WIGS reaction over nanostructured CuO-CeO2 catalysts prepared by hard template method: Characterization, activity and deactivation

被引:37
作者
Djinovic, Petar [1 ]
Batista, Jurka [1 ]
Pintar, Albin [1 ,2 ]
机构
[1] Natl Inst Chem, SI-1001 Ljubljana, Slovenia
[2] Univ Ljubljana, Fac Chem & Chem Technol, SI-1001 Ljubljana, Slovenia
关键词
CuO-CeO2; catalysts; Hard template method; WGS reaction; Carbonates; Catalyst deactivation; WATER-GAS SHIFT; MIXED-OXIDE CATALYSTS; PREFERENTIAL OXIDATION; CARBON-MONOXIDE; CO OXIDATION; RICH H-2; TEMPERATURE; PERFORMANCE; CUO/CEO2; FTIR;
D O I
10.1016/j.cattod.2009.07.009
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
This study focuses on water-gas shift reaction (WGSR) activity Of CuO-CeO2 catalysts containing 10, 15 and 20 mol% CuO synthesized by hard template method with KIT-6 silica acting as a template. The obtained solids were characterized by N-2 adsorption/desorption, XRD, H-2-TPR/TPD, N2O decomposition, in situ DRIFTS and NH3 chemisorption/TPD methods. The catalysts exhibited ordered mesoporous structure, which was identified as the negative replica of KIT-6 silica pore system with CuO dispersion values between 28 and 40%. H-2-TPR/TPD experiments revealed facile and extensive CeO2 reduction in tested samples, which increased with CuO loading, indicating strong interactions between both oxide phases. On the other hand, abundance of surface acidic sites decreased with increasing CuO content. WGS reaction activity was tested at the stoichiometric CO/H2O ratio and low contact times in the temperature range from 250 to 450 degrees C. At reaction temperatures above 375 degrees C, catalyst deactivation was observed, regardless of CuO content. Despite rigorous reaction conditions, CO conversion up to 62% was attained, with H-2 selectivity above 99% in the entire temperature range. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:S191 / S197
页数:7
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