Regeneration of AgXO@SBA-15 for reactive adsorptive desulfurization of fuel
Abstract Adsorbent regeneration is critical for a continuous adsorption–regeneration process and often underestimated. In this work, the regeneration of bifunctional AgXO@SBA-15 for [O]-induced reactive adsorptive desulfurization of liquid fuel is reported and further investigated. The spent AgXO@SB...
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KeAi Communications Co., Ltd.
2018
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oai:doaj.org-article:3f474bc414ef426ab5f5998f0661b18d2021-12-02T10:12:33ZRegeneration of AgXO@SBA-15 for reactive adsorptive desulfurization of fuel10.1007/s12182-018-0264-81672-51071995-8226https://doaj.org/article/3f474bc414ef426ab5f5998f0661b18d2018-10-01T00:00:00Zhttp://link.springer.com/article/10.1007/s12182-018-0264-8https://doaj.org/toc/1672-5107https://doaj.org/toc/1995-8226Abstract Adsorbent regeneration is critical for a continuous adsorption–regeneration process and often underestimated. In this work, the regeneration of bifunctional AgXO@SBA-15 for [O]-induced reactive adsorptive desulfurization of liquid fuel is reported and further investigated. The spent AgXO@SBA-15 was regenerated in various types of solvents followed by calcination and tested in multiple desulfurization–regeneration cycles. The effects of regenerate solvents were also compared systematically. The original and regenerated AgXO@SBA-15 was characterized by X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, N2 adsorption, X-ray photoelectron spectroscopy and atomic absorption spectrometry. The recovery of desulfurization capacity using various solvents follows the order of acetonitrile > acetone > ethanol > methanol > water. Owing to the complete reduction of silver species to Ag0 and severe agglomeration of Ag0, the bifunctional AgXO@SBA-15 demonstrating > 85% (2.60 mg-S/g) of sulfur removal dramatically reduced to < 46% (1.56 mg-S/g) after only 1st-cycle regeneration. It is suggested that polar organic species strongly adsorbed (or residual) on the spent AgXO@SBA-15, in that case, after solvent wash may contribute to the accelerated decomposition of Ag+ to Ag0 in the following calcination step. The desulfurization capacity decreased rather mildly in the later regeneration runs. Cautious choice of regeneration conditions and strategies to rational design stabilized adsorbents is required to avert the adsorbent deactivation.Liqiong WuFeiyan YeDong LeiGuang MiaoBaoyu LiuZhong LiJing XiaoKeAi Communications Co., Ltd.articleBifunctionalRegenerationOxidationAdsorptionDeactivationScienceQPetrologyQE420-499ENPetroleum Science, Vol 15, Iss 4, Pp 857-869 (2018) |
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Bifunctional Regeneration Oxidation Adsorption Deactivation Science Q Petrology QE420-499 |
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Bifunctional Regeneration Oxidation Adsorption Deactivation Science Q Petrology QE420-499 Liqiong Wu Feiyan Ye Dong Lei Guang Miao Baoyu Liu Zhong Li Jing Xiao Regeneration of AgXO@SBA-15 for reactive adsorptive desulfurization of fuel |
description |
Abstract Adsorbent regeneration is critical for a continuous adsorption–regeneration process and often underestimated. In this work, the regeneration of bifunctional AgXO@SBA-15 for [O]-induced reactive adsorptive desulfurization of liquid fuel is reported and further investigated. The spent AgXO@SBA-15 was regenerated in various types of solvents followed by calcination and tested in multiple desulfurization–regeneration cycles. The effects of regenerate solvents were also compared systematically. The original and regenerated AgXO@SBA-15 was characterized by X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, N2 adsorption, X-ray photoelectron spectroscopy and atomic absorption spectrometry. The recovery of desulfurization capacity using various solvents follows the order of acetonitrile > acetone > ethanol > methanol > water. Owing to the complete reduction of silver species to Ag0 and severe agglomeration of Ag0, the bifunctional AgXO@SBA-15 demonstrating > 85% (2.60 mg-S/g) of sulfur removal dramatically reduced to < 46% (1.56 mg-S/g) after only 1st-cycle regeneration. It is suggested that polar organic species strongly adsorbed (or residual) on the spent AgXO@SBA-15, in that case, after solvent wash may contribute to the accelerated decomposition of Ag+ to Ag0 in the following calcination step. The desulfurization capacity decreased rather mildly in the later regeneration runs. Cautious choice of regeneration conditions and strategies to rational design stabilized adsorbents is required to avert the adsorbent deactivation. |
format |
article |
author |
Liqiong Wu Feiyan Ye Dong Lei Guang Miao Baoyu Liu Zhong Li Jing Xiao |
author_facet |
Liqiong Wu Feiyan Ye Dong Lei Guang Miao Baoyu Liu Zhong Li Jing Xiao |
author_sort |
Liqiong Wu |
title |
Regeneration of AgXO@SBA-15 for reactive adsorptive desulfurization of fuel |
title_short |
Regeneration of AgXO@SBA-15 for reactive adsorptive desulfurization of fuel |
title_full |
Regeneration of AgXO@SBA-15 for reactive adsorptive desulfurization of fuel |
title_fullStr |
Regeneration of AgXO@SBA-15 for reactive adsorptive desulfurization of fuel |
title_full_unstemmed |
Regeneration of AgXO@SBA-15 for reactive adsorptive desulfurization of fuel |
title_sort |
regeneration of agxo@sba-15 for reactive adsorptive desulfurization of fuel |
publisher |
KeAi Communications Co., Ltd. |
publishDate |
2018 |
url |
https://doaj.org/article/3f474bc414ef426ab5f5998f0661b18d |
work_keys_str_mv |
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1718397518842167296 |