In the last few years, the use of ionic liquid-based membranes has gained importance in a wide variety of separation processes due to the unique properties of ionic liquids. The aim of this work is to analyze the transport of nutrients through polymer inclusion membranes based on different concentrations of methyltrioctylammonium chloride, in order to broaden the application range of these kinds of membranes. Calcium chloride (CaCl₂) and sodium hydrogen phosphate (Na₂HPO₄) nutrients were used at the concentration of 1 g·L⁻¹ in the feeding phase. The evolution of the concentration in the receiving phase over time (168 h) was monitored and the experimental data fitted to a diffusion-solution transport model. The results show very low permeation values for CaCl₂. By contrast, in the case of Na₂HPO₄ the permeation values were higher and increase as the amount of ionic liquid in the membrane also increases. The surface of the membranes was characterized before and after being used in the separation process by scanning electron microscopy coupled to energy dispersive X-Ray spectroscopy (SEM–EDX) and elemental mapping analysis. The SEM–EDX images show that the polymer inclusion membranes studied are stable to aqueous solution contacting phases and therefore, they might be used for the selective transport of nutrients in separation processes.

The degradation of imazapyr (C₁₃H₁₅N₃O₃), an active element in the aqueous solution of commercial herbicide, was investigated. This study was the first to evaluate in a comprehensive manner the efficiency of advanced oxidation processes for imazapyr degradation. Results showed that Imazapyr degradation is significantly affected by operational conditions such as TiO₂ concentration, ozone concentration, initial concentration of imazapyr and pH. The kinetics of Imazapyr consumption was the first order with respect to Imazapyr concentration and zero order with respect to ozone concentration with a constant rate of 0.247 min⁻¹ and 0.128 min⁻¹ for photocatalytic ozonation and heterogeneous photocatalysis, while it was the first order with respect to Imazapyr and the first order with respect to ozone concentrations when only ozone was used with a constant rate of 0.053 mol L⁻¹ min⁻¹ at pH 7. The results revealed that more than 90 percent of the removal efficiency representing the elimination of imazapyr was held up to 7 μM. Further increase in the concentration of imazapyr leads to a drop in the removal efficiency, however the total imazapyr degradation was reached in 20 min utilizing photocatalytic ozonation for 5 μM of Imazapyr in the presence of 100 mg L⁻¹ of TiO₂, 10 mg L⁻¹ of ozone at pH 7. Photocatalytic ozonation and heterogeneous photocatalysis utilizing TiO₂ as a semiconductor process appeared possible and well suited for the treatment of organic contaminants such as imazapyr herbicides, although at certain dosages of pH and common time for wastewater treatment, imazapyr was not degraded with ozonation on its own. The association of two oxidation processes, ozonation and photocatalysis, has improved oxidation efficiencies for water treatment under optimal conditions, leading to the development of non-selective hydroxyl and more reactive radicals in the oxidation medium, as well as the resulting synergistic effects between photocatalysis and ozonation that react more rapidly with imazapyr herbicide.