Catalytic oxidation of chlorobenzene and PCDD/Fs over V2O5-WO3/TiO2: insights into the component effect and reaction mechanism

被引:14
作者
Qin, Yu [1 ]
Gu, Jun [1 ]
Cai, Wentao [1 ]
Wang, Zhaojia [1 ]
机构
[1] Beijing Bldg Mat Acad Sci Res, State Key Lab Solid Waste Reuse Bldg Mat, Beijing 100041, Peoples R China
关键词
Catalytic oxidation; PCDD; Fs; Chlorobenzene; V2O5; WO3; Reaction mechanism; THERMOCHEMICAL FORMATION; SYNERGETIC INHIBITION; FLUE-GAS; DIOXINS; OXIDE; DECOMPOSITION; REDUCTION; SULFUR; NH3; NOX;
D O I
10.1007/s11356-022-18768-0
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this work, titania supported catalysts (V-W/Ti) with different vanadium-tungsten contents were prepared and evaluated in the catalytic oxidation of chlorobenzene, which was used as the model compound of dioxins. The results showed that V2O5 is the main active component for chlorobenzene oxidation, and doping of WO3 affects the valence distributions of vanadium, contributing a bimetallic synergistic effect. The catalysts were investigated by XRD, SEM-EDS mapping, Raman, and XPS, and the changes in V element valence state and chlorine content on fresh and used catalysts were observed by XPS. Moreover, in situ FTIR studies and chlorine balance were also conducted, the addition of WO3 is helpful to the breakage of C-Cl, and a reaction mechanism for the catalytic oxidation of chlorobenzene was proposed. 3 V-5 W/Ti catalyst with better catalytic activity was selected for catalytic oxidation of PCDD/Fs using a lab scale PCDD/Fs generating and decomposing system. The degradation efficiency was 66.5% at 200 degrees C and 62.2% at 300 degrees C, which indicated that the low reaction temperature of 200 degrees C was conducive to the catalytic degradation of PCDDs, while the high temperature of 300 degrees C was facilitated the degradation of PCDFs.
引用
收藏
页码:42809 / 42821
页数:13
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