Recent advances and future trends in metal oxide photocatalysts for removal of pharmaceutical pollutants from wastewater: a comprehensive review.

The rapid and widespread increase in pharmaceutical micropollutants (PMPs) poses a significant and immediate threat to ecosystems and human health globally. With the demand for clean water becoming increasingly critical, particularly amid escalating global water scarcity challenges, there is an urgent need for innovative approaches. Among the potential solutions, metal oxide photocatalysts such as titanium dioxide-based (TiB) and zinc oxide-based (ZnB) have garnered attention due to their cost-effectiveness, efficient photodegradation capabilities, and inherent stability. This comprehensive review explores recent advancements in the application of TiB and ZnB for the removal of PMPs from wastewater. It examines the multifaceted impacts of PMPs on environmental and public health, evaluates various techniques for their removal, and assesses design strategies aimed at maximizing the photocatalytic efficiency of TiB and ZnB. The mechanisms responsible for the photocatalytic degradation of pharmaceutical micropollutants using TiB and ZnB photocatalysts are comprehensively detailed. Finally, the review outlines the prospects and challenges associated with the use of TiB and ZnB photocatalysts for the removal of PMPs from wastewater. It emphasizes their potential to effectively mitigate PMP contaminants and make substantial contributions to sustainable water management practices in the face of escalating environmental and public health concerns.

Oxidation of antibiotic micropollutants in various water resources through integration of Bi2WO6 and g-C3N4.

Recently, the hazardous effects of antibiotic micropollutants on the environment and human health have become a major concern. To address this challenge, semiconductor-based photocatalysis has emerged as a promising solution for environmental remediation. Our study has developed Bi2WO6/g-C3N4 (BWCN) photocatalyst with unique characteristics such as reactive surface sites, enhanced charge transfer efficiency, and accelerated separation of photogenerated electron-hole pairs. BWCN was utilized for the oxidation of tetracycline antibiotic (TCA) in different water sources. It displayed remarkable TCA removal efficiencies in the following order: surface water (99.8%) > sewage water (88.2%) > hospital water (80.7%). Further, reusability tests demonstrated sustained performance of BWCN after three cycles with removal efficiencies of 87.3, 71.2 and 65.9% in surface water, sewage, and hospital water, respectively. A proposed photocatalytic mechanism was delineated, focusing on the interaction between reactive radicals and TCA molecules. Besides, the transformation products generated during the photodegradation of TCA were determined, along with the discussion on the potential risk assessment of antibiotic pollutants. This study introduces an approach for utilizing BWCN photocatalyst, with promising applications in the treatment of TCA from various wastewater sources.

Photodegradation of ciprofloxacin antibiotic in water by using ZnO-doped g-C3N4 photocatalyst.

Ciprofloxacin antibiotic (CIP) is one of the antibiotics with the highest rate of antibiotic resistance, if used and managed improperly, can have a negative impact on the ecosystem. In this research, ZnO modified g-C3N4 photocatalyst was prepared and applied for the decomposition of CIP antibiotic compounds in water. The removal performance of CIP by using ZnO/g-C3N4 reached 93.8% under pH 8.0 and an increasing amount of catalyst could improve the degradation performance of the pollutant. The modified ZnO/g-C3N4 completely oxidized CIP at a low concentration of 1 mg L-1 and the CIP removal efficiency slightly decreases (around 13%) at a high level of pollutant (20 mg L-1). The degradation rate of CIP by doped sample ZnO/g-C3N4 was 4.9 times faster than that of undoped g-C3N4. The doped catalyst ZnO/g-C3N4 also displayed high reusability for decomposition of CIP with 89.8% efficiency remaining after 3 cycles. The radical species including ·OH, ·O2- and h+ are important in the CIP degradation process. In addition, the proposed mechanism for CIP degradation by visible light-assisted ZnO/g-C3N4 was claimed.