Highly Active Low Cobalt Content-Based Bulk MoS2 Hydrodesulfurization Catalysts with a Unique Impact of H2S

A series of unsupported MoS2, Co9S8, and Co-promoted MoS2 catalysts have been synthesized by tuned impregnation and successive thermal annealing methods using a continuous flow of a mixture of H2 and H2S gases. The resulting catalysts were evaluated in terms of their activity and selectivity for the...

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Main Authors: Hamdy Farag, Abd-Alrahman Embaby, Masahiro Kishida, Abdel-Nasser A. El-Hendawy, Mohamed Mahmoud Nasef
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2018/8076534
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author Hamdy Farag
Abd-Alrahman Embaby
Masahiro Kishida
Abdel-Nasser A. El-Hendawy
Mohamed Mahmoud Nasef
author_facet Hamdy Farag
Abd-Alrahman Embaby
Masahiro Kishida
Abdel-Nasser A. El-Hendawy
Mohamed Mahmoud Nasef
author_sort Hamdy Farag
collection DOAJ
description A series of unsupported MoS2, Co9S8, and Co-promoted MoS2 catalysts have been synthesized by tuned impregnation and successive thermal annealing methods using a continuous flow of a mixture of H2 and H2S gases. The resulting catalysts were evaluated in terms of their activity and selectivity for the hydrodesulfurization of dibenzothiophene (DBT) both in the absence and the presence of H2S. The inclusion of Co onto MoS2 affected both the hydrogenation and direct desulfurization reactions, with the latter (production of biphenyl) being magnified to a much greater degree than the former. Interestingly, low cobalt/molybdenum ratio of ca. 0.05 of the catalyst exhibited outstanding promotion efficiency in the hydrodesulfurization reaction. However, as cobalt is added, the synergy effect drastically decreased. H2S in the reaction mixture led to a remarkable step up in the product from the direct desulfurization reaction route with the most notable increases occurring for the product from the hydrogenation reaction pathway. The HDS activity of such catalysts was much higher than that of the commercial CoMo/Al2O3. The promotion by H2S was discussed.
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institution Kabale University
issn 2090-9063
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language English
publishDate 2018-01-01
publisher Wiley
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series Journal of Chemistry
spelling doaj-art-c986a205a8574c4a9b4e1b0dca55ad782025-02-03T05:54:15ZengWileyJournal of Chemistry2090-90632090-90712018-01-01201810.1155/2018/80765348076534Highly Active Low Cobalt Content-Based Bulk MoS2 Hydrodesulfurization Catalysts with a Unique Impact of H2SHamdy Farag0Abd-Alrahman Embaby1Masahiro Kishida2Abdel-Nasser A. El-Hendawy3Mohamed Mahmoud Nasef4Chemistry Department, Faculty of Science, Mansoura University, Mansoura 35516, EgyptGeology Department, Faculty of Science, Damietta University, Damietta 34517, EgyptDepartment of Material Process Engineering, Graduate School of Engineering, Kyushu University, Motooka 744, Fukuoka 819-0395, JapanPhysical Chemistry Department, National Research Center, 12622 Dokki, Cairo, EgyptChemical Engineering Department, Universiti Teknologi Petronas, 32610 Seri Iskandar, Perak, MalaysiaA series of unsupported MoS2, Co9S8, and Co-promoted MoS2 catalysts have been synthesized by tuned impregnation and successive thermal annealing methods using a continuous flow of a mixture of H2 and H2S gases. The resulting catalysts were evaluated in terms of their activity and selectivity for the hydrodesulfurization of dibenzothiophene (DBT) both in the absence and the presence of H2S. The inclusion of Co onto MoS2 affected both the hydrogenation and direct desulfurization reactions, with the latter (production of biphenyl) being magnified to a much greater degree than the former. Interestingly, low cobalt/molybdenum ratio of ca. 0.05 of the catalyst exhibited outstanding promotion efficiency in the hydrodesulfurization reaction. However, as cobalt is added, the synergy effect drastically decreased. H2S in the reaction mixture led to a remarkable step up in the product from the direct desulfurization reaction route with the most notable increases occurring for the product from the hydrogenation reaction pathway. The HDS activity of such catalysts was much higher than that of the commercial CoMo/Al2O3. The promotion by H2S was discussed.http://dx.doi.org/10.1155/2018/8076534
spellingShingle Hamdy Farag
Abd-Alrahman Embaby
Masahiro Kishida
Abdel-Nasser A. El-Hendawy
Mohamed Mahmoud Nasef
Highly Active Low Cobalt Content-Based Bulk MoS2 Hydrodesulfurization Catalysts with a Unique Impact of H2S
Journal of Chemistry
title Highly Active Low Cobalt Content-Based Bulk MoS2 Hydrodesulfurization Catalysts with a Unique Impact of H2S
title_full Highly Active Low Cobalt Content-Based Bulk MoS2 Hydrodesulfurization Catalysts with a Unique Impact of H2S
title_fullStr Highly Active Low Cobalt Content-Based Bulk MoS2 Hydrodesulfurization Catalysts with a Unique Impact of H2S
title_full_unstemmed Highly Active Low Cobalt Content-Based Bulk MoS2 Hydrodesulfurization Catalysts with a Unique Impact of H2S
title_short Highly Active Low Cobalt Content-Based Bulk MoS2 Hydrodesulfurization Catalysts with a Unique Impact of H2S
title_sort highly active low cobalt content based bulk mos2 hydrodesulfurization catalysts with a unique impact of h2s
url http://dx.doi.org/10.1155/2018/8076534
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AT abdalrahmanembaby highlyactivelowcobaltcontentbasedbulkmos2hydrodesulfurizationcatalystswithauniqueimpactofh2s
AT masahirokishida highlyactivelowcobaltcontentbasedbulkmos2hydrodesulfurizationcatalystswithauniqueimpactofh2s
AT abdelnasseraelhendawy highlyactivelowcobaltcontentbasedbulkmos2hydrodesulfurizationcatalystswithauniqueimpactofh2s
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