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Título : | Effect of H2S inhibition on the hydrodechlorination of polychlorinated biphenyls over Mo/Al2O3 and Co–Mo/ Al2O3 catalysts |
Autor : | De la Rosa, Marjorie Betancourt, Paulino Díaz, Armando Brito, Joaquín L. Pinto-Castilla, Susana |
Palabras clave : | Aroclor 1242 Co–Mo catalyst H2S inhibition Hydrodechlorination Langmuir–Hinshelwood model Polychlorinated biphenyls |
Fecha de publicación : | 28-Sep-2013 |
Editorial : | Springer Science |
Citación : | Reaction Kinetics, Mechanisms and Catalysis |
Citación : | Vol. 111;1 |
Resumen : | The effect of the cobalt addition on the H2S inhibition and subsequently
on the polychlorinated biphenyl (PCB) hydrodechlorination (HDC) activity over
Mo-based catalysts was investigated. The HDC activity over a Mo catalyst containing
cobalt was much higher than that over the same Mo catalyst without cobalt.
On the other hand, the HDC activity of the Co–Mo catalyst was more inhibited by
H2S than that of the Mo catalyst at 300 C. Thus, kinetic parameters were calculated
using a Langmuir–Hinshelwood model to determine the reaction pathway of the
H2S inhibition over Mo and Co–Mo catalysts. We found that the heats of adsorption
of PCB (Aroclor 1242) and H2S on the Co–Mo catalyst was higher than on the Mo
catalyst, indicating that the sulfur-containing species adsorb more strongly on the
catalyst containing cobalt. The results suggested that while the Co–Mo catalyst was
more inhibited by H2S, the Mo–S bonds were more stable on this catalyst than on
the solely Mo catalyst. This Mo–S bond was responsible for the stabilization of the
active phase, which allowed creation of a greater amount of sulfur atoms potentially
labile. Thus, that explained the better HDC activity over the Co–Mo catalyst than
over the Mo catalyst, despite a greater H2S inhibition on the former. |
URI : | http://hdl.handle.net/10872/5755 |
ISSN : | 1878-5190 |
Aparece en las colecciones: | Artículos Publicados
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