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Co3O4/CuMoO4 compound and preparation method and application thereof

A compound and material technology, applied in the direction of metal/metal oxide/metal hydroxide catalyst, hydrogen/synthesis gas production, chemical instruments and methods, etc., can solve the problems of cumbersome operation and high preparation cost, and achieve simple process, The effect of novel method and cheap raw materials

Active Publication Date: 2019-12-20
浙江智胜电子科技有限公司
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] Aiming at the key problems of high preparation cost and cumbersome operation in the above preparation process, the present invention provides a

Method used

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  • Co3O4/CuMoO4 compound and preparation method and application thereof
  • Co3O4/CuMoO4 compound and preparation method and application thereof
  • Co3O4/CuMoO4 compound and preparation method and application thereof

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preparation example Construction

[0034] The invention provides a method for preparing a Co3O4 / CuMoO4 composite, which specifically includes the following methods:

[0035] 1. Take 4.5mmol Co(NO 3 ) 2 ·6H 2 O, 2.25mmol C 6 h 12 N 4 , 1.5mmol Na3 C 6 h 5 o 7 2H 2 O was dissolved in 35mL deionized water and kept stirring until dissolved;

[0036] 2. Transfer the above solution to a 100mL reactor, and react at 95-110°C for 8-24 hours;

[0037] 3. Suction filtration and water washing, drying in a vacuum oven at 40-60°C for 3-6 hours;

[0038] 4. Weigh 90 mg of the above precipitate and disperse it in 40 mL of H 2 O middle;

[0039] 5. Add CuCl 2 (0.5 ~ 2mmol) stirred and dissolved, and then correspondingly add the same amount of H 2 MoO 4 ;

[0040] 6. Dissolve urea (5-20mmol) in 40mL water;

[0041] 7. Add the urea solution to the above solution drop by drop through the sealed funnel, and stir for 30 minutes;

[0042] 8. Transfer to the reaction kettle, react at 150-180°C for 6-10 hours, cool to...

Embodiment 1

[0046] 1. Take 4.5mmol Co(NO 3 ) 2 ·6H 2 O, 2.25mmol C 6 h 12 N 4 , 1.5mmol Na 3 C 6 h 5 o 7 2H 2 O was dissolved in 35mL deionized water, and kept stirring until dissolved; the above solution was transferred to a 100mL reactor, and reacted at 100°C for 24h; filtered and washed with water, and dried in a vacuum oven at 40°C for 3h;

[0047] 2. Weigh 90 mg of the above precipitate and disperse it in 40 mL of H 2 O; add CuCl 2 (0.5mmol) stirring and dissolving, then correspondingly add the same amount of H 2 MoO 4 ;Dissolve urea (5mmol) in 40mL of water, add the urea solution dropwise to the above solution through a sealed funnel, and stir for 30min; transfer to the reaction kettle, react at 160°C for 8h, cool to room temperature after the reaction, collect the precipitate, and wash Vacuum drying after several times; the collected samples were calcined in a muffle furnace at 500°C for 2h with a heating rate of 2°C / min to obtain the final catalyst Co 3 o 4 / CuMoO ...

Embodiment 2

[0060] 1. Take 4.5mmol Co(NO 3 ) 2 ·6H 2 O, 2.25mmol C 6 h 12 N 4 , 1.5mmol Na 3 C 6 h 5 o 7 2H 2 Dissolve O in 35mL deionized water, and keep stirring until dissolved; transfer the above solution to a 100mL reactor, and react at 100°C for 8h; filter and wash with water, and dry in a vacuum oven at 40°C for 3h;

[0061] 2. Weigh 90 mg of the above precipitate and disperse it in 40 mL of H 2 O; add CuCl 2 (0.5mmol) stirring and dissolving, then correspondingly add the same amount of H 2 MoO 4 ;Dissolve urea (5mmol) in 40mL of water, add the urea solution dropwise to the above solution through a sealed funnel, and stir for 30min; transfer to the reaction kettle, react at 160°C for 8h, cool to room temperature after the reaction, collect the precipitate, and wash Vacuum drying after several times; the collected samples were calcined in a muffle furnace at 500°C for 2h, and the heating rate was 2°C / min to obtain the final catalyst Co 3 o 4 / CuMoO 4 ;

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Abstract

The invention discloses a Co3O4 / CuMoO4 compound. The Co3O4 / CuMoO4 compound is an urchin-like Co3O4 / CuMoO4 compound formed by nanorods. The invention further discloses a preparation method of the Co3O4 / CuMoO4 compound. The preparation method of the Co3O4 / CuMoO4 compound comprises the steps that (1), cobalt nitrate, hexamethylene tetramine and trisodium citrate are taken and dissolved in deionized water, and continuous stirring is carried out till dissolution; (2), an obtained solution is transferred to a reactor; (3), suction filtration and water-washing are carried out, and vacuum oven dryingis carried out; (4), a sediment in the step (3) is taken and dispersed in water; (5), CuCl2 is added and stirred to be dissolved, and then H2MoO4 is added; (6), urea is dissolved in water; (7), a ureasolution is dropwise added to the solution and stirred; (8), a mixture is transferred to the reactor, cooling is carried out to room temperature after a reaction is completed, a sediment is collected, and vacuum drying is carried out after multiple times of washing; and (9), collected samples are calcined in a muffle furnace, and a product is obtained. According to the preparation method of the Co3O4 / CuMoO4 compound, an urchin-like catalyst formed by assembling nanowires is successfully prepared by adjusting the doping amount of copper molybdate, the method is simple in a synthetic process, raw materials are cheap and easy to get, the morphology is unique and controllable, and the excellent catalytic activity is shown up in the field of catalysis of ammonia borane hydrolysis.

Description

technical field [0001] The invention relates to the technical field of catalyst synthesis, in particular to a Co 3 o 4 / CuMoO 4 Composite and its preparation method and its application in hydrogen production. Background technique [0002] In response to the current energy crisis and ecological environmental protection, a series of research has emerged, such as photoelectrocatalytic hydrogen evolution, carbon dioxide electroreduction, oxygen reduction, and chemical hydride hydrogen evolution. Development has broad prospects. In these studies, catalysts are often needed to achieve a more ideal situation, so the design and synthesis of catalysts are particularly important. In various fields, precious metals have shown excellent activity, but because of objective factors such as high cost and low crustal content, the commercialization is not worth the loss, thus limiting their wide use, so the vigorous development of non-precious metal catalysts in transition metals has beco...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/885C01B3/06
CPCB01J23/885C01B3/068C01B2203/1076C01B2203/1052Y02E60/36
Inventor 李浩卢东升廖锦云冯裕发王慧泽
Owner 浙江智胜电子科技有限公司