Degradation of methyl tert-butyl ether by catalytic wet air oxidation over Rh/TiO2-CeO2 catalysts

被引:24
作者
Cervantes, A. [1 ]
Del Angel, G. [1 ]
Torres, G. [2 ]
Lafaye, G. [3 ]
Barbier, J., Jr. [3 ]
Beltramini, J. N. [4 ,5 ]
Cabanas-Moreno, J. G. [6 ]
de los Monteros, A. Espinosa [3 ]
机构
[1] Univ Autonoma Metropolitana Unidad Iztapalapa, Dept Quim, Area Catalisis, Mexico City 09340, DF, Mexico
[2] Univ Juarez Autonoma Tabasco, DACB, Lab Catalisis Heterogenea, Cunduacan 86690, Tabasco, Mexico
[3] Univ Poitiers, Catalyse Chim Organ Lab, F-86000 Poitiers, France
[4] Univ Queesland, ARC Ctr Excellence Funct Nanomat, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[5] Univ Queesland, Sch Engn, St Lucia, Qld 4072, Australia
[6] Inst Politecn Nacl, CNMN, UPALM, Mexico City 07738, DF, Mexico
关键词
Catalytic wet air oxidation; Methyl tert-butyl ether; Rh/TiO2; Rh/TiO2-CeO2; HCl effect; Carbon deposition; HERBICIDE 2,4-DICHLOROPHENOXYACETIC ACID; MTBE; WATER; GASOLINE; SOIL;
D O I
10.1016/j.cattod.2012.11.021
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The catalytic wet air oxidation of methyl tert-butyl ether was carried on Rh/TiO2 and Rh/TiO2-CeO2 catalysts. The TiO2-CeO2 (1, 3, 5, 10, and 20 wt% CeO2) mixed oxides were prepared by the sol-gel method. The catalysts were characterized by different techniques: surface adsorption-desorption of N-2 (BET surface area), X-ray diffraction (XRD), Fourier transform infrared of CO adsorption (FTIR-CO), Fourier transformed infrared of pyridine adsorption (FTIR-pyridine), temperature programmed reduction of H-2 (H-2-TPR), total organic compound (TOC) and transmission electron microscopy (TEM). A higher specific surface area BET and Lewis acidity sites were obtained on catalysts containing cerium oxide. Small Rh particles <1.8 nm were obtained in all catalysts. The Rh catalysts containing cerium oxide showed higher activity than the reference Rh/TiO2 and a maximum in activity at 5 wt% loading of CeO2. It is assumed that the acid sites are acting as a tramp for the MTBE molecule increasing the conversion on the Rh particles joined to an additional oxygen supply by cerium oxide redox process. The presence of cerium oxide inhibits the deposit of carbon on the catalyst; the higher cerium oxide concentration, the lower carbon deposited on the Rh surface. The addition of HCl on the initial reaction solution increases the CWAO activity. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:2 / 9
页数:8
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