Ethane dehydrogenation over pore-expanded mesoporous silica-supported chromium oxide: 2. Catalytic properties and nature of active sites

被引:58
|
作者
Rao, T. V. Malleswara [1 ]
Zahidi, El Mamoune [1 ]
Sayari, Abdelhamid [1 ]
机构
[1] Univ Ottawa, Dept Chem, Ottawa, ON K1N 6N5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Ethane dehydrogenation; Chromium oxide; Pore-expanded MCM-41; XPS; ADSORPTION; PROPANE; POLYMERIZATION; SPECTROSCOPY; PARAFFINS; ETHYLENE; BUTANE; SIZE;
D O I
10.1016/j.molcata.2008.12.027
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
Pore-expanded mesoporous MCM-41 silica-supported chromium oxide catalysts with different chromia loadings were synthesized using three different methods. The catalysts were thoroughly characterized and used for ethane dehydrogenation (DH). Reaction studies revealed that the ethane conversion and coke formation on the catalyst depend on the chromia loading and the catalyst preparation method. All catalysts were highly selective toward ethylene. However, among the three catalysts containing 5wt% chromia, the 5wt% Cr/PE-MCM-41 catalyst exhibited the best performance with an ethane conversion of 23% and similar to 99% ethylene selectivity at 650 C(C2H6/N-2 - 0.176 total contact time = 0.0032 g min/mL). The chromia catalysts prepared using as synthesized pore-expanded mesoporous silica (Cr/PE-MCM-41) also exhibited the highest stability. XPS analysis revealed the presence of three different chromium, namely Cr(II), Cr(III) and Cr(VI), whose overall surface concentration as well as relative content varied with the reaction time-on-stream (TOS). Furthermore, the nature and relative amounts of surface chromium species were monitored by in situ XPS measurements as a function of TOS. Correlation of the XPS findings with ethane DH showed clearly that the Cr(III) species are the main active sites. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:159 / 165
页数:7
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