CN1686648A - Preparation method of nano-bronze powder - Google Patents

Preparation method of nano-bronze powder Download PDF

Info

Publication number
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
Authority
CN
China
Prior art keywords
solution
copper
add
ammoniacal liquor
obtains
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
CN 200510049660
Other languages
Chinese (zh)
Other versions
CN1299864C (en
Inventor
黄德欢
李宗全
吕春菊
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CNB200510049660XA priority Critical patent/CN1299864C/en
Publication of CN1686648A publication Critical patent/CN1686648A/en
Application granted granted Critical
Publication of CN1299864C publication Critical patent/CN1299864C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)

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

The preparation method of copper nanoparticle
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.
CNB200510049660XA 2005-04-26 2005-04-26 Preparation method of nano-bronze powder Expired - Fee Related CN1299864C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB200510049660XA CN1299864C (en) 2005-04-26 2005-04-26 Preparation method of nano-bronze powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB200510049660XA CN1299864C (en) 2005-04-26 2005-04-26 Preparation method of nano-bronze powder

Publications (2)

Publication Number Publication Date
CN1686648A true CN1686648A (en) 2005-10-26
CN1299864C CN1299864C (en) 2007-02-14

Family

ID=35304690

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB200510049660XA Expired - Fee Related CN1299864C (en) 2005-04-26 2005-04-26 Preparation method of nano-bronze powder

Country Status (1)

Country Link
CN (1) CN1299864C (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Also Published As

Publication number Publication date
CN1299864C (en) 2007-02-14

Similar Documents

Publication Publication Date Title
CN1299864C (en) Preparation method of nano-bronze powder
CN1299865C (en) Preparation method of nuclear shell structured nano-gold copper powder
DE60125147T2 (en) HOLLOW FULLER ARTICLE NANOPARTICLES AS SOLID LUBRICANTS IN COMPOSITE MATRICES
CN1305618C (en) Method of preparing nano-bronze powder using electric deposition
JP5745035B2 (en) High lubricity solid lubricant
WO2011099823A2 (en) Nano-diamond dispersion solution and method for preparing same
CN101033065A (en) Method of purifying environment-friendly type ultra-fine diamond
WO2019119487A1 (en) Hydroxyl graphene modified clad layer sealant and preparation method therefor
CN108687359B (en) Preparation method of nano copper-coated aluminum composite fuel
CN108017939B (en) Thiadiazole derivative modified graphene and preparation method and application thereof
CN1219439C (en) Nano hud-type bimetal powder of copper and stannum, preparing method and application
CN1305772C (en) Process for preparing nano cuprous oxide powder
CN1275900C (en) Process for preparing composite powder of nano copper-zine oxide
CN1772837A (en) Functional luminescent material and its prepn
Peng et al. Tribological performance of freeze-drying nano-copper particle as additive of paroline oil
CN112779074A (en) Lubricant as well as preparation method and application thereof
Bronusiene et al. Effect of ascorbic acid on the properties of tin sulfide films for supercapacitor application
CN1302882C (en) Method for preparing nano gold solution
CN1155448C (en) Nm-class gold powder and its preparing process
Li et al. Microstructure and properties of MAO composite coatings containing nanorutile TiO2 particles
CN1513588A (en) Modified ceramic microfiltering membrane
CN1908078A (en) Preparation method of nano-copper used as lubricating oil additive
CN108002367B (en) Preparation method of water-soluble fluorinated graphene
Yang et al. Controllable fabrication and self-assembly of Cu nanostructures: the role of Cu 2+ complexes
CN111112639B (en) Nanoscale spherical silver particles with room-temperature antifriction effect and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20070214

Termination date: 20140426