Development of UV-Vis spectroscopy-based analysis method for determination of tin(IV) in epilobium parviflorum (hoary willowherb) tea using deep eutectic solvent based preconcentration.

In this study, a UV-Vis Spectroscopy-based method was developed for the determination of tin(IV) in epilobium parviflorum tea samples after preconcentration. The preconcentration process was carried out using the liquid-liquid microextraction technique. Before starting the analysis, optimization studies were carried out for the variables likely to affect the experimental results. As a result of the analyzes performed under optimum conditions, the detection limit of our method was calculated as 16.83 µg/L. The percent relative standard deviation value was calculated as 1.25% (n = 8) and linearity was found in the range of 10-1000 µg/L. Recovery experiments were performed on epilobium parviflorum tea samples using the matrix matching method. As a result of the analyzes made on teas belonging to three different brands, recovery results ranging from 92 to 117% were obtained.

Accurate and sensitive determination of Sb(III) in water samples using UV-VIS spectrophotometry after simultaneous complexation and preconcentration with deep eutectic solvent/DTZ probe-based liquid-liquid microextraction.

This study describes the determination of trace levels of antimony(III) by UV-Vis spectrophotometer after preconcentration by the deep eutectic solvent/dithizone probe-based liquid-liquid microextraction method. Ditizone was used as a ligand to form the coordinated antimony complex before extraction in the preconcentration process. In the microextraction method developed in the study, deep eutectic solvent was used to dissolve the complexing agent; thus, the complexation was performed at the same time as the extraction of antimony complex by deep eutectic solvent. All variables likely to affect the ligand-antimony(III) complex, extraction efficiency, and spectroscopic measurement were optimized to lower the detection limit. Under the determined optimum conditions, the detection limit for Sb was calculated as 1.6 × 10-3 mg/L. The detection limit obtained with the method is much lower than the value obtained in the Uv-Vis spectrophotometer with the traditional method. In this study, the percent relative standard deviation for the lowest concentration was calculated as 3.12% (n = 8). This value indicates that the analysis performed has high precision. The applicability of the method was determined by performing spiked recovery tests on tap water taken from different regions. Satisfactory recovery results were obtained between 91 and 105% at three different concentrations.

Development of QCM based biosensor for the selective and sensitive detection of paraoxon.

In this study, a quartz crystal microbalance (QCM) based sensor was developed that selectively recognizes and binds the paraoxon molecule. For this purpose, poly (styrene-maleic anhydride) (PSMA) polymer was synthesized to obtain nanofiber. A 30% (wt/wt) PSMA/DMSO solution was prepared for use in the electrospinning process, with operating conditions of 5 kV potential and 1 mL/h flow rate. After obtaining the nanofibers, AChE enzyme was immobilized to nanofiber. The QCM gold electrode surface was coated with AChE immobilized nanofiber. For this purpose, the QCM electrode was first functionalized with 4-aminothiophenol. The quartz electrode coated with the recognition layer was sequentially studied with aqueous solutions containing 50% (v/v) methanol, ranging from 0.1 ppm to 10 ppm of paraoxon. When the electrode interacts with paraoxon, the frequency value decreases. The obtained data were converted to graphs and a calibration graph was obtained. The LOD value was found to be 4.57 × 10-8 and the LOQ value was found to be 1.52 × 10-7 M. These results show us that the developed method can analyze very small quantities of paraoxon samples. The Langmuir adsorption equation was used to study the interaction of the bond between the electrode surface and the paraoxon. For the calculation of the coupling constant Ka, Δm/C (g/M) versus Δm (g) was plotted on the graph. The Ka binding constant of the obtained graphic was found to be 5 × 107 M-1.