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Mutual inhibition effect of sulfur compounds in the hydrodesulfurization of thiophene, 2-ethylthiophene and benzothiophene ternary mixture

The hydrodesulphurization of a model component and equimolar ternary mixture of thiophene, 2-ethylthiophene and benzothiophene over sulphided CoMo/γ-Al(2)O(3) and CoMo/γ-Al(2)O(3)-Nb(2)O(5) catalysts were investigated in a fixed bed flow reactor. The catalysts were prepared by incipient wetness impr...

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Autores principales: Calin, Catalina, Leostean, Cristian, Trifoi, Ancuța Roxana, Oprescu, Elena-Emilia, Wiita, Elizabeth, Banu, Ionut, Doukeh, Rami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463614/
https://www.ncbi.nlm.nih.gov/pubmed/34561507
http://dx.doi.org/10.1038/s41598-021-98552-1
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author Calin, Catalina
Leostean, Cristian
Trifoi, Ancuța Roxana
Oprescu, Elena-Emilia
Wiita, Elizabeth
Banu, Ionut
Doukeh, Rami
author_facet Calin, Catalina
Leostean, Cristian
Trifoi, Ancuța Roxana
Oprescu, Elena-Emilia
Wiita, Elizabeth
Banu, Ionut
Doukeh, Rami
author_sort Calin, Catalina
collection PubMed
description The hydrodesulphurization of a model component and equimolar ternary mixture of thiophene, 2-ethylthiophene and benzothiophene over sulphided CoMo/γ-Al(2)O(3) and CoMo/γ-Al(2)O(3)-Nb(2)O(5) catalysts were investigated in a fixed bed flow reactor. The catalysts were prepared by incipient wetness impregnation method and characterized by textural characteristics, total acidity and chemical species present on the catalysts surface. The characterization results showed that both CoMo/γ-Al(2)O(3)-Nb(2)O(5) and sulphided CoMo/γ-Al(2)O(3) catalysts exhibit a mesoporous structure with cylindrical pores open at both ends, evidenced by the IV type adsorption–desorption isotherm with a H1 hysteresis loop and have an average pore diameter between 3 and 4 nm. The chemical species present on the catalysts surface evaluated by XPS indicated that Co(2+) and Mo(4+) species are present in the sulfide form on both catalysts surfaces. In addition, there are also found oxidic species arising from incomplete reduction and sulphidation. The presence of niobium oxide in the catalytic support had a positive effect in leading to higher specific surface area (170 m(2)/g) and total acidity (0.421 meq/g) compared with CoMo/γ-Al(2)O(3) catalyst (140 m(2)/g and 0.283 meq/g) respectively. The evaluation results from the hydrodesulfurization showed that CoMo/γ-Al(2)O(3)-Nb(2)O(5) catalyst had a higher activity in hydrodesulphurization process of thiophene, 2-ethylthiophene and benzothiophene. The CoMo/γ-Al(2)O(3)-Nb(2)O(5) catalyst eliminated sulfur from the single component feed (corresponding to 2380 ppm S) and reduced below 10 ppm, for the feed consisting in the equimolar ternary mixture of thiophene, 2-ethylthiophene and benzothiophene (2380 ppm S). The reactivity of thiophen compounds was reduced due to competitive adsorption. It was observed that benzothiophene inhibits the transformation of thiophene and 2-ethylthiophene. A mutual inhibition effect between sulfur compounds was also observed when thiophene, 2-ethylthiophene and benzothiophene were combined and tested over the CoMo/γ-Al(2)O(3) catalyst. The inhibition effect had a lower intensity by introducing Nb(2)O(5) in the catalyst support.
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spelling pubmed-84636142021-09-27 Mutual inhibition effect of sulfur compounds in the hydrodesulfurization of thiophene, 2-ethylthiophene and benzothiophene ternary mixture Calin, Catalina Leostean, Cristian Trifoi, Ancuța Roxana Oprescu, Elena-Emilia Wiita, Elizabeth Banu, Ionut Doukeh, Rami Sci Rep Article The hydrodesulphurization of a model component and equimolar ternary mixture of thiophene, 2-ethylthiophene and benzothiophene over sulphided CoMo/γ-Al(2)O(3) and CoMo/γ-Al(2)O(3)-Nb(2)O(5) catalysts were investigated in a fixed bed flow reactor. The catalysts were prepared by incipient wetness impregnation method and characterized by textural characteristics, total acidity and chemical species present on the catalysts surface. The characterization results showed that both CoMo/γ-Al(2)O(3)-Nb(2)O(5) and sulphided CoMo/γ-Al(2)O(3) catalysts exhibit a mesoporous structure with cylindrical pores open at both ends, evidenced by the IV type adsorption–desorption isotherm with a H1 hysteresis loop and have an average pore diameter between 3 and 4 nm. The chemical species present on the catalysts surface evaluated by XPS indicated that Co(2+) and Mo(4+) species are present in the sulfide form on both catalysts surfaces. In addition, there are also found oxidic species arising from incomplete reduction and sulphidation. The presence of niobium oxide in the catalytic support had a positive effect in leading to higher specific surface area (170 m(2)/g) and total acidity (0.421 meq/g) compared with CoMo/γ-Al(2)O(3) catalyst (140 m(2)/g and 0.283 meq/g) respectively. The evaluation results from the hydrodesulfurization showed that CoMo/γ-Al(2)O(3)-Nb(2)O(5) catalyst had a higher activity in hydrodesulphurization process of thiophene, 2-ethylthiophene and benzothiophene. The CoMo/γ-Al(2)O(3)-Nb(2)O(5) catalyst eliminated sulfur from the single component feed (corresponding to 2380 ppm S) and reduced below 10 ppm, for the feed consisting in the equimolar ternary mixture of thiophene, 2-ethylthiophene and benzothiophene (2380 ppm S). The reactivity of thiophen compounds was reduced due to competitive adsorption. It was observed that benzothiophene inhibits the transformation of thiophene and 2-ethylthiophene. A mutual inhibition effect between sulfur compounds was also observed when thiophene, 2-ethylthiophene and benzothiophene were combined and tested over the CoMo/γ-Al(2)O(3) catalyst. The inhibition effect had a lower intensity by introducing Nb(2)O(5) in the catalyst support. Nature Publishing Group UK 2021-09-24 /pmc/articles/PMC8463614/ /pubmed/34561507 http://dx.doi.org/10.1038/s41598-021-98552-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Calin, Catalina
Leostean, Cristian
Trifoi, Ancuța Roxana
Oprescu, Elena-Emilia
Wiita, Elizabeth
Banu, Ionut
Doukeh, Rami
Mutual inhibition effect of sulfur compounds in the hydrodesulfurization of thiophene, 2-ethylthiophene and benzothiophene ternary mixture
title Mutual inhibition effect of sulfur compounds in the hydrodesulfurization of thiophene, 2-ethylthiophene and benzothiophene ternary mixture
title_full Mutual inhibition effect of sulfur compounds in the hydrodesulfurization of thiophene, 2-ethylthiophene and benzothiophene ternary mixture
title_fullStr Mutual inhibition effect of sulfur compounds in the hydrodesulfurization of thiophene, 2-ethylthiophene and benzothiophene ternary mixture
title_full_unstemmed Mutual inhibition effect of sulfur compounds in the hydrodesulfurization of thiophene, 2-ethylthiophene and benzothiophene ternary mixture
title_short Mutual inhibition effect of sulfur compounds in the hydrodesulfurization of thiophene, 2-ethylthiophene and benzothiophene ternary mixture
title_sort mutual inhibition effect of sulfur compounds in the hydrodesulfurization of thiophene, 2-ethylthiophene and benzothiophene ternary mixture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463614/
https://www.ncbi.nlm.nih.gov/pubmed/34561507
http://dx.doi.org/10.1038/s41598-021-98552-1
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