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Sulphate radical oxidation of benzophenone: kinetics, mechanisms and influence of water matrix anions

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Version 2 2020-04-28, 17:30
Version 1 2020-04-15, 09:34
journal contribution
posted on 2020-04-28, 17:30 authored by Jie Ma, Yuan Feng, Xin Yang, Yongxin Wu, Shuo Wang, Congchao Zhang, Quan Shi

Benzophenone (BP) is an emerging contaminant that is widely distributed in soil, groundwater, sediment and surface water. In this study, the degradation kinetics, mechanisms, and influence of anions on thermally activated persulphate (TAP) oxidation of BP were systematically investigated. BP degradation was promoted by elevated temperature. The BP degradation data fitted well to the Arrhenius equation with calculated activation energy of 122.8 kJ/mol. BP degradation was also promoted by alkaline pH and high persulphate concentrations. Radical scavenging experiments suggested that both SO4•− and HO were involved in BP oxidation. Ultra-high-performance liquid chromatography coupled to Orbitrap mass spectrometry (UHPLC-Orbitrap-MS) identified six degradation intermediates. Based on these results, two possible reaction pathways were proposed. Water matrix anions had complex impacts on BP degradation by TAP. Cl had dual effects on the reaction: low concentration promoted it while high concentration inhibited it. Br strongly suppressed the reaction. SO42− and NO3 did not affect the reaction. Overall, this study shows that thermally activated persulphate can effectively remove BP and water matrix anions greatly influence the reaction.

Funding

This work was supported by National Natural Science Foundation of China [grant number 21878332]; Beijing NOVA Program [grant number Z181100006218088]; PetroChina Innovation Foundation [grant number 2018D-5007-0607]; Science Foundation of China University of Petroleum-Beijing [grant number 2462018BJC003, 2462020XKJS04] and Open Project Program of State Key Laboratory of Petroleum Pollution Control [grant number PPC2019019].

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