The activation of peroxydisulfate (PDS) by organic compounds
has
attracted increasing attention. However, some inherent drawbacks including
quick activator decomposition and poor anti-interference capacity
limited the application of organic compound-activated PDS. It was
interestingly found that 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonate)
(ABTS) could act as both activator and electron shuttle for PDS activation
to enhance diclofenac (DCF) degradation over a pH range of 2.0–11.0.
Multiple reactive species of ABTS•+, •OH, and SO4
•– were generated
in the PDS/ABTS system, while only ABTS•+ and •OH directly contributed to DCF degradation. ABTS•+, generated via the reactions of ABTS with PDS, SO4
•–, and •OH, was
the dominant reactive species of DCF degradation. No significant decomposition
of ABTS was observed in the PDS/ABTS system, and ABTS acted as both
activator and electron shuttle. Four possible degradation pathways
of DCF were proposed, and the toxicity of DCF decreased after treatment
with the PDS/ABTS system. The PDS/ABTS system had good anti-interference
capacity to common natural water constituents. Additionally, ABTS
was encapsulated into cellulose to obtain ABTS@Ce beads, and the PDS/ABTS@Ce
system possessed excellent performance on DCF degradation. This study
proposes a new perspective to reconsider the mechanism of activating
PDS with organic compounds and highlights the considerable contribution
of organic radicals on contaminant removal.