Nanocomposites of UiO-66 and graphene oxide (UiO-66_GO) were prepared with different GO contents by a one-step hydrothermal method, and their photocatalytic activities for the degradation of carbamazepine (CBZ) were investigated under ranges of GO loading, catalyst dose, initial pollutant concentration, and solution pH. The UiO-66_GO nanocomposites showed photocatalytic rate constant up to 0.0136 min⁻¹ for CBZ degradation and its high overall removal efficiency (>90%) in 2 h. The photocatalytic rate constant over the UiO-66_GO nanocomposite was about 2.8 and 1.7 times higher than those over pristine GO and UiO-66, respectively. The enhancement of photocatalytic activity by GO was attributed to increased surface area and porosity, improved light absorption, and narrowed band gap. The composite also showed substantial recyclability and stability over five consecutive cycles of photocatalytic degradation. The experimental results indicated that O₂^●− and OH^● are the responsible radicals for photocatalytic degradation, which helped us propose a photocatalytic mechanism for the enhanced CBZ photodegradation. This work provides a reference for the development of GO-based composite photocatalysts and expands the application of UiO-66 as a photocatalyst for the degradation of persistent micropollutants in water.

This work presents the development of titanium dioxide (TiO₂) film immobilized on circular glass sheets for photocatalytic degradation of caffeine under ultraviolet C (UVC) irradiation. TiO₂ was synthesized through the ultrasonic-assisted sol–gel method and immobilized on circular glass sheets by the doctor blade technique. Polyvinylpyrrolidone (PVP) was used to mix with the TiO₂ precursor solution to enhance film adhesion on the glass surface. TiO₂ film was mainly composed of anatase phase with a small amount of rutile phase. Caffeine removal was found to increase with increasing irradiation time. Caffeine (20 mg/L) in the synthetic wastewater could not be detected after 3 h of UVC irradiation. The reaction rate of caffeine degradation followed the pseudo-first-order model. The concentrated caffeine solutions required a longer irradiation time for degradation. The used TiO₂-coated glass sheets could be easily separated from the treated wastewater and reusable. The caffeine removal efficiency of TiO₂-coated glass sheets in each cycle maintained a high level (~100%) during fifteen consecutive cycles.