Catalytic oxidation of toluene in air using manganese incorporated catalyst by non-thermal plasma system

被引:48
作者
Zhang, Xiao [1 ]
Ren, Bin [1 ]
Xu, Yanhua [1 ]
Li, Xi [1 ]
Yu, Peng [1 ]
Sun, Yongjun [2 ]
Zheng, Huaili [3 ]
机构
[1] Nanjing Tech Univ, Sch Environm Sci & Engn, Nanjing 211816, Peoples R China
[2] Nanjing Tech Univ, Coll Urban Construct, Nanjing 211816, Peoples R China
[3] Chongqing Univ, State Minist Educ, Key Lab Three Gorges Reservoir Reg Ecoenvironm, Chongqing 400045, Peoples R China
基金
中国国家自然科学基金;
关键词
Toluene degradation; CO2; selectivity; Non-thermal plasma; Catalytic oxidation; Air pollution control;
D O I
10.1016/j.seppur.2020.117973
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Mn/MCM-41 and imp-Mn/MCM-41 catalysts were prepared in this study through metal heteroatom substitution and impregnation methods, respectively, and their catalytic oxidation performance of toluene under non-thermal plasma (NTP) in a dielectric barrier discharge reactor was studied. The stability of the catalyst and the parameters of catalytic oxidation conditions (initial concentration of toluene, O-2 ratio, and relative humidity of carrier gas) were optimized. Characterization proved that the impregnation method resulted in the existence of manganese in the form of oxides (MnO2, Mn2O3) outside the pores of MCM-41. Meanwhile, the metal heteroatom substitution method implanted manganese into the mesoporous structure and replaced part of it with Si-O-Mn. NTP catalytic oxidation of toluene, ozone emission, and GC-MS by-product analysis confirmed that 60Mn/MCM41 catalyst has high catalytic activity. Moreover, the catalyst affected the production of by-products. The stability test revealed that the 60Mn/MCM-41 catalyst still respectively reached 84.6% and 61% in the conversion of toluene and the selectivity of CO2 under the SED of 558 J/L after 40 h discharge reaction.
引用
收藏
页数:14
相关论文
共 56 条
[21]   Post plasma-catalysis for VOCs degradation over different phase structure MnO2 catalysts [J].
Li, Yizhuo ;
Fan, Zeyun ;
Shi, Jianwei ;
Liu, Zhenyan ;
Shangguan, Wenfeng .
CHEMICAL ENGINEERING JOURNAL, 2014, 241 :251-258
[22]   Plasma-Catalytic Oxidation of Toluene on MnxOy at Atmospheric Pressure and Room Temperature [J].
Lu, Meijuan ;
Huang, Rong ;
Wang, Peitao ;
Chen, Limin ;
Wu, Junliang ;
Fu, Mingli ;
Wen, William ;
Huang, Bichun ;
Ye, Daiqi .
PLASMA CHEMISTRY AND PLASMA PROCESSING, 2014, 34 (05) :1141-1156
[23]  
Ma T, 2016, PLASMA SCI TECHNOL
[24]   In situ study of ozone and hybrid plasma Ag-Al catalysts for the oxidation of toluene: Evidence of the nature of the active sites [J].
Magureanu, Monica ;
Piroi, Daniela ;
Mandache, Nicolae Bogdan ;
Parvulescu, Vasile I. ;
Parvulescu, Viorica ;
Cojocaru, Bogdan ;
Cadigan, Chris ;
Richards, Ryan ;
Daly, Helen ;
Hardacre, Christopher .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2011, 104 (1-2) :84-90
[25]   COMPLETE OXIDATION OF BENZENE ON MANGANESE-DIOXIDE BY OZONE [J].
NAYDENOV, A ;
MEHANDJIEV, D .
APPLIED CATALYSIS A-GENERAL, 1993, 97 (01) :17-22
[26]   Nitrophenol derivatives oxidized by cerium(IV) ammonium nitrate (CAN) and their cytotoxicity [J].
Pan, WB ;
Wei, LM ;
Wei, LL ;
Wu, CC ;
Chang, FR ;
Wu, YC .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 2005, 52 (03) :581-588
[27]   Structural properties and catalytic activity of Mn-MCM-41 mesoporous molecular sieves for single-step amination of benzene to aniline [J].
Parida, K. M. ;
Dash, Saswati Soumya ;
Singha, S. .
APPLIED CATALYSIS A-GENERAL, 2008, 351 (01) :59-67
[28]   Manganese containing MCM-41: Synthesis, characterization and catalytic activity in the oxidation of ethylbenzene [J].
Parida, K. M. ;
Dash, Saswati Soumya .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2009, 306 (1-2) :54-61
[29]   Synthesis, Characterization and Catalytic Performance of Well-Ordered Crystalline Heteroatom Mesoporous MCM-41 [J].
Qin, Jing ;
Li, Baoshan ;
Yan, Dongpeng .
CRYSTALS, 2017, 7 (04)
[30]   Low-temperature catalytic oxidation of toluene over nanocrystal-like Mn-Co oxides prepared by two-step hydrothermal method [J].
Qu, Zhenping ;
Gao, Kang ;
Fu, Qiang ;
Qin, Yuan .
CATALYSIS COMMUNICATIONS, 2014, 52 :31-35