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Chemically activated hydrochar as an effective adsorbent for volatile organic compounds (VOCs).

Authors :
Zhang, Xueyang
Gao, Bin
Fang, June
Zou, Weixin
Dong, Lin
Cao, Chengcheng
Zhang, Jian
Li, Yuncong
Wang, Hailong
Source :
Chemosphere. Mar2019, Vol. 218, p680-686. 7p.
Publication Year :
2019

Abstract

Abstract Hydrochars derived from hickory wood and peanut hull through hydrothermal carbonization were activated with H 3 PO 4 and KOH to improve their performance as a volatile organic compound (VOC) adsorbent. Polar acetone and nonpolar cyclohexane were used as representative VOCs. The VOC adsorptive capacities of the activated hydrochars (50.57–159.66 mg⋅g−1) were greater than that of the nonactivated hydrochars (15.98–25.36 mg⋅g−1), which was mainly caused by the enlargement of surface area. The significant linear correlation (R2 = 0.984 on acetone, and R2 = 0.869 on cyclohexane) between BET surface areas of hydrochars and their VOC adsorption capacities, together with the obvious adsorption exothermal peak of differential scanning calorimetry curve confirmed physical adsorption as the dominating mechanism. Finally, the reusability of activated hydrochar was tested on H 3 PO 4 activated hickory hydrochar (HHP), which had higher acetone and cyclohexane adsorption capacities. After five continuous adsorption desorption cycles, the adsorptive capacities of acetone and cyclohexane on HHP decreased by 6.2% and 7.8%, respectively. The slight decline in adsorption capacity confirmed the reusability of activated hydrochar as a VOC sorbent. Graphical abstract Image Highlights • Chemically activated hydrochars showed good removal of acetone and cyclohexane. • Sorption capacities of the activated hydrochars were 50.57–159.66 mg g−1 • Surface areas of hydrochars and their adsorption capacities had a strong linear correlation. • Physical adsorption was the dominant mechanism. • Activated hydrochar showed good reusability. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
218
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
133781560
Full Text :
https://doi.org/10.1016/j.chemosphere.2018.11.144