Photolysis and photooxidation of typical gaseous VOCs by UV Irradiation: Removal performance and mechanisms

Highlights

UV photodegradation of 27 typical VOCs was systematically investigated.

Contribution of photolysis and photooxidation to VOCs removal was identified.

Gaseous VOC could be partially converted to particles by 185/254 nm UV irradiation.

The mineralization and conversion of 27 VOCs by UV irradiation were reported.

Abstract

Photodegradation by ultraviolet irradiation (UV) is increasingly applied in volatile organic compound (VOC) and odor gas treatments. In this study, 27 typical VOCs, including 11 hydrocarbons and 16 hydrocarbon derivatives, at 150–200 ppm in air and nitrogen gas were treated by a laboratory-scale UV reactor with 185/254 nm irradiation to systematically investigate their removal and conversion by UV irradiation. For the tested 27 VOCs, the VOC removal efficiencies in air were within the range of 13%–97% (with an average of 80%) at a retention time of 53 s, which showed a moderate positive correlation with the molecular weight of the VOCs (R = 0.53). The respective contributions of photolysis and photooxidation to VOC removal were identified for each VOC. According to the CO₂ results, the mineralization rate of the tested VOCs was within the range of 9%–90%, with an average of 41% and were negatively correlated to the molecular weight (R = -0.63). Many of the tested VOCs exhibited high concentration particulate matters in the off-gases with a 3–283 mg/m³ PM₁₀ range and a 2–40 mg/m³ PM_2.5 range. The carbon balance of each VOC during UV irradiation was analyzed based on the VOC, CO₂ and PM₁₀ concentrations. Certain organic intermediates and 23–218 ppm ozone were also identified in the off-gases. Although the UV technique exhibited a high VOC removal efficiency, its drawbacks, specifically low mineralization, particulate matters production, and ozone emission, must be considered prior to its application in VOC gas treatments.

Graphical abstract

Keywords

VOCs / UV photodegradation / Particulate matters / Ozone

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Acknowledgements

This study was supported by the National Natural Science Foundation of China (Grant No.51378286) and the Science and Technology Program for Water Pollution Control (No. 2011ZX07301-003). We thank LetPub (www.letpub.com) for providing linguistic assistance during the preparation of this manuscript.

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