A Metal-Organic Framework (MOF), iron-benzenetricarboxylate (Fe(BTC)), has been studied for the adsorptive removal of azo-dye Orange II from aqueous solutions, where the effect of various parameters was tested and isotherm and kinetic models were suggested. The adsorption capacities of Fe(BTC) were much higher than those of an activated carbon. The experimental data can be best described by the Langmuir isotherm model (R² > 0.997) and revealed the ability of Fe(BTC) to adsorb 435 mg of Orange II per gram of adsorbent at the optimal conditions. The kinetics of Orange II adsorption followed a pseudo-second-order kinetic model, indicating the coexistence of physisorption and chemisorption, with intra-particle diffusion being the rate controlling step. The thermodynamic study revealed that the adsorption of Orange II was feasible, spontaneous and exothermic process (−25.53 kJ·mol⁻¹). The high recovery of the dye showed that Fe(BTC) can be employed as an effective and reusable adsorbent for the removal of Orange II from aqueous solutions and showed the economic interest of this adsorbent material for environmental purposes.

ZnO is an exciting material for photocatalysis applications due to its high activity, easy accessibility of raw materials, low production costs, and nontoxic. Several ZnO nano and microstructures can be obtained, such as nanoparticles, nanorods, micro flowers, microspheres, among others, depending on the preparation method and conditions. ZnO is a wide bandgap semiconductor presenting massive recombination of the generated charge carriers, limiting its photocatalytic efficiency and stability. It is common to mix it with metal, metal oxide, sulfides, polymers, and nanocarbon-based materials to improve its photocatalytic behavior. Therefore, ZnO–nanocarbon composites formation has been a viable alternative that leads to new, more active, and stable photocatalytic systems. Mainly, graphene is a well-known two-dimensional material, which could be an excellent candidate to hybridize with ZnO due to its excellent physical and chemical properties (e.g., high specific surface area, optical transmittance, and thermal conductivity, among others). This review analyses ZnO–graphene nanocomposites’ recent advances, addressing the synthesis methods and the resulting structural, morphological, optical, and electronic properties. Moreover, we examine the ZnO–graphene composites’ role in the photocatalytic degradation of organic/inorganic pollutants.

The FeBTC metal–organic framework (MOF) incorporated with magnetite is proposed as a novel material to solve water contamination with last generation pollutants. The material was synthesized by in situ solvothermal methods, and Fe₃O₄ nanoparticles were added during FeBTC MOF synthesis and used in drug adsorption. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and Raman spectroscopy characterized the materials, with N₂-physisorption at 77 K. Pseudo-second-order kinetic and Freundlich models were used to describe the adsorption process. The thermodynamic study revealed that the adsorption of three drugs was a feasible, spontaneous exothermic process. The incorporation of magnetite nanoparticles in the FeBTC increased the adsorption capacity of pristine FeBTC. The Fe₃O₄–FeBTC material showed a maximum adsorption capacity for diclofenac sodium (DCF), then by ibuprofen (IB), and to a lesser extent by naproxen sodium (NS). Additionally, hybridization of the FeBTC with magnetite nanoparticles reinforced the most vulnerable part of the MOF, increasing the stability of its thermal and aqueous media. The electrostatic interaction, H-bonding, and interactions in the open-metal sites played vital roles in the drug adsorption. The sites’ competition in the multicomponent mixture’s adsorption showed selective adsorption (DCF) and (NS). This work shows how superficial modification with a low-surface-area MOF can achieve significant adsorption results in water pollutants.

There is a need to develop catalysts for the direct ammoxidation of ethane to acetonitrile. This work reports a series of bulk Ni–Nb–O catalysts with increasing niobium content, analysing the structure and the effect on acidity and redox properties and how these relate to Ni–Nb interaction. Niobium doping affects NiO lattice leading to progressively smaller unit cell sizes. The Nb/Ni atomic ratio determines the formation of two Nb–Ni–O mixed phases identified by HRTEM, and which Raman bands are identified near 850 cm⁻¹ and 800 cm⁻¹ for a Nb-poor phase and near 800 cm⁻¹ for a Nb-rich Ni–Nb–O one.