Catalytic wet air oxidation of phenol and acrylic acid over Ru/C and Ru-CeO2/C catalysts

被引:104
作者
Oliviero, L
Barbier-Jr, J
Duprez, D
Guerrero-Ruiz, A
Bachiller-Baeza, B
Rodríguez-Ramos, I
机构
[1] CNRS, Catalyse Chim Organ Lab, UMR6503, F-86022 Poitiers, France
[2] CSIC, Inst Catalisis & Petroleoquim, E-28049 Madrid, Spain
关键词
wet air oxidation; ruthenium catalysts; phenol (catalytic oxidation in water of); acrylic acid (catalytic oxidation in water of);
D O I
10.1016/S0926-3373(99)00141-1
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
Ru/C catalysts promoted, or not, by cerium were prepared by impregnation of an active carbon (961 m(2) g(-1)) with chlorine-free precursors of Ru and Ce, They were characterized by chemisorption of H-2 and of CO and by electron microscopy. TEM and H-2 chemisorption gives coherent results while CO chemisorption overestimates Ru dispersion. Tn Ru-Ce/C, Ce is in close contact with Ru and decreases Ru accessibility. Catalytic wet air oxidation (CWAO) of phenol and of acrylic acid (160 degrees C and 20 bar of O-2) was investigated over these catalysts and their performance (activity, selectivity to intermediate compounds) compared with that of a reference Ru/CeO2 catalyst. Carbon-supported catalysts were very active for the CWAO of phenol but not for acrylic acid. Although high conversions were obtained, phenol was not totally mineralized after 3 h. It was shown that acrylic acid was more strongly adsorbed than phenol. Moreover, the number of contact points between Ru particles and CeO2 crystallites constitutes a key parameter in these reactions. A high surface area of ceria is required to insure O-2 activation when the organic molecule is strongly adsorbed. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:267 / 275
页数:9
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