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Abatement of mixed volatile organic compounds in a catalytic hybrid surface/packed-bed discharge plasma reactor

Author:
Guo, Lianjie, Jiang, Nan, Li, Jie, Shang, Kefeng, Lu, Na, Wu, Yan
Source:
Frontiers of environmental science & engineering 2018 v.12 no.2 pp. 15
ISSN:
2095-2201
Subject:
X-ray photoelectron spectroscopy, adsorption, ambient temperature, benzene, byproducts, carbon dioxide, catalysts, catalytic activity, electrons, mineralization, ozone, relative humidity, toluene, volatile organic compounds, water vapor, xylene
Abstract:
In this study, post plasma-catalysis degradation of mixed volatile organic compounds (benzene, toluene, and xylene) has been performed in a hybrid surface/packed-bed discharge plasma reactor with Ag-Ce/g-Al₂O₃ catalyst at room temperature. The effect of relative air humidity on mixed VOCs degradation has also been investigated in both plasma-only and PPC systems. In comparison to the plasma-only system, a significant improvement can be observed in the degradation performance of mixed VOCs in PPC system with Ag-Ce/γ-Al₂O₃ catalyst. In PPC system, 68% benzene, 89% toluene, and 94% xylene were degraded at 800 J·L–¹, respectively, which were 25%, 11%, and 9% higher than those in plasma-only system. This result can be attributed to the high catalytic activity of Ag-Ce/γ-Al₂O₃ catalyst to effectively decompose O₃ and lead to generating more reactive species which are capable of destructing the VOCs molecules completely. Moreover, the presence of Ag-Ce/γ-Al₂O₃ catalyst in plasma significantly decreased the emission of discharge byproducts (NOₓ and O₃) and promoted the mineralization of mixed VOCs towards CO₂. Adding a small amount of water vapor into PPC system enhanced the degradation efficiencies of mixed VOCs, however, further increasing water vapor had a negative impact on the degradation efficiencies, which was primarily attributed to the quenching of energetic electrons by water vapor in plasma and the competitive adsorption of water vapor on the catalyst surface. Meanwhile, the catalysts before and after discharge were characterized by the Brunauer-Emment-Teller and X-ray photoelectron spectroscopy.
Agid:
5889873