CN1861298A - Method for preparing cube shaped copper particles - Google Patents
Method for preparing cube shaped copper particles Download PDFInfo
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- CN1861298A CN1861298A CN 200510011717 CN200510011717A CN1861298A CN 1861298 A CN1861298 A CN 1861298A CN 200510011717 CN200510011717 CN 200510011717 CN 200510011717 A CN200510011717 A CN 200510011717A CN 1861298 A CN1861298 A CN 1861298A
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- rub
- liter
- concentration
- mantoquita
- reducing agent
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Abstract
A process for preparing cubic Cu particles features that the liquid-phase reduction method is used, in which the Cu salt is reduced by reducer to obtain cubic Cu particles and the size and shell thickness of cubic particle can be controlled by regulating the concentrations of Cu salt and reducer and the reaction temp.
Description
Invention field
The invention belongs to the preparation and the applied technical field of metal photoelectric functional material, particularly relate to the preparation method of cube shaped copper particles.
Background technology
The control of the pattern of metallic particles is the noticeable research direction in nanometer material science field in recent years.The pattern of nano material comprises optics to the physics and the chemical property of nano material, electricity, and performances such as magnetics and catalysis have significant impact.For example, to studies show that of the silver nano-grain of different-shape, triangle, pentagon and spherical particle demonstrate redness, green and blueness [Mock, J.J. respectively under light microscope; Barbic, M.; Smith, D.R; Schultz, D.A.; Schultz, S.J.Chem.Phys.2002,116,6755].The draw ratio of metal rod-shpaed particle directly affects the optical anisotropy of material.In addition, the magnetic of nickel, cobalt nanometer rods is subjected to the influence of pattern [Maillard, M.; Giorgio, S.; Pileni, M.P.J.Phys.Chem.B.2003,107,2466].
Copper is a kind of important metal material, and the electric conductivity in the metal is only second to silver, but its price is more much lower than silver, thereby is widely used in electronics industry.In addition, also can be widely used in aspects such as catalysis, metallurgy, coating, resin, lubricating oil and heat conduction.In recent years, people study the pattern control of copper product, have prepared the copper nano material of multiple patterns such as sphere, corynebacterium.But the preparation of cube shaped copper product yet there are no report.
In our preparation method,, can synthesize cube shaped copper particles with uniform-dimension by the control reaction condition.
Summary of the invention
The object of the present invention is to provide a kind of method for preparing cube shaped copper particles.Adopt this method technology simple, easy to operate, production cost is low.
The objective of the invention is to be achieved through the following technical solutions:
The preparation of employing liquid phase reduction, by reducing agent reduction mantoquita, the copper particle that makes is cube shaped.
The step of concrete grammar is as follows:
(1). prepare the mantoquita and the reducing agent aqueous solution respectively, wherein the concentration of mantoquita is 2 * 10 in the solution
-6～1 * 10
-2Rub/liter, be preferably 2 * 10
-5～5 * 10
-3Rub/liter; The concentration of reducing agent is 5 * 10
-4～1 rub/liter, be preferably 3 * 10
-3～0.5 rub/liter.
(2). with the mantoquita and the reducing agent aqueous solution of step (1) preparation, making the mantoquita concentration of mixing in the solution of back is 1 * 10
-6～5 * 10
-3Rub/liter, be preferably 1 * 10
-5～1 * 10
-3Rub/liter; The concentration of reducing agent is 2 * 10
-5～0.1 rub/liter, be preferably 5 * 10
-4～1 * 10
-2Rub/liter.Stirred 0.5～3 hour down at 20～70 ℃, obtain yellow suspension.Centrifugation obtains cube shaped copper particles, and the particle length of side is yellow mercury oxide at 80～300nm.After the vacuum drying of gained precipitation, obtain the copper functional material.
Described mantoquita comprises copper nitrate, copper chloride, copper sulphate, basic copper carbonate or cupric tartrate.
Described reducing agent comprises organic amine, azanol, polyol, hydrazine hydrate, sodium borohydride, inferior sodium phosphate, formaldehyde or they two or more mixture arbitrarily.
Described organic amine is formamide, p-phenylenediamine (PPD), 4-amino-N-ethyl-N-(Beta-methyl sulfonamide ethyl) meta-aminotoluene list water sulfate, triethanolamine or their mixture etc.; Azanol is a hydroxylamine hydrochloride etc.; Polyol is isopropyl alcohol, ethylene glycol or their mixture etc.
The product purpose that the present invention prepares is extensive, is the important electron industrial materials.Also can be widely used in fields such as catalysis, metallurgy, coating, resin, lubricating oil and heat conduction.
The copper particle that adopts method of the present invention to obtain is cube shaped, as shown in Figure 1.
Method energy consumption of the present invention is low, the product purity height, and evenly and good dispersion, experiment conditions such as concentration that granule-morphology can be by mantoquita and reducing agent and reaction temperature are controlled.
Enforcement principle of the present invention is that reducing agent and mantoquita reaction at first form atomic little primary particle, and then assemble growth by primary particle, thereby obtain end product.When reactant concentration in the system was low, being adsorbed in the gathering growth course of effects of ion played an important role.Because copper ion, makes the growth rate difference of each crystal face in the adsorbance difference of the different crystal faces of primary particle, therefore obtain the end product of different-shape.Under experiment condition of the present invention, because the absorption of copper ion, greater than (100) crystal face, final particle only keeps 6 (100) crystal faces that growth is slower to particle, thereby forms cube structure in the growth rate of (111) crystal face.Control granule-morphology by this method, simple, be convenient to operation.
What this method was significantly different with preparation method in the past is that in the present invention, the simple control of condition by experiment can make cube shaped copper particle.
Description of drawings
Fig. 1. the cube shaped copper particles material electromicroscopic photograph of embodiments of the invention 1.
The specific embodiment
Embodiment 1
(1). prepare the copper chloride and the hydroxylamine hydrochloride aqueous solution respectively, wherein the concentration of copper chloride is 1.5 * 10 in the solution
-3Rub/liter; The concentration of reducing agent is 7.1 * 10
-3Rub/liter.
(2). respectively with the copper chloride and the hydroxylamine hydrochloride aqueous solution of preparation in the step (1), making the copper chloride concentration of mixing in the solution of back is 2.1 * 10
-4Rub/liter; The concentration of hydroxylamine hydrochloride is 5.3 * 10
-3Rub/liter.Stirred 1 hour down at 35 ℃, obtain yellow suspension.Centrifugation obtains cube shaped copper particles, and the particle length of side is yellow mercury oxide at 145nm.After the vacuum drying of gained precipitation, obtain the copper functional material.See accompanying drawing 1.
Embodiment 2
(1). prepare the copper nitrate and the p-phenylenediamine (PPD) aqueous solution respectively, wherein the concentration of copper nitrate is 6.2 * 10 in the solution
-5Rub/liter; The concentration of p-phenylenediamine (PPD) is 7.7 * 10
-3Rub/liter.
(2). respectively with the copper nitrate and the p-phenylenediamine (PPD) aqueous solution of preparation in the step (1), making the copper nitrate concentration of mixing in the solution of back is 2.3 * 10
-5Rub/liter; The concentration of p-phenylenediamine (PPD) is 5 * 10
-4Rub/liter.Stirred 2 hours down at 20 ℃, obtain yellow suspension.Centrifugation obtains cube shaped copper particles, and the particle length of side is yellow mercury oxide at 265nm.After the vacuum drying of gained precipitation, obtain the copper functional material.
Embodiment 3
(1). prepare copper sulphate and hydrazine hydrate aqueous solution respectively, wherein the concentration of copper sulphate is 2 * 10 in the solution
-3Rub/liter; The concentration of hydrazine hydrate is 6 * 10
-2Rub/liter.
(2). copper sulphate and the hydrazine hydrate aqueous solution with preparation in the step (1) mixes respectively, and making the concentration of copper sulfate that mixes in the solution of back is 3.5 * 10
-4Rub/liter; The concentration of hydrazine hydrate is 8 * 10
-3Rub/liter.Stirred 0.5 hour down at 45 ℃, obtain yellow suspension.Centrifugation obtains cube shaped copper particles, and the particle length of side is yellow mercury oxide at 180nm.After the vacuum drying of gained precipitation, obtain the copper functional material.
Embodiment 4
(1). prepare basic copper carbonate and formalin respectively, wherein the concentration of basic copper carbonate is 7.5 * 10 in the solution
-4Rub/liter; The concentration of formaldehyde is 8 * 10
-3Rub/liter.
(2). basic copper carbonate and the formalin with preparation in the step (1) mixes respectively, and making the basic copper carbonate concentration of mixing in the solution of back is 8 * 10
-5Rub/liter; The concentration of formaldehyde is 2.5 * 10
-3Rub/liter.Stirred 1.5 hours down at 60 ℃, obtain yellow suspension.Centrifugation obtains cube shaped copper particles, and the particle length of side is yellow mercury oxide at 110nm.After the vacuum drying of gained precipitation, obtain the copper functional material.
Embodiment 5
(1). prepare copper chloride and sodium borohydride aqueous solution respectively, wherein the concentration of copper chloride is 5 * 10 in the solution
-3Rub/liter; The concentration of sodium borohydride be 0.5 rub/liter.
(2). copper chloride and the sodium borohydride aqueous solution with preparation in the step (1) mixes respectively, and making the copper chloride concentration of mixing in the solution of back is 8 * 10
-4Rub/liter; The concentration of sodium borohydride is 1 * 10
-2Rub/liter.Stirred 2.5 hours down at 70 ℃, obtain yellow suspension.Centrifugation obtains cube shaped copper particles, and the particle length of side is yellow mercury oxide at 240nm.After the vacuum drying of gained precipitation, obtain the copper functional material.
Embodiment 6
(1). prepare cupric tartrate, hydroxylamine hydrochloride and hydrazine hydrate aqueous solution respectively, wherein the concentration of solution mesotartaric acid copper is 3 * 10
-4Rub/liter; The concentration of hydroxylamine hydrochloride is 2.4 * 10
-3Rub/liter; The concentration of hydrazine hydrate is 3.6 * 10
-3Rub/liter.
(2). cupric tartrate, hydroxylamine hydrochloride and the hydrazine hydrate aqueous solution with preparation in the step (1) mixes respectively, and making the cupric tartrate concentration of mixing in the solution of back is 6 * 10
-5Rub/liter; The concentration of hydroxylamine hydrochloride is 5.2 * 10
-4Rub/liter; The concentration of hydrazine hydrate is 6.8 * 10
-4Rub/liter.Stirred 3 hours down at 55 ℃, obtain yellow suspension.Centrifugation obtains cube shaped copper particles, and the particle length of side is yellow mercury oxide at 130nm.After the vacuum drying of gained precipitation, obtain the copper functional material.
Claims (9)
1. the preparation method of a cube shaped copper particles, it is characterized in that: the step of this method comprises:
(1). prepare the mantoquita and the reducing agent aqueous solution respectively;
(2). with the mantoquita and the reducing agent aqueous solution of step (1) preparation, making the mantoquita concentration of mixing in the solution of back is 1 * 10
-6～5 * 10
-3Rub/liter, the concentration of reducing agent is 2 * 10
-5～0.1 rub/liter; Stir, obtain yellow suspension; Centrifugation obtains cube shaped copper particles.
2. the method for claim 1, it is characterized in that: the length of side of described cube shaped copper particles is 80～300nm.
3. the method for claim 1, it is characterized in that: the concentration of mantoquita is 2 * 10 in described step (1) solution
-6～1 * 10
-2Rub/liter; The concentration of reducing agent is 5 * 10
-4～1 rub/liter.
4. method as claimed in claim 3 is characterized in that: the concentration of described mantoquita is 2 * 10
-5～5 * 10
-3Rub/liter, the concentration of reducing agent is 3 * 10
-3～0.5 rub/liter.
5. the method for claim 1, it is characterized in that: the concentration of mantoquita is 1 * 10 in described step (2) solution
-5～1 * 10
-3Rub/liter, the concentration of reducing agent is 5 * 10
-4～1 * 10
-2Rub/liter.
6. as claim 1,2,3,4 or 5 described methods, it is characterized in that: described mantoquita is selected from copper nitrate, copper chloride, copper sulphate, basic copper carbonate or cupric tartrate.
7. as claim 1,2,3,4 or 5 described methods, it is characterized in that: described reducing agent is selected from organic amine, azanol, polyol, hydrazine hydrate, sodium borohydride, inferior sodium phosphate, formaldehyde or they two or more mixture arbitrarily.
8. method as claimed in claim 7 is characterized in that: described organic amine is formamide, p-phenylenediamine (PPD), 4-amino-N-ethyl-N-(Beta-methyl sulfonamide ethyl) meta-aminotoluene list water sulfate, triethanolamine or their mixture; Azanol is a hydroxylamine hydrochloride; Polyol is isopropyl alcohol, ethylene glycol or their mixture.
9. the method for claim 1 is characterized in that: the temperature when described step (2) stirs is 20～70 ℃.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100117177A CN100531973C (en) | 2005-05-13 | 2005-05-13 | Method for preparing cube shaped copper particles |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100117177A CN100531973C (en) | 2005-05-13 | 2005-05-13 | Method for preparing cube shaped copper particles |
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| Publication Number | Publication Date |
|---|---|
| CN1861298A true CN1861298A (en) | 2006-11-15 |
| CN100531973C CN100531973C (en) | 2009-08-26 |
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|---|---|---|---|
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102114545A (en) * | 2011-03-01 | 2011-07-06 | 宁波大学 | Method for preparing copper nanometer granules |
| CN102240813A (en) * | 2010-05-10 | 2011-11-16 | 中国科学院过程工程研究所 | Preparing method for cubic crystallized copper micro powder |
| CN102601380A (en) * | 2011-12-21 | 2012-07-25 | 中国科学院过程工程研究所 | Cubic copper powder and method for preparing same |
| CN104308172A (en) * | 2014-08-11 | 2015-01-28 | 常州大学 | Method for preparing hollow cubic micro-nano metal |
| CN105702774A (en) * | 2016-04-29 | 2016-06-22 | 合肥工业大学 | Self-driven Schottky junction near-infrared photoelectric detector based on silicone nanowire array and preparation method of photoelectric detector |
| CN106853538A (en) * | 2016-12-19 | 2017-06-16 | 北京科技大学 | A kind of quick method for preparing particle diameter and the copper nano-particle of morphology controllable |
| CN108213456A (en) * | 2017-12-08 | 2018-06-29 | 北京有色金属研究总院 | A kind of preparation method of cube copper nanoparticle |
| CN112296347A (en) * | 2019-07-29 | 2021-02-02 | 本田技研工业株式会社 | Method for preparing copper nanocubes by using tributylphosphine as ligand |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107008896B (en) * | 2017-06-16 | 2019-03-12 | 福州大学 | A kind of copper particle and preparation method thereof with multi-angular structure |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3570591B2 (en) * | 1996-03-22 | 2004-09-29 | 株式会社村田製作所 | Production method of copper powder |
| CN1201892C (en) * | 2003-02-19 | 2005-05-18 | 中国科学院理化技术研究所 | Method for preparing homogeneous spherical copper granule by seeding growth |
-
2005
- 2005-05-13 CN CNB2005100117177A patent/CN100531973C/en not_active Expired - Fee Related
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102240813A (en) * | 2010-05-10 | 2011-11-16 | 中国科学院过程工程研究所 | Preparing method for cubic crystallized copper micro powder |
| CN102114545A (en) * | 2011-03-01 | 2011-07-06 | 宁波大学 | Method for preparing copper nanometer granules |
| CN102601380A (en) * | 2011-12-21 | 2012-07-25 | 中国科学院过程工程研究所 | Cubic copper powder and method for preparing same |
| CN102601380B (en) * | 2011-12-21 | 2015-05-20 | 中国科学院过程工程研究所 | Cubic copper powder and method for preparing same |
| CN104308172A (en) * | 2014-08-11 | 2015-01-28 | 常州大学 | Method for preparing hollow cubic micro-nano metal |
| CN105702774B (en) * | 2016-04-29 | 2017-10-03 | 合肥工业大学 | A kind of self-driven schottky junction near infrared photodetector based on silicon nanowire array and preparation method thereof |
| CN105702774A (en) * | 2016-04-29 | 2016-06-22 | 合肥工业大学 | Self-driven Schottky junction near-infrared photoelectric detector based on silicone nanowire array and preparation method of photoelectric detector |
| CN106853538A (en) * | 2016-12-19 | 2017-06-16 | 北京科技大学 | A kind of quick method for preparing particle diameter and the copper nano-particle of morphology controllable |
| CN106853538B (en) * | 2016-12-19 | 2019-03-29 | 北京科技大学 | A method of quickly preparing the copper nano-particle of partial size and morphology controllable |
| CN108213456A (en) * | 2017-12-08 | 2018-06-29 | 北京有色金属研究总院 | A kind of preparation method of cube copper nanoparticle |
| CN108213456B (en) * | 2017-12-08 | 2021-06-15 | 北京有色金属研究总院 | Preparation method of cubic nanometer copper powder |
| CN112296347A (en) * | 2019-07-29 | 2021-02-02 | 本田技研工业株式会社 | Method for preparing copper nanocubes by using tributylphosphine as ligand |
| CN112296347B (en) * | 2019-07-29 | 2023-04-18 | 本田技研工业株式会社 | Method for preparing copper nanocubes by using tributylphosphine as ligand |
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| Publication number | Publication date |
|---|---|
| CN100531973C (en) | 2009-08-26 |
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Granted publication date: 20090826 Termination date: 20130513 |