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Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO(2) Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel

A core-shell Cu-benzene-1,3,5-tricarboxylic acid (Cu-BTC)@TiO(2) was successfully synthesized for photocatalysis-assisted adsorptive desulfurization to improve adsorptive desulfurization (ADS) performance. Under ultraviolet (UV) light irradiation, the TiO(2) shell on the surface of Cu-BTC achieved p...

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Autores principales: Liu, Jing, Li, Xiao-Min, He, Jing, Wang, Lu-Ying, Lei, Jian-Du
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266854/
https://www.ncbi.nlm.nih.gov/pubmed/30405062
http://dx.doi.org/10.3390/ma11112209
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author Liu, Jing
Li, Xiao-Min
He, Jing
Wang, Lu-Ying
Lei, Jian-Du
author_facet Liu, Jing
Li, Xiao-Min
He, Jing
Wang, Lu-Ying
Lei, Jian-Du
author_sort Liu, Jing
collection PubMed
description A core-shell Cu-benzene-1,3,5-tricarboxylic acid (Cu-BTC)@TiO(2) was successfully synthesized for photocatalysis-assisted adsorptive desulfurization to improve adsorptive desulfurization (ADS) performance. Under ultraviolet (UV) light irradiation, the TiO(2) shell on the surface of Cu-BTC achieved photocatalytic oxidation of thiophenic S-compounds, and the Cu-BTC core adsorbed the oxidation products (sulfoxides and sulfones). The photocatalyst and adsorbent were combined using a distinct core-shell structure. The morphology and structure of the fabricated Cu-BTC@TiO(2) microspheres were verified by scanning electron microscopy, high-resolution transmission electron microscopy, energy-dispersive x-ray spectroscopy, X-ray powder diffraction, nitrogen adsorption-desorption and X-ray photoelectron spectroscopy analyses. A potential formation mechanism of Cu-BTC@TiO(2) is proposed based on complementary experiments. The sulfur removal efficiency of the microspheres was evaluated by selective adsorption of benzothiophene (BT) and dibenzothiophene (DBT) from a model fuel with a sulfur concentration of 1000 ppmw. Within a reaction time of 20 min, the BT and DBT conversion reached 86% and 95%, respectively, and achieved ADS capacities of 63.76 and 59.39 mg/g, respectively. The BT conversion and DBT conversion obtained using Cu-BTC@TiO(2) was 6.5 and 4.6 times higher, respectively, than that obtained using Cu-BTC. A desulfurization mechanism was proposed, the interaction between thiophenic sulfur compounds and Cu-BTC@TiO(2) microspheres was discussed, and the kinetic behavior was analyzed.
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spelling pubmed-62668542018-12-17 Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO(2) Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel Liu, Jing Li, Xiao-Min He, Jing Wang, Lu-Ying Lei, Jian-Du Materials (Basel) Article A core-shell Cu-benzene-1,3,5-tricarboxylic acid (Cu-BTC)@TiO(2) was successfully synthesized for photocatalysis-assisted adsorptive desulfurization to improve adsorptive desulfurization (ADS) performance. Under ultraviolet (UV) light irradiation, the TiO(2) shell on the surface of Cu-BTC achieved photocatalytic oxidation of thiophenic S-compounds, and the Cu-BTC core adsorbed the oxidation products (sulfoxides and sulfones). The photocatalyst and adsorbent were combined using a distinct core-shell structure. The morphology and structure of the fabricated Cu-BTC@TiO(2) microspheres were verified by scanning electron microscopy, high-resolution transmission electron microscopy, energy-dispersive x-ray spectroscopy, X-ray powder diffraction, nitrogen adsorption-desorption and X-ray photoelectron spectroscopy analyses. A potential formation mechanism of Cu-BTC@TiO(2) is proposed based on complementary experiments. The sulfur removal efficiency of the microspheres was evaluated by selective adsorption of benzothiophene (BT) and dibenzothiophene (DBT) from a model fuel with a sulfur concentration of 1000 ppmw. Within a reaction time of 20 min, the BT and DBT conversion reached 86% and 95%, respectively, and achieved ADS capacities of 63.76 and 59.39 mg/g, respectively. The BT conversion and DBT conversion obtained using Cu-BTC@TiO(2) was 6.5 and 4.6 times higher, respectively, than that obtained using Cu-BTC. A desulfurization mechanism was proposed, the interaction between thiophenic sulfur compounds and Cu-BTC@TiO(2) microspheres was discussed, and the kinetic behavior was analyzed. MDPI 2018-11-07 /pmc/articles/PMC6266854/ /pubmed/30405062 http://dx.doi.org/10.3390/ma11112209 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Jing
Li, Xiao-Min
He, Jing
Wang, Lu-Ying
Lei, Jian-Du
Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO(2) Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel
title Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO(2) Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel
title_full Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO(2) Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel
title_fullStr Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO(2) Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel
title_full_unstemmed Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO(2) Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel
title_short Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO(2) Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel
title_sort combining the photocatalysis and absorption properties of core-shell cu-btc@tio(2) microspheres: highly efficient desulfurization of thiophenic compounds from fuel
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266854/
https://www.ncbi.nlm.nih.gov/pubmed/30405062
http://dx.doi.org/10.3390/ma11112209
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