EP2060650A1 - Ferritic stainless steel material for automobile exhaust gas passage components - Google Patents
Ferritic stainless steel material for automobile exhaust gas passage components Download PDFInfo
- Publication number
- EP2060650A1 EP2060650A1 EP08019006A EP08019006A EP2060650A1 EP 2060650 A1 EP2060650 A1 EP 2060650A1 EP 08019006 A EP08019006 A EP 08019006A EP 08019006 A EP08019006 A EP 08019006A EP 2060650 A1 EP2060650 A1 EP 2060650A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- temperature
- steel material
- mass
- exhaust gas
- strength
- 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 69
- 229910001220 stainless steel Inorganic materials 0.000 title claims abstract description 22
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 70
- 239000010959 steel Substances 0.000 claims abstract description 70
- 229910052758 niobium Inorganic materials 0.000 claims abstract description 26
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 24
- 238000001556 precipitation Methods 0.000 claims abstract description 19
- 239000000203 mixture Substances 0.000 claims abstract description 13
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 10
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 5
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 5
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 4
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 4
- 239000012535 impurity Substances 0.000 claims abstract description 3
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 3
- 238000000137 annealing Methods 0.000 description 21
- 238000001816 cooling Methods 0.000 description 13
- 239000006104 solid solution Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 10
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 230000001965 increasing effect Effects 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 230000002787 reinforcement Effects 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 238000011835 investigation Methods 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 238000011144 upstream manufacturing Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 230000007704 transition Effects 0.000 description 3
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009863 impact test Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- 229910017060 Fe Cr Inorganic materials 0.000 description 1
- 229910002544 Fe-Cr Inorganic materials 0.000 description 1
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 229910001068 laves phase Inorganic materials 0.000 description 1
- 229910000734 martensite Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/20—Ferrous alloys, e.g. steel alloys containing chromium with copper
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/24—Ferrous alloys, e.g. steel alloys containing chromium with vanadium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/26—Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N2530/00—Selection of materials for tubes, chambers or housings
- F01N2530/02—Corrosion resistive metals
- F01N2530/04—Steel alloys, e.g. stainless steel
Definitions
- the present invention relates to a ferritic stainless steel material for use as automobile exhaust gas passage components, in particular to a ferritic stainless steel material for use as automobile exhaust gas passage components, which has excellent heat resistance and low-temperature toughness favorable for exhaust gas upstream passage components where the material temperature may be over 900°C or further over 950°C, for example, exhaust manifolds, catalyst converters, front pipes and the like.
- two typical ferritic steel species are used properly for automobile exhaust gas passage components, depending on the service temperature range of the components.
- One is a steel species such as typically SUS429 steel mainly applied to the components of which the maximum ultimate temperature of the material may be on a level of 750°C; and the other is a steel species such as typically SUS444 steel mainly applied to the components of which the maximum ultimate temperature of the material may be on a level of 850°C.
- exhaust gas passage upstream components are required to have excellent workability into various shapes.
- the components are required to have excellent workability durable to severe working into complicated shapes.
- exhaust gas passage components are also required to have good low-temperature toughness.
- Patent Reference 1 shows a ferritic stainless steel of which the composition and the texture are so controlled that it may surely have a sufficient amount of solid solution Nb so as to be durable to use in a temperature range over 900°C and may have a tensile strength of 20 MPa at 950°C.
- this has no description relating to 0.2 % yield strength, and the durability of the steel in a case where the material temperature has actually risen up to about 1000°C is not confirmed. In this, any special consideration is not taken for thermal fatigue resistance and low-temperature toughness.
- Patent Reference 2 shows a ferritic stainless steel having excellent high-temperature strength at 900°C and having excellent low-temperature toughness. However, this has no description relating to 0.2 % yield strength, and in this, the measures for sufficiently securing the durability in a case where the material temperature has actually risen up to 1000°C or so could not be said to be always satisfactory.
- Patent Reference 3 describes a ferritic stainless steel having good high-temperature strength at 950°C and good workability. However, this shows nothing relating to 0.2 % yield strength, and in this, it is not certain as to whether or not the material could be actually durable to exposure to about 1000°C or so. No special consideration is taken for low-temperature toughness.
- Patent Reference 4 shows an Fe-Cr alloy of which the thermal expansion coefficient is lowered. However, there is taken no intension of improving the high-temperature strength of the material in a temperature range of about 1000°C or so.
- Patent Reference 5 describes a ferritic stainless steel having excellent thermal fatigue resistance and good low-temperature toughness. In this, however, the material was evaluated for the high-temperature strength in terms of the 0.2 % yield strength thereof at 600°C, and its durability is not clear in a case where the material temperature has actually risen up to about 1000°C.
- Patent Reference 6 shows a ferritic stainless steel for exhaust gas system components to be used at a temperature of not lower than 700°C. Regarding high-temperature strength, however, this shows only the tensile strength data of the material at 600°C and 850°C, and it is not clear as to whether or not the material could be resistant to exposure to temperatures of 1000°C or so. In addition, this has no description relating to low-temperature toughness.
- a method capable of stably realizing a material that exhibits excellent durability when used at a temperature over 900°C and satisfies both good low-temperature toughness and good workability is not as yet established (see the above Patent References).
- An object of the present invention is to provide a ferritic stainless steel material for automobile exhaust gas passage components, which simultaneously satisfies 0.2 % yield strength at high temperature of 1000°C, thermal fatigue resistance, low-temperature toughness and workability all on a high level and which, even when used under the condition where the material temperature actually reaches a high-temperature range of higher than 900°C and even higher than 950°C, still exhibits excellent durability.
- the invention provides a ferritic stainless steel material having excellent heat resistance and low-temperature toughness for automobile exhaust gas passage components, which has a composition essentially containing, in terms of % by mass, at most 0.03 % of C, at most 1 % of Si, from 0.6 to 2 % of Mn, at most 3 % of Ni, from 10 to 25 % of Cr, from 0.3 to 0.7 % of Nb, from more than 1 to 2 % of Cu, from 1 to 2.5 % of Mo, from 1 to 2.5 % of W, at most 0.15 % of Al, from 0.03 to 0.2 % of V, and at most 0.03 % of N, and optionally containing at least one of Ti and Zr in an amount of less than 1 % in total, or further containing at least one of B in an amount of at most 0.02 % and Co in an amount of at most 2 %, or further containing at least one of REM (rare earth element) and Ca in an amount of at most 0.1 % in total
- the element code is substituted with the content of the corresponding element expressed in terms of % by mass.
- “Ferritic stainless steel material for automobile exhaust gas passage components” means a steel material processed for final annealing under heat at a temperature higher than 1000°C (for example, from 1050 to 1100°C) (this may be simply referred to as “final annealing") in a process of producing automobile exhaust gas passage components.
- final annealing a steel material processed for final annealing under heat at a temperature higher than 1000°C (for example, from 1050 to 1100°C) (this may be simply referred to as "final annealing”) in a process of producing automobile exhaust gas passage components.
- final annealing a steel material processed for final annealing under heat at a temperature higher than 1000°C (for example, from 1050 to 1100°C) (this may be simply referred to as "final annealing”) in a process of producing automobile exhaust gas passage components.
- the pipe after the final annealing corresponds to the ferritic stainless steel material for automobile exhaust gas passage components as referred to herein.
- the steel sheet after the final annealing, and the pipe, cylindrical casing or the like obtained by further working the final annealed sheet correspond to the ferritic stainless steel material for automobile exhaust gas passage components.
- a ferritic stainless steel material for automobile exhaust gas passage components which satisfies all the requirements of high-temperature strength durable to exposure to high temperature of 1000°C, good thermal fatigue resistance, good workability and good low-temperature toughness.
- the material meets the recent tendency in the art toward elevated exhaust gas temperatures and brings about an broadened latitude in planning exhaust gas passage upstream components.
- the high-temperature strength (0.2 % yield strength) of the steel material at a level of 1000°C with keeping high the high-temperature strength (0.2 % yield strength) thereof at a level of 600°C. It is extremely effective to make the steel material have high strength both in the two temperature ranges for keeping high the thermal fatigue resistance thereof.
- the 0.2 % yield strength at 600°C and the 0.2 % yield strength at 1000°C of the steel material are both at least 1.5 times higher than the yield strength at the same temperatures of SUS444 steel.
- the 0.2 % yield strength at 600°C of the steel material is at least 200 MPa and the 0.2 % yield strength at 1000°C thereof is at least 15 MPa. It has been found that the material having such high-temperature strength characteristics has good high-temperature fatigue resistance satisfactory for practical use when it receives repeated temperature change between ordinary temperature and 1000°C or so as automobile exhaust gas passage components.
- Cu is used for improving the high-temperature strength of the steel material in a temperature range including 600°C (range of from about 500 to 800°C).
- a temperature range including 600°C range of from about 500 to 800°C.
- an ⁇ -Cu phase is precipitated at a temperature of around 600°C, and this finely disperses in the matrix of the material to thereby express a precipitation-reinforcing phenomenon.
- the steel material can keep the high-temperature strength (0.2 % yield strength) in the temperature range higher by at least about 1.5 times than that of SUS444 steel, it is necessary to take advantage of Nb and Mo solid solution reinforcement in addition to the precipitation of the ⁇ -Cu phase.
- the coefficient of Nb in formula (2) corresponds to the increase in the 0.2 % yield strength (MPa) at 1000°C per 0.1 % by mass of Nb; and the coefficient of Mo and Cu each correspond to the increase in the 0.2 % yield strength (MPa) at 1000°C per 1 % by mass of Nb and Cu, respectively.
- the composition that satisfies the above formula (2) is not enough. More detailed investigations have confirmed that, in particular, it is extremely important to make the steel material have a metal texture in which the Nb and Mo precipitates are reduced as much as possible. Concretely, after final annealing, the steel material must have a texture condition in which the total amount of Nb and Mo existing as a precipitation phase therein is at most 0.2 % by mass.
- the low-temperature toughness and the weldability thereof it is extremely effective to make the steel material have the above-mentioned texture condition after final annealing.
- the amount of Nb or Mo added is considerably large, the amount of the solid solution Mo or the solid solution Nb can be sufficiently secured even when the total amount of Nb and Mo existing as a precipitation phase is more than 0.2 % by mass, and the high-temperature strength of the steel material at 1000°C could be increased owing to their solid solution reinforcement. In this case, however, it is difficult to enhance both the low-temperature toughness and the workability of the steel material.
- Total amount (% by mass) of Nb and Mo existing as a precipitation phase can be determined as follows: The residue of the precipitation phase as extracted out through constant potential electrolysis in an water-free solvent electrolytic solution (SPEED method) is analyzed for elementary quantification, and the total mass of Nb and Mo in the residue is divided by the total mass of the dissolved matrix and the extracted precipitation phase in electrolysis, and this is expressed as percentage.
- the cooling rate from 1050°C to 500°C in the cooling step in the final annealing must be controlled to at least 5°C/sec.
- a steel sheet before formed into a pipe, or after formed into a pipe but before used as the component may be processed at least once for final annealing that comprises soaking under heat at 1050 to 1100°C for from 0 to 10 minutes followed by cooling from 1050°C to 500°C at a cooling rate of at least 5°C/sec.
- any superfluous precipitation phase of Nb and Mo would not form when the automobile exhaust gas passage component formed of the steel material is used under heat at a temperature of 1000°C or so, and practically, therefore, the high-temperature strength and the low-temperature toughness of the steel material would not worsen.
- the alloying ingredients are described below.
- C and N are generally effective for improving creep strength and other high-temperature strength properties but degrade oxidation resistant property, workability, low-temperature toughness and weldability when contained in excess.
- both C and N are limited to a content of at most 0.03 % by mass.
- Si is effective for improving high-temperature oxidation resistance. However, when added in excess, it increases hardness and thus degrades workability and low-temperature toughness.
- the Si content is limited to at most 1 % by mass.
- Mn improves high-temperature oxidation resistance, especially scale peeling resistance.
- the Mn content In order to sufficiently secure high-temperature oxidation resistance on a level of 1000°C, the Mn content must be at least 0.6 % by mass. However, Mn impairs workability and weldability when added in excess. Further, Mn is an austenite-stabilizing element that when added in a large amount facilitates martensite phase formation and thus causes a decline in thermal fatigue resistance and workability.
- the Mn content is therefore limited to at most 2 % by mass, preferably at most 1.5 % by mass, more preferably less than 1.5 % by mass.
- Ni contributes to improvement of low-temperature toughness, but when added too much, it may lower cold elongation.
- the acceptable Ni content is up to 3 % by mass, but more preferably, the Ni content is at most 0.6 % by mass.
- the Cr stabilizes ferrite phase and contributes to improvement of oxidation resistance, an important property of high-temperature materials.
- the Cr content is secured to be at least 15 % by mass for sufficiently exhibiting its effect.
- too much Cr makes the steel material brittle and worsens the workability thereof, and therefore the Cr content is not more than 25 % by mass.
- Nb is effective for increasing high-temperature strength in a temperature range of around 600°C or so by solid solution reinforcement, but the invention takes advantage of the solid solution reinforcing effect of Nb for securing high-temperature strength in a high temperature range of higher than 900°C.
- the Nb content must be at least 0.3 % by mass, and it must satisfy the above-mentioned formula (2).
- the invention must secure the steel texture condition where the total amount of Nb and Mo existing as a precipitation phase is at most 0.2 % by mass.
- Nb has a strong affinity for C and N, therefore readily forming precipitates that may lower high-temperature strength, low-temperature toughness, workability and other properties. Accordingly, the Nb content is limited to at most 0.7 % by mass.
- Cu is an important element in the invention. Specifically, as so mentioned in the above, the invention takes advantage of the fine dispersion precipitation phenomenon of the ⁇ -Cu phase of the steel material to thereby enhance the strength thereof at around 600°C (from about 500 to 850°C) and to improve the thermal fatigue resistance thereof. In a high temperature range over 850°C, Cu further plays a role of assisting the high-temperature strength-enhancing effect of Nb and Mo, based on the solid solution enhancement with Cu. As a result of various studies, the Cu content must be at least more than 1 % by mass for satisfactorily attaining these effects. However, too much Cu worsens workability, low-temperature toughness and weldability, and therefore the uppermost limit of the Cu content is limited to 2 % by mass.
- Mo like Nb
- the high temperature strength in a high temperature range over 900°C must be increased, and Mo addition in an amount of at least 1 % by mass is indispensable.
- the invention must secure the steel texture condition where the total amount of Nb and Mo existing as a precipitation phase is at most 0.2 % by mass. Excess Mo addition may result in formation of carbide and Laves phase (Fe 2 Mo), thereby impairing high temperature strength and low-temperature toughness. Accordingly, the Mo content is limited to at most 2.5 % by mass.
- W is an element effective for increasing high temperature strength in a high temperature range over 900°C, and in the invention, the W content must be at least 1 % by mass. However, excess W addition impairs workability, and therefore, the W content must be at most 2.5 % by mass, more preferably at most 2 % by mass.
- Al is used as a deoxidizer in a steel making, and acts for improving high temperature oxidation resistance.
- too much Al addition has negative influences on surface properties, workability, weldability and low-temperature toughness. Accordingly, Al is added within a range of at most 0.15 % by mass.
- V contributes to improvement of high-temperature strength when added in combination with Nb and Cu.
- V improves workability, low-temperature toughness, resistance to grain boundary corrosion susceptibility, and toughness of weld heat affected zone
- V is added in the invention in an amount of at least 0.03 % by mass.
- excessive addition of V impairs workability and low-temperature toughness. Accordingly, the V content is limited to at most 0.2 % by mass.
- Ti and Zr are elements effective for improving high-temperature strength; and if desired, at least one of these may be added. However, excessive addition impairs toughness. In case where at least one of Ti and Zr is added, the total content thereof must be less than 1 % by mass.
- B and Co like Ni, are elements contributing to low-temperature toughness. If desired, one or two of B and Co may be added. However, excessive addition lowers cold elongation; and therefore, the B content is at most 0.02 % by mass and the Co content is at most 2 % by mass. More effectively, the B content is from 0.0005 to 0.02 % by mass.
- REM rare earth element
- Ca are elements that contribute to high-temperature oxidation resistance. If desired, at least one of these may be added. More effectively, the total content of REM and Ca is at least 0.001 % by mass. However, excessive addition thereof may have some negative influences on producibility, and therefore, the total content of REM and Ca is limited to at most 0.1 % by mass.
- the stainless steel material of the invention may be produced by preparing a stainless steel having a controlled composition as above according to an ordinary steel melting method, then working it into a steel sheet having a predetermined thickness according to an ordinary stainless steel sheet producing method, thereafter welding it into a pipe, or shaping and further working it.
- a controlled composition as above according to an ordinary steel melting method
- a steel sheet having a predetermined thickness according to an ordinary stainless steel sheet producing method
- welding it into a pipe or shaping and further working it.
- the steel could hardly have a texture condition where the total amount of Nb and Mo existing as a precipitation phase is at most 0.2 % by mass, and it may be difficult to enhance the high-temperature strength (0.2 % yield strength) of the steel material at 1000°C stably on a level of at least about 1.5 times that of SUS444. Under the condition, in addition, the low-temperature toughness of the steel material may also be lowered.
- Ferritic stainless steels shown in Table 1 were produced according to a steel melting method, and then worked into cold-rolled annealed steel sheets having a thickness of 2 mm according to a process of hot rolling, annealing of hot-rolled sheets, cold rolling and final annealing.
- the final annealing was attained under the condition as simulated for final annealing of steel materials for exhaust gas passage components.
- the final annealing condition was as follows: After heated at 1050°C with soaking for 1 minute, the steels except some comparative samples (such as No. 21) were cooled from 1000°C to 500°C at a mean cooling rate of at least 5°C/sec. The cooling rate was monitored with a thermocouple attached to the surface of each sample.
- the samples (after final annealing) were tested and analyzed for the total amount of Nb and Mo existing as a precipitation phase therein (this is expressed as "amount of precipitated Nb + precipitated Mo"), and the 0.2 % yield strength at 600°C, the 0.2 % yield strength at 1000°C, the low-temperature toughness and the cold workability thereof in the manner mentioned below.
- a sample is tested though constant potential electrolysis at a potential at which the matrix of the sample dissolves but the precipitation phase thereof does not dissolve, and the residue of the extracted precipitation phase is analyzed for elementary determination.
- the total mass of Nb and Mo in the residue is divided by the total mass of the dissolved matrix and the extracted precipitation phase in electrolysis, and this is expressed as percentage of the amount of precipitated Nb + precipitated Mo.
- used is 10 % acetylacetone + 1 % tetramethylammonium chloride + methyl alcohol solution as a water-free solvent.
- a test piece for tensile strength having a thickness of 2 mm (the pulling direction of the sample is the same as the rolling direction thereof) is tested for tensile strength at 600°C and tensile strength at 1000°C according to JIS G0567.
- a V-notch Charpy impact test piece is cut out of a sample having a thickness of 2 mm (the direction in which the test piece is hit with a hammer is in parallel to the rolling direction of the sample), and tested in a Charpy impact test at a pitch of 25°C within a range of from -75°C to 25°C according to JIS Z2242, thereby determining the ductility-toughness transition temperature of the sample.
- Samples having EL A of at least 30 % are rated G (good in point of the cold workability); and those having EL A of smaller than 30 % are rated NG (not good in point of the cold workability).
- Cooling rate in final annealing means the mean cooling rate from 1050°C to 500°C.
- Table 2 Steel No. Cooling Rate in Final Annealing (°C/sec) Amount of Precipitated Nb + Precipitated Mo (mass%) 0.2 % Yield Strength at 600°C (MPa) 0.2 % Yield Strength at 1000°C (MPa)
- No. 21 is not good, though its composition falls within the scope of the invention. This is because the cooling rate from 1000°C to 500°C in the final annealing was lower than 5°C/sec, and therefore a large amount of Nb and Mo precipitates formed during the cooling step thereby giving a texture condition in which the amount of precipitated Nb + precipitated Mo was too much.
- This comparative sample was poor in the high-temperature strength at 1000°C, the low-temperature toughness and the cold workability.
- the content of Mo and Nb was small; and in No. 23, the Cu content was additionally small. Since these do not satisfy the formulas (1) and (2), their high-temperature strength at 600°C and 1000°C was poor.
- No. 22 the content of Mo and Nb was small.
- the Nb content was high, and in the texture thereof, the amount of precipitated Nb + precipitated Mo was too much, and its cold workability was poor.
- the content of Mo and Nb was high, and in the texture thereof, the amount of precipitated Nb + precipitated Mo was too much, and its low-temperature toughness was poor.
- the Cu content was small, its high-temperature strength at 600°C was low.
- the Mo content was too high, and in the texture of thereof, the amount of precipitated Nb + precipitated Mo was too much.
- the high-temperature strength at 1000°C of the comparative sample was high, but the low-temperature toughness and the cold workability thereof were poor.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Heat Treatment Of Sheet Steel (AREA)
- Heat Treatment Of Steel (AREA)
- Exhaust Silencers (AREA)
Abstract
Description
- The present invention relates to a ferritic stainless steel material for use as automobile exhaust gas passage components, in particular to a ferritic stainless steel material for use as automobile exhaust gas passage components, which has excellent heat resistance and low-temperature toughness favorable for exhaust gas upstream passage components where the material temperature may be over 900°C or further over 950°C, for example, exhaust manifolds, catalyst converters, front pipes and the like.
- Heretofore, two typical ferritic steel species are used properly for automobile exhaust gas passage components, depending on the service temperature range of the components. One is a steel species such as typically SUS429 steel mainly applied to the components of which the maximum ultimate temperature of the material may be on a level of 750°C; and the other is a steel species such as typically SUS444 steel mainly applied to the components of which the maximum ultimate temperature of the material may be on a level of 850°C.
- For satisfying the recent requirements for emission control and mileage regulation, exhaust gas temperatures tend to be higher, and on the presumption that the material temperature in exhaust gas passage upstream components may actually rise up to about 1000°C, the requirements for heat-resistant materials may be expected to increase for those components. Conventional SUS444 steel (18Cr-2Mo-0.5Nb steel) would be difficult to apply to the components that are exposed to such high temperatures. In order that the materials are durable to use at such high temperatures, those merely having high tensile strength at high temperatures are not enough and it is a matter of importance that the 0.2 % yield strength of the materials at high temperature, which is an index of the stress under which the materials begin to undergo plastic deformation, is high.
- With the increase in various devices to be fitted in an engine room, the limitation to the housing space for exhaust gas components is increasing more than before. Accordingly, exhaust gas passage upstream components are required to have excellent workability into various shapes. In particular, not only as plates but also as pipes, the components are required to have excellent workability durable to severe working into complicated shapes. Further, exhaust gas passage components are also required to have good low-temperature toughness.
- Heretofore, various ferritic stainless steels having improved heat resistance such as those mentioned below have been developed and are being put into practical use.
- Patent Reference 1 shows a ferritic stainless steel of which the composition and the texture are so controlled that it may surely have a sufficient amount of solid solution Nb so as to be durable to use in a temperature range over 900°C and may have a tensile strength of 20 MPa at 950°C. However, this has no description relating to 0.2 % yield strength, and the durability of the steel in a case where the material temperature has actually risen up to about 1000°C is not confirmed. In this, any special consideration is not taken for thermal fatigue resistance and low-temperature toughness.
- Patent Reference 2 shows a ferritic stainless steel having excellent high-temperature strength at 900°C and having excellent low-temperature toughness. However, this has no description relating to 0.2 % yield strength, and in this, the measures for sufficiently securing the durability in a case where the material temperature has actually risen up to 1000°C or so could not be said to be always satisfactory.
- Patent Reference 3 describes a ferritic stainless steel having good high-temperature strength at 950°C and good workability. However, this shows nothing relating to 0.2 % yield strength, and in this, it is not certain as to whether or not the material could be actually durable to exposure to about 1000°C or so. No special consideration is taken for low-temperature toughness.
- Patent Reference 4 shows an Fe-Cr alloy of which the thermal expansion coefficient is lowered. However, there is taken no intension of improving the high-temperature strength of the material in a temperature range of about 1000°C or so.
- Patent Reference 5 describes a ferritic stainless steel having excellent thermal fatigue resistance and good low-temperature toughness. In this, however, the material was evaluated for the high-temperature strength in terms of the 0.2 % yield strength thereof at 600°C, and its durability is not clear in a case where the material temperature has actually risen up to about 1000°C.
- Patent Reference 6 shows a ferritic stainless steel for exhaust gas system components to be used at a temperature of not lower than 700°C. Regarding high-temperature strength, however, this shows only the tensile strength data of the material at 600°C and 850°C, and it is not clear as to whether or not the material could be resistant to exposure to temperatures of 1000°C or so. In addition, this has no description relating to low-temperature toughness.
- Patent Reference 1:
JP 2959934 - Patent Reference 2:
JP 2696584 - Patent Reference 3:
JP 3468156 - Patent Reference 4:
JP 2005-206944A - Patent Reference 5:
JP 2006-117985A - Patent Reference 6:
JP 2000-303149A - A method capable of stably realizing a material that exhibits excellent durability when used at a temperature over 900°C and satisfies both good low-temperature toughness and good workability is not as yet established (see the above Patent References).
- An object of the present invention is to provide a ferritic stainless steel material for automobile exhaust gas passage components, which simultaneously satisfies 0.2 % yield strength at high temperature of 1000°C, thermal fatigue resistance, low-temperature toughness and workability all on a high level and which, even when used under the condition where the material temperature actually reaches a high-temperature range of higher than 900°C and even higher than 950°C, still exhibits excellent durability.
- To attain the object as above, the invention provides a ferritic stainless steel material having excellent heat resistance and low-temperature toughness for automobile exhaust gas passage components, which has a composition essentially containing, in terms of % by mass, at most 0.03 % of C, at most 1 % of Si, from 0.6 to 2 % of Mn, at most 3 % of Ni, from 10 to 25 % of Cr, from 0.3 to 0.7 % of Nb, from more than 1 to 2 % of Cu, from 1 to 2.5 % of Mo, from 1 to 2.5 % of W, at most 0.15 % of Al, from 0.03 to 0.2 % of V, and at most 0.03 % of N, and optionally containing at least one of Ti and Zr in an amount of less than 1 % in total, or further containing at least one of B in an amount of at most 0.02 % and Co in an amount of at most 2 %, or further containing at least one of REM (rare earth element) and Ca in an amount of at most 0.1 % in total, with a balance of Fe and inevitable impurities, the composition satisfying the following formulae (1) and (2), and which has a texture where the total amount of Nb and Mo existing as a precipitation phase is at most 0.2 % by mass:
- In the above formulae (1) and (2), the element code is substituted with the content of the corresponding element expressed in terms of % by mass.
- "Ferritic stainless steel material for automobile exhaust gas passage components" means a steel material processed for final annealing under heat at a temperature higher than 1000°C (for example, from 1050 to 1100°C) (this may be simply referred to as "final annealing") in a process of producing automobile exhaust gas passage components. For example, in case where a steel sheet is welded and formed intro a pipe, then shaped and worked, and thereafter processed for final annealing, the pipe after the final annealing corresponds to the ferritic stainless steel material for automobile exhaust gas passage components as referred to herein. In case where a steel sheet is processed for final annealing, the steel sheet after the final annealing, and the pipe, cylindrical casing or the like obtained by further working the final annealed sheet correspond to the ferritic stainless steel material for automobile exhaust gas passage components.
- Of the above-mentioned steel materials, those for use for exhaust gas components that are to be within a material temperature range over 900°C or further over 950°C are especially preferred subjects in the invention.
- According to the invention, there is provided a ferritic stainless steel material for automobile exhaust gas passage components, which satisfies all the requirements of high-temperature strength durable to exposure to high temperature of 1000°C, good thermal fatigue resistance, good workability and good low-temperature toughness. The material meets the recent tendency in the art toward elevated exhaust gas temperatures and brings about an broadened latitude in planning exhaust gas passage upstream components.
- In the invention, it is important to increase the high-temperature strength (0.2 % yield strength) of the steel material at a level of 1000°C with keeping high the high-temperature strength (0.2 % yield strength) thereof at a level of 600°C. It is extremely effective to make the steel material have high strength both in the two temperature ranges for keeping high the thermal fatigue resistance thereof. As a result of various investigations, it is desirable that the 0.2 % yield strength at 600°C and the 0.2 % yield strength at 1000°C of the steel material are both at least 1.5 times higher than the yield strength at the same temperatures of SUS444 steel. Concretely, it is desirable that the 0.2 % yield strength at 600°C of the steel material is at least 200 MPa and the 0.2 % yield strength at 1000°C thereof is at least 15 MPa. It has been found that the material having such high-temperature strength characteristics has good high-temperature fatigue resistance satisfactory for practical use when it receives repeated temperature change between ordinary temperature and 1000°C or so as automobile exhaust gas passage components.
- In the invention, Cu is used for improving the high-temperature strength of the steel material in a temperature range including 600°C (range of from about 500 to 800°C). Specifically, when Cu is added to the steel material, an ε-Cu phase is precipitated at a temperature of around 600°C, and this finely disperses in the matrix of the material to thereby express a precipitation-reinforcing phenomenon. In order that the steel material can keep the high-temperature strength (0.2 % yield strength) in the temperature range higher by at least about 1.5 times than that of SUS444 steel, it is necessary to take advantage of Nb and Mo solid solution reinforcement in addition to the precipitation of the ε-Cu phase. As a result of various investigations, controlling the constitutive ingredients in order that the content of Nb, Mo and Cu could satisfy the formula (1) makes it possible to increase the high-temperature range of at most 800°C strength of the steel material by at least about 1.5 times that of SUS444 steel.
- In a temperature range over 800°C, solid solution of the ε-Cu phase is further promoted, and the effect of Cu to enhance the high-temperature strength of the steel material is weakened. In order to increase the high-temperature strength (0.2 % yield strength) at 1000°C of the steel material by at least about 1.5 times that of SUS444 steel, it is important to fully take advantage of the solid solution reinforcement with Nb and Mo. As the solid solution of Cu is also effective for enhancing the high-temperature strength, it is also utilized. As a result of various investigations, it has been found that the constitutive ingredients must be controlled so as to satisfy the formula (2).
- The coefficient of Nb in formula (2) corresponds to the increase in the 0.2 % yield strength (MPa) at 1000°C per 0.1 % by mass of Nb; and the coefficient of Mo and Cu each correspond to the increase in the 0.2 % yield strength (MPa) at 1000°C per 1 % by mass of Nb and Cu, respectively.
- However, in order to increase the 0.2 % yield strength of the steel material at high temperature of 1000°C by at least about 1.5 times that of SUS444 steel, the composition that satisfies the above formula (2) is not enough. More detailed investigations have confirmed that, in particular, it is extremely important to make the steel material have a metal texture in which the Nb and Mo precipitates are reduced as much as possible. Concretely, after final annealing, the steel material must have a texture condition in which the total amount of Nb and Mo existing as a precipitation phase therein is at most 0.2 % by mass.
- Not only for keeping the high-temperature strength of the steel material but also for keeping well the workability, the low-temperature toughness and the weldability thereof, it is extremely effective to make the steel material have the above-mentioned texture condition after final annealing. In case where the amount of Nb or Mo added is considerably large, the amount of the solid solution Mo or the solid solution Nb can be sufficiently secured even when the total amount of Nb and Mo existing as a precipitation phase is more than 0.2 % by mass, and the high-temperature strength of the steel material at 1000°C could be increased owing to their solid solution reinforcement. In this case, however, it is difficult to enhance both the low-temperature toughness and the workability of the steel material.
- "Total amount (% by mass) of Nb and Mo existing as a precipitation phase" can be determined as follows: The residue of the precipitation phase as extracted out through constant potential electrolysis in an water-free solvent electrolytic solution (SPEED method) is analyzed for elementary quantification, and the total mass of Nb and Mo in the residue is divided by the total mass of the dissolved matrix and the extracted precipitation phase in electrolysis, and this is expressed as percentage.
- For obtaining the texture condition where the total amount of Nb and Mo existing as a precipitation phase is at most 0.2 % by mass, the cooling rate from 1050°C to 500°C in the cooling step in the final annealing must be controlled to at least 5°C/sec. For example, in case where a pipe produced by welding is applied to automobile exhaust gas passage components, a steel sheet before formed into a pipe, or after formed into a pipe but before used as the component, may be processed at least once for final annealing that comprises soaking under heat at 1050 to 1100°C for from 0 to 10 minutes followed by cooling from 1050°C to 500°C at a cooling rate of at least 5°C/sec. Insofar as the steel material is processed once to thereby have the texture condition as above before used as an automobile exhaust gas passage component, any superfluous precipitation phase of Nb and Mo would not form when the automobile exhaust gas passage component formed of the steel material is used under heat at a temperature of 1000°C or so, and practically, therefore, the high-temperature strength and the low-temperature toughness of the steel material would not worsen.
- The alloying ingredients are described below.
- C and N are generally effective for improving creep strength and other high-temperature strength properties but degrade oxidation resistant property, workability, low-temperature toughness and weldability when contained in excess. In the invention, both C and N are limited to a content of at most 0.03 % by mass.
- Si is effective for improving high-temperature oxidation resistance. However, when added in excess, it increases hardness and thus degrades workability and low-temperature toughness. In the invention, the Si content is limited to at most 1 % by mass.
- Mn improves high-temperature oxidation resistance, especially scale peeling resistance. In order to sufficiently secure high-temperature oxidation resistance on a level of 1000°C, the Mn content must be at least 0.6 % by mass. However, Mn impairs workability and weldability when added in excess. Further, Mn is an austenite-stabilizing element that when added in a large amount facilitates martensite phase formation and thus causes a decline in thermal fatigue resistance and workability. The Mn content is therefore limited to at most 2 % by mass, preferably at most 1.5 % by mass, more preferably less than 1.5 % by mass.
- Ni contributes to improvement of low-temperature toughness, but when added too much, it may lower cold elongation. In the invention, the acceptable Ni content is up to 3 % by mass, but more preferably, the Ni content is at most 0.6 % by mass.
- Cr stabilizes ferrite phase and contributes to improvement of oxidation resistance, an important property of high-temperature materials. In the invention, the Cr content is secured to be at least 15 % by mass for sufficiently exhibiting its effect. However, too much Cr makes the steel material brittle and worsens the workability thereof, and therefore the Cr content is not more than 25 % by mass.
- Nb is effective for increasing high-temperature strength in a temperature range of around 600°C or so by solid solution reinforcement, but the invention takes advantage of the solid solution reinforcing effect of Nb for securing high-temperature strength in a high temperature range of higher than 900°C. For this, the Nb content must be at least 0.3 % by mass, and it must satisfy the above-mentioned formula (2). In addition, as so mentioned in the above, the invention must secure the steel texture condition where the total amount of Nb and Mo existing as a precipitation phase is at most 0.2 % by mass. In this connection, Nb has a strong affinity for C and N, therefore readily forming precipitates that may lower high-temperature strength, low-temperature toughness, workability and other properties. Accordingly, the Nb content is limited to at most 0.7 % by mass.
- Cu is an important element in the invention. Specifically, as so mentioned in the above, the invention takes advantage of the fine dispersion precipitation phenomenon of the ε-Cu phase of the steel material to thereby enhance the strength thereof at around 600°C (from about 500 to 850°C) and to improve the thermal fatigue resistance thereof. In a high temperature range over 850°C, Cu further plays a role of assisting the high-temperature strength-enhancing effect of Nb and Mo, based on the solid solution enhancement with Cu. As a result of various studies, the Cu content must be at least more than 1 % by mass for satisfactorily attaining these effects. However, too much Cu worsens workability, low-temperature toughness and weldability, and therefore the uppermost limit of the Cu content is limited to 2 % by mass.
- Mo, like Nb, is effective for increasing high temperature strength by solid solution reinforcement. Especially in the invention, the high temperature strength in a high temperature range over 900°C must be increased, and Mo addition in an amount of at least 1 % by mass is indispensable. As so mentioned in the above, the invention must secure the steel texture condition where the total amount of Nb and Mo existing as a precipitation phase is at most 0.2 % by mass. Excess Mo addition may result in formation of carbide and Laves phase (Fe2Mo), thereby impairing high temperature strength and low-temperature toughness. Accordingly, the Mo content is limited to at most 2.5 % by mass.
- W is an element effective for increasing high temperature strength in a high temperature range over 900°C, and in the invention, the W content must be at least 1 % by mass. However, excess W addition impairs workability, and therefore, the W content must be at most 2.5 % by mass, more preferably at most 2 % by mass.
- Al is used as a deoxidizer in a steel making, and acts for improving high temperature oxidation resistance. However, too much Al addition has negative influences on surface properties, workability, weldability and low-temperature toughness. Accordingly, Al is added within a range of at most 0.15 % by mass.
- V contributes to improvement of high-temperature strength when added in combination with Nb and Cu. When existing along with Nb, V improves workability, low-temperature toughness, resistance to grain boundary corrosion susceptibility, and toughness of weld heat affected zone In order to sufficiently attain all these effects, V is added in the invention in an amount of at least 0.03 % by mass. However, excessive addition of V impairs workability and low-temperature toughness. Accordingly, the V content is limited to at most 0.2 % by mass.
- Ti and Zr are elements effective for improving high-temperature strength; and if desired, at least one of these may be added. However, excessive addition impairs toughness. In case where at least one of Ti and Zr is added, the total content thereof must be less than 1 % by mass.
- B and Co, like Ni, are elements contributing to low-temperature toughness. If desired, one or two of B and Co may be added. However, excessive addition lowers cold elongation; and therefore, the B content is at most 0.02 % by mass and the Co content is at most 2 % by mass. More effectively, the B content is from 0.0005 to 0.02 % by mass.
- REM (rare earth element) and Ca are elements that contribute to high-temperature oxidation resistance. If desired, at least one of these may be added. More effectively, the total content of REM and Ca is at least 0.001 % by mass. However, excessive addition thereof may have some negative influences on producibility, and therefore, the total content of REM and Ca is limited to at most 0.1 % by mass.
- The stainless steel material of the invention may be produced by preparing a stainless steel having a controlled composition as above according to an ordinary steel melting method, then working it into a steel sheet having a predetermined thickness according to an ordinary stainless steel sheet producing method, thereafter welding it into a pipe, or shaping and further working it. In this process, in the final annealing step where the steel is heated at 1050 to 1100°C, it is important to cool the steel from 1050°C to 500°C at a controlled cooling rate of at least 5°C/sec as so mentioned in the above. Overstepping the cooling condition, the steel could hardly have a texture condition where the total amount of Nb and Mo existing as a precipitation phase is at most 0.2 % by mass, and it may be difficult to enhance the high-temperature strength (0.2 % yield strength) of the steel material at 1000°C stably on a level of at least about 1.5 times that of SUS444. Under the condition, in addition, the low-temperature toughness of the steel material may also be lowered.
- Ferritic stainless steels shown in Table 1 were produced according to a steel melting method, and then worked into cold-rolled annealed steel sheets having a thickness of 2 mm according to a process of hot rolling, annealing of hot-rolled sheets, cold rolling and final annealing. The final annealing was attained under the condition as simulated for final annealing of steel materials for exhaust gas passage components. The final annealing condition was as follows: After heated at 1050°C with soaking for 1 minute, the steels except some comparative samples (such as No. 21) were cooled from 1000°C to 500°C at a mean cooling rate of at least 5°C/sec. The cooling rate was monitored with a thermocouple attached to the surface of each sample. Samples of the cold-rolled annealed steel sheets thus obtained after the final annealing were tested and analyzed for various properties of exhaust gas passage components.
Table 1 Steel No. Chemical Ingredients (mass%) Left Side of Formula (1) Left Side of Formula (2) C Si Mn Ni Cr Mo Nb Cu W Al V N Others Invention Steels 1 0.005 0.19 0.65 0.02 17.8 1.35 0.47 1.68 1.55 0.04 0.04 0.009 17.39 10.59 2 0.006 0.25 0.60 0.01 18.2 1.65 0.56 1.05 1.25 0.05 0.04 0.010 15.22 12.23 3 0.007 0.16 0.79 0.02 16.5 1.55 0.56 1.06 1.59 0.01 0.05 0.012 14.78 12.03 4 0.010 0.14 0.80 0.02 24.7 1.98 0.43 1.54 1.84 0.01 0.04 0.009 19.66 11.18 5 0.008 0.08 1.12 0.02 18.0 2.06 0.39 1.48 1.51 0.02 0.05 0.008 Ti:0.08 19.65 10.71 6 0.006 0.09 1.16 0.02 20.4 2.45 0.45 1.45 1.78 0.02 0.12 0.012 Zr:0.09 21.49 12.38 7 0.007 0.12 1.25 0.01 22.5 1.36 0.65 1.39 1.97 0.03 0.04 0.016 15.92 13.17 8 0.009 0.06 1.35 0.02 20.9 2.03 0.69 1.88 1.48 0.03 0.06 0.012 REM:0.04,Ca0.01 22.26 15.35 9 0.010 0.06 0.77 0.03 15.9 2.05 0.45 1.79 1.66 0.04 0.05 0.008 Ti:0.15,Co:0.01 21.53 11.75 10 0.010 0.08 0.60 0.01 18.8 2.16 0.35 1.95 1.74 0.04 0.07 0.007 B:0.0012 22.92 10.55 Comparati ve Steels 21 0.006 0.06 0.75 0.02 18.5 1.22 0.55 1.40 1.88 0.03 0.07 0.011 15.16 11.39 22 0.009 0.12 0.51 0.02 16.5 0.21 0.19 1.46 2.04 0.02 0.05 0.012 Ti:0.15 10.04 4.00 23 0.005 0.24 1.12 0.01 17.2 0.88 0.22 0.68 2.16 0.01 0.04 0.009 8.74 5.40 24 0.005 0.29 1.18 0.01 18.9 1.55 0.58 2.25 2.55 0.03 0.06 0.008 21.95 12.93 25 0.009 0.06 0.69 0.01 20.4 1.30 0.69 0.42 0.18 0.04 0.11 0.009 9.85 13.16 26 0.007 0.12 0.48 0.02 19.2 1.45 0.41 2.08 0.00 0.01 0.06 0.012 20.22 10.09 27 0.008 0.19 0.75 0.02 2.04 2.55 0.12 1.88 0.88 0.02 0.04 0.016 24.17 7.84 28 0.008 0.06 0.69 0.03 22.9 1.68 0.79 1.12 1.24 0.02 0.03 0.015 16.07 15.77 29 0.008 0.08 0.56 0.02 24.8 2.30 0.71 0.78 1.84 0.02 0.05 0.008 B:0.0015 17.03 15.64 30 0.007 0.15 0.84 0.01 15.9 3.58 0.55 1.69 1.05 0.02 0.05 0.009 28.70 16.26 Underlined: Outside the scope of the invention. - The samples (after final annealing) were tested and analyzed for the total amount of Nb and Mo existing as a precipitation phase therein (this is expressed as "amount of precipitated Nb + precipitated Mo"), and the 0.2 % yield strength at 600°C, the 0.2 % yield strength at 1000°C, the low-temperature toughness and the cold workability thereof in the manner mentioned below.
- According to a SPEED method as mentioned above, a sample is tested though constant potential electrolysis at a potential at which the matrix of the sample dissolves but the precipitation phase thereof does not dissolve, and the residue of the extracted precipitation phase is analyzed for elementary determination. The total mass of Nb and Mo in the residue is divided by the total mass of the dissolved matrix and the extracted precipitation phase in electrolysis, and this is expressed as percentage of the amount of precipitated Nb + precipitated Mo. In the SPEED method, used is 10 % acetylacetone + 1 % tetramethylammonium chloride + methyl alcohol solution as a water-free solvent.
- A test piece for tensile strength having a thickness of 2 mm (the pulling direction of the sample is the same as the rolling direction thereof) is tested for tensile strength at 600°C and tensile strength at 1000°C according to JIS G0567. Samples of which the 0.2 % yield strength at 600°C is at least 200 MPa, corresponding to about at least 1.5 times that of SUS444 steel, are good; and those of which the strength is lower than it are not good. Samples of which the 0.2 % yield strength at 1000°C is at least 15 MPa, corresponding to about at least 1.5 times that of SUS444 steel, are good; and those of which the strength is lower than it are not good.
- A V-notch Charpy impact test piece is cut out of a sample having a thickness of 2 mm (the direction in which the test piece is hit with a hammer is in parallel to the rolling direction of the sample), and tested in a Charpy impact test at a pitch of 25°C within a range of from -75°C to 25°C according to JIS Z2242, thereby determining the ductility-toughness transition temperature of the sample. Samples of which the transition temperature is not higher than -25°C are rated G (good in point of the low-temperature toughness); and those of which the transition temperature is higher than -25°C are rated NG (not good in point of the low-temperature toughness).
- Three tensile test pieces (JIS 13B) are cut out of a sample having a thickness of 2 mm in such a manner that the pulling direction thereof could be at an angle of 0°, 45° or 90° relative to the rolling direction thereof. According to JIS 2241, these are tested for tensile strength at break (test times n = 3). The broken pieces are butt-jointed, and the elongation at break (%) thereof is determined. According to the following formula (3), the mean elongation ELA of the sample is computed, and this ELA indicates the cold elongation of the tested sample.
- In this, ELL means the elongation at break of the sample at a pulling direction of 0° (mean value of n = 3); ELD means the elongation at break at a pulling direction of 45° (mean value of n = 3); and ELT means the elongation at break at a pulling direction of 90° (mean value of n = 3). Samples having ELA of at least 30 % are rated G (good in point of the cold workability); and those having ELA of smaller than 30 % are rated NG (not good in point of the cold workability).
- The results are shown in Table 2. In Table 2, "cooling rate in final annealing" means the mean cooling rate from 1050°C to 500°C.
Table 2 Steel No. Cooling Rate in Final Annealing (°C/sec) Amount of Precipitated Nb + Precipitated Mo (mass%) 0.2 % Yield Strength at 600°C (MPa) 0.2 % Yield Strength at 1000°C (MPa) Low-Temperature Toughness Cold Work ability Invention Steels 1 15.2 0.02 230 15 G G 2 10.4 0.20 221 17 G G 3 8.2 0.16 220 17 G G 4 11.2 0.18 254 16 G G 5 8.6 0.05 231 19 G G 6 10.1 0.06 249 20 G G 7 10.6 0.04 230 22 G G 8 5.6 0.05 269 23 G G 9 11.2 0.06 248 20 G G 10 11.5 0.04 264 21 G G Comparative Steels 21 4.8 0.25 204 13 NG NG 22 5.8 0.02 164 8 G G 23 10.2 0.06 176 10 G G 24 10.5 0.16 226 16 G NG 25 10.6 0.04 140 17 G G 26 8.2 0.04 220 11 G G 27 8.5 0.67 230 9 NG G NG 10.7 0.58 205 19 G NG 29 11.5 1.20 150 17 NG G 30 11.6 1.58 220 20 NG NG Underlined: Outside the scope of the invention, or unsatisfactory in point of the properties. - The steel materials of the invention examples that satisfy the requirements for the composition and the amount of precipitated Nb + precipitated Mo all had 0.2 % yield strength at 600°C and 0.2 % yield strength at 1000°C both higher by at least about 1. 5 times than those of SUS444 steel, as known from Table 2; and accordingly, they have excellent high-temperature strength in a high temperature range over 850°C, and have sufficiently good thermal fatigue resistance. In addition, their low-temperature toughness and cold workability are also good.
- In contrast, No. 21 is not good, though its composition falls within the scope of the invention. This is because the cooling rate from 1000°C to 500°C in the final annealing was lower than 5°C/sec, and therefore a large amount of Nb and Mo precipitates formed during the cooling step thereby giving a texture condition in which the amount of precipitated Nb + precipitated Mo was too much. This comparative sample was poor in the high-temperature strength at 1000°C, the low-temperature toughness and the cold workability. In No. 22, the content of Mo and Nb was small; and in No. 23, the Cu content was additionally small. Since these do not satisfy the formulas (1) and (2), their high-temperature strength at 600°C and 1000°C was poor. In No. 24, the W content was too much, and therefore, this was poor in the cold workability. In No. 25, the Cu content was low and this did not satisfy the formula (1), and the high-temperature strength at 600°C of this comparative sample was poor. In No. 26, the Cu content was too much, and this did not satisfy the formula (2). In addition, W was not added to it, and therefore the high-temperature strength at 1000°C of the comparative sample was low. In No. 27, the Mo content was too much, and in the texture thereof, the amount of precipitated Nb + precipitated Mo was too much. Its Nb content was too low, and this did not satisfy the formula (2). Its high-temperature strength at 1000°C and its low-temperature toughness were poor. In No. 28, the Nb content was high, and in the texture thereof, the amount of precipitated Nb + precipitated Mo was too much, and its cold workability was poor. In No. 29, the content of Mo and Nb was high, and in the texture thereof, the amount of precipitated Nb + precipitated Mo was too much, and its low-temperature toughness was poor. In addition, since its Cu content was small, its high-temperature strength at 600°C was low. In No. 30, the Mo content was too high, and in the texture of thereof, the amount of precipitated Nb + precipitated Mo was too much. However, owing to the solid solution of Mo therein, the high-temperature strength at 1000°C of the comparative sample was high, but the low-temperature toughness and the cold workability thereof were poor.
Claims (5)
- A ferritic stainless steel material having excellent heat resistance and low-temperature toughness for automobile exhaust gas passage components, which has a composition comprising, in terms of % by mass, at most 0.03 % of C, at most 1 % of Si, from 0.6 to 2 % of Mn, at most 3 % of Ni, from 10 to 25 % of Cr, from 0.3 to 0.7 % of Nb, from more than 1 to 2 % of Cu, from 1 to 2.5 % of Mo, from 1 to 2.5 % of W, at most 0.15 % of Al, from 0.03 to 0.2 % of V, and at most 0.03 % of N, with a balance of Fe and inevitable impurities, and satisfying the following formulae (1) and (2), and which has a texture where the total amount of Nb and Mo existing as a precipitation phase is at most 0.2 % by mass:
- The steel material as claimed in claim 1, wherein the composition further contains at least one of Ti and Zr in an amount of less than 1 % in total.
- The steel material as claimed in claim 1 or 2, wherein the composition further contains at least one of B in an amount of at most 0.02 % and Co in an amount of at most 2 %.
- The steel material as claimed in any of claims 1 to 3, wherein the composition further contains at least one of REM (rare earth element) and Ca in an amount of at most 0.1 % in total.
- The steel material as claimed in any of claims 1 to 4, which is used for exhaust gas components of which the material temperature is in a temperature range over 900°C.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007294932A JP5178157B2 (en) | 2007-11-13 | 2007-11-13 | Ferritic stainless steel material for automobile exhaust gas path members |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2060650A1 true EP2060650A1 (en) | 2009-05-20 |
EP2060650B1 EP2060650B1 (en) | 2010-12-15 |
Family
ID=40467035
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP08019006A Active EP2060650B1 (en) | 2007-11-13 | 2008-10-30 | Ferritic stainless steel material for automobile exhaust gas passage components |
Country Status (6)
Country | Link |
---|---|
US (1) | US20090120536A1 (en) |
EP (1) | EP2060650B1 (en) |
JP (1) | JP5178157B2 (en) |
CN (1) | CN101435054B (en) |
DE (1) | DE602008003963D1 (en) |
ES (1) | ES2355171T3 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014001644A1 (en) | 2012-06-26 | 2014-01-03 | Outokumpu Oyj | Ferritic stainless steel |
EP2546378A4 (en) * | 2010-03-11 | 2017-08-16 | Nippon Steel & Sumikin Stainless Steel Corporation | Highly oxidation-resistant ferrite stainless steel plate, highly heat-resistant ferrite stainless steel plate, and manufacturing method therefor |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2776892C (en) | 2006-05-09 | 2014-12-09 | Nippon Steel & Sumikin Stainless Steel Corporation | Ferritic stainless steel excellent in resistance to crevice corrosion and formability |
JP5348458B2 (en) * | 2007-04-27 | 2013-11-20 | Jfeスチール株式会社 | Cr-containing steel pipe and manufacturing method thereof |
JP5125600B2 (en) * | 2008-02-25 | 2013-01-23 | Jfeスチール株式会社 | Ferritic stainless steel with excellent high-temperature strength, steam oxidation resistance and workability |
JP5462583B2 (en) * | 2008-10-24 | 2014-04-02 | 新日鐵住金ステンレス株式会社 | Ferritic stainless steel sheet for EGR cooler |
KR101519159B1 (en) | 2009-07-28 | 2015-05-12 | 현대자동차주식회사 | Product method of ferritic stainless steel excellent in thermo-mechanical fatigue property |
CN102822370B (en) * | 2010-03-31 | 2014-09-03 | 日立金属株式会社 | Ferrite heat-resistant cast steel having excellent normal-temperature toughness and exhaust system component formed from the same |
JP5703075B2 (en) * | 2011-03-17 | 2015-04-15 | 新日鐵住金ステンレス株式会社 | Ferritic stainless steel plate with excellent heat resistance |
JP5659061B2 (en) | 2011-03-29 | 2015-01-28 | 新日鐵住金ステンレス株式会社 | Ferritic stainless steel sheet excellent in heat resistance and workability and manufacturing method thereof |
SE1250101A1 (en) * | 2011-04-01 | 2012-10-02 | Scania Cv Ab | Cast iron alloy as well as exhaust gas conducting component |
CN102409259B (en) * | 2011-11-29 | 2013-04-24 | 宁波精磊汽车零部件有限公司 | Alloy steel for braking caliper and preparation method thereof |
CN102433514B (en) * | 2011-11-29 | 2013-08-28 | 宁波精磊汽车零部件有限公司 | Low-alloy steel and preparation method thereof |
JP6037882B2 (en) | 2012-02-15 | 2016-12-07 | 新日鐵住金ステンレス株式会社 | Ferritic stainless steel sheet with excellent scale peel resistance and method for producing the same |
JP6071608B2 (en) * | 2012-03-09 | 2017-02-01 | 新日鐵住金ステンレス株式会社 | Ferritic stainless steel plate with excellent oxidation resistance |
JP5793459B2 (en) | 2012-03-30 | 2015-10-14 | 新日鐵住金ステンレス株式会社 | Heat-resistant ferritic stainless steel cold-rolled steel sheet excellent in workability, ferritic stainless hot-rolled steel sheet for cold-rolled material, and production method thereof |
KR101692660B1 (en) | 2013-03-06 | 2017-01-03 | 닛폰 스틸 앤드 스미킨 스테인레스 스틸 코포레이션 | Ferritic stainless steel sheet having excellent heat resistance |
CA2907970C (en) | 2013-03-27 | 2021-05-25 | Nippon Steel & Sumikin Stainless Steel Corporation | Hot-rolled ferritic stainless-steel plate, process for producing same, and steel strip |
JP6639073B2 (en) * | 2014-02-10 | 2020-02-05 | 日鉄日新製鋼株式会社 | Turbo housing and method of manufacturing the same |
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 |
ES2828466T3 (en) * | 2015-12-18 | 2021-05-26 | Nippon Steel Corp | Heat resistant ferritic steel welding material, heat resistant ferritic steel welding joint and method of producing heat resistant ferritic steel welding joint |
CA3015169C (en) * | 2016-03-24 | 2024-02-20 | Nisshin Steel Co., Ltd. | Ti-containing ferritic stainless steel sheet having good toughness, and flange |
JP6796708B2 (en) | 2017-03-27 | 2020-12-09 | 日鉄ステンレス株式会社 | Ferritic stainless steel sheet and its manufacturing method, and exhaust parts |
WO2018180643A1 (en) * | 2017-03-29 | 2018-10-04 | 新日鐵住金ステンレス株式会社 | Ferrite stainless steel having superior wear resistance at high temperature, production method for ferrite stainless steel sheet, exhaust components, high-temperature sliding components, and turbocharger components |
JP6740974B2 (en) * | 2017-07-14 | 2020-08-19 | 株式会社デンソー | Gas sensor |
CN107675075A (en) * | 2017-09-05 | 2018-02-09 | 王业双 | A kind of high-performance high temperature resistant ferritic stainless steel and preparation method thereof |
KR102020513B1 (en) * | 2017-12-11 | 2019-09-10 | 주식회사 포스코 | Ferritic stainless steel excellent in oxidation resistance at high temperature and manufacturing method thereof |
CN111057947A (en) * | 2019-12-09 | 2020-04-24 | 宁波宝新不锈钢有限公司 | Ferrite stainless steel with good high-temperature strength and preparation method thereof |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0478790A1 (en) * | 1990-03-24 | 1992-04-08 | Nisshin Steel Co., Ltd. | Heat-resistant ferritic stainless steel excellent in low-temperature toughness, weldability and heat resistance |
JP2959934B2 (en) | 1993-09-02 | 1999-10-06 | 新日本製鐵株式会社 | Heat-resistant ferritic stainless steel |
JP2000303149A (en) | 1999-04-16 | 2000-10-31 | Sumitomo Metal Ind Ltd | Ferritic stainless steel for automotive exhaust system parts |
JP2002080943A (en) * | 2000-07-04 | 2002-03-22 | Kawasaki Steel Corp | Ferritic stainless steel having excellent secondary processing brittleness resistance and high temperature fatigue characteristic in weld zone |
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 |
JP2005206944A (en) | 2003-12-26 | 2005-08-04 | Jfe Steel Kk | FERRITIC Cr-CONTAINING STEEL AND ITS PRODUCTION METHOD |
JP2005314740A (en) * | 2004-04-28 | 2005-11-10 | Nippon Steel & Sumikin Stainless Steel Corp | Ferritic stainless steel having excellent heat resistance and workability and its production method |
JP2006117985A (en) | 2004-10-20 | 2006-05-11 | Nisshin Steel Co Ltd | Ferritic stainless steel material superior in thermal fatigue characteristic, and automotive waste-gas path member |
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 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5302214A (en) * | 1990-03-24 | 1994-04-12 | Nisshin Steel Co., Ltd. | Heat resisting ferritic stainless steel excellent in low temperature toughness, weldability and heat resistance |
JP3706428B2 (en) * | 1996-03-15 | 2005-10-12 | 新日鐵住金ステンレス株式会社 | Ferritic stainless steel for automotive exhaust system equipment |
JP4357694B2 (en) * | 2000-04-18 | 2009-11-04 | 日新製鋼株式会社 | Ferritic stainless steel for exhaust gas path members of gas turbines |
EP1176220B9 (en) * | 2000-07-25 | 2004-04-21 | JFE Steel Corporation | Ferritic stainless steel sheet having superior workability at room temperatures and mechanical characteristics at high temperatures, and method of producing the same |
JP5348458B2 (en) * | 2007-04-27 | 2013-11-20 | Jfeスチール株式会社 | Cr-containing steel pipe and manufacturing method thereof |
JP5396752B2 (en) * | 2007-10-02 | 2014-01-22 | Jfeスチール株式会社 | Ferritic stainless steel with excellent toughness and method for producing the same |
-
2007
- 2007-11-13 JP JP2007294932A patent/JP5178157B2/en active Active
-
2008
- 2008-10-30 DE DE602008003963T patent/DE602008003963D1/en active Active
- 2008-10-30 EP EP08019006A patent/EP2060650B1/en active Active
- 2008-10-30 ES ES08019006T patent/ES2355171T3/en active Active
- 2008-11-12 US US12/292,072 patent/US20090120536A1/en not_active Abandoned
- 2008-11-13 CN CN2008101733254A patent/CN101435054B/en active Active
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0478790A1 (en) * | 1990-03-24 | 1992-04-08 | Nisshin Steel Co., Ltd. | Heat-resistant ferritic stainless steel excellent in low-temperature toughness, weldability and heat resistance |
JP2696584B2 (en) | 1990-03-24 | 1998-01-14 | 日新製鋼株式会社 | Ferrite heat-resistant stainless steel with excellent low-temperature toughness, weldability and heat resistance |
JP2959934B2 (en) | 1993-09-02 | 1999-10-06 | 新日本製鐵株式会社 | Heat-resistant ferritic stainless 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 |
JP2000303149A (en) | 1999-04-16 | 2000-10-31 | Sumitomo Metal Ind Ltd | Ferritic stainless steel for automotive exhaust system parts |
JP2002080943A (en) * | 2000-07-04 | 2002-03-22 | Kawasaki Steel Corp | Ferritic stainless steel having excellent secondary processing brittleness resistance and high temperature fatigue characteristic in weld zone |
JP2005206944A (en) | 2003-12-26 | 2005-08-04 | Jfe Steel Kk | FERRITIC Cr-CONTAINING STEEL AND ITS PRODUCTION METHOD |
JP2005314740A (en) * | 2004-04-28 | 2005-11-10 | Nippon Steel & Sumikin Stainless Steel Corp | Ferritic stainless steel having excellent heat resistance and workability and its production method |
JP2006117985A (en) | 2004-10-20 | 2006-05-11 | Nisshin Steel Co Ltd | Ferritic stainless steel material superior in thermal fatigue characteristic, and automotive waste-gas path member |
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 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2546378A4 (en) * | 2010-03-11 | 2017-08-16 | Nippon Steel & Sumikin Stainless Steel Corporation | Highly oxidation-resistant ferrite stainless steel plate, highly heat-resistant ferrite stainless steel plate, and manufacturing method therefor |
WO2014001644A1 (en) | 2012-06-26 | 2014-01-03 | Outokumpu Oyj | Ferritic stainless steel |
EP2864518A4 (en) * | 2012-06-26 | 2015-12-30 | Outokumpu Oy | Ferritic stainless steel |
Also Published As
Publication number | Publication date |
---|---|
JP5178157B2 (en) | 2013-04-10 |
CN101435054B (en) | 2012-09-12 |
US20090120536A1 (en) | 2009-05-14 |
CN101435054A (en) | 2009-05-20 |
EP2060650B1 (en) | 2010-12-15 |
JP2009120894A (en) | 2009-06-04 |
ES2355171T3 (en) | 2011-03-23 |
DE602008003963D1 (en) | 2011-01-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2060650B1 (en) | Ferritic stainless steel material for automobile exhaust gas passage components | |
EP2112245B1 (en) | Ferritic stainless steel for exhaust gas passage member | |
JP4538094B2 (en) | High strength thick steel plate and manufacturing method thereof | |
JP4197492B2 (en) | Ferritic stainless steel for exhaust gas flow path members | |
JP5178156B2 (en) | Ferritic stainless steel material for automobile exhaust gas path members | |
JP4542624B2 (en) | High strength thick steel plate and manufacturing method thereof | |
JP4735167B2 (en) | Method for producing wear-resistant steel sheet with excellent low-temperature toughness | |
EP1081245B1 (en) | Heat resistant Cr-Mo alloy steel | |
EP2166120A1 (en) | Ferritic stainless steel having excellent heat resistance | |
JP5396752B2 (en) | Ferritic stainless steel with excellent toughness and method for producing the same | |
KR20140117686A (en) | Ferritic stainless steel plate having excellent heat resistance and excellent workability | |
WO2011111871A1 (en) | Highly oxidation-resistant ferrite stainless steel plate, highly heat-resistant ferrite stainless steel plate, and manufacturing method therefor | |
JP2007119850A (en) | Wear resistant steel plate with excellent low-temperature toughness, and method for manufacturing the same | |
JP4369612B2 (en) | Steel plate for low quenching or normalizing type low alloy boiler steel pipe excellent in toughness, and method of manufacturing steel pipe using the same | |
JP2010132945A (en) | High-strength thick steel plate having excellent delayed fracture resistance and weldability, and method for producing the same | |
CA3021955A1 (en) | Ti-containing ferritic stainless steel sheet for exhaust pipe flange member, production method, and flange member | |
JP5741454B2 (en) | Ni-added steel sheet excellent in toughness and productivity in which Charpy test value at −196 ° C. is 100 J or more for both base metal and welded joint, and manufacturing method thereof | |
JP2923825B2 (en) | Ferritic stainless steel sheet for heat resistance with excellent high-temperature strength and weldability | |
JP3355711B2 (en) | High Cr ferritic heat resistant steel with excellent high temperature strength and toughness | |
JP3387145B2 (en) | High Cr ferritic steel with excellent high temperature ductility and high temperature strength | |
CN114402088B (en) | Composite steel and method for manufacturing same | |
JP2005200746A (en) | Ferritic stainless steel for automobile exhaust system member | |
JPH06264192A (en) | High strength and high toughness martensitic stainless steel for welding structure and its production | |
JPH0959746A (en) | High chromium ferritic steel excellent in high temperature strength | |
JP2021195602A (en) | Low-alloy heat-resistant 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 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA MK RS |
|
17P | Request for examination filed |
Effective date: 20090624 |
|
17Q | First examination report despatched |
Effective date: 20090723 |
|
AKX | Designation fees paid |
Designated state(s): DE ES FR GB |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C22C 38/26 20060101ALI20100429BHEP Ipc: C22C 38/24 20060101ALI20100429BHEP Ipc: C22C 38/22 20060101ALI20100429BHEP Ipc: C22C 38/20 20060101AFI20100429BHEP |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE ES FR GB |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REF | Corresponds to: |
Ref document number: 602008003963 Country of ref document: DE Date of ref document: 20110127 Kind code of ref document: P |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2355171 Country of ref document: ES Kind code of ref document: T3 Effective date: 20110323 |
|
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 |
|
26N | No opposition filed |
Effective date: 20110916 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602008003963 Country of ref document: DE Effective date: 20110916 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 8 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 9 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 10 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: PLFP Year of fee payment: 11 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: PC2A Owner name: NIPPON STEEL STAINLESS STEEL CORPORATION Effective date: 20220526 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: 732E Free format text: REGISTERED BETWEEN 20220526 AND 20220601 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R081 Ref document number: 602008003963 Country of ref document: DE Owner name: NIPPON STEEL STAINLESS STEEL CORPORATION, JP Free format text: FORMER OWNER: NISSHIN STEEL CO., LTD., TOKIO/TOKYO, JP |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20231020 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20231222 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20231024 Year of fee payment: 16 Ref country code: DE Payment date: 20231020 Year of fee payment: 16 |