Abstract

Increase in the concentration of residual antibiotics in water bodies, including drinking water, has led to developing strategies for their remediation. Here we report a very efficient method of photocatalytic degradation of tetracycline (TC) and ciprofloxacin (CIP) antibiotics in aqueous medium using Z-scheme heterojunction based 0.10SnS2/Bi2WO6 solar photocatalyst. The photocatalyst synthesized by hydrothermal route is thoroughly characterized in terms of its structural, compositional, morphological, and optical properties. About 97% of tetracycline and 93% of ciprofloxacin is degraded in 90 min of sunlight exposure at a photocatalytic rate of 0.027 min−1 and 0.024 min−1, respectively. The total organic carbon estimation of the post-degradation reaction medium corresponded to 80.1% (TC) and 71.1% (CIP) mineralization. The photocatalytic degradation of TC and CIP is attributed to the in-situ generation of reactive oxygen species (ROS), e.g., superoxide radicals, hydroxide radicals, confirmed from ROS scavenging studies. ROS generation is favored by construction of Z-scheme heterojunction, and charge carrier mobility in the photocatalyst. The degradation mechanism has been discussed by analyzing the degradation products via ultra-performance liquid chromatography coupled to quadrupole-Time-of-Flight based mass spectrometry (UPLC-Q-Tof-MS).

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