EP2628814A1 - Ferritic stainless steel excellent in heat resistance and workability - Google Patents

Ferritic stainless steel excellent in heat resistance and workability Download PDF

Info

Publication number
EP2628814A1
EP2628814A1 EP11832650.3A EP11832650A EP2628814A1 EP 2628814 A1 EP2628814 A1 EP 2628814A1 EP 11832650 A EP11832650 A EP 11832650A EP 2628814 A1 EP2628814 A1 EP 2628814A1
Authority
EP
European Patent Office
Prior art keywords
less
content
steel
temperature
mass
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP11832650.3A
Other languages
German (de)
French (fr)
Other versions
EP2628814A4 (en
EP2628814B1 (en
Inventor
Tetsuyuki Nakamura
Hiroki Ota
Yasushi Kato
Hiroyuki Ogata
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Steel Corp
Original Assignee
JFE Steel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by JFE Steel Corp filed Critical JFE Steel Corp
Publication of EP2628814A1 publication Critical patent/EP2628814A1/en
Publication of EP2628814A4 publication Critical patent/EP2628814A4/en
Application granted granted Critical
Publication of EP2628814B1 publication Critical patent/EP2628814B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N13/00Exhaust or silencing apparatus characterised by constructional features ; Exhaust or silencing apparatus, or parts thereof, having pertinent characteristics not provided for in, or of interest apart from, groups F01N1/00 - F01N5/00, F01N9/00, F01N11/00
    • F01N13/16Selection of particular materials
    • 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
    • C21D6/002Heat treatment of ferrous alloys containing Cr
    • 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
    • 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
    • C21D8/0236Cold 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
    • 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
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0273Final recrystallisation annealing
    • 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
    • C22C38/004Very low carbon steels, i.e. having a carbon content of less than 0,01%
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • 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
    • C22C38/20Ferrous alloys, e.g. steel alloys containing chromium with copper
    • 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
    • C22C38/22Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
    • 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
    • C22C38/24Ferrous alloys, e.g. steel alloys containing chromium with vanadium
    • 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
    • C22C38/30Ferrous alloys, e.g. steel alloys containing chromium with cobalt
    • 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
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • 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
    • C21D2211/005Ferrite

Definitions

  • the present invention relates to ferritic stainless steel having high heat resistance (a thermal fatigue property, oxidation resistance and a high-temperature fatigue property) and formability which can be ideally used for the parts of an exhaust system which are used in a high temperature environment such as an exhaust pipe and a catalyst outer cylinder (also called a converter case) of an automobile and a motorcycle and an exhaust air duct of a thermal electric power plant.
  • high heat resistance a thermal fatigue property, oxidation resistance and a high-temperature fatigue property
  • formability which can be ideally used for the parts of an exhaust system which are used in a high temperature environment such as an exhaust pipe and a catalyst outer cylinder (also called a converter case) of an automobile and a motorcycle and an exhaust air duct of a thermal electric power plant.
  • the parts of an exhaust system such as an exhaust manifold, an exhaust pipe, a converter case and a muffler which are used in the environment of the exhaust system of an automobile are required to be excellent in a thermal fatigue property, a high-temperature fatigue property and oxidation resistance (hereinafter, these properties are collectively called heat resistance).
  • the parts such as an exhaust manifold are subjected to heating and cooling due to the repetition of start and stop of engine operation in a state in which they are restrained by the surrounding parts, the thermal expansion and contraction of the material of the parts are restricted, which results in the occurrence of thermal strain.
  • the fatigue phenomenon due to this thermal strain is thermal fatigue.
  • the parts are continuously subjected to vibration while they are heated in the initiation of engine operation.
  • the fatigue phenomenon due to the accumulation of strain caused by this vibration is high-temperature fatigue.
  • the former is low-cycle fatigue and the latter is high-cycle fatigue and both are completely different fatigue phenomena.
  • Type429 containing 14Cr-0.9Si-0.4Nb
  • an exhaust gas temperature has become higher than 900°C with the improvement of engine performance, the thermal fatigue property of Type429 has become unsatisfactory.
  • Patent Literature 2 discloses ferritic stainless steel to be used for the parts of an exhaust gas flow channel of an automobile.
  • Nb 0.50 mass% or less
  • Cu 0.8 mass% or more and 2.0 mass% or less
  • V 0.03 mass% or more and 0.20 mass% or less are added to steel having a Cr content of 10 mass% or more and 20 mass% or less.
  • Patent Literature 3 discloses ferritic stainless steel excellent in a thermal fatigue property.
  • Patent Literatures 3 Ti: 0.05 mass% or more and 0.30 mass% or less, Nb: 0.10 mass% or more and 0.60 mass% or less, Cu: 0.8 mass% or more and 2.0 mass% or less and B: 0.0005 mass% or more and 0.02 mass% or less are added to steel having a Cr content of 10 mass% or more and 20 mass% or less.
  • Patent Literature 4 discloses ferritic stainless steel to be used for the parts of an exhaust gas flow channel of an automobile.
  • Cu: 1 mass% or more and 3 mass% or less is added to steel having a Cr content of 15 mass% or more and 25 mass% or less.
  • the present invention has been completed in view of the situation described above, and an object of the present invention is to provide ferritic stainless steel excellent in heat resistance (oxidation resistance, a thermal fatigue property and a high-temperature fatigue property) and formability, while preventing a decrease in oxidation resistance due to Cu, without adding expensive chemical elements such as Mo and W.
  • the meaning of "excellent in heat resistance” is that oxidation resistance, a thermal fatigue property and a high-temperature fatigue property are equivalent to or better than those of SUS444. Specifically, it means that oxidation resistance at a temperature of 950°C is equivalent to or better than that of SUS444, that a thermal fatigue property when temperature fluctuations repeatedly occur between the temperatures of 100°C and 850°C is equivalent to or better than that of SUS444 and that a high-temperature fatigue property at a temperature of 850°C is equivalent to or better than that of SUS444.
  • the meaning of "excellent in formability" according to the present invention is that a mean elongation in the three directions at room temperature is 36% or more.
  • the present inventors diligently conducted investigations in order to develop ferritic stainless steel excellent in oxidation resistance and a thermal fatigue property by preventing a decrease in oxidation resistance due to Cu which occurs in the conventional methods without adding expensive chemical elements such as Mo or W.
  • a high strength in high-temperature can be achieved by adding the combination of Nb: 0.3 mass% or more and 0.65 mass% or less and Cu: 1.0 mass% or more and 2.5 mass% or less.
  • a thermal fatigue property can be improved in a wide temperature range.
  • the present inventors found that a decrease in oxidation resistance due to the addition of Cu can be prevented by adding an appropriate amount of Al (0.2 mass% or more and 1.0 mass% or less).
  • the present inventors found that, therefore, heat resistance (a thermal fatigue property and oxidation resistnace) equivalent to or better than that of SUS444 can be achieved only by controlling the contents of Nb, Cu and A1 to the appropriate range as described above without adding Mo or W.
  • the present inventors diligently conducted investigations regarding a method for improving oxidation resistance in an environment containing water vapor which is assumed in the case where the ferritic stainless steel is practically used for an exhaust manifold and the like, and found that oxidation resistance in an atmosphere containing water vapor (hereinafter, called water vapor oxidation resistance) also becomes equivalent to or better than that of SUS444 by adjusting a Si content (0.4 mass% or more and 1.0 mass% or less).
  • a fatigue resistance property against vibration in practical service conditions of the parts of the exhaust system of an automobile such as an exhaust manifold is also important. Therefore, the present inventors diligently conducted investigations regarding a method for improving a high-temperature fatigue property, and found that a high-temperature fatigue property also becomes equivalent to or better than that of SUS444 by adjusting the balance of a Si content and an Al content (Si ⁇ Al).
  • the present invention provides ferritic stainless steel excellent in heat resistance and formability having a chemical composition containing, by mass%, C: 0.015% or less, Si: 0.4 % or more and 1.0% or less, Mn: 1.0% or less, P: 0.040% or less, S: 0.010% or less, Cr: 12% or more and less than 16%, N: 0.015% or less, Nb: 0.3% or more and 0.65% or less, Ti: 0.15% or less, Mo: 0.1% or less, W: 0.1% or less, Cu: 1.0% or more and 2.5 % or less and Al: 0.2% or more and 1.0% or less, while the relationship Si ⁇ Al is satisfied, and the balance being Fe and inevitable impurities.
  • the present invention provides ferritic stainless steel excellent in heat resistance and formability having a chemical composition further containing one, two or more chemical elements selected from among, by mass%, B: 0.003% or less, REM: 0.08% or less, Zr: 0.5% or less, V: 0.5% or less, Co: 0.5% or less and Ni: 0.5% or less.
  • ferritic stainless steel having heat resistance (a thermal fatigue property, oxidation resistance and a high-temperature fatigue property) equivalent to or better than that of SUS444 (JIS G 4305) and excellent formability can be obtained without adding expensive Mo or W. Therefore, the steel according to the present invention can be ideally used for the parts of the exhaust system of an automobile.
  • % used when describing chemical composition always denotes mass%.
  • the thermal fatigue life of the specimen was observed by performing a thermal cycle heat treatment in which a restraint ratio was 0.30 and in which heating and cooling were repeated so that temperature fluctuations repeatedly occurred between 100°C and 850°C as illustrated in Fig. 2 .
  • the thermal fatigue life represents as the number of cycles at which the stress first started to continuously decrease from that in the previous cycle.
  • the stress was derived by calculated as the quotient of the load detected at 100°C divided by the cross section area of the soaked parallel portion of a test specimen indicated in Fig. 1 . This number of cycles corresponded to that at which a crack occurred in the test specimen.
  • SUS444 (19%Cr-2%Mo-0.5%Nb steel) for comparison.
  • Fig. 4 illustrates the influence of Cu content on thermal fatigue life in the thermal fatigue test described above. This figure indicates that thermal fatigue life equivalent to or longer than that of SUS444 (about 1350 cycles) can be achieved by setting the Cu content to be 1.0% or more. Therefore, it is necessary that the Cu content be 1.0% or more in order to improve a thermal fatigue property.
  • test specimen of 30 mm ⁇ 20 mm was cut out of the cold rolled steel sheet obtained as described above, then a hole of 4 mm ⁇ was punched in the upper part of the test specimen, then the surface and the edge face of the specimen was polished with a #320 emery paper, then degreased and then used in a continuous oxidation test in air described below.
  • test specimen described above was held in a furnace in air at a temperature of 950°C for duration of 200 hours, and then an increase in weight per unit area due to oxidation (g/m 2 ) was derived from the observed difference in the mass of the test specimen before and after the heating test.
  • Fig. 5 illustrates the influence of Al content on the increase in weight due to oxidation in the continuous oxidation test in air described above. This figure indicates that an oxidation resistance equivalent to or better than that of SUS444 (increase in weight due to oxidation: 19 g/m 2 or less) can be achieved by setting the Al content to be 0.2% or more.
  • the steel ingot was subjected to hot rolling, hot rolled annealing, cold rolling and finishing annealing and made into a cold rolled and annealed steel sheet having a thickness of 2 mm.
  • a test specimen of 30 mm ⁇ 20 mm was cut out of the cold rolled steel sheet obtained as described above. Then a hole of 4 mm ⁇ was punched in the upper part of the test specimen, then the surface and the edge face of the specimen was polished with a #320 emery paper. Then degreased and then used in a continuous oxidation test in water vapor atmosphere described below.
  • test specimen described above was held in a furnace in a water vapor atmosphere in which a gas of 10 vol%CO 2 -20 vol%H 2 O-5 vol%O 2 -bal. N 2 was blown at a rate of 0.5 L/min, and then an increase in weight per unit area due to oxidation (g/m 2 ) was derived from the observed difference in the mass of the specimen before and after the heating test.
  • Fig. 6 illustrates the influence of the Si content on the increase in weight due to oxidation in the oxidation test in water vapor atmosphere described above. This figure indicates that water vapor oxidation resistance equivalent to that of SUS444 (increase in weight due to oxidation: 37g/m 2 or less) cannot be achieved, unless the Si content is set to be 0.4% or more.
  • the high-temperature fatigue property of the test specimen described above was evaluated by using a Schenck type fatigue testing machine and by performing reversed vibration of 22 Hz (1300 rpm) at a temperature of 850°C.
  • a bending stress of 70 MPa was exerted on the surface of the steel sheet during the test, and the fatigue property was evaluated in terms of a number of cycles until fracture occurred.
  • Fig. 7 illustrates the influence of Si - Al on the number of cycles in the high-temperature fatigue test described above. This figure indicates that it is necessary to satisfy the relationship Si ⁇ Al in order to achieve a high-temperature fatigue property equivalent to that of SUS444 (24 ⁇ 10 5 cycles).
  • the steel ingot was subjected to hot rolling, hot rolled annealing, cold rolling and finishing annealing and made into a cold rolled and annealed steel sheet having a thickness of 2 mm.
  • a test specimen of 30 mm ⁇ 20 mm was cut out from the cold rolled steel sheet obtained as described above, then a hole of 4 mm ⁇ was punched in the upper part of the test specimen.
  • the surface and the edge face of the specimen was polished with a #320 emery paper, then degreased and then used in the oxidation test in water vapor atmosphere described above.
  • Fig. 8 illustrates the influence of the Cr content on the increase in weight due to oxidation in the oxidation test in water vapor atmosphere described above. This figure indicates that water vapor oxidation resistance equivalent to that of SUS444 (increase in weight due to oxidation: 37 g/m 2 or less) can be achieved in the case where the Cr content is 12% or more.
  • Tensile tests were conducted at room temperature with tensile test pieces conforming to JIS NO. 13B which were made of these cold rolled and annealed steel sheets.
  • Tensile test pieces had the directions of tension respectively in the rolling direction (L direction), in the direction at right angles to the rolling direction (C direction) and in the direction at a 45° angles to the rolling direction (D direction).
  • a mean elongation was derived from the breaking elongations which were obtained by performing tensile tests in the three directions at room temperature and calculated by the equation below.
  • Fig. 9 illustrates the influence of the Cr content on the mean value of elongations in the three directions (L, C and D directions) in the tensile test. This figure indicates that excellent formability in terms of the mean elongation in the three directions (L, C and D directions) of 36% or more can be achieved in the case where the Cr content is less than 16%.
  • the present invention has been completed by conducting further investigations on the basis of the results of the fundamental experiments described above.
  • ferritic stainless steel according to the present invention will be described in detail hereafter. Firstly, the chemical composition according to the present invention will be described.
  • C 0.015% or less
  • the C content is set to be 0.015% or less.
  • the C content it is preferable that the C content be as small as possible from the viewpoint of achieving formability and that the carbon content be 0.008% or less.
  • the C content it is preferable that the C content be 0.001% or more in order to achieve strength which is required of the parts of an exhaust system, more preferably 0.002% or more and 0.008% or less.
  • Si 0.4% or more and 1.0% or less Si is a chemical element which is important for improving oxidation resistance in a water vapor atmosphere. As Fig. 6 indicates, it is necessary to set Si content to be 0.4% or more in order to achieve water vapor oxidation resistance equivalent to that of SUS444. On the other hand, there is a significant decrease in formability in the case where the Si content is more than 1.0%. Therefore, the Si content is set to be 0.4% or more and 1.0% or less, preferably 0.5% or more and 0.9% or less.
  • the mechanism through which water vapor oxidation resistance is increased in the case where the Si content is 0.4% or more is not clear, it is considered that a dense continuous oxide layer is formed on the surface of a steel sheet in the case where the Si content is 0.4% or more and the penetration of gas elements from outside is prevented, which results in an increase in water vapor oxidation resistance. It is preferable that the Si content be 0.5% or more in the case where there is a necessity of oxidation resistance in a severer environment.
  • Mn 1.0% or less
  • Mn is a chemical element which causes an increase in the strength of steel and which is effective as a deoxidation agent, a ⁇ phase tends to be formed at a high temperature in the case where Mn content is excessively large, the excessive Mn content results in a decrease in heat resistance. Therefore, the Mn content is set to be 1.0% or less, preferably 0.7% or less. It is preferable that the Mn content be 0.05% or more in order to realize the effect of increasing strength and deoxidation.
  • P 0.040% or less Since P is a harmful chemical element which causes a decrease in ductility, it is preferable that P content be as small as possible. Therefore, the P content is set to be 0.040% or less, preferably 0.030% or less.
  • S 0.010% or less Since S is a harmful chemical element which causes a decrease in elongation and an r value. S has a negative influence on formability and S causes a decrease in corrosion resistance which is the basic property of stainless steel. It is preferable that S content be as small as possible. Therefore, the S content is set to be 0.010% or less, preferably 0.005% or less.
  • Cr 12% or more and less than 16%
  • Cr is a chemical element which is effective for increasing corrosion resistance and oxidation resistance, which are the characteristics of stainless steel. Sufficient oxidation resistance cannot be achieved in the case where Cr content is less than 12%.
  • Cr is a chemical element which causes an increase in hardness and a decrease in ductility of steel at room temperature by solid solution strengthening, in particular, these negative influences become significant in the case where the Cr content is 16% or more. Therefore, the Cr content is set to be 12% or more and less than 16%, preferably 12% or more and 15% or less.
  • N 0.015% or less
  • N is a chemical element which causes a decrease in the ductility and the formability of steel, and these negative influences are significant in the case where N content is more than 0.015%. Therefore, the N content is set to be 0.015% or less. Incidentally, it is preferable that the N content be as small as possible from the viewpoint of achieving ductility and formability and that the N content be less than 0.010%.
  • Nb 0.3% or more and 0.65% or less
  • Nb is a chemical element which is effective for increasing corrosion resistance, formability and intergranular corrosion resistance at welds by forming carbide, nitride and carbonitride in combination with C and N.
  • Nb is effective for increasing a thermal fatigue property by increasing high-temperature strength.
  • Mo 0.1% or less Since Mo is an expensive chemical element, additionally in view of the purpose of the present invention, Mo is not added positively. However, Mo may be mixed in from the material of steel such as scrap in the range of 0.1% or less. Therefore, Mo content is set to be 0.1% or less.
  • W 0.1% or less Since W is an expensive chemical element like Mo, additionally in view of the purpose of the present invention, W is not added positively. However, W may be mixed in from the material of steel such as scrap in the range of 0.1% or less. Therefore, W content is set to be 0.1% or less.
  • Cu 1.0% or more and 2.5% or less
  • Cu is a chemical element which is very effective for improving a thermal fatigue property.
  • Fig. 3 indicates, it is necessary that Cu content be 1.0% or more in order to achieve a thermal fatigue property equivalent to or better than that of SUS444.
  • ⁇ -Cu is precipitated when cooling is performed after a heat treatment, which results in an increase in the hardness of steel and results in embrittlement tending to occur when hot work is performed.
  • a thermal fatigue property is improved by adding Cu, contrarily the oxidation resistance of steel is decreased, which results in the deterioration of the overall heat resistance. The reason for this has not been fully identified.
  • the Cu content is set to be 1.0% or more and 2.5% or less, preferably 1.1% or more and 1.8% or less.
  • Ti 0.15% or less Ti is effective for improving corrosion resistance, formability and intergranular corrosion resistance of a welded part by fixing C and N like Nb does. However, this effect saturates and there is an increase in the hardness of steel in the case where Ti content is more than 0.15% in the present invention in which Nb is contained. Therefore, the Ti content is set to be 0.15% or less. Since Ti has higher affinity for N than Nb does, Ti tends to form TiN of a large size. Since TiN of a large size tends to become the origin of a crack and causes a decrease in toughness, it is preferable that the Ti content be 0.01% or less in the case where the toughness of a hot rolled steel sheet is necessary. Incidentally, since it is not necessary to positively add Ti in the present invention, the lower limit of the Ti content includes 0%.
  • Al 0.2% or more and 1.0% or less
  • Al is a chemical element which is essential for increasing the oxidation resistance of Cu containing steel as Fig. 5 indicates.
  • Al is effective as a solid solution strengthening element and, in particular, is effective for increasing high-temperature strength at a temperature of higher than 800°C
  • Al is a chemical element which is important for improving a high-temperature fatigue property in the present invention. It is necessary that Al content be 0.2% or more in order to achieve oxidation resistance equivalent to or better than that of SUS444.
  • the Al content is set to be 0.2% or more and 1.0% or less, preferably 0.3% or more and 1.0% or less, more preferably 0.3% or more and 0.5% or less.
  • Al is effective as a solid solution strengthening element and, in particular, effective for increasing high-temperature strength at a high temperature of higher than 800°C
  • Al is a chemical element which is important for improving a high-temperature fatigue property in the present invention as described above
  • Si is a chemical element which is important for effectively utilizing this effect of solid solution strengthening of Al.
  • the amount of Si is less than that of Al
  • there is a decrease in the amounts of solid solution Al because Al preferentially forms oxides and nitrides at high temperature, which decreases the contribution of Al to strengthening.
  • Si is preferentially oxidized and forms a dense continuous oxide layer on the surface of a steel sheet.
  • One, two or more chemical elements selected from among B, REM, Zr, V, Co and Ni may be further contained in the ferritic stainless steel according to the present invention in addition to the chemical composition described above.
  • B 0.003% or less
  • B is a chemical element which is effective for improving formability, in particular, secondary formability.
  • B content is set to be 0.003% or less. Since the effect described above is realized in the case where the B content is 0.0004% or more, it is more preferable that the B content be 0.0004% or more and 0.003% or less.
  • REM 0.08% or less and Zr: 0.5% or less REM (rare earth elements) and Zr are chemical elements which are effective for improving oxidation resistance and may be added as needed in the present invention.
  • the content of REM is more than 0.080%, the steel become easier to occur the embrittle crack and, in the case where Zr content is more than 0.50%, the steel also become easier to occur the embrittle crack due to the precipitation of a Zr intermetallic compound. Therefore, in the case where REM is contained, the content of REM is set to be 0.080% or less, and, in the case where Zr in contained, the Zr content is set to be 0.50% or less.
  • the content of REM is 0.01% or more and in the case where the Zr content is 0.0050% or more, it is preferable that the content of REM be 0.001% or more and 0.080% or less and that the Zr content be 0.0050% or more and 0.50% or less.
  • V 0.5% or less
  • V is a chemical element which is effective for improving formability and oxidation resistance.
  • V content is set to be 0.50% or less. It is preferable that the V content be 0.15% or more and 0.50% or less in order to realize the effect of improving formability and oxidation resistance, more preferably 0.15% or more and 0.4% or less.
  • Co 0.5% or less
  • Co is a chemical element which is effective for improving toughness.
  • Co is an expensive chemical element and the effect of Co saturates in the case where Co content is more than 0.5%. Therefore, in the case where Co is contained, the Co content is set to be 0.5% or less. Since the effect described above is effectively realized in the case where the Co content is 0.02% or more, it is preferable that the Co content be 0.02% or more and 0.5% or less, more preferably 0.02% or more and 0.2% or less.
  • Ni 0.5% or less
  • Ni is a chemical element which improves toughness.
  • Ni is expensive and a chemical element which strongly forms a ⁇ phase
  • Ni causes a decrease in oxidation resistance by forming a ⁇ phase at a high temperature in the case where Ni content is more than 0.5%. Therefore, in the case where Ni is contained, the Ni content is set to be 0.5% or less. Since the effect described above is effectively realized in the case where the Ni content is 0.05% or more, it is preferable that the Ni content be 0.05% or more and 0.5% or less, more preferably 0.05% or more and 0.4% or less.
  • the remainder of the chemical composition consists of Fe and inevitable impurities.
  • an O content be 0.010% or less, a Sn content be 0.005% or less, a Mg content be 0.005% or less and a Ca content be 0.005% or less, more preferably the O content be 0.005 or less, the Sn content be 0.003% or less, the Mg content be 0.003% or less and the Ca content be 0.003% or less.
  • the method for manufacturing the ferritic stainless steel will be described hereafter.
  • the stainless steel according to the present invention may be manufactured in a common method for manufacturing ferritic stainless steel and there is no particular limitation on manufacturing conditions.
  • Examples of ideal manufacturing methods include smelting steel by using a well-known melting furnace such as a steel converter or an electric furnace, further, optionally, making the steel have the chemical composition according to the present invention described above by performing secondary refining such as ladle refining or vacuum refining, then making a slab of the steel by using a continuous casting method or an ingot casting-blooming rolling method, and then making the slab a cold rolled and annealed steel sheet through the processes such as hot rolling, hot rolled annealing, pickling, cold rolling, finishing annealing, pickling and so forth.
  • the cold rolling described above may be performed one time or repeated two times or more with process annealing in between, and the processes of cold rolling, finishing annealing and pickling may be performed repeatedly.
  • hot rolled annealing may be omitted, and skin pass rolling may be performed after cold rolling or finishing annealing in the case where brightness of a steel sheet is required.
  • Examples of more preferable manufacturing conditions are as follows. It is preferable that some of the conditions of a hot rolling process and a cold rolling process be specified.
  • a steel making process it is preferable to smelt molten steel having the essential chemical composition described above and the optional chemical elements to be added as needed and to perform secondary refining by using a VOD method (Vacuum Oxygen Decurbarization method).
  • VOD method Vauum Oxygen Decurbarization method
  • the smelted molten steel may be made into a steel material by using a well-known method, it is preferable to use a continuous casting method from the viewpoint of productivity and material quality.
  • the steel material obtained through a continuous casting process is heated up to a temperature of, for example, from 1000°C or higher and 1250°C or lower, and then made into a hot rolled steel sheet having a specified thickness. It is needless to say that the steel material may be made into a material of a shape other than a sheet.
  • This hot rolled steel sheet is subjected to, as needed, batch annealing at a temperature of 600°C or higher and 800°C or lower or continuous annealing at a temperature of 900°C or higher and 1100°C or lower, and then made into a hot rolled sheet product after being descaled by performing pickling or the like.
  • descaling may be performed by using a shot blasting method before pickling being performed.
  • the hot rolled and annealed steel sheet obtained as described above is made into a cold rolled steel sheet through a cold rolling process.
  • cold rolling may be performed two times or more with process annealing in between as needed.
  • the total rolling ratio of the cold rolling process, in which cold rolling is performed for one, two or more times, is set to be 60% or more, preferably 70% or more.
  • the cold rolled steel sheet is subjected to continuous annealing (finishing annealing) at a temperature of 900°C or higher and 1150°C or lower, preferably 950°C or higher and 1120°C or lower, and pickling, and then made into a cold rolled and annealed steel sheet.
  • finishing annealing continuous annealing
  • the shape of and the material quality of the steel sheet may be adjusted by performing rolling with a light reduction ratio such as skin pass rolling after cold rolled annealing being performed.
  • the hot rolled sheet product or cold rolled and annealed sheet product obtained as described above are formed into the exhaust pipe of an automobile or a motor bicycle, a material to be used for a catalyst outer cylinder, the exhaust air duct of a thermal electric power plant, or a part related to a fuel cell (such as a separator, an inter connector or a reformer) by performing bending work or other kinds of work in accordance with use application.
  • welding methods for assembling these parts and common arc welding methods such as MIG (Metal Inert Gas), MAG (Metal Active Gas) and TIG (Tungsten Inert Gas), resistance welding methods such as spot welding and seam welding, high-frequency resistance welding methods such as electric resistance welding and high-frequency induction welding methods may be applied.
  • Each of the steel No. 1 through 23 having chemical compositions given in Table 1 was smelted by using a vacuum melting furnace and made into steel ingot of 50 kg, then the steel ingot was subjected to forging, and then the forged ingot was divided into two pieces.
  • each of the divided ingots was heated up to a temperature of 1170°C, then subjected to hot rolling and made into a hot rolled steel sheet having a thickness 5 mm, then subjected to hot rolled annealing, pickling, cold rolling with a rolling ratio of 60%, finishing annealing at a temperature of 1040°C, cooling at a cooling rate of 5°C /sec, pickling and then made into a cold rolled and annealed steel sheet having a thickness of 2 mm.
  • Each of the steel No. 1 through 11 is an example in the range according to the present invention
  • each of the steel No. 12 through 23 is a comparative example out of the range according to the present invention. Incidentally, among the comparative examples, steel No.
  • the cold rolled steel sheets No. 1 through 23 were used in the two kinds of continuous oxidation tests, a high-temperature fatigue test and a tensile test at room temperature as described below.
  • a sample of 30 mm ⁇ 20 mm was cut out of each of the cold rolled and annealed steel sheet obtained as described above, then a hole of 4 mm ⁇ was punched in the upper part of the sample, then the surface and the edge face of the sample was polished with a #320 emery paper, then degreased and then the sample was suspended in a furnace heated up to a temperature of 950°C in air for a holding time of 200 hours. After the test, the mass of the sample was observed, and then an increase in weight due to oxidation (g/m 2 ) was calculated by deriving the difference between the mass observed before and after the test. Incidentally, the test was repeated two times, and oxidation resistance in air was evaluated by using the mean value of the difference in mass.
  • a sample of 30 mm ⁇ 20 mm was cut out from each of the cold rolled and annealed steel sheet obtained as described above. Then a hole of 4 mm ⁇ was punched in the upper part of the sample, then the surface and the edge face of the sample was polished with a #320 emery paper and then degreased. Thereafter, the sample was held in a furnace heated up to a temperature of 950°C in a water vapor atmosphere in which a gas of 10 vol%CO 2 -20 vol%H 2 O-5 vol%O 2 -bal.
  • N 2 was blown at a rate of 0.5 L/min for a holding time of 200 hours, then, after the test, the mass of the sample was observed, and then an increase in weight due to oxidation (g/m 2 ) was calculated by deriving the difference between the mass observed before and after the test.
  • a test specimen illustrated in Fig. 3 was cut out from the cold rolled and annealed steel sheet obtained as described above was subjected to reversed vibration of 1300 rpm (22 Hz) at a temperature of 850°C by using a Schenck type fatigue testing machine. Incidentally, a bending stress of 70 MPa was exerted on the surface of the steel sheet during the test, and evaluation was done in terms of a number of cycles (cycle) until fracture occurred.
  • thermal fatigue life was observed by repeatedly heating and cooling the test specimen between the temperatures of 100°C and 850°C at a restraint ratio of 0.30.
  • a heating rate and a cooling rate were both 10°C/sec
  • a holding time at a temperature of 100°C was 2 minutes
  • a holding time at a temperature of 850°C was 5 minutes.
  • the thermal fatigue life represents as the number of cycles at which the stress first started to continuously decrease from that in the previous cycle.
  • the stress was derived by calculated as the quotient of the load detected at 100°C divided by the cross section area of the soaked parallel portion of a test specimen indicated in Fig. 1 .
  • the steel of the comparative example which is out of the range according to the present invention is poor in either of oxidation resistance, thermal fatigue resistance, a high-temperature fatigue property or formability, which means it has been confirmed that the steel does not satisfy the object of the present invention.
  • the steel according to the present invention can be ideally used not only for the parts of an exhaust system of an automobile but also the parts of an exhaust system of a thermal electric power system and the parts of a solid-oxide fuel cell for which similar properties as that of the parts of an exhaust system of an automobile are required.

Abstract

An object is to provide ferritic stainless steel excellent in heat resistance (oxidation resistance, a thermal fatigue property and a high-temperature fatigue property) and formability, while preventing a decrease in oxidation resistance due to Cu, without adding expensive chemical elements such as Mo and W. Specifically, ferritic stainless steel having a chemical composition containing, by mass%, C: 0.015% or less, Si: 0.4 % or more and 1.0% or less, Mn: 1.0% or less, P: 0.040% or less, S: 0.010% or less, Cr: 12% or more and less than 16%, N: 0.015% or less, Nb: 0.3% or more and 0.65% or less, Ti: 0.15% or less, Mo: 0.1% or less, W: 0.1% or less, Cu: 1.0% or more and 2.5 % or less and Al: 0.2% or more and 1.0% or less, while the relationship Si‰¥Al is satisfied, and the balance being Fe and inevitable impurities.

Description

    [Technical Field]
  • The present invention relates to ferritic stainless steel having high heat resistance (a thermal fatigue property, oxidation resistance and a high-temperature fatigue property) and formability which can be ideally used for the parts of an exhaust system which are used in a high temperature environment such as an exhaust pipe and a catalyst outer cylinder (also called a converter case) of an automobile and a motorcycle and an exhaust air duct of a thermal electric power plant.
  • [Background Art]
  • The parts of an exhaust system such as an exhaust manifold, an exhaust pipe, a converter case and a muffler which are used in the environment of the exhaust system of an automobile are required to be excellent in a thermal fatigue property, a high-temperature fatigue property and oxidation resistance (hereinafter, these properties are collectively called heat resistance). Since the parts such as an exhaust manifold are subjected to heating and cooling due to the repetition of start and stop of engine operation in a state in which they are restrained by the surrounding parts, the thermal expansion and contraction of the material of the parts are restricted, which results in the occurrence of thermal strain. The fatigue phenomenon due to this thermal strain is thermal fatigue. On the other hand, the parts are continuously subjected to vibration while they are heated in the initiation of engine operation. The fatigue phenomenon due to the accumulation of strain caused by this vibration is high-temperature fatigue. The former is low-cycle fatigue and the latter is high-cycle fatigue and both are completely different fatigue phenomena.
  • For applications in which heat resistance are required as described above, nowadays, Cr containing steel to which Nb and Si are added such as Type429 (containing 14Cr-0.9Si-0.4Nb) is often used. However, since an exhaust gas temperature has become higher than 900°C with the improvement of engine performance, the thermal fatigue property of Type429 has become unsatisfactory.
  • In order to solve this problem, Cr containing steel having a high-temperature yield strength increased by adding Nb and Mo, SUS444 ( containing 19Cr-0.5Nb-2Mo) conforming to JIS G 4305 and ferritic stainless steel containing less Cr to which Nb, Mo and W are added and the like have been developed (refer to, for example, Patent Literature 1). However, since the prices of rare metals such as Mo and W have been markedly rising recently, the development of a material having heat resistance equivalent to those of these kinds of steel by using inexpensive raw materials has become to be required.
  • Examples of materials having excellent heat resistance without using expensive chemical elements such as Mo and W are disclosed by Patent Literatures 2 through 4. Patent Literature 2 discloses ferritic stainless steel to be used for the parts of an exhaust gas flow channel of an automobile. In Patent Literatures 2, Nb: 0.50 mass% or less, Cu: 0.8 mass% or more and 2.0 mass% or less and V: 0.03 mass% or more and 0.20 mass% or less are added to steel having a Cr content of 10 mass% or more and 20 mass% or less. Patent Literature 3 discloses ferritic stainless steel excellent in a thermal fatigue property. In Patent Literatures 3, Ti: 0.05 mass% or more and 0.30 mass% or less, Nb: 0.10 mass% or more and 0.60 mass% or less, Cu: 0.8 mass% or more and 2.0 mass% or less and B: 0.0005 mass% or more and 0.02 mass% or less are added to steel having a Cr content of 10 mass% or more and 20 mass% or less. Patent Literature 4 discloses ferritic stainless steel to be used for the parts of an exhaust gas flow channel of an automobile. In Patent Literatures 4, Cu: 1 mass% or more and 3 mass% or less is added to steel having a Cr content of 15 mass% or more and 25 mass% or less. These kinds of disclosed steel are all characterized by having a thermal fatigue property improved by adding Cu.
  • [Citation List] [Patent Literature]
    • [PTL 1] Japanese Unexamined Patent Application Publication No. 2004-018921
    • [PTL 2] International Publication No. W02003/004714
    • [PTL 3] Japanese Unexamined Patent Application Publication No. 2006-117985
    • [PTL 4] Japanese Unexamined Patent Application Publication No. 2000-297355
    [Summary of Invention] [Technical Problem]
  • However, according to investigations carried out by the present inventors, in the case where Cu is added as in the methods disclosed by Patent Literatures 2 through 4, it has been found that, while a thermal fatigue property is improved, contrarily oxidation resistance is decreased, which results in the deterioration of the overall heat resistance.
  • In addition, since a space which an exhaust manifold can occupy in an engine space has become smaller with the weight reduction of an automobile, it has come to be required that an exhaust manifold can be formed into a complex shape.
  • The present invention has been completed in view of the situation described above, and an object of the present invention is to provide ferritic stainless steel excellent in heat resistance (oxidation resistance, a thermal fatigue property and a high-temperature fatigue property) and formability, while preventing a decrease in oxidation resistance due to Cu, without adding expensive chemical elements such as Mo and W.
  • Incidentally, the meaning of "excellent in heat resistance " according to the present invention is that oxidation resistance, a thermal fatigue property and a high-temperature fatigue property are equivalent to or better than those of SUS444. Specifically, it means that oxidation resistance at a temperature of 950°C is equivalent to or better than that of SUS444, that a thermal fatigue property when temperature fluctuations repeatedly occur between the temperatures of 100°C and 850°C is equivalent to or better than that of SUS444 and that a high-temperature fatigue property at a temperature of 850°C is equivalent to or better than that of SUS444. In addition, the meaning of "excellent in formability" according to the present invention is that a mean elongation in the three directions at room temperature is 36% or more.
  • [Solution to Problem]
  • The present inventors diligently conducted investigations in order to develop ferritic stainless steel excellent in oxidation resistance and a thermal fatigue property by preventing a decrease in oxidation resistance due to Cu which occurs in the conventional methods without adding expensive chemical elements such as Mo or W. As a result, the present inventors found that a high strength in high-temperature can be achieved by adding the combination of Nb: 0.3 mass% or more and 0.65 mass% or less and Cu: 1.0 mass% or more and 2.5 mass% or less. By getting the high strength, a thermal fatigue property can be improved in a wide temperature range. The present inventors found that a decrease in oxidation resistance due to the addition of Cu can be prevented by adding an appropriate amount of Al (0.2 mass% or more and 1.0 mass% or less). The present inventors found that, therefore, heat resistance (a thermal fatigue property and oxidation resistnace) equivalent to or better than that of SUS444 can be achieved only by controlling the contents of Nb, Cu and A1 to the appropriate range as described above without adding Mo or W. In addition, the present inventors diligently conducted investigations regarding a method for improving oxidation resistance in an environment containing water vapor which is assumed in the case where the ferritic stainless steel is practically used for an exhaust manifold and the like, and found that oxidation resistance in an atmosphere containing water vapor (hereinafter, called water vapor oxidation resistance) also becomes equivalent to or better than that of SUS444 by adjusting a Si content (0.4 mass% or more and 1.0 mass% or less).
  • In addition, a fatigue resistance property against vibration in practical service conditions of the parts of the exhaust system of an automobile such as an exhaust manifold is also important. Therefore, the present inventors diligently conducted investigations regarding a method for improving a high-temperature fatigue property, and found that a high-temperature fatigue property also becomes equivalent to or better than that of SUS444 by adjusting the balance of a Si content and an Al content (Si≥Al).
  • Moreover, the present inventors diligently conducted investigations regarding the influence of Cr on formability and oxidation resistance, and found that formability can be improved by reducing a Cr content without there being a significant influence on oxidation resistance.
    Although it has been well known in the past that formability can be improved by reducing a Cr content. But there is a decrease in oxidation resistance by reducing a Cr content. The decrease in oxidation resistance has been compensated for by adding Mo and W, instead of Cr, in the past as disclosed by Patent Literature 1. In contrast to this, according to the present invention, it has been found that both excellent oxidation resistance and formability can be achieved by adding an appropriate amount of Al without adding expensive chemical elements such as Mo and W, even if a Cr content is reduced.
  • The present invention has been completed on the basis of the knowledge of the present inventors described above.
  • That is to say, the present invention provides ferritic stainless steel excellent in heat resistance and formability having a chemical composition containing, by mass%, C: 0.015% or less, Si: 0.4 % or more and 1.0% or less, Mn: 1.0% or less, P: 0.040% or less, S: 0.010% or less, Cr: 12% or more and less than 16%, N: 0.015% or less, Nb: 0.3% or more and 0.65% or less, Ti: 0.15% or less, Mo: 0.1% or less, W: 0.1% or less, Cu: 1.0% or more and 2.5 % or less and Al: 0.2% or more and 1.0% or less, while the relationship Si≥Al is satisfied, and the balance being Fe and inevitable impurities.
  • In addition, the present invention provides ferritic stainless steel excellent in heat resistance and formability having a chemical composition further containing one, two or more chemical elements selected from among, by mass%, B: 0.003% or less, REM: 0.08% or less, Zr: 0.5% or less, V: 0.5% or less, Co: 0.5% or less and Ni: 0.5% or less.
  • [Advantageous Effects of Invention]
  • According to the present invention, ferritic stainless steel having heat resistance (a thermal fatigue property, oxidation resistance and a high-temperature fatigue property) equivalent to or better than that of SUS444 (JIS G 4305) and excellent formability can be obtained without adding expensive Mo or W. Therefore, the steel according to the present invention can be ideally used for the parts of the exhaust system of an automobile.
  • [Brief Description of Drawings]
    • [Fig. 1] Fig. 1 is a diagram illustrating a thermal fatigue test specimen.
    • [Fig. 2] Fig. 2 is a diagram illustrating conditions of temperature and constraint in a thermal fatigue test.
    • [Fig. 3] Fig. 3 is a diagram illustrating a high-temperature fatigue test specimen.
    • [Fig. 4] Fig. 4 is a graph illustrating the influence of a Cu content on a thermal fatigue property.
    • [Fig. 5] Fig. 5 is a graph illustrating the influence of an Al content on oxidation resistance (an increase in weight due to oxidation).
    • [Fig. 6] Fig. 6 is a graph illustrating the influence of a Si content on water vapor oxidation resistance (an increase in weight due to oxidation).
    • [Fig. 7] Fig. 7 is a graph illustrating the influence of a Si content - an Al content (Si - Al) on a high-temperature fatigue property.
    • [Fig. 8] Fig. 8 is a graph illustrating the influence of a Cr content on water vapor oxidation resistance (an increase in weight due to oxidation).
    • [Fig. 9] Fig. 9 is a graph illustrating the influence of a Cr content on a mean elongation in the three directions at room temperature.
    [Description of Embodiments]
  • Firstly, the fundamental experiments which led to the completion of the present invention will be described. Hereinafter, % used when describing chemical composition always denotes mass%.
    Steel having a basic chemical composition containing C: 0.005% or more and 0.007% or less, N: 0.004% or more and 0.006% or less, P: 0.02% or more and 0.03% or less, S: 0.002% or more and 0.004% or less, Si: 0.85%, Mn: 0.4%, Cr: 14%, Nb: 0.45%, Al: 0.35%, Ti: 0.007%, Mo: 0.01% or more and 0.03% or less and W: 0.01% or more and 0.03% or less and a Cu content which was adjusted variously in the range of 0% or more and 3% or less was smelted by using an experimental method and made into a steel ingot of 50 kg, then the steel ingot was subjected to forging and a heat treatment into a steel material having a cross section of 35 mm × 35 mm, then a thermal fatigue test specimen having the dimensions illustrated in Fig. 1 was made of the steel material. Then, the thermal fatigue life of the specimen was observed by performing a thermal cycle heat treatment in which a restraint ratio was 0.30 and in which heating and cooling were repeated so that temperature fluctuations repeatedly occurred between 100°C and 850°C as illustrated in Fig. 2. The thermal fatigue life represents as the number of cycles at which the stress first started to continuously decrease from that in the previous cycle. The stress was derived by calculated as the quotient of the load detected at 100°C divided by the cross section area of the soaked parallel portion of a test specimen indicated in Fig. 1. This number of cycles corresponded to that at which a crack occurred in the test specimen. Incidentally, a similar test was performed with SUS444 (19%Cr-2%Mo-0.5%Nb steel) for comparison.
  • Fig. 4 illustrates the influence of Cu content on thermal fatigue life in the thermal fatigue test described above. This figure indicates that thermal fatigue life equivalent to or longer than that of SUS444 (about 1350 cycles) can be achieved by setting the Cu content to be 1.0% or more. Therefore, it is necessary that the Cu content be 1.0% or more in order to improve a thermal fatigue property.
  • Steel having a basic chemical composition containing C: 0.006%, N: 0.007%, P: 0.02% or more and 0.03% or less, S: 0.002% or more and 0.004% or less, Mn: 0.2%, Si: 0.85%, Cr: 14%, Nb: 0.49%, Cu: 1.5%, Ti: 0.007%, Mo: 0.01% or more and 0.03% or less and W: 0.01% or more and 0.03% or less and an Al content which was adjusted variously in the range of 0% or more and 2% or less was smelted by using an experimental method and made into a steel ingot of 50 kg, then the steel ingot was subjected to hot rolling, hot rolled annealing, cold rolling and finishing annealing and made into a cold rolled and annealed steel sheet having a thickness of 2 mm.
    A test specimen of 30 mm × 20 mm was cut out of the cold rolled steel sheet obtained as described above, then a hole of 4 mmφ was punched in the upper part of the test specimen, then the surface and the edge face of the specimen was polished with a #320 emery paper, then degreased and then used in a continuous oxidation test in air described below.
  • <Continuous oxidation test in air>
  • The test specimen described above was held in a furnace in air at a temperature of 950°C for duration of 200 hours, and then an increase in weight per unit area due to oxidation (g/m2) was derived from the observed difference in the mass of the test specimen before and after the heating test.
  • Fig. 5 illustrates the influence of Al content on the increase in weight due to oxidation in the continuous oxidation test in air described above. This figure indicates that an oxidation resistance equivalent to or better than that of SUS444 (increase in weight due to oxidation: 19 g/m2 or less) can be achieved by setting the Al content to be 0.2% or more.
  • Steel having a basic chemical composition containing C: 0.006%, N: 0.007%, P: 0.02% or more and 0.03% or less, S: 0.002% or more and 0.004% or less, Mn: 0.2%, Al: 0.45%, Cr: 14%, Nb: 0.49%, Cu: 1.5%, Ti: 0.007%, Mo: 0.01% or more and 0.03% or less and W: 0.01% or more and 0.03% or less and a Si content which was adjusted variously was smelted by using an experimental method and made into a steel ingot of 50 kg. Then the steel ingot was subjected to hot rolling, hot rolled annealing, cold rolling and finishing annealing and made into a cold rolled and annealed steel sheet having a thickness of 2 mm. A test specimen of 30 mm × 20 mm was cut out of the cold rolled steel sheet obtained as described above. Then a hole of 4 mmφ was punched in the upper part of the test specimen, then the surface and the edge face of the specimen was polished with a #320 emery paper. Then degreased and then used in a continuous oxidation test in water vapor atmosphere described below.
  • <Continuous oxidation test in water vapor atmosphere>
  • The test specimen described above was held in a furnace in a water vapor atmosphere in which a gas of 10 vol%CO2-20 vol%H2O-5 vol%O2-bal. N2 was blown at a rate of 0.5 L/min, and then an increase in weight per unit area due to oxidation (g/m2) was derived from the observed difference in the mass of the specimen before and after the heating test.
  • Fig. 6 illustrates the influence of the Si content on the increase in weight due to oxidation in the oxidation test in water vapor atmosphere described above. This figure indicates that water vapor oxidation resistance equivalent to that of SUS444 (increase in weight due to oxidation: 37g/m2 or less) cannot be achieved, unless the Si content is set to be 0.4% or more.
  • Steel having a basic chemical composition containing C: 0.006%, N: 0.007%, P: 0.02% or more and 0.03% or less, S: 0.002% or more and 0.004% or less, Mn: 0.2%, Cr: 14%, Nb: 0.49%, Cu: 1.5%, Ti: 0.007%, Mo: 0.01% or more and 0.03% or less and W: 0.01% or more and 0.03% or less and the contents of Si and Al which were adjusted variously was smelted by using an experimental method and made into a steel ingot of 50 kg. Then the steel ingot was subjected to hot rolling,
    hot rolled annealing, cold rolling and finishing annealing and made into a cold rolled and annealed steel sheet having a thickness of 2 mm. A high-temperature fatigue test specimen having a shape illustrated in Fig. 3 was made of the cold rolled steel sheet obtained as described above and then used in a high-temperature fatigue test described below.
  • <High-temperature fatigue test>
  • The high-temperature fatigue property of the test specimen described above was evaluated by using a Schenck type fatigue testing machine and by performing reversed vibration of 22 Hz (1300 rpm) at a temperature of 850°C. Here, a bending stress of 70 MPa was exerted on the surface of the steel sheet during the test, and the fatigue property was evaluated in terms of a number of cycles until fracture occurred.
  • Fig. 7 illustrates the influence of Si - Al on the number of cycles in the high-temperature fatigue test described above. This figure indicates that it is necessary to satisfy the relationship Si≥Al in order to achieve a high-temperature fatigue property equivalent to that of SUS444 (24×105 cycles).
  • Steel having a basic chemical composition containing C: 0.006%, N: 0.007%, P: 0.02% or more and 0.03% or less, S: 0.002% or more and 0.004% or less, Mn: 0.2% Si: 0.85%, Al: 0.45%, Nb: 0.49%, Cu: 1.5%, Ti: 0.007%, Mo: 0.01% or more and 0.03% or less and W: 0.01% or more and 0.03% or less and a Cr content which was adjusted variously was smelted by using an experimental method and made into a steel ingot of 50 kg. Then the steel ingot was subjected to hot rolling, hot rolled annealing, cold rolling and finishing annealing and made into a cold rolled and annealed steel sheet having a thickness of 2 mm. A test specimen of 30 mm × 20 mm was cut out from the cold rolled steel sheet obtained as described above, then a hole of 4 mmφ was punched in the upper part of the test specimen. Then the surface and the edge face of the specimen was polished with a #320 emery paper, then degreased and then used in the oxidation test in water vapor atmosphere described above.
  • Fig. 8 illustrates the influence of the Cr content on the increase in weight due to oxidation in the oxidation test in water vapor atmosphere described above. This figure indicates that water vapor oxidation resistance equivalent to that of SUS444 (increase in weight due to oxidation: 37 g/m2 or less) can be achieved in the case where the Cr content is 12% or more.
  • In addition, tensile tests were conducted at room temperature with tensile test pieces conforming to JIS NO. 13B which were made of these cold rolled and annealed steel sheets. Tensile test pieces had the directions of tension respectively in the rolling direction (L direction), in the direction at right angles to the rolling direction (C direction) and in the direction at a 45° angles to the rolling direction (D direction). A mean elongation was derived from the breaking elongations which were obtained by performing tensile tests in the three directions at room temperature and calculated by the equation below. Mean elongation E 1 % = E L + 2 E D + E C / 4 ,
    Figure imgb0001

    where EL: El (%) in L direction, ED: El (%) in D direction and EC: El (%) in C direction.
    Fig. 9 illustrates the influence of the Cr content on the mean value of elongations in the three directions (L, C and D directions) in the tensile test. This figure indicates that excellent formability in terms of the mean elongation in the three directions (L, C and D directions) of 36% or more can be achieved in the case where the Cr content is less than 16%.
  • The present invention has been completed by conducting further investigations on the basis of the results of the fundamental experiments described above.
  • The ferritic stainless steel according to the present invention will be described in detail hereafter.
    Firstly, the chemical composition according to the present invention will be described.
  • C: 0.015% or less
    Although C is a chemical element which is effective for increasing the strength of steel, there is a significant decrease in toughness and formability in the case where C content is more than 0.015%. Therefore, according to the present invention, the C content is set to be 0.015% or less. Incidentally, it is preferable that the C content be as small as possible from the viewpoint of achieving formability and that the carbon content be 0.008% or less. On the other hand, it is preferable that the C content be 0.001% or more in order to achieve strength which is required of the parts of an exhaust system, more preferably 0.002% or more and 0.008% or less.
  • Si: 0.4% or more and 1.0% or less
    Si is a chemical element which is important for improving oxidation resistance in a water vapor atmosphere. As Fig. 6 indicates, it is necessary to set Si content to be 0.4% or more in order to achieve water vapor oxidation resistance equivalent to that of SUS444. On the other hand, there is a significant decrease in formability in the case where the Si content is more than 1.0%. Therefore, the Si content is set to be 0.4% or more and 1.0% or less, preferably 0.5% or more and 0.9% or less. Although the mechanism through which water vapor oxidation resistance is increased in the case where the Si content is 0.4% or more is not clear, it is considered that a dense continuous oxide layer is formed on the surface of a steel sheet in the case where the Si content is 0.4% or more and the penetration of gas elements from outside is prevented, which results in an increase in water vapor oxidation resistance. It is preferable that the Si content be 0.5% or more in the case where there is a necessity of oxidation resistance in a severer environment.
  • Mn: 1.0% or less
    Although Mn is a chemical element which causes an increase in the strength of steel and which is effective as a deoxidation agent, a γ phase tends to be formed at a high temperature in the case where Mn content is excessively large, the excessive Mn content results in a decrease in heat resistance. Therefore, the Mn content is set to be 1.0% or less, preferably 0.7% or less. It is preferable that the Mn content be 0.05% or more in order to realize the effect of increasing strength and deoxidation.
  • P: 0.040% or less
    Since P is a harmful chemical element which causes a decrease in ductility, it is preferable that P content be as small as possible. Therefore, the P content is set to be 0.040% or less, preferably 0.030% or less.
  • S: 0.010% or less
    Since S is a harmful chemical element which causes a decrease in elongation and an r value. S has a negative influence on formability and S causes a decrease in corrosion resistance which is the basic property of stainless steel. It is preferable that S content be as small as possible. Therefore, the S content is set to be 0.010% or less, preferably 0.005% or less.
  • Cr: 12% or more and less than 16%
    Cr is a chemical element which is effective for increasing corrosion resistance and oxidation resistance, which are the characteristics of stainless steel. Sufficient oxidation resistance cannot be achieved in the case where Cr content is less than 12%. On the other hand, Cr is a chemical element which causes an increase in hardness and a decrease in ductility of steel at room temperature by solid solution strengthening, in particular, these negative influences become significant in the case where the Cr content is 16% or more. Therefore, the Cr content is set to be 12% or more and less than 16%, preferably 12% or more and 15% or less.
  • N: 0.015% or less
    N is a chemical element which causes a decrease in the ductility and the formability of steel, and these negative influences are significant in the case where N content is more than 0.015%. Therefore, the N content is set to be 0.015% or less. Incidentally, it is preferable that the N content be as small as possible from the viewpoint of achieving ductility and formability and that the N content be less than 0.010%.
  • Nb: 0.3% or more and 0.65% or less
    Nb is a chemical element which is effective for increasing corrosion resistance, formability and intergranular corrosion resistance at welds by forming carbide, nitride and carbonitride in combination with C and N. Nb is effective for increasing a thermal fatigue property by increasing high-temperature strength. These effects can be realized by setting Nb content to be 0.3% or more. On the other hand, a Laves phase (Fe2Nb) tends to be precipitated in the case where the Nb content is more than 0.65%, which results in the acceleration of embrittlement. Therefore, the Nb content is set to be 0.3% or more and 0.65% or less, preferably 0.4% or more and 0.55% or less.
  • Mo: 0.1% or less
    Since Mo is an expensive chemical element, additionally in view of the purpose of the present invention, Mo is not added positively. However, Mo may be mixed in from the material of steel such as scrap in the range of 0.1% or less. Therefore, Mo content is set to be 0.1% or less.
  • W: 0.1% or less
    Since W is an expensive chemical element like Mo, additionally in view of the purpose of the present invention, W is not added positively. However, W may be mixed in from the material of steel such as scrap in the range of 0.1% or less. Therefore, W content is set to be 0.1% or less.
  • Cu: 1.0% or more and 2.5% or less
    Cu is a chemical element which is very effective for improving a thermal fatigue property. As Fig. 3 indicates, it is necessary that Cu content be 1.0% or more in order to achieve a thermal fatigue property equivalent to or better than that of SUS444. However, in the case where the Cu content is more than 2.5%, ε-Cu is precipitated when cooling is performed after a heat treatment, which results in an increase in the hardness of steel and results in embrittlement tending to occur when hot work is performed. More importantly, while a thermal fatigue property is improved by adding Cu, contrarily the oxidation resistance of steel is decreased, which results in the deterioration of the overall heat resistance. The reason for this has not been fully identified. However, Cu seems to concentrate in a Cr depletion layer where scale has formed thereon and prevent Cr, an element that should improve intrinsic oxidation resistance of stainless steel, from diffusing again. Therefore, the Cu content is set to be 1.0% or more and 2.5% or less, preferably 1.1% or more and 1.8% or less.
  • Ti: 0.15% or less
    Ti is effective for improving corrosion resistance, formability and intergranular corrosion resistance of a welded part by fixing C and N like Nb does. However, this effect saturates and there is an increase in the hardness of steel in the case where Ti content is more than 0.15% in the present invention in which Nb is contained. Therefore, the Ti content is set to be 0.15% or less. Since Ti has higher affinity for N than Nb does, Ti tends to form TiN of a large size. Since TiN of a large size tends to become the origin of a crack and causes a decrease in toughness, it is preferable that the Ti content be 0.01% or less in the case where the toughness of a hot rolled steel sheet is necessary. Incidentally, since it is not necessary to positively add Ti in the present invention, the lower limit of the Ti content includes 0%.
  • Al: 0.2% or more and 1.0% or less
    Al is a chemical element which is essential for increasing the oxidation resistance of Cu containing steel as Fig. 5 indicates. In addition, since Al is effective as a solid solution strengthening element and, in particular, is effective for increasing high-temperature strength at a temperature of higher than 800°C, Al is a chemical element which is important for improving a high-temperature fatigue property in the present invention. It is necessary that Al content be 0.2% or more in order to achieve oxidation resistance equivalent to or better than that of SUS444. On the other hand, there is a decrease in formability due to an increase in the hardness of steel in the case where the Al content is more than 1.0%. Therefore, the Al content is set to be 0.2% or more and 1.0% or less, preferably 0.3% or more and 1.0% or less, more preferably 0.3% or more and 0.5% or less.
  • Si≥Al
    Since Al is effective as a solid solution strengthening element and, in particular, effective for increasing high-temperature strength at a high temperature of higher than 800°C, Al is a chemical element which is important for improving a high-temperature fatigue property in the present invention as described above, and Si is a chemical element which is important for effectively utilizing this effect of solid solution strengthening of Al. In the case where the amount of Si is less than that of Al, there is a decrease in the amounts of solid solution Al, because Al preferentially forms oxides and nitrides at high temperature, which decreases the contribution of Al to strengthening. On the other hand, in the case where the amount of Si is larger than that of Al, Si is preferentially oxidized and forms a dense continuous oxide layer on the surface of a steel sheet. Since this oxide becomes a barrier to the diffusion of oxygen and nitrogen, Al is kept in the state of a solid solution without being oxidized or nitrided, which makes it possible to improve a high-temperature fatigue property by strengthening steel through solid solution strengthening. Therefore, it is necessary that the relationship Si≥Al be satisfied in order to achieve a high-temperature fatigue property equivalent to or better than that of SUS444.
  • One, two or more chemical elements selected from among B, REM, Zr, V, Co and Ni may be further contained in the ferritic stainless steel according to the present invention in addition to the chemical composition described above.
  • B: 0.003% or less
    B is a chemical element which is effective for improving formability, in particular, secondary formability. However, in the case where B content is more than 0.003%, B causes a decrease in formability by forming BN. Therefore, in the case where B is contained, the B content is set to be 0.003% or less. Since the effect described above is realized in the case where the B content is 0.0004% or more, it is more preferable that the B content be 0.0004% or more and 0.003% or less.
  • REM: 0.08% or less and Zr: 0.5% or less
    REM (rare earth elements) and Zr are chemical elements which are effective for improving oxidation resistance and may be added as needed in the present invention. However, in the case where the content of REM is more than 0.080%, the steel become easier to occur the embrittle crack and, in the case where Zr content is more than 0.50%, the steel also become easier to occur the embrittle crack due to the precipitation of a Zr intermetallic compound. Therefore, in the case where REM is contained, the content of REM is set to be 0.080% or less, and, in the case where Zr in contained, the Zr content is set to be 0.50% or less. Since the effect described above is realized in the case where the content of REM is 0.01% or more and in the case where the Zr content is 0.0050% or more, it is preferable that the content of REM be 0.001% or more and 0.080% or less and that the Zr content be 0.0050% or more and 0.50% or less.
  • V: 0.5% or less
    V is a chemical element which is effective for improving formability and oxidation resistance. However, in the case where V content is more than 0.50%, V(C,N) of a large size is precipitated, which results in the deterioration of surface quality. Therefore, in the case where V is contained, the V content is set to be 0.50% or less. It is preferable that the V content be 0.15% or more and 0.50% or less in order to realize the effect of improving formability and oxidation resistance, more preferably 0.15% or more and 0.4% or less.
  • Co: 0.5% or less
    Co is a chemical element which is effective for improving toughness. However, Co is an expensive chemical element and the effect of Co saturates in the case where Co content is more than 0.5%. Therefore, in the case where Co is contained, the Co content is set to be 0.5% or less. Since the effect described above is effectively realized in the case where the Co content is 0.02% or more, it is preferable that the Co content be 0.02% or more and 0.5% or less, more preferably 0.02% or more and 0.2% or less.
  • Ni: 0.5% or less
    Ni is a chemical element which improves toughness. However, since Ni is expensive and a chemical element which strongly forms a γ phase, Ni causes a decrease in oxidation resistance by forming a γ phase at a high temperature in the case where Ni content is more than 0.5%. Therefore, in the case where Ni is contained, the Ni content is set to be 0.5% or less. Since the effect described above is effectively realized in the case where the Ni content is 0.05% or more, it is preferable that the Ni content be 0.05% or more and 0.5% or less, more preferably 0.05% or more and 0.4% or less.
  • The remainder of the chemical composition consists of Fe and inevitable impurities. Among the inevitable impurities, it is preferable that an O content be 0.010% or less, a Sn content be 0.005% or less, a Mg content be 0.005% or less and a Ca content be 0.005% or less, more preferably the O content be 0.005 or less, the Sn content be 0.003% or less, the Mg content be 0.003% or less and the Ca content be 0.003% or less.
  • The method for manufacturing the ferritic stainless steel will be described hereafter.
    The stainless steel according to the present invention may be manufactured in a common method for manufacturing ferritic stainless steel and there is no particular limitation on manufacturing conditions. Examples of ideal manufacturing methods include smelting steel by using a well-known melting furnace such as a steel converter or an electric furnace, further, optionally, making the steel have the chemical composition according to the present invention described above by performing secondary refining such as ladle refining or vacuum refining, then making a slab of the steel by using a continuous casting method or an ingot casting-blooming rolling method, and then making the slab a cold rolled and annealed steel sheet through the processes such as hot rolling, hot rolled annealing, pickling, cold rolling, finishing annealing, pickling and so forth. Incidentally, the cold rolling described above may be performed one time or repeated two times or more with process annealing in between, and the processes of cold rolling, finishing annealing and pickling may be performed repeatedly. Moreover, optionally, hot rolled annealing may be omitted, and skin pass rolling may be performed after cold rolling or finishing annealing in the case where brightness of a steel sheet is required.
  • Examples of more preferable manufacturing conditions are as follows.
    It is preferable that some of the conditions of a hot rolling process and a cold rolling process be specified. In addition, in a steel making process, it is preferable to smelt molten steel having the essential chemical composition described above and the optional chemical elements to be added as needed and to perform secondary refining by using a VOD method (Vacuum Oxygen Decurbarization method). Although the smelted molten steel may be made into a steel material by using a well-known method, it is preferable to use a continuous casting method from the viewpoint of productivity and material quality. The steel material obtained through a continuous casting process is heated up to a temperature of, for example, from 1000°C or higher and 1250°C or lower, and then made into a hot rolled steel sheet having a specified thickness. It is needless to say that the steel material may be made into a material of a shape other than a sheet. This hot rolled steel sheet is subjected to, as needed, batch annealing at a temperature of 600°C or higher and 800°C or lower or continuous annealing at a temperature of 900°C or higher and 1100°C or lower, and then made into a hot rolled sheet product after being descaled by performing pickling or the like. In addition, as needed, descaling may be performed by using a shot blasting method before pickling being performed.
  • Moreover, in order to obtain a cold rolled steel sheet, the hot rolled and annealed steel sheet obtained as described above is made into a cold rolled steel sheet through a cold rolling process. In this cold rolling process, in accordance with manufacturing circumstances, cold rolling may be performed two times or more with process annealing in between as needed. The total rolling ratio of the cold rolling process, in which cold rolling is performed for one, two or more times, is set to be 60% or more, preferably 70% or more. The cold rolled steel sheet is subjected to continuous annealing (finishing annealing) at a temperature of 900°C or higher and 1150°C or lower, preferably 950°C or higher and 1120°C or lower, and pickling, and then made into a cold rolled and annealed steel sheet. In addition, in accordance with use application, the shape of and the material quality of the steel sheet may be adjusted by performing rolling with a light reduction ratio such as skin pass rolling after cold rolled annealing being performed.
  • The hot rolled sheet product or cold rolled and annealed sheet product obtained as described above are formed into the exhaust pipe of an automobile or a motor bicycle, a material to be used for a catalyst outer cylinder, the exhaust air duct of a thermal electric power plant, or a part related to a fuel cell (such as a separator, an inter connector or a reformer) by performing bending work or other kinds of work in accordance with use application. There is no limitation on welding methods for assembling these parts, and common arc welding methods such as MIG (Metal Inert Gas), MAG (Metal Active Gas) and TIG (Tungsten Inert Gas), resistance welding methods such as spot welding and seam welding, high-frequency resistance welding methods such as electric resistance welding and high-frequency induction welding methods may be applied.
  • [EXAMPLES] [EXAMPLE 1]
  • Each of the steel No. 1 through 23 having chemical compositions given in Table 1 was smelted by using a vacuum melting furnace and made into steel ingot of 50 kg, then the steel ingot was subjected to forging, and then the forged ingot was divided into two pieces. Thereafter, one of the divided ingots was heated up to a temperature of 1170°C, then subjected to hot rolling and made into a hot rolled steel sheet having a thickness 5 mm, then subjected to hot rolled annealing, pickling, cold rolling with a rolling ratio of 60%, finishing annealing at a temperature of 1040°C, cooling at a cooling rate of 5°C /sec, pickling and then made into a cold rolled and annealed steel sheet having a thickness of 2 mm. Each of the steel No. 1 through 11 is an example in the range according to the present invention, and each of the steel No. 12 through 23 is a comparative example out of the range according to the present invention. Incidentally, among the comparative examples, steel No. 19 has a chemical composition corresponding to Type429, No. 20 has a chemical composition corresponding to SUS444, and No. 21, No. 22 and No. 23 respectively have chemical compositions corresponding to example 3 of Patent Literature 2, example 3 of Patent Literature 3 and example 5 of Patent Literature 4.
  • The cold rolled steel sheets No. 1 through 23 were used in the two kinds of continuous oxidation tests, a high-temperature fatigue test and a tensile test at room temperature as described below.
  • <Continuous oxidation test in air>
  • A sample of 30 mm × 20 mm was cut out of each of the cold rolled and annealed steel sheet obtained as described above, then a hole of 4 mmφ was punched in the upper part of the sample, then the surface and the edge face of the sample was polished with a #320 emery paper, then degreased and then the sample was suspended in a furnace heated up to a temperature of 950°C in air for a holding time of 200 hours. After the test, the mass of the sample was observed, and then an increase in weight due to oxidation (g/m2) was calculated by deriving the difference between the mass observed before and after the test. Incidentally, the test was repeated two times, and oxidation resistance in air was evaluated by using the mean value of the difference in mass.
  • <Continuous oxidation test in water vapor atmosphere>
  • A sample of 30 mm × 20 mm was cut out from each of the cold rolled and annealed steel sheet obtained as described above. Then a hole of 4 mmφ was punched in the upper part of the sample, then the surface and the edge face of the sample was polished with a #320 emery paper and then degreased. Thereafter, the sample was held in a furnace heated up to a temperature of 950°C in a water vapor atmosphere in which a gas of 10 vol%CO2-20 vol%H2O-5 vol%O2-bal. N2 was blown at a rate of 0.5 L/min for a holding time of 200 hours, then, after the test, the mass of the sample was observed, and then an increase in weight due to oxidation (g/m2) was calculated by deriving the difference between the mass observed before and after the test.
  • <High-temperature fatigue test>
  • A test specimen illustrated in Fig. 3 was cut out from the cold rolled and annealed steel sheet obtained as described above was subjected to reversed vibration of 1300 rpm (22 Hz) at a temperature of 850°C by using a Schenck type fatigue testing machine. Incidentally, a bending stress of 70 MPa was exerted on the surface of the steel sheet during the test, and evaluation was done in terms of a number of cycles (cycle) until fracture occurred.
  • <Tensile test at room temperature>
  • A tensile test piece conforming to JIS No. 13B which had the directions of tension respectively in the rolling direction (L direction), in the direction at right angle to the rolling direction (C direction) and in the direction at 45° angles to the rolling direction (D direction) was cut out from the cold rolled and annealed steel sheet described above. Then tensile tests in these directions were conducted at room temperature, then breaking elongations were observed and then a mean elongation was derived by using the equation below. Mean elongation E 1 % = E L + 2 E D + E C / 4 ,
    Figure imgb0002
    where EL: El (%) in L direction, ED: El (%) in D direction and EC: El (%) in C direction.
  • [EXAMPLE 2]
  • The rest of the pieces which were obtained by dividing the ingot of 50 kg into two pieces in Example 1 was heated up to a temperature of 1170°C, and then hot rolled into a sheet bar having a thickness of 30 mm and a width of 150 mm. Thereafter, this sheet bar was subjected to forging and made into a bar of 35 mm × 35 mm, annealing at a temperature of 1040°C, then machined into a thermal fatigue test specimen having the dimensions illustrated in Fig. 1, and then used in a thermal fatigue test as described below.
  • <Thermal fatigue test>
  • In a thermal fatigue test, a thermal fatigue life was observed by repeatedly heating and cooling the test specimen between the temperatures of 100°C and 850°C at a restraint ratio of 0.30. Here, a heating rate and a cooling rate were both 10°C/sec, a holding time at a temperature of 100°C was 2 minutes and a holding time at a temperature of 850°C was 5 minutes. The thermal fatigue life represents as the number of cycles at which the stress first started to continuously decrease from that in the previous cycle. The stress was derived by calculated as the quotient of the load detected at 100°C divided by the cross section area of the soaked parallel portion of a test specimen indicated in Fig. 1.
  • The results of the continuous oxidation test in air, the continuous oxidation test in water vapor atmosphere, the high-temperature fatigue test and the tensile test at room temperature in Example 1 and those of the thermal fatigue test in Example 2 are summarized in Table 2. As Table 2 indicates, it is clear that any of the steel of the example of the present invention which is within the range of the present invention has heat resistance (oxidation resistance, a thermal fatigue property and a high-temperature fatigue property) equivalent to or better than that of SUS444 and excellent formability in terms of a mean elongation in the three directions (L, C and D direction) at room temperature of 36% or more, which means it has been confirmed that the steel satisfies the object of the present invention. In contrast, the steel of the comparative example which is out of the range according to the present invention is poor in either of oxidation resistance, thermal fatigue resistance, a high-temperature fatigue property or formability, which means it has been confirmed that the steel does not satisfy the object of the present invention.
  • [Industrial Applicability]
  • The steel according to the present invention can be ideally used not only for the parts of an exhaust system of an automobile but also the parts of an exhaust system of a thermal electric power system and the parts of a solid-oxide fuel cell for which similar properties as that of the parts of an exhaust system of an automobile are required.
  • [Table 1]
    mass%
    Sample No. C Si Mn Al P S Cr Cu Nb Ti Mo W N Others Si - Al Note
    1 0.008 0.84 0.25 0.51 0.031 0.002 12.8 1.32 0.48 0.008 0.02 0.02 0.008 0.33 Example
    2 0.007 0.76 0.28 0.40 0.029 0.003 14.5 1.45 0.46 0.007 0.03 0.01 0.009 0.36 Example
    3 0.008 0.91 0.31 0.67 0.030 0.003 15.1 1.48 0.49 0.009 0.02 0.02 0.007 0.24 Example
    4 0.009 0.69 0.29 0.38 0.028 0.003 13.4 1.23 0.47 0.007 0.02 0.03 0.008 0.31 Example
    5 0.006 0.54 0.54 0.31 0.027 0.004 15.2 1.37 0.44 0.006 0.01 0.02 0.008 0.23 Example
    6 0.007 0.89 0.48 0.43 0.028 0.003 14.3 1.54 0.49 0.008 0.01 0.03 0.007 0.46 Example
    7 0.009 0.76 0.24 0.37 0.029 0.003 14.9 1.19 0.46 0.009 0.03 0.02 0.006 0.39 Example
    8 0.007 0.80 0.73 0.45 0.025 0.003 13.7 1.67 0.45 0.007 0.02 0.01 0.007 V: 0.21 0.35 Example
    9 0.007 0.73 0.81 0.4 0.026 0.004 15.5 1.59 0.45 0.008 0.02 0.01 0.007 B: 0.0015 0.33 Example
    10 0.008 0.68 0.89 0.32 0.026 0.002 12.9 1.24 0.43 0.008 0.01 0.02 0.008 Co: 0.09 0.36 Example
    11 0.007 0.94 0.39 0.52 0.028 0.002 13.5 1.55 0.45 0.007 0.01 0.02 0.007 Ni: 0.34 0.42 Example
    12 0.006 1.34 0.5 0.37 0.024 0.003 14.0 1.15 0.48 0.006 0.01 0.03 0.006 0.97 Comparative Example
    13 0.007 0.69 0.44 1.49 0.025 0.002 12.7 1.46 0.47 0.009 0.02 0.02 0.007 -0.8 Comparative Example
    14 0.008 0.92 0.78 0.13 0.027 0.003 15.6 1.29 0.48 0.007 0.02 0.02 0.008 0.79 Comparative Example
    15 0.009 0.47 0.63 0.68 0.029 0.002 14.4 1.51 0.46 0.008 0.03 0.02 0.006 -0.21 Comparative Example
    16 0.008 0.81 0.35 0.54 0.026 0.003 13.9 0.53 0.44 0.007 0.02 0.01 0.008 0.27 Comparative Example
    17 0.008 0.52 0.21 0.39 0.030 0.004 17.1 1.46 0.48 0.003 0.02 0.02 0.008 V: 0.06 0.13 Comparative Example
    18 0.007 0.76 0.84 0.43 0.027 0.003 9.7 1.64 0.43 0.008 0.01 0.03 0.007 0.33 Comparative Example
    19 0.007 0.87 0.33 0.03 0.029 0.002 14.8 0.02 0.44 0.030 0.01 0.01 0.008 0.84 Comparative Example*1
    20 0.008 0.31 0.42 0.02 0.031 0.003 18.7 0.02 0.52 0.003 1.87 0.02 0.008 0.291 Comparative Example*2
    21 0.008 0.32 0.05 0.01 0.028 0.002 17.0 1.93 0.33 0.002 0.01 0.02 0.01 Ni: 0.10, V: 0.10 0.31 Comparative Example*3
    22 0.009 0.46 0.54 0.00 0.029 0.003 18.9 1.36 0.35 0.080 0.01 0.02 0.007 Ni: 0.10, V: 0.03, B: 0.0030 0.458 Comparative Example*4
    23 0.006 0.22 0.05 0.05 0.005 0.005 18.8 1.65 0.42 0.090 0.02 0.02 0.006 Ni: 0.15 0.168 Comparative Example*5
    Underline indicates the value out of the range according to the present invention.
    *1: Type429 *2: SUS444 *3: Example 3 of Patent literature 2
    *4: Example 3 of Patent literature 3 *5: Example 5 of Patent literature 4
  • [Table 2]
    Sample No. Weight gain by oxidation (g/m2) Thermal Fatigue Life (cycle) Weight gain by water vapor oxidation (g/m2) Mean Elongation in Three Directions (%) High-Temperature Fatigue Life at 850°C (x10-5cycles) Note
    1 18 1330 34 36 30 Example
    2 17 1340 34 36 33 Example
    3 16 1350 33 36 26 Example
    4 17 1370 34 37 29 Example
    5 16 1340 35 37 27 Example
    6 16 1310 33 36 32 Example
    7 16 1370 34 37 31 Example
    8 17 1360 34 36 36 Example
    9 16 1340 34 36 27 Example
    10 18 1300 34 37 29 Example
    11 17 1410 33 36 33 Example
    12 17 1280 39 32 30 Comparative Example
    13 18 1380 71 31 9 Comparative Example
    14 55 1400 40 37 15 Comparative Example
    15 17 1290 77 36 11 Comparative Example
    16 15 910 32 38 26 Comparative Example
    17 13 1440 29 34 31 Comparative Example
    18 52 1300 >100 38 14 Comparative Example
    19 45 630 >100 34 8 Comparative Example*1
    20 19 1250 37 31 24 Comparative Example*2
    21 >100 1650 >100 31 15 Comparative Example*3
    22 >100 1380 >100 35 10 Comparative Example*4
    23 >100 1540 >100 34 12 Comparative Example*5
    underline indicates the value out of the range according to the present invention.
    *1: Type429 *2: SUS444 *3: Example 3 of Patent literature 2
    *4: Example 3 of Patent literature 3 *5: Example 5 of Patent literature 4

Claims (2)

  1. Ferritic stainless steel having a chemical composition containing, by mass%, C: 0.015% or less, Si: 0.4 % or more and 1.0% or less, Mn: 1.0% or less, P: 0.040% or less, S: 0.010% or less, Cr: 12% or more and less than 16%, N: 0.015% or less, Nb: 0.3% or more and 0.65% or less, Ti: 0.15% or less, Mo: 0.1% or less, W: 0.1% or less, Cu: 1.0% or more and 2.5 % or less and Al: 0.2% or more and 1.0% or less, while the relationship Si≥Al is satisfied, and the balance being Fe and inevitable impurities.
  2. Ferritic stainless steel having a chemical composition further containing one, two or more chemical elements selected from among, by mass%, B:0.003% or less, REM: 0.08% or less, Zr: 0.5% or less, V: 0.5% or less, Co: 0.5% or less and Ni: 0.5% or less.
EP11832650.3A 2010-10-14 2011-10-12 Ferritic stainless steel excellent in heat resistance and workability Active EP2628814B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2010231562 2010-10-14
JP2011221763A JP5152387B2 (en) 2010-10-14 2011-10-06 Ferritic stainless steel with excellent heat resistance and workability
PCT/JP2011/073980 WO2012050226A1 (en) 2010-10-14 2011-10-12 Ferritic stainless steel excellent in heat resistance and workability

Publications (3)

Publication Number Publication Date
EP2628814A1 true EP2628814A1 (en) 2013-08-21
EP2628814A4 EP2628814A4 (en) 2015-01-21
EP2628814B1 EP2628814B1 (en) 2018-12-05

Family

ID=45938442

Family Applications (1)

Application Number Title Priority Date Filing Date
EP11832650.3A Active EP2628814B1 (en) 2010-10-14 2011-10-12 Ferritic stainless steel excellent in heat resistance and workability

Country Status (10)

Country Link
US (1) US20130183190A1 (en)
EP (1) EP2628814B1 (en)
JP (1) JP5152387B2 (en)
KR (1) KR101581886B1 (en)
CN (1) CN103154294B (en)
ES (1) ES2720733T3 (en)
MX (1) MX339281B (en)
MY (1) MY165138A (en)
TW (1) TWI472629B (en)
WO (1) WO2012050226A1 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5234214B2 (en) * 2011-10-14 2013-07-10 Jfeスチール株式会社 Ferritic stainless steel
JP5304935B2 (en) * 2011-10-14 2013-10-02 Jfeスチール株式会社 Ferritic stainless steel
ES2673216T3 (en) * 2012-05-28 2018-06-20 Jfe Steel Corporation Ferritic stainless steel
JP5904306B2 (en) * 2014-02-05 2016-04-13 Jfeスチール株式会社 Ferritic stainless steel hot-rolled annealed steel sheet, manufacturing method thereof, and ferritic stainless steel cold-rolled annealed steel sheet
MX2016014668A (en) 2014-05-14 2017-03-06 Jfe Steel Corp Ferritic stainless steel.
WO2016068139A1 (en) 2014-10-31 2016-05-06 新日鐵住金ステンレス株式会社 Ferrite-based stainless steel plate, steel pipe, and production method therefor
CN105220074A (en) * 2015-10-22 2016-01-06 山西太钢不锈钢股份有限公司 Chrome ferritic high temperature steel making method in a kind of boiler swing pipe tray use
MX2019007483A (en) * 2016-12-21 2019-08-29 Jfe Steel Corp Ferritic stainless steel.
CN107557693A (en) * 2017-07-26 2018-01-09 邢台钢铁有限责任公司 A kind of wire drawing low-intensity ferrite stainless steel wire rod and its production method

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003160842A (en) * 2001-11-22 2003-06-06 Nisshin Steel Co Ltd Ferritic stainless steel for hydrocarbon fuel reformer
EP1930461A1 (en) * 2006-12-07 2008-06-11 Nisshin Steel Co., Ltd. Ferritic stainless steel for automobile exhaust gas passage components and welded steel pipe
US20080279712A1 (en) * 2007-05-11 2008-11-13 Manabu Oku Ferritic stainless steel sheet with excellent thermal fatigue properties, and automotive exhaust-gas path member
WO2009110641A1 (en) * 2008-03-07 2009-09-11 Jfeスチール株式会社 Ferritic stainless steel with excellent heat resistance and toughness
EP2112245A1 (en) * 2007-02-02 2009-10-28 Nisshin Steel Co., Ltd. Ferritic stainless steel for exhaust gas passage member
JP2010053421A (en) * 2008-08-29 2010-03-11 Jfe Steel Corp Ferritic stainless steel excellent in thermal fatigue property, high temperature fatigue property, oxidation resistance and high temperature salt damage corrosion resistance

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100340568B1 (en) * 1997-12-26 2002-07-18 이구택 A method for setting up annealing condition of high-alloyed ferritic stainless steels
JPH11350081A (en) * 1998-06-11 1999-12-21 Nippon Steel Corp Corrosion resistant steel
JP3468156B2 (en) 1999-04-13 2003-11-17 住友金属工業株式会社 Ferritic stainless steel for automotive exhaust system parts
US20040170518A1 (en) 2001-07-05 2004-09-02 Manabu Oku Ferritic stainless steel for member of exhaust gas flow passage
JP3903855B2 (en) 2002-06-14 2007-04-11 Jfeスチール株式会社 Ferritic stainless steel that is soft at room temperature and excellent in high-temperature oxidation resistance
JP3886933B2 (en) * 2003-06-04 2007-02-28 日新製鋼株式会社 Ferritic stainless steel sheet excellent in press formability and secondary workability and manufacturing method thereof
JP4468137B2 (en) 2004-10-20 2010-05-26 日新製鋼株式会社 Ferritic stainless steel material and automotive exhaust gas path member with excellent thermal fatigue characteristics
JP5208450B2 (en) * 2006-07-04 2013-06-12 新日鐵住金ステンレス株式会社 Cr-containing steel with excellent thermal fatigue properties
JP5297630B2 (en) * 2007-02-26 2013-09-25 新日鐵住金ステンレス株式会社 Ferritic stainless steel plate with excellent heat resistance
KR20090052954A (en) * 2007-11-22 2009-05-27 주식회사 포스코 Low chrome ferritic stainless steel with high corrosion resistance and stretchability and method of manufacturing the same
JP4386144B2 (en) * 2008-03-07 2009-12-16 Jfeスチール株式会社 Ferritic stainless steel with excellent heat resistance
JP5274074B2 (en) * 2008-03-28 2013-08-28 新日鐵住金ステンレス株式会社 Heat-resistant ferritic stainless steel sheet with excellent oxidation resistance
JP4624473B2 (en) * 2008-12-09 2011-02-02 新日鐵住金ステンレス株式会社 High purity ferritic stainless steel with excellent weather resistance and method for producing the same
KR20100075180A (en) * 2008-12-24 2010-07-02 주식회사 포스코 Method for manufacturing ferritic stainless steel
SI2480693T1 (en) * 2009-09-21 2019-04-30 Aperam Stainless steel having local variations in mechanical resistance

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003160842A (en) * 2001-11-22 2003-06-06 Nisshin Steel Co Ltd Ferritic stainless steel for hydrocarbon fuel reformer
EP1930461A1 (en) * 2006-12-07 2008-06-11 Nisshin Steel Co., Ltd. Ferritic stainless steel for automobile exhaust gas passage components and welded steel pipe
EP2112245A1 (en) * 2007-02-02 2009-10-28 Nisshin Steel Co., Ltd. Ferritic stainless steel for exhaust gas passage member
US20080279712A1 (en) * 2007-05-11 2008-11-13 Manabu Oku Ferritic stainless steel sheet with excellent thermal fatigue properties, and automotive exhaust-gas path member
WO2009110641A1 (en) * 2008-03-07 2009-09-11 Jfeスチール株式会社 Ferritic stainless steel with excellent heat resistance and toughness
JP2010053421A (en) * 2008-08-29 2010-03-11 Jfe Steel Corp Ferritic stainless steel excellent in thermal fatigue property, high temperature fatigue property, oxidation resistance and high temperature salt damage corrosion resistance

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2012050226A1 *

Also Published As

Publication number Publication date
KR20130058070A (en) 2013-06-03
JP2012102397A (en) 2012-05-31
TWI472629B (en) 2015-02-11
MX339281B (en) 2016-05-19
KR101581886B1 (en) 2015-12-31
EP2628814A4 (en) 2015-01-21
ES2720733T3 (en) 2019-07-24
WO2012050226A1 (en) 2012-04-19
CN103154294B (en) 2018-11-23
JP5152387B2 (en) 2013-02-27
EP2628814B1 (en) 2018-12-05
CN103154294A (en) 2013-06-12
US20130183190A1 (en) 2013-07-18
TW201221658A (en) 2012-06-01
MY165138A (en) 2018-02-28
MX2013004053A (en) 2013-06-05

Similar Documents

Publication Publication Date Title
EP2474635B1 (en) Ferritic stainless steel having excellent heat resistance
US9157137B2 (en) Ferritic stainless steel excellent in oxidation resistance
EP2628814B1 (en) Ferritic stainless steel excellent in heat resistance and workability
US9290830B2 (en) Ferritic stainless steel
US9365915B2 (en) Ferritic stainless steel
EP2166120A1 (en) Ferritic stainless steel having excellent heat resistance
EP2857538A1 (en) Ferritic stainless steel
KR101899229B1 (en) Ferritic stainless steel
KR101899230B1 (en) Ferritic stainless steel
US20210032731A1 (en) Ferritic stainless steel
JP2023005308A (en) Ferritic stainless steel sheet and method for producing the same
JP2023037686A (en) ferritic stainless steel

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20130510

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
A4 Supplementary search report drawn up and despatched

Effective date: 20150105

RIC1 Information provided on ipc code assigned before grant

Ipc: C22C 38/26 20060101ALI20141218BHEP

Ipc: C22C 38/40 20060101ALI20141218BHEP

Ipc: C21D 6/00 20060101ALI20141218BHEP

Ipc: C22C 38/20 20060101ALI20141218BHEP

Ipc: C22C 38/28 20060101ALI20141218BHEP

Ipc: C21D 8/02 20060101ALI20141218BHEP

Ipc: C22C 38/06 20060101ALI20141218BHEP

Ipc: C21D 9/46 20060101ALI20141218BHEP

Ipc: C22C 38/30 20060101ALI20141218BHEP

Ipc: C22C 38/24 20060101ALI20141218BHEP

Ipc: C22C 38/22 20060101ALI20141218BHEP

Ipc: C22C 38/04 20060101ALI20141218BHEP

Ipc: C22C 38/02 20060101ALI20141218BHEP

Ipc: C22C 38/00 20060101AFI20141218BHEP

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

RIC1 Information provided on ipc code assigned before grant

Ipc: C22C 38/30 20060101ALI20180508BHEP

Ipc: C22C 38/20 20060101ALI20180508BHEP

Ipc: C22C 38/00 20060101AFI20180508BHEP

Ipc: C22C 38/24 20060101ALI20180508BHEP

Ipc: C22C 38/06 20060101ALI20180508BHEP

Ipc: C22C 38/28 20060101ALI20180508BHEP

Ipc: C22C 38/02 20060101ALI20180508BHEP

Ipc: C22C 38/40 20060101ALI20180508BHEP

Ipc: C22C 38/22 20060101ALI20180508BHEP

Ipc: C21D 9/46 20060101ALI20180508BHEP

Ipc: C22C 38/04 20060101ALI20180508BHEP

Ipc: C22C 38/26 20060101ALI20180508BHEP

Ipc: C21D 6/00 20060101ALI20180508BHEP

Ipc: C21D 8/02 20060101ALI20180508BHEP

INTG Intention to grant announced

Effective date: 20180523

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1073148

Country of ref document: AT

Kind code of ref document: T

Effective date: 20181215

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602011054614

Country of ref document: DE

REG Reference to a national code

Ref country code: SE

Ref legal event code: TRGR

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20181205

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1073148

Country of ref document: AT

Kind code of ref document: T

Effective date: 20181205

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190305

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190305

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190306

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2720733

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20190724

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190405

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190405

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602011054614

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

26N No opposition filed

Effective date: 20190906

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: TR

Payment date: 20191008

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20191023

Year of fee payment: 9

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20191012

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20191031

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20191031

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20191012

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602011054614

Country of ref document: DE

Representative=s name: HL KEMPNER PATENTANWAELTE, SOLICITORS (ENGLAND, DE

Ref country code: DE

Ref legal event code: R082

Ref document number: 602011054614

Country of ref document: DE

Representative=s name: HL KEMPNER PATENTANWALT, RECHTSANWALT, SOLICIT, DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20201012

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20111012

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201012

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20201012

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181205

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20230913

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 20230830

Year of fee payment: 13

Ref country code: FR

Payment date: 20230911

Year of fee payment: 13

Ref country code: BE

Payment date: 20230918

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20231102

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20230830

Year of fee payment: 13