Issue 51, 2021, Issue in Progress

Enhanced toluene adsorption/desorption dynamic performances over modified USY zeolites after an aqueous ammonia treatment

Abstract

The dynamic adsorption/desorption performances of modified hierarchical USY zeolites treated with an ammonia solution (NH4OH) at different concentrations were investigated using gas-phase toluene as an indicator. The characterization results indicated that the ammonia treatment could result in the expansion of microporous channels and the formation of a mesoporous structure without evident decrease in crystallinity. The experiment results regarding dynamic adsorption/desorption performances revealed that the mass transfer resistance of modified USY adsorbents were greatly reduced treating with NH4OH. Among the modified samples, the 0.1 mol L−1 NH4OH treated USY adsorbent exhibited large adsorptive capacity and highest desorption rate, which show good cyclic performance that could preserve its adsorbent capacity after 20 cycles. In contrast, pristine USY samples had lost around 28% of the initial adsorption capacity after 20 cycles. Moreover, the NaOH-treated sample showed great crystallinity decline compared to the NH4OH-treated samples due to excessive silicon atom leaching from the USY framework, and had lower adsorption capacity under humid conditions. Therefore, NH4OH-modified USY zeolites could be promising adsorbents for the adsorption/desorption process of volatile organic compounds (VOCs).

Graphical abstract: Enhanced toluene adsorption/desorption dynamic performances over modified USY zeolites after an aqueous ammonia treatment

Supplementary files

Article information

Article type
Paper
Submitted
24 May 2021
Accepted
04 Sep 2021
First published
29 Sep 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 32152-32157

Enhanced toluene adsorption/desorption dynamic performances over modified USY zeolites after an aqueous ammonia treatment

S. Gao, Y. Liao, Y. Zhang, Y. Liu and Z. Wu, RSC Adv., 2021, 11, 32152 DOI: 10.1039/D1RA04034K

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