Polyethylene terephthalate (PET) is widely used material and as such became highly enriched in nature. It is generally considered inert and safe plastic, but due to the recent increased efforts to break-down PET using biotechnological approaches, we realized the scarcity of information about structural analysis of possible degradation products and their ecotoxicological assessment. Therefore, in this study, 11 compounds belonging to the group of PET precursors and possible degradation products have been comprehensively characterized. Seven of these compounds including 1-(2-hydroxyethyl)-4-methylterephthalate, ethylene glycol bis(methyl terephthalate), methyl bis(2-hydroxyethyl terephtahalate), 1,4-benzenedicarboxylic acid, 1,4-bis[2-[[4-(methoxycarbonyl)benzoyl]oxy]ethyl] ester and methyl tris(2-hydroxyethyl terephthalate) corresponding to mono-, 1.5-, di-, 2,5- and trimer of PET were synthetized and structurally characterized for the first time. In-silico druglikeness and physico-chemical properties of these compounds were predicted using variety of platforms. No antimicrobial properties were detected even at 1000 μg/mL. Ecotoxicological impact of the compounds against marine bacteria Allivibrio fischeri proved that the 6 out of 11 tested PET-associated compounds may be classified as harmful to aquatic microorganisms, with PET trimer being one of the most toxic. In comparison, most of the compounds were not toxic on human lung fibroblasts (MRC-5) at 200 μg/mL with inhibiting concentration (IC50) values of 30 μg/mL and 50 μg/mL determined for PET dimer and trimer. Only three of these compounds including PET monomer were toxic to nematode Caenorhabditis elegans at high concentration of 500 μg/mL. In terms of the applicative potential, PET dimer can be used as suitable substrate for the screening, identification and characterization of novel PET-depolymerizing enzymes.The presence of residues of veterinary pharmaceuticals in farm wastewaters such as pig slurry represents a problem that needs to be tackled to avoid further contamination of environmental waters and the development of resistant bacteria. For their monitoring and control, it is necessary the existence of reliable analytical tools. read more The present paper describes for the first time the development and optimization by statistical experimental design of a specifically designed analytical method for the analysis of 21 veterinary drugs, including 18 antibiotics of several families (β-lactams, tetracyclines, fluoroquinolones, sulfonamides, macrolides, among others), 1 antiparasitic, 1 analgesic and 1 hormone, in a complex environmental matrix such as the fresh solid phase of pig slurry. The resulting method, consisted of an ultrasound assisted extraction (UAE) combined with in-situ dispersive solid phase extraction (d-SPE) from a 0.3 g of freeze-dried sample aliquot followed by a preconcentration step by compact solid phase extraction (c-SPE) and subsequent instrumental analysis by ultra-high-performance-liquid-chromatography (UHPLC) coupled to mass spectrometry in tandem (MS/MS) by a triple quadrupole, was successfully validated as a very sensitive (method limit of quantification in the low ng g-1) and reliable method (relative recoveries around 100% and method repeatability featured by a general relative standard deviation below 20%). Provided raw data was intended to be processed by matrix-matched quantification approach. The resulting methodology was applied to the characterization of several pig manures from different Spanish farms sampled across breeding season between 2018 and 2019. Sample precedence showed to have a high impact in the positives, its frequency and concentration.The present work reports the preparation of polyvinyl formal (PVF)/Titanium dioxide (TiO2) nanocomposite films using a solution casting method followed by the characterization of the synthesized PVF/TiO2 nanocomposite films using various analytical techniques namely FTIR, XRD, UV-vis, SEM and TGA analysis. The results obtained from different analyses confirmed that the TiO2 NPs was fine dispersed within the PVF matrix and there exists well compatibility among the polymer matrix and the nanofiller. The pristine TiO2 NPs based fabricated chemiresistive sensor exhibits the maximum sensitivity of 50.25% at 370 °C where as PVF/TiO2 nanocomposite sensor showed the enhanced sensitivity of 83.75% at a relatively low operating temperature of 150 °C towards 600 ppm sulfur dioxide (SO2) gas. The 25 wt% PVF/TiO2 nanocomposite film sensor exhibited good sensitivity (∼83.75%), selectivity, rapid response time (66 s)/recovery time (107 s), and long-term stability of 60 days for SO2 gas detection. The fabricated PVF/TiO2 nanocomposite film sensors in our work possesses the advantages of low power consumption, cost-effective, and distinguished sensing abilities for SO2 detection makes it possible for potential applications. Thus, the fabricated chemiresistive sensors based on TiO2 NPs reinforced PVF nanocomposites films are evaluated and experimental results to show an excellent behavior towards SO2 gas detection for industrial processes control and environmental monitoring applications.Drinking water biofiltration offers the possibility of the removal of trace level micropollutants from source water. Sand, granular activated carbon (GAC), GAC sandwich (a layer of GAC loaded in the middle of sand bed), and anthracite-sand dual biofilters were set-up in duplicate at bench-scale to mimic the filtration process in real drinking water treatment works. During the 3-month system operation, removal of five antibiotics (amoxicillin, clarithromycin, oxytetracycline, sulfamethoxazole, and trimethoprim) and overall biofilter performance were evaluated. Natural surface water spiked with a mixture of the target antibiotics was used as feedwater to the biofilters. Results showed that the target antibiotics were substantially removed (>90%) by GAC-associated biofilters and partially removed (≤20%) by sand alone and anthracite-sand biofilters. In particular, the GAC sandwich biofilter exhibited superior performance compared to sand/anthracite biofilter, and the comparisons among all biofilters indicated that both adsorption and biodegradation contributed to the removal of the target antibiotics in the GAC-associated biofilters.