US20200009651A1 - Use of a Steel for an Additive Manufacturing Process, Method for Producing a Steel Component and Steel Component - Google Patents

Use of a Steel for an Additive Manufacturing Process, Method for Producing a Steel Component and Steel Component Download PDF

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US20200009651A1
US20200009651A1 US16/456,117 US201916456117A US2020009651A1 US 20200009651 A1 US20200009651 A1 US 20200009651A1 US 201916456117 A US201916456117 A US 201916456117A US 2020009651 A1 US2020009651 A1 US 2020009651A1
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steel
content
component
steel powder
powder
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Frank van Soest
Hans-Günter Krull
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Deutsche Edelstahlwerke Specialty Steel GmbH and Co KG
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Deutsche Edelstahlwerke Specialty Steel GmbH and Co KG
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    • B22F1/0011
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/001Ferrous alloys, e.g. steel alloys containing N
    • B22F1/0085
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/05Metallic powder characterised by the size or surface area of the particles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/14Treatment of metallic powder
    • B22F1/142Thermal or thermo-mechanical treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
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    • B22F10/00Additive manufacturing of workpieces or articles from metallic powder
    • B22F10/20Direct sintering or melting
    • B22F10/28Powder bed fusion, e.g. selective laser melting [SLM] or electron beam melting [EBM]
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
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    • B22F10/00Additive manufacturing of workpieces or articles from metallic powder
    • B22F10/60Treatment of workpieces or articles after build-up
    • B22F10/64Treatment of workpieces or articles after build-up by thermal means
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F10/00Additive manufacturing of workpieces or articles from metallic powder
    • B22F10/60Treatment of workpieces or articles after build-up
    • B22F10/66Treatment of workpieces or articles after build-up by mechanical means
    • B22F3/1055
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F8/00Manufacture of articles from scrap or waste metal particles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y70/00Materials specially adapted for additive manufacturing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y80/00Products made by additive manufacturing
    • 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
    • C21D6/004Heat treatment of ferrous alloys containing Cr and Ni
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    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C33/00Making ferrous alloys
    • C22C33/02Making ferrous alloys by powder metallurgy
    • C22C33/0257Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements
    • C22C33/0264Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements the maximum content of each alloying element not exceeding 5%
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/002Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
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    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
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    • 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
    • C22C38/42Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
    • 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
    • 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
    • C22C38/48Ferrous alloys, e.g. steel alloys containing chromium with nickel with niobium or tantalum
    • 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
    • C22C38/50Ferrous alloys, e.g. steel alloys containing chromium with nickel with titanium or zirconium
    • 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
    • C22C38/52Ferrous alloys, e.g. steel alloys containing chromium with nickel with cobalt
    • 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
    • C22C38/54Ferrous alloys, e.g. steel alloys containing chromium with nickel with boron
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F2009/001Making metallic powder or suspensions thereof from scrap particles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2301/00Metallic composition of the powder or its coating
    • B22F2301/05Light metals
    • B22F2301/052Aluminium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2301/00Metallic composition of the powder or its coating
    • B22F2301/05Light metals
    • B22F2301/058Magnesium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2301/00Metallic composition of the powder or its coating
    • B22F2301/10Copper
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2301/00Metallic composition of the powder or its coating
    • B22F2301/15Nickel or cobalt
    • B22F2301/155Rare Earth - Co or -Ni intermetallic alloys
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy
    • B22F2998/10Processes characterised by the sequence of their steps
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B33ADDITIVE MANUFACTURING TECHNOLOGY
    • B33YADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
    • B33Y10/00Processes of additive manufacturing
    • 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
    • C21D2211/001Austenite
    • 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
    • C21D2211/005Ferrite
    • 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
    • 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
    • C21D2211/009Pearlite
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/25Process efficiency

Definitions

  • the invention relates to the use of a steel as a steel powder for producing steel components by additive manufacturing processes, a method for producing a steel component using an additive manufacturing process and a steel component produced through the use of such a steel by using an additive manufacturing process.
  • additive manufacturing process here summarises all manufacturing processes in which a material is added to produce a component. This addition usually takes place in layers. “Additive manufacturing processes”, which are often referred to in the technical language as “generative processes” or generally as “3D printing”, thus stand in contrast to the classic subtractive manufacturing processes, such as the machining processes (for example, milling, drilling, and turning), in which material is removed in order to give shape to the component to be produced. Likewise, additive processes generally differ from conventional solid forming processes, such as forging and the like, in which the respective steel part is formed while retaining the mass of a starting or intermediate product.
  • the components produced by such additive processes are regularly subjected to an after-treatment in order to minimise the residual porosity which is usually still present in the production process.
  • the options available for this purpose are adequately described in the prior art and summarised, for example, in DE 100 39 143 C1.
  • the subject matter of this patent specification is a method for producing precision components by laser sintering of a powder material which comprises a mixture of at least two powder elements.
  • the powder material is formed by the main component, this being iron powder, and other powder alloying elements which are in elemental, pre-alloyed or partially pre-alloyed form.
  • the laser sintering process is controlled in such a way that a powder alloy is formed from the constituents of the powder in the course of the laser sintering process.
  • the powder alloy elements are carbon, silicon, copper, tin, nickel, molybdenum, manganese, chromium, cobalt, tungsten, vanadium, titanium, phosphorus, boron.
  • the content ranges indicated for these components are: C: 0.01-2 wt %, Si: up to 1 wt %, Cu: up to 10 wt %, Sn up to 2 wt %, Ni: up to 10 wt %, Mo: up to 6 wt. %, Mn: up to 2 wt. % or 10-13 wt. %, Cr: up to 5 wt. % or 12-18 wt.
  • Co up to 2 wt %
  • W up to 5 wt %
  • V up to 1 wt %
  • Ti up to 0.5 wt %
  • P up to 1 wt %
  • B up to 1 wt %.
  • a component is also to be specified which consists of steel and can be produced cost-effectively using an additive process.
  • the invention is based on the recognition that a modification of a steel, which is generally already known from EP 3 168 312 A1 for the production of components using forging technology, is also especially suitable as a material for the production of steel components by using an additive manufacturing process.
  • the soft martensitic steels commonly used today for additive manufacturing require high proportions of expensive alloy elements such as Co, Ni and Mo and a subsequent heat treatment to set the degree of hardness.
  • the solutions known from practical experience which are based on steel with an austenitic structure are severely limited in terms of the maximum strength that can be achieved.
  • the invention proposes, in contrast, a material composition for use as a powder for the production of a steel component by additive manufacturing, in which, by a plurality of repetitions of the steps “applying a layer of steel powder to a previously produced steel layer”, “melting the applied steel powder layer”, “cooling the steel layer produced by melting”, the steel component is successively built from a corresponding number of steel layers.
  • This material composition opens a large window for the cooling rate to set a bainitic structure which is less solid than martensite.
  • FIG. 1 shows the TTT diagram of the steel S1 used as steel powder for additive manufacturing.
  • FIG. 2 shows the TTT diagram of the steel S2 used as steel powder for additive manufacturing.
  • a steel in the form of steel powder having a mean grain diameter of 5-150 ⁇ m is used for the production of steel components in an additive process, the steel comprising (in wt %): 0.08-0.35% C, up to 0.80% Si, 0.20-2.00% Mn, up to 4.00% Cr, 0.3-3.0% Mo, 0.004-0.020% N, 0.004-0.050% Al, up to 0.0025% B, at least one element from the group “Nb, Ti, V, S”, with the proviso that the Nb content is 0.003-0.20 wt %, the Ti content is 0.001-0.02 wt %, the V content is 0.02-0.40 wt % and/or the S content is 0.001-0.4 wt %, up to 1.5% Ni, up to 0.3% Cu, up to 2.0% Co, and the remainder being iron and unavoidable impurities, the Al content % Al, the Nb content % Nb, the Ti content % Ti, the V content
  • the unavoidable impurities due to production include all elements which are present in quantities which are ineffective in terms of alloying in respect of the properties of interest here and which enter the steel because of the selected route for producing the steel powder or the selected starting material (scrap).
  • the unavoidable impurities also include P contents of up to 0.0035 wt %.
  • the steel alloy used according to the invention as a powder for additive manufacturing is composed in such a way that there are yield strength-enhancing precipitates of carbides, such as special carbides, carbonitrides or nitrides, as a result of the intrinsic heat treatment required by the additive manufacturing due to heat conduction, said heat treatment resulting from the melting in layers of successively applied and melted powder layers.
  • carbides such as special carbides, carbonitrides or nitrides
  • the steel to be used according to the invention forms a homogeneous bainitic structure which, despite the omission of a separate heat treatment, ensures uniform properties over the volume of the additive-manufactured component.
  • the homogeneous structural state made possible by the steel alloy to be used according to the invention ensures low residual stresses and thus a low risk of cracking.
  • the steel alloy selected according to the invention for use as steel powder for an additive manufacturing process is also particularly suitable insofar as it minimises the critical cooling rate for the formation of the bainitic structure.
  • the “bainitic nose B” obtained in the time-temperature diagram (see FIGS. 1 and 2 ) for the steel to be used according to the invention is shifted towards short cooling times, as are typical for additive manufacturing.
  • alloying the steel to be used according to the invention ensures that, in the course of cooling, no amounts of martensite or ferrite or perlite influencing its properties are formed in the structure.
  • a steel component produced from steel to be used according to the invention is therefore characterised in that it contains at least 80 vol % bainite, wherein the content of non-bainitic structural constituents in steel components produced according to the invention typically is minimised to such an extent that after completion of the additive manufacturing a completely bainitic structure, in the technical sense, is present in the steel component.
  • the steel used according to the invention as steel powder for additive manufacturing may contain up to 0.35 wt % carbon (“C”) to contribute to increasing the strength of the material by carbide formation.
  • C carbon
  • the steel used according to the invention may contain up to 0.35 wt % carbon (“C”) to contribute to increasing the strength of the material by carbide formation.
  • C carbon
  • a respective increase in strength of approximately 70 MPa can be effected.
  • This effect succeeds from a C content of 0.08 wt %, in particular from a content of at least 0.09 wt % C.
  • Limiting the C content to at most 0.35 wt % ensures that a steel to be used according to the invention has good elongation and toughness properties despite its maximised strength.
  • the comparatively low C content in a steel to be used according to the invention also contributes to the acceleration of the bainite transformation, so that the formation of undesired structural constituents is avoided.
  • An optimised effect of the presence of C in the steel to be used according to the invention can be achieved by setting the C content to 0.08-0.25 wt %, in particular 0.09-0.25 wt %.
  • Si Silicon
  • the Si content of a steel to be used according to the invention is therefore limited to at most 0.80 wt %, in particular to at most 0.45 wt %, in order to allow the bainite transformation to take place as early as possible.
  • Si contents up to this upper limit increase the strength due to solid solution strengthening.
  • Molybdenum (“Mo”) is present in the steel to be used according to the invention at contents of 0.3-3.0 wt % to delay the transformation of the structure into ferrite or perlite. This effect occurs in particular when at least 0.6 wt %, in particular more than 0.70 wt % Mo, are present in the steel. At contents of more than 3.0 wt %, in the steel to be used according to the invention there is no economically justifiable further increase in the positive effect of Mo. In addition, above 3.0 wt % Mo, there is a risk of forming a molybdenum-rich carbide phase which may adversely affect the toughness properties.
  • Mo content is at least 0.7 wt %.
  • Manganese (“Mn”) is present at contents of 0.20-2.00 wt % in the steel to be used according to the invention to adjust the tensile strength and yield strength by mixed crystal formation.
  • a minimum content of 0.20 wt % of Mn is required in order to increase the strength. If this effect is to be achieved particularly reliably, then a Mn content of at least 0.35 wt % can be provided. Excessively high Mn contents, however, would delay the bainite transformation and thus lead to a predominantly martensitic transformation. Therefore, the Mn content is limited to at most 2.00 wt %, in particular at most 1.5 wt %. Negative influences of the presence of Mn can be avoided particularly reliably by limiting the Mn content in the steel to be used according to the invention to a maximum of 1.1 wt %.
  • the content of sulphur (“S”) in the steel to be used according to the invention can be up to 0.4 wt %, in particular at most 0.1 wt %, in order to promote the machinability of the steel.
  • S sulphur
  • an S-content of at least 0.001 wt % may be provided.
  • Optimum effects of the presence of S in the steel to be used according to the invention can be achieved at contents of 0.003-0.1 wt %.
  • the fine adjustment of alloying techniques with regard to the mechanical properties and the structure quality of a steel to be used according to the invention is carried out in accordance with the alloying concept to be used according to the invention through a combined microalloying of the elements boron (“B”) in optional contents of up to 0.0025 wt %, in particular at least 0.0005 wt % B, nitrogen (“N”) in contents of 0.004-0.020 wt %, in particular at least 0.006 wt % N or up to 0.0150 wt % N, aluminium (“Al”) in contents of 0.004-0.050 wt % and niobium (“Nb”) in optional contents of up to 0.20 wt %, in particular at least 0.003 wt % or at least 0.005 wt % Nb, wherein the Nb content may in particular also be limited to at most 0.05 wt % Nb, titanium (“Ti”) in optional contents of up to 0.02 wt %, in particular at
  • N in the contents provided according to the invention allows formation of nitrides and carbonitrides to increase the strength and raise the fine grain resistance, without causing embrittlement.
  • Al forms aluminium nitride with N, which contributes to fine grain stability.
  • B delays the formation of ferrite or perlite and thus ensures the formation of the desired bainitic structure in the steel to be used according to the invention.
  • B contents above 0.0025 wt % would entail the risk of embrittlement.
  • the respective micro-alloying elements Nb, Ti and V, which are also optionally present, form carbonitrides and can thus make a significant contribution to optimising the fine grain stability and strength of the steel to be used according to the invention.
  • the micro-alloying elements V, Ti, Nb on the one hand and Al on the other hand may be present respectively in combination with one or more elements from the group “Al, V, Ti, Nb” or alone in amounts above said minimum contents.
  • the nitrogen contained in the steel to be used according to the invention is bound completely via the respectively present contents of Al as well as any additionally added contents of Nb, Ti and V, and boron can thus delay transformation.
  • the binding of N according to the invention makes it possible for the optionally present boron to act as a dissolved element in the matrix of the steel and to suppress the formation of ferrite and/or perlite.
  • Cr chromium
  • at least 0.5 wt % or at least 0.8 wt % of Cr may be provided for this purpose.
  • Cr contents above 4.00 wt % would promote undesirable martensite formation in the structure of the steel to be used according to the invention.
  • Ni contents of up to 1.5 wt % which are also optionally present improve the toughness of the steel to be used according to the invention. If this effect is to be utilised, it occurs from a Ni content of at least 0.1 wt %, in particular at least 0.15 wt %.
  • the alloying elements occurring or deliberately added via the starting material into the steel to be used according to the invention include Cu, whose content is limited to max. 0.3 wt %, in particular less than 0.3 wt %, to avoid negative influences in the steel to be used according to the invention.
  • cobalt optionally present in the steel to be used according to the invention causes a shift in bainite formation to shorter times.
  • the positive influence of Co can be utilised in particular at Co contents of at least 0.1 wt %, in particular at least 0.5 wt %.
  • a method according to the invention for producing a steel component comprises the following steps:
  • the manufacture of the steel powder consisting of steel to be used according to the invention can be carried out in a conventional manner, for example by gas atomisation or by any other suitable method.
  • a steel melt melted according to the invention can be atomised into the steel powder, for example by gas or water atomisation or a combination of these two atomisation methods.
  • the powder particles obtained in this manner can be sieved in order to select those having a suitable grain size for further processing according to the invention.
  • grains having an average diameter of 5-150 ⁇ m have proven to be suitable for the purposes of the invention.
  • a component produced according to the invention is characterised in that it has a structure comprising at least 80 vol % bainite, in particular a completely bainitic structure in the technical sense.
  • the steel powder to be used according to the invention is suitable for any additive manufacturing process of the type known from the prior art and explained at the outset, in which the adjoining particles collected by the heat supplied are fused by local heat input, and thus the steel powder portion treated in this way is solidified during the subsequent cooling in the respective section to be formed of the component to be produced.
  • the known laser melting and laser sintering processes which permit a precisely limited, intensive heating of the steel powder particles and a correspondingly accurate formation of the component to be produced, are suitable for the production of a component according to the invention.
  • the strength and ductility of a steel component produced according to the invention can be set via a conventional heat treatment.
  • This heat treatment may comprise a fine adjustment of the bainitic structure of the steel component produced according to the invention, in which the steel component is heated to an austenitising temperature above the Ac3 temperature and then cooled from the austenitising temperature in air or in oil, the cooling being carried out at a cooling rate of at least 0.5 K/s and less than 300 K/s, in particular 3.0-300 K/s, which is sufficient for setting the bainitic structure, which should be as complete as possible.
  • the steel to be used according to the invention has a B content of 0.0005-0.0025 wt %. The presence of such B contents is particularly effective here in preventing the formation of undesirable ferrite or perlite in the structure of the steel component in the course of the cooling.
  • a tempering treatment may be carried out, in which the steel component is held at a temperature of 450-600° C. over a period of 0.5-6 hours, wherein the specifically provided duration of the tempering treatment can be chosen depending on the size and volume of the steel component, in order to again support, in a targeted manner, the previously mentioned strength increase due to special carbide formation, said strength increase already being obtained in the course of the additive manufacturing.
  • Steel components produced according to the invention after completion of the additive manufacturing (step d), i.e. before step e), already have a tensile strength of at least 900 MPa, in particular at least 1145 MPa, a yield strength of at least 560 MPa, in particular at least 675 MPa, and an elongation at break A5.65 of at least 8%.
  • the mechanical properties of a steel component according to the invention can be improved to such an extent that its tensile strength is at least 1050 MPa, in particular at least 1230 MPa, its yield strength is at least 615 MPa, in particular at least 750 MPa, and its elongation at break A5.65 is at least 8%.
  • melts S1, S2, S3 according to the invention were melted and respectively atomised in a conventional manner in the gas flow into steel powder having a grain size of 5-150 ⁇ m.
  • the composition of melts S1-S3 is given in Table 1.
  • steel components were produced using “Selective Laser Melting” (“3D printing/SLM method”), which were test bodies for determining the optimal parameters for additive manufacturing, namely cubes with approx. 20 mm edge length, and blanks for tensile and impact tests.
  • 3D printing/SLM method Selective Laser Melting
  • the tensile strength Rm_V of the steel components obtained after the additive manufacturing is shown in Table 2.
  • the steel components thus obtained were subjected to a machining operation in order to optimally adapt them to their respectively required final shape.
  • the components each underwent a heat treatment in which they were aged for a period tA at a temperature TA.
  • the respective ageing time tA and ageing temperature TA are also listed in Table 2.
  • Table 2 indicates the tensile strength Rm_N which the components exhibited after mechanical processing and ageing.
  • Table 2 indicates the structure of the components.

Abstract

The production of steel components in an additive process using a steel powder having a mean grain diameter of 5-150 μm, and comprising (in wt % ) 0.08-0.35% C, up to 0.80% Si, 0.20-2.00% Mn, up to 4.00% Cr, 0.3-3.0% Mo, 0.004-0.020% N, 0.004-0.050% Al, up to 0.0025% B, up to 0.20% Nb, up to 0.02% Ti, up 0.40% V, up to 1.5% Ni, up to 0.3% Cu, up to 2.0% Co, at least one of Nb, Ti, V, and S, wherein Nb is 0.003-0.20%, Ti is 0.001-0.02%, V is 0.02-0.40% and/or S is 0.001-0.4%, and the remainder being iron and unavoidable impurities, where % Al/27+% Nb/45+% Ti/48+% V/25>% N/3.5. The steel component has a structure including at least 80 vol % of bainite, with the remainder being retained austenite, ferrite, perlite and/or martensite. and after shaping and before an optional heat treatment, has a tensile strength of ≥900 MPa, a yield strength of ≥560 MPa and an elongation at break A5.65 of ≥8%.

Description

    CROSS-REFERENCE TO RELATED APPLICATION
  • This application claims priority to European Patent Application No. 18182027.5 filed Jul. 5, 2018, the disclosure of which is hereby incorporated by reference in its entirety.
  • BACKGROUND OF THE INVENTION Field of the Invention
  • The invention relates to the use of a steel as a steel powder for producing steel components by additive manufacturing processes, a method for producing a steel component using an additive manufacturing process and a steel component produced through the use of such a steel by using an additive manufacturing process.
  • Description of Related Art
  • If “%” information is given below on alloys or steel compositions, these are respectively based on the weight, unless expressly stated otherwise.
  • All of the mechanical properties mentioned in the present text of the steel to be used according to the invention and of the steels which may be mentioned for comparison have been determined according to DIN EN ISO 6892-1, unless stated otherwise.
  • The term “additive manufacturing process” here summarises all manufacturing processes in which a material is added to produce a component. This addition usually takes place in layers. “Additive manufacturing processes”, which are often referred to in the technical language as “generative processes” or generally as “3D printing”, thus stand in contrast to the classic subtractive manufacturing processes, such as the machining processes (for example, milling, drilling, and turning), in which material is removed in order to give shape to the component to be produced. Likewise, additive processes generally differ from conventional solid forming processes, such as forging and the like, in which the respective steel part is formed while retaining the mass of a starting or intermediate product.
  • The additive manufacturing principle makes it possible to produce geometrically complex structures that cannot be realised or can only be realised with great difficulty using conventional manufacturing processes, such as the aforementioned machining processes or primary moulding processes (casting, forging) (see VDI Status Report “Additive Fertigungsverfahren”, September 2014, published by Verein Deutscher Ingenieure e.V., Fachbereich Produktionstechnik and Fertigungsverfahren (Association of German Engineers, Department of Production Technology and Manufacturing Processes), www.vdi.de/statusadditiv).
  • Further definitions of the methods summarised under the generic term “additive methods” can be found, for example, in VDI Guidelines 3404 and 3405.
  • In practice, powdered steel alloys, which have sufficient weldability due to their carbon contents being below 0.30 wt %, are regularly used today. The steel powder produced is then melted with an electron beam or laser beam in a vacuum and, due to the small liquid quantity compared to the already produced component, rapidly cooled. Due to the high cooling rate, a critical stress state often occurs in the component, which can lead to cracks, especially in the case of elevated carbon contents.
  • In order to minimise the risk of stress cracks, it is common today to use a steel which forms a structural state which is as soft as possible in the case of rapid cooling. Steels which form a structure consisting of soft martensite or lancet martensite are suitable here. Examples of such steels are the “maraging steels”. Typical examples of these steels are standardised under the material numbers 1.2709, 1.6355, 1.4545 and 1.4542 in the StahlEisen-Liste. Alternatively, austenitic steels such as steel 316L (material number 1.4404) are also used as steel powder for additive manufacturing. A disadvantage of these steels is that they require high contents of alloying constituents, which are only available at high costs today.
  • The components produced by such additive processes are regularly subjected to an after-treatment in order to minimise the residual porosity which is usually still present in the production process. The options available for this purpose are adequately described in the prior art and summarised, for example, in DE 100 39 143 C1. The subject matter of this patent specification is a method for producing precision components by laser sintering of a powder material which comprises a mixture of at least two powder elements. The powder material is formed by the main component, this being iron powder, and other powder alloying elements which are in elemental, pre-alloyed or partially pre-alloyed form. At the same time, the laser sintering process is controlled in such a way that a powder alloy is formed from the constituents of the powder in the course of the laser sintering process. The powder alloy elements are carbon, silicon, copper, tin, nickel, molybdenum, manganese, chromium, cobalt, tungsten, vanadium, titanium, phosphorus, boron. Specifically, the content ranges indicated for these components are: C: 0.01-2 wt %, Si: up to 1 wt %, Cu: up to 10 wt %, Sn up to 2 wt %, Ni: up to 10 wt %, Mo: up to 6 wt. %, Mn: up to 2 wt. % or 10-13 wt. %, Cr: up to 5 wt. % or 12-18 wt. %, Co: up to 2 wt %, W: up to 5 wt %, V: up to 1 wt %, Ti: up to 0.5 wt %, P: up to 1 wt %, B: up to 1 wt %.
  • SUMMARY OF THE INVENTION
  • Against this background, the problem has arisen of identifying a steel which is particularly suitable for use as a steel powder in producing components by means of an additive manufacturing process and which can be alloyed cost-effectively.
  • Furthermore, a method based on such a steel powder is to be identified which allows components to be produced reliably using an additive manufacturing process.
  • Finally, a component is also to be specified which consists of steel and can be produced cost-effectively using an additive process.
  • The invention is based on the recognition that a modification of a steel, which is generally already known from EP 3 168 312 A1 for the production of components using forging technology, is also especially suitable as a material for the production of steel components by using an additive manufacturing process. The soft martensitic steels commonly used today for additive manufacturing require high proportions of expensive alloy elements such as Co, Ni and Mo and a subsequent heat treatment to set the degree of hardness. The solutions known from practical experience which are based on steel with an austenitic structure are severely limited in terms of the maximum strength that can be achieved.
  • The invention proposes, in contrast, a material composition for use as a powder for the production of a steel component by additive manufacturing, in which, by a plurality of repetitions of the steps “applying a layer of steel powder to a previously produced steel layer”, “melting the applied steel powder layer”, “cooling the steel layer produced by melting”, the steel component is successively built from a corresponding number of steel layers. This material composition opens a large window for the cooling rate to set a bainitic structure which is less solid than martensite.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 shows the TTT diagram of the steel S1 used as steel powder for additive manufacturing.
  • FIG. 2 shows the TTT diagram of the steel S2 used as steel powder for additive manufacturing.
  • DESCRIPTION OF THE INVENTION
  • According to the invention, a steel in the form of steel powder having a mean grain diameter of 5-150 μm is used for the production of steel components in an additive process, the steel comprising (in wt %): 0.08-0.35% C, up to 0.80% Si, 0.20-2.00% Mn, up to 4.00% Cr, 0.3-3.0% Mo, 0.004-0.020% N, 0.004-0.050% Al, up to 0.0025% B, at least one element from the group “Nb, Ti, V, S”, with the proviso that the Nb content is 0.003-0.20 wt %, the Ti content is 0.001-0.02 wt %, the V content is 0.02-0.40 wt % and/or the S content is 0.001-0.4 wt %, up to 1.5% Ni, up to 0.3% Cu, up to 2.0% Co, and the remainder being iron and unavoidable impurities, the Al content % Al, the Nb content % Nb, the Ti content % Ti, the V content % V and the N content % N of the steel satisfying the following condition: % Al/27+% Nb/45+% Ti/48+% V/25>% N/3.5. In this case, the unavoidable impurities due to production include all elements which are present in quantities which are ineffective in terms of alloying in respect of the properties of interest here and which enter the steel because of the selected route for producing the steel powder or the selected starting material (scrap). In particular, the unavoidable impurities also include P contents of up to 0.0035 wt %.
  • The steel alloy used according to the invention as a powder for additive manufacturing is composed in such a way that there are yield strength-enhancing precipitates of carbides, such as special carbides, carbonitrides or nitrides, as a result of the intrinsic heat treatment required by the additive manufacturing due to heat conduction, said heat treatment resulting from the melting in layers of successively applied and melted powder layers. Thus, in the case of the steel alloy provided according to the invention for use as steel powder for an additive manufacturing process, taking advantage of the process-inherent heat input, an increase in strength occurs through precipitation formation, without the need for a separate heat treatment. In this case, the steel to be used according to the invention forms a homogeneous bainitic structure which, despite the omission of a separate heat treatment, ensures uniform properties over the volume of the additive-manufactured component. The homogeneous structural state made possible by the steel alloy to be used according to the invention ensures low residual stresses and thus a low risk of cracking.
  • Here, the steel alloy selected according to the invention for use as steel powder for an additive manufacturing process is also particularly suitable insofar as it minimises the critical cooling rate for the formation of the bainitic structure. This means that the “bainitic nose B” obtained in the time-temperature diagram (see FIGS. 1 and 2) for the steel to be used according to the invention is shifted towards short cooling times, as are typical for additive manufacturing.
  • As can be understood by way of example with reference to FIGS. 1 and 2, this means that, in the case of a steel to be used according to the invention, a bainitic structure is formed in a particularly wide time window, when the steel is cooled from the heat which is introduced into the layered component during the melting of the processed powder layer. In this case, alloying the steel to be used according to the invention ensures that, in the course of cooling, no amounts of martensite or ferrite or perlite influencing its properties are formed in the structure. A steel component produced from steel to be used according to the invention is therefore characterised in that it contains at least 80 vol % bainite, wherein the content of non-bainitic structural constituents in steel components produced according to the invention typically is minimised to such an extent that after completion of the additive manufacturing a completely bainitic structure, in the technical sense, is present in the steel component.
  • The steel used according to the invention as steel powder for additive manufacturing may contain up to 0.35 wt % carbon (“C”) to contribute to increasing the strength of the material by carbide formation. Thus, by adding respectively 0.01 wt %, a respective increase in strength of approximately 70 MPa can be effected. This effect succeeds from a C content of 0.08 wt %, in particular from a content of at least 0.09 wt % C. Limiting the C content to at most 0.35 wt % ensures that a steel to be used according to the invention has good elongation and toughness properties despite its maximised strength. At the same time, the comparatively low C content in a steel to be used according to the invention also contributes to the acceleration of the bainite transformation, so that the formation of undesired structural constituents is avoided. An optimised effect of the presence of C in the steel to be used according to the invention can be achieved by setting the C content to 0.08-0.25 wt %, in particular 0.09-0.25 wt %.
  • Silicon (“Si”) suppresses cementite formation and shifts ferrite formation to shorter times. The Si content of a steel to be used according to the invention is therefore limited to at most 0.80 wt %, in particular to at most 0.45 wt %, in order to allow the bainite transformation to take place as early as possible. At the same time, Si contents up to this upper limit increase the strength due to solid solution strengthening.
  • Molybdenum (“Mo”) is present in the steel to be used according to the invention at contents of 0.3-3.0 wt % to delay the transformation of the structure into ferrite or perlite. This effect occurs in particular when at least 0.6 wt %, in particular more than 0.70 wt % Mo, are present in the steel. At contents of more than 3.0 wt %, in the steel to be used according to the invention there is no economically justifiable further increase in the positive effect of Mo. In addition, above 3.0 wt % Mo, there is a risk of forming a molybdenum-rich carbide phase which may adversely affect the toughness properties. Optimum effects of Mo in the steel to be used according to the invention can be expected when the Mo content is at least 0.7 wt %. Mo contents of at most 2.0 wt %, in particular at most 1.5 wt % or at most 1.0 wt %, have proved to be particularly effective.
  • Manganese (“Mn”) is present at contents of 0.20-2.00 wt % in the steel to be used according to the invention to adjust the tensile strength and yield strength by mixed crystal formation. A minimum content of 0.20 wt % of Mn is required in order to increase the strength. If this effect is to be achieved particularly reliably, then a Mn content of at least 0.35 wt % can be provided. Excessively high Mn contents, however, would delay the bainite transformation and thus lead to a predominantly martensitic transformation. Therefore, the Mn content is limited to at most 2.00 wt %, in particular at most 1.5 wt %. Negative influences of the presence of Mn can be avoided particularly reliably by limiting the Mn content in the steel to be used according to the invention to a maximum of 1.1 wt %.
  • The content of sulphur (“S”) in the steel to be used according to the invention can be up to 0.4 wt %, in particular at most 0.1 wt %, in order to promote the machinability of the steel. At the same time, the presence of S reduces the interfacial tension of the droplets during atomisation, whereby a finer steel powder is obtained. For this purpose, an S-content of at least 0.001 wt % may be provided. At S-contents above 0.4 wt % there is a risk of red-shortness occurring. Optimum effects of the presence of S in the steel to be used according to the invention can be achieved at contents of 0.003-0.1 wt %.
  • The fine adjustment of alloying techniques with regard to the mechanical properties and the structure quality of a steel to be used according to the invention is carried out in accordance with the alloying concept to be used according to the invention through a combined microalloying of the elements boron (“B”) in optional contents of up to 0.0025 wt %, in particular at least 0.0005 wt % B, nitrogen (“N”) in contents of 0.004-0.020 wt %, in particular at least 0.006 wt % N or up to 0.0150 wt % N, aluminium (“Al”) in contents of 0.004-0.050 wt % and niobium (“Nb”) in optional contents of up to 0.20 wt %, in particular at least 0.003 wt % or at least 0.005 wt % Nb, wherein the Nb content may in particular also be limited to at most 0.05 wt % Nb, titanium (“Ti”) in optional contents of up to 0.02 wt %, in particular at least 0.001 wt % or at least 0.005 wt % Ti, and vanadium (“V”) in optional contents of up to 0.40 wt %, in particular at least 0.01 wt % or at least 0.02 wt % V.
  • The presence of N in the contents provided according to the invention allows formation of nitrides and carbonitrides to increase the strength and raise the fine grain resistance, without causing embrittlement. Al forms aluminium nitride with N, which contributes to fine grain stability.
  • The optional presence of B delays the formation of ferrite or perlite and thus ensures the formation of the desired bainitic structure in the steel to be used according to the invention. B contents above 0.0025 wt % would entail the risk of embrittlement. The respective micro-alloying elements Nb, Ti and V, which are also optionally present, form carbonitrides and can thus make a significant contribution to optimising the fine grain stability and strength of the steel to be used according to the invention.
  • In order to safely use the advantages of the presence of the micro-alloying elements and of aluminium, it may be expedient to adjust the Al content to at least 0.005 wt %, the Ti content to at least 0.001 wt %, the V content to at least 0.02 wt % or the Nb content to at least 0.003 wt %. In this case, the micro-alloying elements V, Ti, Nb on the one hand and Al on the other hand may be present respectively in combination with one or more elements from the group “Al, V, Ti, Nb” or alone in amounts above said minimum contents. At contents of up to 0.01 wt % Ti, up to 0.025 wt % Nb, up to 0.075 wt % V or up to 0.040 wt % Al, the effects of these elements can be utilised particularly effectively in a steel to be used according to the invention. Again, the stated upper limits of the contents of Ti, Nb, V or Al can be maintained alone or in combination with each other in order to achieve the optimal effect of the respective alloying element. The contents % Al, % Nb, % Ti, % V and % N of Al, Nb, Ti, V and N are combined together in the steel to be used according to the invention under the condition

  • %Al/27+%Nb/45+%Ti/48+%V/25>%N/3.5
  • such that the nitrogen contained in the steel to be used according to the invention is bound completely via the respectively present contents of Al as well as any additionally added contents of Nb, Ti and V, and boron can thus delay transformation. In addition, the binding of N according to the invention makes it possible for the optionally present boron to act as a dissolved element in the matrix of the steel and to suppress the formation of ferrite and/or perlite.
  • Optional contents of chromium (“Cr”) of up to 4.00 wt %, in particular up to 3 wt % or up to 2.5 wt %, contribute to the hardenability and corrosion resistance of the steel used according to the invention due to the formation of special carbides and chromium nitrides in an optional nitriding treatment. For example, at least 0.5 wt % or at least 0.8 wt % of Cr may be provided for this purpose. Cr contents above 4.00 wt % would promote undesirable martensite formation in the structure of the steel to be used according to the invention.
  • Contents of Ni of up to 1.5 wt % which are also optionally present improve the toughness of the steel to be used according to the invention. If this effect is to be utilised, it occurs from a Ni content of at least 0.1 wt %, in particular at least 0.15 wt %.
  • The alloying elements occurring or deliberately added via the starting material into the steel to be used according to the invention include Cu, whose content is limited to max. 0.3 wt %, in particular less than 0.3 wt %, to avoid negative influences in the steel to be used according to the invention.
  • At contents of up to 2.0 wt %, cobalt (“Co”) optionally present in the steel to be used according to the invention causes a shift in bainite formation to shorter times. The positive influence of Co can be utilised in particular at Co contents of at least 0.1 wt %, in particular at least 0.5 wt %.
  • In accordance with the above explanations, a method according to the invention for producing a steel component comprises the following steps:
      • a) melting of a steel melt comprising (in wt %): C: 0-0.35%, Si: 0-0.45%, Mn: 0.20-2.00%, Cr: 0-4.00%, Mo: 0.3-3.0%, N: 0.004-0.020%, S: 0-0.40%, Al: 0.004-0.050%, B: 0-0.0025%, Nb: 0-0.20%, Ti: 0-0.02%, V: 0-0.30%, Ni: 0-1.5%, Cu: 0-0.3%, Co: 0-2.0%, remainder iron and unavoidable impurities, and with the Al content % Al, the Nb content % Nb, the Ti content % Ti, the V content % V and the N content % N of the steel meeting the following condition:

  • %Al/27+%Nb/45+%Ti/48+%V/25>%N/3.5
      • b) producing a steel powder from the steel melt melted in step a), wherein the grains of the steel powder have an average diameter of 5-150 μm;
      • c) producing the component by using an additive manufacturing process,
        • c.1) in which at least one portion of the steel powder by volume is exposed to a temporary heat input with subsequent cooling, so that the steel powder particles, which are present in the heated volume portion and respectively adjoin each other, enter into a firmly-bonded connection and are solidified after cooling to form at least one volume portion of the component to be produced;
        • c.2) if necessary, re-applying a further portion of the steel powder to the volume portion solidified in step c.1) and repeating step c.1) with the further portion of the steel powder, wherein steps c.1) and c.2) are repeated until the component to be produced is completely finished;
      • d) optional mechanical, in particular chip-removing, machining to shape the components;
      • e) optional final heat treatment of the resulting component to form strength increasing precipitates in the structure of the component.
  • The manufacture of the steel powder consisting of steel to be used according to the invention can be carried out in a conventional manner, for example by gas atomisation or by any other suitable method. For this purpose, a steel melt melted according to the invention can be atomised into the steel powder, for example by gas or water atomisation or a combination of these two atomisation methods. If necessary, the powder particles obtained in this manner can be sieved in order to select those having a suitable grain size for further processing according to the invention. Here, grains having an average diameter of 5-150 μm have proven to be suitable for the purposes of the invention.
  • As explained, by setting the alloying of the steel used according to the invention as a steel powder, the structure of the steel component produced according to the invention can be determined. Here, a component produced according to the invention is characterised in that it has a structure comprising at least 80 vol % bainite, in particular a completely bainitic structure in the technical sense.
  • The steel powder to be used according to the invention is suitable for any additive manufacturing process of the type known from the prior art and explained at the outset, in which the adjoining particles collected by the heat supplied are fused by local heat input, and thus the steel powder portion treated in this way is solidified during the subsequent cooling in the respective section to be formed of the component to be produced. In particular, the known laser melting and laser sintering processes which permit a precisely limited, intensive heating of the steel powder particles and a correspondingly accurate formation of the component to be produced, are suitable for the production of a component according to the invention.
  • Optionally, the strength and ductility of a steel component produced according to the invention can be set via a conventional heat treatment. This heat treatment may comprise a fine adjustment of the bainitic structure of the steel component produced according to the invention, in which the steel component is heated to an austenitising temperature above the Ac3 temperature and then cooled from the austenitising temperature in air or in oil, the cooling being carried out at a cooling rate of at least 0.5 K/s and less than 300 K/s, in particular 3.0-300 K/s, which is sufficient for setting the bainitic structure, which should be as complete as possible. In this heat treatment, it proves to be particularly advantageous if the steel to be used according to the invention has a B content of 0.0005-0.0025 wt %. The presence of such B contents is particularly effective here in preventing the formation of undesirable ferrite or perlite in the structure of the steel component in the course of the cooling.
  • Optionally, as an alternative or in addition to the fine adjustment of the structure, which is also optionally carried out as explained above, a tempering treatment may be carried out, in which the steel component is held at a temperature of 450-600° C. over a period of 0.5-6 hours, wherein the specifically provided duration of the tempering treatment can be chosen depending on the size and volume of the steel component, in order to again support, in a targeted manner, the previously mentioned strength increase due to special carbide formation, said strength increase already being obtained in the course of the additive manufacturing.
  • Steel components produced according to the invention, after completion of the additive manufacturing (step d), i.e. before step e), already have a tensile strength of at least 900 MPa, in particular at least 1145 MPa, a yield strength of at least 560 MPa, in particular at least 675 MPa, and an elongation at break A5.65 of at least 8%.
  • By virtue of the respective optional heat treatment steps (step e), the mechanical properties of a steel component according to the invention can be improved to such an extent that its tensile strength is at least 1050 MPa, in particular at least 1230 MPa, its yield strength is at least 615 MPa, in particular at least 750 MPa, and its elongation at break A5.65 is at least 8%.
  • Three melts S1, S2, S3 according to the invention were melted and respectively atomised in a conventional manner in the gas flow into steel powder having a grain size of 5-150 μm. The composition of melts S1-S3 is given in Table 1.
  • From the steel powders obtained, steel components were produced using “Selective Laser Melting” (“3D printing/SLM method”), which were test bodies for determining the optimal parameters for additive manufacturing, namely cubes with approx. 20 mm edge length, and blanks for tensile and impact tests.
  • The tensile strength Rm_V of the steel components obtained after the additive manufacturing is shown in Table 2.
  • The steel components thus obtained were subjected to a machining operation in order to optimally adapt them to their respectively required final shape.
  • Subsequently, the components each underwent a heat treatment in which they were aged for a period tA at a temperature TA. The respective ageing time tA and ageing temperature TA are also listed in Table 2.
  • Likewise, Table 2 indicates the tensile strength Rm_N which the components exhibited after mechanical processing and ageing.
  • In addition, Table 2 indicates the structure of the components.
  • It can be seen from the TTT diagrams displayed in FIGS. 1 and 2 for steels S1 (FIG. 1) and S2 (FIG. 2) that in steels S1, S2 the initially austenitic structure transforms completely into bainite, in particular in a bainitic transformation stage, during the cooling from the high temperature which the steel powders produced from steels S1 and S2 reach during melting in the course of additive manufacturing. This results, largely independently of the cooling rate, in a nearly constant hardness in the bainite region.
  • TABLE 1
    Data in wt %, remainder
    iron and unavoidable impurities
    Melt: Si S2 S3
    C 0.10 0.17 0.20
    Si 0.78 0.33 0.35
    Mn 1.42 0.72 0.50
    Mo 0.52 0.70 0.72
    Ni 0.17 0.24 0.17
    Al 0.025 0.025 0.031
    Ti 0.01 0.01 0.01
    Cu 0.05 0.05 0.03
    Cr 0.4 2.00 1.80
    Co 0.01 0.01 0.82
    N 0.01 0.01 0.01
    S 0.02 0.005 0.004
    B 0.0011 0.0012 0.0
    Nb 0.01 0.02 0.02
    V 0.04 0.10 0.10
  • TABLE 2
    Rm_V tA TA Rm_N
    Melt [MPa] [h] [°C.] [MPa] Structure [vol %]
    S1 1080 4 450 1125 100% bainite
    S2 1110 1 600 1213 3% tempered martensite,
    97% bainite
    S3 1135 1 575 1245 100% bainite

Claims (17)

1. A steel powder for the production of steel components by an additive manufacturing process which comprises (in wt %):
C: 0.08-0.35%,
Si: 0-0.80%,
Mn: 0.20-2.00%,
Cr: 0-4.00%,
Mo: 0.3-3.0%,
N: 0.004-0.020%,
Al: 0.004-0.050%,
B: 0-0.0025%,
Cu: 0-0.3%,
Co: 0-2.0%,
at least one element from the group consisting of Nb, Ti, V, and S, wherein
the Nb content is 0.003-0.20 wt %,
the Ti content is 0.001-0.02 wt %,
the V content is 0.02-0.40 wt %
and/or
the S content is 0.001-0.4 wt %,
with the remainder being iron and unavoidable impurities,
wherein the Al content % Al, the Nb content % Nb, the Ti content % Ti, the V content % V and the N content % N of the steel satisfy the following condition:

%Al/27+%Nb/45+%Ti/48+%V/25>%N/3.5,
and wherein the grains of the steel powder have an average diameter of 5-150 μm.
2. The steel powder according to claim 1, wherein the steel powder has a C content of at least 0.09 wt %.
3. The steel powder according to claim 1, wherein the steel powder has a Cr content of at least 0.5 wt %.
4. The steel powder according to claim 1, wherein the S content of the steel powder is at least 0.003 wt %.
5. The steel powder according to claim 1, wherein the S content of the steel powder is at most 0.1 wt %.
6. The steel powder according to claim 1, wherein the steel powder has a B content of at least 0.0005 wt %.
7. The steel powder according to claim 1, wherein the steel powder has an N content of at least 0.006 wt %.
8. The steel powder according to claim 1, wherein the steel powder has a Cu content of less than 0.3 wt %.
9. The steel powder according to claim 1, wherein the steel powder has an Mo content of less than 0.7 wt %.
10. A method for producing a steel component, comprising:
a) melting a steel which comprises (in wt %):
C: 0.08-0.35%,
Si: 0-0.80%,
Mn: 0.20-2.00%,
Cr: 0-4.00%,
Mo: 0.3-3.0%,
N: 0.004-0.020%,
Al: 0.004-0.050%,
B: 0-0.0025%,
Cu: 0-0.3%,
Co: 0-2.0%,
at least one element from the group consisting of Nb, Ti, V, and S, wherein
the Nb content is 0.003-0.20 wt %,
the Ti content is 0.001-0.02 wt %,
the V content is 0.02-0.40 wt %
and/or
the S content is 0.001-0.4 wt %,
with the remainder being iron and unavoidable impurities,
wherein the Al content % Al, the Nb content % Nb, the Ti content % Ti, the V content % V and the N content % N of the steel satisfy the following condition:

%Al/27+%Nb/45+%Ti/48+%V/25>%N/3.5;
b) producing a steel powder from the steel melted in step a), wherein the grains of the steel powder have an average diameter of 5-150 μm;
c) producing the component by using an additive manufacturing process, wherein
c.1) at least one portion of the steel powder by volume is exposed to a temporary heat input with subsequent cooling, so that the steel powder particles, which are present in the heated volume portion and respectively adjoin each other, enter into a firmly-bonded connection and are solidified after cooling to form at least one volume portion of the component to be produced; and
c.2) optionally, re-applying a further portion of the steel powder to the volume portion solidified in step c.1) and repeating step c.1) with the further portion of the steel powder, wherein steps c.1) and c.2) are repeated until the component to be produced is completely finished.
11. A steel component produced according to the method of claim 10.
12. The steel component according to claim 11, wherein a structure of the steel component comprises at least 80 vol % bainite and the remainder of the structure comprises retained austenite, ferrite, perlite and/or martensite.
13. The steel component according to claim 11, wherein before the optional step e), the steel component has a tensile strength of at least 900 MPa, a yield strength of at least 560 MPa and an elongation at break A5.65 of at least 8%.
14. The steel component according to claim 11, wherein after the optional step e), the steel component has a tensile strength of at least 1050 MPa, a yield strength of at least 615 MPa and an elongation at break A5.65 is at least 8%.
15. The method according to claim 11, further comprising machining the produced component to shape.
16. The method according to claim 11, further comprising final heat treating the resulting produced component to form strength increasing precipitates in the structure of the component.
17. The method according to claim 16, wherein the heat treating is an ageing process in which the component is held at a temperature of 450-600° C. over a period of 0.5-6 hours.
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