Removal of chlorobenzene using a sequential adsorption–plasma catalytic system over Ag‐, Ce‐ and Mn‐modified activated carbon catalysts
BACKGROUND: A dielectric barrier discharge reactor coupled with a series of activated carbon (AC) catalysts was applied to remove low concentrations of chlorobenzene. The catalysts were prepared via an impregnation method and their adsorption capacity and plasma-catalytic ability examined in a seque...
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sg-ntu-dr.10356-1054122020-06-01T10:21:25Z Removal of chlorobenzene using a sequential adsorption–plasma catalytic system over Ag‐, Ce‐ and Mn‐modified activated carbon catalysts Jiang, Liying Cao, Xiang Chen, Jianmeng Guo, Haiqian Chen, Zhong Li, Sha School of Materials Science & Engineering Chlorobenzene DRNTU::Engineering::Materials AC Catalysts BACKGROUND: A dielectric barrier discharge reactor coupled with a series of activated carbon (AC) catalysts was applied to remove low concentrations of chlorobenzene. The catalysts were prepared via an impregnation method and their adsorption capacity and plasma-catalytic ability examined in a sequential adsorption–plasma oxidation process. RESULTS: Ag/AC had the longest breakthrough time and highest breakthrough capacity among the catalysts studied. At the discharge stage, the Ag/AC catalyst had the highest CO2 yield, chlorobenzene mineralization rate and carbon balance, and the lowest emission of chlorobenzene when compared with the other catalysts under the same conditions. However, the Ag/AC catalyst exhibited the worst reducing ozone generation performance, while the Mn/AC catalyst showed the best ozone decomposition ability. The organic intermediates produced using Ag/AC and Ce/AC were simpler and in lower concentrations than those formed using Mn/AC.The adsorption capacity and catalytic activity of the Ag/AC catalyst showed no obvious decrease after five cycles. Fourier transform infrared and scanning electron microscopy–energy dispersive spectroscopy analyses after the reaction showed that some nitrogen organic intermediates and chlorine substances produced via the degradation of chlorobenzene were adsorbed onto the catalyst surface. CONCLUSIONS: Ag/AC exhibited a longer breakthrough time, higher breakthrough capacity, higher CO2 yield, less chlorobenzene emission and better carbon balance when compared with the other catalysts. 2019-06-12T06:17:32Z 2019-12-06T21:50:43Z 2019-06-12T06:17:32Z 2019-12-06T21:50:43Z 2019 Journal Article Jiang, L., Cao, X., Chen, J., Guo, H., Chen, Z., & Li, S. (2019). Removal of chlorobenzene using a sequential adsorption–plasma catalytic system over Ag‐, Ce‐ and Mn‐modified activated carbon catalysts. Journal of Chemical Technology & Biotechnology, 94(6), 1788-1799. doi:10.1002/jctb.5944 0268-2575 https://hdl.handle.net/10356/105412 http://hdl.handle.net/10220/48674 10.1002/jctb.5944 en Journal of Chemical Technology & Biotechnology © 2019 Society of Chemical Industry. All rights reserved. |
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Chlorobenzene DRNTU::Engineering::Materials AC Catalysts Jiang, Liying Cao, Xiang Chen, Jianmeng Guo, Haiqian Chen, Zhong Li, Sha Removal of chlorobenzene using a sequential adsorption–plasma catalytic system over Ag‐, Ce‐ and Mn‐modified activated carbon catalysts |
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BACKGROUND: A dielectric barrier discharge reactor coupled with a series of activated carbon (AC) catalysts was applied to remove low concentrations of chlorobenzene. The catalysts were prepared via an impregnation method and their adsorption capacity and plasma-catalytic ability examined in a sequential adsorption–plasma oxidation process. RESULTS: Ag/AC had the longest breakthrough time and highest breakthrough capacity among the catalysts studied. At the discharge stage, the Ag/AC catalyst had the highest CO2 yield, chlorobenzene mineralization rate and carbon balance, and the lowest emission of chlorobenzene when compared with the other catalysts under the same conditions. However, the Ag/AC catalyst exhibited the worst reducing ozone generation performance, while the Mn/AC catalyst showed the best ozone decomposition ability. The organic intermediates produced using Ag/AC and Ce/AC were simpler and in lower concentrations than those formed using Mn/AC.The adsorption capacity and catalytic activity of the Ag/AC catalyst showed no obvious decrease after five cycles. Fourier transform infrared and scanning electron microscopy–energy dispersive spectroscopy analyses after the reaction showed that some nitrogen organic intermediates and chlorine substances produced via the degradation of chlorobenzene were adsorbed onto the catalyst surface. CONCLUSIONS: Ag/AC exhibited a longer breakthrough time, higher breakthrough capacity, higher CO2 yield, less chlorobenzene emission and better carbon balance when compared with the other catalysts. |
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School of Materials Science & Engineering |
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School of Materials Science & Engineering Jiang, Liying Cao, Xiang Chen, Jianmeng Guo, Haiqian Chen, Zhong Li, Sha |
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Jiang, Liying Cao, Xiang Chen, Jianmeng Guo, Haiqian Chen, Zhong Li, Sha |
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Jiang, Liying |
title |
Removal of chlorobenzene using a sequential adsorption–plasma catalytic system over Ag‐, Ce‐ and Mn‐modified activated carbon catalysts |
title_short |
Removal of chlorobenzene using a sequential adsorption–plasma catalytic system over Ag‐, Ce‐ and Mn‐modified activated carbon catalysts |
title_full |
Removal of chlorobenzene using a sequential adsorption–plasma catalytic system over Ag‐, Ce‐ and Mn‐modified activated carbon catalysts |
title_fullStr |
Removal of chlorobenzene using a sequential adsorption–plasma catalytic system over Ag‐, Ce‐ and Mn‐modified activated carbon catalysts |
title_full_unstemmed |
Removal of chlorobenzene using a sequential adsorption–plasma catalytic system over Ag‐, Ce‐ and Mn‐modified activated carbon catalysts |
title_sort |
removal of chlorobenzene using a sequential adsorption–plasma catalytic system over ag‐, ce‐ and mn‐modified activated carbon catalysts |
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2019 |
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https://hdl.handle.net/10356/105412 http://hdl.handle.net/10220/48674 |
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1681057271894769664 |