EP0568863A1 - Poudre métallique finement divisée - Google Patents
Poudre métallique finement divisée Download PDFInfo
- Publication number
- EP0568863A1 EP0568863A1 EP93106466A EP93106466A EP0568863A1 EP 0568863 A1 EP0568863 A1 EP 0568863A1 EP 93106466 A EP93106466 A EP 93106466A EP 93106466 A EP93106466 A EP 93106466A EP 0568863 A1 EP0568863 A1 EP 0568863A1
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- European Patent Office
- Prior art keywords
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- powders
- reactor
- metal powder
- powder according
- 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.)
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Classifications
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- 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
-
- 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
- B22F9/28—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from gaseous metal compounds
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- 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
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/05—Metallic powder characterised by the size or surface area of the particles
- B22F1/052—Metallic 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
-
- 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
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/14—Treatment of metallic powder
- B22F1/145—Chemical treatment, e.g. passivation or decarburisation
-
- 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 finely divided powders of the metals B, Al, Si, Ti, Zr, Hf, V, Nb, Ta and / or Cr with a defined particle size between 1.0 nm and less than 3 ⁇ m.
- the properties of the starting powder are of decisive importance for the mechanical properties of powder-metallurgically manufactured components.
- a narrow particle size distribution, high powder purity and a lack of coarse particles or agglomerates have a positive effect on the properties of corresponding components.
- the particle size and particle size of the powders produced cannot be exactly controlled, and the reaction conditions usually lead to a wide particle size distribution and to the occurrence of individual particles whose diameter is a multiple of the average particle size.
- EP-A 0 290 177 describes the decomposition of transition metal carbonyls for the production of fine metallic powders. Here, up to 200 nm fine powders can be obtained
- the noble gas condensation process enables the production of the finest metal powders in the lower nanometer range. However, only quantities on a milligram scale can be obtained here. In addition, the powders produced in this way do not have a narrow particle size distribution.
- the invention relates to finely divided powders of the metals B, Al, Si, Ti, Zr, Hf, V, Nb, Ta and / or Cr with a defined particle size between 1.0 nm and less than 3 ⁇ m, less than 1% of the individual particles a deviation of more than 40% and no individual particles have a deviation of more than 60% from the average grain size.
- the individual particles Preferably, less than 1% of the individual particles have a deviation of more than 20% and no individual particles have a deviation of more than 50% from the mean grain size. Particularly preferably less than 1% of the individual particles have a deviation of more than 10% and no individual particles Deviation of more than 40% from the average grain size.
- the powders according to the invention preferably have particle sizes from 1 to less than 500 nm, particularly preferably from 1 to less than 100 nm and very particularly preferably from 1 to less than 50 nm.
- the metal powders according to the invention are notable for their high purity. They preferably have an oxygen content of less than 5,000 ppm and particularly preferably less than 1,000 ppm.
- Particularly pure metal powders according to the invention are characterized in that they have an oxygen content of less than 100 ppm, preferably less than 50 ppm.
- the non-oxide impurities are also very low.
- the sum of their impurities, with the exception of the oxidic impurities, is preferably less than 5,000 ppm, particularly preferably less than 1,000 ppm.
- the sum of their impurities, with the exception of the oxide impurities, is less than 200 ppm.
- the powders according to the invention are available on an industrial scale. They are preferably present in amounts of more than 1 kg.
- the powders according to the invention are obtainable in a process for the production of finely divided metal powders by reacting corresponding metal compounds and corresponding reactants in the gas phase -CVR-, the metal compound (s) and the other reactants being reacted in a gaseous state, directly from the gas phase condensed homogeneously with the exclusion of any wall reaction and then separated from the reaction medium, which is characterized in that the metal compounds and the reactants are introduced into the reactor separately from one another at at least the reaction temperature.
- the respective gas mixtures should be selected so that no reaction occurs during the heating process. which leads to solid reaction products.
- This process can be carried out particularly advantageously in a tubular reactor. It is particularly favorable if the metal compounds, the reactants and the product particles flow through the reactor in a laminar manner.
- the location of the nucleation can be limited by separately preheating the process gases to at least the reaction temperature.
- the laminar flow in the reactor ensures a narrow residence time distribution of the germs or the particles. A very narrow grain size distribution can be achieved in this way.
- the metal compounds and the reactants should therefore preferably be introduced into the reactor as coaxial laminar partial streams.
- a preferred embodiment of this method therefore consists in that the coaxial, laminar partial streams of the metal compound (s) and the reactants are mixed in a defined manner by means of a Karman vortex street.
- the reaction medium is preferably shielded from the reaction wall by an inert gas layer.
- an inert gas layer This can be done by introducing an inert gas stream into the reactor wall through specially shaped annular gaps, which is applied to the reactor wall via the Coanda effect.
- the metal powder particles created in the reactor by a homogeneous separation from the gas phase with typical residence times between 10 and 300 msec leave this together with the gaseous reaction products (e.g. HCl), the unreacted reactants and the inert gases, which act as carrier gas, purge gas and for the purpose of reduction the HCl adsorption are blown in. Yields, based on the metal component, of up to 100% can be achieved by the process according to the invention.
- the metal powders are then preferably separated off at temperatures above the boiling or sublimation temperatures of the metal compounds used, reactants and / or forced products formed during the reaction.
- the separation can advantageously be carried out in a blow-back filter. If this at high temperatures of e.g. 600 ° C is operated, the adsorption of the gases, especially the non-inert gases such as HCl on the very large surface of the powder can be kept low.
- the remaining interfering substances adsorbed on the powder surfaces can be added in a downstream Vacuum containers are further removed, preferably again at temperatures of about 600 ° C.
- the finished powders should then be discharged from the system in the absence of air.
- Preferred metal compounds for the purposes of this invention are one or more from the group consisting of metal halides, partially hydrogenated metal halides, metal hydrides, metal alcoholates, metal alkyls, metal amides, metal azides and metal carbonyls.
- Hydrogen is used as a further reaction partner.
- Other characteristics of the powders are their high purity, high surface purity and good reproducibility.
- the powders according to the invention can be very sensitive to air or pyrophoric. In order to eliminate this property, these powders can be surface-modified in a defined manner by exposure to gas / steam mixtures.
- Fig. 1 is a schematic representation of a device with which the powders according to the invention can be produced. The implementation of this method is explained below with reference to FIG. 1. The process, material and / or device parameters explicitly mentioned here represent only selected options among many and thus do not limit the invention.
- the solid, liquid or gaseous metal compounds are metered into an outside evaporator (1) or inside the high temperature furnace (1a), evaporated there at temperatures from 200 ° C to 2000 ° C and with an inert carrier gas (N2, Ar or He) transported into the gas preheater (2a).
- the further reactant (3) H2 is also heated in a gas preheater (2).
- the turbulent individual flow threads emerging from the gas preheaters (2) are formed into two coaxial, laminar and rotationally symmetrical flow threads in a nozzle (5).
- the middle flow thread (6) which contains the metal component
- the enveloping flow thread (7) which contains the hydrogen, mix under defined conditions.
- the reaction occurs at temperatures between 500 ° C and 2000 ° C, for example according to the following case examples; TaCl5 + 2 1/2 H2 ⁇ Ta + 5 HCl BCl3 + 1 1/2 H2 ⁇ B + 3 HCl
- a Karman vortex street can be created by installing a disturbing body (17) in the otherwise strictly laminar flow.
- the two coaxial flow threads are separated by a weak inert gas flow (16) at the nozzle outlet in order to prevent growth at the nozzle (5).
- the blow-back filter (10) is operated at temperatures between 300 ° C and 1000 ° C, whereby the adsorption of the gases, especially the non-inert gases such as HCl on the very large surface of these powders is kept at a low level.
- the residues of the adsorbed gases on the powders are further reduced by preferably alternately applying a vacuum and flooding with various gases at 300 ° C. to 1000 ° C. Good effects are achieved when gases such as N2, Ar or Kr are used. SF6 is particularly preferably used.
- Metastable material systems are obtained by setting very high cooling rates in the lower part of the reactor.
- the particles with a core / shell structure are obtained by introducing additional reaction gases into the lower part of the reactor.
- the powders reach the cooling container (12) from the evacuation container (11) before they pass through the lock (13) into the collection and shipping container (14).
- the particle surfaces can be surface-modified in a defined manner in the cooling container (12) by blowing in various gas / steam mixtures
- Coated graphite in particular fine-grain graphite, can preferably be used as the material for those components which are exposed to temperatures of up to 2000 ° C. and more, such as heat exchangers (2) and (3), nozzle (5), reactor (4) and reactor jacket tube (15). be used.
- a coating can e.g. be necessary if the necessary chemical resistance of the graphite against the gases used such as metal chlorides, HCl, H2 and N2, is not sufficient at the given temperatures or if the erosion is very considerable at higher flow rates (0.5 to 50 m / sec) or if the gas tightness of the graphite can be increased as a result or if the surface roughness of the reactor components can thus be reduced.
- layers e.g. SiC, B4C, TiN, TiC and Ni can be used. Combinations of different layers, e.g. with an "own" top layer are possible. These layers can advantageously be applied by means of CVD, plasma spraying and electrolysis (Ni).
- a major advantage of the variability of the temperature-residence time profile is the possibility of decoupling the nucleation zone from the nucleation zone. This makes it possible to produce "coarser” powders at a very low temperature and with a short residence time (ie small reactor cross section for one certain length) to allow the formation of only a few nuclei, which can then grow into "coarse” particles at high temperature and a long residence time (large reactor cross section). It is also possible to produce very “fine” powders: in a region of high temperature and a relatively long residence time, a large number of nuclei are formed, which only grow slightly in the further reactor at low temperatures and a short residence time (small reactor cross section). It is possible to set all transitions between the borderline cases shown here qualitatively.
- the cooling container (12) In the cooling container (12), a passivation of the partly. very air sensitive to pyrophoric powder possible.
- the particle surfaces of these metal powders can be coated with an oxide layer of defined thickness as well as with suitable organic compounds such as higher alcohols, amines or sintering aids such as paraffins in an inert carrier gas stream.
- suitable organic compounds such as higher alcohols, amines or sintering aids such as paraffins in an inert carrier gas stream.
- the coating can also be carried out with regard to the further processing possibilities of the powders.
- the nanoscale powders according to the invention are suitable for the production of novel sensors, actuators, structural metals and cermets.
- Ta became according to the reaction equation TaCl5 + 2 1/2 H2 ⁇ Ta + 5HCl 1 in an apparatus, with an excess of H2 was maintained.
- the turbulent individual flow threads emerging from the gas preheaters (2) were formed in the outer part of the nozzle (5) to form a homogeneous, rotationally symmetrical and laminar ring flow.
- the gas stream emerging from the gas preheater (2a) was also laminarized in the nozzle (5) and introduced into the ring flow.
- the nozzle (5) consisted of three sub-nozzles arranged coaxially to one another.
- An inert gas stream (16) emerged from the middle part nozzle, which moved the location of the start of the reaction, ie the meeting of the two partial flows (6) and (7) away from the nozzle into the reaction tube.
- the tube reactor had a total length of 1100 mm at the nozzle outlet with an inner diameter of 40 mm, 200 mm below the nozzle with an inner diameter of 30 mm and 50 mm at the outlet.
- the reaction tube (4) was composed of 18 segments, the segments each being connected by a spacer and centering ring. An annular gap (8) was implemented at each of these locations.
- the temperature of the reaction tube (4) was set at 1230 ° C., measured on the outer wall of the reactor, 400 mm below the nozzle, using the W5Re-W26Re thermocouple (19).
- the pressure in the reaction tube (4) was practically identical to the pressure in the blow-back filter (10). This was 250 mbar overpressure.
- the reactor wall was flushed through 18 ring gaps (8) with 200 Nl / min Ar. If the reactor wall is not flushed with an inert gas, accretions can occur which can sometimes lead to the reactor closure and thus to the process being terminated very quickly; in any case, because of the changing reactor geometry, a likewise changing product is produced.
- 200 Nl / min Ar was blown into the reaction tube (4) through the 6th annular gap from below with an additional gas inlet device.
- the product (Ta with a uniform particle size of ⁇ 25 nm) was separated from the gases (H2, HCl, Ar) in the blow-back filter (10) at a temperature of 600 ° C.
- This temperature was selected in order to keep the primary coverage of the very large particle surfaces (18 m2 / g) with HCl at a low level ( ⁇ 0.8% Cl).
- the Ta produced in this way was collected in the blow-back filter for 40 min (ie 2000 g), in order to then be transferred to the evacuation container (11). 8 pump-flood cycles with a final vacuum of 0.1 mbar abs were carried out in this container over a period of 35 min . run through.
- the container was filled with Ar up to a pressure of 1100 mbar abs. flooded, after 35 min. the Ta powder thus treated was transferred to the cooling container (12).
- Targeted surface tailoring is also possible in this container by blowing in various gas / steam mixtures. After the powder had cooled to ⁇ 50 ° C., it was transferred through the lock (13) into the collection and shipping container without contact with the outside air.
- the pyrophoric Ta powder showed an extremely narrow particle size distribution at a specific surface area of 17 m2 / g, according to BET, measured according to the N2-1-point method (DIN 66 131), corresponding to 25 nm.
- a SEM image of this Ta powder with a specific surface area of 25 m2 / g showed the very narrow distribution of the particle dimensions and the absence of oversize particles. According to this, less than 1% of the individual particles have a deviation of more than 10% and no individual particles have a deviation of more than 40% from the mean grain size. According to the current state of measurement technology, reliable statements about a Particle size distribution of such extremely fine powders can only be obtained using imaging methods (e.g. B, SEM, TEM).
- This Ta powder showed an oxygen content of 70 ppm and the sum of the non-oxide impurities was 430 ppm.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Powder Metallurgy (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4214722A DE4214722C2 (de) | 1992-05-04 | 1992-05-04 | Feinteilige Metallpulver |
DE4214722 | 1992-05-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0568863A1 true EP0568863A1 (fr) | 1993-11-10 |
EP0568863B1 EP0568863B1 (fr) | 1997-02-26 |
Family
ID=6458139
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP93106466A Expired - Lifetime EP0568863B1 (fr) | 1992-05-04 | 1993-04-21 | Poudre métallique finement divisée |
Country Status (6)
Country | Link |
---|---|
US (1) | US5407458A (fr) |
EP (1) | EP0568863B1 (fr) |
JP (1) | JP3356325B2 (fr) |
KR (1) | KR100251664B1 (fr) |
AT (1) | ATE149110T1 (fr) |
DE (2) | DE4214722C2 (fr) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4337336C1 (de) * | 1993-11-02 | 1994-12-15 | Starck H C Gmbh Co Kg | Feinteilige Metall-, Legierungs- und Metallverbindungspulver |
US5964963A (en) * | 1994-08-25 | 1999-10-12 | Turchan; Manuel C. | Brazing paste |
JP3434041B2 (ja) * | 1994-09-28 | 2003-08-04 | スタルクヴイテック株式会社 | タンタル粉末及びそれを用いた電解コンデンサ |
US5876480A (en) * | 1996-02-20 | 1999-03-02 | The United States Of America As Represented By The Secretary Of The Navy | Synthesis of unagglomerated metal nano-particles at membrane interfaces |
JPH09316504A (ja) * | 1996-05-27 | 1997-12-09 | Res Dev Corp Of Japan | Al超微粒子 |
US6344271B1 (en) | 1998-11-06 | 2002-02-05 | Nanoenergy Corporation | Materials and products using nanostructured non-stoichiometric substances |
US6652967B2 (en) * | 2001-08-08 | 2003-11-25 | Nanoproducts Corporation | Nano-dispersed powders and methods for their manufacture |
US6933331B2 (en) * | 1998-05-22 | 2005-08-23 | Nanoproducts Corporation | Nanotechnology for drug delivery, contrast agents and biomedical implants |
US5788738A (en) * | 1996-09-03 | 1998-08-04 | Nanomaterials Research Corporation | Method of producing nanoscale powders by quenching of vapors |
US5905000A (en) * | 1996-09-03 | 1999-05-18 | Nanomaterials Research Corporation | Nanostructured ion conducting solid electrolytes |
DE69733660T2 (de) * | 1996-11-04 | 2006-05-18 | Materials Modification, Inc. | Mikrowellenplasma chemischen synthese von ultrafeinen pulvern |
US6391494B2 (en) | 1999-05-13 | 2002-05-21 | Nanogram Corporation | Metal vanadium oxide particles |
US5984997A (en) * | 1997-08-29 | 1999-11-16 | Nanomaterials Research Corporation | Combustion of emulsions: A method and process for producing fine powders |
US6051044A (en) | 1998-05-04 | 2000-04-18 | Cabot Corporation | Nitrided niobium powders and niobium electrolytic capacitors |
EP2055412B1 (fr) * | 1998-05-06 | 2012-08-22 | H.C. Starck GmbH | Poudre de niobum ou tantale produite par la réduction des oxydes avec un metal gazeux |
DE19831280A1 (de) * | 1998-07-13 | 2000-01-20 | Starck H C Gmbh Co Kg | Verfahren zur Herstellung von Erdsäuremetallpulvern, insbesondere Niobpulvern |
JP3871824B2 (ja) | 1999-02-03 | 2007-01-24 | キャボットスーパーメタル株式会社 | 高容量コンデンサー用タンタル粉末 |
US6375704B1 (en) † | 1999-05-12 | 2002-04-23 | Cabot Corporation | High capacitance niobium powders and electrolytic capacitor anodes |
US6520402B2 (en) | 2000-05-22 | 2003-02-18 | The Regents Of The University Of California | High-speed direct writing with metallic microspheres |
US6562099B2 (en) * | 2000-05-22 | 2003-05-13 | The Regents Of The University Of California | High-speed fabrication of highly uniform metallic microspheres |
EP1286789A4 (fr) * | 2000-05-22 | 2004-06-16 | Univ California | Fabrication a haute vitesse de microspheres metalliques a tres petite echelle |
US6491737B2 (en) | 2000-05-22 | 2002-12-10 | The Regents Of The University Of California | High-speed fabrication of highly uniform ultra-small metallic microspheres |
US6602523B1 (en) * | 2000-08-17 | 2003-08-05 | Technology Holding, Llc. | Composite material and process for increasing bioavailability and activity of a beneficial agent |
JP2002121601A (ja) * | 2000-10-16 | 2002-04-26 | Aisin Seiki Co Ltd | 軟磁性金属粉末粒子、軟磁性金属粉末粒子の処理方法、軟磁性成形体、軟磁性成形体の製造方法 |
US6780218B2 (en) * | 2001-06-20 | 2004-08-24 | Showa Denko Kabushiki Kaisha | Production process for niobium powder |
US6855426B2 (en) * | 2001-08-08 | 2005-02-15 | Nanoproducts Corporation | Methods for producing composite nanoparticles |
JP4187953B2 (ja) | 2001-08-15 | 2008-11-26 | キャボットスーパーメタル株式会社 | 窒素含有金属粉末の製造方法 |
US20030064086A1 (en) | 2001-08-31 | 2003-04-03 | Danuvio Carrion | Cosmetic compositions comprising nanoparticles and processes for using the same |
US7442227B2 (en) | 2001-10-09 | 2008-10-28 | Washington Unniversity | Tightly agglomerated non-oxide particles and method for producing the same |
JP3610942B2 (ja) * | 2001-10-12 | 2005-01-19 | 住友金属鉱山株式会社 | ニオブおよび/またはタンタルの粉末の製造法 |
US7708974B2 (en) * | 2002-12-10 | 2010-05-04 | Ppg Industries Ohio, Inc. | Tungsten comprising nanomaterials and related nanotechnology |
US6955703B2 (en) * | 2002-12-26 | 2005-10-18 | Millennium Inorganic Chemicals, Inc. | Process for the production of elemental material and alloys |
WO2005096785A2 (fr) * | 2004-04-09 | 2005-10-20 | Synergy Innovations, Inc. | Systeme et procede de fabrication de particules spheriques dispersees d'une seule taille |
KR20150063590A (ko) * | 2007-08-02 | 2015-06-09 | 다우 글로벌 테크놀로지스 엘엘씨 | 열경화성 중합체의 성능을 개선시키기 위한 양친매성 블록 공중합체 및 무기 나노충진제 |
US20160104580A1 (en) | 2013-06-13 | 2016-04-14 | Ishihara Chemical Co., Ltd. | Ta powder, production method therefor, and ta granulated powder |
US10329644B2 (en) | 2014-09-11 | 2019-06-25 | Ishihara Chemical Co., Ltd. | Ta—Nb alloy powder and anode element for solid electrolytic capacitor |
DE202017102288U1 (de) * | 2017-04-18 | 2018-07-20 | Powder Light Metals GmbH | Mittel zum Verschweißen bzw. Löten von Komponenten aus Aluminiummaterial |
KR20190037466A (ko) | 2017-09-29 | 2019-04-08 | 손이혁 | 생리대 |
Citations (3)
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GB919954A (en) * | 1960-11-10 | 1963-02-27 | Union Carbide Corp | Improvements in and relating to the production of ultra fine metal powders |
GB950148A (en) * | 1961-05-03 | 1964-02-19 | Union Carbide Corp | Improvements in or relating to the production of ultrafine metal particles |
US4383852A (en) * | 1980-09-13 | 1983-05-17 | Toho Aen Kabushiki Kaisha | Process for producing fine powdery metal |
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DE3119635A1 (de) * | 1981-05-16 | 1982-12-02 | Degussa Ag, 6000 Frankfurt | "verfahren und vorrichtung zur herstellung von silberpulver" |
JPS6039106A (ja) * | 1983-08-10 | 1985-02-28 | Res Dev Corp Of Japan | 微粒子の製造方法 |
US4994107A (en) * | 1986-07-09 | 1991-02-19 | California Institute Of Technology | Aerosol reactor production of uniform submicron powders |
US4740238A (en) * | 1987-03-26 | 1988-04-26 | Fansteel Inc. | Platelet-containing tantalum powders |
US4808216A (en) * | 1987-04-25 | 1989-02-28 | Mitsubishi Petrochemical Company Limited | Process for producing ultrafine metal powder |
US4769064A (en) * | 1988-01-21 | 1988-09-06 | The United States Of America As Represented By The United States Department Of Energy | Method for synthesizing ultrafine powder materials |
DE3820960A1 (de) * | 1988-06-22 | 1989-12-28 | Starck Hermann C Fa | Feinkoernige hochreine erdsaeuremetallpulver, verfahren zu ihrer herstellung sowie deren verwendung |
DE3937740A1 (de) * | 1989-11-13 | 1991-05-16 | Rudolf C Dr Alberti | Verfahren zur herstellung von nanokristallinen pulvern aus metallen, legierungen bzw. keramikwerkstoffen |
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1992
- 1992-05-04 DE DE4214722A patent/DE4214722C2/de not_active Expired - Fee Related
-
1993
- 1993-04-21 AT AT93106466T patent/ATE149110T1/de not_active IP Right Cessation
- 1993-04-21 DE DE59305509T patent/DE59305509D1/de not_active Expired - Lifetime
- 1993-04-21 EP EP93106466A patent/EP0568863B1/fr not_active Expired - Lifetime
- 1993-04-26 US US08/051,888 patent/US5407458A/en not_active Expired - Lifetime
- 1993-04-28 JP JP12499593A patent/JP3356325B2/ja not_active Expired - Fee Related
- 1993-04-30 KR KR1019930007411A patent/KR100251664B1/ko not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB919954A (en) * | 1960-11-10 | 1963-02-27 | Union Carbide Corp | Improvements in and relating to the production of ultra fine metal powders |
GB950148A (en) * | 1961-05-03 | 1964-02-19 | Union Carbide Corp | Improvements in or relating to the production of ultrafine metal particles |
US4383852A (en) * | 1980-09-13 | 1983-05-17 | Toho Aen Kabushiki Kaisha | Process for producing fine powdery metal |
Non-Patent Citations (2)
Title |
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY Bd. 109, Nr. 8, August 1962, MANCHESTER, NEW HAMPSHIRE US Seiten 713 - 716 H.LAMPREY ET AL 'ultrafine tungsten and molybdenum powders' * |
PATENT ABSTRACTS OF JAPAN vol. 12, no. 219 (C-506)22. Juni 1988 & JP-A-63 016 041 ( KAWASAKI STEEL CORP ) * |
Also Published As
Publication number | Publication date |
---|---|
DE59305509D1 (de) | 1997-04-03 |
DE4214722A1 (de) | 1993-11-11 |
JPH0625701A (ja) | 1994-02-01 |
JP3356325B2 (ja) | 2002-12-16 |
US5407458A (en) | 1995-04-18 |
ATE149110T1 (de) | 1997-03-15 |
DE4214722C2 (de) | 1994-08-25 |
EP0568863B1 (fr) | 1997-02-26 |
KR930023095A (ko) | 1993-12-18 |
KR100251664B1 (ko) | 2000-04-15 |
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