12·10-4, LOQ = 7.04·10-4 mg/L). PET quantification involves depolymerization, in this case by alkaline hydrolysis, followed by HPLC analysis of its comonomer terephthalic acid. Eight sludge samples from four WWTPs in Italy showed contamination in the 29.3-215.3 ppm and 10.6-134.6 ppm range for nylon 6 and nylon 6,6, respectively, and in the 520-1470 ppm range for PET.Persistent organic pollutants (mainly aromatic compounds) such as bromophenol and diethyl phthalate are dangerous and act as primary contaminants in aqueous system. In this study, efficient reduced graphene oxide zinc oxide (rGO-ZnO) nanocomposites were synthesized by using a simple and facile method for photocatalytic degradation of 4-Bromophenol (4-BP) and diethyl phthalate (DEP). The rGO-ZnO (rGZ) nanocomposites (NCs) with different weight ratio of rGO and ZnO (coded as rGZ-1, rGZ-2, rGZ-5 and rGZ-10) were synthesized via high temperature refluxing method. The crystalline structure and phase, surface morphological study, optical properties, crystal defects and existence of functional groups in rGZ NCs were studied by X-ray diffraction (XRD), field-emission-scanning electron microscope (FE-SEM), UV-Visible diffuse reflectance spectroscopy (DRS), Raman spectroscopy and FT-IR analysis, respectively. The elimination of 4-BP and DEP from water by UV-light exposure was considered to estimate the photocatalytic efficiency of prepared rGZ NCs. The maximum elimination of 4-BP and DEP via photodegradation (advanced oxidation process) was found about 99.04% and 98.63% over rGZ NCs after 180 min UV irradiation, respectively. The photodegradation study was examined by using high performance liquid chromatography (HPLC) technique. This study confirms the efficient photocatalytic activity of rGZ-5 towards degradation of 4-BP and DEP. Finally, degradation mechanism has been proposed for the degradation of 4-BP and DEP.The occurrence of Pharmaceutical and Personal Care Products (PPCPs) in the aquatic environment has raised concerns due to their accumulation in the ecosystem. This study aims to explore the feasibility of using a Revolving Algal Biofilm (RAB) reactor for PPCPs removal from waterbody. Five model PPCP compounds including ibuprofen, oxybenzone, triclosan, bisphenol A and N, N-diethyl-3-methylbenzamide (DEET) were mixed and added to the culture medium. It shows that PPCP removal efficiencies of the RAB reactor ranged from 70% to 100%. The degradation of PPCPs by the RAB reactor contributed > 90% PPCP removal while less then 10% PPCPs removal was due to accumulation in the algal biomass.  https://www.selleckchem.com/products/unc-3230.html  The nutrients removal performance of the RAB reactor was not affected by exposing to the PPCPs. The extracellular polysaccharides content of the biomass increased when exposing to PPCPs, while the extracellular proteins content remained constant. The Chl a content maintained constant in the PPCPs-treated biomass, but decreased in the biomass without PPCP treatment. It was also found that the microbial consortium of the RAB reactor was enriched with PPCPs degradation microorganisms with the progressing of feeding PPCPs. Collectively, this work demonstrates that the RAB system is a promising technology for removing PPCPs from wastewater.This work presents a systematical experimental and density functional theory (DFT) studies to reveal the mechanism of NO reduction by H2 reaction over platinum nanoparticles (NPs) deposited on boron-doped graphene (denoted as Pt/BG) catalyst. Both characterizations and DFT calculations identified boron (in Pt/BG) as an additional NO adsorption site other than the widely recognized Pt NPs. Moreover, BG led to a decrease of Pt NPs size in Pt/BG, which facilitated hydrogen spillover. The mathematical and physical criteria of the Langmuir-Hinshelwood dual-site kinetic model over the Pt/BG were satisfied, indicating that adsorbed NO on boron (in Pt/BG) was further activated by H-spillover. On the other hand, Pt/graphene (Pt/Gr) demonstrated a typical Langmuir-Hinshelwood single-site mechanism where Pt NPs solely served as active sites for NO adsorption. This work helps understand NO-H2 reaction over Pt/BG and Pt/Gr catalysts in a closely mechanistic view and provides new insights into roles of active sites for improving the design of catalysts for NO abatement.Experimental studies suggested per- and polyfluoroalkyl substances (PFASs) may disrupt estrogens in animals, however, the epidemiological evidence on the associations of PFASs with estrogens is sparse. We investigated the associations of legacy PFASs and their alternatives, including F-53B, the perfluorooctane sulfonate (PFOS) replacement that is specifically and commonly used in China, with estrogen concentrations in newborns. We quantified six PFASs and three estrogens in the cord sera of 942 newborns from a birth cohort in Wuhan, China, between 2013 and 2014. After adjusting for confounders and correcting for multiple comparisons, we observed that both legacy PFASs and their alternatives were associated with higher serum levels of estradiol (E2). Some of the PFASs were associated with increasing levels of estrone (E1) and estriol (E3). Analysis of PFASs in mixture using weighted quantile sum regressions showed that F-53B contributed 20.1% and 48.5% to the associations between PFASs and E1 and E2, respectively. This study provided epidemiological data on the associations between common PFAS exposures and estrogens in newborns. Additional toxicology studies are needed to fully understand the effects of PFASs on estrogens and the mechanisms.MoS2@Kaolin was prepared by facile one-step hydrothermal method for the efficient adsorption of Pb(II) from aqueous solution. XRD, TG, SEM, BET, XPS and FTIR were used to characterize the phase and structure of composite before and after the adsorption of Pb(II). The results showed that MoS2 nanosheets were successfully assembled on kaolinite surface to form MoS2@Kaolin, and the adsorption capacity of the MoS2@Kaolin is 1.74 and 16.95 times than that of single MoS2 and kaolinite, respectively. MoS2@Kaolin composite exhibited a fast adsorption rate for Pb(II) and an excellent adsorption efficiency for Pb(II) in a wide pH range (2-5.5). The adsorption process followed the Langmuir isotherm model and maximum adsorption capacity was 280.39 mg/g. The adsorption kinetics of MoS2@Kaolin composite to Pb(II) fitted well with the pseudo-second-order kinetics models, which showed that the adsorption process was controlled by chemical sorption. MoS2@Kaolin showed excellent regeneration and maintained high selectivity adsorption with co-existence metal ions.