CN1693204A - Process for preparing nano cuprous oxide powder - Google Patents
Process for preparing nano cuprous oxide powder Download PDFInfo
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- CN1693204A CN1693204A CN 200510049661 CN200510049661A CN1693204A CN 1693204 A CN1693204 A CN 1693204A CN 200510049661 CN200510049661 CN 200510049661 CN 200510049661 A CN200510049661 A CN 200510049661A CN 1693204 A CN1693204 A CN 1693204A
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- cuprous oxide
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Abstract
A process for preparing the cuprous oxide nanoparticles includes such steps as dissolving copper salt in deionized water, adding polyvinyl pyrrolidone and sodium laurylsulfate, stirring while adding the aqueous solution of dyrazine hydrate until pH=6.8-7.2, adding atoleine or lubricating oil, stirring, ageing, centrifugal separation, washing and drying.
Description
Technical field
The present invention relates to the preparation method of nano cuprous oxide powder.
Background technology
Lubricant (comprising lubricating oil, lubricating grease) is widely used in mechanical component, to reduce the friction and wear between the mechanical component.Along with the development of industrial technology, also just more and more higher to the requirement of lubricant.For this reason, in lubricant, add suitable slip additive, improve the anti-friction wear-resistant ability of lubricant.
Red copper oxide belongs to cubic crystal structure, and four copper atoms constitute tetrahedron, and a Sauerstoffatom occupies the tetrahedron center.Such copper-oxygen tetrahedron interconnects in the mode that is total to the summit, forms cuprous oxide crystal.The composition of Red copper oxide and structure make it can be used as slip additive.
Summary of the invention
The object of the present invention is to provide a kind of preparation method of nano cuprous oxide powder, particularly prepare the method for nano cuprous oxide powder with chemical method.
The preparation method of nano cuprous oxide powder of the present invention, its step is as follows:
1) in deionized water, adds mantoquita, compound concentration is the copper salt solution of 0.005～0.5mol/L, treat that mantoquita dissolving back adds polyvinylpyrrolidone and sodium lauryl sulphate, the mass ratio of mantoquita, polyvinylpyrrolidone, sodium lauryl sulphate is 0.01～5.0: 0.02～10.0: 0.0001～5.0;
2) in the stirring, with concentration is that 0.01～1.5% hydrazine hydrate aqueous solution joins in the mixing solutions that step 1) obtains, when the pH value reaches 6.8～7.2, stop to add hydrazine hydrate aqueous solution, and add solution amount thousandth to ten thousand/ whiteruss or lubricating oil, continue to stir 20～60 minutes, ageing is 10～40 hours then, obtains containing the suspension of nano cuprous oxide;
3) with step 2) suspension that obtains carries out centrifugation, cleans with deionized water and ethanol;
4) nano cuprous oxide powder after will cleaning 40～80 ℃ dry down, get final product.
Above-mentioned mantoquita can be copper sulfate or cupric nitrate.Said lubricating oil can be the lubricating oil of any trade mark.
Preparation technology of the present invention is simple, and cost is low, and the particle of the nano cuprous oxide that makes is little, and granularity is 10 to 100nm.Experiment shows, after the nano cuprous oxide powder that the present invention is made adds lubricating oil, lubricating grease to, can improve the anti-friction wear-resistant ability of lubricant greatly, the work-ing life of improving mechanical component.
Description of drawings
Fig. 1 is the X-ray diffractogram of the nano cuprous oxide powder of embodiment 1 preparation;
Fig. 2 is the X-ray diffractogram of the nano cuprous oxide powder of embodiment 2 preparations.
Embodiment
Embodiment 1
1) in the 100mL deionized water, adds cupric nitrate, compound concentration is the copper nitrate solution of 0.005mol/L, treat that cupric nitrate dissolving back adds 0.5g polyvinylpyrrolidone, 0.001g sodium lauryl sulphate, the mass ratio of cupric nitrate, polyvinylpyrrolidone, sodium lauryl sulphate is 0.094: 0.5: 0.001;
2) stirring, is that 1.0% hydrazine hydrate aqueous solution joins in the mixing solutions that step 1) obtains, when the pH value reaches 7.0 with concentration, stop to add hydrazine hydrate aqueous solution, add the 0.01ml whiteruss, continue to stir 50 minutes, ageing is 10 hours then, obtains containing the suspension of nano cuprous oxide;
3) with step 2) suspension that obtains carries out centrifugation, cleans 3 times with ethanol with deionized water, back earlier;
4) nano cuprous oxide powder after will cleaning is put into baking oven, 70 ℃ dry down, obtain nano cuprous oxide.
Fig. 1 is the X-ray diffractogram of the nano cuprous oxide powder of present embodiment preparation, and the granularity of Red copper oxide is 12nm, and the diffraction peak of Red copper oxide marks in the drawings.
Embodiment 2
1) in the 100mL deionized water, adds cupric nitrate, compound concentration is the copper nitrate solution of 0.01mol/L, treat that cupric nitrate dissolving back adds 2.5g polyvinylpyrrolidone, 0.001g sodium lauryl sulphate, the mass ratio of cupric nitrate, polyvinylpyrrolidone, sodium lauryl sulphate is 0.19: 2.5: 0.001;
2) stirring, is that 1.0% hydrazine hydrate aqueous solution joins in the mixing solutions that step 1) obtains, when the pH value reaches 7.0 with concentration, stop to add hydrazine hydrate aqueous solution, add the 0.01ml whiteruss, continue to stir 60 minutes, ageing is 24 hours then, obtains containing the suspension of nano cuprous oxide;
3) with step 2) suspension that obtains carries out centrifugation, cleans 3 times with ethanol with deionized water, back earlier;
4) nano cuprous oxide after will cleaning is put into baking oven, 70 ℃ dry down, obtain nano cuprous oxide powder.
Fig. 2 is the X-ray diffractogram of the nano cuprous oxide powder of present embodiment preparation, and the granularity of Red copper oxide is 10nm.The diffraction peak of Red copper oxide marks in the drawings.
Embodiment 3
1) in the 100mL deionized water, adds cupric nitrate, compound concentration is the copper nitrate solution of 0.02mol/L, treat that cupric nitrate dissolving back adds 2.0g polyvinylpyrrolidone, 0.5g sodium lauryl sulphate, the mass ratio of cupric nitrate, polyvinylpyrrolidone, sodium lauryl sulphate was respectively 0.38: 2.0: 0.5;
2) stirring, is that 1.0% hydrazine hydrate aqueous solution joins in the mixing solutions that step 1) obtains, when the pH value reaches 7.0 with concentration, stop to add hydrazine hydrate aqueous solution, add the 0.02ml whiteruss, continue to stir 60 minutes, ageing is 20 hours then, obtains containing the suspension of nano cuprous oxide;
3) with step 2) suspension that obtains carries out centrifugation, cleans 3 times with deionized water and ethanol;
4) nano cuprous oxide after will cleaning is put into baking oven, 60 ℃ dry down, obtain nano cuprous oxide powder, the granularity of Red copper oxide is 20nm.
Embodiment 4
1) in the 100mL deionized water, adds copper sulfate, compound concentration is the copper-bath of 0.01mol/L, treat that copper sulfate dissolving back adds 2.0g polyvinylpyrrolidone, 1.0g sodium lauryl sulphate, the mass ratio of copper sulfate, polyvinylpyrrolidone, sodium lauryl sulphate is 0.19: 2.0: 1.0;
2) stirring, is that 0.8% hydrazine hydrate aqueous solution joins in the mixing solutions that step 1) obtains, when the pH value reaches 7.0 with concentration, stop to add hydrazine hydrate aqueous solution, add 0.02ml lubricating oil, continue to stir 60 minutes, ageing is 15 hours then, obtains containing the suspension of nano cuprous oxide;
3) with step 2) suspension that obtains carries out centrifugation, cleans 3 times with deionized water and ethanol;
4) nano cuprous oxide after will cleaning is put into baking oven, 70 ℃ dry down, obtain nano cuprous oxide powder, the granularity of Red copper oxide is 18nm.
Claims (2)
1. the preparation method of nano cuprous oxide powder is characterized in that comprising step:
1) in deionized water, adds mantoquita, compound concentration is the copper salt solution of 0.005～0.5mol/L, treat that mantoquita dissolving back adds polyvinylpyrrolidone and sodium lauryl sulphate, the mass ratio of mantoquita, polyvinylpyrrolidone, sodium lauryl sulphate is 0.01～5.0: 0.02～10.0: 0.0001～5.0;
2) in the stirring, with concentration is that 0.01～1.5% hydrazine hydrate aqueous solution joins in the mixing solutions that step 1) obtains, when the pH value reaches 6.8～7.2, stop to add hydrazine hydrate aqueous solution, and add solution amount thousandth to ten thousand/ whiteruss or lubricating oil, continue to stir 20～60 minutes, ageing is 10～40 hours then, obtains containing the suspension of nano cuprous oxide;
3) with step 2) suspension that obtains carries out centrifugation, cleans with deionized water and ethanol;
4) nano cuprous oxide powder after will cleaning 40～80 ℃ dry down, get final product.
2. the preparation method of nano cuprous oxide powder according to claim 1 is characterized in that mantoquita is copper sulfate or cupric nitrate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100496614A CN1305772C (en) | 2005-04-26 | 2005-04-26 | Process for preparing nano cuprous oxide powder |
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| Application Number | Priority Date | Filing Date | Title |
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| CNB2005100496614A CN1305772C (en) | 2005-04-26 | 2005-04-26 | Process for preparing nano cuprous oxide powder |
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| CN1693204A true CN1693204A (en) | 2005-11-09 |
| CN1305772C CN1305772C (en) | 2007-03-21 |
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| CNB2005100496614A Expired - Fee Related CN1305772C (en) | 2005-04-26 | 2005-04-26 | Process for preparing nano cuprous oxide powder |
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Cited By (5)
| 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 |
| CN101905899A (en) * | 2010-08-16 | 2010-12-08 | 河北工业大学 | Method for preparing ordered nano cuprous oxide polycrystalline powder |
| CN103172104A (en) * | 2013-04-03 | 2013-06-26 | 浙江理工大学 | Preparation method of nano cuprous oxide |
| CN105695070A (en) * | 2014-11-23 | 2016-06-22 | 武汉鸿信通科技有限公司 | Liquid lubricant |
| CN105858710A (en) * | 2016-03-31 | 2016-08-17 | 合肥工业大学 | Method for preparing purple cuprous oxide |
Family Cites Families (4)
| 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 |
| CN1027803C (en) * | 1990-03-12 | 1995-03-08 | 烟台市金河化工厂 | Method for making cuprous oxide |
| JPH05221637A (en) * | 1992-02-10 | 1993-08-31 | Sumitomo Metal Ind Ltd | Production of cuprous oxide powder and copper powder |
| CN1249276C (en) * | 2003-07-11 | 2006-04-05 | 华中师范大学 | Method for preparing stable nanometer cuprous oxide whiskers with chemical precipitation method |
-
2005
- 2005-04-26 CN CNB2005100496614A patent/CN1305772C/en not_active Expired - Fee Related
Cited By (8)
| 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 |
| CN101890506B (en) * | 2010-07-31 | 2013-04-24 | 太原理工大学 | Method for preparing nano-copper |
| CN101905899A (en) * | 2010-08-16 | 2010-12-08 | 河北工业大学 | Method for preparing ordered nano cuprous oxide polycrystalline powder |
| CN101905899B (en) * | 2010-08-16 | 2012-01-04 | 河北工业大学 | Method for preparing ordered nano cuprous oxide polycrystalline powder |
| CN103172104A (en) * | 2013-04-03 | 2013-06-26 | 浙江理工大学 | Preparation method of nano cuprous oxide |
| CN105695070A (en) * | 2014-11-23 | 2016-06-22 | 武汉鸿信通科技有限公司 | Liquid lubricant |
| CN105858710A (en) * | 2016-03-31 | 2016-08-17 | 合肥工业大学 | Method for preparing purple cuprous oxide |
| CN105858710B (en) * | 2016-03-31 | 2017-05-17 | 合肥工业大学 | Method for preparing purple cuprous oxide |
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|---|---|
| CN1305772C (en) | 2007-03-21 |
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Granted publication date: 20070321 Termination date: 20140426 |