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Removal of toluene by sequential adsorption-plasma oxidation: Mixed support and catalyst deactivation.
Qin, Caihong; Huang, Xuemin; Zhao, Junjie; Huang, Jiayu; Kang, Zhongli; Dang, Xiaoqing.
Afiliação
  • Qin C; School of Environment & Municipal Engineering, Xi'an University of Architecture & Technology, Xi'an 710055, China.
  • Huang X; School of Environment & Municipal Engineering, Xi'an University of Architecture & Technology, Xi'an 710055, China.
  • Zhao J; School of Environment & Municipal Engineering, Xi'an University of Architecture & Technology, Xi'an 710055, China.
  • Huang J; Research Center of Air Pollution Control Technology, Chinese Research Academy of Environmental Sciences, Beijing 100012, China.
  • Kang Z; School of Environment & Municipal Engineering, Xi'an University of Architecture & Technology, Xi'an 710055, China.
  • Dang X; School of Environment & Municipal Engineering, Xi'an University of Architecture & Technology, Xi'an 710055, China. Electronic address: xiaoqingdang@hotmail.com.
J Hazard Mater ; 334: 29-38, 2017 Jul 15.
Article em En | MEDLINE | ID: mdl-28384555
ABSTRACT
A sequential adsorption-plasma oxidation system was used to remove toluene from simulated dry air using γ-Al2O3, HZSM-5, a mixture of the two materials or their supported Mn-Ag catalyst as adsorbents under atmospheric pressure and room temperature. After 120min of plasma oxidation, γ-Al2O3 had a better carbon balance (∼75%) than HZSM-5, but the CO2 yield of γ-Al2O3 was only ∼50%; and there was some desorption of toluene when γ-Al2O3 was used. When a mixture of HZSM-5 and γ-Al2O3 with a mass ratio of 1/2 was used, the carbon balance was up to 90% and 82% of this was CO2. The adsorption performance and electric discharge characteristics of the mixed supports were tested in order to rationalize this high COx yield. After seven cycles of sequential adsorption-plasma oxidation, support and Mn-Ag catalyst deactivation occurred. The support and catalyst were characterized before and after deactivation by SEM, a BET method, XRD, XPS and GC-MS in order to probe the mechanism of their deactivation. 97.6% of the deactivated supports and 76% of the deactivated catalysts could be recovered by O2 temperature-programmed oxidation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article