WO2004000491A2 - Highly pure metallic nano-powders and their production - Google Patents
Highly pure metallic nano-powders and their production Download PDFInfo
- Publication number
- WO2004000491A2 WO2004000491A2 PCT/IL2003/000522 IL0300522W WO2004000491A2 WO 2004000491 A2 WO2004000491 A2 WO 2004000491A2 IL 0300522 W IL0300522 W IL 0300522W WO 2004000491 A2 WO2004000491 A2 WO 2004000491A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- powder
- metal
- silver
- alloy
- chemicals
- 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.)
- Ceased
Links
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
- B22F9/16—Making metallic powder or suspensions thereof using chemical processes
-
- 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
- B22F1/054—Nanosized particles
-
- 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
- B22F1/10—Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
- B22F1/102—Metallic powder coated with organic material
-
- 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
-
- 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
- B22F2998/10—Processes characterised by the sequence of their steps
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
Definitions
- the present invention generally relates to a method for the production of highly pure metallic nano-powders and to powders produced thereof. More specifically, the present invention relates to metallic silver, metal elements, copper, platinum, nickel, palladium, titanium, gold, cobalt and blends comprising such metals (alloys) nano-powders wherein the particle size is in the range of 1 to 100 nm.
- Nano-powders are single or multi-phase polycrystals comprises particles with sizes of 1 to 100 nm in at least one direction.
- Various methods were suggested in the literature for the production of well-defined nano-powders. Some of them, such as presented in U.S. Pat. No. 6,312,643 to Upadhya et al. are respectively tedious and costly operation, comprises no less then 21 steps, treating the material in all solid, liquid and gas phases; wherein gas is evacuated from one processing chamber to less then 10 "3 Torr, and then pressed in another processing chamber to at least 10 3 psi, heated to some 550°C etc.
- U.S. Pat. No. 6,054,495 to Markowitz et al. presents a powder of un-agglomerated metallic particles, made by making at least four dispersions of surfactants vesicles in the presence of metal ions, and then freeze-drying the obtained lipid phase.
- This costly method requires the operator to continuously control this very delicate, inflammable, multi-phase and complicated system, decreasing its compatibility with full-scale operations.
- U.S. Pat. 5,476,535 to the applicant present a method for the production of nano-powders, especially of silver.
- This process comprising the steps of (a) forming an aluminum-silver alloy of a specific blend composition; (b) leaching the aluminum ingredient by a series of consequent leaching steps wherein a fresh leaching agent is reacting the treated solid material, providing a gradually porous and homogeneous silver alloy.
- Ultrasonic oscillations are applied in step (c), disintegrating the agglomerate and enhancing the penetration of the leaching agent into the ever growing porous of the alloy by the application of a plurality of ultrasonic oscillations.
- the leaching agent is leaving silver agglomerate in step (d), and then the agglomerate is washed and dried in a final step.
- the object of the present invention to provide a useful and novel method for the production of metallic nano-powders, comprising the steps: (a) forming an alloy comprising a first metal or metal, preferably silver, copper, platinum, palladium, titanium, nickel, gold, cobalt and blends comprising such metals (alloys), yet not limited to said metals, and at least one another second soluble metal or metals, preferably, yet not limited to aluminum, magnesium, zinc or tin.
- a first metal or metal preferably silver, copper, platinum, palladium, titanium, nickel, gold, cobalt and blends comprising such metals (alloys), yet not limited to said metals, and at least one another second soluble metal or metals, preferably, yet not limited to aluminum, magnesium, zinc or tin.
- This method is based on gradually single leaching step and plurality of few thermal treatings, avoid using ulrasonic processes, and comprising a novel technique of coating the powder with predetermined chemicals which provides the obtained powder better de-agglomeration properties and de-agglomeration process.
- the first metal is selected from atoms of group I, IV, V, VI, VII and VIII of the periodic table of elements. More specifically, said first metal is selected from, copper, nickel, cobalt, titanium, silver, palladium, platinum, gold and iridium. Most particularly, silver is said first metal.
- various alloys comprising a blend of the said silver and at least one other metal, selected from atoms of group I, IV, V, VI, VII and VIII of the periodic table of elements. More specifically, cooper, aluminum, nickel, cobalt, titanium, palladium, platinum, gold, iridium or - any mixture thereof is suitable to be comprised in the aforementioned alloy.
- the at least one soluble metal is selected from aluminum, zinc, magnesium, tin, copper and silver.
- the concentration of the at least one soluble metal is near saturation.
- the present invention relates thus to a method to produce a nano-powder, wherein silver is the first metal and aluminum is the soluble metal.
- the preferred concentration of the soluble metal ingredient of the said processed alloy is in the range between 5 to 90 % w/w.
- the method according to the present invention comprises at least one step of leaching.
- Suitable leaching agents are preferably selected from sodium hydroxide, potassium hydroxide, acetic acid, hydrochloric acid, formic acid, sulfuric acid, hydrofluoric acid, nitric acid or any combination thereof. It is acknowledged that a sequent of few leaching steps useful to extract the soluble metal from the alloy, wherein in each leaching step comprising different leaching agent at possibly different concentration.
- the hereto-defined method may additionally comprise at least one step of surface cleansing wherein the obtained strips are treated by means of at least one cleaning agent.
- Those cleansing agents are preferably selected from nitric acid, potassium hydroxide, sodium hydroxide or a mixture thereof.
- the term 'heat treatment' is defined as any heating, cooling, smelting, fusing or melting, amalgamating, liquidating, sustaining a substrate in a predetermined temperature and for a predetermined period or any combination thereof. It is thus in the scope of the present invention, wherein the temperature ranges of first thermal treatment is about 400°C for 2 to 4 hours, or alternatively, until a homogenized alloy is obtained.
- the term 'cold work' is defined as any work or force provided on the substrate. This work is selected, yet not limited to pressing, compressing, squashing, mashing, pulverizing, grinding, milling or any combination thereof.
- the aforementioned method comprises a step of cold work as defined above, useful for applying the obtained strip a thickness in the range of 0.3 to 1.0 mm or thinner.
- the above mentioned second thermal treatment is adapted to the range of 460°C to 610°C.
- Said method according to the present invention may additionally comprising a step of quenching steps, wherein the strips obtained from the oven are to be treated by means of immersing them in cold water, so the predetermined phase composition obtained during the heat treatment is provided.
- sodium hydroxide is a useful leaching agent, adapted to be effective wherein the leaching temperature is between 36°C to 80°C.
- silver is the first metal and aluminum is the soluble metal.
- concentration of the aforementioned sodium hydroxide is between 25 to 55 % (w/w) and the molar ratio of the aluminum to the said sodium hydroxide is between 5 to 6.
- the obtained powder is preferably to be filtered and washed by water so pH in the range of 6 to 7 is provided and further wherein at a maximum temperature of 45°C, the powder to a LOD weight ratio is lower 1%.
- the present invention relates to various chemical compositions, some of them are wieldy known in the art in their trademark name. Those terms are denoted in the present invention according their definitions introduced in Table 1 below:
- Glyceryl monostearate glyceryl monostearate
- chemicals hereby defined, yet not limited to this list are selected from sorbitan esters, polyoxyethylene esters, alcohols, glycerin, polyglycols, organic acids salts and esters, thiols, phosphines, acrylics and polyesters or any other suitable low molecular weight polymers or combination thereof were found to comprise superior effectively.
- chemicals for coating the powder are admixed to the range of 1 to 5%, weight-by- weight based on the metal. Alternatively, least two different chemicals are to be used for coating the powder.
- At least one primary chemical is admixed in the range 1% to 5%
- at least one secondary chemical is admixed in the range of 0.1 to 2.5% weight by weight based on the metal.
- Table 2 presents an extracted list of useful combinations of both primary and secondary chemicals.
- the method for the production of the said metallic nano-powers additionally comprises the following steps: a. dissolving the chemicals in a solvent; b. admixing the dissolved chemicals with the metal powder by an efficient mean; and then, c. drying the slurry in an oven at low temperature.
- the above-mentioned solvent is preferably selected from of low boiling temperature solvent, and more specifically from methanol, ethanol, isopropanol, acetone, water or combination thereof. It is also suggested according to use a ball mill to admixed the dissolved chemicals with the metal powder.
- said de-agglomeration of the said coated powder is enabled by means of a dry process, using at least one jet mill.
- said de-agglomerating of the coated powder is also enabled by means of a wet process, using effective means selected from of any suitable mechanical dispersers, mechanical homogenizes, ultra sonic homogenizes or any combination thereof.
- means selected from, yet not limited to rotor/stator; rotors; dispersing elements; mechanical homogenizers; ultra-sonic homogenizers; ball milling and/or any other suitable de-agglomeration means are acknowledged as useful.
- said metal is selected from the group I, IV, V, VI, VII and VIII of the periodic table of elements. More specifically, the said metal powder is selected from silver, cooper, nickel, cobalt, titanium, silver, palladium, platinum, gold and iridium.
- said produced nano-powder comprises metal that is preferably selected from alloys comprising a blend of silver and at least one other metal, selected from atoms of group I, IV, V, VI, VII and VIII of the periodic table of elements.
- a metallic nano-powder comprising silver, silver-cooper, silver palladium, silver-platinum, and cooper was produced by the method of forming an alloy comprising said first metal and at least one soluble metal, selected from aluminum, zinc and magnesium, applying first thermal treatment in the manner homogenized alloy is obtained; applying a cold work to the homogenized alloy so thin strips are obtained; applying a second thermal treatment to the previously leached alloy until a phase composition of predetermined characteristics is obtained; subjecting the said alloy to a leaching agent (i.e., sodium hydroxide, hydrochloride, formic acid and sulfuric acid) adapted to effectively leach out the least one soluble metal; filtering and washing the powder; drying the powder; coating the powder with chemicals; and then, de-agglomerating the coated powder by various means (e.g., using the commercial available Kinematica or jet mills): Exp No Powder Auxiliary First Leaching
- Table 4 Nine different coating systems to produce nano-metal particles according to this invention.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nanotechnology (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Composite Materials (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Powder Metallurgy (AREA)
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN038142791A CN1662331B (zh) | 2002-06-19 | 2003-06-19 | 制造高纯金属纳米粉末的方法 |
| US10/518,227 US7544229B2 (en) | 2002-06-19 | 2003-06-19 | Method for the production of highly pure metallic nano-powders |
| EP03732985A EP1515817B1 (en) | 2002-06-19 | 2003-06-19 | Highly pure metallic nano-powders and their production |
| AU2003238645A AU2003238645A1 (en) | 2002-06-19 | 2003-06-19 | Highly pure metallic nano-powders and their production |
| JP2004515403A JP2005530048A (ja) | 2002-06-19 | 2003-06-19 | 高純度金属ナノ粉末の製造方法及びこの方法により製造されたナノ粉末 |
| AT03732985T ATE468189T1 (de) | 2002-06-19 | 2003-06-19 | Hochreine metallische nanopulver sowie ihre herstellung |
| DE60332625T DE60332625D1 (de) | 2002-06-19 | 2003-06-19 | Hochreine metallische nanopulver sowie ihre herstellung |
| CN038142791A CN1662331A (zh) | 2002-06-19 | 2003-06-19 | 制造高纯金属纳米粉末的方法以及由此制造的纳米粉末 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IL150325A IL150325A (en) | 2002-06-19 | 2002-06-19 | Method for the production of highly pure metallic nano-powders and nano-powders produced thereby |
| IL150325 | 2002-06-19 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2004000491A2 true WO2004000491A2 (en) | 2003-12-31 |
| WO2004000491A3 WO2004000491A3 (en) | 2004-05-06 |
Family
ID=28053383
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IL2003/000522 Ceased WO2004000491A2 (en) | 2002-06-19 | 2003-06-19 | Highly pure metallic nano-powders and their production |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7544229B2 (enExample) |
| EP (1) | EP1515817B1 (enExample) |
| JP (2) | JP2005530048A (enExample) |
| KR (1) | KR100989881B1 (enExample) |
| CN (2) | CN1662331B (enExample) |
| AT (1) | ATE468189T1 (enExample) |
| AU (1) | AU2003238645A1 (enExample) |
| DE (1) | DE60332625D1 (enExample) |
| IL (1) | IL150325A (enExample) |
| WO (1) | WO2004000491A2 (enExample) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1760043A1 (en) | 2005-09-06 | 2007-03-07 | ETH Zürich, ETH Transfer | Reducing flame spray pyrolysis method for the production of metal, non-oxidic, ceramic and reduced metal oxide powders and nano-powders |
| US7274458B2 (en) | 2005-03-07 | 2007-09-25 | 3M Innovative Properties Company | Thermoplastic film having metallic nanoparticle coating |
| US7566360B2 (en) | 2002-06-13 | 2009-07-28 | Cima Nanotech Israel Ltd. | Nano-powder-based coating and ink compositions |
| US7601406B2 (en) | 2002-06-13 | 2009-10-13 | Cima Nanotech Israel Ltd. | Nano-powder-based coating and ink compositions |
| US7736693B2 (en) | 2002-06-13 | 2010-06-15 | Cima Nanotech Israel Ltd. | Nano-powder-based coating and ink compositions |
| US20110194106A1 (en) * | 2010-02-10 | 2011-08-11 | Makoto Murakami | method and apparatus to prepare a substrate for molecular detection |
| US8142743B2 (en) | 2009-06-25 | 2012-03-27 | Industrial Technology Research Institute | Method and apparatus for forming zinc oxide |
| US8633474B2 (en) | 2007-12-20 | 2014-01-21 | Cima Nanotech Israel Ltd. | Photovoltaic device having transparent electrode formed with nanoparticles |
| EP2883607A4 (en) * | 2012-08-08 | 2016-03-30 | Mitsubishi Gas Chemical Co | OXYGEN ABSORPTION MATERIAL |
| CN110014143A (zh) * | 2018-12-27 | 2019-07-16 | 江苏博迁新材料股份有限公司 | 铜磷包覆粉的制备方法 |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7311754B2 (en) * | 1998-10-26 | 2007-12-25 | University Of Utah Research Foundation | Molecular decomposition processes for the synthesis of nanosize metallic powders |
| DE102006014067A1 (de) * | 2006-03-27 | 2007-10-04 | Universität Bremen | Goldhaltiger Katalysator mit poröser Struktur |
| JP2008108539A (ja) * | 2006-10-25 | 2008-05-08 | Fujitsu Ltd | 導電性ペーストおよびその製造方法 |
| US8101005B2 (en) * | 2007-12-21 | 2012-01-24 | Cima Nanotech Israel Ltd. | Process of making metal nanoparticles |
| CN100553833C (zh) * | 2008-01-14 | 2009-10-28 | 重庆大学 | 制备金属单质纳米晶体材料的方法 |
| WO2009137680A1 (en) * | 2008-05-09 | 2009-11-12 | Cima Nanotech Israel Ltd. | Process for producing powders of germanium |
| DE112010005261B4 (de) | 2010-02-12 | 2021-04-29 | Audi Ag | Platin-Nanopartikel mit hohlen Skelettstrukturen und Herstellungsverfahren |
| DE112010005263B4 (de) | 2010-02-12 | 2022-07-21 | Audi Ag | Platin-Monoschicht auf hohlen, porösen Nanopartikeln mit großen Oberflächen-Flächen und Herstellungsverfahren |
| TWI573846B (zh) | 2010-03-09 | 2017-03-11 | 西瑪奈米技術以色列有限公司 | 形成具有燒結添加物之透明導電塗層的方法 |
| WO2012098643A1 (ja) * | 2011-01-18 | 2012-07-26 | Dowaエレクトロニクス株式会社 | 金属粒子粉末およびそれを用いたペースト組成物 |
| TWI584485B (zh) | 2011-10-29 | 2017-05-21 | 西瑪奈米技術以色列有限公司 | 於基材上對齊的網路 |
| CN102974833B (zh) * | 2012-11-20 | 2015-03-18 | 宁波广博纳米新材料股份有限公司 | 片状银粉的制备方法 |
| CN104994952A (zh) | 2012-12-03 | 2015-10-21 | 奥迪股份公司 | 核壳催化剂及钯基核颗粒的制备方法 |
| CN102989463B (zh) * | 2012-12-04 | 2014-10-01 | 昆明理工大学 | 甲醇合成用CuZnO催化剂的高能球磨制备方法 |
| CN103240420B (zh) * | 2013-05-24 | 2015-12-02 | 苏州大学 | 一种金双锥结构纳米粒子的提纯方法 |
| US20160228951A1 (en) * | 2013-09-12 | 2016-08-11 | Cima Nanotech Israel Ltd. | Process for producing a metal nanoparticle composition |
| CN107344239A (zh) * | 2017-09-08 | 2017-11-14 | 张家港创博金属科技有限公司 | 一种纳米级金属粉末的制备方法 |
| CN109763128B (zh) * | 2019-03-23 | 2020-07-03 | 昆明理工大学 | 一种合金腐蚀法制备超细鳞片状铜粉的方法 |
| CN112207285B (zh) * | 2020-03-12 | 2022-05-20 | 赵远云 | 粉体材料的制备方法及其应用 |
| KR102323009B1 (ko) * | 2020-07-09 | 2021-11-10 | 한국생산기술연구원 | 적층제조용 티타늄 분말의 유동성 향상을 위한 표면처리 방법 및 이에 의해 제조된 적층제조용 티타늄 분말 |
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| IL106958A (en) * | 1993-09-09 | 1996-06-18 | Ultrafine Techn Ltd | Method of producing high-purity ultra-fine metal powder |
| JP2955985B2 (ja) * | 1994-08-31 | 1999-10-04 | ナノパウダース インダストリーズ(イスラエル)リミテッド | 高純度超微粒金属粉を製造する方法 |
| EP0761348B1 (en) * | 1995-09-07 | 1999-12-22 | Nanopowders Industries (Israel) Limited | Method of producing high-purity ultra-fine metal powder by leaching |
| 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 |
| US5922403A (en) * | 1996-03-12 | 1999-07-13 | Tecle; Berhan | Method for isolating ultrafine and fine particles |
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| JP3244652B2 (ja) * | 1997-08-22 | 2002-01-07 | 科学技術振興事業団 | 金属含有量の高い金属・有機ポリマー複合構造体および多孔体ならびにその製造方法 |
| US6312643B1 (en) * | 1997-10-24 | 2001-11-06 | The United States Of America As Represented By The Secretary Of The Air Force | Synthesis of nanoscale aluminum alloy powders and devices therefrom |
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| JP2000178610A (ja) * | 1998-12-16 | 2000-06-27 | Nikko Rika Kk | 金属超微粒子の製造方法 |
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-
2002
- 2002-06-19 IL IL150325A patent/IL150325A/en not_active IP Right Cessation
-
2003
- 2003-06-19 WO PCT/IL2003/000522 patent/WO2004000491A2/en not_active Ceased
- 2003-06-19 AT AT03732985T patent/ATE468189T1/de not_active IP Right Cessation
- 2003-06-19 DE DE60332625T patent/DE60332625D1/de not_active Expired - Lifetime
- 2003-06-19 EP EP03732985A patent/EP1515817B1/en not_active Expired - Lifetime
- 2003-06-19 JP JP2004515403A patent/JP2005530048A/ja active Pending
- 2003-06-19 AU AU2003238645A patent/AU2003238645A1/en not_active Abandoned
- 2003-06-19 CN CN038142791A patent/CN1662331B/zh not_active Expired - Fee Related
- 2003-06-19 KR KR1020047020672A patent/KR100989881B1/ko not_active Expired - Fee Related
- 2003-06-19 US US10/518,227 patent/US7544229B2/en not_active Expired - Fee Related
- 2003-06-19 CN CN038142791A patent/CN1662331A/zh active Granted
-
2010
- 2010-12-02 JP JP2010269337A patent/JP5575622B2/ja not_active Expired - Fee Related
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7566360B2 (en) | 2002-06-13 | 2009-07-28 | Cima Nanotech Israel Ltd. | Nano-powder-based coating and ink compositions |
| US7601406B2 (en) | 2002-06-13 | 2009-10-13 | Cima Nanotech Israel Ltd. | Nano-powder-based coating and ink compositions |
| US7736693B2 (en) | 2002-06-13 | 2010-06-15 | Cima Nanotech Israel Ltd. | Nano-powder-based coating and ink compositions |
| US7274458B2 (en) | 2005-03-07 | 2007-09-25 | 3M Innovative Properties Company | Thermoplastic film having metallic nanoparticle coating |
| EP1760043A1 (en) | 2005-09-06 | 2007-03-07 | ETH Zürich, ETH Transfer | Reducing flame spray pyrolysis method for the production of metal, non-oxidic, ceramic and reduced metal oxide powders and nano-powders |
| US8633474B2 (en) | 2007-12-20 | 2014-01-21 | Cima Nanotech Israel Ltd. | Photovoltaic device having transparent electrode formed with nanoparticles |
| US8795462B2 (en) | 2007-12-20 | 2014-08-05 | Cima Nanotech Israel Ltd. | Transparent conductive coating with filler material |
| US8142743B2 (en) | 2009-06-25 | 2012-03-27 | Industrial Technology Research Institute | Method and apparatus for forming zinc oxide |
| US20110194106A1 (en) * | 2010-02-10 | 2011-08-11 | Makoto Murakami | method and apparatus to prepare a substrate for molecular detection |
| US8836941B2 (en) * | 2010-02-10 | 2014-09-16 | Imra America, Inc. | Method and apparatus to prepare a substrate for molecular detection |
| EP2883607A4 (en) * | 2012-08-08 | 2016-03-30 | Mitsubishi Gas Chemical Co | OXYGEN ABSORPTION MATERIAL |
| US9387973B2 (en) | 2012-08-08 | 2016-07-12 | Mitsubishi Gas Chemical Company, Inc. | Oxygen absorbing agent |
| CN110014143A (zh) * | 2018-12-27 | 2019-07-16 | 江苏博迁新材料股份有限公司 | 铜磷包覆粉的制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| IL150325A0 (en) | 2002-12-01 |
| WO2004000491A3 (en) | 2004-05-06 |
| JP2011089205A (ja) | 2011-05-06 |
| US7544229B2 (en) | 2009-06-09 |
| EP1515817B1 (en) | 2010-05-19 |
| CN1662331B (zh) | 2013-08-28 |
| AU2003238645A1 (en) | 2004-01-06 |
| IL150325A (en) | 2010-12-30 |
| DE60332625D1 (de) | 2010-07-01 |
| EP1515817A2 (en) | 2005-03-23 |
| KR100989881B1 (ko) | 2010-10-26 |
| KR20060035548A (ko) | 2006-04-26 |
| JP5575622B2 (ja) | 2014-08-20 |
| CN1662331A (zh) | 2005-08-31 |
| US20060112785A1 (en) | 2006-06-01 |
| ATE468189T1 (de) | 2010-06-15 |
| JP2005530048A (ja) | 2005-10-06 |
| AU2003238645A8 (en) | 2004-01-06 |
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