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Chitosan-modified activated coke in-situ loaded nano-gold catalyst and its preparation method

A technology of activated coke and chitosan, which is applied in chemical instruments and methods, organic compound/hydride/coordination complex catalysts, preparation of organic compounds, etc., can solve catalyst activity decline, environmental secondary pollution, nano-gold Poor dispersion and other problems, to achieve the effect of improving mechanical stability, stable chemical properties, and developed void structure

Active Publication Date: 2020-03-17
HUNAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Based on the above problems, researchers try to load nano-gold particles on the carrier to improve the activity and stability of the catalyst, among which carbon materials such as carbon nanotubes, carbon nanofibers, graphene (graphene oxide), mesoporous carbon, etc. are often used as Nanogold carrier materials, but these carrier materials have problems such as high cost, low mechanical strength, and underdeveloped pore structure, and the acquisition methods of these carbon materials are relatively complicated and difficult to obtain. The weak interaction force of gold makes it challenging to load nano-gold. For example, nano-gold is easy to lose, the catalyst activity drops significantly, and the cycle stability is not high. Therefore, can the binding force between nano-gold and carbon support be further enhanced? It is one of the issues that are currently concerned about supported nano-gold catalysts.
In addition, the existing preparation methods of supported nano-gold catalysts include impregnation method, deposition-precipitation method, co-precipitation method, chemical vapor deposition method, etc. These methods have the following disadvantages: incomplete loading of nano-gold catalysts, poor repeatability of the preparation process, and easy Affected by the solvation effect and the cluster effect of metal components, resulting in poor dispersion of gold nanoparticles, unstable catalyst structure (poor stability), high amount of precious metals, and the addition of chemical reagents such as sodium borohydride and hydrazine during the preparation process , and these chemical reagents will cause secondary pollution to the environment, which does not meet the theme of green chemistry
In addition, the existing deposition-precipitation method, impregnation method and other methods are difficult to achieve high dispersion of gold nanoparticles on carbon support materials.

Method used

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  • Chitosan-modified activated coke in-situ loaded nano-gold catalyst and its preparation method
  • Chitosan-modified activated coke in-situ loaded nano-gold catalyst and its preparation method
  • Chitosan-modified activated coke in-situ loaded nano-gold catalyst and its preparation method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] A chitosan-modified activated coke in-situ supported nano-gold catalyst, including activated coke, chitosan and nano-gold particles, wherein the chitosan modification forms a chitosan / active coke complex on the surface of the active coke, and the chitosan / The active coke composite is loaded with nano-gold particles.

[0038] In this example, in the chitosan-modified activated coke in-situ loaded nano-gold catalyst, the mass percentage of nano-gold particles was 0.84 wt%, and the mass ratio of chitosan to activated coke was 0.5.

[0039] In this embodiment, the average particle size of the gold nanoparticles is 5.27 ± 2.02 nm.

[0040] A kind of preparation method of the above-mentioned chitosan modified active coke in situ loaded nano-gold catalyst of the present embodiment, comprises the following steps:

[0041] (1) Pretreatment of active coke:

[0042] The active coke was cleaned with ultrapure water, and dried in a vacuum drying oven; the dried active coke was ba...

Embodiment 2

[0051] A chitosan-modified active coke in-situ loaded nano-gold catalyst is basically the same as the chitosan-modified active coke in-situ loaded nano-gold catalyst in Example 1, the only difference being: Chitosan-modified active coke in Example 2 The mass percentage of gold nanoparticles in the in situ supported nano-gold catalyst was 1.68 wt%, and the average particle size of gold nanoparticles was 6.78 ± 2.31 nm.

[0052] A kind of preparation method of the above-mentioned chitosan modified active coke in-situ loading nano-gold catalyst of the present embodiment is basically the same as the preparation method of embodiment 1, the difference is only: the input of chloroauric acid solution in the preparation method of embodiment 2 The dosage is 0.7mL.

[0053] The chitosan-modified active coke prepared in Example 2 supported nano-gold catalyst in situ, numbered as Au NPs / CTS / AC (2) .

Embodiment 3

[0055] A chitosan-modified active coke in-situ loaded nano-gold catalyst, which is basically the same as the chitosan-modified active coke in-situ loaded nano-gold catalyst in Example 1, the only difference being: Chitosan-modified active coke in Example 3 The mass percentage of gold nanoparticles in the in situ loaded nano-gold catalyst was 3.35 wt%, and the average particle size of gold nanoparticles was 13.05 ± 5.82 nm.

[0056] A kind of preparation method of the above-mentioned chitosan modified activated coke in-situ loading nano-gold catalyst of the present embodiment is basically the same as the preparation method of embodiment 1, the difference is only: the input of chloroauric acid solution in the preparation method of embodiment 3 The dosage is 1.4mL.

[0057] The chitosan-modified active coke prepared in Example 3 supports nano-gold catalyst in situ, and the number is Au NPs / CTS / AC (3) .

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Abstract

The invention discloses a chitosan-modified activated coke loaded with nano-gold catalyst in-situ and a preparation method thereof. The chitosan-modified activated coke loaded with nano-gold catalyst in-situ includes activated coke, chitosan and nano-gold particles. The activated coke The surface modified chitosan forms a chitosan / activated coke complex, and the chitosan / activated coke complex is loaded with gold nanoparticles. The preparation method includes preparing a chitosan / active coke composite and loading nano-gold on the chitosan / active coke composite. The catalyst of the present invention has the advantages of good dispersion of nano-gold particles, high mechanical strength, good catalytic activity, good stability, etc. It is a new type of supported nano-gold catalyst and has high application value and wide application range. The preparation method has the advantages of simple preparation process, easy operation, cheap raw materials, short production cycle, low production cost, green and environmental protection, etc. It can realize large-scale preparation at normal temperature and is suitable for industrial production.

Description

technical field [0001] The invention belongs to the technical field of nano-metal catalyst preparation, and relates to a chitosan-modified activated coke in-situ loaded nano-gold catalyst and a preparation method thereof. [0002] technical background [0003] In the existing nano-gold catalyst, due to the small particle size and high surface activation energy of the nano-gold, it is easy to agglomerate, so that the reaction activity is significantly reduced. Based on the above problems, researchers try to load nano-gold particles on the carrier to improve the activity and stability of the catalyst, among which carbon materials such as carbon nanotubes, carbon nanofibers, graphene (graphene oxide), mesoporous carbon, etc. are often used as Nanogold carrier materials, but these carrier materials have problems such as high cost, low mechanical strength, and underdeveloped pore structure, and the acquisition methods of these carbon materials are relatively complicated and diffic...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J31/06B01J35/10C07C213/02C07C215/76
CPCC07C213/02B01J31/06B01J2231/64B01J35/393B01J35/61C07C215/76
Inventor 曾光明符玉葵赖萃秦蕾何江凡易欢李敏芳李玲黄芳龙
Owner HUNAN UNIV
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