This paper investigated ultraviolet
A light-emitting diode (UVA-LED)
irradiation to activate Fe(VI) for the degradation of micropollutants
(e.g., sulfamethoxazole (SMX), enrofloxacin, and trimethoprim). UVA-LED/Fe(VI)
could significantly promote the degradation of micropollutants, with
rates that were 2.6–7.2-fold faster than for Fe(VI) alone.
Comparatively, UVA-LED alone hardly degraded selected micropollutants.
The degradation performance was further evaluated in SMX degradation
via different wavelengths (365–405 nm), light intensity, and
pH. Increased wavelengths led to linearly decreased SMX degradation
rates because Fe(VI) has a lower molar absorption coefficient at higher
wavelengths. Higher light intensity caused faster SMX degradation,
owing to the enhanced level of reactive species by stronger photolysis
of Fe(VI). Significantly, SMX degradation was gradually suppressed
from pH 7.0 to 9.0 due to the changing speciation of Fe(VI). Scavenging
and probing experiments for identifying oxidative species indicated
that high-valent iron species (Fe(V)/Fe(IV)) were responsible for
the enhanced degradation. A kinetic model involving target compound
(TC) degradation by Fe(VI), Fe(V), and Fe(IV) was employed to fit
the TC degradation kinetics by UVA-LED/Fe(VI). The fitted results
revealed that Fe(IV) and Fe(V) primarily contributed to TC degradation
in this system. In addition, transformation products of SMX degradation
by Fe(VI) and UVA-LED/Fe(VI) were identified and the possible pathways
included hydroxylation, self-coupling, bond cleavage, and oxidation
reactions. Removal of SMX in real water also showed remarkable promotion
by UVA-LED/Fe(VI). Overall, these findings could shed light on the
understanding and application of UVA-LED/Fe(VI) for eliminating micropollutants
in water treatments.