WO2020157665A1 - A high strength-high ductile steel and a method of manufacturing thereof - Google Patents
A high strength-high ductile steel and a method of manufacturing thereof Download PDFInfo
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- WO2020157665A1 WO2020157665A1 PCT/IB2020/050670 IB2020050670W WO2020157665A1 WO 2020157665 A1 WO2020157665 A1 WO 2020157665A1 IB 2020050670 W IB2020050670 W IB 2020050670W WO 2020157665 A1 WO2020157665 A1 WO 2020157665A1
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- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/56—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering characterised by the quenching agents
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- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
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- 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
- C21D8/021—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips involving a particular fabrication or treatment of ingot or slab
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- 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
- C21D8/0221—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
- C21D8/0226—Hot rolling
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- 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
- C21D8/0247—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
- C21D8/0263—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment following hot rolling
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- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
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- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
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- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/34—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of silicon
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- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/42—Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
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- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/44—Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/46—Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
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- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/52—Ferrous alloys, e.g. steel alloys containing chromium with nickel with cobalt
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- 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
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- 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
- C21D2211/008—Martensite
Definitions
- the present disclosure in general relates to a field of material science and metallurgy. Particularly, but not exclusively, the present disclosure relates to a high strength-high ductile steel. Further embodiments of the disclosure disclose a method for manufacturing the a high strength-high ductile steel.
- Steel is an alloy of iron, carbon and other elements such as Phosphorous (P), Sulphur (S), Nitrogen (N), Manganese (Mn), Silicon (Si), Chromium (Cr), etc. Because of its high tensile strength and low cost, steel may be considered as a major component in wide variety of applications. Some of the applications of the steel may include buildings, ships, tools, automobiles, machines, bridges and numerous other applications. The steel obtained from steel making process may not possess all the desired properties. Therefore, the steel may be subjected to secondary processes such as heat treatment for controlling material properties to meet various needs in the intended applications.
- heat treatment may be carried out using techniques including but not limiting to annealing, normalising, hot rolling, quenching, and the like.
- the material undergoes a sequence of heating and cooling operations, thus, the microstructures of the steel may be modified during such operation.
- the steel undergo phase transformation, influencing mechanical properties like strength, ductility, toughness, hardness, drawability etc.
- the purpose of heat treatment is to increase service life of a product by improving its strength, hardness etc., or prepare the material for improved manufacturability.
- the present disclosure is directed to overcome one or more limitations stated above or any other limitation associated with the prior arts.
- a method for manufacturing high strength- high ductile steel comprising soaking, a steel comprising of a composition in weight percentage (wt%) of: Carbon (C) at about 0.4 wt% to about 0.42 wt%.
- Carbon (C) at about 0.4 wt% to about 0.42 wt%.
- Manganese (Mn) at about 0.5 wt% to about lwt %, Sulphur (S) up-to 0.02 wt%.
- Phosphorus (P) up-to 0.02 wt%.
- Iron (Fe) optionally along with incidental elements
- the high strength-high ductile steel primarily comprises a martensitic microstructure.
- the high strength-high ductile steel exhibits ultimate tensile strength ranging from about 1850 MPa to 1936 MPa, and the ductility ranging from about 17% to about 19%.
- the high-strength-high ductile steel comprises a martensitic microstructure and a retained austinite microstructure.
- the re-heating, soaking, and tempering are carried out in a furnace, and the cooling is normal air cooling. Further, the isothermal quenching is carried out in a hot water bath.
- the steel is maintained in the hot water bath for about 5 minutes to achieve equilibrium temperature.
- the first pre-determined temperature is about 1250 °C
- the second pre- detennined temperature is about 100°C
- the third pre-determined temperature ranging from about 100°C to about 160°C.
- volume fraction of the retained austinite in the microstructure of the high strength-high ductile steel increases gradually with increase in the third pre-determined temperature.
- the first pre-set period of time is about 3 hours
- the second pre-set period of time is about 45 minutes
- the third pre-set period of time is about 24 hours.
- the first hot working process is a forging process
- the second hot working process is a rolling process.
- the rolling process is carried out at least five to six times on the steel, and wherein, the temperature of the steel drops to a range of about 900°C to about 950°C during the rolling process.
- the method comprises, cooling the steel to a room temperature in air after the tempering.
- the method comprises cleaning the steel by acid pickling at the temperature below 50°C, preferably at room temperature.
- the steel is produced by casting alloy in at least one of air-melting furnace, and vaccum furace.
- a high strength-high ductile steel comprising of a composition in weight percentage (wt%) of: Carbon (C) at about 0.4 wt% to about 0.42 wt%.
- Manganese (Mn) at about 0.5 wt% to about lwt %, Sulphur (S) up-to 0.02 wt%, Phosphorus (P) up-to 0.02 wt%, Nitrogen (N) up-to 0.01 wt%, Silicon (Si) at about 1.5 wt% to about 2 wt %, Vanadium (V) at about 0.05 wt% to about 0.08 wt%, Aluminum (Al) at about 0.5 wt% to about 1 wt %, Chromium (Cr) at about 0.8 wt% to about 1 wt%, Nickel (Ni) at about 3 wt% to about 3.5 wt %, Cobalt (Co) at about 1.5 wt%) of: Carbon (C) at about 0.4
- the high strength-high ductile comprises martensitic microstructure and retained austinite microstructure.
- the microstructure of the high strength-high ductile steel forms a twin in stable austenite when subjected to tensile straining.
- a method for manufacturing high strength-high ductile steel comprising: casting a steel of composition comprising: of a composition in weight percentage (wt%) of: Carbon (C) at about 0.4 wt% to about 0.42 wt%, Manganese (Mn) at about 0.5 wt% to about lwt %, Sulphur (S) up-to 0.02 wt%, Phosphorus (P) up-to 0.02 wt%, Nitrogen (N) up-to 0.01 wt%, Silicon (Si) at about 1.5 wt% to about 2 wt %, Vanadium (V) at about 0.05 wt% to about 0.08 wt%, Aluminum (Al) at about 0.5 wt% to about 1 wt %, Chromium (Cr) at about 0.8 wt% to about 1 wt%, Nickel (Ni) at about 3 wt% to about 3.5 wt %,
- C Carbon
- Mn Manganese
- the method further includes tempering, the steel at a third predetermined temperature for a third pre-set period of time, to obtain high strength-high ductile steel.
- the high strength-high ductile steel primarily comprises martensitic microstructure. Ill an embodiment, the high-strength-high ductile steel comprises martensitic microstructure and retained austinite microstructure.
- an automotive light weight structural part comprising a high- strength-high ductile steel as described above is disclosed.
- Figure.1 is a flowchart illustrating a method for producing high strength-high ductile steel, according to an exemplary embodiment of the present disclosure.
- Figure.2 is graphical flow diagram illustrating a method for producing high strength-high ductile steel, according to an exemplary embodiment of the present disclosure.
- Figure. 3 illustrates microstructure of the high strength-high ductile steel manufactured by the method of figure. 1, which is only quenched, according to an exemplary embodiment of the present disclosure.
- Figures. 4-7 illustrates microstructure of the high strength-high ductile steel manufactured by the method of figure. 1, which is quenched and tempered at different temperatures, in accordance with some embodiments of the present disclosure.
- Figure. 8a illustrates a graphical representation of results of X-ray Diffraction analysis carried out on the high strength-high ductile steel sample hot rolled-quenched at 100°C, and tempered at 100°C for a period of 24 hours, according to an exemplary embodiment of the present disclosure.
- Figures. 8b illustrates a graphical representation of results of X-ray Diffraction analysis carried out on the high strength-high ductile steel sample hot rolled-quenched at 100°C, and tempered at 160°C for a period of 24 hours, according to an exemplary embodiment of the present disclosure.
- Figure. 9 is graphical representation of stress versus elongation, obtained during tensile test of the high-strength high ductile steel tempered for the time period of about 24 hours at various temperatures, according to an exemplary embodiment of the present disclosure.
- Embodiments of the present disclosure discloses a high strength and high ductile steel and a method for manufacturing or producing a high strength and high ductile steel.
- Ductility is an important property for the mass industrial application of high strength material like steel.
- high strength and high ductile steels are produced as TWIP steel.
- high strength bainitic steel is used for specific application like in armor vehicle, however, not being used for mass scale industrial manufacturing type application because of its poor ductility.
- high manganese content in TWIP steel limits its mass industrial and commercial applications due to constraints associated with processing and higher production cost.
- the present disclosure provides a method for manufacturing high strength- high ductile steel in which ferritic-bainite phase is replaced by fine martensitic strip which can incorporate higher strength value. It is expected that the fine martensite plates will contribute little positively to the ductility of the steel in comparison to the transformed martensite from blocky retained austenite. Additionally, the presence of mechanically stable thin-film retained austenite (RA) in-between the lath martensite plate and interior of the martensite strip play a major role to impart ductility to the martensite base current steel.
- RA thin-film retained austenite
- the austenite phase needs to be at lower SFE (stacking fault energy) range to promote twin in the retained austenite. This would be a more effective option to incorporate the additional strength without impairing ductility.
- the steel with martensitic microstructure with retained austinite may be produced.
- steels with twin formation in the microstructure are preferred due to their enhanced mechanical properties.
- the mechanical properties include but are not limited to strength, ductility, torsion, hardness and toughness.
- the present disclosure forms a twin in stable austenite when subjected to tensile straining. This improves ductility of the steel.
- steel comprising desired composition may be, formed by any manufacturing process, including but not limiting to casting. Then the steel is initially soaked at a first predetermined temperature for a first pre-set period of time in the furnace. In an embodiment, the first pre-determined temperature is about 1250°C. The hot steel is then subjected to a first hot working process and followed by normal air cooling. In an embodiment, the first hot working process is a forging process. The cooled steel is reheated to the first pre-determined temperature and annealed for a second pre-set period of time. In an embodiment, the time period for which the steel ingot is annealed is about 45 minutes.
- the steel is subjected to a second hot working process like a rolling process.
- the steel is rolled for at least five times between the one or more pair of rollers.
- the steel is then isothermally quenched to a second predetermined temperature of about 100°C, and cooled to a room temperature.
- the steel is tempered in a third predetermined temperature for a third pre-set time of about 24 hours, and cooled to a room temperature.
- the third predetermined temperature may be about 100°C to about 160°C.
- the steel obtained by the method of the present disclosure will have remarkably high plasticity and strength combination. Therefore, the steel may be used in wide variety of industrial applications where structural components require some amount of formability. As an example, the application may include but not limiting to automotive industry.
- Figures.1 and 2 are exemplary embodiments of the present disclosure illustrating a flowchart depicting and a process flow diagram of a method for manufacturing high strength-high ductile steel.
- mechanical properties such as strength and ductility of the final microstructure of the steel may be improved.
- the steel produced by the method of the present disclosure includes a martensitic microstructure and a retained austinite microstructure.
- the method is now described with reference to the flowchart blocks and is as below. The order in which the method is described is not intended to be construed as a limitation, and any number of the described method blocks can be combined in any order to implement the method. Additionally, individual blocks may be deleted from the methods without departing from the scope of the subject matter described herein.
- the method is particularly applicable to high-strength -high ductile steel and it may also be extended to other type of steels as well.
- a steel of desired alloy composition is formed by any of the manufacturing process.
- the steel is further processed to form high strength-high ductile steel.
- the steel is made in the form of ingots, and the alloy may be prepared in at least one of air-melting furace, and vaccum furnace .
- the steel ingot may have composition of in weight percentage (wt%) of: Carbon (C) at about 0.4 wt% to about 0.42 wt%, Manganese (Mn) at about 0.5 wt% to about Iwt %, Sulphur (S) up-to 0.02 wt%, Phosphorus (P) up-to 0.02 wt%, Nitrogen (N) up-to 0.01 wt%, Silicon (Si) at about 1.5 wt% to about 2 wt %, Vanadium (V) at about 0.05 wt% to about 0.08 wt%, Aluminum (Al) at about 0.5 wt% to about 1 wt %, Chromium (Cr) at about 0.8 wt% to about 1 wt%.
- C Carbon
- Mn Manganese
- S Sulphur
- P Phosphorus
- Silicon (Si) at about 1.5 wt% to about 2
- the method comprises of soaking the steel in the form of ingots.
- the steel ingots may be subjected for soaking in the first predetermined temperature for a first pre-set period of time in an annealing furnace.
- the first pre -determined temperature ranges from about 1220 °C to 1280 °C, preferably 1250 °C. Further, in an embodiment, the first pre-set period of time is around 3 hours.
- the method includes a step or a stage of hot working the steel ingot by a first hot working process [shown in block 103] immediately after soaking.
- the first hot working process is a forging process.
- Forging is a mechanical process in which the components may be reshaped by applying localized compressive stresses.
- the localized compressive stresses may be induced using a 0.5 ton motor driven hammer. Blows are delivered by the hammer on to the steel ingot in order to induce localized compressive stresses, which may result in internal grain deformation, thus enhancing strength and stiffness of the structure.
- the steel ingot is allowed to cool.
- the cooling of the steel ingot is carried out by normal air cooling.
- the method comprises of re-heating the steel ingot to a first pre -determined temperature of around 1220 °C to 1280 °C, preferably 1250 °C.
- the method comprises of annealing the steel ingot for a second pre-set period of time.
- the second pre-set period of time is about 45 minutes.
- Annealing is a heat treatment process, which involves heating the structure above the re-crystallization temperature and maintaining the temperature for a suitable time and cooling. During annealing, atoms migrate in the crystal lattice and the number of dislocations decreases, which result in improving mechanical properties of the structure.
- the annealing is carried out in an argon gas atmosphere.
- the method comprises of hot working the steel ingot by a second hot working process.
- the second hot working process may be a rolling process.
- the rolling is a mechanical process, which involves passing the metal stock through one or more pairs of rolls to refine the grain size in the structure.
- the steel ingot may be passed through the one or more pair of rolls for at least 5 to 6 times.
- the temperature of the steel ingot reduces below the first pre-detennined temperature i.e. the temperature reduces from about 900°C to about 950°C.
- the steel ingot is isothermally quenched [shown in block 107] to a second predetennined temperature.
- the second pre-detennined temperature is about 100°C.
- the isothermal quenching of the steel ingot may be carried out in hot water maintained at 100 °C and kept for 5 minutes to achieve equilibrium temperature. After quenching, the steel ingot is cooled to room temperature by air cooling as shown in step 108. Subsequently, the steel ingot is subjected for tempering at third predetermined temperature for a third predetermined time as shown in block 109.
- the third predetennined temperature may range from about 100°C to about 160°C, and the third predetermined time may be about 24 hours.
- tempering may be carried out in a muffle furnace.
- the steel ingot may be taken out of the muffle furace and cooled in air to room temperature.
- the steel ingot processed by the method of the present disclosure results in microstructural changes to form high strength-high ductile steel.
- the steel comprises a substantially martensitic microstructure with retained austinite (RA).
- the method optionally comprises cleaning the steel by acid pickling at the temperature below 50 °C, preferably at room temperature.
- the high strength-high ductile steel exhibits ultimate tensile strength ranging from about 1850 MPa tol936 MPa, and ductility ranging from about 17% to about 19%.
- the transfer from annealing furnace to rolling mill took about 7 seconds, the five reduction passes took about 30 seconds and transfer from rolling mill to water quench at 100° C took less than 2 seconds. This signifies the processing is much faster when compared to the conventional processes.
- the following portions of the present disclosure provides details about the proportion of each alloying element in a composition of the steel and their role in enhancing properties.
- Carbon (C) may be used in the range between 0.4 to 0.42 wt%. Carbon is an austenite stabilizer and controls the martensite formation. Excessive carbon may promote carbide precipitates in the interface of martensite and austenite and may vary the precipitation formation as the cooling rate varies, this may affect the constant strength over a wide range of cooling rate. Silicon (Si) may be used minimum in the range of 1.5 to 2 wt%. Silicon suppress the carbide formation in the steel when it is added to about 1.5 wt%. It leads to carbide free matrix which eventually improve the ductility and impact toughness of the steel.
- Manganese (Mn) may be used in the range of 0.5 to 1.0 wt%. Lower content of manganese may retain the toughness and lower the possibility of carbide formation aiming to produce carbide free matrix to improve the ductility. However, the hardenability may decrease as a result of reducing (Mn). The (Mn) content limit may be considered low or high as per extent of hardenability required with carbide free matrix.
- Chromium (Cr) may be used in the range 0.8 to 1 wt%. This addition may substantially increase the strength and hardenability of the steel. It may vary beyond above range for customized strength and hardenability requirement.
- Nickel may be used in the range 3 - 3.5 wt.% . This increases the strength and toughness.
- Molybdenum (Mo) may be used in the range of 0.24 to 0.27 wt%. The addition of small quantity reduces the impurity embrittlement and to increases hardenability. Excess addition may reduce the carbon content in austenite. It increases the room temperature strength in steel.
- Vanadium (V) may be added in range 0.06 to 0.07 wt%. This addition may reduce the stacking faults in the austenite. It also act as solid solution strengthener.
- Co Co
- Co Co
- Co Co
- the addition of cobalt may effectively decrease the stacking fault energy of austenite.
- Aluminum (Al) may be added in between 1 to 1.06 wt%. This addition improves strength and ductility. It can also be added more or less as a solid solution strengthener. Copper (Cu) may be added in the range of 0.18 to 0.20wt%. Thus addition may increase the solid solution strengthening and aiming to boost up the toughness. This can be added more to increase the strength and toughness.
- Figures. 3-7 show the microstructure of the quenched, and the quenched and tempered (at different temperature) sample. This consists of clear lath-martensite plates separated by thin retained austenite (RA) film with overall homogeneity in microstructure and granular the retained austenite (RA) in the interior of lath-m artsite .
- RA retained austenite
- FIG. 3 which shows microstructure of the steel which is quenched to 100 °C, and not tempered.
- This microstructure clearly shows the presence of lath-martensite with thin retained austenite (RA) and granular retained austenite (RA) in the interior of lath-martensite .
- Figure. 4 shows microstructure of the steel which is quenched to 100 °C and subjected to tempering for 24 hour at 100 °C. It is evident from Figure. 4 that, microstructure of lath-martensite with thin retained austenite (RA) and granular retained austenite (RA) is present in the interior of lath-martensite.
- RA thin retained austenite
- RA granular retained austenite
- the final microstructure of the steel fonned by the method described above includes matristic microstructure and retained austinite (RA) microstructure.
- RA retained austinite
- the final product could then be used in a wide range of industrial and commercial applications with optimum processing cost.
- FIGS. 8a and 8b are exemplary embodiments of the present disclosure, illustrating graphical representation of the results of XRD analyses carried out on the steel sample i.e. hot rolled-quenched to 100 °C and tempered at 100 °C for 24 hours and tempered at 160 °C for 24 hours respectively.
- the parent material i.e. only quenched steel exhibits martensitic microstructure (see Figure.3) with low content of granular retained austenite (RA) in the interior of martensite plate. Thin film may be observed in between martensitic plate.
- the presence of retained austenite (RA) may be confirmed by the XRD results ( Figures 8a and 8b).
- the results indicate that there is a gradual increase in the volume fraction of the retained austenite (RA) as the tempering temperature is changing from 100°C to 160°C temperature.
- volume fraction of retained austinite is about 5.5% and 8.1% respectively for tempered at 100 °C for 24 hours and tempered at 160 °C for 24 hours. Also, there are no such apparent microstructural changes that can be observed with the change in the tempering temperature. It is expected that carbon diffusion to austenite controls the ductility without lowering the considerable amount of strength of the material. It may be assumed that, the rule of phase mixture which may be applicable here, thus contribute to mechanical properties accordingly. The carbon diffusion from martensite may decrease the strength a little. This diffused carbon simultaneously harden the retained austenite (RA).
- retained austinite will always be surrounded by hard martensitic phase which will not allow retained austinite (RA) to be transformed to martensite since it is limited by volume expansion and remain in highly stressed condition (as demonstrated by austenite peak-shift in the Figures. 8a and 8b). This may contribute to the mechanical stability of the retained austinite (RA).
- M100T Hot rolled-Quenched (100 °C water) and Tempered at 100 °C for 24 Hrs.
- M120T Hot rolled-Quenched (100 °C water) and Tempered at 120 °C for 24 Hrs.
- M140T Hot rolled-Quenched (100 °C water) and Tempered at 140 °C for 24 Hrs.
- M160T Hot rolled-Quenched (100 °C water) and Tempered at 160 °C for 24 Hrs.
- the tensile test may be carried using standard tensile test samples of the steel tempered for 24 hours at various temperatures like 100 °C, 120 °C, 140 °C, and 160 °C.
- the test sample may be with a gauge length of 25mm and
- the method of the present disclosure is most easiest processing route compared to others available method, and the method achieves about 2 GPa strength and ductility raging between 17 to 19% in the steel.
- the present disclosure discloses a method for producing a high strength-high ductile steel is disclosed.
- the method may be useful from industrial point.
- the method according to this embodiment includes steps of casting a steel of composition comprising: of a composition in weight percentage (wt%) of: Carbon (C) at about 0.4 wt% to about 0.42 wt%.
- the steel slab may undergo defonnation, and then subsequently the steel slab may be subjected for quenching.
- the quenching may be done in a hot water for the second predetermined time.
- the steel slab may be subjected for second hot working process such as rolling process.
- the method further includes tempering, the steel at a third predetermined temperature for a third pre-set period of time, to obtain high strength-high ductile steel.
- the high strength-high ductile steel primarily comprises martensitic microstructure.
- the high strength-high ductile steel of the present disclosure may be used any application including but not limiting to automotive applications to manufacture structural components like chassis, pillars, outer and inner panels, and the like.
- the high strength-high ductile steel may be used in any other industrial structural applications.
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US11718890B2 (en) * | 2021-10-15 | 2023-08-08 | Jiangxi University Of Science And Technology | High-strength and high-plasticity TWIP steel and preparation method thereof |
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