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This study is focused on the optimization and application of an analytical methodology for the determination of 15 selected pesticides in three substrates during the vinification process. QuEChERS extraction was used followed by GC-MS to develop a simple and rapid method for the determination of these compounds. The optimized methodology was validated, providing for all selected pesticides excellent linearity, recoveries ranging between 60.9% and 95.0% and LOQs lower than 50 ng g−1 f for all substrates. The developed methodology was tested on real samples of grapes, must and wine obtained from a winery in the Epirus region. The results indicated the existence of some of the selected pesticides at comparatively low levels in contrast to the valid MRLs. [ABSTRACT FROM AUTHOR]

Traditionally, antibiotics have been used to treat human and animal diseases caused by pathogenic bacteria. The aquaculture industry, which is massively expanding currently, also makes use of several antibiotic classes, resulting in potential antibiotic residues in the surrounding aquatic environment, as well as the cultured products raising bacterial resistance. The aim of this study was the optimization, validation, and application of a solid-phase extraction (SPE) method in combination with liquid chromatography (LC)-LTQ/Orbitrap mass spectrometry in order to determine the most commonly used antibiotics in waters sampled from fish farms, both saltwater and freshwater, located in Greece. Under optimum conditions, the method was validated, achieving recoveries in the range of 57.7% (for sulfamethoxazole in river water) to 95.8% (for florfenicol in river water). The method quantification limits were within the range of 0.25 and 10 ng·L−1 in all cases, with relative standard deviations (RSDs) < 15.9%. The application of the proposed methodology revealed the presence of oxytetracycline and trimethoprim traces. Finally, an assessment of the environmental risk posed by the detected antibiotics was performed, calculating either the risk quotient (RQ) for three trophic levels (8.013 × 10−6 < RQ < 0.496) or the mixture RQ (0.005 < RQ < 0.682), proving that in all cases, the risk was medium to low. [ABSTRACT FROM AUTHOR]

Today, the pollution caused by a multitude of pharmaceuticals used by humans has been recognized as a major environmental problem. The objective of this study was to evaluate and compare the photocatalytic degradation of ten target psychiatric drugs in hospital wastewater effluents using g-C3N4 and 1%MoS2/g-C3N4 (1MSCN) as photocatalytic materials. The experiments were performed using real wastewater samples collected from hospital wastewater treatment plant (WWTP) secondary effluent in spiked and inherent pharmaceutical concentration levels. The photocatalytic experiments were performed in a laboratory-scale pilot plant composed of a stainless-steel lamp reactor (46 L) equipped with ten UVA lamps and quartz filters connected in series with a polypropylene recirculation tank (55–100 L). In addition, experiments were carried out in a solar simulator apparatus Atlas Suntest XLS+ at a 500 Wm−2 irradiation intensity. The analysis of the samples was accomplished by solid-phase extraction, followed by liquid chromatography-Orbitrap high-resolution mass spectrometry. Results showed that the photocatalytic degradation of pharmaceutical compounds followed first-order kinetics. In all cases, 1MSCN presented higher photocatalytic performance than g-C3N4. The removal rates of the pharmaceutical compounds were determined above 30% and 54% using g-C3N4 and 1MSCN, respectively. Parallel to kinetic studies, the transformation products (TPs) generated during the treatment were investigated. [ABSTRACT FROM AUTHOR]

The objective of this work was to evaluate the efficiency of a solar photocatalytic process using g-C3N4 as photocatalyst on the degradation of pharmaceutical compounds detected in hospital wastewater treatment plant secondary effluents. A compound parabolic collector pilot plant, established in the secondary effluent stream of the Ioannina city hospital wastewater treatment plant, was used for the photocatalytic experiments. The analysis of the samples before and after the photocatalytic treatment was accomplished using solid phase extraction (SPE), followed by UHPLC-LTQ/Orbitrap HRMS. Initial effluent characterization revealed the presence of ten pharmaceutical compounds. Among these, amisulpride, O-desmethyl venlafaxine, venlafaxine and carbamazepine were detected in all experiments. Initial concentrations ranged from 73 ng L−1 for citalopram to 2924.53 ng L−1 for O-desmethyl venlafaxine. The evolution of BOD5 and COD values were determined before and after the photocatalytic treatment. All detected pharmaceuticals were removed in percentages higher than 54% at an optimum catalyst loading ranging between 200 and 300 mg L−1. The potential of the catalyst to be reused without any treatment for two consecutive cycles was studied, showing a significant efficiency decrease. [ABSTRACT FROM AUTHOR]