EP3155137B1 - Verfahren zur herstellung einer niedriglegierten stahlbarren - Google Patents

Verfahren zur herstellung einer niedriglegierten stahlbarren Download PDF

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Publication number
EP3155137B1
EP3155137B1 EP15727949.8A EP15727949A EP3155137B1 EP 3155137 B1 EP3155137 B1 EP 3155137B1 EP 15727949 A EP15727949 A EP 15727949A EP 3155137 B1 EP3155137 B1 EP 3155137B1
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Prior art keywords
equal
content
electrode
less
weight
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English (en)
French (fr)
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EP3155137A1 (de
Inventor
Laurent Ferrer
Nicolas Binot
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Safran Aircraft Engines SAS
Safran Landing Systems SAS
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Safran Aircraft Engines SAS
Safran Landing Systems SAS
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Priority to EP19169956.0A priority Critical patent/EP3536815A1/de
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B9/00General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
    • C22B9/16Remelting metals
    • C22B9/20Arc remelting
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D27/00Treating the metal in the mould while it is molten or ductile ; Pressure or vacuum casting
    • B22D27/02Use of electric or magnetic effects
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D27/00Treating the metal in the mould while it is molten or ductile ; Pressure or vacuum casting
    • B22D27/04Influencing the temperature of the metal, e.g. by heating or cooling the mould
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B9/00General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
    • C22B9/04Refining by applying a vacuum
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • 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
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/44Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/46Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F27FURNACES; KILNS; OVENS; RETORTS
    • F27BFURNACES, KILNS, OVENS, OR RETORTS IN GENERAL; OPEN SINTERING OR LIKE APPARATUS
    • F27B3/00Hearth-type furnaces, e.g. of reverberatory type; Tank furnaces
    • F27B3/10Details, accessories, or equipment peculiar to hearth-type furnaces
    • F27B3/28Arrangement of controlling, monitoring, alarm or the like devices
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F27FURNACES; KILNS; OVENS; RETORTS
    • F27DDETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
    • F27D19/00Arrangements of controlling devices

Definitions

  • the invention relates to methods for manufacturing low alloy steel ingots and to steel parts obtainable by such methods.
  • the minimum design curves depend not only on the average value but also on the dispersion of results. This is particularly true for parts used in the aeronautical field with which a statistical analysis is generally taken into account. Reducing the dispersion of the results therefore makes it possible to trace the minimum dimensioning curves and, consequently, to improve the performances of the parts, for example by making it possible to lighten the parts, to extend their service life or to to increase the constraints to which they may be exposed. The reduction of the dispersion of the results advantageously makes it possible to confer a competitive technical differentiation as well as an economic gain in the material used.
  • the service life during oligo-cyclic fatigue stresses may depend, on the one hand, on the energy consumed at the moment of initiation on one of the particles present in the metallic material leading to a microcracking and, on the other hand, the propagation of the crack.
  • a dispersion in the types of primers can induce a large dispersion of the priming energy reductions and can, therefore, further reduce the curve enveloping the minimum points (lowering of the mean and increase of the standard deviation).
  • each reflow oven has a certain dispersion, inducing a dispersion of the sizes of these primers and, consequently, disparities in the lifetimes of the products obtained.
  • Low-alloy steel means a steel for which no alloying element is present in a mass content greater than 5.00%. In other words, in a low-alloy steel, each of the chemical elements, other than iron, is present in a mass content less than or equal to 5.00%.
  • the "molten bath” comprises the liquid part obtained after melting the electrode and the pasty part situated between the liquid part and the ingot obtained.
  • average speed of solidification during step b) is meant the ratio (distance traveled by the solidification front during step b)) / (duration of step b)).
  • the solidification front corresponds to the boundary between the ingot obtained and the pasty zone of the molten bath.
  • the distance traveled by the solidification front is equal to the distance, measured along the longitudinal axis of the crucible, which is traversed by the bottom of the molten bath (ie by the point of the molten bath closest to the bottom of the crucible and situated at the contact of the solidification front).
  • the duration of step b) is the time during which solidification of the melt is performed.
  • the invention advantageously makes it possible to obtain low alloy steel ingots with reduced inclusions of size and alignment.
  • the invention advantageously makes it possible to obtain low alloy steel ingots having a dispersion of the inclusion population obtained during the reduced production compared to the ingots manufactured by the methods of the state of the art.
  • the ingots obtained by the process according to the invention advantageously have mechanical properties as well as improved lifetimes compared to ingots made by known processes.
  • a solidification rate of the melt sufficiently low is imposed so that all or part of the inclusions present in the melt "up" faster to the surface of the melt than the solidification front.
  • the average solidification rate is chosen to be less than the flotation rate (i.e. the rate of rise to the surface of the melt) of all or part of the inclusions present in the melt.
  • vF K . r 2 . ⁇ MV
  • K is a physical constant describing the constant of gravitational acceleration and dynamic viscosity at a given temperature
  • r the radius of inclusion
  • ⁇ (MV) is the density difference between inclusion and melted bath.
  • Equation 1 shows that small inclusions take longer to rise to the surface than larger inclusions in a radius-to-square ratio. In addition, equation 1 shows that an increase in the density difference increases the flotation rate.
  • the flotation time of all or part of the inclusions present in the melt is less than the duration of step b).
  • the average rate of solidification imposed during step b) may advantageously be less than the flotation rate of all or part of the nonmetallic inclusions present in the melt.
  • the average rate of solidification imposed during step b) may advantageously be less than the flotation rate of inclusions present in the melt and able to crystallize in the melt but not in the ingot obtained.
  • the average rate of solidification imposed during step b) may advantageously be less than the flotation rate of alumina Al 2 O 3 and / or the flotation rate of lime aluminates of formula [(Al 2 O 3 ) x (CaO) y ] present in the melt.
  • the flotation rates and, therefore, the flotation times can be similar.
  • the flotation times may, for example, be less than 60 minutes.
  • the duration of step b) may, for example, be greater than or equal to 60 minutes, for example 100 minutes.
  • the method according to the invention may further comprise after step b) a step c) of homogenizing the alloying elements present in the ingot obtained.
  • Step c) may, for example, comprise a heat treatment of the ingot obtained by submitting the ingot at a temperature below its melting temperature.
  • Such a step is advantageous insofar as it makes it possible to diffuse the alloying elements from a zone heavily loaded with alloying elements to a zone weakly loaded with alloying elements.
  • the method according to the invention may, furthermore, comprise, after step c), a step d) of shaping to hot ingot.
  • Step d) may make it possible to obtain from the ingot a semi-finished product, for example in the form of a bar or a sheet.
  • the average speed of solidification imposed during step b) may preferably be less than or equal to 40 ⁇ m / s, preferably 35 ⁇ m / s, preferably 30 ⁇ m / s, particularly preferably 25 ⁇ m / s. .
  • the reflow oven can have instabilities which can lead to the return to the bottom of the molten bath of rafts of inclusions.
  • the presence of such instabilities may lead to an increase in the time required for the inclusions to rise to the surface of the melt and remain there.
  • Operating at such average rates of solidification advantageously makes it possible to further increase the difference between the time required to solidify the melt and the time required for an inclusion to rise to the surface. Consequently, the negative impact of the instabilities of the reflow oven is advantageously reduced because the solidification is slower, thus leaving time for the inclusions possibly returned to the bottom of the molten bath to rise to the surface.
  • the flotation time of all or part of the inclusions present in the melt may advantageously be less than or equal to two-thirds, or even half, of the duration of step b).
  • the diameter of the electrode before fusion can, for example, be between 650 mm and 1200 mm.
  • electrode diameter is meant the largest dimension of the electrode measured perpendicular to the longitudinal axis of the electrode.
  • the electrode may, before melting, be of cylindrical shape.
  • a cylindrical electrode advantageously makes it possible, after merging, to obtain an upward movement of the inclusions within the molten bath essentially directed along the longitudinal axis of the crucible. This advantageously allows to further limit the amount of inclusions trapped in the ingot obtained after solidification due to a rise of inclusions more direct to the surface of the molten bath.
  • the invention is not limited to the implementation of a cylindrical electrode before melting. Indeed, the electrode may, alternatively, be of conical or parallelepipedal shape before melting.
  • the diameter of the molten bath may, for example, be between 650 mm and 1200 mm.
  • the diameter of the molten bath can be between 700 mm and 950 mm.
  • the diameter of the molten bath can be between 650 mm and 950 mm.
  • the diameter of the molten bath can be between 700 mm and 1200 mm.
  • the diameter of the molten bath corresponds to its largest dimension measured perpendicularly to the longitudinal axis of the crucible.
  • the diameter of the molten bath is measured perpendicular to the height of the cylinder.
  • the diameter of the melt is measured without taking into account the thickness of the side wall of the crucible.
  • the average speed of solidification imposed during step b) may be greater than or equal to 9 ⁇ m / s and more preferably greater than or equal to 14 ⁇ m / s.
  • the cooling fluid may, for example, be a coolant.
  • the combination of a cooling liquid and a cooling gas can be used during step b) to achieve the heat exchange.
  • the cooling gas may be chosen from: helium, argon or nitrogen.
  • the cooling liquid may, for example, be selected from: water, a polymer fluid or molten sodium.
  • the water used as coolant may optionally include additives such as anti-scale and / or anti-bacterial additives.
  • the cooling fluid may, for example, be in motion relative to the crucible during all or part of step b).
  • the circulation velocity of the cooling fluid performing the heat exchange may, for example, be greater than or equal to 1000 l / min, preferably between 2000 and 6000 l / min, during all or part of step b).
  • the cooling fluid may, before the start of the heat exchange, be at a temperature of less than or equal to 80 ° C.
  • the crucible may, for example, comprise, in particular consist of, a heat-transfer metal.
  • the crucible may, for example, comprise, in particular consist of, copper or brass.
  • the carbon may be present in the electrode before melting in a mass content of between 0.09% and 1.00%.
  • the electrode may further comprise before chromium melting in a mass content of between 0.10% and 5.50%.
  • the electrode may further comprise before molybdenum melting at a mass content less than or equal to 5.00%, for example between 0.05% and 5.00%.
  • Such a part according to the invention advantageously has improved fatigue strength compared to the parts of the state of the art.
  • the piece is obtained by implementing a method as described above.
  • the part may include non-metallic inclusions.
  • the part may correspond to the ingot obtained at the end of step b) or possibly of step c) described above.
  • the part may also correspond to the half-product obtained after implementation of step d) described above.
  • the carbon may be present in the part in a mass content of between 0.09% and 1.00%.
  • the part may further comprise chromium in a mass content of between 0.05% and 5.00%.
  • the part may further comprise molybdenum in a mass content less than or equal to 5.00%, for example between 0.05% and 5.00%.
  • the part according to the invention may, for example, comprise different alloying elements in the proportions indicated in Table 1 given below.
  • Table 1 ⁇ / u> % C % Mn %Or %Yes % Cr % Mo V% Room 1 0.13 0.2 3.4 0.2 4.1 4.3 1.2 Room 2 0.15 0.5 3.2 0.3 1.0 0.3 ⁇ 0.1 Exhibit 3 0.20 0.5 3.2 0.3 1.0 0.3 ⁇ 0.1 Room 4 0.32 0.7 ⁇ 0.4 0.3 3.3 2.0 0.3 Exhibit 5 0.35 0.5 3.9 0.3 1.8 0.4 ⁇ 0.1 Room 6 0.40 ⁇ 0.5 1.8 ⁇ 0.5 0.8 0.3 ⁇ 0.1 Exhibit 7 0.40 0.5 ⁇ 0.4 0.2 3.2 1.0 0.2 Exhibit 8 0.40 0.3 ⁇ 0.4 0.9 5.0 1.3 0.5 Exhibit 9 0.41 0.8 1.8 1.7 0.8 0.4 0.08 Exhibit 10 0.81 0.2 ⁇ 0.4 0.2 4.1 4.3 1.0
  • the part may have a cylindrical shape.
  • the part may, for example, have a conical or parallelepiped shape.
  • the patent further discloses a low alloy steel part comprising iron and carbon and obtainable by carrying out a method as described above.
  • Such a piece may, for example, have the same constituents present at the same mass contents as for the piece described above.
  • the electrode 1 intended to be melted is present in the interior volume delimited by the crucible 10.
  • the electrode 1 may, previously, have been developed by any means known as air preparation or elaboration by vacuum induction.
  • the electrode 1 may, as shown, have a cylindrical shape before melting. As explained above, it is not beyond the scope of the present invention if an electrode having another form before fusion is implemented.
  • the crucible 10 is, for example, copper.
  • the crucible 10 extends along a longitudinal axis X.
  • a generator G imposes a potential difference between the crucible 10 and the electrode 1.
  • a first terminal of the generator G can, as shown, be connected to the electrode 1 and a second terminal of the generator G may, as shown, be connected to the bottom 11 of the crucible 10.
  • the potential difference imposed between the crucible 10 and the electrode 1 by the generator G makes it possible to create electric arcs 3 in the space 2 in which there is a void. These electric arcs 3 make it possible to melt the electrode 1 and to carry out step a).
  • the molten portion of the electrode 1 is collected in the crucible 10 and thus forms a melt 20.
  • the melt 20 comprises a liquid portion 21 located on the electrode side 1 and a pasty portion 22 located between the liquid portion 21 and the ingot 30.
  • the ingot 30 is obtained by cooling the molten portion of the electrode.
  • the solidification front 34 separates the resulting ingot from the melt 20 and propagates during step b) to the free surface of the melt bath 20. Water circulates around the crucible 10 to continuously cool the crucible 10 as well as the melt 20 and to ensure the solidification of the latter.
  • a cooling channel 13 is present within the side wall 12 and the bottom wall 14 of the crucible 10.
  • a coolant can circulate within the cooling channel 13 to also participate in the solidification of the melt 20 .
  • the ingot 30 is present, during step b), between the melt 20 and the bottom 11 of the crucible 10 as well as between the melt 20 and the side wall 12 of the crucible 10.
  • at least a portion of the peripheral surface 31 of the ingot 30 may not be in contact with the side wall 12 of the crucible 10 and be separated from the latter by a space 33.
  • a gas for example He , Ar, N 2
  • He , Ar, N 2 can be injected to improve cooling.
  • the resulting ingot 30 may have a cylindrical shape.
  • the figure 2 provides a simplified representation of certain details of the method according to the invention.
  • the electrode 1 comprises before fusion inclusions 40. These inclusions 40 may be non-metallic inclusions.
  • the end 1a of the electrode 1 is, during melting, melted by the energy of the electric arcs 3. Molten electrode drops are produced which will be collected by the crucible 10.
  • the crucible 10 is , as explained above, cooled with water.
  • the melt 20 has a diameter d equal to the internal diameter of the crucible 10.
  • the melt 20 may, as shown, have during all or part of step b) a hemispherical shape. Such a shape can for example be obtained when using a crucible 10 of cylindrical shape.
  • the melt 20 may take other forms, for example a semi-quasi-ovoid shape. Such a shape can for example be obtained when using a parallelepiped shaped crucible.
  • the distance e between the free surface of the melt 20 and the electrode 1 is advantageously kept constant during step b).
  • This distance e can be driven either in voltage (V) or in pulses 5.
  • the electrode 1 is during step b) moved along the longitudinal axis X of the crucible 10 in order to maintain the distance e constant.
  • the drops 5 fall and are collected by the crucible 10.
  • the drops 5 may include inclusions 40 which were initially present in the electrode 1. Once introduced into the melt 20, the inclusions 40 may be entrained towards the bottom 26 of the melt 20 (ie the point of the melt 20 closest to the bottom 11 of the crucible and in contact with the solidification front 34).
  • the melt 20 has an axial portion having a temperature greater than that of its peripheral portion. This leads to a natural convection, corresponding to the engaged forces of buoyancy, which starts from the bottom 26 of the melt 20, joins the free surface 25 of the melt 20 and goes to the edge 27 of the molten bath 20. This convection is shown schematically in FIG. the figure 2 by the arrows 28a and 28b.
  • the inclusions 40 either solid or liquids of lower density than that of the melt 20 will tend to rise to the surface 25 with some velocity by flotation mechanisms as explained above.
  • aggregates 41 formed of agglomerated inclusions 40. These aggregates 41 are driven towards the periphery of the ingot 30 where they will be fixed.
  • the solidification front 34 propagates from the bottom 11 of the crucible 10 to the free surface 25 of the molten bath.
  • the solidification front 34 propagates during step b) along the longitudinal axis X of the crucible 10 as shown by the arrow 35.
  • the solidification front 34 may retain its shape during all or part of the step b).
  • the average rate of rise of the solidification front 34 is controlled so as to be less than the rate of rise to the surface of all or part of the inclusions 40 as explained above.
  • the diameter of the electrode before fusion was 920mm.
  • the molten electrode drops are collected in a crucible with a diameter of 975 mm and form a molten bath in the copper crucible.
  • the melted bath is then solidified by heat exchange between the molten bath and water circulating at 3000 l / minute with a temperature thermostated at 38 ° C. at the inlet and a continuous injection of He at 20mbar.
  • the heat exchange achieved makes it possible to impose a mean solidification rate during step b) equal to 24 ⁇ m / s.
  • the diameter of the electrode before fusion was 550mm.
  • the molten electrode drops are collected in a crucible with a diameter of 600 mm and form a molten bath in the copper crucible.
  • the melted bath is then solidified by heat exchange between the molten bath and water circulating at 1500 l / min with a temperature thermostated at 38 ° C. at the inlet and without gas injection.
  • the heat exchange achieved makes it possible to impose a mean solidification rate during step b) equal to 49 ⁇ m / s.

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  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Organic Chemistry (AREA)
  • Metallurgy (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Physics & Mathematics (AREA)
  • Plasma & Fusion (AREA)
  • General Engineering & Computer Science (AREA)
  • Manufacture And Refinement Of Metals (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)
  • Investigating And Analyzing Materials By Characteristic Methods (AREA)
  • Treatment Of Steel In Its Molten State (AREA)

Claims (15)

  1. Verfahren zur Herstellung eines Barrens (30) aus niedriglegiertem Stahl, umfassend die folgenden Schritte:
    a) Schmelzen einer ganzen Elektrode (1) oder eines Teils davon durch ein Vakuumlichtbogenumschmelzverfahren, wobei die Elektrode (1) vor dem Schmelzen Eisen und Kohlenstoff enthält, wobei der geschmolzene Teil der Elektrode in einem Schmelztiegel (10) gesammelt wird, wodurch in dem Schmelztiegel (10) ein Schmelzbad (20) gebildet wird, und
    b) Erstarren des Schmelzbades (20) durch Wärmeaustausch zwischen dem Schmelzbad (20) und einem Kühlmittel, wobei der vollzogene Wärmeaustausch ermöglicht, während des Schrittes b) eine mittlere Erstarrungsgeschwindigkeit von weniger als oder gleich 45 µm/s aufzuerlegen und einen Barren (30) aus niedriglegiertem Stahl zu erhalten.
  2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, dass der Kohlenstoff in der Elektrode (1) vor deren Schmelzen in einem Massengehalt im Bereich zwischen 0,09 % und 1,00 % vorliegt.
  3. Verfahren nach einem der Ansprüche 1 und 2, dadurch gekennzeichnet, dass die Elektrode (1) vor dem Schmelzen ferner Chrom in einem Massengehalt im Bereich zwischen 0,10 % und 5,50 % aufweist.
  4. Verfahren nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, dass die Elektrode (1) vor dem Schmelzen ferner Molybdän in einem Massengehalt von weniger als oder gleich 5,00 % enthält.
  5. Verfahren nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, dass die Elektrode (1) vor dem Schmelzen Eisen sowie
    • Kohlenstoff in einem Massengehalt im Bereich zwischen 0,09 % und 1,00 %,
    • Mangan in einem Massengehalt von weniger als oder gleich 6,00 %,
    • Nickel in einem Massengehalt von weniger als oder gleich 5,50 %,
    • Silizium in einem Massengehalt von weniger als oder gleich 3,00 %,
    • Chrom in einem Massengehalt im Bereich zwischen 0,10 % und 5,50 %,
    • Molybdän in einem Massengehalt von weniger als oder gleich 5,00 %, und
    • Vanadium in einem Massengehalt von weniger als oder gleich 5,00 % enthält.
  6. Verfahren nach einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, dass der Durchmesser (d) des Schmelzbades (20) im Bereich zwischen 650 mm und 1200 mm liegt.
  7. Verfahren nach einem der Ansprüche 1 bis 6, dadurch gekennzeichnet, dass die Elektrode (1) vor dem Schmelzen eine zylindrische Form aufweist.
  8. Verfahren nach einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, dass die während des Schrittes b) auferlegte mittlere Erstarrungsgeschwindigkeit des Schmelzbades (20) weniger als oder gleich 40 µm/s beträgt.
  9. Verfahren nach einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, dass die während des Schrittes b) auferlegte mittlere Erstarrungsgeschwindigkeit mehr als oder gleich 9 µm/s beträgt.
  10. Teil (30) aus niedriglegiertem Stahl mit Eisen und Kohlenstoff, das durch Durchführen eines Verfahrens nach einem der Ansprüche1 bis 9 erhalten wird, wobei sich das Teil (30) entlang einer Längsachse erstreckt, wobei das Teil (30) derart ist, dass wenn es entsprechend dem Verfahren D der Norm ASTME 45-10 bewertet wird, die folgenden Ergebnisse hinsichtlich der Analyse entlang der Längsachse erhalten werden:
    • die Anzahl von Feldern mit Einschlüssen des Typs D mit einem Schweregrad gleich 0,5 beträgt weniger als 5.
    • es wird kein Feld mit Einschlüssen des Typs D mit einem Schweregrad von 1 erhalten, und
    • es wird kein Feld mit Einschlüssen des Typs B mit einem Schweregrad gleich 0,5 erhalten.
  11. Teil (30) nach Anspruch 10, dadurch gekennzeichnet, dass wenn es entsprechend dem Verfahren D der Norm ASTME 45-10 bewertet wird, durch Addieren der drei Messergebnisse, welche entlang der Längsachse des Teils und entlang der beiden zu dieser Längsachse senkrechten Achsen erzielt werden, das folgende Ergebnis erhalten wird:
    • die Gesamtanzahl von Feldern mit Einschlüssen des Typs D mit einem Schweregrad gleich 0,5 beträgt weniger als oder gleich 15.
  12. Teil (30) nach einem der Ansprüche 10 und 11, dadurch gekennzeichnet, dass der Kohlenstoff in einem Massengehalt im Bereich zwischen 0,09 % und 1,00 % vorliegt.
  13. Teil (30) nach einem der Ansprüche 10 bis 12, dadurch gekennzeichnet, dass es ferner Chrom in einem Massengehalt im Bereich zwischen 0,05 % und 5,00 % enthält.
  14. Teil (30) nach einem der Ansprüche 10 bis 13, dadurch gekennzeichnet, dass es ferner Molybdän in einem Massengehalt von weniger als oder gleich 5,00 % umfasst.
  15. Teil (30) nach einem der Ansprüche 10 bis 14, dadurch gekennzeichnet, dass es Eisen sowie:
    • Kohlenstoff in einem Massengehalt im Bereich zwischen 0,09 % und 1,00 %,
    • Mangan in einem Massengehalt von weniger als oder gleich 5,00 %,
    • Nickel in einem Massengehalt von weniger als oder gleich 5,00 %,
    • Silizium in einem Massengehalt von weniger als oder gleich 3,00 %,
    • Chrom in einem Massengehalt im Bereich zwischen 0,05 % und 5,00 %,
    • Molybdän in einem Massengehalt von weniger als oder gleich 5,00 % und
    • Vanadium in einem Massengehalt von weniger als oder gleich 5,00 % enthält.
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EP3536815A1 (de) 2019-09-11
US20170130297A1 (en) 2017-05-11
CN106574321B (zh) 2019-01-18
CA2951574C (fr) 2022-06-28
FR3021977B1 (fr) 2017-10-06
CA2951574A1 (fr) 2015-12-17
US20190309390A1 (en) 2019-10-10
US10364479B2 (en) 2019-07-30
RU2695682C2 (ru) 2019-07-25
FR3055340A1 (fr) 2018-03-02
RU2017100062A (ru) 2018-07-18
BR112016028856A2 (pt) 2017-08-22
JP2017524828A (ja) 2017-08-31
FR3021977A1 (fr) 2015-12-11
FR3055340B1 (fr) 2021-07-30
EP3155137A1 (de) 2017-04-19
CN106574321A (zh) 2017-04-19
US11560612B2 (en) 2023-01-24
RU2017100062A3 (de) 2019-05-30
WO2015189083A1 (fr) 2015-12-17

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