Abstract

In this study, a nano-sheet C3N4-WO3 composite (nsCW21) was applied as a visible-light active photocatalyst to degrade natural organic matter (NOM). The nsCW21 photocatalyst exhibited a higher removal efficiency for NOM than the bare host and other composite counterparts due to the effective separation of the charge carriers in the Z-scheme pathway. The addition of H2O2 resulted in the enhanced photocatalytic performance via the generation of hydroxyl radicals from the catalyst with an NOM removal rate of up to 71% for 5 h. The catalyst showed a considerable stability, which held a good NOM degradation efficiency during five cycle runs. The complex NOM removal behavior was unraveled by using a fluorescence excitation emission matrix-parallel factor analysis and a two-dimensional correlation spectroscopy (2D-COS) combined with Fourier-transform infrared spectroscopy (FT-IR). The large sized and the terrestrial humic-like component exhibited a high adsorption tendency toward the catalyst and was degraded primarily by h+, while a typical humic-like component, which is mainly removed by .OH, displayed a high degradation rate constant (k = 0.159 h−1). The 2D-COS revealed the sequence of the preferable removal among the different NOM functional groups in the nsCW21 system with H2O2 addition, which occurred in the order of open ring reaction > oxygenated functional groups > the transformation into aliphatic compounds/inorganic moieties. Meanwhile, the hybrid system that employed ultrafiltration as a post-treatment demonstrated synergetic effects on the improved effectiveness for NOM removal in the overall system, which was a total of 91%, of the residuals from the precedent photocatalysis as well as alleviating the membrane fouling.

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