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EP4198156A1 - Tungsten carbide reinforced manganese steel - Google Patents

Tungsten carbide reinforced manganese steel Download PDF

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Publication number
EP4198156A1
EP4198156A1 EP21215683.0A EP21215683A EP4198156A1 EP 4198156 A1 EP4198156 A1 EP 4198156A1 EP 21215683 A EP21215683 A EP 21215683A EP 4198156 A1 EP4198156 A1 EP 4198156A1
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Prior art keywords
composite material
manganese steel
zone
reinforcing
previous
Prior art date
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EP21215683.0A
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German (de)
French (fr)
Inventor
Latifa MELK
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Sandvik SRP AB
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Sandvik SRP AB
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Publication date
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Priority to EP21215683.0A priority Critical patent/EP4198156A1/en
Priority to PCT/EP2022/086051 priority patent/WO2023111132A1/en
Priority to US18/719,416 priority patent/US20250051887A1/en
Priority to EP22839250.2A priority patent/EP4448819A1/en
Priority to CN202280082148.7A priority patent/CN118339320A/en
Priority to AU2022410342A priority patent/AU2022410342A1/en
Priority to CA3239333A priority patent/CA3239333A1/en
Publication of EP4198156A1 publication Critical patent/EP4198156A1/en
Priority to CL2024001807A priority patent/CL2024001807A1/en
Withdrawn legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C29/00Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
    • C22C29/02Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
    • C22C29/06Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
    • C22C29/08Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
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    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1036Alloys containing non-metals starting from a melt
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D19/00Casting in, on, or around objects which form part of the product
    • B22D19/0081Casting in, on, or around objects which form part of the product pretreatment of the insert, e.g. for enhancing the bonding between insert and surrounding cast metal
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D19/00Casting in, on, or around objects which form part of the product
    • B22D19/02Casting in, on, or around objects which form part of the product for making reinforced articles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D19/00Casting in, on, or around objects which form part of the product
    • B22D19/14Casting in, on, or around objects which form part of the product the objects being filamentary or particulate in form
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D21/00Casting non-ferrous metals or metallic compounds so far as their metallurgical properties are of importance for the casting procedure; Selection of compositions therefor
    • B22D21/02Casting exceedingly oxidisable non-ferrous metals, e.g. in inert atmosphere
    • B22D21/025Casting heavy metals with high melting point, i.e. 1000 - 1600 degrees C, e.g. Co 1490 degrees C, Ni 1450 degrees C, Mn 1240 degrees C, Cu 1083 degrees C
    • 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
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/02Compacting only
    • 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
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/24After-treatment of workpieces or articles
    • B22F3/26Impregnating
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/04Making non-ferrous alloys by powder metallurgy
    • C22C1/05Mixtures of metal powder with non-metallic powder
    • C22C1/051Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor
    • C22C1/053Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor with in situ formation of hard compounds
    • C22C1/055Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor with in situ formation of hard compounds using carbon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1036Alloys containing non-metals starting from a melt
    • C22C1/1057Reactive infiltration
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C29/00Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
    • C22C29/005Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides comprising a particular metallic binder
    • 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
    • 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
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/22Ferrous alloys, e.g. steel alloys containing chromium 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
    • C22C38/38Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of 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
    • C22C38/58Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
    • 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
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/24After-treatment of workpieces or articles
    • B22F2003/248Thermal after-treatment
    • 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
    • B22F2301/20Refractory metals
    • 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
    • B22F2302/00Metal Compound, non-Metallic compound or non-metal composition of the powder or its coating
    • B22F2302/40Carbon, graphite
    • 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
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2999/00Aspects linked to processes or compositions used in powder metallurgy
    • CCHEMISTRY; METALLURGY
    • 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
    • C22C33/0278Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5%
    • C22C33/0292Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements with at least one alloying element having a minimum content above 5% with more than 5% preformed carbides, nitrides or borides

Definitions

  • the present invention relates to a composite material based on reinforced manganese steel, a wear part made thereof and a method for making the same.
  • a particular category of wear resistant steels is typically referred to as manganese steel or Hatfield steel. These materials are suitable for applications where a high toughness and a moderate abrasion resistance are required including for example use as wear parts for crushers that are subjected to strong abrasion and dynamic surface pressures due to the rock crushing action. Abrasion results when the rock material contacts the wear part and strips-off material from the wear part surface. Additionally, the surface of the wear part is subjected to significantly high surface pressures that cause wear part fatigue and breakage.
  • Manganese or Hadfield steel is typically characterised by having an amount of manganese, usually above 11% by weight.
  • the problem with manganese steel is that it is typically too ductile for wear parts in modern crushers that are subject to extreme operating conditions, meaning the at the lifetime of the wear parts is reduced and the maintenance costs are increased. Therefore, the problem to be solved is to provide a manganese steel with enhanced wear resistance.
  • WO20200222662 discloses a composite material, however the problem with this material is that is not provide an optimal balance between wear resistance and impact resistance and an even more significant problem is that there is poor bonding between the reinforcing particle and the manganese steel matrix and poor bonding between reinforced and non-reinforced zones, which leads reduced wear resistance and premature failure of the wear parts.
  • a “catalysis” is a metal powder or mixture of metal powders which during the reaction in the self-propagating high temperature synthesis (SHS) undergo melting and form a matrix of the composite zone.
  • SHS self-propagating high temperature synthesis
  • the fundamental role of catalysis is to reduce the amount of dissipated energy in the SHS process.
  • a "compact” is a densified powder composition.
  • the objective is achieved by providing a composite material comprising: at least one reinforcing zone comprising tungsten carbide (WC) and a manganese steel matrix; a manganese steel zone that surrounds each of the reinforcing zones; and an interface layer positioned between each of the reinforcing zones and the manganese steel zone; characterized in that: the average grain size of the WC particles in each of the reinforcing zone(s) is between 7-12 ⁇ m, preferably between 7-10 ⁇ m.
  • WC tungsten carbide
  • this produces a composite material that has both increased wear resistance and structural integrity. Therefore, when the material is used on areas of wear parts that are highly exposed to wear the lifetime of the parts is increased. If the average grain size of the WC grains is too large, then the composite material will be too brittle. If the average grain size of the WC grains in too small the wear resistance will be reduced.
  • the composite material comprises between 70-98 wt% of WC in each of the reinforcing zones. Preferably between 80-95 wt%, even more preferably between 90-95 wt%.
  • this provides the optimal balance between wear resistance and impact resistance. If the wt% of WC in each of the reinforcing zones in too high the composite material will be too brittle and more prone to failure. If the wt% of the WC in each of the reinforcing zones is too low, then composite material will have low hardness and therefore it will not have sufficient wear resistance.
  • the composition of the manganese steel in manganese steel zone has the chemical composition by weight of: carbon: 0.5 to 2.0%; manganese: 11 to 22%; silicon: 0.2 to 1.0%; chromium: 1 to 2%; nickel: up to 0.6%; molybdenum: up to 0.5%; and a balance of Iron.
  • this steel composition is characterized by the addition of micro-alloying elements such as chromium, nickel and molybdenum in good amounts which induce high yield strength and high hardness resulting in increase in wear resistance of manganese steel.
  • the Vickers hardness of the reinforcing zones is between 580-780 HV1 and the hardness of the manganese steel zone is between 200 - 300 HV1 before work hardening.
  • the increased hardness in the reinforcing zones leads to a more wear resistant material.
  • the thickness of each of the interface layer is between 90-300 ⁇ m, preferably between 130-200, even more preferably between 250-300 ⁇ m.
  • this thickness of interface layer or thickness of contact area between manganese and composite zone is an indication of an increase in the reaction propagation rate and the amount of heat generated due to the high combustion temperature taking place at the contact between the molten manganese steel and the insert. A high combustion temperature leads to the precipitation of large grains at the interface. If the thickness is too large the heat conductivity increases in the composite zone which results in a faster heat dissipation towards the inside of the composite zone resulting in high nucleation rate of WC particles. If the thickness is too small the heat conductivity is less which favours growth, consequently less nucleation of WC particles.
  • the interface layer is free of defects.
  • the absence of any defects in the interface layer means that there is good bonding between the manganese steel zone and each of the reinforcing zones and consequently the structural integrity of the composite material is improved, meaning that the lifetime of the wear parts that the materials is used in is increased.
  • the absence of the presence of any pores is an indication that the composition has the ability to absorb the excess heat and gases from the SHS process and so therefore signifies that the synthesis reaction has been successful.
  • the wettability between the WC grains and the manganese steel in the reinforcing zone (s) is >99%, preferably >99.5%, even more preferably >99.9%.
  • good wettability induces an excellent bonding between the composite zone and Manganese steel preventing defects such as pores and cracks to form and consequently the wear resistance increases.
  • the each of the reinforcing zones has a volume of between 30-75 cm 3 .
  • this size provides the optimal balance between wear resistance and impact resistance.
  • the WC grains in the reinforcing zones have a triangular prismatic shape.
  • the triangular prismatic shape of WC will contribute to crack deflection and stop crack propagation increasing the ductility and high wear resistance of the reinforcing zone.
  • the distance between two neighbouring reinforcing zones is between 1-20 ⁇ m, preferably between 1-5 mm, more preferably between 1-3 mm.
  • this provides the optimal balance between wear resistance and impact resistance. If the reinforcing zones are spaced too far apart then the wear resistance will not be high enough. If the reinforcing zones are spaced to close together then the impact resistance will not be high enough.
  • Another aspect of the present invention relates to a wear part comprising the composite material as described hereinbefore or hereinafter.
  • the presence of the reinforcing zones within the manganese zone will improve the wear resistance and therefore the lifetime of the wear parts which in turn increases profitability.
  • Another aspect of the present invention relates to a method of producing the composite material as described hereinbefore or hereinafter comprising the steps of: a) mixing together 60-95 wt% tungsten, 3-8wt% carbon and 0-40 % catalysis powders; b) compacting the mixed powders together to form at least one compact; c) positioning and optionally fixing at least one compact into the interior of a mold; d) pouring molten casting manganese steel into the mold to surround the at least one compact to initiate a self-propagating high temperature synthesis (SHS) reaction to produce a cast; e) heat treating the cast; f) quenching the cast; characterized in that: in step b) the powders are compacting with a pressure of between 400-700 MPa, preferably between 500-600 MPa, more preferably between 550-600 MPa.
  • SHS high temperature synthesis
  • the compacts have a low density which enables the manganese steel to more easily infiltrate between the WC grains and consequently results in improved bonding between the WC grains and the manganese steel. Further it avoids the creation of defects which would lead to premature failure of the wear parts that the composite material is used in.
  • the catalysis is selected from Fe, Mn, Ni, Mo, Cr, W, Al, or a mixture thereof.
  • he addition of a catalysis in a specific amount will contribute to a strong stabilization to austenite phase within the microstructure in addition to good mechanical properties and high wear resistance.
  • the catalysis addition will also act as a grain growth inhibitor which results in a fine microstructure.
  • Figure 1 shows a composite material 2 comprising at least one reinforcing zone 4 comprising tungsten carbide (WC) and a manganese steel matrix; a manganese steel zone 6 that surrounds each of the reinforcing zones 4 ; and an interface layer 8 positioned between each of the reinforcing zones 4 and the manganese steel zone 6.
  • the WC acts to reinforce the manganese steel matrix.
  • the average grain size of the WC particles in each of the reinforcing zone(s) (4) is between 7-12 ⁇ m, preferably between 7-10 ⁇ m, preferably between 7-9 ⁇ m.
  • the average grain size of the WC grains is measured by Scanning Electron Microscopy (SEM) analysis where several and different areas from the samples were analysed and particle sizes were measured. Then, the average particle size was calculated.
  • SEM Scanning Electron Microscopy
  • Each interface layer 8 comprises WC and manganese steel and can be distinguished from the reinforcing zones 4 as the shape and size of the WC grains are different.
  • the interface layer(s) 8 can be distinguished from the reinforcing zone(s) 4 can either: comparing the geometry and / or comparing the average grain size. If the geometry is being compared, the reinforcing zone(s) 4 comprise >90% WC grains having a triangular prismatic geometry whereas the interface layer(s) 8 comprise ⁇ 5% WC grains having a triangular prismatic geometry. A WC grain is considered to have triangular prismatic geometry if the grains have 3 sharp edges. If the grain size is being compared the average WC grain size of in the interface layer(s) 8 is at least 5% less than the average WC grain size on the reinforcing zone(s) 4.
  • Figure 2 shows a Scanning Electron microscope image using MIRA3 TESCAN equipment.
  • a secondary electron detector (SE) with a high voltage of 15 KV and a working distance of 9 mm configuration were used.
  • Figure 3 shows an SEM image of the WC grains in the interface layer 8. The different WC grain geometry and size can be clearly be seen when comparing these two figures.
  • the wt% of WC in each of the reinforcing zones 4 is between 70-98 %, more preferably between 80-95 %, even more preferably between 90-95%.
  • the composition of the manganese steel in manganese steel zone 6 has the chemical composition by weight of: carbon: 0.5 to 2.0%; manganese: 11 to 22%; silicon: 0.2 to 1.0% ; chromium: 1 to 2%; nickel: up to 0.6%, molybdenum: up to 0.5% and a balance of Fe.
  • the chemical composition of the manganese steel in each of the reinforcing zones 4 has the chemical composition by weight of: 1-1.5 % C, 11-14 % Mn, 0.4-0.8 % Si, 1.3-2.0 % Cr, 0.6 % Ni, 0.065 % P.
  • the hardness of the reinforcing zones 4 is between 580-780 HV1, preferably between 600-700.
  • the hardness of the manganese steel zone 6 is between 200 - 300 HV1.
  • Hardness is measured using Vickers hardness mapping on polished samples using a 1 kgf and a holding time of 15 seconds. A micro-hardness tester, Matsuzawa, model MXT was used. Hardness measurement profiles are performed starting from the non-reinforce zone, moving to the interface layer and then to the reinforced zone.
  • the interface layer 6 is between 90-300 ⁇ m wide, preferably between 130-200 ⁇ m .
  • Figure 4 shows an SEM image taken at 15.0 kV, 563 magnification of the reinforced zone 4, the manganese steel zone 6 and the interface layer 8.
  • the width of the interface layer 6 is measured from a start point 10, which is defined as being adjacent to the manganese steel zone 6 and the point at where the WC grains are present.
  • the end point 12 for measuring where the interface layer 8 ends, and therefore where the reinforcing zone 8 starts is considered to be where the average grain size of the WC grains has increased by 20% compared average WC grains measured at the start point 10 and / or where the percentage of WC grains having a triangular prismatic shape increases above 90%.
  • the interface layer 8 is free of defects. Defects are considered to be cracks or pores.
  • the wettability between the WC grains and the manganese steel in the reinforcing zones 4 is >99%, preferably >99.5%, more preferably >99.9%, most preferably 100%. Wettability is measured by a Scanning Electron Microscope where the contact area and the bonding between the WC grains and the manganese steel have been evaluated.
  • each of the reinforcing zones 4 has a volume of between 30-75 cm 3 .
  • the reinforcing zone(s) 4 could have a length of between 100-200 mm, preferably between 100-150 mm, a width of between 20-30 mm, preferably between 20-25 mm and a thickness between 15-30 mm, preferably between 15-25 mm.
  • >95%, preferably >98%, more preferably >99% of the WC grains in the reinforcing zones 4 have a triangular prismatic shape.
  • the WC grains are uniformly distributed in the manganese steel in the reinforcing zone(s).
  • Figure 5 shows an example of a wear part 14 comprising the composite material 2 as described hereinabove or hereinafter.
  • the wear part 2 could be, but not limited to, a cone crusher or a stationary jaw crusher or a mobile jaw crusher that is configured to crush material or other material/rock processing unit.
  • the reinforcing zone(s) 4 are positions on the wear parts 14 in the locations that are most subjected to high wear, for example on a crushing zone 18 of a cone crusher 16.
  • the method for producing the composite material 2 as described hereinbefore or hereinafter comprising the steps of: a) Mixing together 60-95 wt%, preferably 75-95 tungsten; 3-8 wt%, preferably 4-5% carbon and 0-40 %, preferably 10-20 % catalysis powders; b) compacting the mixed powders together to form at least one compact using a compacting pressure of between 400-700 MPa, preferably 500-600 MPa more preferably 550-600 MPa ; c) positioning and optionally fixing at least one compact into the interior of a mold; d) pouring molten casting manganese steel into the mold to surround the at least one compact to initiate a self-propagating high temperature synthesis (SHS) reaction to produce a cast; e) heat treating the cast; and then f) quenching the cast.
  • SHS self-propagating high temperature synthesis
  • the cast is treated at a temperature of between 1400-1500°C, the cast is quenched using water.
  • the catalysis is selected from Fe, Co, Ni, Mo, Cr, W, Al, or a mixture thereof.
  • Carbon could be added in the form of graphite, amorphous graphite, a carbonaceous material or mixtures thereof.
  • the compacts could for example be held in place using me a metallic fixation system to hold them in place during casting.
  • Sample A is a comparative sample of non-reinforced manganese steel having the composition 1-1.5 % C, 11-14 % Mn, 0.4-0.8 % Si, 1.3-2.0 % Cr, 0.6 % Ni, 0.065 % P.
  • Samples B-K are samples of composite materials produced by mixing together powders of tungsten, carbon and a catalysis powder. The compacting the mixed powders to form compacts which were then positioned in a mold and then molten manganese steel having a composition of 1-1.5 % C, 11-14 % Mn, 0.4-0.8 % Si, 1.3-2.0 % Cr, 0.6 % Ni, 0.065 % was poured into the mold to surround the compacts which initiated a SHS reaction, the cast was then heat treated at a temperature of 1450 °C and then quenching with water.
  • Table 1 shows a summary of the reinforced samples: Table 1: Summary of samples Sample Compacting pressure used (MPa) Average WC grain size in reinforced zone ( ⁇ m) WC content in reinforced zone (wt%) Wettability (%) B (invention) 600 12 78 100 C (comparative) 600 13 74 100 D (comparative) 600 14 73 5 E (comparative) 600 13 76 10 F (comparative) 600 5 75 80 H (invention) 600 10 86 100 I (invention) 600 10 87 100 J (comparative) 600 5 74 100 K (invention) 600 7 90 100
  • Vickers hardness was measured by a micro-hardness tester, Matsuzawa, model MXT using 1 kgf and a holding time of 15 seconds. Hardness measurement profiles are performed starting from the non-reinforce zone, moving to the interface layer and then to the reinforced zone.
  • inventive samples have an increased hardness in reinforced zones compared to the comparative samples.
  • Wear was tested using a standard wear test using a lab jaw crusher.
  • the wear test procedure consists on using fixed amount of rocks from 1 Ton up to 4 Ton of rocks.
  • the reference plates are based on Weldox type of material.
  • the calculation of wear is based on the difference in volume loss of the test plates compared to the reference plates. All plates were weighed before and after wear test. Then volume loss is calculated using the density of 7.85 g/cm 3 and 7.6 g/cm 3 for the reference and test plates respectively.
  • the total wear ratio (WR) is calculated according to ASTM G81-97a(2013).
  • Table 4 Defects Sample Defects in the reinforced zone Defects in the interface layer Thickness of the interface layer ( ⁇ m) B (inventive) none none 170 C (comparative) pores cracks 93.5 D (comparative) none cracks 0 E (comparative) pores cracks 190 F (comparative) none none 138.5 H (inventive) none none 232 I (inventive) none none 292 J (comparative) none none none 158 K (inventive) none none 293
  • Figure 6 shows an examples of cracking in the interface layer in comparative samples D and E, whereas figure 4 shows inventive sample K, where there is no cracking.
  • inventive samples have optimal grain sizes, optimal hardness, wear resistance, optimal interface layer thickness, good wettability and are free of cracks and pores, whereas the comparative samples have one or more of low hardness, non-optimal interface layer thickness, poor wettability, low wear resistance, pores and / or cracks.

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Abstract

A composite material comprising: at least one reinforcing zone comprising tungsten carbide (WC) and a manganese steel matrix; a manganese steel zone that surrounds each of the reinforcing zones; and an interface layer positioned between each of the reinforcing zones and the manganese steel zone characterized in that: the average grain size of the WC particles in each of the reinforcing zone(s) is between 7-12 µm.

Description

    TECHNICAL FIELD
  • The present invention relates to a composite material based on reinforced manganese steel, a wear part made thereof and a method for making the same.
  • BACKGROUND
  • A particular category of wear resistant steels is typically referred to as manganese steel or Hatfield steel. These materials are suitable for applications where a high toughness and a moderate abrasion resistance are required including for example use as wear parts for crushers that are subjected to strong abrasion and dynamic surface pressures due to the rock crushing action. Abrasion results when the rock material contacts the wear part and strips-off material from the wear part surface. Additionally, the surface of the wear part is subjected to significantly high surface pressures that cause wear part fatigue and breakage.
  • Manganese or Hadfield steel is typically characterised by having an amount of manganese, usually above 11% by weight. However, the problem with manganese steel is that it is typically too ductile for wear parts in modern crushers that are subject to extreme operating conditions, meaning the at the lifetime of the wear parts is reduced and the maintenance costs are increased. Therefore, the problem to be solved is to provide a manganese steel with enhanced wear resistance.
  • A known solution is to reinforce at least part of the manganese steel with particles having an increased hardness. WO20200222662 discloses a composite material, however the problem with this material is that is not provide an optimal balance between wear resistance and impact resistance and an even more significant problem is that there is poor bonding between the reinforcing particle and the manganese steel matrix and poor bonding between reinforced and non-reinforced zones, which leads reduced wear resistance and premature failure of the wear parts.
  • Therefore, the problem to be solved to provide a composite material that can be used for wear parts having an optimal balance between wear resistance and impact resistance, wherein there is improved bonding between the reinforcing particles and the manganese matrix and the bonding between the reinforced and non-reinforced zones in order to reduce defects and cracking that would lead to premature failure of the wear parts.
  • DEFINITIONS
  • A "catalysis" is a metal powder or mixture of metal powders which during the reaction in the self-propagating high temperature synthesis (SHS) undergo melting and form a matrix of the composite zone. The fundamental role of catalysis is to reduce the amount of dissipated energy in the SHS process.
  • A "compact" is a densified powder composition.
  • SUMMARY OF INVENTION
  • It is an objective of this invention to provide a novel and improved composite material for wear parts. The objective is achieved by providing a composite material comprising: at least one reinforcing zone comprising tungsten carbide (WC) and a manganese steel matrix; a manganese steel zone that surrounds each of the reinforcing zones; and an interface layer positioned between each of the reinforcing zones and the manganese steel zone; characterized in that: the average grain size of the WC particles in each of the reinforcing zone(s) is between 7-12 µm, preferably between 7-10 µm.
  • Advantageously, this produces a composite material that has both increased wear resistance and structural integrity. Therefore, when the material is used on areas of wear parts that are highly exposed to wear the lifetime of the parts is increased. If the average grain size of the WC grains is too large, then the composite material will be too brittle. If the average grain size of the WC grains in too small the wear resistance will be reduced.
  • Preferably, the composite material comprises between 70-98 wt% of WC in each of the reinforcing zones. Preferably between 80-95 wt%, even more preferably between 90-95 wt%. Advantageously, this provides the optimal balance between wear resistance and impact resistance. If the wt% of WC in each of the reinforcing zones in too high the composite material will be too brittle and more prone to failure. If the wt% of the WC in each of the reinforcing zones is too low, then composite material will have low hardness and therefore it will not have sufficient wear resistance.
  • Preferably, the composition of the manganese steel in manganese steel zone has the chemical composition by weight of: carbon: 0.5 to 2.0%; manganese: 11 to 22%; silicon: 0.2 to 1.0%; chromium: 1 to 2%; nickel: up to 0.6%; molybdenum: up to 0.5%; and a balance of Iron. Advantageously, this steel composition is characterized by the addition of micro-alloying elements such as chromium, nickel and molybdenum in good amounts which induce high yield strength and high hardness resulting in increase in wear resistance of manganese steel.
  • Preferably, the Vickers hardness of the reinforcing zones is between 580-780 HV1 and the hardness of the manganese steel zone is between 200 - 300 HV1 before work hardening. Advantageously, the increased hardness in the reinforcing zones leads to a more wear resistant material.
  • Preferably, the thickness of each of the interface layer is between 90-300 µm, preferably between 130-200, even more preferably between 250-300 µm. Advantageously, this thickness of interface layer or thickness of contact area between manganese and composite zone is an indication of an increase in the reaction propagation rate and the amount of heat generated due to the high combustion temperature taking place at the contact between the molten manganese steel and the insert. A high combustion temperature leads to the precipitation of large grains at the interface. If the thickness is too large the heat conductivity increases in the composite zone which results in a faster heat dissipation towards the inside of the composite zone resulting in high nucleation rate of WC particles. If the thickness is too small the heat conductivity is less which favours growth, consequently less nucleation of WC particles.
  • Preferably, the interface layer is free of defects. Advantageously, the absence of any defects in the interface layer means that there is good bonding between the manganese steel zone and each of the reinforcing zones and consequently the structural integrity of the composite material is improved, meaning that the lifetime of the wear parts that the materials is used in is increased. Further, the absence of the presence of any pores is an indication that the composition has the ability to absorb the excess heat and gases from the SHS process and so therefore signifies that the synthesis reaction has been successful.
  • Preferably, the wettability between the WC grains and the manganese steel in the reinforcing zone (s) is >99%, preferably >99.5%, even more preferably >99.9%. Advantageously, good wettability induces an excellent bonding between the composite zone and Manganese steel preventing defects such as pores and cracks to form and consequently the wear resistance increases.
  • Preferably, the each of the reinforcing zones has a volume of between 30-75 cm3. Advantageously, this size provides the optimal balance between wear resistance and impact resistance.
  • Preferably, at least 95 % of the WC grains in the reinforcing zones have a triangular prismatic shape. Advantageously, the triangular prismatic shape of WC will contribute to crack deflection and stop crack propagation increasing the ductility and high wear resistance of the reinforcing zone.
  • Preferably, the distance between two neighbouring reinforcing zones is between 1-20 µm, preferably between 1-5 mm, more preferably between 1-3 mm. Advantageously, this provides the optimal balance between wear resistance and impact resistance. If the reinforcing zones are spaced too far apart then the wear resistance will not be high enough. If the reinforcing zones are spaced to close together then the impact resistance will not be high enough.
  • Another aspect of the present invention relates to a wear part comprising the composite material as described hereinbefore or hereinafter. Advantageously, the presence of the reinforcing zones within the manganese zone will improve the wear resistance and therefore the lifetime of the wear parts which in turn increases profitability.
  • Another aspect of the present invention relates to a method of producing the composite material as described hereinbefore or hereinafter comprising the steps of: a) mixing together 60-95 wt% tungsten, 3-8wt% carbon and 0-40 % catalysis powders; b) compacting the mixed powders together to form at least one compact; c) positioning and optionally fixing at least one compact into the interior of a mold; d) pouring molten casting manganese steel into the mold to surround the at least one compact to initiate a self-propagating high temperature synthesis (SHS) reaction to produce a cast; e) heat treating the cast; f) quenching the cast; characterized in that: in step b) the powders are compacting with a pressure of between 400-700 MPa, preferably between 500-600 MPa, more preferably between 550-600 MPa.
  • Advantageously, if this pressing pressure is used the compacts have a low density which enables the manganese steel to more easily infiltrate between the WC grains and consequently results in improved bonding between the WC grains and the manganese steel. Further it avoids the creation of defects which would lead to premature failure of the wear parts that the composite material is used in.
  • Preferably, the catalysis is selected from Fe, Mn, Ni, Mo, Cr, W, Al, or a mixture thereof. Advantageously, he addition of a catalysis in a specific amount will contribute to a strong stabilization to austenite phase within the microstructure in addition to good mechanical properties and high wear resistance. The catalysis addition will also act as a grain growth inhibitor which results in a fine microstructure.
  • BRIEF DECRSIPTION OF DRAWINGS
    • Figure 1: Shows a line drawing of the composition of the composite material.
    • Figure 2: Shows an SEM image taken of the reinforced zone with low magnification on the left and high magnification on the right.
    • Figure 3: Shows an SEM image taken of the interface layer with low magnification on the left and high magnification on the right.
    • Figure 4: Shows an SEM image of the composite material.
    • Figure 5: Shows a perspective drawing of a wear part.
    • Figure 6: Shows SEM images of the cracking at the interface layer for comparative sample.
    DETAILED DESCRIPTION
  • Figure 1 shows a composite material 2 comprising at least one reinforcing zone 4 comprising tungsten carbide (WC) and a manganese steel matrix; a manganese steel zone 6 that surrounds each of the reinforcing zones 4 ; and an interface layer 8 positioned between each of the reinforcing zones 4 and the manganese steel zone 6. In each of the reinforcing zones, the WC acts to reinforce the manganese steel matrix.
  • The average grain size of the WC particles in each of the reinforcing zone(s) (4) is between 7-12 µm, preferably between 7-10 µm, preferably between 7-9 µm.
  • The average grain size of the WC grains is measured by Scanning Electron Microscopy (SEM) analysis where several and different areas from the samples were analysed and particle sizes were measured. Then, the average particle size was calculated.
  • Each interface layer 8 comprises WC and manganese steel and can be distinguished from the reinforcing zones 4 as the shape and size of the WC grains are different. The interface layer(s) 8 can be distinguished from the reinforcing zone(s) 4 can either: comparing the geometry and / or comparing the average grain size. If the geometry is being compared, the reinforcing zone(s) 4 comprise >90% WC grains having a triangular prismatic geometry whereas the interface layer(s) 8 comprise <5% WC grains having a triangular prismatic geometry. A WC grain is considered to have triangular prismatic geometry if the grains have 3 sharp edges. If the grain size is being compared the average WC grain size of in the interface layer(s) 8 is at least 5% less than the average WC grain size on the reinforcing zone(s) 4.
  • Figure 2 shows a Scanning Electron microscope image using MIRA3 TESCAN equipment. A secondary electron detector (SE) with a high voltage of 15 KV and a working distance of 9 mm configuration were used. SEM image of the WC grains in the reinforcing zone 4. Figure 3 shows an SEM image of the WC grains in the interface layer 8. The different WC grain geometry and size can be clearly be seen when comparing these two figures.
  • In one embodiment the wt% of WC in each of the reinforcing zones 4 is between 70-98 %, more preferably between 80-95 %, even more preferably between 90-95%.
  • In one embodiment, the composition of the manganese steel in manganese steel zone 6 has the chemical composition by weight of: carbon: 0.5 to 2.0%; manganese: 11 to 22%; silicon: 0.2 to 1.0% ; chromium: 1 to 2%; nickel: up to 0.6%, molybdenum: up to 0.5% and a balance of Fe.
  • In one embodiment, the chemical composition of the manganese steel in each of the reinforcing zones 4 has the chemical composition by weight of: 1-1.5 % C, 11-14 % Mn, 0.4-0.8 % Si, 1.3-2.0 % Cr, 0.6 % Ni, 0.065 % P.
  • In one embodiment, the hardness of the reinforcing zones 4 is between 580-780 HV1, preferably between 600-700. The hardness of the manganese steel zone 6 is between 200 - 300 HV1.
  • Hardness is measured using Vickers hardness mapping on polished samples using a 1 kgf and a holding time of 15 seconds. A micro-hardness tester, Matsuzawa, model MXT was used. Hardness measurement profiles are performed starting from the non-reinforce zone, moving to the interface layer and then to the reinforced zone.
  • In one embodiment, the interface layer 6 is between 90-300 µm wide, preferably between 130-200 µm . Figure 4 shows an SEM image taken at 15.0 kV, 563 magnification of the reinforced zone 4, the manganese steel zone 6 and the interface layer 8. The width of the interface layer 6 is measured from a start point 10, which is defined as being adjacent to the manganese steel zone 6 and the point at where the WC grains are present. The end point 12 for measuring where the interface layer 8 ends, and therefore where the reinforcing zone 8 starts is considered to be where the average grain size of the WC grains has increased by 20% compared average WC grains measured at the start point 10 and / or where the percentage of WC grains having a triangular prismatic shape increases above 90%.
  • In one embodiment, the interface layer 8 is free of defects. Defects are considered to be cracks or pores.
  • In one embodiment, the wettability between the WC grains and the manganese steel in the reinforcing zones 4 is >99%, preferably >99.5%, more preferably >99.9%, most preferably 100%. Wettability is measured by a Scanning Electron Microscope where the contact area and the bonding between the WC grains and the manganese steel have been evaluated.
  • In one embodiment each of the reinforcing zones 4 has a volume of between 30-75 cm3. For example, but not limited to the reinforcing zone(s) 4 could have a length of between 100-200 mm, preferably between 100-150 mm, a width of between 20-30 mm, preferably between 20-25 mm and a thickness between 15-30 mm, preferably between 15-25 mm.
  • In one embodiment >95%, preferably >98%, more preferably >99% of the WC grains in the reinforcing zones 4 have a triangular prismatic shape. Preferably, the WC grains are uniformly distributed in the manganese steel in the reinforcing zone(s).
  • In one embodiment, there are a plurality of reinforcing zones 4 with its interface zone 8 and the distance between two neighbouring reinforcing zones 4 with its interface layer 8 is between 1-5 mm, preferably between 1-3 mm, more preferably between 1-2 mm.
  • Figure 5 shows an example of a wear part 14 comprising the composite material 2 as described hereinabove or hereinafter. For example, the wear part 2 could be, but not limited to, a cone crusher or a stationary jaw crusher or a mobile jaw crusher that is configured to crush material or other material/rock processing unit. The reinforcing zone(s) 4 are positions on the wear parts 14 in the locations that are most subjected to high wear, for example on a crushing zone 18 of a cone crusher 16.
  • The method for producing the composite material 2 as described hereinbefore or hereinafter comprising the steps of: a) Mixing together 60-95 wt%, preferably 75-95 tungsten; 3-8 wt%, preferably 4-5% carbon and 0-40 %, preferably 10-20 % catalysis powders; b) compacting the mixed powders together to form at least one compact using a compacting pressure of between 400-700 MPa, preferably 500-600 MPa more preferably 550-600 MPa ; c) positioning and optionally fixing at least one compact into the interior of a mold; d) pouring molten casting manganese steel into the mold to surround the at least one compact to initiate a self-propagating high temperature synthesis (SHS) reaction to produce a cast; e) heat treating the cast; and then f) quenching the cast.
  • Preferably, the cast is treated at a temperature of between 1400-1500°C, the cast is quenched using water. Preferably, the catalysis is selected from Fe, Co, Ni, Mo, Cr, W, Al, or a mixture thereof. Carbon could be added in the form of graphite, amorphous graphite, a carbonaceous material or mixtures thereof. The compacts could for example be held in place using me a metallic fixation system to hold them in place during casting.
  • EXAMPLES Example 1 - Samples
  • Sample A is a comparative sample of non-reinforced manganese steel having the composition 1-1.5 % C, 11-14 % Mn, 0.4-0.8 % Si, 1.3-2.0 % Cr, 0.6 % Ni, 0.065 % P.
  • Samples B-K are samples of composite materials produced by mixing together powders of tungsten, carbon and a catalysis powder. The compacting the mixed powders to form compacts which were then positioned in a mold and then molten manganese steel having a composition of 1-1.5 % C, 11-14 % Mn, 0.4-0.8 % Si, 1.3-2.0 % Cr, 0.6 % Ni, 0.065 % was poured into the mold to surround the compacts which initiated a SHS reaction, the cast was then heat treated at a temperature of 1450 °C and then quenching with water. Table 1 shows a summary of the reinforced samples: Table 1: Summary of samples
    Sample Compacting pressure used (MPa) Average WC grain size in reinforced zone (µm) WC content in reinforced zone (wt%) Wettability (%)
    B (invention) 600 12 78 100
    C (comparative) 600 13 74 100
    D (comparative) 600 14 73 5
    E (comparative) 600 13 76 10
    F (comparative) 600 5 75 80
    H (invention) 600 10 86 100
    I (invention) 600 10 87 100
    J (comparative) 600 5 74 100
    K (invention) 600 7 90 100
  • It can be seen if the compacting pressure is not high enough then the wettability is reduced.
  • Example 2 - Hardness
  • Vickers hardness was measured by a micro-hardness tester, Matsuzawa, model MXT using 1 kgf and a holding time of 15 seconds. Hardness measurement profiles are performed starting from the non-reinforce zone, moving to the interface layer and then to the reinforced zone.
  • The hardness measurement results are shown in Table 2 below:
    Sample Hardness in manganese steel zone (HV1) Hardness in interface zone Hardness in reinforced zone
    A (comparative) 240 N/A N/A
    B (invention) 288 560 600
    C (comparative) 259 581 584
    E (comparative) - 572 619
    F (comparative) 253.5 576 609
    H (invention) 326.5 625 709
    I (invention) 261 611 731
    J (comparative) 241.7 521 582
    K (invention) 264.1 740 770
    Table 2: Hardness measurement
  • It can be seen that the inventive samples have an increased hardness in reinforced zones compared to the comparative samples.
  • Example 3 - Wear test
  • Wear was tested using a standard wear test using a lab jaw crusher. The wear test procedure consists on using fixed amount of rocks from 1 Ton up to 4 Ton of rocks. Four plates, two stationary and two moving, were placed inside the jaw crusher. Reference plates were also mounted in both positions. The reference plates are based on Weldox type of material.
  • The calculation of wear is based on the difference in volume loss of the test plates compared to the reference plates. All plates were weighed before and after wear test. Then volume loss is calculated using the density of 7.85 g/cm3 and 7.6 g/cm3 for the reference and test plates respectively. The total wear ratio (WR) is calculated according to ASTM G81-97a(2013).
  • The wear test results are shown in table 3 below: Table 3: Wear test results
    Sample Wear ratio rate
    C (comparative) 0.5
    K (inventive) 0.3
  • It can be seen that the wear rate for the inventive sample is reduced.
  • Example 4 - Defects
  • Table 4: Defects
    Sample Defects in the reinforced zone Defects in the interface layer Thickness of the interface layer (µm)
    B (inventive) none none 170
    C (comparative) pores cracks 93.5
    D (comparative) none cracks 0
    E (comparative) pores cracks 190
    F (comparative) none none 138.5
    H (inventive) none none 232
    I (inventive) none none 292
    J (comparative) none none 158
    K (inventive) none none 293
  • Defects were assessed by using Scanning Electron microscopy analysis where cracks and pores are identified. It can be seen that the inventive samples are free of defects.
  • Figure 6 shows an examples of cracking in the interface layer in comparative samples D and E, whereas figure 4 shows inventive sample K, where there is no cracking.
  • It can be seen from tables 1-4, that inventive samples have optimal grain sizes, optimal hardness, wear resistance, optimal interface layer thickness, good wettability and are free of cracks and pores, whereas the comparative samples have one or more of low hardness, non-optimal interface layer thickness, poor wettability, low wear resistance, pores and / or cracks.

Claims (13)

  1. A composite material (2) comprising:
    at least one reinforcing zone (4) comprising tungsten carbide (WC) and a manganese steel matrix;
    a manganese steel zone (6) that surrounds each of the reinforcing zones (4); and
    an interface layer (8) positioned between each of the reinforcing zones (4) and the manganese steel zone (6);
    characterized in that:
    the average grain size of the WC particles in each of the reinforcing zone(s) (4) is between 7-12 µm.
  2. The composite material (2) according to claim 1 wherein the wt% of WC in each of the reinforcing zones (4) is between 70-98.
  3. The composite material (2) according to claim 1 or claim 2 wherein the composition of the manganese steel in manganese steel zone (6) has the chemical composition by weight of:
    carbon: 0.5 to 2.0%;
    manganese: 11 to 22%;
    silicon: 0.2 to 1.0% ;
    chromium: 1 to 2%;
    nickel: up to 0.6%
    molybdenum: up to 0.5%
    and a balance of iron.
  4. The composite material (2) according to any of the previous claims wherein the hardness of the reinforcing zones (4) is between 580-780 HV1 and the hardness of the manganese steel zone (6) is between 200 - 300 HV1 before work hardening.
  5. The composite material (2) according to any of the previous claims wherein the thickness of each of the interface layer (6) is between 90-295 µm.
  6. The composite material (2) according to any of the previous claims wherein the interface layer 8 is free of defects.
  7. The composite material (2) according to any of the previous claims wherein wettability between the WC grains and the manganese steel in the reinforcing zones (4) is >99%.
  8. The composite material (2) according to any of the previous claims wherein each of the reinforcing zones has a volume of between 30-75 cm3.
  9. The composite material (2) according to any of the previous claims wherein at least 95% of the WC grains in the reinforcing zones (4) have a triangular prismatic shape.
  10. The composite material (2) according to any of the previous claims wherein there are a plurality of reinforcing zones (4) and the distance between two neighbouring reinforcing zones is between 1-5 mm.
  11. A wear part (14) comprising the composite material (2) according to any of claims 1-10.
  12. A method of producing the composite material (2) according to any of claims 1-10 comprising the steps of:
    a) mixing together 60-95wt% tungsten, 3-8 wt% carbon and 0-40 % catalysis powders;
    b) compacting the mixed powders together to form at least one compacts (20);
    c) positioning and optionally fixing at least one compact (20) into the interior of a mold (22);
    d) pouring molten casting manganese steel (24) into the mold (22) to surround the at least one compact (20) to initiate a self-propagating high temperature synthesis (SHS) reaction to produce a cast (26);
    e) heat treating the cast (26)
    f) quenching the cast (26)
    characterized in that:
    in step b) the powders are compacting with a pressure of between 400-700 mPa.
  13. The method according to claim 12 wherein the catalysis is selected from iron, cobalt, nickel, molybdenum, chromium, tungsten , aluminum or a mixture thereof.
EP21215683.0A 2021-12-17 2021-12-17 Tungsten carbide reinforced manganese steel Withdrawn EP4198156A1 (en)

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US18/719,416 US20250051887A1 (en) 2021-12-17 2022-12-15 Tungsten carbide reinforced manganese steel
EP22839250.2A EP4448819A1 (en) 2021-12-17 2022-12-15 Tungsten carbide reinforced manganese steel
CN202280082148.7A CN118339320A (en) 2021-12-17 2022-12-15 Tungsten carbide reinforced manganese steel
AU2022410342A AU2022410342A1 (en) 2021-12-17 2022-12-15 Tungsten carbide reinforced manganese steel
CA3239333A CA3239333A1 (en) 2021-12-17 2022-12-15 Tungsten carbide reinforced manganese steel
CL2024001807A CL2024001807A1 (en) 2021-12-17 2024-06-14 Manganese steel reinforced with tungsten carbide.

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180369905A1 (en) * 2015-11-12 2018-12-27 Innerco Sp. Z O.O. Powder Composition For The Manufacture Of Casting Inserts, Casting Insert And Method Of Obtaining Local Composite Zones In Castings
CN111455249A (en) * 2020-03-18 2020-07-28 内蒙古科技大学 Manganese steel-based complex-phase particle reinforced metal ceramic surface composite material, casting and manufacturing method thereof
WO2020222662A1 (en) 2019-04-30 2020-11-05 Innerco Sp. Z O.O, Composite material based on alloys, manufactured in situ, reinforced with tungsten carbide and methods of its production

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101376931A (en) * 2008-09-24 2009-03-04 上海大学 Preparation of cemented carbide containing block tabular tungsten carbide crystal grain
US10112200B2 (en) * 2015-04-29 2018-10-30 Spokane Industries Composite milling component
AU2020457247A1 (en) * 2020-07-07 2023-02-02 Sandvik Srp Ab A crushing or wear part having a localized composite wear zone
CN113416891B (en) * 2021-05-21 2022-07-08 宁国市开源电力耐磨材料有限公司 A wear-resistant excavator bucket tooth and its manufacturing process

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180369905A1 (en) * 2015-11-12 2018-12-27 Innerco Sp. Z O.O. Powder Composition For The Manufacture Of Casting Inserts, Casting Insert And Method Of Obtaining Local Composite Zones In Castings
WO2020222662A1 (en) 2019-04-30 2020-11-05 Innerco Sp. Z O.O, Composite material based on alloys, manufactured in situ, reinforced with tungsten carbide and methods of its production
CN111455249A (en) * 2020-03-18 2020-07-28 内蒙古科技大学 Manganese steel-based complex-phase particle reinforced metal ceramic surface composite material, casting and manufacturing method thereof

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