CN101041119A - Application of nanometer copper oxide and the method of preparing the same - Google Patents
Application of nanometer copper oxide and the method of preparing the same Download PDFInfo
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- CN101041119A CN101041119A CN 200710071896 CN200710071896A CN101041119A CN 101041119 A CN101041119 A CN 101041119A CN 200710071896 CN200710071896 CN 200710071896 CN 200710071896 A CN200710071896 A CN 200710071896A CN 101041119 A CN101041119 A CN 101041119A
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Abstract
The invention relates to an application of nanometer copper oxide and the preparing method, belonging to an application of compound and the preparing method. Before the invention, there are not reports that single nanometer copper oxide is used as ambient temperature desulfurizer and the purity of nanometer copper oxide prepared by prior preparing method for nanometer copper oxide is low. In the invention, the nanometer copper oxide is used as the ambient temperature desulfurizer and the nanometer copper oxide is the only component of ambient temperature desulfuizer. The preparation of nanometer copper oxide is that sodium hydroxide is added in the copper nitrate solution and then it is filtered, dried and baked or the preparation of nanometer copper oxide is that sodium hydroxide is added in the copper nitrate solution and then it is filtered and dried. The desulfurization accuracy of nanometer copper oxide in the invention is high in ambient temperature condition and the sulfur capacity is high to 18.3%-28.7%. The purity of nanometer copper oxide prepared in the invention is higher than 99.9%. It is provided with simple preparing process, low demand for machining equipment, small energy consumption and low production cost. It is easy to be developed and implemented.
Description
Technical field
The present invention relates to a kind of application of compound and preparation method thereof.
Background technology
Hydrogen sulfide gas has huge harm to industrial equipment and environment, all needs to be controlled in productive life, and desulfurizing agent is widely used in fields such as chemical industry, metallurgy, electronics, weaving, machinery, aerospace, environmental protection.Desulfurizing agent can be divided into high temperature desulfuration agent, middle low-temp desulfurization agent and ambient temperature desulfuration agent according to application of temperature.Desulfurization can be saved a large amount of energy under the normal temperature condition, but because reactant is difficult to break through energy barrier under the normal temperature condition, the material that only possesses specific physical performance and chemical property just can reach the control target of normal temperature desulfurization, desulfurizing agent desulfurization performance under normal temperature condition that exploitation at present is used for high temperature non-activity even that can significantly descend; And the desulfurizing agent overwhelming majority in the market is by mixing and load raising reactivity, preparation method's complexity often, and Sulfur capacity is low.And do not see have up to now with the report of single nano cupric oxide as ambient temperature desulfuration agent.
The nano cupric oxide purity that present nano cupric oxide preparation method is made is low.
Summary of the invention
Never have with the report of single nano cupric oxide before the present invention, and the nano cupric oxide purity that present nano cupric oxide preparation method is made is low as ambient temperature desulfuration agent; Therefore the invention provides application of a kind of nano cupric oxide and preparation method thereof.
Nano cupric oxide is used as ambient temperature desulfuration agent among the present invention, and nano cupric oxide is the unique component of ambient temperature desulfuration agent.
Above-mentioned nano cupric oxide prepares according to the following steps: (one) is that 1: 0.5～3 water-ethanol liquid is solvent with volume ratio, and copper nitrate is a solute, is mixed with the copper nitrate solution that concentration is 0.2mol/L; (2) 2.0～2.2 times by copper ion molal quantity in the copper nitrate solution add NaOH in copper nitrate solution, and stir 0.5～1h, leave standstill 1 ± 0.1h then; (3) filter, solid formation spends deionised water 5～8 times, places 60 ± 2 ℃ the dry 1～2h of environment again; (4) solid formation of drying roasting 1 ± 0.1h under 185～260 ℃ condition promptly obtains the nano cupric oxide that particle diameter is 10～30nm.The another kind of preparation method of above-mentioned nano cupric oxide: (one) is that 1: 0.5～3 water-ethanol liquid is solvent with volume ratio, and copper nitrate is a solute, is mixed with the copper nitrate solution that concentration is 0.2mol/L; (2) copper nitrate solution is slowly poured in the sodium hydroxide solution that concentration is 0.1～1mol/L, made that the mol ratio of copper ion and hydroxide ion is 1: 2.04～2.2 in the mixed liquor, and stir 0.5～1h, leave standstill 1 ± 0.1h then; (3) filter, solid formation spends deionised water 5～8 times, places 60 ± 2 ℃ the dry 1～2h of environment again, promptly obtains nano cupric oxide.
Nano cupric oxide of the present invention is (25～30 ℃) desulfurization precision height under normal temperature condition, and Sulfur capacity is up to 18.3%～28.7%.The nano cupric oxide purity that the present invention prepares is higher than 99.9%, and preparation technology is simple, and process equipment requires low, and energy consumption is little, and production cost is low, is easy to promotion and implementation.
The specific embodiment
The specific embodiment one: the present embodiment nano cupric oxide is used as ambient temperature desulfuration agent, and nano cupric oxide is the unique component of ambient temperature desulfuration agent.
The specific embodiment two: the difference of the present embodiment and the specific embodiment one is: the particle diameter of nano cupric oxide is 10～30nm.Other is identical with embodiment one.
Present embodiment is carried out the desulfurization contrast experiment under the condition of normal temperature (25～30 ℃), 1 standard atmospheric pressure, experimental data is as shown in table 1.
Table 1
| The desulfurization thing | Desulfurization thing particle diameter (nm) | Air speed (h -1) | 20ppmv breakthrough point Sulfur capacity (%) | The concentration of hydrogen sulfide of giving vent to anger before the breakthrough point |
| Analyze pure zirconia copper | 200～500 | 3000 | 0.44 | ＞10ppmv |
| Nano zine oxide | 14.3 | 3000 | 3.76 | ＞0.1ppmv |
| Nano cupric oxide and nano zine oxide combination (mol ratio 1: 18.40) | 6.2-11.1 | 3000 | 7.71 | ＞0.1ppmv |
| The present embodiment nano cupric oxide | 10～30 | 3000 | 18.3～28.7 | ＞0.04ppmv |
Desulfurization contrast experiment data declaration present embodiment nano cupric oxide has excellent desulfurized effect under normal temperature (25～30 ℃) condition.The present embodiment nano cupric oxide is 7000h in normal temperature (25～30 ℃), air speed
-1Condition under still have higher desulfurization precision and Sulfur capacity, desulfurization precision can reach 0.5ppm, Sulfur capacity also can reach more than 10%.
The specific embodiment three: the present embodiment nano cupric oxide prepares according to the following steps: (one) is that 1: 0.5～3 water-ethanol liquid is solvent with volume ratio, and copper nitrate is a solute, is mixed with the copper nitrate solution that concentration is 0.2mol/L; (2) 2.0～2.2 times by copper ion molal quantity in the copper nitrate solution add NaOH in copper nitrate solution, and stir 0.5～1h, leave standstill 1 ± 0.1h then; (3) filter, solid formation spends deionised water 5～8 times, places 60 ± 2 ℃ the dry 1～2h of environment again; (4) solid formation of drying roasting 1 ± 0.1h under 185～260 ℃ condition promptly obtains the nano cupric oxide that particle diameter is 10～30nm.
The nano cupric oxide of present embodiment preparation is through the X-ray detection, and its particle diameter is 10～40nm, and wherein the nano cupric oxide grain diameter more than 95% is less than 30nm.
The specific embodiment four: the difference of the present embodiment and the specific embodiment three is: be that 1: 1～2.5 water-ethanol liquid is solvent with volume ratio in the step ().Other step and parameter are identical with embodiment three.
The specific embodiment five: the difference of the present embodiment and the specific embodiment three is: be that 1: 1.5～2 water-ethanol liquid is solvent with volume ratio in the step ().Other step and parameter are identical with embodiment three.
The specific embodiment six: the difference of the present embodiment and the specific embodiment three is: be that 1: 1 water-ethanol liquid is solvent with volume ratio in the step ().Other step and parameter are identical with embodiment three.
The specific embodiment seven: the difference of the present embodiment and the specific embodiment three is: extraordinarily go into NaOH by 2.08～2.15 of copper ion molal quantity in the copper nitrate solution in the step (two).Other step and parameter are identical with embodiment three.
The specific embodiment eight: the difference of the present embodiment and the specific embodiment three is: extraordinarily go into NaOH by 2.10～2.13 of copper ion molal quantity in the copper nitrate solution in the step (two).Other step and parameter are identical with embodiment three.
The specific embodiment nine: the difference of the present embodiment and the specific embodiment three is: place 60 ℃ the dry 1.2～1.8h of environment in the step (three).Other step and parameter are identical with embodiment three.
The specific embodiment ten: the difference of the present embodiment and the specific embodiment three is: place 60 ℃ the dry 1.5h of environment in the step (three).Other step and parameter are identical with embodiment three.
The specific embodiment 11: the difference of the present embodiment and the specific embodiment three is: solid formation roasting 1h under 200～250 ℃ condition of drying in the step (four).Other step and parameter are identical with embodiment three.
The specific embodiment 12: the difference of the present embodiment and the specific embodiment three is: solid formation roasting 1h under 220～230 ℃ condition of drying in the step (four).Other step and parameter are identical with embodiment three.
The specific embodiment 13: the present embodiment nano cupric oxide prepares according to the following steps: (one) is that 1: 0.5～3 water-ethanol liquid is solvent with volume ratio, and copper nitrate is a solute, is mixed with the copper nitrate solution that concentration is 0.2mol/L; (2) copper nitrate solution is slowly poured in the sodium hydroxide solution that concentration is 0.1～1mol/L, made that the mol ratio of copper ion and hydroxide ion is 1: 2.04～2.2 in the mixed liquor, and stir 0.5～1h, leave standstill 1 ± 0.1h then; (3) filter, solid formation spends deionised water 5～8 times, places 60 ± 2 ℃ the dry 1～2h of environment again, promptly obtains nano cupric oxide.Other step and parameter are identical with embodiment three.
Present embodiment nano cupric oxide preparation method is more simple, power consumption is lower, and production cost is lower.The nano cupric oxide of present embodiment preparation is through the X-ray detection, and its particle diameter is 10～40nm, and wherein the nano cupric oxide grain diameter more than 95% is less than 30nm.
The specific embodiment 14: the difference of the present embodiment and the specific embodiment 13 is: be that 1: 1～2.5 water-ethanol liquid is solvent with volume ratio in the step ().Other step and parameter are identical with embodiment 13.
The specific embodiment 15: the difference of the present embodiment and the specific embodiment 13 is: be that 1: 1.5～2 water-ethanol liquid is solvent with volume ratio in the step ().Other step and parameter are identical with embodiment 13.
The specific embodiment 16: the difference of the present embodiment and the specific embodiment 13 is: be that 1: 1 water-ethanol liquid is solvent with volume ratio in the step ().Other step and parameter are identical with embodiment 13.
The specific embodiment 17: the difference of the present embodiment and the specific embodiment 13 is: the mol ratio of copper ion and hydroxide ion is 1: 2.08～2.15 in the middle mixed liquor of step (two).Other step and parameter are identical with embodiment 13.
The specific embodiment 18: the difference of the present embodiment and the specific embodiment 13 is: the mol ratio of copper ion and hydroxide ion is 1: 2.10～2.13 in the middle mixed liquor of step (two).Other step and parameter are identical with embodiment 13.
The specific embodiment 19: the difference of the present embodiment and the specific embodiment 13 is: place 60 ℃ the dry 1.5h of environment in the step (three).Other step and parameter are identical with embodiment 13.
Claims (10)
1, the application of nano cupric oxide it is characterized in that nano cupric oxide uses as ambient temperature desulfuration agent, and nano cupric oxide is the unique component of ambient temperature desulfuration agent.
2, the application of nano cupric oxide according to claim 1, the particle diameter that it is characterized in that nano cupric oxide is 10～30nm.
3, the preparation method of nano cupric oxide according to claim 1, it is characterized in that nano cupric oxide prepares according to the following steps: (one) is that 1: 0.5～3 water-ethanol liquid is solvent with volume ratio, copper nitrate is a solute, is mixed with the copper nitrate solution that concentration is 0.2mol/L; (2) 2.0～2.2 times by copper ion molal quantity in the copper nitrate solution add NaOH in copper nitrate solution, and stir 0.5～1h, leave standstill 1 ± 0.1h then; (3) filter, solid formation spends deionised water 5～8 times, places 60 ± 2 ℃ the dry 1～2h of environment again; (4) solid formation of drying roasting 1 ± 0.1h under 185～260 ℃ condition promptly obtains nano cupric oxide.
4, the preparation method of nano cupric oxide according to claim 3 is characterized in that in the step () with volume ratio being that 1: 1～2.5 water-ethanol liquid is solvent.
5, the preparation method of nano cupric oxide according to claim 3 is characterized in that in the step () with volume ratio being that 1: 1 water-ethanol liquid is solvent.
6, the preparation method of nano cupric oxide according to claim 3 is characterized in that extraordinarily going into NaOH by 2.08～2.15 of copper ion molal quantity in the copper nitrate solution in the step (two).
7, the preparation method of nano cupric oxide according to claim 3 is characterized in that extraordinarily going into NaOH by 2.10～2.13 of copper ion molal quantity in the copper nitrate solution in the step (two).
8, the preparation method of nano cupric oxide according to claim 3 is characterized in that placing in the step (three) 60 ℃ the dry 1.2～1.8h of environment.
9, the preparation method of nano cupric oxide according to claim 3 is characterized in that solid formation roasting 1h under 200～250 ℃ condition of drying in the step (four).
10, the preparation method of nano cupric oxide according to claim 1, it is characterized in that nano cupric oxide prepares according to the following steps: (one) is that 1: 0.5～3 water-ethanol liquid is solvent with volume ratio, copper nitrate is a solute, is mixed with the copper nitrate solution that concentration is 0.2mol/L; (2) copper nitrate solution is slowly poured in the sodium hydroxide solution that concentration is 0.1～1mol/L, made that the mol ratio of copper ion and hydroxide ion is 1: 2.04～2.2 in the mixed liquor, and stir 0.5～1h, leave standstill 1 ± 0.1h then; (3) filter, solid formation spends deionised water 5～8 times, places 60 ± 2 ℃ the dry 1～2h of environment again, promptly obtains nano cupric oxide.
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| CNB2007100718962A CN100490940C (en) | 2007-03-16 | 2007-03-16 | Application method of nanometer copper oxide |
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| CNB2007100718962A CN100490940C (en) | 2007-03-16 | 2007-03-16 | Application method of nanometer copper oxide |
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| CN100490940C CN100490940C (en) | 2009-05-27 |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102923756A (en) * | 2012-11-21 | 2013-02-13 | 东江环保股份有限公司 | Manufacturing technique for electroplated level copper oxide |
| CN105579400A (en) * | 2013-07-18 | 2016-05-11 | 麦拓公司 | Composite coatings of oxidized and/or phosphorous copper |
| CN112279291A (en) * | 2020-11-11 | 2021-01-29 | 湖南师范大学 | Nano copper oxide and preparation method and application thereof |
| CN113735157A (en) * | 2021-09-18 | 2021-12-03 | 武汉大学 | Preparation method of petal-shaped copper oxide nanosheet and application of petal-shaped copper oxide nanosheet |
-
2007
- 2007-03-16 CN CNB2007100718962A patent/CN100490940C/en not_active Expired - Fee Related
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102923756A (en) * | 2012-11-21 | 2013-02-13 | 东江环保股份有限公司 | Manufacturing technique for electroplated level copper oxide |
| CN105579400A (en) * | 2013-07-18 | 2016-05-11 | 麦拓公司 | Composite coatings of oxidized and/or phosphorous copper |
| CN105579400B (en) * | 2013-07-18 | 2017-07-11 | 麦拓公司 | The composite coating of oxidation and/or phosphorous copper |
| CN112279291A (en) * | 2020-11-11 | 2021-01-29 | 湖南师范大学 | Nano copper oxide and preparation method and application thereof |
| CN113735157A (en) * | 2021-09-18 | 2021-12-03 | 武汉大学 | Preparation method of petal-shaped copper oxide nanosheet and application of petal-shaped copper oxide nanosheet |
| CN113735157B (en) * | 2021-09-18 | 2022-06-03 | 武汉大学 | Preparation method of petal-shaped copper oxide nanosheet and application of petal-shaped copper oxide nanosheet |
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| CN100490940C (en) | 2009-05-27 |
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