Bisphenol A (BPA) is a chemical compound used in the manufacturing of plastics and resins whose presence in the body in low concentrations can cause serious health problems. Due to this, there is a growing interest in the scientific community to develop analytical methods that allow quantifying trace concentrations of BPA in different types of samples. The determination of this compound in toys made of plastics that can be manipulated by children leads to an extra concern, because it is possible for BPA to enter the body by introducing these toys into the mouth. This work presents a novel procedure to the quickly and easily quantification of trace levels of BPA in samples of toys and pacifiers according to the current demanding regulations. The determination of very low levels of BPA was carried out by ionic liquid dispersive liquid–liquid microextraction (IL-DLLME) followed by high-performance liquid chromatography (HPLC). The formation in situ of the ionic liquid (IL) 1-octyl-3-methylimidazolium bis((trifluoromethane)sulfonyl)imide ([C₈MIm] [NTf₂]), was achieved by mixing 1-octyl-3-methylimidazolium chloride ([C₈MIm]Cl) and lithium bis(trifluoromethanesulfonyl)imide ([NTf₂]Li) aqueous solutions, reaching an instant dispersion whose cloud of microdrops allows the total extraction of BPA in the IL from aqueous solutions. After centrifugation, BPA concentration in the sedimented phase was determined by HPLC. The optimal experimental conditions for the microextraction and determination of BPA in the IL were studied. The total extraction was achieved at pH 4, heating the sample at 30 °C for 5 min, using 100 µL of IL precursor volume, and spinning after the formation of dispersion at 3000 rpm for 10 min. The enrichment factor (EF) and detection limit (LOD) reached with the procedure were 299 and 0.19 µg L⁻¹, respectively. The relative standard deviation for ten replications at the 0.5 µg L⁻¹ level was 5.2%. Recovery studies showed a mean value for BPA recovery percentage in the samples of 99%. Additionally, a hybrid model was applied to characterize the extraction kinetics. This simple, low cost and fast method simplifies traditional microextraction techniques, representing an outstanding alternative.

This paper presents a novel procedure for the treatment of contaminated water with high concentrations of nitrates, which are considered as one of the main causes of the eutrophication phenomena. For this purpose, magnetic nanoparticles functionalized with silver (Fe₃O₄@AgNPs) were synthesized and used as an adsorbent of nitrates. Experimental conditions, including the pH, adsorbent and adsorbate dose, temperature and contact time, were analyzed to obtain the highest adsorption efficiency for different concentration of nitrates in water. A maximum removal efficiency of 100% was reached for 2, 5, 10 and 50 mg/L of nitrate at pH = 5, room temperature, and 50, 100, 250 and 500 µL of Fe₃O₄@AgNPs, respectively. The characterization of the adsorbent, before and after adsorption, was performed by energy dispersive X-ray spectroscopy, scanning electron microscopy, Brunauer-Emmett-Teller analysis and Fourier-transform infrared spectroscopy. Nitrates can be desorbed, and the adsorbent can be reused using 500 µL of NaOH solution 0.01 M, remaining unchanged for the first three cycles, and exhibiting 90% adsorption efficiency after three regenerations. A deep study on equilibrium isotherms reveals a pH-dependent behavior, characterized by Langmuir and Freundlich models at pH = 5 and pH = 1, respectively. Thermodynamic studies were consistent with physicochemical adsorption for all experiments but showed a change from endothermic to exothermic behavior as the temperature increased. Interference studies of other ions commonly present in water were carried out, enabling this procedure as very selective for nitrate ions. In addition, the method was applied to real samples of seawater, showing its ability to eliminate the total nitrate content in eutrophized waters.

Fast and effective location of the switching point between kinetic and thermodynamic regimes by means of the NSM approach provides comprehensive control over the product composition.

This work presents a novel procedure for the removal of Cu²⁺ from water, an essential element in human nutrition considered toxic in high concentrations, based on a microextraction technique involving the formation of a micellar phase. To achieve the total elimination of copper from aqueous samples, a Cu²⁺-complexing reagent based on silver nanoparticles functionalized with sodium mercaptoethane sulfonate (AgNPs@MESNa) was used. The complex formed by Cu²⁺ and the reagent was extracted into a micellar microphase formed by Triton X-114, a harmless surfactant. Volumes of 200 µL of the 10⁻⁴ mol L⁻¹ suspension of AgNPs@MESNa and 100 µL of a solution of Triton X-114 at 30% m/m were employed to successfully remove 10 mg L⁻¹ of Cu from 20 mL of water samples. The time and temperature needed to achieve 100% microextraction efficiency were 10 min and 40 °C, respectively. The procedure is considered environmentally friendly due to the low volume of the extracting phase and the simple experimental conditions that achieve total removal of Cu²⁺ from water samples.

In this work we present a rapid and easy method to remove the totality of bisphenol A from aqueous solutions using ionic liquid (IL). Dispersive liquid–liquid microextraction is employed. The IL 1-octyl-3-methylimidazolium bis((trifluoromethane)sulfonyl)imide ([C₈C₁im] [NTf₂]) is formed in situ because of the mixture of 1-octyl-3-methylimidazolium chloride ([C₈C₁im]Cl) and lithium bis(trifluoromethanesulfonyl)imide (Li[NTf₂]) aqueous solutions. A cloud of microdroplets of IL formed by the dispersion generated through the precursors metathesis reaction allows the rapid and total extraction of bisphenol A (BPA). After centrifugation, the formed IL phase is deposited at the bottom of the flask and the total amount of BPA is extracted in the sedimented phase. The volume of IL is very low, in the order of microliters, which enables us to remove all the BPA from the solution. The technique studied is highly efficient, cost-effective, and presents less environmental impact than other extraction techniques, thus becoming an outstanding alternative to the most commonly used methods. BPA concentration is determined by high performance liquid chromatography by injecting the IL phase directly. An extraction kinetic model for the kinetic profile has been tested for this method, which allows to infer the ideal experimental conditions to execute the extraction method.