Photocatalytic degradation
is a sustainable technique for reducing
the environmental hazards created by the overuse of antibiotics in
the food and pharmaceutical industries. Herein, a layer of MoS2/g-C3N4 nanocomposite is introduced
to zirconium oxide (ZrO2) nanoparticles to form a “particle-embedded-layered”
structure. Thus, a narrow band gap (2.8 eV) starts developing, deliberated
as a core photodegradation component. Under optimization, a high photocatalytic
activity of 20 mg/L TC at pH 3 with ZrO2@MoS2/g-C3N4 nanocomposite was achieved with 94.8%
photocatalytic degradation in 90 min. A photocatalytic degradation
rate constant of 0.0230 min–1 is determined, which
is 2.3 times greater than the rate constant for bare ZrO2 NPs. The superior photocatalytic activity of ZrO2@MoS2/g-C3N4 is due to the dual charge-transfer
channel between the MoS2/g-C3N4 and
ZrO2 nanoparticles, which promotes the formation of photogenerated
e–/h+ pairs. Charge recombination produces
many free electron–hole pairs, which aid photocatalyst reactions
by producing superoxide and hydroxyl radicals via electron–hole
pair generation. The possible mechanistic routes for TC were investigated
in-depth, as pointed out by the liquid chromatography–mass
spectrometry (LC–MS) investigation. Overall, this work shows
that photocatalysis is a feasible sorbent approach for environmental
antibiotic wastewater treatment.