Metal–organic frameworks (MOFs) have garnered significant attention for water purification in recent years. In particular, UiO-66 (a member of the UiO-MOF family, developed at the University of Oslo) has emerged as a promising water purification material. UiO-66 exhibits excellent adsorption through electrostatic interaction, π–π stacking and Lewis acid–base coordination mechanisms. The photocatalytic degradation property was enhanced through metal doping, composite with semiconductor materials, defect engineering, etc., and the removal efficiency of pollutants was significantly improved. This review systematically describes the structure of UiO-66 and the synthesis methods of UiO-66, including solvothermal, microwave-assisted, mechanized and electrochemical methods, as well as the application of UiO-66 in the adsorption and photocatalytic degradation of various pollutants.

Water pollution, driven by industrial wastewater, agricultural runoff, and domestic sewage, introduces organic pollutants (e.g., dyes and antibiotics) and heavy metal ions (e.g., Pb²⁺ and Cr(VI)), threatening ecosystems and human health. Although traditional water treatment technologies have now matured, they still have some deficiencies in terms of specific pollutants. Metal–organic frameworks (MOFs), particularly zeolite imidazole frame-67 (ZIF-67)—a cobalt-based MOF with high surface area, tunable pores, and robust chemical stability—show excellent adsorption capacity for pollutants and have emerged as promising candidates for water treatment due to their efficacy in adsorption, catalysis, and photocatalysis. This review examines ZIF-67’s synthesis, functionalization strategies, and applications in removing organic pollutants and heavy metals. It explores its mechanisms, composite designs, and recyclability, while highlighting challenges and future directions for developing efficient, sustainable water treatment technologies.

ZIF-67 nanoparticles were synthesized by a simple method at room temperature and used to remove chlortetracycline hydrochloride (CTC) and doxycycline hydrochloride (DOX) from water. ZIF-67 was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), fourier transform infrared spectroscopy (FT-IR), Brunauer-Emmett-Teller (BET) surface area, X-ray photoelectron spectroscopy (XPS), thermogravimetry (TGA) and zeta potential analyzer. The morphology and chemical composition of the synthesized ZIF-67 were characterized. The effects of key parameters such as pH, dosage, temperature, contact time, different initial concentrations and coexisting ions on the adsorption behavior were systematically studied. The results of batch adsorption experiments indicate that the adsorption process conforms to the pseudo-second-order kinetic model and Sips model. At 303K, the removal rates of CTC and DOX at 150 mg/L reached 99.16 % and 97.61 %, and the maximum adsorption capacity of CTC and DOX reached 1411.68 and 1073.28 mg/g, respectively. At the same time, ZIF-67 has excellent stability and reusability. Most importantly, the possible adsorption mechanism is proposed by exploring the changes of SEM, TEM, BET and FT-IR characterization results before and after the reaction, which mainly includes pore filling, electrostatic interaction and π-π interaction. The prepared ZIF-67 has a large specific surface area (1495.967 m² g^-1), achieves a high removal rate within a short time frame, and maintains a high removal rate across a wide pH range. These characteristics make ZIF-67 a potentially promising adsorbent for removing antibiotics from aqueous solutions.

In this study, an Fe₃O₄/Bi₂MoO₆/g-C₃N₄ magnetic composite photocatalyst was synthesized for the visible-light-driven photocatalytic degradation of sulfonamide antibiotics, specifically sulfamerazine (SM1). Characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), photoluminescence spectroscopy (PL), UV-vis diffuse reflectance spectra (UV-vis), and the use of a vibrating sample magnetometer (VSM), were employed to analyze the fabricated samples. The composite exhibited efficient visible-light absorption and charge separation, with optimal photocatalytic performance achieved at a pH value of 9.0. The study reveals the importance of solution pH in the degradation process and the potential applicability of the composite for efficient magnetic separation and recycling in photocatalytic processes. The Fe₃O₄/Bi₂MoO₆/g-C₃N₄ magnetic composite photocatalyst demonstrated exceptional stability and recyclability, maintaining a high degradation efficiency of over 87% after five consecutive cycles. An XRD analysis conducted after the cycling tests confirmed that the composite’s composition and chemical structure remained unchanged, further supporting its chemical stability. This investigation offers valuable insights into the photocatalytic degradation of sulfonamide antibiotics using magnetic composite photocatalysts and highlights the potential of the Fe₃O₄/Bi₂MoO₆/g-C₃N₄ composite for practical applications in environmental remediation.

The extensive use of oxytetracycline (OTC) poses significant threats to aquatic ecosystems, necessitating efficient removal strategies. While photocatalytic technology is a promising approach, single catalysts, like UiO-66-NH₂ and Bi₂MoO₆, suffer from rapid photogenerated carrier recombination and narrow light absorption. To address this, a Z-scheme heterojunction photocatalyst, Bi₂MoO₆/UiO-66-NH₂, was synthesized via a solvothermal method to enhance OTC degradation. Characterization results showed that the composite expanded visible-light absorption and improved electron-hole separation. Under simulated sunlight, the optimized composite (BUN80) achieved an OTC removal efficiency of 87.68% within 120 min under optimized conditions. The catalyst retained photocatalytic activity over five consecutive cycles, although a decrease in removal efficiency was observed. Radical trapping experiments indicated that h⁺ and •O₂⁻ were the main reactive species, and a proposed Z-scheme charge transfer pathway was suggested based on band structure analysis and photoelectrochemical results. LC-MS analysis identified 17 intermediate products, and ECOSAR-based toxicity prediction suggested a decreasing trend in aquatic toxicity during the degradation process. These findings indicate that Bi₂MoO₆/UiO-66-NH₂ is a promising photocatalyst for OTC degradation in water.