Performance of carbon nanofibres, high surface area graphites, and activated carbons as supports of Pd-based hydrodechlorination catalysts

被引:22
作者
Bueres, Ruben F. [1 ]
Asedegbega-Nieto, Esther [1 ]
Diaz, Eva [1 ]
Ordonez, Salvador [1 ]
Diez, Fernando V. [1 ]
机构
[1] Univ Oviedo, Dept Chem Engn & Environm Technol, E-33006 Oviedo, Spain
关键词
Tetrachloroethylene; Hydrodechlorination; Pd catalyst; Carbon nanofibres; High surface area graphites; LIQUID-PHASE HYDRODECHLORINATION; ADSORPTION PROPERTIES; PD/AL2O3; CATALYST; HYDROGENATION; DEACTIVATION; NANOTUBES; CINNAMALDEHYDE; PLATINUM;
D O I
10.1016/j.cattod.2009.05.020
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Palladium catalysts (1 wt%) supported on three different carbonaceous supports (activated carbon, AC; carbon nanofibre, CNF; and high surface area graphite, HSAG) were prepared and tested for tetrachloroethylene (TTCE) catalytic hydrodechlorination at 523 K and 195 h(-1) space velocity (WHSV). Organic solutions (0.9 mol/L of TTCE in toluene) were used as feed, simulating real chlorinated wastes. Pd/activated carbon and Pd/CNF have shown a fast deactivation on stream, whereas the HSAG-supported catalyst showed the best performance. Characterization of fresh and used catalysts by BET, TEM, XRD and XPS revealed that the deactivation of Pd/AC catalyst is caused by the micropore blockage because of coke formation, whereas in the case of Pd/CNF, deactivation is caused by a combination of coke deposition (in lower extent than in the case of activated carbon). active phase sintering and chlorine poisoning. The best behaviour of the HSAG-based catalysts is caused by the absence of sintering and coke formation, although chlorine poisoning is still present. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:16 / 21
页数:6
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