Lamgrady7008

Amoxicillin transformation products, penilloic acid (285-8047 ng/L) and penicilloic acid (107 ng/L), were confirmed for the first time with reference standards in wastewater samples from India, Sweden, and U.S. This workflow provides an efficient approach to broad-scale identification of emerging contaminants using publicly-available databases for suspect screening and prioritization.Considering dissolved organic matter (DOM) molecules, the present study is an attempt to unravel the individual removal targets of nine advanced treatment technologies for bio-stabilized landfill leachate. For the eight DOM molecular subcategories, preferable technologies and removal rates were as follows lipids ‒ powdered activated carbon (PAC) adsorption (97%) and Fenton (97%); proteins ‒ extended electrolysis (92%) and Fenton (92%); and lignins/carboxylic rich alicyclic molecules (CRAM)-like organics ‒ Fenton (90%) and extended electrolysis (75%). As to individual technologies, Fenton, PAC adsorption, extended electrolysis, and reverse osmosis (RO) had the highest removal rates based on the intensity and abundance of DOM. selleck products As to the improved technology combinations, "Fenton with PAC adsorption" and "PAC adsorption with reverse osmosis" were then recommended according to the target complementarity in compound intensity and abundance. The study suggested that the treatment strategy of an unknown recalcitrantly biodegraded wastewater could be designed in a tailored way based on the subcategorized DOM characteristics of the refractory wastewater.Exploring novel sensing materials enabling selective discrimination of trace ambient H2S at lower temperature is of utmost importance for diverse practical applications. Herein, heterostructural (Sr0.6Bi0.305)2Bi2O7/ZnO (SBO/ZnO) nanomaterials were proposed. Synergetic effect of promoting analyte adsorption (via multiplying oxygen vacancy defects) and reversible sulfuration-desulfuration reaction induced unique band alignment among SBO/ZnO/ZnS, contributes to the sensitive and selective response toward H2S molecules. Novel SBO/ZnO (10%) sensor possesses excellent sensing H2S performances, including a high response (107.6 for 10 ppm), low limit of detection of 20 ppb, good selectivity and long-term stability. Together with the merits of low operation temperature of 75 °C and weak humidity dependence (endowed by the hydrophobic SBO), present heterostructural SBO/ZnO sensor paves the way for the practical monitoring of trace H2S pollutants in diverse workplaces including petroleum and natural gas industries.The biomedical applications of graphene-based nanomaterials (GBN) have significantly grown in the last years. Many of these applications suppose their intravenous exposure and, in this way, GBN could encounter blood cells triggering an immunological response of unknown effects. Consequently, understanding the relationships between GBN and the immune system response should be a prerequisite for its adequate use in biomedicine. In the present study, we have conducted a little explored ex vivo exposure method in order to study the complexity of the secretome given by the interactions between GBN and blood cells. Blood samples from different healthy donors were exposed to three different types of GBN widely used in the biomedical field. In this sense, graphene oxide (GO), graphene nanoplatelets (GNPs), graphene nanoribbons (GNRs) and a panel of 105 proteins representatives of the blood secretome were evaluated. The results show broad changes in both the cytokines number and the expression levels, with important changes in inflammatory response markers. Furthermore, the indirect soft-agar assay was used as a tool to unravel the global functional impact of the found secretome changes. Our results indicate that the GBN-induced altered secretome can modify the natural anchorage-independent growth capacity of HeLa cells, used as a model. As a conclusion, this study describes an innovative approach to study the potential harmful effects of GBN, providing relevant data to be considered in the biomedical context when GBN are planned to be used in patients.Competitive adsorption of arsenate (AsO43-) and phosphate (PO43-) on α-FeOOH, LaOOH, and nano-TiO2 was studied using batch adsorption experiments and in-situ flow cell ATR-FTIR coupled with two-dimensional correlation spectroscopy (2D-COS) for the first time. With a higher temporal resolution, our results found a highly dynamic adsorption sequence for AsO43- and PO43-. When AsO43- and PO43- were simultaneously exposed to the adsorbents at the same concentrations, AsO43- was preferentially adsorbed by α-FeOOH and TiO2, but PO43- adsorption was dominant on LaOOH. The results implied that the PO43- adsorbed on LaOOH had to be remobilized to allow for AsO43- adsorption, but that PO43- adsorption on α-FeOOH and TiO2 was hindered by faster AsO43- adsorption. Crystal orbital Hamilton population (COHP) analysis revealed that AsO43- complexes bonded more strongly on α-FeOOH and TiO2, whereas PO43- complexes were more stable on LaOOH. Different adsorption sequences and the stability of the complexes were attributed to the diverse geometric configurations of AsO43- and PO43- on metal oxides surfaces with specific bonding chemistry. The presence of Ca2+ did not affect AsO43- and PO43- adsorption sequence on α-FeOOH or LaOOH, but it reversed the adsorption sequence on TiO2 due to the formation of ternary surface complexes on TiO2 surfaces.In this work, fibrous silica-titania (FST) was successfully prepared by the microemulsion method prior to the addition of three types of carbonaceous materials graphitic-carbon nitride, g-C3N4 (CN), graphene nanoplatelets (GN), and multi-wall carbon nanotubes, MWCNT (CNT), via a solid-state microwave irradiation technique. The catalysts were characterized using XRD, FESEM, TEM, FTIR, UV-Vis DRS, N2 adsorption-desorption, XPS and ESR, while their photoactivity was examined on the degradation of toxic 2-chlorophenol (2-CP). The result demonstrated that the initial reaction rate was in the following order CNFST (5.1 × 10-3 mM min-1) > GNFST (2.5 × 10-3 mM min-1) > CNTFST (2.3 × 10-3 mM min-1). The best performance was due to the polymeric structure of g-C3N4 with a good dispersion of C and N on the surface FST. This dispersion contributed towards an appropriate quantity of defect sites, as a consequence of the greater interaction between g-C3N4 and the FST support, that led to narrowed of band gap energy (2.98 eV to 2.10 eV). The effect of scavenger and ESR studies confirmed that the photodegradation over CNFST occurred via a Z-scheme mechanism. It is noteworthy that the addition of green carbonaceous materials on the FST markedly enhanced the photodegradation of toxic 2-CP.Tetrabromobisphenol A (TBBPA) is one of the most extensively used brominated flame retardants and is universally detected in the environment. However, information related to its transgenerational toxicity is sparse. Using zebrafish as a study model, adult fish were exposed to TBBPA at different concentrations (0, 3, 30, or 300 μg/L) for 42 d and then, the exposed adults were spawned in TBBPA-free water. The neurobehavior of adults and larval offspring was evaluated, and the levels of thyroxine (T4), triiodothyronine (T3) and neurotransmitters (acetylcholine, dopamine and gamma-aminobutyric acid) were quantified in larvae and embryos. Our results showed that TBBPA was detected in embryo and the locomotor activity of larval offspring was significantly reduced, suggesting that TBBPA can transfer to offspring and result in neurotoxicity in larval offspring. Furthermore, a reduction in T3 levels was observed in both the larvae and embryos. We also found a significantly decreased content of dopamine in larval offspring, accompanied by downregulated mRNA expression of rdr2b and drd3. Our results demonstrated that TBBPA can be transferred to offspring embryos, and subsequently induce neurotoxicity in larval offspring by affecting the amount of T3 transferred from the parents to embryos and the production of dopamine in larvae.Analytical methods were validated for the evaluation of acetaldehyde and formaldehyde, which are harmful chemicals, using solid-phase microextraction-gas chromatography/mass spectrometry in four different matrices. Typical home-cooking methods including boiling, pan-frying, and stir-frying, were applied to beef, rapeseed oil, canned pork ham, egg, and rice wine. In addition, monosaccharides, disaccharides, alanine, and glycine were heated for the formation of both aldehydes. All validation parameters, including accuracy, precision, limit of detection, limit of quantification, and uncertainty, for four different matrices were within recommended ranges, confirming the validity of the current method. Acetaldehyde contents ranged from undetectable to 17.92 μg/g and formaldehyde contents ranged from undetectable to 0.27 μg/g. Generally, boiling decreased both aldehydes except acetaldehyde in egg. Pan- and stir-frying increased both aldehyde content substantially in rapeseed oil whereas pan-frying increased acetaldehyde content in canned pork ham and egg. Fructose and sucrose produced higher content of both aldehydes than maltose and glucose when heated. Depending on food type, the cooking process had slightly different effects on the contents of acetaldehyde and formaldehyde.A photoelectrochemical (PEC) biosensor was constructed for 5-formylcytosine (5fC) nucleotide detection based on Ag2S@WS2 photoactive material and FeVO4 catalytic signal quenching. After Ag2S@WS2 was modified onto the ITO substrate surface, 5fC recognition reagent of Au@4-amino3hydrazino5mercapto-1,2,4-triazol (Au@AHMT) was further modified through electrostatic adsorption. Afterwards, based on the specific chemical reaction between -NH2 and -CHO, 5fC can be selectively recognized and captured. Subsequently, the nanoenzyme of FeVO4 was recognized based on the specific reaction between the phosphate group of 5fC nucleotide and Fe3+. Under the catalysis of FeVO4, the 4-chloro-1-naphthol in the detection solution can be oxidized to generate a precipitate, which will be retained on the electrode surface to inhibit the PEC signal. The developed method presented a widely dynamic range from 0.1 to 400 nM. The detection limit was 0.062 nM (3σ). This method also showed good detection selectivity, reproducibility and stability. The applicability was verified by investigating 5fC content change in genomic DNA of rice tissues after incubated with heavy metals. Moreover, the inhibited influence of hydrochar towards heavy metals was also assessed.A preparation of colloidal activated carbon (CAC) for phenol remediation from groundwater was introduced. The CAC prepared by a simple pulverization technique was an excellent metal-free catalyst for persulfate (PS) activation due to high contact surface area. The removal efficiency of phenol in the PS/CAC system (~100%) was higher than that in the PS/activated carbon (AC) system (90.1%) and was superior to the conventional PS/Fe2+ system (27.9%) within 30 min. The phenol removal reaction occurred both in bulk solution and at the surface of the CAC, as confirmed by Langmuir-Hinshelwood (L-H) kinetic model fitting, FT-IR, and electron spin resonance (ESR) analyses. The downsizing of particle size from AC to CAC played a critical role in the radical oxidation mechanism by leading to the formation of predominant superoxide radical (O2•-) species in the PS/CAC system. Anions NO3-, SO42-, and Cl- slightly inhibited the phenol removal efficiency, whereas CO32-, HCO3- and PO43- did not. Ferulic acid (C10H10O4) was detected as an organic byproduct of phenol oxidation.