Ciprofloxacin (CIP) is a commonly used antibiotic, however, once in the environment, it is highly toxic with a poor biodegradability. Given these attributes, an effective strategy for the removal of CIP is urgently needed for the protection of water resources. Herein, a novel copper metal-organic framework (Cu_xO/MOF) multifunctional material has been produced, in this work, by the calcination of Cu-MOF urea at 300 °C, in the presence of a 5% H₂ atmosphere. The morphological, structural, and thermal properties of the prepared Cu_xO/MOF were determined through various techniques, and its photocatalytic behavior was investigated for the degradation of CIP under visible-light irradiation. The prepared Cu_xO/MOF bifunctional material is presented as a graphitic carbon-layered structure with a particle size of 9.2 ± 2.1 nm. The existence of CuO-Cu₂O-C, which was found on the Cu_xO/MOF surface, enhanced the adsorption efficiency and increased the photosensitivity of Cu_xO/MOF, towards the degradation of CIP in aqueous solutions. The tailored Cu_xO/MOF, not only shows an excellent CIP degradation efficiency of up to 92% with a constant kinetic rate (k_obs) of 0.048 min⁻¹ under visible light, but it can also retain the stable photodegradation efficiency of >85%, for at least six cycles. In addition, Cu_xO/MOF has an excellent adsorption capacity at pH 6.0 of the maximum Langmuir adsorption capacity of 34.5 mg g⁻¹ for CIP. The results obtained in this study demonstrate that Cu_xO/MOF is a reliable integrated material and serves as an adsorbent and photocatalyst, which can open a new pathway for the preparation of visible-light-responsive photocatalysts, for the removal of antibiotics and other emerging pollutants.

Photoelectrochemical (PEC) water splitting is a promising strategy to improve the efficiency of oxygen evolution reactions (OERs). However, the efficient adsorption of visible light as well as long-term stability of light-harvesting electrocatalysis is the crucial issue in PEC cells. Metal–organic framework (MOF)-derived bimetallic electrocatalysis with its superior performance has wide application prospects in OER and PEC applications. Herein, we have fabricated a nickel and iron bimetallic organic framework (FeNi-MOF) deposited on top of anodized TiO₂ nanotube arrays (TNTA) for PEC and OER applications. The FeNi-MOF/TNTA was incorporated through the electrochemical deposition of Ni²⁺ and Fe³⁺ onto the surface of TNTA and then connected with organic ligands by the hydrothermal transformation. Therefore, FeNi-MOF/TNTA demonstrates abundant photoelectrocatalytic active sites that can enhance the photocurrent up to 1.91 mA/cm² under 100 mW/cm² and a negligible loss in activity after 180 min of photoreaction. The FeNi-MOF-doped photoanode shows predominant photoelectrochemical performance due to the boosted excellent light-harvesting ability, rapid photoresponse, and stimulated interfacial energy of charge separation under the UV-visible light irradiation conditions. The results of this study give deep insight into MOF-derived bimetallic nanomaterial synthesis for photoelectrochemical OER and provide guidance on future electrocatalysis design.

Adsorbent made by carbonization of biomass under oxygen-limited conditions has become a promising material for wastewater treatment owing to its cost-effective, simple, and eco-friendly processing method. Ultrasound is considered a green technique to modify carbon materials because it uses water as the solvent. In this study, a comparison of Reactive Black 5 (RB5) adsorption capacity between biochar (BC) generated by pyrolysis of water bamboo (Zizania latifolia) husks at 600 °C and ultrasound-assisted biochar (UBC) produced by pyrolysis at 600 °C assisted by ultrasonic irradiation was performed. UBC showed a greater reaction rate and reached about 80% removal efficiency after 4 h, while it took 24 h for BC to reach that level. Scanning electron microscope (SEM) images indicated that the UBC morphology surface was more porous, with the structure of the combination of denser mesopores enhancing physiochemical properties of UBC. By Brunauer, Emmett, and Teller (BET), the specific surface areas of adsorbent materials were analyzed, and the surface areas of BC and UBC were 56.296 m²/g and 141.213 m²/g, respectively. Moreover, the pore volume of UBC was 0.039 cm³/g, which was higher than that of BC at 0.013 cm³/g. The adsorption isotherms and kinetics revealed the better fits of reactions to Langmuir isotherm and pseudo-second-order kinetic model, indicating the inclination towards monolayer adsorption and chemisorption of RB5 on water bamboo husk-based UBC.

Recycling and reusing glass fiber waste (GFW) has become an environmental concern, as the means of disposal are becoming limited as GFW production increases. Therefore, this study developed a novel, cost-effective method to turn GFW into a mesoporous zeolite-like nanomaterial (MZN) that could serve as an environmentally benign adsorbent and efficient remover of methylene blue (MB) from solutions. Using the Taguchi optimizing approach to hydrothermal alkaline activation, we produced analcime with interconnected nanopores of about 11.7 nm. This MZN had a surface area of 166 m² g⁻¹ and was negatively charged with functional groups that could adsorb MB ranging from pH 2 to 10 and all with excellent capacity at pH 6.0 of the maximum Langmuir adsorption capacity of 132 mg g⁻¹. Moreover, the MZN adsorbed MB exothermically, and the reaction is reversible according to its thermodynamic parameters. In sum, this study indicated that MZN recycled from glass fiber waste is a novel, environmentally friendly means to adsorb cation methylene blue (MB), thus opening a gateway to the design and fabrication of ceramic-zeolite and tourmaline-ceramic balls and ceramic ring-filter media products. In addition, it has environmental applications such as removing cation dyes and trace metal ions from aqueous solutions and recycling water.

The new technology development for municipal solid waste incineration fly ash treatment and reuse is urgent due to landfill shortage and environmental effect of leached hazardous substances. Chlorine (Cl) is worth considering due to its high levels in fly ash. In this study, a treatment process of ultrasound combined with organic acid was used to eliminate Cl from fly ash to enhance its properties for reuse. Taguchi methodology was implemented to design the experiments by controlling four impact factors and the contribution of each factor was evaluated by the ANOVA analysis of variance. Following two treatment steps within 5 min with a solid/liquid ratio of 1:10 at 165 kHz, 98.8% of Cl was eliminated. Solid/liquid ratio was the most prominent factor that contributed to the Cl removal with more than 90%, according to the ANOVA analysis of variance. Tert-butyl alcohol (tBuOH), an ^•OH radical scavenger, was utilized to examine different effects of ultrasonic cavitation on Cl removal efficiency. A 20 kHz ultrasound was used to explore the influence of multi-frequency ultrasound with different mechanical and sonochemical effects on the fly ash dechlorination. This ultrasonic-assisted organic acid treatment was found to be a time and cost-effective pathway for fly ash Cl removal.