Hydrochlorination of acetylene using supported bimetallic Au-based catalysts

被引:241
|
作者
Conte, Marco [1 ]
Carley, Albert F. [1 ]
Attard, Gary [1 ]
Herzing, Andrew A. [2 ,3 ]
Kiely, Christopher J. [2 ]
Hutchings, Graham J. [1 ]
机构
[1] Cardiff Univ, Sch Chem, Cardiff CF10 3AT, S Glam, Wales
[2] Lehigh Univ, Dept Mat Sci & Engn, Bethlehem, PA 18015 USA
[3] Natl Inst Stand & Technol, Surface & Microanal Sci Div, Gaithersburg, MD 20899 USA
基金
美国国家科学基金会; 英国工程与自然科学研究理事会;
关键词
cold catalysis; acetylene hydrochlorination; supported bimetallic catalysts; gold alloy nanoparticles;
D O I
10.1016/j.jcat.2008.04.024
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A detailed study of the hydrochlorination of acetylene using supported gold and gold-based bimetallic catalysts is described and discussed. Carbon-sup ported Au-Pd catalysts were studied in detail, because Au and Pd can form a continuous solid solution across all alloy compositions. The addition of <= 5 at% Pd to Au increased the initial activity but with a significant loss of selectivity. In addition, all Au-Pd/C catalysts deactivated rapidly due to coke deposition. Pt-Au catalysts behaved in a similar manner. In contrast, Au-catalysts doped with It and Rh demonstrated enhanced activity with little change in selectivity. The addition of Ru had no significant effect. The observations are rationalized in terms (i) of the relative solubilities of the second metal in Au, which were explored by detailed STEM-XEDS analysis, and (ii) the dehydrochlorination and oligomerization activity of the dopant metal. These results confirm that the most active known catalyst for the hyd rochlori nation of acetylene for long-term use is undoped Au, and that the activity of the catalyst correlates with the standard electrode potential. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:190 / 198
页数:9
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