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Coating TiO2 with MIL-101(Fe) to decarboxylate D-Glu and D-MeAsp of microcystin-LR from HA-rich water: Diminishing the inhibitory effect of humic acids
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•MIL-101(Fe)/TiO2 (M/P) was constructed using surface-coated FeOOH as the precursor.•MC-LR could be efficiently removed by M/P from HA-rich Water.•HA exerted non-inhibitory effect on MC-LR removal by M/P.•The key toxicity functional groups of MC-LR were destroyed by M/P with or without HA.
Humic acids (HA) released during algal bloom poses a key challenge for efficient photocatalytic degradation of Microcystin-LR (MC-LR) due to their scavenging function on active species. Herein, MIL-101(Fe)/TiO2-P25 (M/P) was constructed to diminish the inhibitory effect of HA on the photocatalytic degradation of MC-LR. Results showed that MC-LR could be efficiently removed assigning to the photogenerated holes (h+) and superoxide radical (O2•−) oxidation under visible light irradiation, where the carboxy groups of D-glutamic acid (Glu) and methyl-D-aspartic acid (MeAsp), and Adda side chain related to MC-LR biotoxicity were selectively destroyed to achieve MC-LR detoxication. More importantly, HA exerted non-inhibitory effect on MC-LR removal by M/P. The counteracting mechanisms were studied. Firstly, the location of TiO2 in the pore structure of MIL-101(Fe) could occupy the adsorption sites of HA, and decrease the HA adsorption on M/P. Furthermore, XPS analyses suggested the coordination of unsaturated Fe metal sites on the surface of M/P hybrids complexed with –OH and –COOH of HA, which could accelerate the electron transfer and reduce hole consumption. Thus, the inhibitory effect of HA was alleviated during photocatalytic MC-LR treatment. This work offers a possible way to remove MC-LR in an abundant HA matrix water system efficiently.