New alternatives for the removal of transition metal ions that present an environmental risk are required. The chemical adsorption of these ions on surfaces with chemisorbent properties represents a promising area of research. In this work, manganite (γ-MnOOH) nanorods were synthesized, with a surface area of 20.22 m² g⁻¹, pore size of 32.18 nm and pore volume of 0.1627 cm³ g⁻¹. After chemical and structural characterization of the manganite sample, it was evaluated as an adsorbent of Cu(II) from aqueous solution. The equilibrium adsorption data were well fitted by the Langmuir isotherm, and the results indicated that the maximum adsorption capacity of Cu(II) was 11.926 mg g⁻¹. Cu(II) ion adsorption on the manganite surface is a spontaneous and exothermic process (ΔG°< 0 and ΔH°< 0). The negative value of ΔS° suggests the stability of the adsorption process without structural change at the manganite–aqueous solution interface. A scheme for chemisorption of Cu(II) ions on the hydroxylated surface of manganite is proposed.

Solar energy is one of the most promising and developed technologies in recent years, due to its high efficiency and low cost. Perovskite-type solar cells have been the focus of attention by the world scientific community. The main objective of this article is to present an (PSCs) analysis of the various investigations reported on the development of ABX3 inorganic halide perovskite-based solar cells, with emphasis in the effect that temperature and humidity have on their chemical and crystal structure stability. The main methods that are used to obtain ABX3 inorganic halide perovskites are also presented and analyzed. An analysis about the structure of these photovoltaic cells and how to improve their efficiency (PCS), fill factor (FF), short circuit current density (Jsc) and open circuit voltage (Voc) of these devices is presented. As a conclusion, a relationship of the methods, synthesis variables, and type of inorganic halide perovskite used for the development of devices with the best efficiencies is presented; the trends towards which this area of science is heading are also highlighted.

Las estructuras metal-orgánicas (MOFs) son polímeros de coordinación que se componen por un centro metálico y un ligando orgánico, que pueden diseñarse empleando iones metálicos biocompatibles (Fe+3, Zn+2, Mg+2, Ca+2 y Mo+6) y ligandos orgánicos bioactivos, permitiendo la modulación de la estructura y propiedades a escala nanométrica. El objetivo del presente trabajo es dar a conocer un panorama de los materiales empleados en la liberación de fármacos, enfatizando las ventajas, avances y retos en la liberación de fármacos con MOFs nanoestructurados, así como su mecanismo de liberación, degradación y actividad antimicrobiana.

The goal of the present work was to compare the partitioning behavior of chitinase and laminarinase (from Trichoderma spp.) in soya lecithin liposomes at different temperatures and examine the activity of the resulting microencapsulated enzymes against Fusarium oxysporum. In both cases the partition coefficients (K_o/w) were greater than 1, indicating affinity of the enzymes for microencapsulation in liposomes. Enthalpy calculations indicated that the process was endothermic in the case of laminarinase and exothermic in the case of chitinase. Soya lecithin liposomes were stable for more than 20 days. The stability of the immobilized enzyme was increased in the case of chitinase, but was not changed in the case of laminarinase. Although the antifungal effects of individual immobilized preparations decreased after microencapsulation compared with non-immobilized enzymes, they were increased by the synergistic effect of both encapsulated enzymes. The application of free or immobilized enzymes was also shown to enhance the inhibitory effect of the chemical fungicide, thiabendazole, on F. oxysporum.