Quantification of the electron donating capacity and UV absorbance of dissolved organic matter during ozonation of secondary wastewater effluent by an assay and an automated analyzer

摘要

Ozonation of secondary wastewater treatment plant effluent for the abatement of organic micropollutants requires an accurate process control, which can be based on monitoring ozone-induced changes in dissolved organic matter (DOM). This study presents a novel automated analytical system for monitoring changes in the electron donating capacity (EDC) and UV absorbance of DOM during ozonation. In a first step, a quantitative photometric EDC assay was developed based on electron-transfer reactions from phenolic moieties in DOM to an added chemical oxidant, the radical cation of 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonate) (ABTS(center dot+)). The assay is highly sensitive (limit of quantification similar to 0.5 mg(DOC.)L(-1)) and EDC values of model DOM isolates determined by this assay were in good agreement with values determined previously by mediated electrochemical oxidation (slope = 1.01 +/- 0.07, R-2 = 0.98). In a second step, the photometric EDC measurement method was transferred onto an automated fluidic system coupled to a photometer (EDC analyzer). The EDC analyzer was then used to monitor changes in EDC and UV absorbance of secondary wastewater effluent treated with ozone. While both parameters exhibited a dose-dependent decrease, a more pronounced decrease in EDC as compared to UV absorbance was observed at specific ozone doses up to 0.4 mg(O3)center dot g(DOC)(-1). The concentration of 17 alpha-ethinylestradiol, a phenolic micropollutant with a high ozone reactivity, decreased proportionally to the EDC decrease. In contrast, abatement of less ozone-reactive micropollutants and bromate formation started only after a pronounced initial decrease in EDC. The on-line EDC analyzer presented herein will enable a comprehensive assessment of the combination of EDC and UV absorbance as control parameters for full-scale ozonation. (C) 2020 The Authors. Published by Elsevier Ltd.