TY - JOUR
T1 - Effect of H2S inhibition on the hydrodechlorination of polychlorinated biphenyls over Mo/Al2O3 and Co-Mo/Al 2O3 catalysts
AU - De La Rosa, Marjorie
AU - Betancourt, Paulino
AU - Díaz, Armando
AU - Brito, Joaquín L.
AU - Pinto-Castilla, Susana
PY - 2014/2
Y1 - 2014/2
N2 - 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.
AB - 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.
KW - Aroclor 1242
KW - Co-Mo catalyst
KW - HS inhibition
KW - Hydrodechlorination
KW - Langmuir-Hinshelwood model
KW - Polychlorinated biphenyls
UR - http://www.scopus.com/inward/record.url?scp=84893241945&partnerID=8YFLogxK
U2 - 10.1007/s11144-013-0635-5
DO - 10.1007/s11144-013-0635-5
M3 - Artículo
AN - SCOPUS:84893241945
SN - 1878-5190
VL - 111
SP - 277
EP - 292
JO - Reaction Kinetics, Mechanisms and Catalysis
JF - Reaction Kinetics, Mechanisms and Catalysis
IS - 1
ER -