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EP2103704A1 - Hot-rolled long product and method for its manufacture - Google Patents

Hot-rolled long product and method for its manufacture Download PDF

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Publication number
EP2103704A1
EP2103704A1 EP08004335A EP08004335A EP2103704A1 EP 2103704 A1 EP2103704 A1 EP 2103704A1 EP 08004335 A EP08004335 A EP 08004335A EP 08004335 A EP08004335 A EP 08004335A EP 2103704 A1 EP2103704 A1 EP 2103704A1
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EP
European Patent Office
Prior art keywords
content
hot
long product
product according
rolled long
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EP08004335A
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German (de)
French (fr)
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EP2103704B1 (en
Inventor
Hans Roelofs
Ulrich Urlau
Mirkka Lembke
Guido Olschewski
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Swiss Steel AG
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Swiss Steel AG
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Priority to EP08004335A priority Critical patent/EP2103704B1/en
Priority to ES08004335T priority patent/ES2391312T3/en
Priority to PL08004335T priority patent/PL2103704T3/en
Priority to SI200830770T priority patent/SI2103704T1/en
Publication of EP2103704A1 publication Critical patent/EP2103704A1/en
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    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/002Heat treatment of ferrous alloys containing Cr
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/005Heat treatment of ferrous alloys containing Mn
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/008Heat treatment of ferrous alloys containing Si
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226Hot rolling
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/002Bainite
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/004Dispersions; Precipitations
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/008Martensite

Definitions

  • the invention relates to a hot-rolled long product according to the preamble of claim 1 and a method for its production.
  • tempered steels are generally used. With tempered steels it is possible to achieve tensile strengths of more than 1 000 MPa with simultaneous necking of more than 45%.
  • the necessary heat treatment heat treatment, quenching, tempering
  • expensive post-processing straightening, grinding
  • Pre-tempered steels have significant disadvantages in machining (long chips, low tool life). These processing disadvantages can be somewhat reduced by the addition of a maximum of 0.04 wt.% Sulfur. Higher levels of sulfur degrade the manufacturability and microscopic purity of these Al-alloyed steels.
  • the tempered steels are alloyed with at least 0.015% aluminum.
  • hard and abrasive Al 2 O 3 -containing oxide inclusions are produced, which have a detrimental effect on tool life.
  • these inclusions In order to achieve good machinability, these inclusions must be converted into less abrasive calcium aluminate inclusions by adding calcium in a complex metallurgical process.
  • ferritic-martensitic dual-phase steels were developed.
  • the structure of these steels is via a thermomechanical Treatment achieved during hot rolling.
  • good toughness properties can only be set as long as the stored martensite islands remain small enough.
  • the achievable tensile strength is thereby limited to below 1'000 MPa.
  • Steels for pipe production must be characterized in particular by good toughness and weldability. For this to be achieved, a low carbon content of less than 0.13 wt% is required.
  • the desired high-strength, tough structure is achieved by accelerated cooling from the rolling heat. In the temperature range of 800 to 500 ° C (range of conversion) cooling rates of 10 to 40 K / s are used.
  • the structure of these steels then consists of allotriomorphic ferrite and bainite (at least 20%).
  • the low carbon content of the accelerated cooling guarantees the avoidance of high martensite content, which enables good toughness properties.
  • the tensile strength is thereby limited to below 1'000 MPa.
  • EP 0845544 (C ⁇ 0.12%) describes a microalloyed bainitic steel which has a tensile strength of more than 1000 MPa at room temperature. To achieve these properties, the steel is austenitized again after rolling and then quenched at a cooling rate of 17 to 150 K / s. These cooling rates are well above the air cooled long products in conventional rolling mills.
  • An easily machinable bainitic-martensitic complex phase steel for the production of air-cooled conventionally hot-rolled long products in a size range of 5.0 to 70 mm is not yet available.
  • the material concept must be designed in such a way that the dimensional differences in the cooling rate of approx. 0.1 to 8.0 K / s do not lead to any significant fluctuations in the mechanical-technological properties of the final product.
  • the object of the invention is to provide an improved hot-rolled long product, with which in particular the above disadvantages are avoided.
  • Another object of the invention is to provide a process for producing a hot-rolled long product.
  • the alloying components are selected such that, at conventional cooling rates from 0.1 to 8.0 K / s, a bainitic-martensitic microstructure always results with a tensile strength level of 1'000 to 1400 MPa, without costly alloying elements and / or or special equipment for accelerated cooling from the rolling heat must be used.
  • the lower limit of the carbon content to 0.20% ensures, in combination with manganese and chromium, that only small amounts of ferrite are present in the microstructure. Ferrite levels above 10% affect both the strength level and impact strength of the product.
  • the upper limit of the carbon to 0.25% ensures that the tensile strength does not rise above 1400 MPa. Higher strength values degrade machinability in the downstream drawing or machining process. Higher carbon contents also promote the formation of carbides, which adversely affects ductility.
  • Silicon affects the carbon activity and slows down the precipitation of carbides.
  • the selected silicon concentration allows a one-hour annealing treatment at 400 ° C without degrading the ductility due to carbide precipitations (based on the description of the carbide-free bainite in WO 96/22396 ). Since silicon is an efficient solid solution hardener in bainite, its content must be limited to 1.35% in order not to exceed the maximum desired tensile strength of 1400 MPa.
  • the manganese content is too high, the manganese segregations are pronounced and the microstructure becomes very inhomogeneous. For this reason, the "free”, ie not bound in manganese sulfides, manganese content ( ⁇ total manganese content - 1.72 Sulfur content) to 1.50%.
  • the so determined manganese content is not sufficient to achieve a bainitic-martensitic structure after air cooling from the rolling heat.
  • the product must also contain so much chromium that chromium content + (manganese content - 1.72 sulfur content)> 2.6% by weight applies. Together with a carbon content of at least 0.20%, a bainitic-martensitic microstructure with ⁇ 10% ferrite is ensured.
  • Molybdenum is said to prevent the precipitation of iron carbides at the primary grain boundaries and associated loss of toughness. For cost reasons, the molybdenum content should be as low as necessary: 0.1 to 0.5% molybdenum.
  • the steel should contain at least 0.04%, preferably 0.12 to 0.17% sulfur.
  • the sulfur combines with manganese to form manganese sulfide precipitates, thus improving both chip breaking and tool life. Since these precipitates also reduce the transverse toughness of the hot-rolled long product, the addition of sulfur should be limited to 0.25%.
  • the aluminum content should be limited to 0.01%.
  • oxide inclusions should be set with an Al 2 O 3 content of ⁇ 50%.
  • the metallurgical treatment is carried out so that soft, glassy silicate inclusions are formed with the following relative proportions by weight: 20 to 50% CaO, 35 to 65% SiO 2 and less than 25% Al 2 O 3 . The tool life of the tools used in machining is then significantly extended.
  • the good machinability of the hot-rolled long product produced according to the invention can be further improved according to claim 3 or 4 by the addition of 0.05 to 0.3% lead or 0.05 to 0.3% bismuth.
  • the austenite grain size before the structural transformation and the cooling rate during structural transformation in a temperature range between 800 and 500 ° C. are of crucial importance.
  • a fine austenite grain leads to a finer final structure with better toughness values.
  • the austenite grain after the last forming step according to claim 7 should not be greater than 50 ⁇ m.
  • the cooling rates should be between 0.1 and 8.0 K / s.
  • the upper value is given by the possibilities of conventional cooling of accelerated air.
  • the lower limit of 0.1 K / s is to ensure that no ferrite> 10% occur. Large bar dimensions that cool down inside the bar much slower than 0.1 K / s can not be produced with this technology.
  • a heat treatment for 0.5 to 2 hours at 300 to 500 ° C according to claim 8 may be useful.
  • the high silicon content of the product delays the rearrangement of carbon atoms in the microstructure. This is desirable to suppress the formation of coarse carbide precipitates.
  • also in connection with carbon known aging processes that begin immediately after the hot rolling slowed down. In particular, the maximum ductility of the structure sets in only after a few weeks. In cases where the rolled long product is to be further processed immediately, a heat treatment is therefore recommended.
  • a molten steel was poured and then rolled into steel bars of various dimensions.
  • the molten steel was produced by the electrical steel process with a secondary metallurgical treatment on a ladle and subsequent casting to 150 ⁇ 150 mm 2 sticks in a continuous casting plant.
  • the billets were then reheated in a walking beam oven to 1'150 to 1'200 ° C and then to bar steel in the dimensions 22 (cooling rate is about 1.5 K / s) and 52 mm (cooling rate is about 0.4 K / s) rolled.
  • the cooling of the rods after rolling was carried out in air.
  • the steel was made 0.22% carbon 0.94% silicon 00:07% nickel 0.14% to molybdenum 00:15% sulfur 0.003% aluminum 0.012% phosphorus ⁇ 0.001% boron 0.011% titanium ⁇ 0.003% lead ⁇ 0.003% bismuth 0.013% nitrogen 1.60% manganese 1:34% Manganese - 1.72 Sulfur 1:54% chrome 2.88% Chromium + (manganese - 1.72 sulfur) and other impurities caused by melting.
  • the high sulfur content of 0.15% ensures good chip breaking and improves tool life.
  • the low aluminum content suppresses the formation of hard, abrasive, clay-containing oxide inclusions.
  • the metallographic micrographs at 200x magnification are in the Fig. 1 shown.
  • the microstructure is a very fine mixed structure.
  • the bainite and martensite fractions could not be reliably quantified.
  • the pictures as well as the obtained strength level show that the structure consists primarily (>> 50%) of bainite.
  • the structure of the 52 mm rod is slightly coarser than the structure of the 22 mm rod due to the low cooling rate from the rolling heat.
  • manganese sulphides which can serve as nucleating sites for ferrite formation
  • isolated ferrite grains can be recognized.
  • the ferrite content is extremely low ( ⁇ 10%).
  • the determination of the residual austenite quantity in the X-ray diffractometer showed 5.1 ⁇ 0.45% for the 22 mm rod and 4.4 ⁇ 1.34% for the 52 mm rod.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Heat Treatment Of Steel (AREA)

Abstract

Hot-rolled longitudinal product contains (in wt.%) 0.20-0.25 carbon, 0.90-1.35 silicon, up to 0.20 nickel, up to 0.50 molybdenum, 0.04-0.25 sulfur, up to 0.01 aluminum, up to 0.035 phosphorus, up to 0.0008 boron, up to 0.02 titanium, up to 0.3 lead, up to 0.3 bismuth, up to 1.93 manganese, up to 4.0 chromium, up to 0.02 nitrogen and up to 0.01 oxygen bound in oxidic inclusions. Manganese content - 1.72 sulfur content 1.50% and chromium content + (manganese content - 1.72 sulfur content) 2.6 wt.%. The product has the following constituents: 50-90% bainite, up to 50% martensite, up to 10% ferrite and up to 10% residual austenite. An independent claim is also included for a method for the production of a hot-rolled longitudinal product.

Description

Technisches GebietTechnical area

Die Erfindung betrifft ein warmgewalztes Langprodukt gemäss dem Oberbegriff des Anspruchs 1 sowie ein Verfahren zu dessen Herstellung.The invention relates to a hot-rolled long product according to the preamble of claim 1 and a method for its production.

Stand der TechnikState of the art

Um aus Stahl gefertigte Bauteile mit gleichzeitig hoher Festigkeit und hoher Zähigkeit herstellen zu können, kommen in der Regel Vergütungsstähle zum Einsatz. Mit Vergütungsstählen lassen sich Zugfestigkeiten von über 1'000 MPa bei gleichzeitiger Brucheinschnürung von über 45% realisieren. Die notwendige Wärmebehandlung (Erwärmen, Abschrecken, Anlassen) ist kostenintensiv und umweltbelastend. Falls sie am fertigen Bauteil durchgeführt wird, kann aufgrund von Verzug eine teure Nachbearbeitung (Richten, Schleifen) notwendig werden. Vorvergütete Stähle weisen deutliche Nachteile in der zerspanenden Bearbeitung auf (lange Späne, niedrige Werkzeugstandzeiten). Diese Bearbeitungsnachteile können durch die Zugabe von maximal 0.04 Gew.% Schwefel etwas gemindert werden. Höhere Schwefelgehalte verschlechtern die Herstellbarkeit und den mikroskopischen Reinheitsgrad dieser Al-legierten Stählen.In order to be able to produce steel components with high strength and high toughness, tempered steels are generally used. With tempered steels it is possible to achieve tensile strengths of more than 1 000 MPa with simultaneous necking of more than 45%. The necessary heat treatment (heating, quenching, tempering) is cost-intensive and polluting. If carried out on the finished component, expensive post-processing (straightening, grinding) may be necessary due to distortion. Pre-tempered steels have significant disadvantages in machining (long chips, low tool life). These processing disadvantages can be somewhat reduced by the addition of a maximum of 0.04 wt.% Sulfur. Higher levels of sulfur degrade the manufacturability and microscopic purity of these Al-alloyed steels.

Um eine Austenitkornvergröberung während der notwendigen Wärmebehandlung zu vermeiden, werden die Vergütungsstähle mit mindestens 0.015% Aluminium legiert. Während der Stahlherstellung entstehen dann harte und im Zerspanungsprozess abrasive Al2O3-haltige Oxideinschlüsse, welche sich nachteilig auf die Werkzeugstandzeiten auswirken. Um eine gute Zerspanbarkeit zu erreichen müssen diese Einschlüsse in einem aufwendigen metallurgischen Prozess durch Zugabe von Kalzium in weniger abrasive Kalziumaluminateinschlüsse umgewandelt werden.In order to avoid austenitic grain coarsening during the necessary heat treatment, the tempered steels are alloyed with at least 0.015% aluminum. During steel production, hard and abrasive Al 2 O 3 -containing oxide inclusions are produced, which have a detrimental effect on tool life. In order to achieve good machinability, these inclusions must be converted into less abrasive calcium aluminate inclusions by adding calcium in a complex metallurgical process.

Alternativ zu den Vergütungsstählen wurden ferritisch-martensitische Dualphasenstähle entwickelt. Das Gefüge dieser Stähle wird über eine thermomechanische Behandlung während des Warmwalzens erreicht. Mit diesen Stählen lassen sich nur dann gute Zähigkeitseigenschaften einstellen, solange die eingelagerten Martensitinseln klein genug bleiben. Die erreichbare Zugfestigkeit wird dadurch auf unter 1'000 MPa limitiert.As an alternative to tempered steels, ferritic-martensitic dual-phase steels were developed. The structure of these steels is via a thermomechanical Treatment achieved during hot rolling. With these steels, good toughness properties can only be set as long as the stored martensite islands remain small enough. The achievable tensile strength is thereby limited to below 1'000 MPa.

Eine weitere Entwicklung sind die direkthärtenden weichmartensitischen Stähle. Nachteilig an diesen Stählen ist, dass das erforderliche martensitische Gefüge erst über eine beschleunigte Abkühlung mit hoher Abschreckgeschwindigkeit aus der Umformwärme erreicht wird. Aus diesem Grund findet dieses Verfahren hauptsächlich bei dünnwandigen Teilen (Schmiedteile, Rohre) seine Anwendung. Bei Produkten mit mittlerer oder grosser Ausdehnung wird das eingestellte Gefüge über den Querschnitt unakzeptabel inhomogen. Für die Herstellung von warmgewalzten Langprodukten wie Walzdraht und Stabstahl in konventionellen Abmessungen eignen sich diese Stähle deshalb nicht.Another development is the direct-hardening soft-martensitic steels. A disadvantage of these steels is that the required martensitic structure is achieved only by accelerated cooling with high quenching rate from the forming heat. For this reason, this method is mainly used in thin-walled parts (forgings, pipes) its application. For products with medium or large expansion, the set structure is unacceptably inhomogeneous across the cross section. For the production of hot-rolled long products such as wire rod and steel bars in conventional dimensions, these steels are therefore not suitable.

Eine andere Entwicklungsrichtung wird mit den AFP(ausscheidungshärtende ferritisch-perlitischen)-Stählen eingeschlagen. Durch eine geregelte Abkühlung aus der Umformhitze werden Karbonitride der Elemente Titan, Vanadium und Niob ausgeschieden. Diese führen dann wegen der Dispersionshärtung zu einer höheren Festigkeit des Grundwerkstoffs. Im Vergleich zu den Vergütungsstählen besitzen sie eine niedrige Streckgrenze und geringe Zähigkeiten. Für die Anwendung im Bereich hoher Belastungen sind sie daher ungeeignet. Eine kontrollierte Einstellung der Ausscheidungsprodukte verlangt enge Analysenvorgaben für den Stahl und eine genaue Steuerung der Abkühlung aus der Umformhitze.Another development direction is taken with the AFP (precipitation-hardening ferritic-pearlitic) steels. By a controlled cooling from the forming heat carbonitrides of the elements titanium, vanadium and niobium are eliminated. These then lead due to the dispersion hardening to a higher strength of the base material. Compared to tempered steels, they have a low yield strength and low toughness. For use in the field of high loads, they are therefore unsuitable. A controlled adjustment of the waste products requires tight analysis specifications for the steel and precise control of the cooling from the forming heat.

Neuere Entwicklungen zeigen, dass sich schon mit Luftabkühlung direkt aus der Umformhitze sehr gute Eigenschaftskombinationen mit Komplexphasenstählen erreichen lassen. Diese Stähle weisen in der Regel ein bainitisch-martensitisches Gefüge mit Restanteilen von Ferrit und Restaustenit auf.Recent developments show that very good combinations of properties with complex phase steels can be achieved even with air cooling directly from the forming heat. These steels usually have a bainitic-martensitic structure with residual amounts of ferrite and retained austenite.

Erste Anwendungen von Komplexphasenstählen findet man heute bei der Herstellung von Rohren aus Flachstahl sowie bei der Herstellung von Schienen.First applications of complex phase steels are found today in the production of tubes of flat steel as well as in the production of rails.

Stähle für die Rohrherstellung müssen sich insbesondere durch eine gute Zähigkeit und Verschweissbarkeit auszeichnen. Damit dies erreicht werden kann, ist ein tiefer Kohlenstoffgehalt von unter 0.13 Gew.% erforderlich. Das gewünschte hochfeste, zähe Gefüge wird über eine beschleunigte Abkühlung aus der Walzhitze erreicht. Im Temperaturbereich von 800 bis 500°C (Bereich der Umwandlung) werden Kühlraten von 10 bis 40 K/s angewendet. Das Gefüge dieser Stähle besteht dann aus allotriomorphem Ferrit und Bainit (mindestens 20%). Der tiefe Kohlenstoffgehalt garantiert bei der beschleunigten Abkühlung die Vermeidung von hohen Martensitanteilen, was die guten Zähigkeitseigenschaften erst ermöglicht. Die Zugfestigkeit wird dadurch auf unter 1'000 MPa begrenzt.Steels for pipe production must be characterized in particular by good toughness and weldability. For this to be achieved, a low carbon content of less than 0.13 wt% is required. The desired high-strength, tough structure is achieved by accelerated cooling from the rolling heat. In the temperature range of 800 to 500 ° C (range of conversion) cooling rates of 10 to 40 K / s are used. The structure of these steels then consists of allotriomorphic ferrite and bainite (at least 20%). The low carbon content of the accelerated cooling guarantees the avoidance of high martensite content, which enables good toughness properties. The tensile strength is thereby limited to below 1'000 MPa.

Bei der Herstellung von Schienenstahl spielen insbesondere die Verschleiss- und Ermüdungsfestigkeit eine wichtige Rolle. In WO 96/22396 wird die Herstellung einer bainitischen Schiene mit konventioneller kontinuierlicher Abkühlung aus der Walzhitze beschrieben. Damit die gewünschte Verschleissfestigkeit erreicht wird, muss die Bildung von groben Zementitteilchen unterdrückt werden ("karbid-freier Bainit"). Dies kann durch die Zugabe von Silizium geschehen. Die Kinetik der Zementitausscheidung wird dadurch verlangsamt. Für die zerspanende Bearbeitung sind diese Stähle nicht geeignet.In particular, the wear and fatigue strength play an important role in the production of rail steel. In WO 96/22396 describes the production of a bainitic rail with conventional continuous cooling from the rolling heat. To achieve the desired wear resistance, the formation of coarse cementite particles must be suppressed ("carbide-free bainite"). This can be done by the addition of silicon. The kinetics of cementite excretion is thereby slowed down. These steels are not suitable for machining.

Der in CN 1477226 beschriebene bainitisch-martensitischer Stahl (C = 0.15 bis 0.34%) erreicht eine Zugfestigkeit von über 900 MPa. Es sind Mangangehalte von über 1.8% vorgesehen. Dieser hohe Mangangehalt erleichtert zwar die Einstellung des bainitischen Gefüges bei für das Warmwalzen konventionellen Kühlraten. Er führt jedoch gleichzeitig zu schwer kontrollierbaren Seigerungproblemen, die sich in unerwünschten Martensitzeilen äussern. Die mechanisch-technologischen Eigenschaften unterliegen für konventionelle warmgewalzte Langprodukte deshalb unakzeptablen Schwankungen. Die zerspanende Bearbeitung wird durch die unregelmässig vorhandenen Martensitzeilen stark beeinträchtigt.The in CN 1477226 bainitic-martensitic steel (C = 0.15 to 0.34%) described achieves a tensile strength of over 900 MPa. Manganese levels in excess of 1.8% are foreseen. Although this high manganese content facilitates the adjustment of the bainitic structure at conventional cooling rates for hot rolling. At the same time, however, it leads to difficult to control seeding problems, which manifest themselves in undesirable martenseats. The mechanical-technological properties are therefore subject to unacceptable fluctuations for conventional hot-rolled long products. The machining is severely impaired by the irregularly present martensite parts.

In EP 0845544 (C ≤ 0.12%) wird ein mikrolegierter bainitischer Stahl beschrieben, der bei Raumtemperatur eine Zugfestigkeit von über 1'000 MPa aufweist. Um diese Eigenschaften zu erreichen, wird der Stahl nach der Walzung wieder austenitisiert und anschliessend mit einer Abkühlrate von 17 bis 150 K/s abgeschreckt. Diese Abkühlraten liegen deutlich über den an Luft abgekühlten Langprodukten in konventionellen Walzwerken.In EP 0845544 (C ≤ 0.12%) describes a microalloyed bainitic steel which has a tensile strength of more than 1000 MPa at room temperature. To achieve these properties, the steel is austenitized again after rolling and then quenched at a cooling rate of 17 to 150 K / s. These cooling rates are well above the air cooled long products in conventional rolling mills.

DE 102005052069 beschreibt einen B/Ti-legierten bainitisch-martensitischen Stahl für warmgewalzte Langprodukte. Der geforderte N-Gehalt erfordert eine zusätzliche Entgasungsbehandlung. Der beschriebene Stahl ist für dünne Drahtabmessungen mit Luftabkühlung oder für dickere Drahtabmessungen mit beschleunigter Abkühlung geeignet. Im Vergleich zu ferritisch-perlitischen Vergütungsstählen ist mit einer deutlich schlechteren Bearbeitbarkeit in der Zerspanung zu rechnen. Das Legierungskonzept limitiert (wegen der Bildung von Titankarbosulfiden) den Einsatz von zerspanungsverbessernden Zusätzen wie Schwefel. Aus diesem Grund ist der wirtschaftliche Einsatz auf die Massivumformung begrenzt. DE 102005052069 describes a B / Ti-alloyed bainitic-martensitic steel for hot-rolled long products. The required N content requires an additional degassing treatment. The described steel is suitable for thin wire dimensions with air cooling or for thicker wire dimensions with accelerated cooling. Compared to ferritic-pearlitic tempered steels, significantly lower machinability in machining can be expected. The alloy concept limits (because of the formation of titanium carbosulfides) the use of machining additives such as sulfur. For this reason, the economic use is limited to the massive forming.

Ein in der Zerspanung gut bearbeitbarer bainitisch-martensitischer Komplexphasenstahl für die Herstellung von mit Luftabkühlung konventionell warmgewalzten Langprodukten in einem Abmessungsbereich von 5.0 bis 70 mm steht heute noch nicht zur Verfügung. Das Werkstoffkonzept muss dabei so ausgelegt sein, dass die abmessungsbedingten Unterschiede in der Abkühlrate von ca. 0.1 bis 8.0 K/s zu keinen gravierenden Schwankungen der mechanisch-technologischen Eigenschaften am Endprodukt führen.An easily machinable bainitic-martensitic complex phase steel for the production of air-cooled conventionally hot-rolled long products in a size range of 5.0 to 70 mm is not yet available. The material concept must be designed in such a way that the dimensional differences in the cooling rate of approx. 0.1 to 8.0 K / s do not lead to any significant fluctuations in the mechanical-technological properties of the final product.

Darstellung der ErfindungPresentation of the invention

Aufgabe der Erfindung ist es, ein verbessertes warmgewalztes Langprodukt bereitzustellen, mit dem insbesondere die obigen Nachteile vermieden werden. Eine weitere Aufgabe der Erfindung besteht darin, ein Verfahren zur Herstellung eines warmgewalzten Langprodukts anzugeben.The object of the invention is to provide an improved hot-rolled long product, with which in particular the above disadvantages are avoided. Another object of the invention is to provide a process for producing a hot-rolled long product.

Gelöst werden diese Aufgaben durch das im Anspruch 1 definierte warmgewalzte Langprodukt sowie das im Anspruch 6 definierte Herstellverfahren.These objects are achieved by the defined in claim 1 hot rolled long product and defined in claim 6 manufacturing process.

Die nachfolgenden Gehaltsangaben in Prozent (%) bzw. in Teilen pro Million ("parts per million, ppm") beziehen sich - sofern nicht ausdrücklich anders angegeben - auf Gewichtsanteile.The following percentages by weight (%) or parts per million (ppm) refer to parts by weight unless expressly stated otherwise.

Das erfindungsgemässe warmgewalzte Langprodukt weist einen Gewichtsanteil von

  • 0.20 bis 0.25% Kohlenstoff,
  • 0.90 bis 1.35% Silizium,
  • bis zu 0.20% Nickel,
  • 0.1 bis 0.5% Molybdän,
  • 0.04 bis 0.25% Schwefel,
  • bis zu 0.01% Aluminium,
  • bis zu 0.035% Phosphor,
  • bis zu 0.0008% Bor,
  • bis zu 0.02% Titan,
  • bis zu 0.3% Blei,
  • bis zu 0.3% Wismut,
  • bis zu 1.93% Mangan
  • bis zu 4.0% Chrom
  • bis zu 0.02% Stickstoff und
  • bis zu 0.01% in oxidischen Einschlüssen gebundener Sauerstoff
sowie weitere stahlübliche Beimengungen auf, wobei
(Mangangehalt - 1.72 Schwefelgehalt) < 1.50% und
Chromgehalt + (Mangangehalt - 1.72 Schwefelgehalt) > 2.6 Gew.% sein soll und folgende Gefügebestandteile vorliegen:
  • 50 bis 90% Bainit,
  • bis 50% Martensit,
  • bis zu 10% Ferrit und
  • bis zu 10% Restaustenit.
The inventive hot-rolled long product has a weight fraction of
  • 0.20 to 0.25% carbon,
  • 0.90 to 1.35% silicon,
  • up to 0.20% nickel,
  • 0.1 to 0.5% molybdenum,
  • 0.04 to 0.25% sulfur,
  • up to 0.01% aluminum,
  • up to 0.035% phosphorus,
  • up to 0.0008% boron,
  • up to 0.02% titanium,
  • up to 0.3% lead,
  • up to 0.3% bismuth,
  • up to 1.93% manganese
  • up to 4.0% chrome
  • up to 0.02% nitrogen and
  • Up to 0.01% oxygen bound in oxidic inclusions
and other customary admixtures on, wherein
(Manganese content - 1.72 sulfur content) <1.50% and
Chromium content + (manganese content - 1.72 sulfur content)> 2.6% by weight should be and the following structural components are present:
  • 50 to 90% bainite,
  • up to 50% martensite,
  • up to 10% ferrite and
  • up to 10% retained austenite.

Bei dem erfindungsgemäss hergestellten Produkt sind die Legierungskomponenten so gewählt, dass bei üblichen Abkühlraten aus der Walzhitze von 0.1 bis 8.0 K/s immer ein bainitisch-martensitisches Gefüge mit Zugfestigkeitsniveau von 1'000 bis 1'400 MPa resultiert, ohne dass kostspielige Legierungselemente und/oder spezielle Einrichtungen zur beschleunigten Abkühlung aus der Walzhitze verwendet werden müssen.In the product produced according to the invention, the alloying components are selected such that, at conventional cooling rates from 0.1 to 8.0 K / s, a bainitic-martensitic microstructure always results with a tensile strength level of 1'000 to 1400 MPa, without costly alloying elements and / or or special equipment for accelerated cooling from the rolling heat must be used.

Durch die untere Begrenzung des Kohlenstoffgehalts auf 0.20% wird in Kombination mit Mangan und Chrom sichergestellt, dass nur noch geringe Ferritanteile im Gefüge vorliegen. Ferritanteile über 10% beeinträchtigen sowohl das Festigkeitsniveau wie auch die Kerbschlagzähigkeit des Produkts.The lower limit of the carbon content to 0.20% ensures, in combination with manganese and chromium, that only small amounts of ferrite are present in the microstructure. Ferrite levels above 10% affect both the strength level and impact strength of the product.

Durch die obere Begrenzung des Kohlenstoffs auf 0.25% wird gewährleistet, dass die Zugfestigkeit nicht über 1'400 MPa ansteigt. Höhere Festigkeitswerte verschlechtern die Bearbeitbarkeit im nachgelagerten Ziehprozess oder Zerspanungsprozess. Höhere Kohlenstoffgehalte fördern ausserdem die Bildung von Karbiden, was die Duktilität nachteilig beeinflusst.The upper limit of the carbon to 0.25% ensures that the tensile strength does not rise above 1400 MPa. Higher strength values degrade machinability in the downstream drawing or machining process. Higher carbon contents also promote the formation of carbides, which adversely affects ductility.

Silizium beeinflusst die Kohlenstoffaktivität und verlangsamt die Ausscheidung von Karbiden. Die gewählte Siliziumkonzentration erlaubt eine einstündige Anlassbehandlung bei 400°C, ohne dass sich die Duktilität wegen Karbidausscheidungen verschlechtert (in Anlehnung an die Beschreibung des karbid-freien Bainits in WO 96/22396 ). Da Silizium ein effizienter Mischkristallverfestiger im Bainit ist, muss sein Gehalt auf 1.35% begrenzt werden, um die maximal gewünschte Zugfestigkeit von 1'400 MPa nicht zu überschreiten.Silicon affects the carbon activity and slows down the precipitation of carbides. The selected silicon concentration allows a one-hour annealing treatment at 400 ° C without degrading the ductility due to carbide precipitations (based on the description of the carbide-free bainite in WO 96/22396 ). Since silicon is an efficient solid solution hardener in bainite, its content must be limited to 1.35% in order not to exceed the maximum desired tensile strength of 1400 MPa.

Bei einem zu hohen Mangangehalt werden die Manganseigerungen ausgeprägt und das Gefüge wird sehr inhomogen. Aus diesem Grund muss der "freie", d.h. nicht in Mangansulfiden gebundene, Mangangehalt (≈ total Mangangehalt - 1.72 Schwefelgehalt) auf 1.50% begrenzt werden.If the manganese content is too high, the manganese segregations are pronounced and the microstructure becomes very inhomogeneous. For this reason, the "free", ie not bound in manganese sulfides, manganese content (≈ total manganese content - 1.72 Sulfur content) to 1.50%.

Der so festgelegte Mangangehalt reicht nicht aus, um ein bainitisch-martensitisches Gefüge nach Luftabkühlung aus der Walzhitze zu erreichen. Das Produkt muss zusätzlich soviel Chrom enthalten, dass Chromgehalt + (Mangangehalt - 1.72 Schwefelgehalt) > 2.6 Gew.% gilt. Zusammen mit einem Kohlenstoffgehalt von mindestens 0.20% wird so ein bainitisch-martensitisches Gefüge mit < 10% Ferrit sichergestellt.The so determined manganese content is not sufficient to achieve a bainitic-martensitic structure after air cooling from the rolling heat. The product must also contain so much chromium that chromium content + (manganese content - 1.72 sulfur content)> 2.6% by weight applies. Together with a carbon content of at least 0.20%, a bainitic-martensitic microstructure with <10% ferrite is ensured.

Molybdän soll die Ausscheidung von Eisenkarbiden an den Primärkorngrenzen und einen damit verbundenen Zähigkeitsverlust verhindern. Aus Kostengründen ist der Molybdängehalt so niedrig wie notwendig zu wählen: 0.1 bis 0.5% Molybdän.Molybdenum is said to prevent the precipitation of iron carbides at the primary grain boundaries and associated loss of toughness. For cost reasons, the molybdenum content should be as low as necessary: 0.1 to 0.5% molybdenum.

Um eine deutliche Verbesserung der Zerspanbarkeit zu erreichen, soll der Stahl mindestens 0.04%, vorzugsweise 0.12 bis 0.17 % Schwefel enthalten. Der Schwefel verbindet sich mit Mangan zu Mangansulfidausscheidungen, so sowohl den Spanbruch als auch die Werkzeugstandzeit verbessern. Da diese Ausscheidungen gleichzeitig auch die Querzähigkeit des warmgewalzten Langprodukts vermindern, ist die Schwefelzugabe auf 0.25% zu begrenzen.To achieve a significant improvement in machinability, the steel should contain at least 0.04%, preferably 0.12 to 0.17% sulfur. The sulfur combines with manganese to form manganese sulfide precipitates, thus improving both chip breaking and tool life. Since these precipitates also reduce the transverse toughness of the hot-rolled long product, the addition of sulfur should be limited to 0.25%.

Dem erfindungsgemäss hergestellten Produkt wurde kein Aluminium zugegeben. Um die Bildung von harten, abrasiven Oxideinschlüssen vom Typ Korund zu vermeiden, soll der Aluminiumgehalt auf 0.01% begrenzt sein. In Kombination mit dem hohen Siliziumgehalt und einer geringen Kalziumzugabe am Ende der metallurgischen Behandlung sollen gemäss Anspruch 2 Oxideinschlüsse mit einem Al2O3-Gehalt von < 50% eingestellt werden. Vorzugsweise wird die metallurgische Behandlung so vorgenommen, dass weiche, glasartige Silikateinschlüsse mit folgenden relativen Gewichtsanteilen entstehen: 20 bis 50% CaO, 35 bis 65% SiO2 und weniger als 25% Al2O3. Die Werkzeugstandzeit der in der Zerspanung eingesetzten Werkzeuge wird dann deutlich verlängert.No aluminum was added to the product prepared according to the invention. In order to avoid the formation of hard, abrasive oxide inclusions of the corundum type, the aluminum content should be limited to 0.01%. In combination with the high silicon content and a low calcium addition at the end of the metallurgical treatment according to claim 2 oxide inclusions should be set with an Al 2 O 3 content of <50%. Preferably, the metallurgical treatment is carried out so that soft, glassy silicate inclusions are formed with the following relative proportions by weight: 20 to 50% CaO, 35 to 65% SiO 2 and less than 25% Al 2 O 3 . The tool life of the tools used in machining is then significantly extended.

Die gute Zerspanbarkeit des erfindungsgemäss hergestellten warmgewalzten Langprodukts kann gemäss Anspruch 3 bzw. 4 weiter durch die Zugabe von 0.05 bis 0.3% Blei bzw. 0.05 bis 0.3% Wismut verbessert werden.The good machinability of the hot-rolled long product produced according to the invention can be further improved according to claim 3 or 4 by the addition of 0.05 to 0.3% lead or 0.05 to 0.3% bismuth.

Zur erfindungsgemässen Herstellung des warmgewalzten Langprodukts sind die Austenitkorngrösse vor der Gefügeumwandlung, sowie die Abkühlrate während der Gefügeumwandlung in einem Temperaturreich zwischen 800 und 500°C von entscheidender Bedeutung. Ein feines Austenitkorn führt zu einem feineren Endgefüge mit besseren Zähigkeitswerten. Aus diesem Grund soll das Austenitkorn nach dem letzten Umformschritt gemäss Anspruch 7 nicht grösser sein als 50µm. Die Abkühlraten sollen zwischen 0.1 und 8.0 K/s liegen. Der obere Wert ist durch die Möglichkeiten der konventionellen Abkühlung an beschleunigter Luft gegeben. Durch die untere Begrenzung von 0.1 K/s soll sichergestellt werden, dass keine Ferritanteile > 10% vorkommen. Grosse Stabstahlabmessungen, die im Stabinnern deutlich langsamer (als 0.1 K/s) abkühlen, können mit dieser Technologie nicht gefertigt werden.For the production according to the invention of the hot-rolled long product, the austenite grain size before the structural transformation and the cooling rate during structural transformation in a temperature range between 800 and 500 ° C. are of crucial importance. A fine austenite grain leads to a finer final structure with better toughness values. For this reason, the austenite grain after the last forming step according to claim 7 should not be greater than 50μm. The cooling rates should be between 0.1 and 8.0 K / s. The upper value is given by the possibilities of conventional cooling of accelerated air. The lower limit of 0.1 K / s is to ensure that no ferrite> 10% occur. Large bar dimensions that cool down inside the bar much slower than 0.1 K / s can not be produced with this technology.

Vor der weiteren Bearbeitung des warmgewalzten Langprodukts kann eine Wärmebehandlung für 0.5 bis 2 Stunden bei 300 bis 500 °C gemäss Anspruch 8 sinnvoll sein. Der hohe Siliziumgehalt des Produkts verzögert die Umlagerung von Kohlenstoffatomen im Gefüge. Dies ist wünschenswert, um das Entstehen von groben Karbidausscheidungen zu unterdrücken. Andererseits werden auch in Verbindung mit Kohlenstoff bekannte Alterungsprozesse, die unmittelbar nach der Warmwalzung einsetzen, verlangsamt. Insbesondere stellt sich die maximale Duktilität des Gefüges erst nach einigen Wochen ein. In Fällen, bei denen das gewalzte Langprodukt unmittelbar weiterverarbeitet werden soll, ist deshalb eine Wärmebehandlung empfehlenswert.Before the further processing of the hot-rolled long product, a heat treatment for 0.5 to 2 hours at 300 to 500 ° C according to claim 8 may be useful. The high silicon content of the product delays the rearrangement of carbon atoms in the microstructure. This is desirable to suppress the formation of coarse carbide precipitates. On the other hand, also in connection with carbon known aging processes that begin immediately after the hot rolling, slowed down. In particular, the maximum ductility of the structure sets in only after a few weeks. In cases where the rolled long product is to be further processed immediately, a heat treatment is therefore recommended.

Wege zur Ausführung der ErfindungWays to carry out the invention

Ausführungsbeispiele der Erfindung werden nachfolgend anhand der Zeichnungen näher beschrieben, dabei zeigen:

Fig. 1
Gefügebilder nach 200-facher Vergrösserung (Ätzmittel: HNO3 2%-ig), für (a) 22 mm Stabstahl, (b) 52 mm Stabstahl;
Fig. 2
eine schematische Darstellung der Entnahme der B8x40 mm- Zugproben;
Fig. 3
dem Verlauf der Vickers Härte über den Querschnitt eines 22 mm und eines 52 mm Stabs (von der Oberfläche bis zum Kern).
Exemplary embodiments of the invention will be described in greater detail below with reference to the drawings, in which:
Fig. 1
Micrographs after 200-fold magnification (etchant: HNO 3 2% strength), for (a) 22 mm bar steel, (b) 52 mm bar steel;
Fig. 2
a schematic representation of the removal of the B8x40 mm tensile specimens;
Fig. 3
the progression of Vickers hardness across the cross section of a 22 mm and a 52 mm rod (from the surface to the core).

Im Rahmen eines Ausführungsbeispiels wurde eine Stahlschmelze vergossen und anschliessend zu Stabstahl in verschiedenen Abmessungen verwalzt. Die Herstellung der Stahlschmelze erfolgte nach dem Elektrostahl-Verfahren mit einer sekundärmetallurgischen Behandlung an einem Pfannenstand und anschliessendem Vergiessen zu 150x150 mm2-Knüppeln in einer kontinuierlichen Stranggussanlage. Die Knüppel wurden danach in einem Hubbalkenofen auf 1'150 bis 1'200°C wieder erwärmt und anschliessend zu Stabstahl in den Abmessungen 22 (Kühlrate ist ca. 1.5 K/s) und 52 mm (Kühlrate ist ca. 0.4 K/s) gewalzt. Die Abkühlung der Stäbe nach der Walzung erfolgte an Luft. Der Stahl bestand aus 0.22% Kohlenstoff 0.94% Silizium 0.07% Nickel 0.14% Molybdän 0.15% Schwefel 0.003% Aluminium 0.012% Phosphor <0.001% Bor 0.011 % Titan <0.003% Blei <0.003% Wismut 0.013% Stickstoff 1.60% Mangan 1.34% Mangan - 1.72 Schwefel 1.54% Chrom 2.88% Chrom + (Mangan - 1.72 Schwefel) sowie weiterer erschmelzungsbedingter Verunreinigungen.In the context of one embodiment, a molten steel was poured and then rolled into steel bars of various dimensions. The molten steel was produced by the electrical steel process with a secondary metallurgical treatment on a ladle and subsequent casting to 150 × 150 mm 2 sticks in a continuous casting plant. The billets were then reheated in a walking beam oven to 1'150 to 1'200 ° C and then to bar steel in the dimensions 22 (cooling rate is about 1.5 K / s) and 52 mm (cooling rate is about 0.4 K / s) rolled. The cooling of the rods after rolling was carried out in air. The steel was made 0.22% carbon 0.94% silicon 00:07% nickel 0.14% to molybdenum 00:15% sulfur 0.003% aluminum 0.012% phosphorus <0.001% boron 0.011% titanium <0.003% lead <0.003% bismuth 0.013% nitrogen 1.60% manganese 1:34% Manganese - 1.72 Sulfur 1:54% chrome 2.88% Chromium + (manganese - 1.72 sulfur) and other impurities caused by melting.

Der hohe Schwefelgehalt von 0.15% gewährleistet den guten Spanbruch und verbessert die Werkzeugstandzeit. Der tiefe Aluminiumgehalt unterdrückt die Bildung harter, abrasiver tonerdehaltige Oxideinschlüsse.The high sulfur content of 0.15% ensures good chip breaking and improves tool life. The low aluminum content suppresses the formation of hard, abrasive, clay-containing oxide inclusions.

Die metallographische Gefügebilder bei 200-facher Vergrösserung sind in der Fig. 1 gezeigt. Bei dem Gefüge handelt es sich um ein sehr feines Mischgefüge. Die Bainit- und Martensitanteile konnten bisher nicht sicher quantifiziert werden. Die Bilder sowie das erhaltene Festigkeitsniveau zeigen jedoch, dass das Gefüge primär (>>50%) aus Bainit besteht. Das Gefüge des 52 mm Stabs ist aufgrund der geringen Abkühlrate aus der Walzhitze etwas gröber als das Gefüge beim 22 mm Stab. In der Umgebung von Mangansulfiden (die als Keimstellen für die Ferritbildung dienen können) sind vereinzelt Ferritkörner zu erkennen. Der Ferritanteil ist äusserst gering (<<10%). Die Bestimmung der Restaustenitmenge im Röntgendiffraktometer ergab 5.1 ± 0.45% für den 22 mm Stab und 4.4 ± 1.34% für den 52 mm Stab.The metallographic micrographs at 200x magnification are in the Fig. 1 shown. The microstructure is a very fine mixed structure. The bainite and martensite fractions could not be reliably quantified. However, the pictures as well as the obtained strength level show that the structure consists primarily (>> 50%) of bainite. The structure of the 52 mm rod is slightly coarser than the structure of the 22 mm rod due to the low cooling rate from the rolling heat. In the vicinity of manganese sulphides (which can serve as nucleating sites for ferrite formation), isolated ferrite grains can be recognized. The ferrite content is extremely low (<< 10%). The determination of the residual austenite quantity in the X-ray diffractometer showed 5.1 ± 0.45% for the 22 mm rod and 4.4 ± 1.34% for the 52 mm rod.

Da die Proben für die Zugversuche unmittelbar nach der Warmumformung genommen wurden, wurden sie zur Beschleunigung der natürlichen Alterung vor dem Zugversuch eine Stunde bei 300°C unter Schutzgas gelagert. Trotz der unterschiedlichen Abkühlbedingungen aus der Walzhitze bei 22 und 53 mm Stabstahl liegen die Festigkeitswerte für den erfindungsgemäss hergestellten Stahl innerhalb einer Spanne von 100 MPa (Tabelle 1). Tabelle 1: Festigkeitswerte 22 mm 52 mm Rp0.2 886 MPa 842 MPa Rm 1168 MPa 1'064 MPa A5 14.2 % 11.8% Since the samples were taken for the tensile tests immediately after hot working, they were stored for one hour at 300 ° C under inert gas to accelerate the natural aging before the tensile test. Despite the different cooling conditions from the rolling heat at 22 and 53 mm bars the strength values for the steel produced according to the invention are within a range of 100 MPa (Table 1). Table 1: Strength values 22 mm 52 mm Rp0.2 886 MPa 842 MPa rm 1168 MPa 1,064 MPa A5 14.2% 08.11%

Beim 52 mm Stabstahl wurden an verschiedenen Stellen Zugproben (siehe Fig. 2) entnommen, um die Gleichmässigkeit der Eigenschaften nachweisen zu können. Die Ergebnisse sind aus der nachfolgenden Tabelle 2 zu entnehmen. Tabelle 2: Ergebnisse der Zugproben Abstand von Kern 5 mm 13 mm 20 mm Rp0.2 777 MPa 842 MPa 862 MPa Rm 1029 MPa 1064 MPa 1071 MPa A5 10.4% 11.8% 12.9% For 52 mm steel bars, tensile specimens were used at various points (see Fig. 2 ) to demonstrate the uniformity of the properties can. The results are shown in Table 2 below. Table 2: Results of tensile tests Distance from core 5 mm 13 mm 20 mm Rp0.2 777 MPa 842 MPa 862 MPa rm 1029 MPa 1064 MPa 1071 MPa A5 10.04% 08.11% 09.12%

Die hohe Gleichmässigkeit der Härte über den Stabquerschnitt wurde für einen 22 mm und einen 52 mm Stabstahl an nicht-ausgelagerten Proben mittels HV1-Messungen bestätigt (Fig. 3). Aufgrund der schnelleren Abkühlrate ist die Härte bzw. die Festigkeit beim 22 mm etwas höher als beim 52 mm Stabstahl.The high uniformity of hardness across the bar cross-section was confirmed for a 22 mm and a 52 mm bar steel on non-outsourced samples by HV1 measurements ( Fig. 3 ). Due to the faster cooling rate, the hardness or strength of the 22 mm is slightly higher than that of the 52 mm steel bar.

Eine einstündige Auslagerung der 52 mm Stabstahlproben bei 300, 400 und 500°C ergab keine wesentliche Veränderung der mechanischen Eigenschaften (hier an einer bei R/2 entnommene B8x40 mm- Probe ermittelt): Tabelle 3: Mechanische Eigenschaften nach Auslagerung Auslagerung 1 Stunde bei 300°C 400°C 500°C Rp0.2 842 MPa 878 MPa 815 MPa Rm 1064 MPa 1068 MPa 1124 MPa A5 11.8% 13.4% 12.0% A one-hour aging of the 52 mm bar steel samples at 300, 400 and 500 ° C showed no significant change in the mechanical properties (determined here on a B8x40 mm sample taken from R / 2): Table 3: Mechanical properties after aging Outsourcing for 1 hour 300 ° C 400 ° C 500 ° C Rp0.2 842 MPa 878 MPa 815 MPa rm 1064 MPa 1068 MPa 1124 MPa A5 08.11% 04.13% 12.0%

Die vorstehenden Daten zeigen, dass die mechanischen Eigenschaften des erfindungsgemäss hergestellten Produkts über einen grossen Abmessungsbereich nahezu konstant sind. Es wird eine für Vergütungsstähle typische Zugfestigkeit von >1'000 MPa bei einer gleichzeitig guten Bruchdehnung von >11% ohne notwendige Vergütungsbehandlung erreicht. Der reduzierte Aluminiumgehalt sowie der erhöhte Schwefelgehalt im Vergleich zu den Vergütungsstählen gewährleistet eine deutlich bessere Zerspanbarkeit.The above data show that the mechanical properties of the product produced according to the invention are almost constant over a large dimensional range. A tensile strength of> 1 000 MPa typical for tempered steels is achieved with a simultaneously good elongation at break of> 11% without the necessary tempering treatment. The reduced aluminum content and the increased sulfur content compared to the tempered steels ensure a significantly better machinability.

Claims (8)

Warmgewalztes Langprodukt mit einem Gewichtsanteil von 0.20 bis 0.25% Kohlenstoff, 0.90 bis 1.35% Silizium, bis zu 0.20% Nickel, bis 0.5% Molybdän, 0.04 bis 0.25% Schwefel, bis zu 0.01 % Aluminium, bis zu 0.035% Phosphor, bis zu 0.0008% Bor, bis zu 0.02% Titan, bis zu 0.3% Blei, bis zu 0.3% Wismut, bis zu 1.93% Mangan bis zu 4.0% Chrom bis zu 0.02% Stickstoff und bis zu 0.01% in oxidischen Einschlüssen gebundener Sauerstoff sowie weitere stahlübliche Beimengungen, wobei (Mangangehalt - 1.72 Schwefelgehalt) < 1.50 % und Chromgehalt + (Mangangehalt - 1.72 Schwefelgehalt) > 2.6 Gew.-% ist, mit folgenden Gefügebestandteilen: 50 bis 90% Bainit, bis 50%Martensit, bis zu 10% Ferrit und bis zu 10% Restaustenit. Hot rolled long product with a weight fraction of 0.20 to 0.25% carbon, 0.90 to 1.35% silicon, up to 0.20% nickel, up to 0.5% molybdenum, 0.04 to 0.25% sulfur, up to 0.01% aluminum, up to 0.035% phosphorus, up to 0.0008% boron, up to 0.02% titanium, up to 0.3% lead, up to 0.3% bismuth, up to 1.93% manganese up to 4.0% chrome up to 0.02% nitrogen and Up to 0.01% oxygen bound in oxidic inclusions and other common steel admixtures, wherein (Manganese content - 1.72 sulfur content) <1.50% and Chromium content + (manganese content - 1.72 sulfur content)> 2.6 wt .-%, with the following structural components: 50 to 90% bainite, up to 50% martensite, up to 10% ferrite and up to 10% retained austenite. Warmgewalztes Langprodukt nach Anspruch 1, dadurch gekennzeichnet, dass es oxidische Einschlüsse enthält mit weniger als 50 Gew.-% Al2O3, vorzugsweise liegen oxidische Einschlüsse mit folgenden relativen Gewichtsanteilen vor: 20 bis 50% CaO, 35 bis 65% SiO2 und weniger als 25% Al2O3.Hot rolled long product according to claim 1, characterized in that it contains oxide inclusions with less than 50 wt .-% Al 2 O 3 , preferably are oxide inclusions with the following relative proportions before: 20 to 50% CaO, 35 to 65% SiO 2 and less than 25% Al 2 O 3 . Warmgewalztes Langprodukt nach Anspruch 1 oder 2, mit einem Bleigehalt von 0.05 bis 0.3 Gew.-%.Hot rolled long product according to claim 1 or 2, with a lead content of 0.05 to 0.3 wt .-%. Warmgewalztes Langprodukt nach einem der Ansprüche 1 bis 3, mit einem Wismutgehalt von 0.05 bis 0.3 Gew.-%.Hot rolled long product according to one of claims 1 to 3, having a bismuth content of 0.05 to 0.3 wt .-%. Warmgewalztes Langprodukt nach einem der Ansprüche 1 bis 4, mit einer Zugfestigkeit Rm von 1'000 bis 1'400 MPa.Hot rolled long product according to one of claims 1 to 4, having a tensile strength Rm of 1'000 to 1400 MPa. Verwendung eines Langprodukts nach einem der Ansprüche 1 bis 5 für die spanabhebende Bearbeitung.Use of a long product according to any one of claims 1 to 5 for machining. Verfahren zur Herstellung eines warmgewalzten Langprodukts nach einem der Ansprüche 1 bis 5, wobei: - die mittlere Austenitkorngrösse nach dem letzten Warmumformungschritt kleiner ist wie 50 µm; - die Abkühlung aus der Umformhitze an ruhender oder bewegter Luft so geschieht, dass der Temperaturbereich zwischen 800 und 500°C mit einer Kühlrate von 0.1 bis 8.0 K/s durchlaufen wird. A process for producing a hot-rolled long product according to any one of claims 1 to 5, wherein: the mean austenite grain size after the last hot forming step is less than 50 μm; - The cooling from the forming heat to stationary or moving air is done so that the temperature range between 800 and 500 ° C with a cooling rate of 0.1 to 8.0 K / s is passed through. Verfahren zur Herstellung eines warmgewalzten Langprodukts nach Anspruch 7, wobei die Alterung des Stahlgefüges nach dem Warmwalzen über eine anschliessende, zusätzliche Wärmebehandlung für 0.5 bis 2 Stunden bei 300 bis 500°C beschleunigt wird.A process for producing a hot-rolled long product according to claim 7, wherein aging of the steel structure after hot rolling is accelerated by subsequent heat treatment at 300 to 500 ° C for 0.5 to 2 hours.
EP08004335A 2008-03-10 2008-03-10 Hot-rolled long product and method for its manufacture Active EP2103704B1 (en)

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ES08004335T ES2391312T3 (en) 2008-03-10 2008-03-10 Longitudinal hot rolled product and manufacturing process
PL08004335T PL2103704T3 (en) 2008-03-10 2008-03-10 Hot-rolled long product and method for its manufacture
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EP2453027A1 (en) * 2010-11-10 2012-05-16 Swiss Steel AG Thermoformed product and method for producing same
EP2453026A1 (en) * 2010-11-10 2012-05-16 Swiss Steel AG Thermoformed steel product and method for producing same
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EP3061837A1 (en) 2015-02-27 2016-08-31 Swiss Steel AG Blank bainite long product and method for producing the same
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US20230416858A1 (en) * 2017-06-07 2023-12-28 Voestalpine Schienen Gmbh Track part and method for producing a track part
WO2019180563A1 (en) * 2018-03-23 2019-09-26 Arcelormittal Forged part of bainitic steel and a method of manufacturing thereof
RU2763027C1 (en) * 2018-03-23 2021-12-24 Арселормиттал Forged part made of bainite steel and its manufacturing method
JP2021517609A (en) * 2018-03-23 2021-07-26 アルセロールミタル Forged parts of bainite steel and its manufacturing method
CN111836908A (en) * 2018-03-23 2020-10-27 安赛乐米塔尔公司 Forged parts of bainitic steel and method for manufacturing same
WO2019180492A1 (en) * 2018-03-23 2019-09-26 Arcelormittal Forged part of bainitic steel and a method of manufacturing thereof
US12203156B2 (en) 2018-03-23 2025-01-21 Arcelormittal Forged part of bainitic steel and a method of manufacturing thereof

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EP2103704B1 (en) 2012-07-11

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