4.8 Article

Generality and diversity on the kinetics, toxicity and DFT studies of sulfate radical-induced transformation of BPA and its analogues

Journal

WATER RESEARCH
Volume 219, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2022.118506

Keywords

Bisphenol analogues; Density functional theory; Steady-state kinetic model; Toxity assessment; Transformation pathway

Funding

  1. National Natural Science Foundation of China [51878422, 42177060]
  2. Science & Technology Bureau of Chengdu [2017-GH02-00010-HZ]
  3. Innovation Spark Project in Sichuan University [2082604401254]
  4. High Performance Computing Cluster System of Changzhou University (HPCCS-CCZU)

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This study examined the chemical oxidation of BPA and its alternatives in a UV-activated persulfate system. The findings revealed similar removal characteristics, degradation mechanisms, and influencing trends of different BPs. The results provide valuable information for assessing the potential environmental risks of using BPA alternatives.
The international campaign to ban bisphenol A (BPA) has resulted in increasing application of BPA substitutes. However, investigations have mainly been confined to the removal of single contaminant from the water, resulting in an inefficient burden. Furthermore, systematic study and synthetical discussion of bisphenol analogues (BPs) kinetics and transformation pathways were largely underemphasized. Chemical oxidation of BPA and four typical alternatives (i.e., bisphenol AF, bisphenol E, bisphenol F and bisphenol S) in a UV-activated persulfate system was examined in this study. The effects of persulfate (PS) dosage, pH and water matrix constituents (i.e., bicarbonate, chloride and natural organic matter) were comprehensively examined using a combination of laboratory experiments and mathematical modeling. According to our findings, the removal characteristics of different BPs employing SO4 center dot(-)-induced removal technology, including degradation mechanisms and influencing trends by water matrix, revealed similarly. The second order-rate constants of SO4 center dot (-) reacting with BPs served as the main variables mediating the variation in degradation kinetics. Frontier molecular orbital theory and density functional theory suggested BPs molecules possessed the same susceptible positions to free radicals. In the UV-activated PS process, transformation pathways included hydroxylation, electron-transfer, substitution, and rearrangement triggered by ortho-cleavage, with certain intermediates exhibiting higher toxicity than the parent chemicals. The findings of this study provided valuable information to estimate potential environmental risks of using BPA alternatives.

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