The oxygen reduction reaction (ORR)
was an unavoidable
side reaction
in the electro-activating persulfate (PS) process, especially on the
ORR-active carbon materials, which has usually been ignored in previous
reports. In this work, the O2/N2-involved electro-activation
of the PS system was constructed to confirm the role of side-reactive
ORR on oxidized carbon black (OCB) for sulfamethoxazole (SMX) degradation.
With O2 involvement, 820.8 μM •OH was produced by PDS electro-activation, over 7 times more than
115.8 μM under N2 aeration, leading to a high SMX
removal of 90.6% (only 67.8% under N2 aeration). Such a
huge difference in •OH yield and SMX removal performance
was mainly attributed to side-reactive 2e– ORR,
in which as-generated H2O2 was electro-activated
to produce abundant •OH and form an advanced homogeneous •OH/SO4
•– oxidation
system via mutual transformation with gradual acidification. Meanwhile,
the introduction of oxygen functional groups and defects on the surface
of carbon black calcined at 600 °C (CB600) also contributed to
the improvement of SMX removal performance, attributing to their enhancing
effects on SMX electro-adsorption, PDS electro-activation, and O2 electro-reduction. Thus, side-reactive oxygen reduction played
the spontaneous and synergistic oxidation roles in the O2-involved electro-activating PS process, helping to design highly
effective advanced oxidation systems in the future.