Insight Into the Role of Ceria on OMS-2 and OL Materials for Catalytic Degradation of Toluene

被引:2
|
作者
Yue, Lin [1 ,2 ]
Hu, Minghua [1 ]
Tian, Mingjiao [2 ]
Liao, Xu [3 ]
Xu, Zhihua [1 ]
Shi, Ling [1 ]
He, Chi [2 ]
机构
[1] Jianghan Univ, Hubei Key Lab Ind Fume & Dust Pollut Control, Wuhan, Hubei, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Energy & Power Engn, State Key Lab Multiphase Flow Power Engn, Xian, Shaanxi, Peoples R China
[3] Chinese Acad Sci, Inst Urban Environm, Key Lab Urban Environm & Hlth, Xiamen, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Volatile organic compounds; Ce/MnOx; toluene; catalytic oxidation; reaction mechanism; OCTAHEDRAL MOLECULAR-SIEVES; METHYL-ETHYL-KETONE; MANGANESE OXIDE; TOTAL OXIDATION; BENZYL ALCOHOL; CE; PERFORMANCE; ETHANOL; OXYGEN;
D O I
10.3389/fenvc.2020.599349
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Catalytic oxidation is one of the most efficient approaches for industrial volatile organic compounds (VOCs) elimination. MnOx-based catalysts have attracted much attention due to their remarkable low-temperature catalytic activity. Here, octahedral layered birnessite-type manganese oxide (OL-1) with layer spacing of 7 & Aring; and cryptomelane type manganese oxide (OMS-2) with tunneled pore diameter of 4.6 & Aring;x 4.6 & Aring; were synthesized by a reflux method. Following this, Ce-doped OL-1 and OMS-2 were further prepared by an impregnation method with target to improve catalytic performance in toluene oxidation. Results reveal that the OMS-2 material exhibits the best catalytic activity with 90% of toluene decomposed at 224 degrees C owing to the presence of a large quantity of active lattice oxygen species. Interestingly, the introduction of Ce leads to the formation of large amounts of acidic sites, which limit the oxidation process and enhance the yield of benzoic acid by-product. The findings in the present work are meaningful for deepening our understanding of the role of ceria on metal oxide catalysts and helping us to design effective catalysts for VOC destruction.
引用
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页数:11
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