Exploring the fate of dissolved organic matter at the molecular level in the reactive electrochemical ceramic membrane system using fluorescence spectroscopy and FT-ICR MS

Abstract

This research evaluated the performance of reactive electrochemical ceramic membrane (REM) in treating secondary effluent and investigated the fate of dissolved organic matter (DOM) at the molecular level. The role of adsorption, electrosorption, and oxidation in DOM removal was comprehensively elucidated based on fluorescence spectroscopy and high-resolution mass spectrometry (FT-ICR MS). Among the fluorescence components (C1-C3) in secondary effluent, microbial humic-like C2 showed fewer adsorption on the REM surface without applying an electrical potential. The electrosorption helped an enhanced uptake of all DOM components and transformed them onto the electrode surface. The fluorescence components and all three fractions (hydrophilic, transphilic, and hydrophobic) were rapidly degraded, and finished water with stable DOM was obtained. The leading degradation phenomena were the change of the unsaturated compounds to the aliphatic and transformation of large-sized molecules to medium and small-sized ones. Above 70% of the compounds in the secondary effluent acted as precursors, which were mineralized/degraded and transformed products were found on the REM surface and in the finished water. The compounds containing sulfur (CHOS) were easily and preferably degraded/mineralized, followed by the compounds containing nitrogen (CHON) and CHO. The oxidation of DOM led to the extensive formation of organo-chlorinated compounds, which contributed above 80% in products. Overall, the combination of fluorescence spectroscopy and FT-ICR MS provided unique behavior of DOM in the secondary effluent toward electro-oxidation in the REM system. These findings could help explore the potential of REM for different water matrices to project the possible composition of DOM in the finished water.