Degradation of trichloroethylene by hydrodechlorination using formic acid as hydrogen source over supported Pd catalysts

被引:28
|
作者
Yu, Xin [1 ,2 ]
Wu, Ting [1 ]
Yang, Xue-Jing [1 ]
Xu, Jing [1 ]
Auzam, Jordan [3 ]
Semiat, Raphael [4 ]
Han, Yi-Fan [1 ]
机构
[1] E China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[2] Harbin Normal Univ, Coll Chem & Chem Engn, Harbin 150025, Peoples R China
[3] Univ Western Ontario, Dept Chem & Biochem Engn, London, ON N6A 5B9, Canada
[4] Technion Israel Inst Technol, Wolfson Dept Chem Engn, IL-32000 Haifa, Israel
基金
美国国家科学基金会;
关键词
Trichloroethylene (TCE); Formic acid (FA); Pd/MCM-41; Hydrodechlorination; Kinetics; ZERO-VALENT IRON; PHOTOCATALYTIC DEGRADATION; CHLORINATED HYDROCARBONS; BIMETALLIC PARTICLES; ORGANIC-COMPOUNDS; ZEROVALENT IRON; WATER; PALLADIUM; NANOPARTICLES; KINETICS;
D O I
10.1016/j.jhazmat.2015.11.025
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
An advanced method for the degradation of trichloroethylene (TCE) over Pd/MCM-41 catalysts through a hydrogen-transfer was investigated. Formic acid (FA) was used instead of gaseous H-2 as the hydrogen resource. As a model H-carrier compound, FA has proven to yield less by-products and second-hand pollution during the reaction. Several factors have been studied, including: the property of catalyst supports, Pd loading and size, temperature, initial concentrations of FA and TCE (potential impact on the reaction rates of TCE degradation), and FA decomposition. The intrinsic kinetics for TCE degradation were measured, while the apparent activation energies and the reaction orders with respect to TCE and FA were calculated through power law models. On the basis of kinetics, we assumed a plausible reaction pathway for TCE degradation in which the catalytic degradation of TCE is most likely the rate-determining step for this reaction.(C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:178 / 189
页数:12
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