Issue 22, 2015

An Au–Cu bimetal catalyst for acetylene hydrochlorination with renewable γ-Al2O3 as the support

Abstract

The bimetal catalyst gold(III) chloride–copper(II) chloride (AuCl3–CuCl2) was prepared with several different gamma-aluminium oxide (γ-Al2O3) supports and its catalytic properties towards acetylene hydrochlorination were assessed in a fixed-bed reactor. The comparison indicated that one of the catalysts attained the highest activity with an acetylene conversion of 97%, which was far higher than the others. Catalysts were characterized using detailed X-ray diffraction, nitrogen-Brunauer, Emmett and Teller surface area analysis (N2-BET), ammonia temperature-programmed desorption, Fourier-transform infrared spectroscopy and carbon dioxide temperature-programmed desorption analysis. It is proposed that the base site contributed to its high catalyst activity compared with the other catalysts, instead of the acid site or the textural properties on the support, therefore, the activity and the life of the catalysts can be improved significantly by treating the supports with potassium hydroxide. In addition, the results of N2-BET, thermogravimetric analysis and scanning electron microscopy indicated that the catalysts deactivated rapidly because of carbon deposition, and the actual amount of coke deposition was 18.0% after the reaction. AuCl3–CuCl2/γ-Al2O3 was easily regenerated for reuse as a catalyst by burning off in an air atmosphere for 10 min. The activity of the regenerated catalyst nearly reached the level of the fresh catalyst.

Graphical abstract: An Au–Cu bimetal catalyst for acetylene hydrochlorination with renewable γ-Al2O3 as the support

Supplementary files

Article information

Article type
Paper
Submitted
02 Nov 2014
Accepted
21 Jan 2015
First published
21 Jan 2015

RSC Adv., 2015,5, 16727-16734

Author version available

An Au–Cu bimetal catalyst for acetylene hydrochlorination with renewable γ-Al2O3 as the support

J. Zhao, J. Zeng, X. Cheng, L. Wang, H. Yang and B. Shen, RSC Adv., 2015, 5, 16727 DOI: 10.1039/C4RA13648A

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