Effect of catalyst pre-reduction temperature on the reaction of 1,2-dichloroethane and H2 catalyzed by SiO2-supported PtCu bimetallics

被引:8
作者
Akonwie, Lindney N. [1 ]
Kazachkin, D. V. [1 ]
Luebke, D. R. [1 ]
d'Itri, Julie L. [1 ]
机构
[1] Univ Pittsburgh, Dept Chem Engn, Pittsburgh, PA 15261 USA
关键词
Bimetallics; PtCu bimetallics; Adsorbate-induced surface enrichment; Dual site mechanism; 1,2-Dichloroethane dechlorination; Catalyst pretreatment; ENERGY ION-SCATTERING; ADSORBATE-INDUCED SEGREGATION; SILICA-SUPPORTED PLATINUM; CARBON-MONOXIDE; SURFACE-COMPOSITION; ADSORPTION EQUILIBRIUM; COPPER-CATALYSTS; CU ALLOYS; HYDROGEN CHEMISORPTION; INFRARED-SPECTROSCOPY;
D O I
10.1016/j.apcata.2011.12.002
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 combination of reaction kinetics experiments, temperature-programmed investigations and FTIR CO adsorption studies were used to understand the effect of catalyst pretreatment on the reaction of 1,2-dichloroethane and H-2 catalyzed by SiO2 supported PtCu bimetallics prepared from metal chloride precursors. Higher initial and steady-state selectivities towards ethylene were obtained for catalysts with a Cu to Pt atomic ratio of 1, 2, and 3 after pre-reduction at 220 degrees C than after pre-reduction at 500 degrees C. For catalysts with a Cu to Pt atomic ratio of 4 and 5, the initial ethylene selectivity was higher after the 220 degrees C pre-reduction. but the steady-state ethylene selectivities were essentially the same. Based on the catalyst characterization results, the low temperature pre-reduction yields supported particles with Pt-rich cores covered with Cu-rich layers that are still well-chlorinated, whereas the high temperature pre-reduction yields particles both more metallic and with surfaces richer in Pt. The factors governing the evolution of the catalysts during the two different pretreatments are discussed as well as the impact catalyst pretreatment has on the macroscopic performance behavior. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:59 / 69
页数:11
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