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The elimination of volatile organic compounds (VOCs) via vacuum ultraviolet (VUV) photolysis is greatly limited by low removal efficiency and gaseous byproducts generation, while photocatalytic oxidation of VOCs suffers from catalytic deactivation. Herein, a coupled process of gaseous VUV photolysis with aqueous photocatalytic oxidation with P25 as the catalyst was firstly proposed for efficient aromatic VOCs removal (VUV/P25). The removal efficiency of toluene reached 86.2% in VUV/P25 process, but was only 33.6% and 58.1% in alone gaseous VUV photolysis and aqueous ultraviolet photocatalytic oxidation (UV/P25) process, respectively. Correspondingly, the outlet CO 2 concentration in VUV/P25 process reached 132 ppmv. Toluene was firstly destructed by high-energy photons generated from gaseous VUV photolysis, resulting in its incomplete oxidation to form soluble intermediates including acids, aldehydes, esters. These soluble intermediates would be further degraded and mineralized into CO 2 in subsequent aqueous UV/P25 process. Notably, the concentrations of intermediates in VUV/P25 were much lower than those in VUV photolysis, indicating the synergy effect of VUV photolysis and UV/P25 process. The stability tests proved that VUV/P25 process maintained an excellent toluene degradation performance and P25 did not suffer from catalytic deactivation. In addition to toluene, the VUV/P25 system also achieved the efficient and sustainable degradation of styrene and chlorobenzene, suggesting its good application prospect in industrial VOCs treatment. This study proposes an efficient and promising strategy for deep oxidation of multiple aromatic VOCs in industries., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The traditional treatment processes for volatile organic compounds (VOCs) removal generally suffered several disadvantages, such as secondary air-pollutants. To overcome these issues, wet scrubber coupled with heterogeneous UV/Fenton was developed for gaseous VOCs (i.e. toluene) removal. ZSM-5 supported iron oxide (Fe/ZSM-5) was prepared as a multifunctional catalyst for activation of H 2 O 2 and enhancement of gas-liquid mass transfer. Toluene was removed efficiently by this coupled process with the removal efficiency of 85% during 120 min. Many intermediates were detected in the solution by GC-MS while no intermediates were observed in the outlet gas, suggesting that wet scrubber coupled with heterogeneous UV/Fenton could significantly reduce secondary air pollutants. The possible mechanism of toluene oxidation was proposed including the physical adsorption by Fe/ZSM-5 and OH oxidation. This study provides an environmentally benign and highly efficient chemical scrubbing process for gaseous VOCs removal., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Ag/TiO 2 catalysts were prepared via in-situ synthesis and impregnation methods. The effect of redox state of Ag species on catalytic activity of Ag/TiO 2 catalysts was studied. The Ag-i-300 catalyst with partially oxidized state of Ag species shows superior catalytic activity, keeping HCHO removal efficiency at an extraordinary level of 100% during the 200 min's reaction. The Ag/TiO 2 catalysts were characterized by XPS, UV-Vis, BET, XRD, TEM, and in-situ DRIFTS technologies. XPS and TEM results exhibit that the partially oxidized state of Ag δ+ (0 < δ < 1) and high dispersion of Ag species are beneficial for the oxidation of HCHO over Ag/TiO 2 catalysts. According to the above results, a reaction pathway for HCHO oxidation over Ag-i-300 catalyst was also proposed., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

A novel 3-D heterojunction photocatalyst Ag 2 CO 3 /BiVO 4 was successfully fabricated. It exhibits excellent photocatalytic performances for the photocatalytic oxidation of crystal violet and reduction of Cr 6+ , which is ascribed to the suppression of charge recombination, and increasing lifetime of the charge carriers confirmed by the result of time-resolved fluorescence emission decay spectra and photoelectrochemical measures. The electron spin resonance result also suggests that heterojunction structure can improve separation efficiency of photogenerated carriers and favor to form •OH radicals. Moreover, ten intermediates and products for the photocatalytic oxidation degradation of crystal violet are identified by GC-MS., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Volatile organic compounds (VOCs) are regarded as the major contributors to air pollution, and should be strictly regulated. Photocatalytic oxidation (PCO) is of great interest for the removal of VOCs owing to its strong oxidation capability. However, its application is greatly limited by catalytic deactivation. Vacuum Ultraviolet (VUV) irradiation provides a novel way to improve the photocatalytic activity while much O 3 will be generated which may cause secondary pollution. In this study, a multi-functional catalyst of Mn/TiO 2 /activated carbon (AC) was developed to eliminate and utilize O 3 , as well as enhance catalytic oxidation of VOC degradation via ozone-assisted catalytic oxidation (OZCO). The results indicate that Mn modified TiO 2 /AC (i.e. 0.1%Mn/20%TiO 2 /AC) achieved a toluene removal efficiency of nearly 86% with 100% elimination rate of O 3 . With the help of Mn/TiO 2 /AC catalyst, O 3 was catalytically decomposed and transformed into active species of O ( 1 D) and OH, thus enhancing toluene removal. The combination of VUV irradiation with multi-functional catalyst provides a novel and efficient way for the degradation of VOCs., (Copyright © 2018 Elsevier Ltd. All rights reserved.)