The photoactivity of complexation of DOM and copper in aquatic system: Implication on the photodegradation of TBBPA

The photoactivity of dissolved organic matter (DOM) has a great impact on the photodegradation of organic pollutants in natural waters. In this study, the photodegradation of TBBPA was investigated under simulated sunlight irradiation in the presence of copper ion (Cu2+), dissolved organic matter (DOM) and Cu-DOM complexation (Cu-DOM) to illustrate the effect of Cu2+ on photoactivity of DOM. The rate of photodegradation of TBBPA in the presence of Cu-DOM complex was 3.2 times higher than that in pure water. The effects of Cu2+, DOM and Cu-DOM on the photodegradation of TBBPA were highly pH dependent and hydroxyl radical(center dot OH) responded for the acceleration ef-fect. Spectral and radical experiments indicated that Cu2+ had high affinity to fluorescence components of DOM, and acted as both the cation bridge and electron shuttle, resulting the aggregation of DOM and increasing of steady-state concentration of center dot OH (center dot OHss). Simultaneously, Cu2+ also inhibited intramolecular energy transfer leading to the de-crease of steady-state concentration singlet oxygen (1O2ss) and triplet of DOM (3DOM*ss). The interaction between Cu2+ and DOM followed the order of conjugated carbonyl C_O, COO- or C\\O stretching in phenolic groups and carbohydrate or alcoholic C\\O groups. With these results, a comprehensive investigation on the photodegradation of TBBPA in the presence of Cu-DOM was conducted, and the effect of Cu2+ on the photoactivity of DOM was illus-trated. These findings helped to understanding the potential mechanism of interaction among metal cation, DOM and organic pollutants in sunlit surface water, especially for the DOM-induced photodegradation of organic pollutants.

Automated summary

The effect of copper ion (Cu2+) on the photoactivity of dissolved organic matter (DOM) was investigated in the photodegradation of TBBPA under simulated sunlight irradiation. The presence of Cu-DOM complex resulted in a 3.2 times higher rate of TBBPA photodegradation compared to pure water. The interaction between Cu2+ and DOM influenced the aggregation of DOM, the concentration of hydroxyl radical (center dot OH), as well as the concentration of singlet oxygen (1O2ss) and triplet of DOM (3DOM*ss).