Junkerbille8028

However, the highest (56.38%) pyrene removal efficiency (PRE) was achieved near electrodes due to the synergistic effect of electric filed and PDM, and PRE was positively correlated with the PDM number in soil away from electrodes. The increasing application of Quantum Dots (QDs) is cause of concern for the potential negative effects for the ecosystem, especially in soils that may act as a sink. In this study, soil leaching experiments were performed in quartz sand packed columns to investigate the behavior of core-shell CdSe/ZnS QDs coated with either small ligands (TGA-QDs) or more complex polymers (POAMA-QDs). Fluorescence emission was compared to mass spectrometric measurements to assess the nanoparticles (NPs) state in both the leachate (transported species) and porous media (deposited amounts). Although both QDs were strongly retained in the column, large differences were observed depending on their capping ligand stability. Specifically, for TGA-QDs elution was negligible and the retained fraction accumulated in the top-columns. Furthermore, 74% of the NPs were degraded and 38% of the Se was found in the leachate in non-NPs state. Conversely, POAMA-QDs were recovered to a larger extent (78.1%), and displayed a higher transport along the soil profile. Further experiments with altered NPs showed that homo-aggregation of the QDs prior injection determined a reduced mobility but no significant changes in their stability. Eventually, ageing of the NPs in the column (15 days) caused the disruption of up to 92% of the original QDs and the immobilization of NPs and metals. These results indicate that QDs will accumulate in top-soils, where transformations phenomena will determine the overall transport, persistency and degradation of these chemicals. Once accumulated, they may act as a source for potentially toxic Cd and Se metal species displaying enhanced mobility. Hydrochar, the product of hydrothermal carbonization of biomass, is a sustainable alternative to other carbonaceous environmental sorbents. However, its use has been limited due to its low surface area. A one-pot biomass/metal salt co-hydrothermal synthesis method might improve its sorptive properties while retaining its efficient production characteristic. Thus, bamboo sawdust and zinc chloride (ZnCl2) were combined in a hydrothermal reactor (200 °C, 7 h) for preparing modified hydrochar. Compared to the non-modified hydrochar, the hydrochar produced with the addition of ZnCl2 during hydrothermal treatment was more fully carbonized (C content increased from 54% to 64%), of higher surface area after acid washing (30 versus 1.7 m2 g-1), and enriched in O-containing functional groups and of greater aromaticity (according to FTIR and XRD analysis). Because of these improved properties, Methylene blue adsorption capacity of the modified hydrochar increased by nearly 90% and by 257% after it was rinsed with acid. This study highlights the potential of this one-pot co-hydrothermal treatment of biomass in presence of metal salt to provide a simple and effective hydrochar with properties suitable for environmental remediation and water treatment. Two 1, 8-naphthalimide derivatives, 2-(2-ethylhexyl)-6-(2-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)benzylidene)hydrazinyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione (named as NAOZ) and 2-(2-ethylhexyl)-6-(2-(4-(5-phenyl-1,3,4-thiadiazol-2-yl)benzylidene)hydrazinyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione (named as NATZ), containing hydrazone and thiadiazole/oxadiazole, were successfully synthesized. Compounds NAOZ and NATZ were further served as efficient reversible colorimetric and fluorescent chemosensors for fluoride ion over a wide range of other anions (Cl-, Br-, I-, NO3-, ClO4-, HSO4-, BF4-, and PF6- as their (C4H9)4N+ salts) because fluoride ion can deprotonate the hydrazone moiety, leading to the observed long-wavelength color change. Interestingly, CO2 can recover the charge transfer (CT) absorption and photoluminescence intensities of compound NAOZ/NATZ + F-, because CO2 can react with a small amount of water to form acids, which can provide protons. V.Remote identification of illegal plantations of Cannabis sativa Linnaeus is an important task for the Brazilian Federal Police. The current analytical methodology is expensive and strongly dependent on the expertise of the forensic investigator. A faster and cheaper methodology based on automatic methods can be useful for the detection and identification of Cannabis sativa L. in a reliable and objective manner. In this work, the high potential of Near Infrared Hyperspectral Imaging (HSI-NIR) combined with machine learning is demonstrated for supervised detection and classification of Cannabis sativa L. This plant, together with other plants commonly found in the surroundings of illegal plantations and soil, were directly collected from an illegal plantation. find more Due to the high correlation of the NIR spectra, sparse Principal Component Analysis (sPCA) was implemented to select the most important wavelengths for identifying Cannabis sativa L. One class Soft Independent Class Analogy model (SIMCA) was built, considering just the spectral variables selected by sPCA. Sensitivity and specificity values of 89.45% and 97.60% were, respectively, obtained for an external validation set subjected to the s-SIMCA. The results proved the reliability of a methodology based on NIR hyperspectral cameras to detect and identify Cannabis sativa L., with only four spectral bands, showing the potential of this methodology to be implemented in low-cost airborne devices. Seeking novel strategies for designing superatoms is of significance for the potential applications in cluster-assembled nanomaterials. Herein, by employing the density functional theory (DFT) calculations, the effect of the oriented external electronic field (OEEF) on the electronic and photoelectron spectroscopic properties of the superatom-polymeric Zr3O3 cluster was explored. We present the evidence that the increment of the OEEF along all directions results in the remarkable enhancement of the electron affinity (EA) of Zr3O3, which turns it into superhalogen with an EA value of 4.02 eV under 0.020 au OEEF along +y direction. Strikingly, this EA value is larger than that of any halogen atoms in the periodic table. The downward shift of the electronic spectrum induced by the OEEF was confirmed to be the origin of the observed EA enhancement. Furthermore, the investigation of the OEEF's effect on the molecular orbitals (MOs) and photoelectron spectra (PES) of the cluster reveals that the OEEF could alter the electron distribution as well as promoting the blue shift of the PES without changing the spacings between different energetic levels.