Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite

被引:8
作者
Regenhardt, S. A. [1 ]
Meyer, C. I. [1 ]
Trasarti, A. F. [1 ]
Monzon, A. [2 ]
Garetto, T. F. [1 ]
机构
[1] FIQ UNL CONICET, GICIC Inst Invest Catalisis & Petroquim INCAPE, RA-3000 Santa Fe, Argentina
[2] Univ Zaragoza, INA, Dept Chem & Environm Engn, E-50009 Zaragoza, Spain
关键词
Carbon tetrachloride combustion; Exchanged Y-zeolite; Co-zeolite; Langmuir-Hinshelwood mechanism; Kinetic modeling; DECOMPOSITION; COMBUSTION; DESTRUCTION; MECHANISM;
D O I
10.1016/j.cej.2012.05.055
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this contribution we present the results of a kinetic study of the catalytic combustion of carbon tetrachloride over several catalysts of Y-zeolite exchanged with Cr, Co, Mn and Fe. The catalysts were prepared by ion exchange and characterized, before and after catalytic tests, by atomic absorption, N-2 physisorption (BET surface measurement) and X-ray diffraction. The experimental results have been analyzed using both empirical, -power-law pseudo-homogenous-. and mechanistical -Langmuir-Hinshelwood-models. The catalytic results indicate the following order of activity: Y-Co > Y-Cr >> Y-Fe congruent to Y-Mn. According to the mechanism assumed to explain the kinetic results obtained, the oxygen molecule adsorbs over the surface Co++ species, and the carbon tetrachloride interacts with the H+ ion on the Bronsted acid site. It was also obtained that the presence of water in the feed is necessary to avoid the deactivation of the catalyst. This effect is probably due to the capacity of water to restore the Bronsted acid sites depleted during the reaction. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:18 / 26
页数:9
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