Aquatic photochemistry of Cu(II) in the presence of As(III): Mechanistic insights from Cu(III) production and As(III) oxidation under neutral pH conditions

Surface complexation between arsenite (As(III)) and colloidal metal hydroxides plays an important role not only in the immobilization and oxidation of As(III) but also in the cycle of the metal and the fate of their ligands. However, the photochemical processes between Cu(II) and As(III) are not sufficiently understood. In this work, the photooxidation of As(III) in the presence of Cu(II) under neutral pH conditions was investigated in water containing 200 mu M Cu(II) and 5 mu M As(III) under simulated solar irradiation consisting of UVB light. The results confirmed the complexation between As(III) and Cu(II) hydroxides, and the photooxidation of As(III) is attrib-uted to the ligand-to-metal charge transfer (LMCT) process and Cu(III) oxidation. The light-induced LMCT process results in simultaneous As(III) oxidation and Cu(II) reduction, then produced Cu(I) undergoes autoox-idation with O2 to produce O2 center dot- and H2O2, and further the Cu(I)-Fenton reaction produces Cu(III) that can oxidize As(III) efficiently (kCu(III)+As(III) = 1.02 x 109 M-1 s-1). The contributions from each pathway (rho rCu(II)-As(III)+hv = 0.62, rho rCu(III)+As(III) = 0.38) were obtained using kinetic analysis and simulation. Sunlight experiments showed that the pH range of As(III) oxidation could be extended to weak acidic conditions in downstream water from acid mine drainage (AMD). This work helps to understand the environmental chemistry of Cu(II) and As(III) regarding their interaction and photo-induced redox reactions.

Automated summary

The photooxidation process of As(III) in the presence of Cu(II) under neutral pH conditions was investigated. The study confirmed that the photooxidation is attributed to the ligand-to-metal charge transfer process and Cu(III) oxidation. The findings help understand the environmental chemistry of Cu(II) and As(III) and their interaction in photo-induced redox reactions.