Hybrid clay composites were prepared from Kaolinite clay and Carica papaya seeds via modification with chitosan, Alum, NaOH, and ZnCl2 in different ratios, using solvothermal and surface modification techniques. Several composite adsorbents were prepared, and the most efficient of them for the removal of gram negative enteric bacteria was the hybrid clay composite that was surface-modified with chitosan, Ch-nHYCA 1:5 (Chitosan: nHYCA = 1:5). This composite adsorbent had a maximum adsorption removal value of 4.07 × 106 cfu/mL for V. cholerae after 120 min, 1.95 × 106 cfu/mL for E. coli after ∼180 min and 3.25 × 106 cfu/mL for S. typhi after 270 min. The Brouers-Sotolongo model was found to better predict the maximum adsorption capacity (qmax ) of Ch-nHYCA1:5 composite adsorbent for the removal of E. coli with a qmax of 103.07 mg/g (7.93 × 107 cfu/mL) and V. cholerae with a qmax of 154.18 mg/g (1.19 × 108 cfu/mL) while the Sips model best described S. typhi adsorption by Ch-nHYCA 1:5 composite with an estimated qmax of 83.65 mg/g (6.43 × 107 cfu/mL). These efficiencies do far exceed the alert/action levels of ca. 500 cfu/mL in drinking water for these bacteria. The simplicity of the composite preparation process and the availability of raw materials used for its preparation underscore the potential of this low-cost chitosan-modified composite adsorbent (Ch-nHYCA 1:5 ) for water treatment.

The incessant release of pharmaceuticals into the aquatic environment continues to be a subject of increasing concern. This is because of the growing demand for potable water sources and the potential health hazards which these pollutants pose to aquatic animals and humans. The inability of conventional water treatment systems to remove these compounds creates the need for new treatment systems in order to deal with these class of compounds. This review focuses on advanced oxidation processes that employ graphene-based composites as catalysts for the degradation of pharmaceuticals. These composites have been identified to possess enhanced catalytic activity due to increased surface area and reduced charge carrier recombination. The techniques employed in synthesizing these composites have been explored and five different advanced oxidation processes—direct degradation process, chemical oxidation process, photocatalysis, electrocatalyis processes and sonocatalytic/sono-photocatalytic processes—have been studied in terms of their enhanced catalytic activity. Finally, a comparative analysis of the processes that employ graphene-based composites was done in terms of process efficiency, reaction rate, mineralization efficiency and time required to achieve 90% degradation.

The release of common medications and illegal drugs into the environment could be potentially harmful to the ecosystem and hamper the behavior and growth of plants and animals. These pollutants gain access to water through sewage and factory discharges and have been found to exceed safety limits in water bodies. Therefore, there is an urgent need for improved wastewater purification systems. In this study, semiconductor-based heterojunction photocatalyst CuInS₂/CeO₂, synthesized through a facile solvothermal process, was explored for the photocatalytic degradation of ciprofloxacin, commonly used antibiotics. Studies on the electronic properties of the heterojunction revealed interfacial characteristics that were suitable for enhanced charge carrier separation and transport and a potential S-scheme charge transfer mechanism. The heterojunction achieved ∼90% efficiency for the degradation of CIP compared to 60% and 12% reported for CeO₂ and CuInS₂, respectively. This shows an improvement in the activity, which results from the improved charge carrier properties of the heterojunction. Further investigation of the charge transfer mechanism through radical scavenging experiments identified ^•OH, O2^•-, and h⁺ as active species contributing to the catalyst's efficacy. Based on X-ray photoelectron spectroscopy analysis, a proposed S-scheme charge transfer mechanism was suggested for the CuInS₂/CeO₂ heterojunction. The findings indicate the potential of the CuInS₂/CeO₂ heterojunction as a promising photocatalyst for treating waste effluents from the pharmaceutical industry.

ZnO and TiO₂ nanoparticles were prepared through a plant-extract mediated hydrothermal synthesis. X-ray diffraction (XRD) study confirmed the crystalline nature and the phase characteristic of the obtained nanoparticles. X-ray diffraction profile analysis models such as Williamson–Hall analysis, size-strain plot and Rietveld analysis were further used in evaluating the microstructural parameters of the obtained materials. The calculated particle size for all the models was in great agreement, with values in the range of 55.46–87.6 nm recorded for ZnO, while for TiO₂, the crystallite size was in the range of 33.82–41.9 nm. The calculated crystal microstrain varied based on the model, while the stress in the ZnO and TiO₂ nanoparticles was evaluated at 3.8 and 13.7 MPa, respectively. Furthermore, TiO₂ nanoparticles had a higher energy density of 8.96 × 10^–8 KJ m⁻³ compared to 7.12 × 10^–8 KJ m⁻³ obtained for ZnO.