Evaluation of lanthanide-group promoters on Co-Ni/Al2O3 catalysts for CH4 dry reforming

被引:79
作者
Foo, Say Yei [1 ]
Cheng, Chin Kui [1 ]
Tuan-Huy Nguyen [1 ]
Adesina, Adesoji A. [1 ]
机构
[1] Univ New S Wales, Sch Chem Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, Australia
基金
澳大利亚研究理事会;
关键词
CO2 reforming of CH4; Lanthanide promoter; Cobalt-nickel catalyst; Pauling electronegativity; GEL NI/AL2O3 CATALYSTS; CARBON-DIOXIDE; SYNTHESIS GAS; BIMETALLIC CATALYSTS; SUPPORTED COBALT; METHANE; CO2; DEACTIVATION; PERFORMANCE; OXIDATION;
D O I
10.1016/j.molcata.2011.04.018
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
The influence of lanthanide group (Ce, Pr and Sm) promoters on alumina-supported bimetallic Co-Ni catalysts for CH4 dry reforming in a fixed-bed reactor was investigated. Lanthanide doping did not appear to affect CH4 and CO2 consumption rate, however, H-2 and CO production rates increased suggesting better utilisation of surface carbonaceous species. Carbon deposition on the promoted catalysts was substantially reduced (by up to 50%), with Ce providing the greatest anti-coking resistance followed by Pr and Sm. The beneficial effects of the promoted catalysts may be attributed to the interaction of the deposited but unconverted CxH1-x species with the lanthanide oxide in redox reactions, as well as smaller active particle size of the promoted catalysts which was unfavourable for carbon formation. In general, the study shows that attributes (such as product (H-2 and CO) formation rate constants and the associated reaction orders as well as the enthalpy and entropy of CH4 adsorption) of the promoted catalysts compared favourably to those of the unpromoted counterpart and are reasonably correlated with the Pauling electronegativity of the dopants. TPR-TPO of used catalysts suggests the presence two types of carbonaceous deposits - a reactive species which is lower in the promoted catalysts, and a relatively unreactive carbon which is present in similar quantities for all the catalysts. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 36
页数:9
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