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A kind of dendritic cu/c-cusio3 nanostructure hydrogenation catalyst preparation method

A technology of hydrogenation catalyst and nanostructure, applied in the direction of metal/metal oxide/metal hydroxide catalyst, physical/chemical process catalyst, chemical instrument and method, etc. Stability and other issues, to achieve the effect of specific surface area and pore volume increase, high gas flux

Inactive Publication Date: 2019-08-09
SICHUAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Aiming at the problem of deactivation caused by crystal grain migration, sintering and unstable valence state of copper active components during the high-temperature hydrogenation reaction of copper-based catalysts, the present invention uses conventional oxides, silicates and other materials to develop a low-cost, The dendritic core-sheath structure copper-based catalyst is easy to operate, and the unique structure of the dendrite is coupled to the promotion of the active components of the catalyst and the synergistic effect between the components, so as to achieve the purpose of improving the reaction activity and stability

Method used

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  • A kind of dendritic cu/c-cusio3 nanostructure hydrogenation catalyst preparation method
  • A kind of dendritic cu/c-cusio3 nanostructure hydrogenation catalyst preparation method
  • A kind of dendritic cu/c-cusio3 nanostructure hydrogenation catalyst preparation method

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Experimental program
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Effect test

Embodiment 1

[0025] 0.16g of cetyltrimethylammonium bromide (CTAB), 30mL of deionized water, 100mL of absolute ethanol, and 2mL of ammonia water with a mass fraction of 25-28wt% were mixed and stirred uniformly at room temperature. While vigorously stirring, 0.1 g of carbon nanotubes CNTs (DI=20-40 nm) was added, followed by ultrasonic dispersion for 480 min. An alcohol solution of ethyl orthosilicate (0.6 mL TEOS dissolved in 20 mL absolute ethanol) was added dropwise to the above suspension, and the vigorous stirring was continued at room temperature for 12 h. The obtained intermediate product was washed 3 times with water, and the alcoholic solution of ammonium nitrate (8 g of ammonium nitrate dissolved in 400 mL of absolute ethanol) was washed 3 times. Put 0.2g CNT@SiO 2 Disperse in 40mL deionized water, ultrasonically disperse evenly. Add 2 mL of ammonia water (mass fraction 25-28%) under low-speed stirring, add 1.2 mL of copper nitrate with a concentration of 0.1 M dropwise into th...

Embodiment 2

[0027] This embodiment is to change the ratio of raw materials on the basis of embodiment 1.

[0028] 0.16g of cetyltrimethylammonium bromide (CTAB), 30mL of deionized water, 100mL of absolute ethanol, and 2mL of ammonia water with a mass fraction of 25-28wt% were mixed and stirred uniformly at room temperature. While vigorously stirring, 0.1 g of carbon nanotubes CNTs (DI=20-40 nm) was added, followed by ultrasonic dispersion for 480 min. An alcohol solution of ethyl orthosilicate (0.9 mL TEOS dissolved in 20 mL absolute ethanol) was added dropwise to the above suspension, and the vigorous stirring was continued at room temperature for 12 hours. The obtained intermediate product was washed 3 times with water, and the alcoholic solution of ammonium nitrate (8 g of ammonium nitrate dissolved in 400 mL of absolute ethanol) was washed 3 times. Put 0.2g CNT@SiO 2 Disperse in 40mL deionized water, ultrasonically disperse evenly. Add 3 mL of ammonia water (25-28% by mass) under l...

Embodiment 3

[0030] In this example, on the basis of Example 1, the type and loading amount of the loaded active components are changed.

[0031] 0.16g of cetyltrimethylammonium bromide (CTAB), 30mL of deionized water, 100mL of absolute ethanol, and 2mL of ammonia water with a mass fraction of 25-28wt% were mixed and stirred uniformly at room temperature. While vigorously stirring, 0.1 g of carbon nanotubes CNTs (DI=20-40 nm) was added, followed by ultrasonic dispersion for 480 min. An alcohol solution of ethyl orthosilicate (0.6 mL TEOS dissolved in 20 mL absolute ethanol) was added dropwise to the above suspension, and the vigorous stirring was continued at room temperature for 12 h. The obtained intermediate product was washed 3 times with water, and the alcoholic solution of ammonium nitrate (8 g of ammonium nitrate dissolved in 400 mL of absolute ethanol) was washed 3 times. Put 0.2g CNT@SiO2 Disperse in 40mL deionized water, ultrasonically disperse evenly. Add 2 mL of ammonia water...

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Abstract

The invention discloses a dendritic Cu / C-CuSiO 3 Nanostructured hydrogenation catalyst and preparation method thereof. This dendritic Cu / C‑CuSiO 3 The preparation process of the nanostructured hydrogenation catalyst is as follows: first, a silica coating layer is formed by hydrolyzing ethyl orthosilicate on the surface of monodispersed carbon nanotubes; then, the silica coating layer is combined with the hydrothermal condition The copper ammonia complex ion reacts to generate a copper silicate needle array outside the carbon nanotube; finally, metal nano-copper particles are loaded on the inner and outer surfaces of the material to adjust the content of metallic copper and copper silicate. Dendritic Cu / C‑CuSiO prepared by this method 3 Nanostructured hydrogenation catalysts can achieve stable coexistence and ratio adjustment of Cu(I) and Cu(0) active components in copper-based catalysts. At the same time, the tubular structure formed by the copper silicate needle array can obtain a large specific surface area and gas Flux can effectively solve the problems of deactivation caused by grain migration, sintering and unstable valence state of copper active components of copper-based catalysts during high-temperature hydrogenation reactions, improve the performance of catalytic hydrogenation reactions, and has broad application prospects.

Description

technical field [0001] The invention relates to a dendritic Cu / C-CuSiO 3 A nanostructured hydrogenation catalyst and a preparation method thereof, the catalyst has a high dispersion of copper metal, a stable morphology structure and surface Cu(I) / Cu(0) dual active components, and can be used to catalyze hydrogenation reactions. Background technique [0002] Catalytic hydrogenation is one of the most important reactions in organic reactions, and it is of great significance to industrial production applications. Copper-based catalysts have become the main catalysts used in many catalytic hydrogenation processes because of their low price and easy availability. At present, most of the copper-based catalysts used in industrial hydrogenation reactions are prepared by traditional loading methods such as impregnation method and coprecipitation method. The preparation process of simple supported catalysts tends to cause low dispersion of active components and exist in the body. pha...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J23/72
CPCB01J23/72B01J35/396B01J35/00B01J35/30
Inventor 岳海荣丁明月李静梁斌刘长军唐思扬
Owner SICHUAN UNIV