CN1686648A - Preparation method of nano-bronze powder - Google Patents
Preparation method of nano-bronze powder Download PDFInfo
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- CN1686648A CN1686648A CN 200510049660 CN200510049660A CN1686648A CN 1686648 A CN1686648 A CN 1686648A CN 200510049660 CN200510049660 CN 200510049660 CN 200510049660 A CN200510049660 A CN 200510049660A CN 1686648 A CN1686648 A CN 1686648A
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Abstract
A process for preparing the copper nanoparticles includes dissolving copper salt in distilled water, slowly adding ammonia water until the solution becomes clear, adding polyvinyl pyrrolidone and sodium laurylsulfate, heating, stirring while adding the aqueous solution of hydrazine hydrate until pH=8.5-9.5, adding atoleine or lubricating oil, stirring, ageing, centrifugal separation in N2 or argon atmosphere, washing and vacuum drying.
Description
Technical field
The present invention relates to the preparation method of copper nanoparticle.
Background technology
Copper is the sliding bearing basic material of using always, and copper and some other material are (as graphite, MoS
2Deng) the compound copper radical self-lubricating composite that becomes.Studies show that in recent years adds nanometer copper particle in the lubricating oil, copper particle plays skeleton function, prevents the excess flow of lubricating oil in the friction process, improves bearing capacity, reduces the real contact area between friction surface, thereby reduces coefficient of friction, reduces wearing and tearing.Therefore, the lubricated oil additive of nanometer copper particle conduct can increase substantially the lubricating ability and the usefulness of lubricating oil, and copper nanoparticle is with a wide range of applications, and the preparation of copper nanoparticle is the basis of its application.
Summary of the invention
The object of the present invention is to provide a kind of preparation method of copper nanoparticle.
The preparation method of copper nanoparticle of the present invention, its step is as follows:
1) in distilled water, adds mantoquita, compound concentration is the copper salt solution of 0.005~0.05mol/L, slowly adds concentration and be 0.5~15.0% ammoniacal liquor, solution becomes muddiness when beginning to add ammoniacal liquor, adding with ammoniacal liquor clears up gradually, and stops to add ammoniacal liquor when solution becomes fully after limpid;
2) in the solution that step 1) obtains, add polyvinylpyrrolidone and lauryl sodium sulfate, the mass ratio of mantoquita, polyvinylpyrrolidone, lauryl sodium sulfate is 0.01~5.0: 0.02~10.0: 0.0001~5.0, mixed solution is heated to 50~80 ℃;
3) in the stirring, with temperature is that 25~80 ℃, concentration are that 0.01~5.0% hydrazine hydrate aqueous solution joins step 2) in the mixed solution that obtains, when the pH value reaches 8.5~9.5, stop to add hydrazine hydrate aqueous solution, in solution, add solution amount one thousandth to ten thousand/ atoleine or lubricating oil, continue to stir 20~100 minutes, ageing is 20~50 hours then, obtains containing the suspension of nanometer copper;
4) under nitrogen or argon gas atmosphere, suspension is carried out centrifugation, clean with distilled water and ethanol;
5) copper nanoparticle after will cleaning gets final product in 40~80 ℃ of following vacuum drying.
Above-mentioned mantoquita can be copper sulphate or copper nitrate.Said lubricating oil can be the lubricating oil of any trade mark.
Technology of the present invention is simple, and the copper nanoparticle particle that makes is little, and its granularity is 10 to 100nm; Under protective atmosphere, separate, clean and drying, be difficult for taking place oxidation.
Description of drawings
Fig. 1 is the electronic microscopic image of the copper nanoparticle that makes of embodiment 1, and the particle diameter of copper particle is 13nm, and the illustration in the upper left corner is the electron diffraction diagram of copper nanoparticle among the figure;
Fig. 2 is the X-ray diffractogram of the copper nanoparticle that makes of embodiment 2, and the particle diameter of copper particle is 42nm;
Fig. 3 is the X-ray diffractogram of the copper nanoparticle that makes of embodiment 3, and the particle diameter of copper particle is 55nm.
The specific embodiment
Embodiment 1
1) be the copper nitrate aqueous solution 100ml of 0.01mol/L with the distilled water compound concentration, slowly add concentration and be 5.0% ammoniacal liquor, solution becomes muddiness when beginning to add ammoniacal liquor clears up gradually with the adding of ammoniacal liquor, stops to add ammoniacal liquor when solution becomes fully after limpid;
2) in the solution that step 1) obtains, add 2.5g polyvinylpyrrolidone, 1g lauryl sodium sulfate, mixed solution is heated to 60 ℃;
3) in the stirring, with temperature is that 60 ℃, concentration are that 2.5% hydrazine hydrate aqueous solution joins step 2) in the mixed solution that obtains, when the pH value reaches 9, stop to add hydrazine hydrate aqueous solution, in solution, add the 0.01ml atoleine, continue to stir 60 minutes, ageing is 20 hours then, obtains containing the suspension of nanometer copper;
4) under argon gas atmosphere, suspension is carried out centrifugation, clean 3 times with ethanol with distilled water, back earlier;
5) copper nanoparticle after the step 4) cleaning is put into vacuum drying chamber, dry down at 70 ℃.
Fig. 1 is the electronic microscopic image of the copper nanoparticle that makes, and the particle diameter of copper particle is 13nm.
Embodiment 2
1) be the copper nitrate aqueous solution 100ml of 0.01mol/L with the distilled water compound concentration, slowly add concentration and be 5.0% ammoniacal liquor, solution becomes muddiness when beginning to add ammoniacal liquor clears up gradually with the adding of ammoniacal liquor, stops to add ammoniacal liquor when solution becomes fully after limpid;
2) solution that obtains in step 1) adds 1g polyvinylpyrrolidone, 0.001g lauryl sodium sulfate, and mixed solution is heated to 70 ℃;
3) in the stirring, with temperature is that 70 ℃, concentration are that 2.5% hydrazine hydrate aqueous solution joins step 2) in the mixed solution that obtains, when the pH value reaches 9, stop to add hydrazine hydrate aqueous solution, in solution, add the 0.01ml atoleine, continue to stir 60 minutes, ageing is 20 hours then, obtains containing the suspension of nanometer copper;
4) suspension is carried out centrifugation under argon gas atmosphere, clean 3 times with ethanol with distilled water, back earlier;
5) copper nanoparticle after the step 4) cleaning is put into vacuum drying chamber, dry down at 70 ℃.
Fig. 2 is the X-ray diffractogram of the copper nanoparticle that makes, and the particle diameter of copper particle is 42nm.
Embodiment 3
1) be the copper sulfate solution 100ml of 0.03mol/L with the distilled water compound concentration, slowly add concentration and be 10.0% ammoniacal liquor, solution becomes muddiness when beginning to add ammoniacal liquor clears up gradually with the adding of ammoniacal liquor, stops to add ammoniacal liquor when solution becomes fully after limpid;
2) solution that obtains in step 1) adds 1g polyvinylpyrrolidone, 0.01g lauryl sodium sulfate, and mixed solution is heated to 80 ℃;
3) in the stirring, with temperature is that 80 ℃, concentration are that 2.5% hydrazine hydrate aqueous solution joins step 2) in the mixed solution that obtains, when the pH value reaches 10, stop to add hydrazine hydrate aqueous solution, in solution, add the 0.01ml atoleine, continue to stir 60 minutes, ageing is 20 hours then, obtains containing the suspension of nanometer copper;
4) suspension that step 3) is obtained carries out centrifugation under argon gas atmosphere, cleans 3 times with ethanol with distilled water, back earlier;
5) copper nanoparticle after the step 4) cleaning is put into vacuum drying chamber, dry down at 80 ℃.
Fig. 3 is the X-ray diffractogram of the copper nanoparticle that makes, and the particle diameter of copper particle is 55nm.
Embodiment 4
1) be the copper nitrate aqueous solution 100ml of 0.04mol/L with the distilled water compound concentration, slowly add concentration and be 5.0% ammoniacal liquor, solution becomes muddiness when beginning to add ammoniacal liquor clears up gradually with the adding of ammoniacal liquor, stops to add ammoniacal liquor when solution becomes fully after limpid;
2) solution that obtains in step 1) adds 0.1g polyvinylpyrrolidone, 2g lauryl sodium sulfate, and mixed solution is heated to 70 ℃;
3) in the stirring, with temperature is that 70 ℃, concentration are that 2.5% hydrazine hydrate aqueous solution joins step 2) in the mixed solution that obtains, when the pH value reaches 9, stop to add hydrazine hydrate aqueous solution, in solution, add 0.01ml lubricating oil, continue to stir 60 minutes, ageing is 30 hours then, obtains containing the suspension of nanometer copper;
4) suspension that step 3) is obtained carries out centrifugation, cleans 3 times with ethanol with distilled water, back earlier under argon gas atmosphere;
5) copper nanoparticle after the step 4) cleaning is put into vacuum drying chamber, dry under 70 ℃, obtain copper nanoparticle, the particle diameter of copper particle is 45nm.
Claims (2)
1. the preparation method of copper nanoparticle, its step is as follows:
1) in distilled water, adds mantoquita, compound concentration is the copper salt solution of 0.005~0.05mol/L, slowly adds concentration and be 0.5~15.0% ammoniacal liquor, solution becomes muddiness when beginning to add ammoniacal liquor, adding with ammoniacal liquor clears up gradually, and stops to add ammoniacal liquor when solution becomes fully after limpid;
2) in the solution that step 1) obtains, add polyvinylpyrrolidone and lauryl sodium sulfate, the mass ratio of mantoquita, polyvinylpyrrolidone, lauryl sodium sulfate is 0.01~5.0: 0.02~10.0: 0.0001~5.0, mixed solution is heated to 50~80 ℃;
3) in the stirring, with temperature is that 25~80 ℃, concentration are that 0.01~5.0% hydrazine hydrate aqueous solution joins step 2) in the mixed solution that obtains, when the pH value reaches 8.5~9.5, stop to add hydrazine hydrate aqueous solution, in solution, add solution amount one thousandth to ten thousand/ atoleine or lubricating oil, continue to stir 20~100 minutes, ageing is 20~50 hours then, obtains containing the suspension of nanometer copper;
4) under nitrogen or argon gas atmosphere, suspension is carried out centrifugation, clean with distilled water and ethanol;
5) copper nanoparticle after will cleaning gets final product in 40~80 ℃ of following vacuum drying.
2. the preparation method of copper nanoparticle according to claim 1 is characterized in that said mantoquita is copper sulphate or copper nitrate.
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Cited By (11)
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CN101890506A (en) * | 2010-07-31 | 2010-11-24 | 太原理工大学 | Method for preparing nano-copper |
CN101104205B (en) * | 2006-07-10 | 2011-06-01 | 三星电机株式会社 | Method for manufacturing copper nano granule |
CN102198513A (en) * | 2011-05-27 | 2011-09-28 | 中南大学 | Method for preparing nano copper particle |
CN102371358A (en) * | 2011-11-18 | 2012-03-14 | 复旦大学 | Aqueous-phase preparation method for re-dispersible nano-copper particles |
CN102560500A (en) * | 2012-02-03 | 2012-07-11 | 昆山市洁驰环保科技发展有限公司 | Method for producing nanometer copper powder by use of waste alkaline etching solution which can be regenerated and apparatus thereof |
CN102601381A (en) * | 2012-03-11 | 2012-07-25 | 郭雨 | Copper nano powder and preparation method of copper nano powder |
CN101607317B (en) * | 2009-07-16 | 2012-10-17 | 复旦大学 | Preparation method of nano-copper |
CN103769598A (en) * | 2013-10-08 | 2014-05-07 | 东江环保股份有限公司 | Method for stably preparing nano-copper powder |
CN105945302A (en) * | 2016-05-20 | 2016-09-21 | 金陵科技学院 | Preparation method for antioxidant copper nanopowder |
CN107116229A (en) * | 2016-02-25 | 2017-09-01 | 新材料与产业技术北京研究院 | A kind of copper nanoparticle and preparation method thereof |
CN107812954A (en) * | 2017-12-01 | 2018-03-20 | 深圳市中金岭南科技有限公司 | The preparation method and its preparation facilities of a kind of copper powder |
Family Cites Families (6)
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JP2728726B2 (en) * | 1989-05-10 | 1998-03-18 | 正同化学工業株式会社 | Method for producing fine copper powder |
US5179056A (en) * | 1991-05-06 | 1993-01-12 | Union Carbide Chemicals & Plastics Technology Corporation | Production of alkenyl alkanoate catalysts |
JPH05221637A (en) * | 1992-02-10 | 1993-08-31 | Sumitomo Metal Ind Ltd | Production of cuprous oxide powder and copper powder |
CN1191142C (en) * | 2003-08-12 | 2005-03-02 | 北京科技大学 | Method for mfg nano copper powder |
CN1241706C (en) * | 2004-01-13 | 2006-02-15 | 上海大学 | Method for manufacturing nano-copper |
CN1247354C (en) * | 2004-11-23 | 2006-03-29 | 北京科技大学 | Method for preparing nanometer copper powder by chemical reduction in water solution |
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CN101104205B (en) * | 2006-07-10 | 2011-06-01 | 三星电机株式会社 | Method for manufacturing copper nano granule |
CN101607317B (en) * | 2009-07-16 | 2012-10-17 | 复旦大学 | Preparation method of nano-copper |
CN101890506A (en) * | 2010-07-31 | 2010-11-24 | 太原理工大学 | Method for preparing nano-copper |
CN101890506B (en) * | 2010-07-31 | 2013-04-24 | 太原理工大学 | Method for preparing nano-copper |
CN102198513A (en) * | 2011-05-27 | 2011-09-28 | 中南大学 | Method for preparing nano copper particle |
CN102371358A (en) * | 2011-11-18 | 2012-03-14 | 复旦大学 | Aqueous-phase preparation method for re-dispersible nano-copper particles |
CN102560500A (en) * | 2012-02-03 | 2012-07-11 | 昆山市洁驰环保科技发展有限公司 | Method for producing nanometer copper powder by use of waste alkaline etching solution which can be regenerated and apparatus thereof |
CN102601381A (en) * | 2012-03-11 | 2012-07-25 | 郭雨 | Copper nano powder and preparation method of copper nano powder |
CN102601381B (en) * | 2012-03-11 | 2014-01-29 | 郭雨 | Preparation method of copper nano powder |
CN103769598A (en) * | 2013-10-08 | 2014-05-07 | 东江环保股份有限公司 | Method for stably preparing nano-copper powder |
CN107116229A (en) * | 2016-02-25 | 2017-09-01 | 新材料与产业技术北京研究院 | A kind of copper nanoparticle and preparation method thereof |
CN105945302A (en) * | 2016-05-20 | 2016-09-21 | 金陵科技学院 | Preparation method for antioxidant copper nanopowder |
CN105945302B (en) * | 2016-05-20 | 2017-11-28 | 金陵科技学院 | A kind of preparation method of Anti-Oxidation Copper Nanopowders |
CN107812954A (en) * | 2017-12-01 | 2018-03-20 | 深圳市中金岭南科技有限公司 | The preparation method and its preparation facilities of a kind of copper powder |
CN107812954B (en) * | 2017-12-01 | 2020-08-21 | 深圳市中金岭南科技有限公司 | Preparation method and preparation device of copper powder |
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