Catalytic oxidation at pilot-scale: Efficient degradation of volatile organic compounds in gas phase

被引:10
|
作者
Borges Ribeiro, Barbara Maria [1 ]
Pinto, Jefferson Ferreira [2 ]
Suppino, Raphael Soeiro [1 ]
Marcola, Lucas [1 ]
Landers, Richard [3 ]
Tomaz, Edson [1 ]
机构
[1] Univ Estadual Campinas, Sch Chem Engn, Dept Proc Engn, Ave Albert Einstein 500, BR-13083852 Campinas, SP, Brazil
[2] Fac Paulinia, R Nelson Prodocimo 495, BR-13145004 Paulinia, SP, Brazil
[3] Univ Estadual Campinas, Gleb Wataghin Inst Phys, Dept Appl Phys, Surface Phys Lab, BR-13083859 Campinas, SP, Brazil
关键词
Air pollution control; Volatile organic compound; Catalytic oxidation; Commercial catalyst; Pilot-scale; PALLADIUM CATALYSTS; PD/AL2O3; CATALYST; O-XYLENE; TOLUENE; COMBUSTION; VOCS; PD; PLATINUM; REMOVAL; BENZENE;
D O I
10.1016/j.jhazmat.2018.11.030
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Volatile organic compounds (VOCs) are responsible for environmental problems and may affect human health. Several treatment technologies minimize VOCs emissions; among those, catalytic oxidation appears as a promising alternative. In this study, a pilot-scale catalytic reactor was developed and the influence of process parameters on toluene degradation were investigated. Inlet gases were heated by electrical resistances and the catalyst employed was a honeycomb shape commercial automotive catalyst (Umicore, model AFT). Toluene degradation higher than 99% was achieved for several conditions and temperature showed to be the most important process variable for it. For all concentrations, it was observed that when increasing temperature led to a decrease on the space time. At 800 ppmv, varying from 543 K to 633 K, the space time decreased from 0.121 s to 0.08 s, respectively. At 1600 ppmv for the same temperature range, space time was reduced from 0.098 s to 0.040 s, respectively. At 2400 ppmv, varying from 543 K to 633 K, space time decreased from 0.081 s to 0.048 s. The catalytic reactor developed proved to be efficient for VOCs treatment, showing a high potential of application at industrial emission sources.
引用
收藏
页码:581 / 589
页数:9
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