RESUMEN

In the present investigation of copper ferrite, a CuFe2O4 nanocomposite adsorbent was synthesized using the sol-gel method, and its relevance in the adsorptive elimination of the toxic Congo red (CR) aqueous phase was examined. A variety of structural methods were used to analyze the CuFe2O4 nanocomposite; the as-synthesized nanocomposite had agglomerated clusters with a porous, irregular, rough surface that could be seen using FE-SEM, and it also contained carbon (23.47%), oxygen (44.31%), copper (10.21%), and iron (22.01%) in its elemental composition by weight. Experiments were designed to achieve the most optimized system through the utilization of a central composite design (CCD). The highest uptake of CR dye at equilibrium occurred when the initial pH value was 5.5, the adsorbate concentration was 125 mg/L, and the adsorbent dosage was 3.5 g/L. Kinetic studies were conducted, and they showed that the adsorption process followed a pseudo-second-order (PSO) model (regression coefficient, R2 = 0.9998), suggesting a chemisorption mechanism, and the overall reaction rate was governed by both the film and pore diffusion of adsorbate molecules. The process through which dye molecules were taken up onto the particle surface revealed interactions involving electrostatic forces, hydrogen bonding, and pore filling. According to isotherm studies, the equilibrium data exhibited strong agreement with the Langmuir model (R2 = 0.9989), demonstrating a maximum monolayer adsorption capacity (qmax) of 64.72 mg/g at pH 6 and 302 K. Considering the obtained negative ΔG and positive ΔHads and ΔSads values across all tested temperatures in the thermodynamic investigations, it was confirmed that the adsorption process was characterized as endothermic, spontaneous, and feasible, with an increased level of randomness. The CuFe2O4 adsorbent developed in this study is anticipated to find extensive application in effluent treatment, owing to its excellent reusability and remarkable capability to effectively remove CR in comparison to other adsorbents.

RESUMEN

A cerium-based metal-organic framework with MOF-76 topology has been synthesized by a very simple and fast solvothermal method that has been tested for a one gram yield. Variable-temperature powder XRD and X-ray absorption data, analyzed by Rietveld and multiple-scattering extended X-ray absorption fine-structure methods, revealed high thermal stability and the presence of three different stable structures. X-ray absorption near-edge structure and FTIR spectroscopy probed the presence of cerium(III), which was characterized by coordinatively unsaturated sites that, however, played no major role in carbon dioxide adsorption. The material revealed excellent carbon dioxide adsorption properties: the highest gravimetric capacity of 15 wt% was observed at 1.1 bar in the case of the sample activated at 250 °C in vacuum, whereas the strongest interaction energy of 35 kJ mol(-1) was observed for the sample activated at 150 °C. Negligible nitrogen uptake of the sample activated at 150 °C indicates that this material is a promising candidate for nitrogen/carbon dioxide separation purposes.

Asunto(s)

RESUMEN

A series of mixed-ligand [1,4-benzenedicarboxylic acid (BDC)/2-amino-1,4-benzenedicarboxylic acid (ABDC)] UiO-66 metal-organic frameworks (MOFs) synthesized through two different methods (low (LT) and high temperature (HT)) have been investigated for their carbon dioxide adsorption properties from 0 to 1 bar to clarify the role of amino loading on carbon dioxide uptake. Volumetric CO2 isotherms show that the CO2 capacity (normalized to the Langmuir surface area) increases with a degree of functionalization of about 46%; for similar NH2 contents, the same values are found for both synthetic procedures. Microcalorimetric isotherms reveal that amino-functionalized materials have a larger differential heat of adsorption (q(diff) ) towards CO2 ; reaching 27(25) and 20(22) kJ mol(-1) on HT(LT)-UiO-66-NH2 and UiO-66, respectively, at the lowest equilibrium pressures used in this study. All experimental results are supported by values obtained through quantum mechanical calculations.

Asunto(s)

RESUMEN

A series of amine-functionalized mixed-linker metal-organic frameworks (MOFs) of idealized structural formula Zr6O4(OH)4(BDC)(6-6X)(ABDC)6X (where BDC = benzene-1,4-dicarboxylic acid, ABDC = 2-aminobenzene-1,4-dicarboxylic acid) has been prepared by solvothermal synthesis. The materials have been characterized by thermogravimetric analysis (TGA), powder X-ray diffraction (PXRD), and Fourier transform infrared (FTIR) spectroscopy with the aim of elucidating the effect that varying the degrees of amine functionalization has on the stability (thermal and chemical) and porosity of the framework. This work includes the first application of ultraviolet-visible light (UV-vis) spectroscopy in the quantification of ABDC in mixed-linker MOFs.

RESUMEN

New catalytic systems based on ceria have been used in the direct carboxylation of ethanol. The catalytic behavior of Al(2)O(3) and Nb(2)O(5) loaded ceria is compared, the latter showing a better performance. A morphological and structural study has been carried out on Nb(2)O(5)/CeO(2) catalysts in order to explain their behavior in catalysis. Pervaporation membranes have been used for water separation. The synthesis of diethylcarbonate (DEC) has been carried out either in a liquid phase (ethanol) pressurized with CO(2) or in supercritical conditions. A set-up has been developed that allows the production of quite pure DEC (>90%) with recycling of CO(2) and ethanol.