Water is life, and clean-water demand is increasing daily as a result of rapid population growth and industrial evolution. Nevertheless, due to the inadequate supply and availability of new water sources, there is a need for effective, sustainable removal of contaminants for wastewater reuse. Several treatment approaches that include chemical, physical, and biological methods have been thoroughly tested, with biological treatment being regarded as the most cost-effective and environmentally friendly method. However, the presence of heavy metals and complicated chemicals that are nonbiodegradable limits the use of this cost-effective approach. In this paper, we review the sustainable application of a cheap, water-stable metal-organic framework, the zeolitic imidazolate framework (ZIF-8), with an easier synthesis approach for heavy-metal removal in aqueous solutions. In this review, we discuss the removal efficiency in terms of adsorption capacity, describe the underlying mechanism behind the adsorption capacity of ZIF-8, present a sustainable synthesis approach, and make vital suggestions to aid in the future application of ZIF-8 for the removal of heavy metals.

In this study, a series of g-C3N4 nanosheets were prepared by various thermal oxidative etching times from four different precursors (urea, melamine, dicyandiamide and thiourea). The physicochemical properties of these g-C3N4 nanosheets were analyzed in detail using scanning electron microscopy (SEM), X-ray diffraction (XRD), photoluminescence emission spectra, Fourier transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET) analysis and ultraviolet-visible diffuse reflectance. The results revealed that the g-C3N4 nanosheets obtained a thinner layer thickness and larger specific surface area, with an extension of thermal oxidative etching time. Meanwhile, sulfamethazine (SMZ), one of the most widely used sulfonamides, was used to evaluate the photocatalyst activity of the g-C3N4 nanosheets prepared in this study. Compared to other g-C3N4 nanosheets, urea-derived g-C3N4 nanosheets under 330 min thermal oxidative etching showed the highest photocatalytic activity for SMZ under visible light. In conclusion, our study provides detailed insights into the synthesis and characterization of g-C3N4 nanosheets prepared from various precursors and highlights the importance of thermal oxidative etching time in determining the photocatalytic activity of these materials.

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.

In this study, a series of Bi2MoO6/g-C3N4 composites were prepared through a wet-impregnation method, and their photocatalytic properties were investigated for the degradation of sulfadiazine (SDZ) under visible light irradiation. Physical and chemical characterizations were carried out using X-ray diffraction (XRD), scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FT-IR), photoluminescence spectroscopy (PL), UV-vis diffuse reflectance spectra (UV-vis), and electrochemical impedance spectra (EIS). Compared to pure g-C3N4, the introduction of Bi2MoO6 significantly enhanced the visible light responsive photocatalytic activity, with the 1:32 Bi2MoO6/g-C3N4 composite exhibiting the highest photodegradation efficiency towards SDZ under visible light irradiation with a photocatalytic efficiency of 93.88% after 120 min of visible light irradiation. The improved photocatalytic activity can be attributed to the formation of a heterojunction between Bi2MoO6 and g-C3N4, which promotes the transfer of photogenerated electron-hole pairs, thereby elevating its photocatalytic activity. The results suggest that Bi2MoO6/g-C3N4 composites have potential application for the degradation of sulfonamides in aquatic environments.

Highly efficient visible-light-driven heterogeneous photocatalyst Ag3PO4/g-C3N4 with different weight ratios from Ag3PO4 to g-C3N4 were synthesized by a facile in situ hydrothermal method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectrometry (FTIR), photoluminescence spectra (PL), UV–vis diffuse reflectance spectra (UV-Vis), and electrochemical impedance spectra (EIS). Under visible light irradiation, Ag3PO4/g-C3N4 showed very excellent photocatalytic activity for sulfapyridine (SP) which is one of the widely used sulfonamide antibiotics. When the ratio from Ag3PO4 to g-C3N4 was 1:2, the degradation rate of SP at 120 min was found to be 94.1%, which was superior to that of pure Ag3PO4 and pure g-C3N4. Based on the experimental results, the possible enhanced photocatalytic mechanism of Ag3PO4/g-C3N4 was proposed.