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EP1079950A1 - Poudres de metal et d'alliage pour le frittage, a utiliser dans la metallurgie des poudres, leur procede de production et leur utilisation - Google Patents

Poudres de metal et d'alliage pour le frittage, a utiliser dans la metallurgie des poudres, leur procede de production et leur utilisation

Info

Publication number
EP1079950A1
EP1079950A1 EP99923562A EP99923562A EP1079950A1 EP 1079950 A1 EP1079950 A1 EP 1079950A1 EP 99923562 A EP99923562 A EP 99923562A EP 99923562 A EP99923562 A EP 99923562A EP 1079950 A1 EP1079950 A1 EP 1079950A1
Authority
EP
European Patent Office
Prior art keywords
metal
carboxylic acid
aqueous
alloy powder
precipitation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP99923562A
Other languages
German (de)
English (en)
Other versions
EP1079950B1 (fr
Inventor
Bernd Mende
Gerhard Gille
Benno Gries
Peter Aulich
Jörg MÜNCHOW
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
HC Starck GmbH
Original Assignee
HC Starck GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by HC Starck GmbH filed Critical HC Starck GmbH
Publication of EP1079950A1 publication Critical patent/EP1079950A1/fr
Application granted granted Critical
Publication of EP1079950B1 publication Critical patent/EP1079950B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00—Making metallic powder or suspensions thereof
    • B22F9/16—Making metallic powder or suspensions thereof using chemical processes
    • B22F9/18—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
    • B22F9/20—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from solid metal compounds
    • B22F9/22—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from solid metal compounds using gaseous reductors
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy

Definitions

  • the present invention relates to metal powder consisting of one or more of the elements Fe, Ni, Co, Cu, Sn and possible additions of Al, Cr, Mn, Mo and W, a process for their preparation and their use.
  • Alloy powders have diverse applications for the production of sintered materials by powder metallurgy.
  • the main feature of powder metallurgy is that corresponding powdered alloy or metal powder is pressed and then sintered at an elevated temperature.
  • This method has been introduced on an industrial scale for the production of complicated molded parts that can otherwise only be produced with a high degree of elaborate finishing.
  • the sintering can be carried out as solid phase sintering or to form a liquid phase, e.g. with hard or heavy metals.
  • a very important application of alloy and pure metal powders are tools for metal, stone and wood processing. In these cases, it is a matter of two-phase materials, whereby the hardness carriers (e.g. carbides or diamonds) are embedded in a metallic matrix, which ensures the required toughness properties of these
  • the element cobalt plays a special role because it is used as a metallic matrix
  • Diamond and carbide tools have some special properties. Because it wets tungsten carbide and diamonds particularly well, it is traditionally preferred for both types of tools.
  • the use of cobalt for the metallic binder phase in composite materials based on tungsten carbide or diamond achieves particularly good adhesion of the hardness carrier in the metallic binder phase. What is important here is the fact that in the case of cobalt the tendency for the formation of carbides of the type Co3W3C ("eta phases"), which lead to embrittlement in hard metals, is less pronounced than, for example, in the case of iron. Co also attacks diamonds less than, for example, iron, which easily forms Fe 3 C. For these technical reasons, cobalt is traditionally used in the carbide and diamond tool industry.
  • cobalt metal powders 0.8 to 2 ⁇ m FSSS (ASTM B330) are generally used, which together with the hard materials, pressing aids and a grinding fluid are subjected to mixed grinding in air gates or ball mills, which contain hard metal balls as grinding media become.
  • the suspension obtained is then separated from the grinding media, spray-dried, and the granules obtained are pressed into molds.
  • the subsequent liquid phase sintering at temperatures above the melting point of the W-Co-C eutectic results in dense sintered bodies (hard metals).
  • An important property of the hard metals produced in this way is their strength
  • Porosity is weakened.
  • Industrial hard metals have a porosity better than or equal to A02B00C00 according to ASTM B276 (or DIN ISO 4505).
  • the A-porosity is the microporosity
  • the B-porosity is the macroporosity.
  • cobalt metal powders are ductile and are not crushed during mixed grinding, but plastically deformed or the existing agglomerates disassembled. If the cobalt metal powder used contains large, sintered, large agglomerates, they are transferred into the spray granules in deformed form and result in A and B porosity in the sintered hard metal, often associated with local enrichment of the binder phase.
  • Diamond tools as a second important application group contain sintered parts (segments) as cutting or grinding active components, which consist mainly of diamonds, embedded in a metallic binder phase, mainly cobalt.
  • sintered parts consist mainly of diamonds, embedded in a metallic binder phase, mainly cobalt.
  • hard materials or other metal powders are optionally added to match the wear behavior of the bond on the diamond and the materials to be machined.
  • segments Metal powder, diamonds and possibly hard material powder mixed, optionally granulated and densely sintered in hot presses at elevated pressure and temperature.
  • the requirements placed on the binder metal powder in addition to the necessary chemical purity are: good compactibility, the highest possible sintering activity, one that is tailored to the diamond and the medium to be processed
  • the porosity decreases with increasing sintering temperature, i.e. the density of the
  • Binding after sintering is very inhomogeneous, since the sintering temperature and time at Homogenization is not enough.
  • high pressing forces occur, which wear out the pressing tools and lead to low strengths of the green compacts (eg edge breakouts).
  • This is also due to the cubic, body-centered grating type of iron, which has fewer sliding planes than the cubic, face-centering types of cobalt and
  • Nickel or copper metal powder contains high amounts of carbon, which can lead to a loss of strength in the segment.
  • Atomized metal powders or alloys do not have sufficient sintering activity, so that the temperatures that are acceptable for diamonds are still insufficiently compacted.
  • the object of the invention is to provide metal and alloy powders containing at least one of the metals iron, copper, tin, cobalt or nickel which meet the requirements mentioned for binder metals for hard metals and diamond tools.
  • the metal and alloy powders according to the invention can be modified by doping with the elements Al, Cr, Mn, Mo and / or W in a minor amount and adapted to special requirements.
  • the invention firstly relates to a method for producing the metal
  • Alloy powder by mixing aqueous metal salt solutions with a carboxylic acid solution, separating the precipitate from the mother liquor and
  • the precipitate is preferably washed with water and dried.
  • the precipitation product is preferably reduced in a hydrogen-containing atmosphere at temperatures between 400 and 600 ° C.
  • the reduction can take place in the indirectly heated rotary kiln or in the push-through furnace with little bed cover.
  • Other options for carrying out the reduction are readily known to the person skilled in the art, such as in the deck oven or in the fluidized bed.
  • the dried precipitation product is calcined at temperatures between 250 and 500 ° C. before the reduction in an oxygen-containing atmosphere.
  • the calcination has the effect that the precipitation product consisting of polycrystalline particles or agglomerates is comminuted by the gases released during the decomposition of the carboxylic acid residue by decrepitation, so that a larger surface area is available for the subsequent gas phase reaction (reduction) and a finer end product is obtained.
  • calcination in an oxygen-containing atmosphere results in the formation of a metal or alloy powder which has a significantly reduced porosity compared to direct reduction.
  • the (mixed) metal carboxylic acid salt is converted to the metal or alloy powder, there is a considerable reduction in the volume of the particles, which leads to the inclusion of pores.
  • the (mixed) metal carboxylic acid salt is first converted into the (mixed) metal oxide and annealed, so that pre-compression takes place with the healing of lattice defects.
  • the subsequent reduction in a hydrogen-containing atmosphere only the volume shrinkage from oxide to metal has to be overcome.
  • the intermediate calcination step leads to a gradual volume shrinkage achieved, each with structural stabilization of the crystals after each shrinkage stage.
  • Suitable carboxylic acids are aliphatic or aromatic, saturated or unsaturated mono- or dicarboxylic acids, in particular those with 1 to 8 carbon atoms. Because of their reducing effect, formic acid, oxalic acid, acrylic acid and crotonic acid are preferred, and because of their availability, formic and oxalic acid in particular. Oxalic acid is particularly preferably used. The excess of reducing carboxylic acids prevents the formation of Fe (III) ions, which would lead to problems during the precipitation.
  • the carboxylic acid is preferably used in a 1.1- to 1.6-fold stoichiometric excess, based on the metals. A 1.2- to 1.5-fold excess is particularly preferred.
  • the carboxylic acid solution is used as a suspension which contains undissolved carboxylic acid in suspension.
  • the preferably used carboxylic acid suspension contains a deposit of undissolved carboxylic acid, from which the carboxylic acid withdrawn by precipitation of the solution is replaced, so that a high concentration of carboxylic acid is maintained in the mother liquor throughout the precipitation reaction.
  • the concentration of dissolved carboxylic acid in the mother liquor should preferably be at least 20% of the saturation concentration of the carboxylic acid in water at the end of the precipitation reaction.
  • the concentration of dissolved carboxylic acid in the mother liquor should particularly preferably still be 25 to 50% of the saturation concentration of the carboxylic acid in water.
  • a chloride solution is preferably used as the metal salt solution.
  • the concentration of the metal salt solution is preferably about 1.6 to 2.5 mol per liter.
  • the metal salt solution preferably has a content of 10 to 90% by weight of iron, based on the total metal content and at least one further of the elements Copper, tin, nickel or cobalt.
  • the content of iron in the metal salt solution is particularly preferably at least 20% by weight, more preferably at least 25% by weight, very particularly preferably at least 50% by weight, but less than 80% by weight, very particularly preferably less than 60 wt .-%, each based on the total metal content.
  • the metal salt solutions further preferably contain 10 to 70% by weight, particularly preferably up to 45% by weight, of cobalt, based on the total metal content.
  • the nickel content of the metal salt solution is preferably 0 to 50% by weight, particularly preferably up to 16% by weight.
  • Copper and / or tin can be used in amounts of up to 30% by weight, preferably up to 10% by weight, based on the total metal content.
  • the metal salt solution is gradually added to the carboxylic acid suspension in the
  • the metal salt solution is particularly preferably added gradually such that the concentration of dissolved carboxylic acid does not fall below 80% of the solubility in until the suspended carboxylic acid has dissolved
  • a concentrated carboxylic acid solution has "activity 1", and only a half-concentrated carboxylic acid solution has "activity 0.5".
  • the activity of the mother liquor should accordingly preferably not fall below 0.8 during the addition of the metal salt solution.
  • the solubility of the oxalic acid which is preferably used in water is approximately 1 mol per liter of water (room temperature), corresponding to 126 g of oxalic acid (2 molecules of water of crystallization).
  • the oxalic acid should be introduced as an aqueous suspension which contains 2.3 to 4.5 mol of oxalic acid per liter of water.
  • This suspension contains about 1.3 to 3.5 moles of undissolved oxalic acid per liter of water.
  • the content of oxalic acid in the mother liquor should still be 20 to 55 g / l of water.
  • the oxalic acid consumed for the precipitation is constantly replaced by the dissolution of suspended oxalic acid.
  • the mother liquor is constantly stirred to homogenize it.
  • the metal salt solution is added gradually such that the oxalic acid concentration in the mother liquor does not drop below 75 g, particularly preferably not less than 100 g, per liter of mother liquor during the addition. This has the effect that a sufficiently high supersaturation is constantly achieved during the addition of the metal salt solution
  • Nucleation i.e. is sufficient to generate further precipitation particles. This on the one hand ensures a high nucleation rate, which leads to correspondingly small particle sizes, and on the other hand largely prevents agglomeration of the particles due to dissolution due to the low metal ion concentration present in the mother liquor.
  • the high carboxylic acid concentration, which is preferred according to the invention, during the precipitation also has the effect that the precipitation product has the same composition as the metal salt solution in terms of the relative contents of metals, i.e. that there is a homogeneous precipitation product with respect to its composition and thus alloy metal powder.
  • the invention further relates to metal and alloy powders which contain at least one of the elements iron, copper, tin, nickel or cobalt and which can optionally be doped in a minor amount by one or more of the elements Al, Cr, Mn, Mo, W. , and the average grain size according to ASTM B330 (FSSS) from 0.5 to 5 ⁇ , preferably below 3 ⁇ m.
  • the alloy powders according to the invention are characterized in that they have no fracture surfaces produced by grinding. They are available with this grain size immediately after reduction.
  • Preferred metal or alloy particles according to the invention have a very low carbon content of less than
  • Metal or alloy powders preferred according to the invention furthermore have an oxygen content of less than 1% by weight, preferably less than 0.5% by weight.
  • the preferred composition of the alloy powders according to the invention corresponds to the preferred relative metal contents of the metal salt solutions used, as stated above.
  • the metal and alloy powders according to the invention are outstandingly suitable as binder metals for hard metals or diamond tools. They are also suitable for the powder metallurgical production of components.
  • the metal and alloy powders according to the invention show higher sintering activity, more complete alloy formation and better wetting with the hardness carrier in the production of hard metals due to their finely dispersed distribution and thus lead to non-porous hard metals.
  • the metal and alloy powders according to the invention are also distinguished by the fact that they can be sintered to very dense sintered bodies even at a comparatively low temperature.
  • the invention accordingly also relates
  • Metal and alloy powders which, after sintering at a temperature of 650 ° C and exposure to a pressure of 35 MPa for 3 minutes, form a sintered body which has more than 96%, preferably more than 97%, of the theoretical material density.
  • Particularly preferred alloy powders according to the invention already achieve more than 97% of the theoretical material density at a sintering temperature of 620 ° C.
  • “theoretical material density” is to be understood as the density of an alloy with a corresponding composition produced by melting in a vacuum.
  • a hard metal test was carried out on this metal powder under identical conditions as in Examples 1 to 4.
  • the oxalate precipitation was carried out as in Example 5, but a chloride solution with 42.7 g / 1 Co and 56.3 g / 1 Fe was used.
  • the calcination in the muffle furnace was carried out at 250 ° C.
  • the three-stage reduction under hydrogen was carried out at 520/550/570 ° C.
  • An iron-cobalt-copper oxalate was precipitated, washed and dried analogously to Example 1, using a metal chloride solution containing about 45 g / 1 Fe, 45 g / 1 Co and 10 g / 1 Cu.
  • the metal powders had the properties shown in Table 3. Table 3

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Powder Metallurgy (AREA)
  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)
  • Manufacture And Refinement Of Metals (AREA)
EP99923562A 1998-05-20 1999-05-08 Poudres de metal et d'alliage pour le frittage, a utiliser dans la metallurgie des poudres, leur procede de production et leur utilisation Expired - Lifetime EP1079950B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19822663A DE19822663A1 (de) 1998-05-20 1998-05-20 Sinteraktive Metall- und Legierungspulver für pulvermetallurgische Anwendungen und Verfahren zu deren Herstellung und deren Verwendung
DE19822663 1998-05-20
PCT/EP1999/003170 WO1999059755A1 (fr) 1998-05-20 1999-05-08 Poudres de metal et d'alliage pour le frittage, a utiliser dans la metallurgie des poudres, leur procede de production et leur utilisation

Publications (2)

Publication Number Publication Date
EP1079950A1 true EP1079950A1 (fr) 2001-03-07
EP1079950B1 EP1079950B1 (fr) 2003-08-13

Family

ID=7868428

Family Applications (1)

Application Number Title Priority Date Filing Date
EP99923562A Expired - Lifetime EP1079950B1 (fr) 1998-05-20 1999-05-08 Poudres de metal et d'alliage pour le frittage, a utiliser dans la metallurgie des poudres, leur procede de production et leur utilisation

Country Status (10)

Country Link
US (1) US6554885B1 (fr)
EP (1) EP1079950B1 (fr)
JP (2) JP4257690B2 (fr)
KR (1) KR100543834B1 (fr)
CN (1) CN1254339C (fr)
AT (1) ATE246976T1 (fr)
AU (1) AU4039399A (fr)
CA (1) CA2332889C (fr)
DE (2) DE19822663A1 (fr)
WO (1) WO1999059755A1 (fr)

Cited By (2)

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DE102006045339B3 (de) * 2006-09-22 2008-04-03 H.C. Starck Gmbh Metallpulver
DE102007004937A1 (de) 2007-01-26 2008-07-31 H.C. Starck Gmbh Metallformulierungen

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SE521488C2 (sv) 2000-12-22 2003-11-04 Seco Tools Ab Belagt skär med järn-nickel-baserad bindefas
WO2003083150A1 (fr) * 2002-03-29 2003-10-09 Umicore Poudres de liaison prealliees
US7799141B2 (en) * 2003-06-27 2010-09-21 Lam Research Corporation Method and system for using a two-phases substrate cleaning compound
WO2005117763A2 (fr) * 2004-05-28 2005-12-15 Smith & Nephew, Inc. Tige intramedullaire cannelee
CN1868637B (zh) * 2005-05-25 2010-04-21 成都平和同心金属粉末有限公司 铜合金包覆粉及制取方法
CN100509219C (zh) * 2005-10-10 2009-07-08 中国科学院金属研究所 一种铁基扩散合金粉末的制备方法
FR2892957B1 (fr) * 2005-11-09 2009-06-05 Eurotungstene Poudres Soc Par Poudre polymetallique et piece frittee fabriquee a partir de cette poudre
CN100393454C (zh) * 2005-11-25 2008-06-11 河南卡斯通科技有限公司 用于制备金刚石工具专用预合金粉的共沉淀法
CN101096053B (zh) * 2006-06-29 2010-05-26 王世荣 一种钴铁超细合金粉的制备方法
DE102006045481B3 (de) * 2006-09-22 2008-03-06 H.C. Starck Gmbh Metallpulver
DE102006057004A1 (de) * 2006-12-02 2008-06-05 H.C. Starck Gmbh Metallpulver
DE102007047312A1 (de) * 2007-10-02 2009-04-09 H.C. Starck Gmbh Werkzeug
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CN101428348B (zh) * 2008-07-29 2010-09-08 张建玲 一种水热处理制备球形超细金属粉末的工艺方法
WO2010046224A2 (fr) * 2008-10-20 2010-04-29 H.C. Starck Gmbh Poudre métallique
DE102008052559A1 (de) 2008-10-21 2010-06-02 H.C. Starck Gmbh Metallpulver
JP5546120B2 (ja) * 2008-11-26 2014-07-09 京セラ株式会社 サーメット製スローアウェイチップ
US8216340B2 (en) * 2009-03-03 2012-07-10 E. I. Du Pont De Nemours And Company Method for producing dispersed, crystalline, stable to oxidation copper particles
JP5530270B2 (ja) * 2010-06-29 2014-06-25 Ｊｘ日鉱日石金属株式会社 コバルト粉末及びその製造方法
EP2527480B1 (fr) 2011-05-27 2017-05-03 H.C. Starck GmbH Liant NiFe ayant une application universelle
CN102218709B (zh) * 2011-06-03 2013-01-09 福建万龙金刚石工具有限公司 防脱落的金刚石布拉及其制作工艺
US20130178360A1 (en) * 2012-01-06 2013-07-11 California Institute Of Technology Nickel-based electrocatalytic photoelectrodes
JP5991645B2 (ja) * 2012-12-28 2016-09-14 住友電気工業株式会社 金属粉末の製造方法
JP6568104B2 (ja) * 2014-05-13 2019-08-28 ザ ユニバーシティ オブ ユタ リサーチ ファウンデイション 実質的に球状の金属粉末の製造
CN104874807A (zh) * 2015-06-17 2015-09-02 北京科技大学 一种具有体心立方结构纳米铁钴固溶体合金粉末的制备方法
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102006045339B3 (de) * 2006-09-22 2008-04-03 H.C. Starck Gmbh Metallpulver
DE102007004937A1 (de) 2007-01-26 2008-07-31 H.C. Starck Gmbh Metallformulierungen
DE102007004937B4 (de) * 2007-01-26 2008-10-23 H.C. Starck Gmbh Metallformulierungen

Also Published As

Publication number Publication date
EP1079950B1 (fr) 2003-08-13
US6554885B1 (en) 2003-04-29
ATE246976T1 (de) 2003-08-15
KR100543834B1 (ko) 2006-01-23
JP2009001908A (ja) 2009-01-08
CN1301205A (zh) 2001-06-27
JP2002515543A (ja) 2002-05-28
DE19822663A1 (de) 1999-12-02
AU4039399A (en) 1999-12-06
CA2332889A1 (fr) 1999-11-25
CA2332889C (fr) 2010-04-06
WO1999059755A1 (fr) 1999-11-25
KR20010052366A (ko) 2001-06-25
JP4257690B2 (ja) 2009-04-22
CN1254339C (zh) 2006-05-03
DE59906598D1 (de) 2003-09-18

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