Heliyon (Mar 2024)
Spectrophotometric determination of phenol impurity in phenoxyethanol and phenol index of drinking water and municipal wastewater effluent after salting-out assisted liquid phase microextraction (SA-LPME)
Abstract
In this study, a novel and convenient analytical method based on salting-out-assisted liquid phase microextraction (SA-LPME) has been developed. A spectrophotometric technique was employed to quantify the concentration of phenol in drinking water and treated wastewater, as well as the phenol impurity in 2-phenoxyethanol (PE). To accomplish this, a solution containing dissolved PE was supplemented with 4-aminoantipyrine (4-AAP) and hexacyanoferrate. Subsequently, NaCl was added to induce the formation of a two-phase system, consisting of fine droplets of PE as an extractant phase in the aqueous phase. The resulting red derivative was then extracted into the extractant phase and separated through centrifugation. Finally, the absorbance of the extracted derivative was measured at 520 nm. The Response Surface Methodology (RSM) based on the Box-Behnken Design (BBD) was employed to optimize the influential factors, namely 4-Aminoantipyrine (4-AAP), buffer (pH = 10), hexacyanoferrate, and NaCl. By utilizing the optimal conditions (buffer: 50 μL, 4-AAP (1% w/v): 80 μL, hexacyanoferrate (10% w/v): 65 μL, and NaCl: 0.7 g per 10 mL of the sample), the limit of detection was determined to be 0.7 ng mL−1 and 0.22 μg g−1 for water and PE samples, respectively. The relative standard deviation (RSD) and correlation of determination (r2) obtained fell within the range of 2.4–6.8% and 0.9983–0.9994, respectively. Moreover, an enrichment factor of 65 was achieved for a sample volume of 10 mL. The phenol concentration in two PE samples (PE-1, PE-2), provided by a pharmaceutical company (Pars Sadra Fanavar, Iran), were determined to be 0.83 ± 0.05 μg g−1 and 2.70 ± 0.14 μg g−1, respectively. Additionally, the phenol index in drinking water and treated municipal wastewater was found to be 3.60 ± 1.06 ng mL−1 and 4.60 ± 1.17 ng mL−1, respectively. These mentioned samples were spiked in order to evaluate the potential influence of the matrix. The relative recoveries from PE-1, PE-2 samples, drinking water, and treated municipal wastewater samples were measured as 104.5%, 97.5%, 101.6%, and 107.8%, respectively, indicating no matrix effect.
