WO2020043718A1 - Modified high speed steel particle, powder metallurgy method using the same, and sintered part obtained therefrom - Google Patents

Modified high speed steel particle, powder metallurgy method using the same, and sintered part obtained therefrom Download PDF

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Publication number
WO2020043718A1
WO2020043718A1 PCT/EP2019/072829 EP2019072829W WO2020043718A1 WO 2020043718 A1 WO2020043718 A1 WO 2020043718A1 EP 2019072829 W EP2019072829 W EP 2019072829W WO 2020043718 A1 WO2020043718 A1 WO 2020043718A1
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Prior art keywords
weight
hss
particles
particle
modified
Prior art date
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PCT/EP2019/072829
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French (fr)
Inventor
Denis Oshchepkov
Christophe Szabo
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Höganäs Ab (Publ)
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Publication date
Priority to US17/269,164 priority Critical patent/US20210262050A1/en
Application filed by Höganäs Ab (Publ) filed Critical Höganäs Ab (Publ)
Priority to KR1020217008614A priority patent/KR20210038691A/en
Priority to EP19756210.1A priority patent/EP3844315A1/en
Priority to JP2021510771A priority patent/JP2021535282A/en
Priority to BR112021002876-5A priority patent/BR112021002876A2/en
Priority to CN201980056348.3A priority patent/CN112639150A/en
Publication of WO2020043718A1 publication Critical patent/WO2020043718A1/en

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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/005Heat treatment of ferrous alloys containing Mn
    • CCHEMISTRY; METALLURGY
    • 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
    • C22C33/0207Using a mixture of prealloyed powders or a master alloy
    • C22C33/0221Using a mixture of prealloyed powders or a master alloy comprising S or a sulfur compound
    • 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%
    • 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
    • C22C38/20Ferrous alloys, e.g. steel alloys containing chromium 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
    • C22C38/22Ferrous 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
    • C22C38/24Ferrous alloys, e.g. steel alloys containing chromium 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
    • C22C38/38Ferrous 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
    • C22C38/46Ferrous 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
    • C22C38/58Ferrous alloys, e.g. steel alloys containing chromium with nickel 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
    • C22C38/60Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
    • 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
    • B22F1/052Metallic powder characterised by the size or surface area of the particles characterised by a mixture of particles of different sizes or by the particle size distribution
    • 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
    • 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
    • B22F9/02Making metallic powder or suspensions thereof using physical processes
    • B22F9/06Making metallic powder or suspensions thereof using physical processes starting from liquid material
    • B22F9/08Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
    • B22F9/082Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/004Dispersions; Precipitations

Definitions

  • the present invention relates to particles made from a High Speed Steel (HSS) that is modified to contain dispersed precipitations of manganese sulfide (MHSS), and to a Powder Metallurgy (PM) method using the same. It also relates to a part produced by the PM process using the modified HSS particles.
  • HSS High Speed Steel
  • PM Powder Metallurgy
  • High Speed Steel is a highly alloyed steel and is conventionally used in a variety of applications due to its high hardness at high temperature, flexural strength and durability.
  • a typical application of HSS alloys is cutting equipment for machining apparatuses or valve seat inserts (VSI) for combustion engines.
  • VSI valve seat inserts
  • WO 93/19875 describes a method for the manufacture of a sintered ferrous-based material that comprises the steps of making a mixture of a ferrous-based powder, the mixture including a compound containing at least one metal from the group comprising manganese and the alkaline-earth series of metals; at least one sulphur donating material; pressing the powder mixture and sintering the pressed mixture so as to cause the formation by reaction during sintering of at least one stable metal sulfide within the sintered material. Materials and articles made by the method are also described.
  • the physical properties of the High Speed Steel, in particular strength, are not impaired at all as compared to a High Speed Steel not including the means of the present invention.
  • the part obtained from the PM should be suitable for applications that require final machining prior to use yet should possess properties that withstand harsh conditions of use, such as present in a combustion engine.
  • MnS is known to cause serious eye irritation, skin irritation for the human exposed to it (https://echa.europa.eu/registration- dossier/-/registered-dossier/10223/2/1. It is hence a further object of the present invention to provide a material that has improved machinability with a reduced health risk.
  • the present inventors found that forming a melt of a HSS and 1) Mn or a Mn- containing compound and 2) S or an S-containing compound, followed by an atomization process to form particles, is able to modify an HSS particle to contain dispersed sulfide precipitations containing mainly manganese sulfide.
  • the amount of Mn and S are chosen such that the weight ratio of Mn to S (Mn/S), in wt-% of the total weight of the particle, is in the range of 8.0 - 1.0, preferably 5.5 to 3.0, such as from 5.5 to 3.5 or from 5.5 to 4.1 .
  • manufacturing method using the particles has improved machinability as compared to a an article prepared from a corresponding non-modified HSS to which 1 ) Mn or a Mn-containing compound and 2) S or an S-containing compound were not added.
  • the physical properties of the article obtained from the modified HSS particles are not or not significantly impaired as compared to an article that is prepared from corresponding non-modified HSS particles.
  • the material of present invention does not contain free MnS particles therefore MnS dusting and abovementioned hazards are dramatically reduced.
  • a High Speed Steel (HSS) particle that is modified to contain dispersed precipitations of manganese sulfide, wherein the weight ratio of Mn to S (Mn/S), in wt-% of the total weight of the particle, is in the range of 8.0 - 1.0, preferably 5.5 to 3.0, such as from 5.5 to 3.5 or from 5.5 to 4.1.
  • High Speed Steel particle that is modified to contain dispersed
  • composition consisting of, in weight%,
  • HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to any one of items 1 to 3, wherein the total amount of Mn and S (Mn+S) is from 0.10 - 3.80 % by weight, preferably from 0.10 -3.00% by weight, further preferably from 0.20 - 2.50% by weight, such as from 0.30- 2.00 % by weight.
  • Method for forming a powder metallurgy product which comprises the steps of: a . Providing a multitude of particles as defined in any one of items 1 to 8; b . Compacting a composition comprising the particles to form a green part; c . Sintering the green part, and
  • step c optionally heat-treating the part obtained from step c;
  • forming particles from the melt preferably by water atomization or gas atomization.
  • a.3. optionally annealing the particles in vacuum, inert or reducing atmosphere.
  • Sintered part obtainable from the particles as defined by in any one of items 1 to 9 or by the process as defined in any one of items 9 and 10.
  • Sintered part according to item 1 1 which is a part for a combustion engine, preferably a valve seat insert.
  • any given range referred to by a lower and upper limit such as for example“2 to 5” or“between 2 and 5”, includes the lower and the upper value, as any value in between. Values greater than the lower limit or lower than the upper limit are explicitly included. The term is thus to be understood as abbreviation for the expression“[lower limit] or greater, but [upper limit] or lower”.
  • the lower and upper limits can be freely combined.
  • the phrase“5 to 10, preferably 6 to 8" also includes the ranges of 5 to 8 and 6 to 10.
  • the term“about” means that the amount or value in question may be the specific value designated or some other value in its neighborhood, generally within a range of ⁇ 5% of the indicated value. As such, for instance the phrase“about 100” denotes a range of 100 ⁇ 5, and the phrase“about 60” denotes a range of 60 ⁇ 3.
  • composition comprising certain components thus may comprise other components besides the ones listed.
  • the term also includes the more restrictive meanings“consisting of and“consisting essentially of.
  • Consisting essentially of allows for the presence of up to and including 10 weight%, preferably up to and including 5% of materials other than those listed for the respective composition, which other materials may also be completely absent. In the latter case, the composition“consists of the recited components.
  • High Speed Steel denotes an alloy as defined by its composition in Table 1 of ASTM 600-92a(2010), not including the Intermediate High Speed Steels M50 and M52, or an alloy having a composition as disclosed in W02009/040369, which is hereby incorporated in its entirety be reference.
  • This alloy may be in any form, e.g.
  • a pre-alloyed water atomized iron-based powder in the form of a pre-alloyed water atomized iron-based powder, and it has a composition comprising 10 to less than 18% by weight of Cr, 0.5 - 5 % by weight of at least one of Mo, W, V, and Nb, 0.5 - 2 % by weight, preferably 0.7 - 2 % by weight, more preferably 1 - 2 % by weight of C, optionally 0 - 2 % by weight of Si, the remainder being Fe.
  • the alloy according to this definition is not limited in structure, yet it may comprise a matrix containing less than 10% by weight of Cr, as well as large chromium carbides having an average size of 8 - 45 pm, preferably 8 - 30 pm, and smaller and harder chromium carbides having an average size of less than 8 pm.
  • the large chromium carbides are more preferably present in an amount of 10 - 30% by volume, and the smaller and harder chromium carbides are preferably present in an amount of 3 - 10% by volume.
  • a Modified High Speed Steel refers to an alloy that satisfies the compositions as defined in Table 1 of ASTM 600-92a(2010) or defined above with reference to W02009/040369 except for the amounts of manganese (Mn) and sulfur (S), which are higher for a modified High Speed Steel as compared to the corresponding High Speed Steel.
  • the present invention relates to a High Speed Steel (HSS) particle that is modified to contain dispersed precipitations of manganese sulfide.
  • HSS High Speed Steel
  • MHSS s Modified High Speed Steel
  • Such a particle can be obtained by the method of the present invention that will be described later, and is generally obtainable by adding Mn or an Mn-containing compound and S or an S-containing compound to a melt of HSS as defined in ASTM 600-92a(2010) or an alloy as disclosed above with reference to
  • Mn-containing compound and S-containing compound can be replaced by a compound containing both Mn and S, such as MnS. It is however necessary to form a homogeneous melt of the HSS and the material(s) that are added in order to increase the Mn and S content as compared to the HSS on which the MHSS is based, as adding MnS to HSS particles is unable to form the structure of the particles of the present invention containing dispersed precipitations of manganese sulfide.
  • the HSS on which the MHSS is based is not particular limited, but is in one embodiment preferably a M-type HSS, such as M2 (regular or high C), M3 (class 1 or class 2) or M35.
  • M2 regular or high C
  • M3 class 1 or class 2
  • M35 M35
  • Other HSS on which the MHSS may be bases include OB1 , available from Hoganas AB, Sweden, and T15.
  • the MHSS consists of, in weight%,
  • V 1.75 - 4.50, preferably 3.00-3.80
  • the unavoidable impurities include any element not listed above, such as P or Si.
  • the lower limit of Mn can also be 0.50, and/or the lower limit of S can also be 0.100.
  • the MHSS particle of the present invention has precipitations of manganese sulfide. This, however, does not mean that elements other than Mn and S are completely absent in these precipitations. If a precipitate is analyzed by e.g. SEM / EDS mapping on 50 or more precipitations (point analysis).
  • the amount of Mn is 40 at.% or more, in a normalized connotation wherein the amounts of the elements Si, S, V Cr, Mn, Fe, Mo and W (insofar present) form 100 at.%.
  • Si silicon
  • S vanadium
  • Mn manganese
  • Mo manganese
  • W insofar present
  • the size of the precipitations is not particularly limited, but is typically not too large in order not to disturb the structure of the HSS too much and to provide dispersed regions that are believed to improve machinability.
  • the longest axis of all precipitates, as observed by SEM on the surface of the particles, is typically 10 pm or less, such as 1 to 8 pm and typically from 1 to 5 or from 2 to 5 pm.
  • the total amount of Mn and S (Mn+S) is generally from 0.10 - 3.80 % by weight, preferably from 0.10 -3.00% by weight, further preferably from 0.20 - 2.50% by weight, such as from 0.30- 2.00 % by weight, relative to the weight of the MHSS particle.
  • the lower limit in each of these ranges can however also be 0.50, 0.60, 0.70, 0.80 or 0.90% by weight or more, such as 0.95% by weight or more.
  • the weight ratio of Mn to S i.e. weight of Mn / weight of S, in wt-% of the total weight of the MHSS particle
  • the first reason is that this ratio is required to obtain a proper structure. If the relative amount of Mn (i.e. the weight ratio of Mn to S) is too high, excess Mn may lead to distortions. If the ratio is too low, excess S may form sulfide layers at grain boundaries, which may potentially lead to an impairment of physical properties, such as rupture strength of an article obtained by a PM process using the MHSS particles.
  • the present inventors have surprisingly found that adjusting the ratio of Mn and S allows avoiding a substantial loss of sulfur from the melt, as would generally be expected due to the relatively high vapor pressure of sulfur at elevated temperatures.
  • the sulfur immediately reacts with (or associates with) the manganese. Thereby the amount of elementary sulfur that could get lost due to its high vapor pressure is thus minimized. This is turn avoids or minimizes the need for maintenance work for removing sublimed sulfur, lowers the environmental burden and also makes the MHSS cheaper and easier to produce.
  • the weight ratio of Mn to S (Mn/S), in wt-% of the total weight of the particle is in the range of 8.0 - 1.0, more preferably 5.5 to 3.0, such as from 5.5 to 3.5 or from 5.5 to 4.1.
  • the Mn content in HSS is mostly 0.15 - 0.40% by weight or less, depending on the type of HSS as listed in Table 1 of ASTM A600-92a (2010).
  • the Mn content is higher than that, and is in one embodiment 3.00% by weight or less, preferably 2.00 % by weight or less, but 0.41 % by weight or more, such as 0.45% by weight or more, or even 0.50% by weight or more or 0.75% by weight or more.
  • the amount of S is also higher as in corresponding HSS, wherein it is limited to 0.03% by weight.
  • the amount of S is 0.05 % by weight or higher, such as 0.10% by weight or higher or 0.15 % by weight or higher.
  • the upper limit is not particularly limited, but may be 0.50% by weight or lower, such as 0.30% by weight or lower or 0.25% by weight or lower.
  • HSS alloys contain more than one of Mo, W, V and Cr in different amounts, depending on the type of HSS.
  • the MHSS particle contains 4.00% by weight or more of at least one element selected from Mo, W, V and Cr, and in one embodiment contains 4.00% by weight or more of two or more of these elements.
  • the MHSS particle may contain 4.00 % by weight or more of each of Mo, W and Cr.
  • the MHSS particle of the present invention can be used in a PM manufacturing process, and to this end, a multitude of MHSS particles are needed.
  • 98% by weight or more of the particles have an particle size of 0 to 300 pm, wherein the amount of particles bigger than 300 pm is 2% by weight or less, as determined by sieve analysis according to IS04497:1983.
  • the amount of particles bigger than 300 mih can also be 1 % by weight or less, or such particles can be completely absent.
  • 98% by weight or more of the particles have a particle size of 0 to 200 pm and the amount of particles bigger than 200 pm is 2% by weight or less.
  • the amount of particles bigger than 200 pm can also be 1 % by weight or less, or such particles can be completely absent.
  • the MHSS particles of the present invention can be formed by providing a melt of the raw components, typically a commercially available HSS, S and Mn (or compounds comprising S and Mn), followed by atomization from the melt by a conventional technique.
  • the raw components may be HSS scrap, but could also involve virgin raw materials such as Fe, FeCr, FeV etc.
  • the atomization can be effected by e.g. gas atomization or water atomization, with water atomization being preferred.
  • the MHSS particles can be annealed in vacuum or protective atmosphere in order to reduce hardness and improve compressibility. Such an annealing can be conducted under conditions that are generally known, such as at 900-1 100 °C for 15-72 hours.
  • the MHSS particles are suitable for use in PM manufacturing process. They possess suitable powder compressibility and are able to provide a low dimensional change during sintering.
  • the method for forming a powder metallurgy product of the present invention comprises the steps: a . Providing a multitude of MHSS particles as described above;
  • step c optionally heat-treating the part obtained from step c;
  • step e optionally machining the sintered part obtained from step c. or from step d.
  • steps are conventional in the field of PM manufacturing methods. Any suitable conventional method can be employed in the present invention.
  • the composition referred to in step b. may consist of the MHSS particles only, but may optionally also contain other metal or alloy components, such us graphite powder (up to 1 %), iron powder, low alloyed iron powder, Cu powder, hard additives, such as Tribaloy, and may also contain other additives such as a glidant (e.g. amide wax) in an amount of e.g. 1 % by weight.
  • the MHSS particles of the present invention typically form 90% by weight or more, such as 95% by weight or more or 99% by weight or more of the composition of step b.
  • Sintering step“c” can optionally be carried out with the presence of an Cu based alloy.
  • Cu based alloy is placed in contact with the green part in the sintering furnace. At sintering temperature the infiltrating alloy is melted. The liquid Cu alloy will penetrate into the pores by capillary forces and form a nearly fully dense composite material. Infiltrating alloys typically contain at least 95% Cu and optionally further elements for improving infiltration behavior, as is well known in the art. Cu infiltration increases the hardness and strength of the final PM component and improves the thermal conductivity.
  • the sintered part of the present invention is a part that is obtainable by using a composition comprising or consisting of the MHSS particles as described above in a PM manufacturing process, e.g. the process described above.
  • the sintered part of the present invention obtainable by using the composition comprising or consisting of the MHSS particles as described above has improved machinability as compared to a sintered part made from the corresponding HSS under the same conditions. Surprisingly, the sintered part of the present invention has still very satisfactory properties. In particular, the sintered part may still have the same hardness and strength.
  • the present invention is particularly suitable for providing sintered parts (parts produced by a PM manufacturing method) for use under harsh conditions.
  • the sintered part of the present invention is thus in one embodiment a part for a combustion engine, such as a valve seat insert (VSI) or valve guide.
  • VSI valve seat insert
  • MHSS particles with the following compositions were prepared (balance: Fe and unavoidable impurities):
  • Melts of the materials were prepared by adding Mn and S to virgin materials, including Fe and alloy thereof such as ferrochromium, ferrovanadium,
  • the vacuum annealed powders were investigated by SEM. It was observed that precipitates of manganese sulfide having a longest axis of 2 - 5 pm had been formed.
  • the compacted parts (green parts) were then sintered at 1120°C for 20 minutes in nitrogen with Thereafter, the particles were sub-zero cooled dipping in liquid nitrogen for 20 minutes in order to transform retained austenite.
  • the machinability of the sintered parts was evaluated by using ring shaped samples of 55*45*15 mm under the following cutting parameters:
  • Sandvik CNGA120404T010208B material - CBN, radius of cutting tip: 0.4mm Cutting Depth: 0.4 mm
  • the material of Ref2 achieved cutting distance 2834 m until the tool tip was broken.
  • the MHSS material of Example 2 could be machined up to 6720 m. Tool tip wear was about 0.18 mm.
  • the machinability was evaluated in the same manner as in Examples 1 and 2.
  • the machinability was at the same level for Comp. Ex 2 as for Example 2.
  • Example 2 and Comp. Ex. 1 provided a tool life of at least 3 times as Ref 2.
  • admixing of MnS in Comparative Example 1 resulted in a considerable reduction of material strength, which was not observed for the material of Example 2.

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  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
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  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
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  • Crystallography & Structural Chemistry (AREA)
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Abstract

The present invention relates to particles made from a High Speed Steel (HSS) that is modified to contain dispersed precipitations of manganese sulfide (MHSS), and to a Powder Metallurgy (PM) method using the same. It also relates to a part produced by the PM process using the modified HSS particles. It has been found that by forming a melt of a HSS and 1 ) Mn or a Mn-containing compound and 2) S or an S-containing compound, followed by an atomization process, modified HSS particle can be obtained containing dispersed sulfide precipitations containing mainly manganese sulfide. The amount of Mn and S are chosen such that the weight ratio of Mn to S (Mn/S), in wt-% of the total weight of the particle, is in the range of 8.0 - 1.0, preferably 5.5 to 3.0, such as from 5.5 to 3.5 or from 5.5 to 4.1. An article obtained by a PM manufacturing method using the particles has improved machinability as compared to a an article prepared from a corresponding non-modified HSS to which 1) Mn or a Mn-containing compound and 2) S or an S-containing compound were not added. Surprisingly, the physical properties of the article obtained from the modified HSS particles are not or not significantly impaired as compared to an article that is prepared from corresponding non-modified HSS particles.

Description

MODIFIED HIGH SPEED STEEL PARTICLE, POWDER METALLURGY
METHOD USING THE SAME, AND SINTERED PART OBTAINED THEREFROM
Field of the Invention
The present invention relates to particles made from a High Speed Steel (HSS) that is modified to contain dispersed precipitations of manganese sulfide (MHSS), and to a Powder Metallurgy (PM) method using the same. It also relates to a part produced by the PM process using the modified HSS particles.
Background of the Invention
High Speed Steel is a highly alloyed steel and is conventionally used in a variety of applications due to its high hardness at high temperature, flexural strength and durability. A typical application of HSS alloys is cutting equipment for machining apparatuses or valve seat inserts (VSI) for combustion engines.
Due to its high hardness, machining or cutting of HSS itself is a costly and wear- intensive operation. Yet, such operations are typically required even for articles manufactured by powder metallurgy in order to obtain an article having exactly the required dimensions, such as for a VSI.
It is further known to add additives that improve machinability to alloys other than HSS. For instance, WO 93/19875 describes a method for the manufacture of a sintered ferrous-based material that comprises the steps of making a mixture of a ferrous-based powder, the mixture including a compound containing at least one metal from the group comprising manganese and the alkaline-earth series of metals; at least one sulphur donating material; pressing the powder mixture and sintering the pressed mixture so as to cause the formation by reaction during sintering of at least one stable metal sulfide within the sintered material. Materials and articles made by the method are also described.
Another approach is described in an article by L.G. Roy et al in“Prealloyed Mn/S powders for improved machinability in P/M parts”, Progress in Powder Metallurgy A. 1987, vol. 43, pp. 489-499. The authors describe the pre-alloyed Mn/S iron powder MP 37S and its predecessor MP 36S, from which it differs with respect to its higher Mn/S ratio. In these materials, Mn and S were added to form manganese sulphide (MnS) inclusions in order to improve the machinability of iron powders. These inclusions are deformed in the shear plane in the flow zone adjacent to a tool surface, they contribute to higher cutting speeds, longer tool life, good surface finish of machined parts, lower tool forces. However, the document also emphasizes that for powders used for PM processes, a variety of additional requirements need to be met, such as growth characteristics of the powder during sintering, as well as the mechanical properties of the sintered part. The authors thus investigated the effect of increasing the Mn/S ratio on the machinability, dimensional change and strength of the sintered part. From a chemical analysis, it was also found that the inclusions in MR 36S and MP37 not only contain MnS, but also MnFeO, Si02, S, and/or FeS.
For High Speed Steels, the high hardness and strength needs to be maintained. It is thus believed that adding additives that improve the machinability, such as M0S2 or MnS, may possibly improve machinability, but will at the same time be accompanied by an impairment of other properties, such as a reduction in hardness and strength.
Objects of the Invention
It is an object of the present invention to provide a means for improving the machinability of High Speed Steel materials, and to provide a High Speed Steel based material- having improved machinability.
It is a further object of the invention to provide a means for improving the machinability of High Speed Steel materials without significantly impairing the physical properties of the High Speed Steel. Preferably, the physical properties of the High Speed Steel, in particular strength, are not impaired at all as compared to a High Speed Steel not including the means of the present invention.
It is yet another object of the present invention to provide a material that is suitable for a Powder Metallurgy (PM) Manufacturing Process and a PM method using the same. The part obtained from the PM should be suitable for applications that require final machining prior to use yet should possess properties that withstand harsh conditions of use, such as present in a combustion engine. Manganese sulfide powder which is commonly used in powder metallurgy mixes for machinability improvement has mean particle size D50=4-6pm, for example MnS-E commercially produced by Hoganas AB. This makes the powder and mixes containing it very prone to dusting. MnS is known to cause serious eye irritation, skin irritation for the human exposed to it (https://echa.europa.eu/registration- dossier/-/registered-dossier/10223/2/1. It is hence a further object of the present invention to provide a material that has improved machinability with a reduced health risk.
Summary of the Invention
The present inventors found that forming a melt of a HSS and 1) Mn or a Mn- containing compound and 2) S or an S-containing compound, followed by an atomization process to form particles, is able to modify an HSS particle to contain dispersed sulfide precipitations containing mainly manganese sulfide. The amount of Mn and S are chosen such that the weight ratio of Mn to S (Mn/S), in wt-% of the total weight of the particle, is in the range of 8.0 - 1.0, preferably 5.5 to 3.0, such as from 5.5 to 3.5 or from 5.5 to 4.1 . An article obtained by a PM
manufacturing method using the particles has improved machinability as compared to a an article prepared from a corresponding non-modified HSS to which 1 ) Mn or a Mn-containing compound and 2) S or an S-containing compound were not added. Surprisingly, the physical properties of the article obtained from the modified HSS particles are not or not significantly impaired as compared to an article that is prepared from corresponding non-modified HSS particles.
The material of present invention does not contain free MnS particles therefore MnS dusting and abovementioned hazards are dramatically reduced.
The present invention includes the following aspects. Further aspects and features of the invention will become more apparent in view of the following detailed description.
1. A High Speed Steel (HSS) particle that is modified to contain dispersed precipitations of manganese sulfide, wherein the weight ratio of Mn to S (Mn/S), in wt-% of the total weight of the particle, is in the range of 8.0 - 1.0, preferably 5.5 to 3.0, such as from 5.5 to 3.5 or from 5.5 to 4.1. High Speed Steel particle that is modified to contain dispersed
precipitations of manganese sulfide according to item 1 , having a
composition consisting of, in weight%,
C: 0.75-1.40
Mn: 0.41-2.00
Si: 0.10-0.45
Cr: 3.75-5.00
Ni: up to 0.20
Mo: 4.50 - 6,50
W: 5.50-7.50
V: 1.75 - 4.50
Cu: up to 0.20
S: 0.050 - 0.300
the balance being Fe and unavoidable impurities in an amount of up to 0.5% by weight, preferably 0.2 % by weight. HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to item 1 , wherein the longest axis of the manganese sulfide precipitations is from 1 to 10 pm, as determined by SEM image analysis, preferably 1 to 8 pm, more preferably 1 to 5 pm. HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to any one of items 1 to 3, wherein the total amount of Mn and S (Mn+S) is from 0.10 - 3.80 % by weight, preferably from 0.10 -3.00% by weight, further preferably from 0.20 - 2.50% by weight, such as from 0.30- 2.00 % by weight.
HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to any one of items 1 to 4, wherein the amount of Mn in the overall particle is 3.00% by weight or less, preferably 2.00 % by weight or less. HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to any one of items 1 to 5, wherein the particle contains 4.00% by weight or more of at least one element selected from Mo, W, V and Cr. HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to any one of items 1 to 6, wherein the amount of S is 0.10% by weight or more, and the amount of Mn is 0.45% by weight or more. A multitude of HSS particles that are modified to contain dispersed precipitations of manganese sulfide as defined in any one of items 1 to 7, wherein 98% by weight or more of the particles have an particle size of 0 to 300 pm and wherein the a mount of particles bigger than 300 pm is 2% by weight or less, as determined by sieve analysis according to IS04497:1983; and wherein preferably 98% by weight or more of the particles have a particle size of 0 to 200pm and the amount of particles bigger than 200 pm is 2% by weight or less. Method for forming a powder metallurgy product, which comprises the steps of: a . Providing a multitude of particles as defined in any one of items 1 to 8; b . Compacting a composition comprising the particles to form a green part; c . Sintering the green part, and
d . optionally heat-treating the part obtained from step c; and
e . optionally machining the sintered part obtained from step c. or from step d. 10. A method for forming a powder metallurgy product according to item 9, wherein the step a. of providing the particles includes the steps of:
a.1-1 adding Mn or an Mn-containing compound and S or an S- containing compound to HSS material, and melting the obtained mixture; or a.1-2 adding Mn or an Mn-containing compound and S or an S- containing compound to a melt of HSS;
a.2. forming particles from the melt, preferably by water atomization or gas atomization.
a.3. optionally annealing the particles in vacuum, inert or reducing atmosphere.
11. Sintered part, obtainable from the particles as defined by in any one of items 1 to 9 or by the process as defined in any one of items 9 and 10.
12. Sintered part according to item 1 1 , which is a part for a combustion engine, preferably a valve seat insert.
13. Use of a combination of Mn or a Mn-containing compound and S or an S- containing compound for improving the machinability of products made from HSS, preferably powder metallurgy products, the use including the formation of dispersed precipitations of manganese sulfide in a HSS.
14. Use according to item 13, wherein the formation of dispersed precipitations of manganese sulfide in a HSS is achieved by forming a melt of HSS and Mn or a Mn-containing compound and S or an S-containing compound.
Definitions
The following terms and definitions will be used and apply in the following detailed description: Any given range referred to by a lower and upper limit, such as for example“2 to 5” or“between 2 and 5”, includes the lower and the upper value, as any value in between. Values greater than the lower limit or lower than the upper limit are explicitly included. The term is thus to be understood as abbreviation for the expression“[lower limit] or greater, but [upper limit] or lower”.
Whenever reference is made to ranges and more preferred ranges, the lower and upper limits can be freely combined. As one example, the phrase“5 to 10, preferably 6 to 8" also includes the ranges of 5 to 8 and 6 to 10.
In the present invention, all physical parameters are measured at room
temperature (20°C) and at atmospheric pressure (105Pa), unless indicated differently or prescribed differently by a standard such as ISO or ASTM. In case there should be a discrepancy between a standard method and the methods described and referred to in the following description, the present description prevails.
As used herein, the indefinite article“a” indicates one as well as more than one and does not necessarily limit its reference noun to the singular.
The term“about” means that the amount or value in question may be the specific value designated or some other value in its neighborhood, generally within a range of ±5% of the indicated value. As such, for instance the phrase“about 100” denotes a range of 100 ± 5, and the phrase“about 60” denotes a range of 60 ± 3.
The term and/or means that either all or only one of the elements indicated is present. For instance,“a and/or b” denotes“only a”, or“only b”, or“a and b together”. In the case of“only a” the term also covers the possibility that b is absent, i.e.“only a, but not b”.
The term“comprising” as used herein is intended to be non-exclusive and open- ended. A composition comprising certain components thus may comprise other components besides the ones listed. However, the term also includes the more restrictive meanings“consisting of and“consisting essentially of. The term “consisting essentially of allows for the presence of up to and including 10 weight%, preferably up to and including 5% of materials other than those listed for the respective composition, which other materials may also be completely absent. In the latter case, the composition“consists of the recited components.
In the present invention, the term High Speed Steel (HSS) denotes an alloy as defined by its composition in Table 1 of ASTM 600-92a(2010), not including the Intermediate High Speed Steels M50 and M52, or an alloy having a composition as disclosed in W02009/040369, which is hereby incorporated in its entirety be reference. This alloy may be in any form, e.g. in the form of a pre-alloyed water atomized iron-based powder, and it has a composition comprising 10 to less than 18% by weight of Cr, 0.5 - 5 % by weight of at least one of Mo, W, V, and Nb, 0.5 - 2 % by weight, preferably 0.7 - 2 % by weight, more preferably 1 - 2 % by weight of C, optionally 0 - 2 % by weight of Si, the remainder being Fe. The alloy according to this definition is not limited in structure, yet it may comprise a matrix containing less than 10% by weight of Cr, as well as large chromium carbides having an average size of 8 - 45 pm, preferably 8 - 30 pm, and smaller and harder chromium carbides having an average size of less than 8 pm. The large chromium carbides are more preferably present in an amount of 10 - 30% by volume, and the smaller and harder chromium carbides are preferably present in an amount of 3 - 10% by volume.
A Modified High Speed Steel (MHSS) refers to an alloy that satisfies the compositions as defined in Table 1 of ASTM 600-92a(2010) or defined above with reference to W02009/040369 except for the amounts of manganese (Mn) and sulfur (S), which are higher for a modified High Speed Steel as compared to the corresponding High Speed Steel.
Detailed Description of the Invention . Modified High Speed Steel particle
In one aspect, the present invention relates to a High Speed Steel (HSS) particle that is modified to contain dispersed precipitations of manganese sulfide. Such a particle is also referred to a s Modified High Speed Steel (MHSS) particle. Such a particle can be obtained by the method of the present invention that will be described later, and is generally obtainable by adding Mn or an Mn-containing compound and S or an S-containing compound to a melt of HSS as defined in ASTM 600-92a(2010) or an alloy as disclosed above with reference to
W02009/040369, or by melting HSS together with Mn or an Mn-containing compound and S or an S-containing compound, followed by atomization in order to form particles. Of course, the Mn-containing compound and the S-containing compound can be replaced by a compound containing both Mn and S, such as MnS. It is however necessary to form a homogeneous melt of the HSS and the material(s) that are added in order to increase the Mn and S content as compared to the HSS on which the MHSS is based, as adding MnS to HSS particles is unable to form the structure of the particles of the present invention containing dispersed precipitations of manganese sulfide.
The HSS on which the MHSS is based is not particular limited, but is in one embodiment preferably a M-type HSS, such as M2 (regular or high C), M3 (class 1 or class 2) or M35. Other HSS on which the MHSS may be bases include OB1 , available from Hoganas AB, Sweden, and T15.
In one embodiment, the MHSS consists of, in weight%,
C: 0.75 - 1.40, preferably 1.00-1.25
Mn: 0.41-2.00
Si 0.10-0.45
Cr 3.75-5.00
Ni: up to 0.20
Mo: 4.50 - 6.50, preferably 5.00-6.50
W: 5.50-7.50
V: 1.75 - 4.50, preferably 3.00-3.80
Cu: up to 0.20
S: 0.050 - 0.300 the balance being Fe and unavoidable impurities in an amount 0.5% by weight or less, preferably 0.2 % by weight or less. Herein, the unavoidable impurities include any element not listed above, such as P or Si. The lower limit of Mn can also be 0.50, and/or the lower limit of S can also be 0.100. The MHSS particle of the present invention has precipitations of manganese sulfide. This, however, does not mean that elements other than Mn and S are completely absent in these precipitations. If a precipitate is analyzed by e.g. SEM / EDS mapping on 50 or more precipitations (point analysis). In such an SEM/EDS mapping, the amount of Mn is 40 at.% or more, in a normalized connotation wherein the amounts of the elements Si, S, V Cr, Mn, Fe, Mo and W (insofar present) form 100 at.%. Herein, Fe typically forms 15 to 25 at.%, and S typically forms 25 - 35 at.%.
The size of the precipitations is not particularly limited, but is typically not too large in order not to disturb the structure of the HSS too much and to provide dispersed regions that are believed to improve machinability. The longest axis of all precipitates, as observed by SEM on the surface of the particles, is typically 10 pm or less, such as 1 to 8 pm and typically from 1 to 5 or from 2 to 5 pm.
The total amount of Mn and S (Mn+S) is generally from 0.10 - 3.80 % by weight, preferably from 0.10 -3.00% by weight, further preferably from 0.20 - 2.50% by weight, such as from 0.30- 2.00 % by weight, relative to the weight of the MHSS particle. The lower limit in each of these ranges can however also be 0.50, 0.60, 0.70, 0.80 or 0.90% by weight or more, such as 0.95% by weight or more.
It has been found that the weight ratio of Mn to S (i.e. weight of Mn / weight of S, in wt-% of the total weight of the MHSS particle) is of relevance for at least the following two reasons.
The first reason is that this ratio is required to obtain a proper structure. If the relative amount of Mn (i.e. the weight ratio of Mn to S) is too high, excess Mn may lead to distortions. If the ratio is too low, excess S may form sulfide layers at grain boundaries, which may potentially lead to an impairment of physical properties, such as rupture strength of an article obtained by a PM process using the MHSS particles.
Secondly, the present inventors have surprisingly found that adjusting the ratio of Mn and S allows avoiding a substantial loss of sulfur from the melt, as would generally be expected due to the relatively high vapor pressure of sulfur at elevated temperatures. Without wishing to be bound by theory, it is believed that when there is an sufficiently enough manganese in relation to sulfur, the sulfur immediately reacts with (or associates with) the manganese. Thereby the amount of elementary sulfur that could get lost due to its high vapor pressure is thus minimized. This is turn avoids or minimizes the need for maintenance work for removing sublimed sulfur, lowers the environmental burden and also makes the MHSS cheaper and easier to produce.
For the above at least two reasons, the weight ratio of Mn to S (Mn/S), in wt-% of the total weight of the particle, is in the range of 8.0 - 1.0, more preferably 5.5 to 3.0, such as from 5.5 to 3.5 or from 5.5 to 4.1.
The Mn content in HSS is mostly 0.15 - 0.40% by weight or less, depending on the type of HSS as listed in Table 1 of ASTM A600-92a (2010). In the MHSS particle of the present invention, the Mn content is higher than that, and is in one embodiment 3.00% by weight or less, preferably 2.00 % by weight or less, but 0.41 % by weight or more, such as 0.45% by weight or more, or even 0.50% by weight or more or 0.75% by weight or more.
In the MHSS particle, the amount of S is also higher as in corresponding HSS, wherein it is limited to 0.03% by weight. In one embodiment of the present invention, the amount of S is 0.05 % by weight or higher, such as 0.10% by weight or higher or 0.15 % by weight or higher. The upper limit is not particularly limited, but may be 0.50% by weight or lower, such as 0.30% by weight or lower or 0.25% by weight or lower.
HSS alloys contain more than one of Mo, W, V and Cr in different amounts, depending on the type of HSS. In one embodiment of the present invention, the MHSS particle contains 4.00% by weight or more of at least one element selected from Mo, W, V and Cr, and in one embodiment contains 4.00% by weight or more of two or more of these elements. For instance, the MHSS particle may contain 4.00 % by weight or more of each of Mo, W and Cr.
The MHSS particle of the present invention can be used in a PM manufacturing process, and to this end, a multitude of MHSS particles are needed. In one embodiment of the multitude of MHSS particles of the present invention, 98% by weight or more of the particles have an particle size of 0 to 300 pm, wherein the amount of particles bigger than 300 pm is 2% by weight or less, as determined by sieve analysis according to IS04497:1983.The amount of particles bigger than 300 mih can also be 1 % by weight or less, or such particles can be completely absent.
In one embodiment, 98% by weight or more of the particles have a particle size of 0 to 200 pm and the amount of particles bigger than 200 pm is 2% by weight or less. The amount of particles bigger than 200 pm can also be 1 % by weight or less, or such particles can be completely absent.
The MHSS particles of the present invention can be formed by providing a melt of the raw components, typically a commercially available HSS, S and Mn (or compounds comprising S and Mn), followed by atomization from the melt by a conventional technique. The raw components may be HSS scrap, but could also involve virgin raw materials such as Fe, FeCr, FeV etc. The atomization can be effected by e.g. gas atomization or water atomization, with water atomization being preferred.
The MHSS particles can be annealed in vacuum or protective atmosphere in order to reduce hardness and improve compressibility. Such an annealing can be conducted under conditions that are generally known, such as at 900-1 100 °C for 15-72 hours.
The MHSS particles are suitable for use in PM manufacturing process. They possess suitable powder compressibility and are able to provide a low dimensional change during sintering.
2. Method for forming a powder metallurgy product
The method for forming a powder metallurgy product of the present invention comprises the steps: a . Providing a multitude of MHSS particles as described above;
b . Compacting a composition comprising the particles to form a green part; c . Sintering the green part, and
d . optionally heat-treating the part obtained from step c; and
e . optionally machining the sintered part obtained from step c. or from step d. Other than the MHSS particles described above, the steps are conventional in the field of PM manufacturing methods. Any suitable conventional method can be employed in the present invention.
The composition referred to in step b. may consist of the MHSS particles only, but may optionally also contain other metal or alloy components, such us graphite powder (up to 1 %), iron powder, low alloyed iron powder, Cu powder, hard additives, such as Tribaloy, and may also contain other additives such as a glidant (e.g. amide wax) in an amount of e.g. 1 % by weight. The MHSS particles of the present invention typically form 90% by weight or more, such as 95% by weight or more or 99% by weight or more of the composition of step b.
Sintering step“c” can optionally be carried out with the presence of an Cu based alloy. In this case Cu based alloy is placed in contact with the green part in the sintering furnace. At sintering temperature the infiltrating alloy is melted. The liquid Cu alloy will penetrate into the pores by capillary forces and form a nearly fully dense composite material. Infiltrating alloys typically contain at least 95% Cu and optionally further elements for improving infiltration behavior, as is well known in the art. Cu infiltration increases the hardness and strength of the final PM component and improves the thermal conductivity.
3. Sintered part
The sintered part of the present invention is a part that is obtainable by using a composition comprising or consisting of the MHSS particles as described above in a PM manufacturing process, e.g. the process described above.
The sintered part of the present invention obtainable by using the composition comprising or consisting of the MHSS particles as described above has improved machinability as compared to a sintered part made from the corresponding HSS under the same conditions. Surprisingly, the sintered part of the present invention has still very satisfactory properties. In particular, the sintered part may still have the same hardness and strength.
Due to these beneficial properties, the present invention is particularly suitable for providing sintered parts (parts produced by a PM manufacturing method) for use under harsh conditions. The sintered part of the present invention is thus in one embodiment a part for a combustion engine, such as a valve seat insert (VSI) or valve guide.
Examples Examples 1 and 2
MHSS particles with the following compositions were prepared (balance: Fe and unavoidable impurities):
Table 1 :
Chemical Composition of MHSS particles of Examples 1 and 2
Figure imgf000015_0001
Melts of the materials were prepared by adding Mn and S to virgin materials, including Fe and alloy thereof such as ferrochromium, ferrovanadium,
ferrotungsten and ferromolybdenum and melting the composition, followed by atomization and sieving using a -212 pm screen. Reference materials, in the following referred to as Ref1 and Ref2, were prepared in the same manner, except for no addition of Mn and S. The powders were vacuum annealed. The particles had the following particle size distribution:
Table 2:
Figure imgf000015_0002
The vacuum annealed powders were investigated by SEM. It was observed that precipitates of manganese sulfide having a longest axis of 2 - 5 pm had been formed.
An elemental mapping (point chemical analysis) using EDS was performed on more than 200 precipitates. The following results were obtained:
Table 3:
Composition of precipitations in Examples 1 and 2 (at.-%, normalized)
Figure imgf000016_0002
25 kg of the powders of Examples 1 and 2 and of the non-modified HSS powders were admixed with 1 % amide wax as a lubricant and used in a PM manufacturing process. The compressibility of modified and non-modified HSS particles was identical, compacted parts showing similar porosities after compaction at 800 MPa and 50°C.
The compacted parts (green parts) were then sintered at 1120°C for 20 minutes in nitrogen with
Figure imgf000016_0001
Thereafter, the particles were sub-zero cooled dipping in liquid nitrogen for 20 minutes in order to transform retained austenite.
Thereafter, a final tempering at 560°C in N2 was performed for 2 hours.
The dimensional change and the hardness of the sintered materials obtained from the MHSS particles (Examples 1 and 2) and the corresponding HSS particles (Ref1 and Ref2) are shown in Table 4 below. Table 4:
Properties of sintered parts
Figure imgf000017_0001
The hardness values given in Table 4 overlap in their margin of error (± 15). It is thus concluded that the modification of the present invention does not impair important properties of the sintered part, including hardness. Further, all sintered parts obtained from the MHSS of Examples 1 and 2 showed similar porosity as compared to the sintered part obtained from the respective reference particles made from HSS without addition of Mn or S.
The machinability of the sintered parts was evaluated by using ring shaped samples of 55*45*15 mm under the following cutting parameters:
Cutting Tool:
Sandvik CNGA120404T010208B, material - CBN, radius of cutting tip: 0.4mm Cutting Depth: 0.4 mm
Cutting Speed: 120 m/minute
Radial Feed Rate: 0.07 mm/rev.
The wear (mm) of the tool tip wear or breakage was used as a criterion for machinability. The test was repeated two times for each material. The results are given in Table 5.
Table 5:
Results of machinability evaluation.
Figure imgf000018_0001
The material of Ref2 achieved cutting distance 2834 m until the tool tip was broken. The MHSS material of Example 2 could be machined up to 6720 m. Tool tip wear was about 0.18 mm.
The material of Ref1 could not be machined given that the tool tip was broken shortly after beginning of the test. A variation in the cutting conditions to 400 m/min and a reduction of the radial feed rate could slightly improve the situation, but still the tip broke after 48 cuts (538 m, data shown in Table 5). Comparative Example 1
In order to evaluate whether the addition of MnS to particles of HSS has the same effect, the HSS material of Ref2 was admixed with MnS powder (D50 = 5 pm) to prepare the powder of Comp. Ex. 1. Then, sintered parts were prepared in the same manner as described above. The following results were obtained:
Table 6:
Properties of materials after sintering and heat treatment
Figure imgf000019_0001
The machinability was evaluated in the same manner as in Examples 1 and 2. The machinability was at the same level for Comp. Ex 2 as for Example 2. Example 2 and Comp. Ex. 1 provided a tool life of at least 3 times as Ref 2. Yet, admixing of MnS in Comparative Example 1 resulted in a considerable reduction of material strength, which was not observed for the material of Example 2.

Claims

Claims
1. A High Speed Steel (HSS) particle that is modified to contain dispersed
precipitations of manganese sulfide, wherein the weight ratio of Mn to S (Mn/S), in wt-% of the total weight of the particle, is in the range of 8.0 - 1.0, preferably 5.5 to 3.0, such as from 5.5 to 3.5 or from 5.5 to 4.1 .
2. High Speed Steel particle that is modified to contain dispersed precipitations of manganese sulfide according to claim 1 , having a composition consisting of, in weight%,
C: 0.75-1.40
Mn: 0.41 -2.00
Si: 0.10-0.45
Cr: 3.75-5.00
Ni: up to 0.20
Mo: 4.50 - 6,50
W: 5.50-7.50
V: 1.75 - 4.50
Cu: up to 0.20
S: 0.050 - 0.300
the balance being Fe and unavoidable impurities in an amount of up to 0.5% by weight, preferably 0.2 % by weight.
3. HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to claim 1 , wherein the longest axis of the manganese sulfide precipitations is from 1 to 10 pm, as determined by SEM image analysis, preferably 1 to 8 pm, more preferably 1 to 5 pm.
4. HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to any one of claims 1 to 3, wherein the total amount of Mn and S (Mn+S) is from 0.10 - 3.80 % by weight, preferably from 0.10 -3.00% by weight, further preferably from 0.20 - 2.50% by weight, such as from 0.30- 2.00 % by weight.
5. HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to any one of claims 1 to 4, wherein the amount of Mn in the overall particle is 3.00% by weight or less, preferably 2.00 % by weight or less.
6. HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to any one of claims 1 to 5, wherein the particle contains 4.00% by weight or more of at least one element selected from Mo, W, V and Cr.
7. HSS particle that is modified to contain dispersed precipitations of manganese sulfide according to any one of claims 1 to 6, wherein the amount of S is 0.10% by weight or more, and the amount of Mn is 0.45% by weight or more.
8. A multitude of HSS particles that are modified to contain dispersed
precipitations of manganese sulfide as defined in any one of claims 1 to 7, wherein 98% by weight or more of the particles have an particle size of 0 to 300 pm and wherein the a mount of particles bigger than 300 pm is 2% by weight or less, as determined by sieve analysis according to IS04497:1983; and wherein preferably 98% by weight or more of the particles have a particle size of 0 to 200pm and the amount of particles bigger than 200 pm is 2% by weight or less.
9. Method for forming a powder metallurgy product, which comprises the steps of: a. Providing a multitude of particles as defined in any one of claims 1 to 8; b. Compacting a composition comprising the particles to form a green part; c. Sintering the green part, and
d. optionally heat-treating the part obtained from step c; and
e. optionally machining the sintered part obtained from step c. or from step d.
10. A method for forming a powder metallurgy product according to claim 9,
wherein the step a. of providing the particles includes the steps of: a.1 -1 adding Mn or an Mn-containing compound and S or an S- containing compound to HSS material, and melting the obtained mixture; or a.1 -2 adding Mn or an Mn-containing compound and S or an S- containing compound to a melt of HSS;
a.2. forming particles from the melt, preferably by water atomization or gas atomization.
a.3. optionally annealing the particles in vacuum, inert or reducing atmosphere.
1 1. Sintered part, obtainable from the particles as defined by in any one of claims 1 to 9 or by the process as defined in any one of claims 9 and 10.
12. Sintered part according to claim 1 1 , which is a part for a combustion engine, preferably a valve seat insert.
13. Use of a combination of Mn or a Mn-containing compound and S or an S- containing compound for improving the machinability of products made from HSS, preferably powder metallurgy products, the use including the formation of dispersed precipitations of manganese sulfide in a HSS.
14. Use according to claim 13, wherein the formation of dispersed precipitations of manganese sulfide in a HSS is achieved by forming a melt of HSS and Mn or a Mn-containing compound and S or an S-containing compound.
PCT/EP2019/072829 2018-08-31 2019-08-27 Modified high speed steel particle, powder metallurgy method using the same, and sintered part obtained therefrom WO2020043718A1 (en)

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BR112021002876-5A BR112021002876A2 (en) 2018-08-31 2019-08-27 modified high speed steel particle, powder metallurgy method using the same, and sintered part obtained therefrom
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