Enhanced Oxidation of Xylene Using Plasma Activation of an Mn/Al2O3 Catalyst

被引:11
|
作者
Wu, Zuliang [1 ]
Zhou, Weili [1 ]
Zhu, Zhoubin [2 ]
Hao, Xiaodong [2 ]
Zhang, Xuming [3 ]
机构
[1] Zhejiang Gongshang Univ, Sch Environm Sci & Engn, Hangzhou 310018, Peoples R China
[2] Focused Photon Inc, Hangzhou 310052, Peoples R China
[3] Zhejiang Sci Tech Univ, State Prov Joint Engn Lab Fluid Transmiss Syst, Hangzhou 310018, Peoples R China
基金
中国国家自然科学基金;
关键词
Catalyst; dielectric barrier discharge (DBD); organic compounds; oxidation; plasma; NONTHERMAL PLASMA; CE CATALYSTS; P-XYLENE; REMOVAL; DECOMPOSITION; DISCHARGE; AIR; REACTOR; TOLUENE; PHASE;
D O I
10.1109/TPS.2019.2959698
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
Non-thermal plasma technology has great potential for the removal of the emission of volatile organic compounds (VOCs). However, the plasma-alone process may produce various undesired by-products that cause secondary pollutions. Here, a coaxial dielectric barrier discharge (DBD) reactor has been developed for the removal of xylene over an Al2O3-based catalyst (Mn/Al2O3, Co/Al2O3, Ce/Al2O3) at low temperatures. Compared with the plasma-alone process and other plasma-catalytic combined process, the combination of plasma and the Mn/Al2O3 catalyst obviously enhanced xylene conversion and substantially restrained the formation of by-product organic aerosol (up to 100%), and what is more is that our setup was more efficient than those in other studies. In the meantime, ozone could be effectively converted by the Mn/Al2O3 catalyst; as the main active group with a long period of existence during discharge, ozone adsorbed onto the surface of the catalyst under the action of Mn/Al2O3 and participated in the oxidation of xylene. Mn4+ and the high lattice oxygen content were the reasons for the highest efficiency of 1% Mn.
引用
收藏
页码:163 / 172
页数:10
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