EP2366035B1 - Feuillard d'acier au manganèse à teneur accrue en phosphore et son procédé de fabrication - Google Patents
Feuillard d'acier au manganèse à teneur accrue en phosphore et son procédé de fabrication Download PDFInfo
- Publication number
- EP2366035B1 EP2366035B1 EP09760726.1A EP09760726A EP2366035B1 EP 2366035 B1 EP2366035 B1 EP 2366035B1 EP 09760726 A EP09760726 A EP 09760726A EP 2366035 B1 EP2366035 B1 EP 2366035B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- steel strip
- manganese steel
- rolled
- hot
- cold
- 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.)
- Not-in-force
Links
- 229910000617 Mangalloy Inorganic materials 0.000 title claims description 43
- 229910052698 phosphorus Inorganic materials 0.000 title claims description 34
- 238000000034 method Methods 0.000 title claims description 30
- 230000008569 process Effects 0.000 title claims description 28
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title description 21
- 239000011574 phosphorus Substances 0.000 title description 21
- 229910000831 Steel Inorganic materials 0.000 claims description 92
- 239000010959 steel Substances 0.000 claims description 92
- 238000000137 annealing Methods 0.000 claims description 31
- 238000005096 rolling process Methods 0.000 claims description 29
- 239000000047 product Substances 0.000 claims description 27
- 238000001816 cooling Methods 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 23
- 229910052799 carbon Inorganic materials 0.000 claims description 22
- 239000000126 substance Substances 0.000 claims description 22
- 239000011572 manganese Substances 0.000 claims description 21
- 229910052710 silicon Inorganic materials 0.000 claims description 20
- 238000005097 cold rolling Methods 0.000 claims description 19
- 238000004519 manufacturing process Methods 0.000 claims description 19
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 17
- 229910052782 aluminium Inorganic materials 0.000 claims description 17
- 229910052757 nitrogen Inorganic materials 0.000 claims description 16
- 238000005266 casting Methods 0.000 claims description 9
- 229910052804 chromium Inorganic materials 0.000 claims description 9
- 229910052742 iron Inorganic materials 0.000 claims description 9
- 229910052721 tungsten Inorganic materials 0.000 claims description 8
- 238000005098 hot rolling Methods 0.000 claims description 7
- 239000012535 impurity Substances 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 238000001953 recrystallisation Methods 0.000 claims description 7
- 229910052750 molybdenum Inorganic materials 0.000 claims description 5
- 229910052758 niobium Inorganic materials 0.000 claims description 5
- 239000011265 semifinished product Substances 0.000 claims description 5
- 229910052719 titanium Inorganic materials 0.000 claims description 5
- 239000010960 cold rolled steel Substances 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims 4
- 229910052720 vanadium Inorganic materials 0.000 claims 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- 230000015572 biosynthetic process Effects 0.000 description 15
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 14
- 239000002245 particle Substances 0.000 description 14
- 239000010703 silicon Substances 0.000 description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 13
- 229910052748 manganese Inorganic materials 0.000 description 12
- 229910000734 martensite Inorganic materials 0.000 description 12
- 239000011651 chromium Substances 0.000 description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 10
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 10
- 239000013078 crystal Substances 0.000 description 10
- 230000007246 mechanism Effects 0.000 description 10
- 238000005275 alloying Methods 0.000 description 9
- 229910001566 austenite Inorganic materials 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- 230000009467 reduction Effects 0.000 description 7
- 238000007792 addition Methods 0.000 description 6
- 229910001567 cementite Inorganic materials 0.000 description 6
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 6
- 239000006104 solid solution Substances 0.000 description 6
- 230000035882 stress Effects 0.000 description 6
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 150000001247 metal acetylides Chemical class 0.000 description 5
- 239000010955 niobium Substances 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- 238000005336 cracking Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000012467 final product Substances 0.000 description 4
- 238000011835 investigation Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 4
- 239000010937 tungsten Substances 0.000 description 4
- 238000005246 galvanizing Methods 0.000 description 3
- 238000009847 ladle furnace Methods 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 238000005482 strain hardening Methods 0.000 description 3
- 230000009466 transformation Effects 0.000 description 3
- 229910000805 Pig iron Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910000794 TRIP steel Inorganic materials 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000029142 excretion Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 description 1
- 229910001339 C alloy Inorganic materials 0.000 description 1
- 229910000914 Mn alloy Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 206010003549 asthenia Diseases 0.000 description 1
- 229910001563 bainite Inorganic materials 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000009749 continuous casting Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000010891 electric arc Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000000635 electron micrograph Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QMQXDJATSGGYDR-UHFFFAOYSA-N methylidyneiron Chemical compound [C].[Fe] QMQXDJATSGGYDR-UHFFFAOYSA-N 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 238000004881 precipitation hardening Methods 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 238000007634 remodeling Methods 0.000 description 1
- 239000008137 solubility enhancer Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 238000009849 vacuum degassing Methods 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING 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
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/005—Heat treatment of ferrous alloys containing Mn
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING 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
- C21D6/00—Heat treatment of ferrous alloys
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING 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
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING 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
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0205—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips of ferrous alloys
-
- 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
- C21—METALLURGY OF IRON
- C21D—MODIFYING 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
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/001—Austenite
Definitions
- the invention relates to an austenitic manganese steel strip and to a method for producing austenitic manganese steel strips. Furthermore, the invention relates to a manganese steel sheet with a deformed, in particular stretched or deep-drawn sheet steel section.
- Manganese austenites are lightweight structural steels that are particularly strong and elastic at the same time.
- the weight reduction afforded by the higher strength makes manganese austenite a material of great potential in the automotive industry. Because through lighter bodies fuel consumption can be reduced, with a high elasticity and stability for the production of the body parts and their crash behavior are important.
- TRIP-steels (TRANSformation Induced Plasticity), which are increasingly used in the automotive industry, are already known.
- High-alloyed TRIP steels reach high tensile strengths of up to more than 1000 MPa and can have elongations of up to about 30%. Due to these high mechanical properties thinner plates and thus a reduction in body weight can be achieved in vehicle construction.
- TRIP steel consists of several phases of iron-carbon alloys, mainly ferrite, bainite and carbon-rich residual austenite.
- the TRIP effect is based on the deformation-induced transformation of residual austenite into martensite. This remodeling of the crystal structure results in a simultaneous increase in strength and formability in product manufacture or in product use in the event of a crash.
- the TRIP effect can be specifically influenced by admixing the alloying elements aluminum and silicon.
- TWIP TWinning Induced Plasticity
- the particular ductility of TWIP steels can be caused by different mechanisms in the crystal structure.
- the extensibility can be promoted by lattice defects in the crystal structure, at which the crystal structure can fold-induced induced, whereby the folding mechanism runs on a mirror plane and regularly mirrored crystal areas (so-called twins) arise.
- twins Different types of twins can be distinguished.
- further effects such as the occurrence of slip bands can influence the mechanical properties.
- TWIP steels Due to their high ductility, TWIP steels are excellently suited for the production of metal sheets in the automotive industry, especially for accident-relevant areas of the body. TWIP steels have an austenitic structure and are characterized by a high manganese content (usually over 25%) and relatively high alloying additions of aluminum and silicon.
- hot and cold rolled austenitic manganese steel tapes are from the US 2008/0035248 A1 which have a maximum phosphorus content of 0.05% and whose mean particle sizes are given as ⁇ 10 ⁇ m for hot-rolled manganese steel or ⁇ 5 ⁇ m for cold-rolled manganese steel.
- One object of the invention is to provide a steel with improved mechanical properties.
- good weldability of the steel and / or good formability should be achievable.
- the invention aims to provide a method for producing a steel with improved mechanical properties, in particular high ductility in combination with high tensile strength, and in particular a good weldability and a good formability.
- the steel according to the invention is characterized, inter alia, by the fact that with a carbon content in% by weight of about 0.4% ⁇ C ⁇ 1.2%, a manganese content of about 12.0% ⁇ Mn ⁇ 25.0 % is available.
- the percentages of chemical constituents in this document always refer to percentages by weight, phosphorus, which increases the yield strength or tensile strength, reduces the elongation at break, promotes brittleness, lowers austenite stability, hampers cementite precipitation, and usually weldability decreases, is alloyed according to the invention in a relatively high proportion of at least 0.03%. It turned out in the case of an extensive omission of the alloying element aluminum (Al ⁇ 0.05%) with this alloy concept, high mechanical properties and a surprisingly good weldability with very good formability of the manganese steel strip produced can be achieved.
- a product of elongation at break in MPa and tensile strength in percent of over 65,000 MPa%, especially over 70,000 MPa% can be obtained.
- this product is above 75,000 MPa% and may be above 80,000 MPa%, in particular also above 85,000 MPa%, preferably above 100,000 MPa%.
- the bake-hardening effect can also be used to increase the yield strength.
- the bake hardening values were determined according to the European standard EN 10325.
- the high levels of interstitially dissolved alloying elements ensure an increased bake-hardening potential and can further improve the mechanical properties of the final product.
- the manganese content of an austenitic manganese steel tape according to the invention may preferably be in the range of 14% ⁇ Mn ⁇ 18.0%, in particular 14% ⁇ Mn ⁇ 16.5%.
- the grain size can be influenced in a targeted manner by the ratio of N to Al.
- AlN aluminum nitride
- a high grain size can be made possible with an austenitic manganese steel strip.
- the Al content can be kept very low in the alloying concept pursued here, as much carbon is available for the deoxidation of the liquid steel.
- the manganese steel according to the invention can have the lowest possible aluminum content, which is limited only by unavoidable impurities in the production process (ie no aluminum addition). In the case of the steel strip according to the invention, this results in maximum grain size growth during recrystallization (ie during hot rolling or during annealing).
- appropriately high phosphorus contents of 0.03% ⁇ P, in particular 0.05% ⁇ P, 0.06% ⁇ P, 0.07% ⁇ P, 0.08% ⁇ P and also 0.10% ⁇ P are used. It may even be provided a phosphorus content 0.20% ⁇ P.
- a high phosphorus content can increase the tensile strength and especially the yield strength at higher particle sizes. Surprisingly, no significant reduction in elongation at break and no significant deterioration in weldability were observed with an increase in phosphorus content.
- the tensile strength and the yield strength as well as the elongation at break of the produced steel strip can be changed in a targeted manner.
- the larger the grain the lower the tensile strength and the yield strength and the higher the elongation at break.
- Medium particle sizes of more than 5 ⁇ m or more than 10 ⁇ m can be set.
- the manganese steel according to the invention preferably has a very low silicon content (Si ⁇ 1.0%, in particular Si ⁇ 0.2%, particularly preferably Si ⁇ 0.05%), which is optionally limited only by unavoidable impurities in the production process (ie in this case no addition of silicon, the Si content may then be below Si ⁇ 0.03%).
- silicon has an influence on deformation mechanisms. Silicon impairs twinning, ie a low silicon concentration facilitates the formation of twins and possibly the formation of small micro-twins or nano-twins.
- the silicon content of the manganese steel of the present invention can be set low, preferably as low as possible.
- the silicon content can be kept very low, as much carbon is available for the deoxidation of the liquid steel, and because the strength of the steel (silicon causes an increase in strength) by other measures such as high concentrations of C and / or P. is guaranteed.
- Niobium (Nb), vanadium (V) and titanium (Ti) are elements that form precipitates (carbides, nitrides, carbonitrides) and may optionally be added to improve strength through precipitation hardening.
- these elements have a grain-fine effect, which is why their concentration should be kept low, if a high grain size is to be ensured.
- Nickel can stabilize the austenite phase (so-called ⁇ -stabilizer). Nickel may optionally be added in larger amounts (e.g., over 1% to 5% or even 10%).
- the solid solution strengthener chromium (Cr) stabilizes the ⁇ -ferrites. Additions of chromium up to 10% by weight prefer the formation of ⁇ -martensite and / or ⁇ '-martensite, resulting in higher tensile strength and lower ductility.
- the proportion of chromium should therefore be limited. For example, Cr ⁇ 5%, in particular Cr ⁇ 0.2%, can preferably be set.
- Molybdenum (Mo) and tungsten (W) also show a grain-refining angle. Tungsten has a high affinity for carbon and forms the hard and very stable carbides W 2 C and WC steel. The proportion of tungsten should be limited.
- W ⁇ 1% in particular W ⁇ 0.02%
- Tungsten is an even better solid solubility enhancer than chromium and also forms carbides (but to a lesser extent than chromium).
- Mo ⁇ 1%, in particular, Mo ⁇ 0.02% is set.
- the grain size of a hot-rolled steel strip is also greatly influenced by the final rolling temperature during hot rolling.
- the steel strip according to the invention can be rolled with a final rolling temperature of between 750 ° C and 1050 ° C, preferably between 800 ° C and 900 ° C. For a given chemical composition can be adjusted by the choice of the final rolling temperature, the average grain size.
- the tensile strength of the hot-rolled steel may preferably be above 1050 MPa.
- Cold rolling can increase the mechanical properties of the hot rolled austenitic manganese steel strip.
- the grain size of a cold-rolled steel strip is strongly influenced by the annealing temperature.
- the annealing performed after the cold rolling may be carried out at an annealing temperature between 750 ° C and 1050 ° C, and in particular, the annealing temperature may be greater than 900 ° C.
- Tensile strengths of more than 1100 MPa, in particular more than 1200 MPa can be achieved with an elongation at break of more than 75%, in particular over 80%.
- a manganese steel sheet according to the invention with the said chemical compositions has a reshaped, in particular stretched or deep-drawn sheet steel section whose microstructure micro-twins having an average thickness of less than 30 nm, in particular less than 20 nm and nano-twins having an average thickness of less than 10 nm.
- these micro- and nano-twins form during the forming process, whereby the high mechanical properties of the starting material are presumably due - at least in part - to this deformation mechanism.
- the semi-finished product is heated to a temperature above 1100 ° C after casting a semi-finished steel.
- the heated semi-finished product is rolled at a final rolling temperature between 750 ° C and 1050 ° C, preferably between 800 ° C and 900 ° C.
- the rolled steel strip is cooled at a rate of 20 ° C./s or higher.
- rapid cooling of the hot rolled steel strip is performed at a rate of 50 ° C / s or higher, more preferably 200 ° C / s or higher. Rapid cooling helps to provide high solids solubility of C, N and P elements in the granules.
- the rapid cooling leads to a "freezing" of the dissolved elements without or with only little excretion formation.
- the excretion formation can be largely prevented by a rapid cooling.
- the occurrence of grain boundary carbides as well as embrittlement (grain boundary segregation) of the steel structure caused by high phosphorus contents can be prevented by a rapid cooling.
- the higher the cooling rate the better and more uniformly can carbon and phosphorus be kept in solution. Cooling rates of over 100 ° C / s to 400 ° C / s were used. Cooling rates of more than 400 ° C / s to even more than 600 ° C / s are also possible. If necessary, before the rapid cooling an intermediate phase of several seconds, in particular 1 to 4 seconds, persist, in which the steel strip slowly cools in air to improve the recrystallization of the phosphorus-alloyed steel strip.
- the hot rolled steel strip is cold rolled and then annealed for recrystallization.
- the annealing temperature may be between 750 ° C and 1150 ° C and in particular greater than 900 ° C.
- the grain size can be changed again, after annealing, a grain size of about 15 ⁇ m, especially about 20 microns may be provided to achieve a high elongation at break and possibly an improvement in the solid solubility of carbon, phosphorus and optionally nitrogen , A high tensile strength can be ensured in particular by a relatively high proportion of phosphorus (and carbon).
- the rolled steel strip is cooled at a rate of 20 ° C / s or higher.
- rapid cooling of the cold-rolled steel strip is conducted at a rate of 50 ° C / sec or higher, more preferably 200 ° C / sec or higher.
- a rapid cooling also contributes to effecting a high and uniform solid solubility of carbon, phosphorus and nitrogen in the grains and thereby to achieve a high tensile strength even with large grains. Cooling rates of over 100 ° C / s to 400 ° C / s were used. Cooling rates of more than 400 ° C / s to even more than 600 ° C / s are also possible. If necessary, before the rapid cooling an intermediate phase of several seconds, in particular 1 to 6 seconds, persist, in which the steel strip slowly cools in air to improve the recrystallization of the phosphorus-alloyed steel strip.
- pig iron is produced in the blast furnace or with a smelting reduction process such as Corex or Finex.
- the Tecnored process is also possible.
- the pig iron is then converted into steel, for example, in an oxygen inflation process (eg in an LD (Linz-Donawitz) / BOF (Bottom Oxygen Furnace) process).
- a vacuum degassing eg according to the Ruhrstahl-Heraeus process (RH)
- RSH Ruhrstahl-Heraeus process
- a second production route which may be particularly suitable for manganese steels, uses an electric arc furnace (EAF) for steelmaking and an AOD converter for decarburizing the liquid steel. Again, prior to casting the steel, a ladle furnace can be used to heat and alloy the molten metal.
- EAF electric arc furnace
- AOD converter AOD converter
- the steel thus produced can be further processed by means of various casting techniques such as block casting, casting rolls, thin strip casting or continuous casting.
- the steel body produced during casting is called semifinished and may e.g. be realized in the form of slabs, billets or blocks.
- the slab is further processed in hot strip mills to hot strip.
- rolling mills for narrow strip width less than 100 mm
- middle strip width between 100 mm and 600 mm
- broadband width greater 600 mm
- blocks and billets to profiles, pipes or wires is possible.
- a rolling temperature between about 1100 ° C and 1300 ° C, optionally also higher, can be used.
- the rolling end temperature may for example be between 750 ° C and 1050 ° C and in particular between 800 ° C and 900 ° C.
- Different rolling end temperatures result in different average particle sizes of the hot-rolled steel strip according to the dynamic recrystallization at the prevailing temperature. The lower the final rolling temperature, the smaller the average particle size obtained for a given chemical composition. With a reduction of the mean grain size, the tensile strength decreases and the breaking strength of the hot-rolled steel strip, the elongation at break decreases.
- roller end temperature is too low, however, there is the risk that the high grain refining in manganese steels causes a loss of plastic deformability as a result of the increased strength. Furthermore, due to the phase stability, low cementation temperatures increasingly lead to the formation of cementite ((Fe, Mn) 3 C), which may affect the mechanical properties. The cementite precipitates reached a particle size at rolling end temperatures below 740 ° C., which significantly impaired the mechanical properties.
- the mean grain size of the hot strip steel strip is further influenced by the content of aluminum and nitrogen. It is known that manganese increases the solubility of nitrogen in liquid iron. Nitrogen dissolved in liquid iron forms aluminum nitride precipitates with aluminum, which hinder the migration of grain boundaries and thus grain growth. Aluminum nitride may further cause hot working cracking. It has been found that by targeted control of the aluminum and nitrogen content in steel low Endwalztemperaturen well below 950 ° C and especially below 900 ° C down to 750 ° C are possible without causing cracking occurs. However, the formation of large cementite particles, which begins with a lowering of the final rolling temperature below about 740 ° C to 800 ° C, to avoid. Particularly preferred final rolling temperatures in the hot rolling process can therefore be in the range of 800 ° C to 900 ° C.
- the avoidance of cracking has been achieved at said final rolling temperatures in the range of 800 ° C to 900 ° C with chemical compositions in which an extremely small amount of aluminum up to 0.008% or 0.010% in combination with a low content of nitrogen to eg 0.030% or 0.036% were used.
- the respective concentrations of the elements are interdependent. If less nitrogen is used, more aluminum is allowed and vice versa. In this respect, higher nitrogen contents than stated above are possible with a low aluminum content.
- rapid cooling of the hot strip is performed at as high a cooling rate as possible (e.g., above 50 ° C / s or higher).
- the cooling can be done by applying the hot strip with water.
- the hot strip is then removed in a continuous pickling plant e.g. cleaned with sulfuric acid (descaled).
- the hot strip may have a thickness of 1.5 to 2.0 mm, for example.
- An annealing step is usually not carried out in the hot strip products produced here. In a particular embodiment, however, such an annealing step is carried out and causes a grain coarsening as well as an increase in the elongation at break.
- the hot strip produced in the manner described above can be further processed by cold rolling and annealing to the cold strip product.
- cold rolling the hot strip is further reduced in thickness and the mechanical and technological properties of the band are set.
- low strip thicknesses in the range of about 0.7 mm to 1.75 mm of the cold strip can be produced.
- Cold-strip products with such small thicknesses are of particular interest in the automotive sector for crash-absorbing components.
- the cold rolling is preferably carried out using high rolling forces.
- Roll stands with 2 to 20 rolls can be used.
- a Sendzimir rolling mill with 12 rolls consists for example of a symmetrical arrangement of each of 3 back rolls, 2 intermediate rolls and 1 roller defining the nip pressure roller.
- a Sendzimir rolling mill with 20 rolls for example, consists of a symmetrical arrangement of 4 back rolls, 3 outer intermediate rolls, 2 inner intermediate rolls and 1 roller defining the nip pressure roller. It showed a surprisingly good rolling and low cracking compared to other manganese steels.
- the percent reduction in thickness (cold rolling degree) achieved during cold rolling may be above 40%, e.g. between 40% and 60%.
- Cold rolling was also carried out with cold rolling degrees above 60%, especially above 80%. It was cold rolled with and without train.
- the steel strip is annealed for recrystallization.
- the annealing may e.g. be carried out after the continuous annealing or annealing process.
- the solidification of the microstructure occurring during cold rolling is reduced again. It comes here about nucleation and grain growth to a rebuilding of the structure.
- the annealing can be carried out at temperatures between 750 ° C and 1250 ° C, in particular 750 ° C to 1150 ° C and about 5 seconds to 5 minutes, in particular 2 to 5 minutes to annealing temperature persist.
- the annealing time is sufficient to heat the band substantially full volume to the respective annealing temperature.
- the hot steel strip is rapidly cooled, preferably quenched by exposure to water or in the gas stream (Gasjet). It has been found that a particularly rapid cooling is helpful to a high solids solubility of the elements C, N and P in the grains too cause. In particular, the embrittlement (grain boundary segregation) critical with a high phosphorus content could be largely or completely prevented by increasing the cooling rate. Cooling rates of over about 50 ° C or over 100 ° C per second are advantageous. Furthermore, cooling rates of more than 200 ° C., 300 ° C. or 400 ° C. per second may preferably also be provided, whereby experiments with cooling rates above 500 ° C. and above 600 ° C. per second have also been successfully carried out.
- cold-rolling After cold-rolling, annealing and cooling, cold-rolling can be carried out to set a suitable flatness of the cold-rolled strip.
- thickness reductions e.g. 0.5%, 1.5%, 5%, 25% and more than 40%, or appropriate intermediate values.
- galvanizing for example hot-dip galvanizing or electrolytic galvanizing
- the chemical composition of the steel may vary over a wide range in other alloying elements. As upper limit values are provided: 0.5% ⁇ V, 0.5% ⁇ Nb, 0.5% ⁇ Ti, 10% ⁇ Cr, 10% ⁇ Ni, 1% ⁇ W, 1% ⁇ Mo, 3% ⁇ Cu, 0.02% ⁇ B, the rest as mentioned iron and production-related impurities.
- Table 1 shows the chemical composition of four steel strips X80Mn16-0.01P, X80Mn16-0.03P, X80Mn16-0.08P and X80Mn16-0.1.0P with a phosphorus concentration between 0.011 and 0.102% by weight.
- the hot strip process was carried out in each case as described above.
- the used final rolling temperatures (between 750 ° C and 1030 ° C) as well as the obtained mechanical properties of the produced hot rolled products X80Mn16-0.01P, X80Mn16-0.03P, X80Mn16-0.08P and X80Mn16-0.10P are given in Table 2.
- the mechanical values obtained in the tensile tests were determined according to European standard "EUROPEAN STANDARD EN 10002-1, July 2001", which is hereby incorporated by reference into the disclosure of this document. All values given in Table 2 are also disclosed as lower limits on the size to which they relate.
- the hot strip (WB) can optionally be further processed into a cold strip (KB).
- the cold strip processing was carried out with the processing parameters given in Table 3.
- Table 3 The mechanical properties of the cold-rolled products of the chemical compositions X80Mn16-0.01P, X80Mn16-0.03P, X80Mn16-0.08P and X80Mn16-0.10P prepared in this way are given in Table 3. All values given in Table 3 are also disclosed as lower limits on the size to which they relate.
- the cold-rolled products with the KB numbers 1 to 3 are therefore based on approximately the hot-rolled product with the WB number 2 (the final rolling temperatures differ only by 10 ° C) and the cold-rolled products with the KB numbers 4 to 6 is approximately based on the hot-rolled product with the WB number 5 (the final rolling temperatures differ only by 30 ° C).
- Table 3 shows that tensile strengths Rm over 1100 MPa and even above 1200 MPa are attained, and that even with large average particle sizes (15 ⁇ m in the case of X80Mn16-0.03P (KB no. 6) and X80Mn16-0.10P (KB No. 10) as well as over 20 ⁇ m or possibly even 25 ⁇ m in the case of the other samples), tensile strengths Rm above 1000 MPa can still be achieved.
- the tensile strength Rm is defined as the stress occurring at maximum tensile force on the workpiece.
- the elongation at break A 50 given in Table 3 is the percentage permanent change in length after breakage of the tensile test specimen (according to EN 10002-1), based on the initial measuring length, based on an initial measuring length of 50 mm.
- EN 10002-1 the percentage permanent change in length after breakage of the tensile test specimen
- Another important parameter for the mechanical properties of steel strips is the product of tensile strength and elongation at break. Especially with large average particle sizes, high product values are achieved. The reason for this is that large grains lead to higher elongation at break values and the tensile strength, which usually decreases markedly with increasing grain size, is maintained as far as possible according to the invention by the relatively high carbon and / or phosphorus content.
- Table 4 gives the results of a study of the weldability of the steels of the chemical compositions X80Mn16-0.01P, X80Mn16-0.03P, X80Mn16-0.08P and X80Mn16-0.10P: Table 4 - Investigation of weldability - composition Imine (n / a) Imax (n / a) deltaI (n / a) X80Mn16-0.01P 5.2 6.3 1.1 X80Ma16-0.03P 4.7 5.8 1.1 X80Mn16-0.08P 5.2 6.4 1.2 X80Mn16-0.08P 5.3 6.6 1.3 X80Mn16-0.10P 5.2 6.4 1.2 X80Mn16-0.10P 5.1 6.6 1.5
- Fig. 1 the mean grain size of the aluminum nitride-poor cold-rolled steel strips specified in Table 3 with the chemical compositions X80Mn16-0.01P, X80Mn16-0.03P, X80Mn16-0.08P and X80Mn16-0.10P is shown as a function of the annealing temperature during the cold strip process.
- the cold-rolled strip products shown here were based on a final rolling temperature of 900 ° C in the hot strip process.
- the graph it can be seen that the steel bands and X80Mn16-0.01P X80Mn16-0.03P at annealing temperatures of about 920 ° C achieve average grain sizes more than 15 ⁇ m.
- the phosphorus-rich steel strips of the chemical compositions X80Mn16-0.08P and X80Mn16-0.10P achieved even larger average particle sizes at comparable annealing temperatures.
- the mean particle sizes were determined by light microscopic investigations on micrographs.
- Fig. 2 shows a graph in which the work hardening n (here the n 10/20 value) of the steel strips mentioned above, which is also referred to as solidification exponent , compared with the vertical anisotropy (r 0/15 -, r 45/15 -, and r 90/15 value) is shown.
- the n value was determined in accordance with standard ISO 10275, issue 2006-07, which is hereby incorporated by reference into the disclosure of this document.
- the vertical anisotropy is in accordance with standard ISO 10113, edition 2006-09 which is hereby incorporated by reference into the disclosure of this document. Since the mechanical properties of a larger dispersion than those in Fig. 1 having shown average grain size, several samples of said steel strips were examined.
- n 10/20 values above 0.5 can be achieved at a r 0/15 , r 45/15 and r 90/15 value in the range from 0.6 to 1.5 .
- the phosphorus-rich steel strips of the chemical compositions X80Mn16-0.08P and X80Mn16-0.10P achieve slightly higher n-values than the steel strips of the chemical compositions X80Mn16-0.01P and X80Mn16-0.03P.
- the steel strips according to the invention have a good cold workability, which is particularly important for further processing in drawing and deep drawing processes.
- FIGS. 3A-C show schematic representations of microstructures observed in electron beam microscopic studies on reshaped samples of the steels of the invention.
- Fig. 3A shows one direction activated System with conventional twinning, where lines 1 represent the mirror lines of the twins.
- Fig. 3B shows a unidirectional system with micro- or nano-twins 2.
- the micro- or nano-twins 2 are lath-shaped and often arranged side by side in larger numbers.
- the lath thickness is referred to as the thickness d of the micro- or nano-twins 2 and is typically much smaller than the thickness of common twins.
- Fig. 3C shows a bi-directionally activated micro- or nano-twin system 2. It can be seen that bi-directional micro- or nano-twins 2 occur.
- Fig. 4 shows an electron micrograph of a steel structure according to the invention after a deformation or tensile stress. A large number of pale-shaped micro- and nano-twins are recognizable in the bright field.
- Fig. 5 shows a microsection of the weld nugget of a steel structure according to the invention after a weld.
- X80Mn16-0.10P samples were used. It can be seen that the basic hardness as well as the maximum hardness in the heat-affected zones and the hardness in the weld nugget agree well and have only slight deviations. These deviations are in the range of the measuring tolerance. It is further recognized that there are no cracks or martensite in the structure.
- the n-value is largely determined by the chemical composition. That is, the strength of the final product that can be achieved by deformation depends on how easily dislocations can travel in the crystal. In the fcc crystal lattice, the solid solubility of C and N is greater than in the bcc crystal lattice.
- the increase in tensile strength caused by solid solution of C and P is utilized, whereby in recent investigations tensile strength values of 1100 MPa could be measured with an extremely high breaking elongation of 95%.
- the hardening achieved by solid solution of said elements makes it possible to increase the n-value considerably. As a result, the highest reported product values of tensile strength and elongation at break are achieved. This is particularly due to the use of high phosphorus concentrations and the associated increase in strength - especially at relatively large mean particle sizes - attributed.
- the hot strip or cold strip is cut in further processing into steel sheets, e.g. be used in automotive technology for the production of body parts.
- steel according to the invention can also be used in rails, switches, in particular switch hearts, rod material, pipes, hollow profiles or high-strength wires.
- the steel sheets are brought by forming processes such as deep drawing in the desired shape and then further processed into the final products (eg body part).
- the forming process at least portions of the steel sheets are subjected to a mechanical stress (usually tensile stress), so that in these areas, the deformation mechanisms described above are effective.
- a mechanical stress usually tensile stress
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Heat Treatment Of Sheet Steel (AREA)
- Heat Treatment Of Steel (AREA)
Claims (15)
- Bande d'acier austénitique au manganèse laminée à chaud, présentant une composition chimique, en données pondérales, de
Al ≤ 0,05%, V ≤ 0,5%, Nb ≤ 0,5%, Ti ≤ 0,5%, Cr ≤ 10%, Ni ≤ 10%, W ≤ 1%, Mo ≤ 1%, Cu ≤ 3%, B ≤ 0,02%, N ≤ 0,04%, le reste étant du fer et des impuretés liées à la production, et présentant une grosseur moyenne de grain supérieure à 13 µm, un produit de l'allongement à la rupture en % et de la résistance à la traction en MPa supérieur à 65.000, en particulier supérieur à 70.000 MPa% étant obtenu. - Bande d'acier austénitique au manganèse laminée à chaud selon la revendication 1, présentant comme propriété qu'un échantillon de la bande d'acier au manganèse, après avoir été soumis à un procédé de formage, présente, dans sa structure, des micromacles présentant une épaisseur moyenne inférieure à 30 nm, en particulier inférieure à 20 nm, en particulier inférieure à 10 nm.
- Bande d'acier austénitique au manganèse, laminée à chaud selon l'une quelconque des revendications précédentes, présentant une teneur en P ≥ 0,05%, en particulier P ≥ 0,06%, en particulier P ≥ 0,08%, plus particulièrement P ≥ 0,10%.
- Bande d'acier austénitique au manganèse, laminée à chaud selon l'une quelconque des revendications précédentes, présentant une teneur en Si ≤ 1,0%, en particulier Si ≤ 0,2%, plus particulièrement Si ≤ 0,05%.
- Bande d'acier austénitique au manganèse, laminée à chaud selon l'une quelconque des revendications précédentes, présentant une grosseur moyenne de grain supérieure à 18 µm, en particulier supérieure à 20 µm.
- Bande d'acier austénitique au manganèse laminée à froid, présentant une composition chimique, en données pondérales, de
Al ≤ 0,05%, V ≤ 0,5%, Nb ≤ 0,5%, Ti ≤ 0,5%, Cr ≤ 10%, Ni ≤ 10%, W ≤ 1%, Mo ≤ 1%, Cu ≤ 3%, B ≤ 0,02%, N ≤ 0,04%, le reste étant du fer et des impuretés liées à la production, et présentant une grosseur moyenne de grain supérieure à 5 µm, un produit de l'allongement à la rupture en % et de la résistance à la traction en MPa supérieur à 75.000, en particulier supérieur à 80.000 MPa% étant obtenu. - Bande d'acier austénitique au manganèse laminée à froid selon la revendication 6, présentant comme propriété qu'un échantillon de la bande d'acier au manganèse, après avoir été soumis à un procédé de formage, présente, dans sa structure, des micromacles présentant une épaisseur moyenne inférieure à 30 nm, en particulier inférieure à 20 nm, en particulier inférieure à 10 nm.
- Bande d'acier austénitique au manganèse, laminée à froid selon l'une quelconque des revendications 6 ou 7, présentant une teneur en P ≥ 0,06%, en particulier P ≥ 0,06%, en particulier P ≥ 0,08%, plus particulièrement P ≥ 0,10%.
- Bande d'acier austénitique au manganèse, laminée à froid selon l'une quelconque des revendications 6 à 8, présentant une teneur en Si ≤ 1,0%, en particulier Si ≤ 0,2%, plus particulièrement Si ≤ 0,05%.
- Bande d'acier austénitique au manganèse, laminée à froid selon l'une quelconque des revendications 6 à 9, présentant une grosseur moyenne de grain supérieure à 15 µm, en particulier supérieure à 20 µm.
- Bande d'acier au manganèse, présentant une composition chimique, en données pondérales, de
Al ≤ 0,05%, V ≤ 0,5%, Nb ≤ 0,5%, Ti ≤ 0,5%, Cr ≤ 10%, Ni ≤ 10%, W ≤ 1%, Mo ≤ 1%, Cu ≤ 3%, B ≤ 0,02%, N ≤ 0,04%, le reste étant du fer et des impuretés provoquées par la production et présentant une section en tôle d'acier étirée sur forme ou emboutie, dont la structure présente des micromacles présentant une épaisseur inférieure à 30 nm, en particulier inférieure à 20 nm. - Procédé pour la production d'une bande d'acier austénitique au manganèse laminée à chaud, présentant une composition chimique, en données pondérales, de
le reste étant du fer et des impuretés provoquées par la production, présentant les étampes :coulée d'un produit semi-fini en acier ;chauffage du produit semi-fini à une température supérieure à 1100°C ;laminage du produit semi-fini à une température de fin de laminage entre 750°C et 1050°C, la grosseur moyenne de grain après le laminage à chaud étant supérieure à 13 µm ;et refroidissement de la bande d'acier laminée à une vitesse de 20°C/s ou plus. - Procédé selon la revendication 12, la grosseur moyenne de grain après le laminage à chaud étant supérieure à 20 µm.
- Procédé pour la production d'une bande d'acier austénitique au manganèse laminée à froid, présentant les étapes :mise à disposition d'une bande d'acier laminée à chaud produite selon un procédé des revendications 12 ou 13 ;laminage à froid de la bande d'acier ; etrecuit de la bande d'acier laminée à froid pour sa recristallisation.
- Procédé selon la revendication 14, la température de recuit étant située entre 750°C et 1150°C et en particulier supérieure à 900°C.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008056844A DE102008056844A1 (de) | 2008-11-12 | 2008-11-12 | Manganstahlband und Verfahren zur Herstellung desselben |
| PCT/EP2009/008065 WO2010054813A1 (fr) | 2008-11-12 | 2009-11-12 | Feuillard d'acier au manganèse à teneur accrue en phosphore et son procédé de fabrication |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2366035A1 EP2366035A1 (fr) | 2011-09-21 |
| EP2366035B1 true EP2366035B1 (fr) | 2017-07-05 |
Family
ID=41796429
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP09760726.1A Not-in-force EP2366035B1 (fr) | 2008-11-12 | 2009-11-12 | Feuillard d'acier au manganèse à teneur accrue en phosphore et son procédé de fabrication |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9677146B2 (fr) |
| EP (1) | EP2366035B1 (fr) |
| KR (1) | KR101387040B1 (fr) |
| CN (1) | CN102216474B (fr) |
| DE (1) | DE102008056844A1 (fr) |
| ES (1) | ES2642891T3 (fr) |
| WO (1) | WO2010054813A1 (fr) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102011000089A1 (de) * | 2011-01-11 | 2012-07-12 | Thyssenkrupp Steel Europe Ag | Verfahren zum Herstellen eines warmgewalzten Stahlflachprodukts |
| CN102296232B (zh) * | 2011-09-08 | 2012-12-26 | 上海交通大学 | 超高强度高塑性低碳相变与孪晶诱发塑性热轧钢板及制法 |
| JP5879448B2 (ja) * | 2011-12-28 | 2016-03-08 | ポスコ | 溶接熱影響部の靱性に優れた耐磨耗オーステナイト系鋼材及びその製造方法 |
| DE112013001144A5 (de) * | 2012-02-25 | 2014-10-30 | Technische Universität Bergakademie Freiberg | Verfahren zur Herstellung hochfester Formteile aus hochkohlenstoff- und hochmanganhaltigem austenitischem Stahlguss mit TRIP/TWIP-Eigenschaften |
| ITRM20120647A1 (it) * | 2012-12-19 | 2014-06-20 | Ct Sviluppo Materiali Spa | ACCIAIO INOSSIDABILE AUSTENITICO AD ELEVATA PLASTICITÀ INDOTTA DA GEMINAZIONE, PROCEDIMENTO PER LA SUA PRODUZIONE, E SUO USO NELLÂeuro¿INDUSTRIA MECCANICA. |
| JP6140836B2 (ja) * | 2012-12-26 | 2017-05-31 | ポスコPosco | 溶接熱影響部の靭性に優れた高強度オーステナイト系鋼材及びその製造方法 |
| US20140261918A1 (en) * | 2013-03-15 | 2014-09-18 | Exxonmobil Research And Engineering Company | Enhanced wear resistant steel and methods of making the same |
| EP2824213A1 (fr) * | 2013-07-12 | 2015-01-14 | Voestalpine Stahl GmbH | Procédé d'amélioration de l'adhérence sur une tôle d'acier dotée d'un revêtement de protection |
| US10597760B2 (en) * | 2013-07-26 | 2020-03-24 | Nippon Steel Corporation | High-strength steel material for oil well and oil well pipes |
| IN201617022707A (fr) | 2014-01-06 | 2016-08-31 | Nippon Steel & Sumitomo Metal Corp | |
| US10774405B2 (en) | 2014-01-06 | 2020-09-15 | Nippon Steel Corporation | Steel and method of manufacturing the same |
| AR101904A1 (es) * | 2014-09-29 | 2017-01-18 | Nippon Steel & Sumitomo Metal Corp | Material de acero y tuberías expansibles para la industria del petróleo |
| CN106795603B (zh) * | 2014-10-01 | 2019-07-23 | 日本制铁株式会社 | 高强度油井用钢材和油井管 |
| KR101665810B1 (ko) * | 2014-12-24 | 2016-10-13 | 주식회사 포스코 | 표면경도가 우수한 오스테나이트계 강재 및 이의 제조방법 |
| JP6693217B2 (ja) * | 2015-04-02 | 2020-05-13 | 日本製鉄株式会社 | 極低温用高Mn鋼材 |
| CA3009463C (fr) * | 2015-12-22 | 2020-09-22 | Posco | Materiau en acier austenitique presentant une excellente resistance a la fragilisation par l'hydrogene |
| WO2017169811A1 (fr) * | 2016-03-30 | 2017-10-05 | 新日鐵住金株式会社 | Matériau d'acier de haute résistance et son procédé de fabrication |
| WO2017203315A1 (fr) | 2016-05-24 | 2017-11-30 | Arcelormittal | Tôle mince en acier laminée à froid et recuite, son procédé de production et utilisation d'un tel acier pour produire des pièces de véhicule |
| CN106282804B (zh) * | 2016-11-10 | 2017-12-26 | 钢铁研究总院 | 一种Cr‑Al‑Nb‑V合金化的高耐磨高锰铸钢 |
| RU2659542C2 (ru) * | 2016-12-09 | 2018-07-02 | федеральное государственное бюджетное образовательное учреждение высшего образования "Уфимский государственный авиационный технический университет" | Сверхпрочная высокомарганцевая сталь, полученная за счет комбинирования механизмов упрочнения |
| KR101940874B1 (ko) * | 2016-12-22 | 2019-01-21 | 주식회사 포스코 | 저온인성 및 항복강도가 우수한 고 망간 강 및 제조 방법 |
| KR101920973B1 (ko) * | 2016-12-23 | 2018-11-21 | 주식회사 포스코 | 표면 특성이 우수한 오스테나이트계 강재 및 그 제조방법 |
| KR20190138835A (ko) * | 2017-04-11 | 2019-12-16 | 티센크루프 스틸 유럽 악티엔게젤샤프트 | 벨형 노에서 어닐링 처리된 냉간 압연한 평강 제품 및 그 제조 방법 |
| CN107574376A (zh) * | 2017-09-07 | 2018-01-12 | 北京科技大学 | 一种低成本高强塑型高锰twip/trip效应共生钢及其制备方法 |
| CN107574377B (zh) * | 2017-09-07 | 2019-05-03 | 北京科技大学 | 一种基于纳米结构的高吸能型高锰twip钢及其制备方法 |
| KR102109270B1 (ko) * | 2017-10-18 | 2020-05-12 | 주식회사 포스코 | 표면품질이 우수한 저온용 고 망간강재 및 제조방법 |
| WO2019186906A1 (fr) | 2018-03-29 | 2019-10-03 | 日本製鉄株式会社 | Tôle d'acier austénitique résistante à l'abrasion |
| US11285529B2 (en) | 2018-04-24 | 2022-03-29 | Nucor Corporation | Aluminum-free steel alloys and methods for making the same |
| WO2020085852A1 (fr) * | 2018-10-25 | 2020-04-30 | 주식회사 포스코 | Acier austénitique à haute teneur en manganèse ayant une haute limite d'élasticité et son procédé de fabrication |
| CN113308626B (zh) * | 2020-02-27 | 2022-03-18 | 南京理工大学 | 一种含有梯度纳米结构的镍基合金及其制备方法 |
| CN111659732B (zh) * | 2020-06-08 | 2022-04-19 | 首钢集团有限公司 | 一种解决高锰热成型钢酸洗后锈蚀的方法 |
| CN112522624B (zh) * | 2020-11-30 | 2021-11-16 | 湖南华菱涟源钢铁有限公司 | 高锰奥氏体耐磨钢及其制造方法 |
| CN112877606B (zh) * | 2021-01-12 | 2022-03-08 | 钢铁研究总院 | 一种超高强全奥氏体低密度钢及制备方法 |
| EP4532785A1 (fr) * | 2022-06-02 | 2025-04-09 | ArcelorMittal | Acier laminé à chaud à haute teneur en manganèse et son procédé de production |
| CN115572800B (zh) * | 2022-10-31 | 2024-10-22 | 昆明理工大学 | 一种复合析出相提高高锰钢性能的处理方法 |
| CN116815050B (zh) * | 2023-06-01 | 2025-02-07 | 湖南华菱涟源钢铁有限公司 | 一种基于罩式退火的450MPa级冷轧钢板、制备方法及应用 |
| CN117512462B (zh) * | 2023-10-26 | 2025-11-18 | 南京钢铁股份有限公司 | 一种铁路辙叉用高锰钢及其生产方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4968357A (en) | 1989-01-27 | 1990-11-06 | National Science Council | Hot-rolled alloy steel plate and the method of making |
| BR9205689A (pt) | 1991-12-30 | 1994-05-24 | Po Hang Iron & Steel | Aço austenitico de elevado manganês com uma melhor conformabilidade, resistência e soldabilidade, e o correspondente processo de fabricaçao |
| KR970001324B1 (ko) * | 1994-03-25 | 1997-02-05 | 김만제 | 열간가공성이 우수한 고망간강 및 그 열간압연 방법 |
| DE19727759C2 (de) | 1997-07-01 | 2000-05-18 | Max Planck Inst Eisenforschung | Verwendung eines Leichtbaustahls |
| FR2796083B1 (fr) | 1999-07-07 | 2001-08-31 | Usinor | Procede de fabrication de bandes en alliage fer-carbone-manganese, et bandes ainsi produites |
| DE10259230B4 (de) | 2002-12-17 | 2005-04-14 | Thyssenkrupp Stahl Ag | Verfahren zum Herstellen eines Stahlprodukts |
| FR2857980B1 (fr) | 2003-07-22 | 2006-01-13 | Usinor | Procede de fabrication de toles d'acier austenitique fer-carbone-manganese, a haute resistance, excellente tenacite et aptitude a la mise en forme a froid, et toles ainsi produites |
| FR2876708B1 (fr) * | 2004-10-20 | 2006-12-08 | Usinor Sa | Procede de fabrication de toles d'acier austenitique fer-carbone-manganese laminees a froid a hautes caracteristiques mecaniques, resistantes a la corrosion et toles ainsi produites |
| JP2008519160A (ja) * | 2004-11-03 | 2008-06-05 | ティッセンクルップ スチール アクチェンゲゼルシャフト | Twip特性をもつ高強度の鋼ストリップ又はシートの製造方法、コンポーネント及び高強度鋼ストリップ又はシートの製造方法 |
| FR2878257B1 (fr) * | 2004-11-24 | 2007-01-12 | Usinor Sa | Procede de fabrication de toles d'acier austenitique, fer-carbone-manganese a tres hautes caracteristiques de resistance et d'allongement, et excellente homogeneite |
| FR2881144B1 (fr) | 2005-01-21 | 2007-04-06 | Usinor Sa | Procede de fabrication de toles d'acier austenitique fer-carbone-manganese a haute resistance a la fissuration differee, et toles ainsi produites |
| JP5318421B2 (ja) | 2005-02-02 | 2013-10-16 | タタ、スティール、アイモイデン、ベスローテン、フェンノートシャップ | 高い強度および成型性を有するオーステナイト系鋼、該鋼の製造方法およびその使用 |
| KR100711361B1 (ko) * | 2005-08-23 | 2007-04-27 | 주식회사 포스코 | 가공성이 우수한 고망간형 고강도 열연강판 및 그 제조방법 |
| DE202005021771U1 (de) | 2005-12-20 | 2010-02-18 | Salzgitter Flachstahl Gmbh | Umformbarer Leichtbaustahl |
| KR100742833B1 (ko) | 2005-12-24 | 2007-07-25 | 주식회사 포스코 | 내식성이 우수한 고 망간 용융도금강판 및 그 제조방법 |
| KR100742823B1 (ko) | 2005-12-26 | 2007-07-25 | 주식회사 포스코 | 표면품질 및 도금성이 우수한 고망간 강판 및 이를 이용한도금강판 및 그 제조방법 |
| EP1878811A1 (fr) | 2006-07-11 | 2008-01-16 | ARCELOR France | Procede de fabrication d'une tole d'acier austenitique fer-carbone-manganese ayant une excellente resistance a la fissuration differee, et tole ainsi produit |
| DE102006039307B3 (de) | 2006-08-22 | 2008-02-21 | Thyssenkrupp Steel Ag | Verfahren zum Beschichten eines 6-30 Gew.% Mn enthaltenden warm- oder kaltgewalzten Stahlbands mit einer metallischen Schutzschicht |
-
2008
- 2008-11-12 DE DE102008056844A patent/DE102008056844A1/de not_active Withdrawn
-
2009
- 2009-11-12 EP EP09760726.1A patent/EP2366035B1/fr not_active Not-in-force
- 2009-11-12 WO PCT/EP2009/008065 patent/WO2010054813A1/fr not_active Ceased
- 2009-11-12 ES ES09760726.1T patent/ES2642891T3/es active Active
- 2009-11-12 CN CN200980145236.1A patent/CN102216474B/zh not_active Expired - Fee Related
- 2009-11-12 KR KR1020117013287A patent/KR101387040B1/ko not_active Expired - Fee Related
-
2011
- 2011-05-11 US US13/067,137 patent/US9677146B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20110308673A1 (en) | 2011-12-22 |
| US9677146B2 (en) | 2017-06-13 |
| WO2010054813A1 (fr) | 2010-05-20 |
| DE102008056844A1 (de) | 2010-06-02 |
| EP2366035A1 (fr) | 2011-09-21 |
| CN102216474B (zh) | 2014-08-20 |
| KR101387040B1 (ko) | 2014-04-18 |
| CN102216474A (zh) | 2011-10-12 |
| KR20110083735A (ko) | 2011-07-20 |
| ES2642891T3 (es) | 2017-11-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2366035B1 (fr) | Feuillard d'acier au manganèse à teneur accrue en phosphore et son procédé de fabrication | |
| EP2864517B1 (fr) | Acier multiphase à haute résistance et procédé pour la fabrication d'une bande faite de cet acier présentant une résistance à la traction minimale de 580 mpa | |
| DE69226946T2 (de) | Austenitischer manganstahlblech mit hoher verformbarkeit, festichkeit und schweissbarkeit und verfahren | |
| EP3504349B1 (fr) | Procédé de fabrication d'une bande d'acier à résistance très élevée présentant des propriétés améliorées lors du traitement ultérieur et une telle bande d'acier | |
| EP3027784B1 (fr) | Acier multiphase à haute résistance, micro-allié et contenant du silicium, présentant une résistance minimale à la traction de 750 mpa et des propriétés améliorées et procédé de fabrication d'une bande à partir de cet acier | |
| EP3655560B1 (fr) | Produit plat en acier possédant une bonne résistance au vieillissement et son procédé de fabrication | |
| EP3535431B1 (fr) | Produit d'acier à teneur en manganèse intermédiaire pour application à basse température et son procédé de fabrication | |
| DE60300835T2 (de) | Kaltgewalztes Stahlblech mit ultrafeinem Korngefüge und Verfahren zu dessen Herstellung | |
| EP3976838B1 (fr) | Composant fait à partir d'un produit plat en acier, et son procédé de fabrication | |
| EP3221483B1 (fr) | Acier multiphases autotrempant en profondeur à haute résistance mécanique avec excellent aptitude au faconnage et procédé de fabrication d'une bande de cet acier | |
| EP2905348B1 (fr) | Produit en acier plat de haute résistance avec une structure bainitique-martensitique et procédé de fabrication d'un tel produit acier plat | |
| EP3221484B1 (fr) | Procédé de production d'une bande en acier polyphasé, durcissant à l'air, ayant une haute résistance et ayant d'excellentes propriétés de mise en oeuvre | |
| EP3692178B1 (fr) | Procede de fabrication d'une bande d'acier a partir d'un acier multiphase a tres haute resistance | |
| EP0352597A1 (fr) | Procédé de fabrication de feuillard laminé à chaud ou tôles fortes | |
| EP4298255A1 (fr) | Produit plat en acier laminé à chaud à haute résistance ayant une aptitude au formage à froid locale élevée et procédé de production d?un tel produit plat en acier | |
| DE102014017275A1 (de) | Hochfester lufthärtender Mehrphasenstahl mit hervorragenden Verarbeitungseigenschaften und Verfahren zur Herstellung eines Bandes aus diesem Stahl | |
| EP2009120B1 (fr) | Utilisation d'un alliage d'acier très solide destiné à la fabrication de tuyaux en acier très résistants et ayant une bonne déformabilité | |
| WO2023020931A1 (fr) | Acier ayant des propriétés de traitement améliorées pour travailler à des températures élevées | |
| DE3881002T2 (de) | Durch wärmrbehandlung härtbares warmgewalztes stahlfeinblech mit ausgezeichneter kaltverformbarkeit und verfahren zu seiner herstellung. | |
| EP1399598A1 (fr) | Procede pour fabriquer des produits en acier de grande resistance et de bonne malleabilite, formes a froid a partir d'un feuillard lamine a chaud | |
| EP4301885A1 (fr) | Produit plat en acier, son procédé de production, et utilisation d'un tel produit plat en acier | |
| WO2020038883A1 (fr) | Produit plat en acier laminé à chaud n'ayant pas subi un traitement par trempe et revenu, laminé à chaud ayant subi un traitement par trempe et revenu, ainsi que procédé de production associé | |
| EP3872194B1 (fr) | Procédé de fabrication d'un produit plat en acier laminé à chaud et produit plat en acier | |
| WO2023025635A1 (fr) | Produit plat en acier laminé à froid et son procédé de production | |
| EP4174207A1 (fr) | Produit plat en acier ayant des propriétés de traitement améliorées |
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: 20110610 |
|
| 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 MK MT NL NO PL PT RO SE SI SK SM TR |
|
| RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: MRACZEK, KLEMENS Inventor name: ARENHOLZ, ENNO Inventor name: SCHNEIDER, REINHOLD Inventor name: SAMEK, LUDOVIC |
|
| DAX | Request for extension of the european patent (deleted) | ||
| 17Q | First examination report despatched |
Effective date: 20151124 |
|
| GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
| INTG | Intention to grant announced |
Effective date: 20170127 |
|
| 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): 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 SE SI SK SM TR |
|
| REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D Free format text: NOT ENGLISH |
|
| 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: 906658 Country of ref document: AT Kind code of ref document: T Effective date: 20170715 |
|
| REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D Free format text: LANGUAGE OF EP DOCUMENT: GERMAN |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 502009014128 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: 20170705 |
|
| REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2642891 Country of ref document: ES Kind code of ref document: T3 Effective date: 20171120 |
|
| REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D Ref country code: FR Ref legal event code: PLFP Year of fee payment: 9 |
|
| 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: 20170705 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: 20170705 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: 20170705 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: 20170705 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: 20171005 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20171005 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: 20170705 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: 20171105 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: 20171006 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: 20170705 |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 502009014128 Country of ref document: DE |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20170705 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: 20170705 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: 20170705 |
|
| 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: 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: 20170705 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: 20170705 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: 20170705 |
|
| 26N | No opposition filed |
Effective date: 20180406 |
|
| 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: 20170705 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20171130 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20171130 |
|
| 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: 20171112 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: 20170705 |
|
| REG | Reference to a national code |
Ref country code: BE Ref legal event code: MM Effective date: 20171130 |
|
| REG | Reference to a national code |
Ref country code: IE Ref legal event code: MM4A |
|
| 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: 20170705 |
|
| 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: 20171112 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20171130 |
|
| REG | Reference to a national code |
Ref country code: AT Ref legal event code: MM01 Ref document number: 906658 Country of ref document: AT Kind code of ref document: T Effective date: 20171112 |
|
| 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 NON-PAYMENT OF DUE FEES Effective date: 20171112 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20091112 |
|
| 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 NON-PAYMENT OF DUE FEES Effective date: 20170705 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20170705 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20191127 Year of fee payment: 11 Ref country code: DE Payment date: 20191127 Year of fee payment: 11 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20191125 Year of fee payment: 11 Ref country code: IT Payment date: 20191125 Year of fee payment: 11 Ref country code: ES Payment date: 20191202 Year of fee payment: 11 |
|
| 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 FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20170705 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20191127 Year of fee payment: 11 |
|
| 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: 20170705 |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 502009014128 Country of ref document: DE |
|
| REG | Reference to a national code |
Ref country code: SE Ref legal event code: EUG |
|
| GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20201112 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20201113 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20201130 Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20201112 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20210601 Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20201112 |
|
| REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20220201 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20201113 |