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A kind of metal-supported catalyst and its preparation method and application

A supported catalyst and metal technology, which is applied in catalyst activation/preparation, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problems of complex material synthesis steps and high catalyst cost, and achieve stable catalytic performance and improve activity. Effect

Active Publication Date: 2021-05-14
ZHEJIANG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] The purpose of the present invention is to provide a simple and effective ternary non-precious metal-supported composite catalyst and its preparation method for the existing problems of high catalyst cost and complicated material synthesis steps.

Method used

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  • A kind of metal-supported catalyst and its preparation method and application
  • A kind of metal-supported catalyst and its preparation method and application
  • A kind of metal-supported catalyst and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Ternary non-noble metal Cu 0.8 Ni 0.1 co 0.1Preparation of @MIL-101 nanocatalyst:

[0038] (1) Weigh terephthalic acid (0.82g, 5.0mmol), chromium nitrate nonahydrate (2.06g, 5.0mmol), NaAC (0.11g, 0.125mmol) and deionized water (25mL), stir for 30min and transfer to Put it into a 50mL stainless steel reaction kettle lined with polytetrafluoroethylene, seal it and transfer it to a constant temperature of 180°C for 18 hours. After the reaction was completed, it was cooled to room temperature to obtain a green suspension. Transfer the suspension into a centrifuge tube, add DMF, heat to 70°C, shake and wash, and then centrifuge twice. Wash the obtained green product with deionized water twice at room temperature and then centrifuge. Put the obtained green product at 70°C Drying for 12 hours under the hood to obtain MIL-101 green powder.

[0039] (2) Weigh 50.0 mg of the above MIL-101 powder and disperse it in 5 ml of absolute ethanol, and disperse it by ultrasonic for ...

Embodiment 2

[0044] Ternary non-noble metal Cu 0.4 Ni 0.3 co 0.3 Preparation of @MIL-101 nanocatalyst:

[0045] Weigh 50.0 mg of the MIL-101 powder prepared in Example 1 and disperse it in 5 ml of absolute ethanol, and disperse it ultrasonically for 30 min. Weigh 2.05mg CuCl 2 2H 2 O, 2.2mg NiCl 2 ·6H 2 O, 2.2 mg CoCl 2 ·6H 2 O was added to the above MIL-101 solution, and ultrasonic dispersion was continued for 30 minutes. After the sonication is completed, transfer to a 60°C water bath and heat and stir until the solvent is completely evaporated to obtain a dry green block.

[0046] Weigh 111.4 mg NaBH 4 Dissolve in 5ml deionized water, NaBH 4 The aqueous solution was added to the above-mentioned green block at one time to reduce the metal ions, and the stirring was continued for 1 h after the addition was completed. After the obtained solution was centrifuged with deionized water, the obtained green block was vacuum-dried overnight to obtain dark green ternary Cu 0.4 Ni 0.3...

Embodiment 3

[0048] Ternary non-noble metal Cu 0.6 Ni 0.2 co 0.2 Preparation of @MIL-101 nanocatalyst:

[0049] Weigh 50.0 mg of the MIL-101 powder prepared in Example 1 and disperse it in 5 ml of absolute ethanol, and disperse it ultrasonically for 30 min. Weigh 3.08mg CuCl 2 2H 2 O, 1.5mg NiCl 2 ·6H 2 O, 1.5 mg CoCl 2 ·6H 2 O was added to the above MIL-101 solution, and ultrasonic dispersion was continued for 30 minutes. After the sonication is completed, transfer to a 60°C water bath and heat and stir until the solvent is completely evaporated to obtain a dry green block.

[0050] Weigh 111.4 mg NaBH 4 Dissolve in 5ml deionized water, NaBH 4 The aqueous solution was added to the above-mentioned green block at one time to reduce the metal ions, and the stirring was continued for 1 h after the addition was completed. After the obtained solution was centrifuged with deionized water, the obtained green block was vacuum-dried overnight to obtain dark green ternary Cu 0.6 Ni 0.2...

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Abstract

The invention discloses a metal-loaded catalyst, a preparation method thereof and an application in hydrogen production by hydrolysis of ammonia borane. The metal-supported catalyst uses the metal-organic framework material MIL-101 as a carrier, and the Cu, Ni, and Co precursors are completely adsorbed in the pores of the MIL-101 by the solvent evaporation method according to the control ratio, and then passed through NaBH 4 A ternary metal-supported nanocatalyst Cu‑Ni‑Co@MIL‑101 with excellent catalytic performance was obtained through reduction. The obtained catalyst has the characteristics of uniform distribution of metal particles, large specific surface area, and many catalytic active sites. Compared with traditional noble metal catalysts, it has low cost, simple preparation, easy-to-obtain raw materials, and is suitable for industrial production. catalyst.

Description

technical field [0001] The invention belongs to the field of hydrogen storage materials, and relates to a ternary metal-loaded catalyst with high catalytic activity for the hydrolysis of ammonia borane, a preparation method and application thereof. Background technique [0002] With the excessive exploitation and use of traditional primary energy, the available traditional energy on the earth has become less and less. It is particularly important to develop clean secondary energy sources that are non-polluting and highly efficient. As a clean secondary energy source, hydrogen has the advantages of high energy density and no pollution to the environment. However, the efficient preparation and storage of hydrogen is still an important difficulty in the application of hydrogen energy. [0003] Ammoniaborane (NH 3 BH 3 , AB), is a lightweight hydrogen storage material with high application prospects. It has a hydrogen content as high as 19.6 wt%, is non-toxic, and has good c...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J31/22B01J37/16B01J37/34B01J37/02C01B3/06
CPCB01J31/1691B01J31/2213B01J37/0201B01J37/0236B01J37/16B01J37/343C01B3/065Y02E60/36
Inventor 肖学章梁子俊陈立新李露李寿权葛红卫
Owner ZHEJIANG UNIV