%を超えると、耐食性の低下、溶接時の高温割れ、さらには加工性の低下を招く。Mn含有量の上限は6%であることが好ましく、4%であることがさらに好ましい。また、Mnの上記の効果を確実に得るためには、Mn含有量は0.5%以上であることが好ましく、1.0%以上であることがさらに好ましい。
[Mn: 10% or less]
Mn is a stabilizing element of the austenite phase and is also contained as a deoxidizing agent. If the Mn content exceeds 10%, the corrosion resistance decreases, hot cracking during welding, and further the workability decreases. The upper limit of the Mn content is preferably 6%, and more preferably 4%. Moreover, in order to acquire the said effect of Mn reliably, it is preferable that Mn content is 0.5% or more, and it is further more preferable that it is 1.0% or more.

 [sol.Al:0.03%以下]
 Alは、脱酸剤として鋼中に含まれるが、Alを過剰に含有すると有害な介在物を生成するため、sol.Alの含有量は0.03%以下とする。
[Sol.Al: 0.03% or less]
Al is contained in the steel as a deoxidizing agent. However, since excessive inclusion of Al generates harmful inclusions, the content of sol.Al is set to 0.03% or less.

 [P:0.03%以下、S:0.03%以下]
 PおよびSは、いずれも、耐食性、溶接性に有害な元素であり、それぞれの含有量は低いほど好ましい。そこで、P含有量は0.03%以下、S含有量は0.03%以下とする。
[P: 0.03% or less, S: 0.03% or less]
P and S are both elements harmful to corrosion resistance and weldability, and the lower the content of each, the better. Therefore, the P content is 0.03% or less, and the S content is 0.03% or less.

 [N:0.035%以下]
 Nは、Nb、Ti、Ta、Zrとの親和性が高く、これらの元素によるCの固定を阻害することから、N含有量はできるだけ低い方が好ましい。そこで、N含有量は0.035%以下とする。
[N: 0.035% or less]
N has a high affinity with Nb, Ti, Ta, and Zr, and inhibits the fixation of C by these elements. Therefore, the N content is preferably as low as possible. Therefore, the N content is set to 0.035% or less.

 [Nb、Ti、Ta、Zrの一種または2種以上の合計:0.05~0.7%]
 Nb、Ti、Ta、Zrは、いずれも、Cを固定して鋭敏化による粒界耐食性の低下を抑制する効果があり、特に溶接熱影響部の耐食性改善に有効な元素である。これらの元素の合計含有量が0.05%未満では、耐粒界腐食性の改善効果を得られず、さらに低融点Ni-Si系金属間化合物の形成による熱間加工割れが大きくなる。一方、これらの元素の合計含有量0.7%を超えると加工性がする。そこで、これらの元素の含有量は、1種または複数種の合計で0.05%以上0.7%以下とする。
[One or more of Nb, Ti, Ta and Zr: 0.05 to 0.7%]
Nb, Ti, Ta, and Zr all have an effect of fixing C and suppressing the decrease in intergranular corrosion resistance due to sensitization, and are particularly effective elements for improving the corrosion resistance of the weld heat affected zone. If the total content of these elements is less than 0.05%, the effect of improving the intergranular corrosion resistance cannot be obtained, and hot working cracks due to the formation of a low melting point Ni—Si intermetallic compound become large. On the other hand, if the total content of these elements exceeds 0.7%, workability is obtained. Therefore, the content of these elements is 0.05% or more and 0.7% or less in total of one or more kinds.

 [製造条件]
 本発明に係るオーステナイト系ステンレス鋼の製造方法は、上記化学組成を有するステンレス鋼のスラブを、熱間圧延時の加熱温度をThとし、(1)式:Th=1135-90Si-2.9Cr+40Ni-ΔT中のΔTが30℃以上である加熱温度Thに加熱して熱間圧延を行う熱間圧延工程と、好ましくはさらに1100~1160℃の温度範囲で熱処理した後、100℃/分以上の冷却速度で冷却を行う熱処理工程(焼鈍工程)とからなる。
[Production conditions]
Method of manufacturing austenitic stainless steel according to the present invention, a slab of stainless steel having the above chemical composition, the heating temperature during the hot rolling and T h, (1) formula: T h = 1135-90Si-2. a hot rolling step of performing hot rolling 9Cr + 40Ni-ΔT ΔT in is heated to a heating temperature T h at 30 ° C. or higher, after heat treatment at preferably a temperature range of more 1100 ~ 1160 ℃, 100 ℃ / min It consists of a heat treatment step (annealing step) for cooling at the above cooling rate.

 「熱間圧延工程」
 熱間圧延に最適な加熱温度範囲を明らかにするため、高温捩り試験によって化学組成と高温変形能との関係を調べた。それにより熱間圧延におけるゼロ延性を調査することができる。
"Hot rolling process"
In order to clarify the optimum heating temperature range for hot rolling, the relationship between chemical composition and high temperature deformability was investigated by high temperature torsion test. Thereby, the zero ductility in hot rolling can be investigated.

 高温捩り試験では、平行部直径8mm、長さ30mmの試験片の一方を固定して、所定の温度に保持した状態で回転速度300rpm(歪速度4.2sec-1)、軸力0kgfで一方向に捩りを加えて破断するまでの回転数を捩り回数とした。 In the high-temperature torsion test, one of the test pieces having a parallel part diameter of 8 mm and a length of 30 mm is fixed and held at a predetermined temperature, with a rotational speed of 300 rpm (strain speed of 4.2 sec −1 ) and an axial force of 0 kgf in one direction. The number of rotations until twisting was applied and breaking was taken as the number of twists.

 一例として、表1に供試鋼1として示す化学組成を有する高Siステンレス鋼の試験片を用いて高温戻り試験を実施した結果を、加熱温度と捩り回数との関係として図1に示す。 As an example, FIG. 1 shows the relationship between the heating temperature and the number of twists as a result of conducting a high temperature return test using a test piece of high Si stainless steel having the chemical composition shown in Table 1 as test steel 1.

Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001

 図1において、捩り回数は1100℃付近で極大を示し、それよりも高温では捩り回数が著しい低下傾向を示し、1275℃では捩り始めると同時に破断した。すなわち、表1に供試鋼1として示す高Siステンレス鋼の延性がゼロになる温度(以下、「ゼロ延性温度」という)は、おおむね1275℃であることがわかる。 In FIG. 1, the number of twists showed a maximum at around 1100 ° C., and the number of twists decreased significantly at a temperature higher than that, and at 1275 ° C., it started to twist and broke at the same time. That is, it can be seen that the temperature at which the ductility of the high Si stainless steel shown as the test steel 1 in Table 1 becomes zero (hereinafter referred to as “zero ductility temperature”) is approximately 1275 ° C.

 同様の方法を用いてNb、Ta、Ti、Zrの1種又は2種以上を含有する種々の化学組成からなる高Siステンレス鋼について上記高温捩り試験を行い、ゼロ延性温度を調べた。その結果、ゼロ延性温度(T0)は、Si、Cr、Ni濃度との関係として下記回帰式(2)により表すことができることを見出した。 Using the same method, the high-temperature torsion test was conducted on high-Si stainless steels having various chemical compositions containing one or more of Nb, Ta, Ti, and Zr, and the zero ductility temperature was examined. As a result, it was found that the zero ductility temperature (T 0 ) can be expressed by the following regression equation (2) as the relationship with the Si, Cr, Ni concentration.

  T0=1135-90Si-2.9Cr+40Ni ・・・ (2)
 熱間加工における加熱温度(Th)をゼロ延性温度(T0)よりも30℃以上低くすること、すなわち、加熱温度(Th)を、下記(1)式:
  Th=1135-90Si-2.9Cr+40Ni-ΔT ・・・ (1)
におけるΔTが30℃以上となる温度に設定することによって、Ni-Si-X三元系(X=Nb、Ta、Ti、Zr)金属間化合物を起点とする割れは起き難くなり、ヘゲ疵は減少する。ヘゲ疵が少なくなれば、簡便な表面手入れで次工程へと進めることができるため、経済性に優れる。
T 0 = 1135-90Si-2.9Cr + 40Ni (2)
The heating temperature (T h ) in the hot working is made 30 ° C. lower than the zero ductility temperature (T 0 ), that is, the heating temperature (T h ) is expressed by the following formula (1):
T h = 1135-90Si-2.9Cr + 40Ni-ΔT (1)
By setting the temperature at ΔT to 30 ° C. or higher, cracking starting from the Ni—Si—X ternary system (X = Nb, Ta, Ti, Zr) intermetallic compound is less likely to occur. Decrease. If the amount of lashes is reduced, it is possible to proceed to the next process with simple surface care, which is excellent in economic efficiency.

 鍛造スラブを所定の温度で加熱した後に、熱間圧延により4mm厚とした。その後、酸洗によりスケールを除去した後、以下の方法でヘゲ疵発生率を調査した。 After the forging slab was heated at a predetermined temperature, the thickness was 4 mm by hot rolling. Thereafter, the scale was removed by pickling, and then the rate of occurrence of baldness was investigated by the following method.

 鋼板表面を100mm単位のメッシュに区切り、調査した全体のメッシュ数のうち、ヘゲ疵が存在するメッシュ数の比率をヘゲ疵発生率(%)とした。ヘゲ疵発生率が5%以下であれば簡便な手直しで次工程へと進めることができる。 The steel plate surface was divided into 100 mm unit meshes, and the ratio of the number of meshes with scabs in the total number of meshes investigated was defined as the scab generation rate (%). If the rate of occurrence of lashes is 5% or less, it is possible to proceed to the next step with a simple rework.

 表1に示す供試鋼1の成分から、(2)式によりゼロ延性温度T0=1275℃が得られる。図2に、供試鋼1(表1)のΔTとヘゲ疵発生率との関係を示す。 From the components of the test steel 1 shown in Table 1, the zero ductility temperature T 0 = 1275 ° C. is obtained by the equation (2). FIG. 2 shows the relationship between ΔT of the test steel 1 (Table 1) and the rate of occurrence of lashes.

 図2のグラフに示すように、ΔT≧30℃を満足するように熱間圧延の加熱温度Thを設定することにより、ヘゲ疵発生率が5%以下となる。一方、ΔTが30℃よりも小さく、ゼロ延性温度に近くなるほど、ヘゲ疵の発生率は急激に高くなった。 As shown in the graph of FIG. 2, by setting the heating temperature T h of hot rolling so as to satisfy the [Delta] T ≧ 30 ° C., scab defect occurrence rate of 5% or less. On the other hand, as ΔT was smaller than 30 ° C. and closer to the zero ductility temperature, the rate of occurrence of lashes rapidly increased.

 すなわち、ヘゲ疵を最小限にするためには、ΔTが30℃以上、望ましくは60℃以上となるように、熱間圧延の加熱温度Thを設定すればよい。この加熱温度への保持時間は特に制限されない。本発明では、加熱温度は圧延後のヘゲ疵発生を防止するために設定されるので、スラブの表面温度が所定の温度になればよい。しかし、熱間圧延に支障をきたさないようにするには、スラブ中心部までほぼ均一な温度になるまで加熱することが好ましい。これに要する加熱時間はスラブの大きさにもよるが、一般には加熱時間を60分間以上とすることが好ましい。 That is, in order to minimize the scab defect is, [Delta] T is 30 ° C. or more, preferably such that 60 ° C. or higher may be set the heating temperature T h of the hot rolling. The holding time to this heating temperature is not particularly limited. In the present invention, the heating temperature is set in order to prevent the occurrence of baldness after rolling, so that the surface temperature of the slab may be a predetermined temperature. However, in order not to interfere with hot rolling, it is preferable to heat the slab to the center until the temperature is substantially uniform. The heating time required for this depends on the size of the slab, but in general, the heating time is preferably 60 minutes or more.

 ΔTの上限は特に規定しない。通常の熱間圧延設備では熱間圧延終止温度が700℃以上であれば熱間圧延を実施することが可能である。望ましくはこの終止温度を950℃以上とする。 The upper limit of ΔT is not specified. In a normal hot rolling facility, hot rolling can be performed if the hot rolling end temperature is 700 ° C. or higher. Desirably, the end temperature is set to 950 ° C. or higher.

 熱間圧延は一段または多段で実施することができる。多段圧延の場合、必要であれば圧延スタンド間で加熱することができる。この時の加熱温度は、上記のΔTが30℃以上となる温度にする必要は特段ないが、好ましくはΔTが30℃以上となる温度にする。それにより、その後の熱間圧延時に表面の結晶粒径が細粒化するため、割れの伝播が起こりにくく、ヘゲの発生がさらに抑制される。熱間圧延後は一般に常法により酸洗して圧延材表面の酸化スケールを除去する。 Hot rolling can be performed in one or more stages. In the case of multi-stage rolling, if necessary, it can be heated between rolling stands. The heating temperature at this time is not particularly required to be a temperature at which ΔT is 30 ° C. or higher, but is preferably a temperature at which ΔT is 30 ° C. or higher. Thereby, since the crystal grain size of the surface is refined during the subsequent hot rolling, the propagation of cracks hardly occurs, and the occurrence of lashes is further suppressed. After hot rolling, pickling is generally performed by a conventional method to remove oxide scale on the surface of the rolled material.

 [熱処理工程]
 熱間圧延により得られたステンレス鋼板は、焼鈍のための熱処理を行うことによって機械的特性(伸び、耐力)を調整することができるので、熱間圧延後に熱処理を実施することが好ましい。熱処理温度を高くすると、伸びは上昇するものの耐力が低下する。熱処理後の冷却速度が遅いと、クロム炭化物が析出するため、耐食性が劣化する。したがって、熱処理温度およびその後の冷却速度は、伸びと耐力を両立でき、かつ鋭敏化を防ぐように設定する必要がある。
[Heat treatment process]
Since the stainless steel plate obtained by hot rolling can adjust mechanical characteristics (elongation, yield strength) by performing a heat treatment for annealing, it is preferable to perform the heat treatment after the hot rolling. When the heat treatment temperature is increased, the proof stress is reduced although the elongation is increased. When the cooling rate after the heat treatment is slow, chromium carbide precipitates, and the corrosion resistance deteriorates. Therefore, it is necessary to set the heat treatment temperature and the subsequent cooling rate so as to achieve both elongation and yield strength and prevent sensitization.

 図3には、供試鋼1の熱処理温度と0.2%耐力および伸びとの関係を示す。図3のグラフにおける丸プロットは0.2%耐力(MPa)を、四角プロットは伸び(%)をそれぞれ示す。 FIG. 3 shows the relationship between the heat treatment temperature of the test steel 1, the 0.2% proof stress and the elongation. The circle plot in the graph of FIG. 3 shows 0.2% yield strength (MPa), and the square plot shows elongation (%).

 図3に示すように、1100℃以上1160℃以下で熱処理することによって、良好な伸び性と十分な耐力、具体的には、伸び:50~53%,0.2%耐力:325~290MPaを示すステンレス鋼を得ることができる。 As shown in FIG. 3, by performing heat treatment at 1100 ° C. or more and 1160 ° C. or less, good elongation and sufficient yield strength, specifically, elongation: 50 to 53%, 0.2% yield strength: 325 to 290 MPa The stainless steel shown can be obtained.

 さらに、熱処理後の冷却速度が遅いと鋭敏化が起こり、粒界腐食感受性が高まる。冷却速度を100℃/分以上とすることによって、鋭敏化も生じず、良好な硝酸耐食性を示すステンレス鋼となる。 Furthermore, when the cooling rate after heat treatment is slow, sensitization occurs and the susceptibility to intergranular corrosion increases. By setting the cooling rate to 100 ° C./min or more, sensitization does not occur, and the stainless steel exhibits good nitric acid corrosion resistance.

 このように、本発明によれば、熱間圧延の過程でヘゲ疵を発生することなく、高温、高濃度硝酸環境中で使用するのに好適な高Si含有オーステナイト系ステンレス鋼を確実に製造することができる。 Thus, according to the present invention, a high Si content austenitic stainless steel suitable for use in a high-temperature, high-concentration nitric acid environment can be reliably produced without generating lashes in the hot rolling process. can do.

 上記表1に示す成分供試鋼1~5を高周波電気炉溶解した10kg鋳塊より鍛造して得たスラブを、表2に示す所定温度で120分間加熱して、2段圧延機で厚さ4mmまで熱間圧延した。得られたステンレス鋼板を酸洗してスケールを除去した状態で、鋼板表面のヘゲ疵発生率を前述した方法で調査した。結果を表2にまとめて示す。 A slab obtained by forging a 10 kg ingot in which the component test steels 1 to 5 shown in Table 1 above were melted by a high-frequency electric furnace was heated at a predetermined temperature shown in Table 2 for 120 minutes, and the thickness was measured with a two-stage rolling mill Hot rolled to 4 mm. In the state where the obtained stainless steel plate was pickled and the scale was removed, the rate of occurrence of lashes on the surface of the steel plate was investigated by the method described above. The results are summarized in Table 2.

Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000002

 表2に示すように、熱間圧延時の加熱温度を成分から計算されるゼロ延性温度T0(℃)よりも30℃以上低くしたものは、ヘゲ疵発生率が5%以下であった。 As shown in Table 2, when the heating temperature at the time of hot rolling was lower by 30 ° C. or more than the zero ductility temperature T 0 (° C.) calculated from the components, the rate of occurrence of whipping was 5% or less. .

 これに対し、加熱温度が成分から計算されるゼロ延性温度T0(℃)よりも30℃低い温度より高くなった場合には、ヘゲ疵発生率が5%を越え、熱間圧延の過程でヘゲ疵を発生することなく、高温、高濃度硝酸環境中で使用するのに好適な高Si含有オーステナイト系ステンレス鋼を確実に製造することができなかった。 On the other hand, when the heating temperature is higher than a temperature that is 30 ° C. lower than the zero ductility temperature T 0 (° C.) calculated from the components, the rate of occurrence of whipping exceeds 5%, and the hot rolling process Thus, a high Si content austenitic stainless steel suitable for use in a high-temperature, high-concentration nitric acid environment could not be reliably produced without generating baldness.

Claims (2)

 質量%で、C:0.04%以下、Cr:7~20%、Ni:10~22%、Si:2.5~7%、Mn:10%以下、sol.Al:0.03%以下、P:0.03%以下、S:0.03%以下、N:0.035%以下、Nb、Ti、Ta、Zrのうち1種または2種以上の合計:0.05~0.7%を含有し、残部がFeおよび不純物からなる化学組成を有するステンレス鋼のスラブを、熱間圧延時の加熱温度をThとし、下記(1)中のΔTが30℃以上である加熱温度Thに加熱して熱間圧延を行う熱間圧延工程を含むことを特徴とするオーステナイト系ステンレス鋼の製造方法。
  Th=1135-90Si-2.9Cr+40Ni-ΔT ・・・ (1)
In mass%, C: 0.04% or less, Cr: 7-20%, Ni: 10-22%, Si: 2.5-7%, Mn: 10% or less, sol.Al: 0.03% or less , P: 0.03% or less, S: 0.03% or less, N: 0.035% or less, total of one or more of Nb, Ti, Ta, Zr: 0.05 to 0.7 % containing, a slab of stainless steel having a chemical composition the balance being Fe and impurities, the heating temperature during the hot rolling and T h, the heating temperature T [Delta] T in the following (1) is 30 ° C. or higher A method for producing an austenitic stainless steel, comprising a hot rolling step of heating to h and performing hot rolling.
T h = 1135-90Si-2.9Cr + 40Ni-ΔT (1)
 前記熱間圧延で得られたオーステナイト系ステンレス鋼を1100~1160℃の温度範囲で熱処理し、次いで100℃/分以上の冷却速度で冷却を行う熱処理工程をさらに含む、請求項1に記載の方法。 The method according to claim 1, further comprising a heat treatment step of heat-treating the austenitic stainless steel obtained by the hot rolling in a temperature range of 1100 to 1160 ° C and then cooling at a cooling rate of 100 ° C / min or more. .
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JP (1) JP5418734B2 (en)
KR (1) KR101495483B1 (en)
CN (1) CN103826766B (en)
SI (1) SI2737961T1 (en)
WO (1) WO2013018628A1 (en)

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JP2016079481A (en) * 2014-10-20 2016-05-16 新日鐵住金株式会社 High Si austenitic stainless steel containing composite non-metallic inclusions
JP2020104145A (en) * 2018-12-27 2020-07-09 ヤマコー株式会社 Method of forming high silicon stainless steel

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CN110257690B (en) * 2019-06-25 2021-01-08 宁波宝新不锈钢有限公司 Resource-saving austenitic heat-resistant steel and preparation method thereof

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JP2020104145A (en) * 2018-12-27 2020-07-09 ヤマコー株式会社 Method of forming high silicon stainless steel

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JP5418734B2 (en) 2014-02-19
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SI2737961T1 (en) 2017-05-31
EP2737961A1 (en) 2014-06-04
EP2737961A4 (en) 2015-06-03
KR20140037969A (en) 2014-03-27
JPWO2013018628A1 (en) 2015-03-05
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KR101495483B1 (en) 2015-02-24
EP2737961B1 (en) 2016-12-14

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