Effect of cobalt precursors on the dispersion, reduction, and CO oxidation of CoOx/γ-Al2O3 catalysts calcined in N2

被引:61
作者
Zhang, Lingling [2 ]
Dong, Lihui [2 ]
Yu, Wujiang [2 ]
Liu, Lianjun [2 ]
Deng, Yu [1 ]
Liu, Bin [2 ]
Wan, Haiqin [2 ]
Gao, Fei [1 ]
Sun, Keqin [3 ]
Dong, Lin [1 ,2 ]
机构
[1] Nanjing Univ, Ctr Modern Anal, Nanjing 210093, Jiangsu Prov, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Nanjing 210093, Peoples R China
[3] SE Univ, Sch Energy & Environm, Nanjing 211102, Peoples R China
基金
中国国家自然科学基金;
关键词
Cobalt precursors; Dispersion capacity; Incorporation model; CO oxidation; FISCHER-TROPSCH CATALYSTS; SUPPORTED COBALT; CO/AL2O3; CATALYSTS; ALUMINA CATALYSTS; OXIDE CATALYSTS; CARBON-MONOXIDE; NO REDUCTION; TEMPERATURE; SURFACE; DECOMPOSITION;
D O I
10.1016/j.jcis.2010.11.076
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
The present work tentatively investigated the effect of cobalt precursors (cobalt acetate and cobalt nitrate) on the physicochemical properties of CoOx/gamma-Al2O3 catalysts calcined in N-2. XRD, Raman, XPS, FTIR, and UV-vis DRS results suggested that CoO/gamma-Al2O3 was obtained from cobalt acetate precursors and CoO was dispersed on gamma-Al2O3 below its dispersion capacity of 1.50 mmol/(100 m(2) gamma-Al2O3), whereas Co3O4/gamma-Al2O3 was obtained from cobalt nitrate precursors and Co3O4 preferred to agglomerate above the dispersion capacity of 0.15 mmol/(100 m(2) gamma-Al2O3). Compared with Co3O4/gamma-Al2O3, CoO/gamma-Al2O3 catalysts were difficult to be reduced and easy to desorb oxygen species at low temperatures and presented high activities for CO oxidation as proved by H-2-TPR, O-2-TPD, and CO oxidation model reaction results. A surface incorporation model was proposed to explain the dispersion and reduction properties of CoO/gamma-Al2O3 catalysts. Crown Copyright (C) 2010 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:464 / 471
页数:8
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