Mechanistic Insight into the Effect of Metal Ions on Photogeneration of Reactive Species from Dissolved Organic Matter

摘要

The photogeneration of reactive species (RS) from dissolved organic matter (DOM) exhibits a great impact on the attenuation of pollutants in natural waters. However, the effect of metal ions on the photogeneration of excited triplet-state DOM ((DOM)-D-3*), singlet oxygen (O-1(2)), and hydroxyl radical ((OH)-O-center dot) by effluent organic matter (EfOM), fulvic acid (FA), and humic acid (HA) is poorly understood. Here, we provided the first evidence that the quenching of (DOM)-D-3* was positively correlated with the complexation capacity of metal ions with DOM. Generally, the paramagnetic metal ions (Cr3+, Mn2+, Fe3+, and Cu2+) exhibited higher conditional stability constants (log K-ML) with DOM and stronger inhibition for RS than the others (Mg2+, Ca2+, Al3+, and Zn2+). For DOM of different sources, the metal binding capacity increased in the order of EfOM HA FA and the humic substances were more susceptible to metal ions. The inhibition was attributed to both static and dynamic quenching of (DOM)-D-3* by metal ions. The dynamic quenching rate constants of metal ions for (DOM)-D-3* were estimated as similar to 10(9) M-1 s(-1), which was positively related to the corresponding log K-ML. These findings highlight crucial links between metal-DOM complexation and (DOM)-D-3* quenching and, consequently, the inhibition of RS.