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Kinetic studies of dye removal from aqueous solutions by the as-prepared cross-linked networks indicate that the dye removal proceeds via pseudo-second-order kinetics. The study of adsorption isotherm of the removal process indicates that the adsorption follows the Langmuir isotherm model. In this present work, we have thoroughly evaluated the influence of PEG chain length on several physical properties and toxic cationic dye removal efficiencies of thiol-norbornene photo-cross-linked networks. Copyright © 2020 American Chemical Society.Investigating how grain structure affects the functional properties of nanoparticles requires a robust method for nanoscale grain mapping. In this study, we directly compare the grain mapping ability of transmission Kikuchi diffraction (TKD) in a scanning electron microscope to automated crystal orientation mapping (ACOM) in a transmission electron microscope across multiple nanoparticle materials. Analysis of well-defined Au, ZnO, and ZnSe nanoparticles showed that the grain orientations and GB geometries obtained by TKD are accurate and match those obtained by ACOM. For more complex polycrystalline Cu nanostructures, TKD provided an interpretable grain map whereas ACOM, with or without precession electron diffraction, yielded speckled, uninterpretable maps with orientation errors. Acquisition times for TKD were generally shorter than those for ACOM. Our results validate the use of TKD for characterizing grain orientation and grain boundary distributions in nanoparticles, providing a framework for the broader exploration of how microstructure influences nanoparticle properties. Copyright © 2020 American Chemical Society.We developed a novel substrate for the collection of volatile organic compounds (VOCs) emitted from either living or dried plant material to be analyzed by surface-enhanced Raman spectroscopy (SERS). We demonstrated that this substrate can be utilized to differentiate emissions from blends of three teas, and to differentiate emissions from healthy cotton plants versus caterpillar-infested cotton plants. The substrate we developed can adsorb VOCs in static headspace sampling environments, and VOCs naturally evaporated from three standards were successfully identified by our SERS substrate, showing its ability to differentiate three VOCs and to detect quantitative differences according to collection times. In addition, volatile profiles from plant materials that were either qualitatively different among three teas or quantitatively different in abundance between healthy and infested cotton plants were confirmed by collections on Super-Q resin for dynamic headspace and solid-phase microextraction for static headspace sampling, respectively, followed by gas chromatography to mass spectrometry. Our results indicate that both qualitative and quantitative differences can also be detected by our SERS substrate although we find that the detection of quantitative differences could be improved. Copyright © 2020 American Chemical Society.A green composite of organically modified bentonite supported by Co3O4 nanoparticles (OB/Co) was successfully fabricated and investigated as a potential eco-friendly, low-cost adsorbent and photocatalyst for promising removal of both malachite green dye (MG.D) and Cr(VI) ions. The composite showed high adsorption properties and achieved experimental q max values of 223 and 139 mg/g for MG.D and Cr(VI) after equilibration times of 360 min and 480 min for the inspected contaminants, respectively. The kinetic and equilibrium inspection reflected the best description of their adsorption behaviors by the pseudo-first-order kinetic model and the Langmuir isotherm model, respectively. This revealed favorable and homogeneous uptake of both MG.D and Cr(VI) in a monolayer form with theoretical Langmuir q max values of 343.6 and 194.5 mg/g, respectively. The theoretical adsorption energies of MG.D (0.6 kJ/mol) and Cr(VI) (0.5 kJ/mol) from the Dubinin-Radushkevich (D-R) model revealed physisorption properties that might be resulted from some types of Coulombic attractive forces, achieving theoretical q max values of 226.5 and 144.6 mg/g, respectively. The suggested adsorption mechanism was confirmed by the main mathematical parameters of thermodynamic studies that revealed physical, spontaneous, and exothermic uptake processes. Also, the composite showed high photocatalytic performance under visible light, which resulted in a 100% removal percentage of 100 mg/L of MG.D and Cr(VI) after about 180 and 240 min, respectively, from the adsorption equilibrium time. Copyright © 2020 American Chemical Society.How the methyl torsion transition energy in unsaturated systems is affected by its environment is investigated. selleck inhibitor It is strongly influenced by both its immediate neighborhood, (the number of methyl groups present in the molecule) and the intermolecular interactions. It is clear that the intermolecular interactions have a major influence on the torsion transition energy, as demonstrated unambiguously previously for mesitylene and also seen here for other systems. In part, this may be caused by the fact that the methyl torsion is rarely a pure mode (unless enforced by symmetry). Where the crystal structure is available, the assignments have been supported by CASTEP calculations of the unit cell. The agreement between the observed and calculated spectra is generally good, although not perfect, toluene being a case in point, and highlights just how demanding it is to obtain accurate transition energies for low energy modes. The disagreement between observed and calculated inelastic neutron scattering spectra for meta-xylene and 9,10 dimethylanthracene is so severe that it would suggest that there are additional phases to those presently known. Comparison between the full periodic calculations and those for the isolated molecule shows that intermolecular interactions raise the methyl torsion transition energy by at least 8% and in some cases by more than 50%. The presence of more than one methyl group in the molecule generally raises the average torsion energy from the less then 100 cm-1 seen for single methyl groups to 150-200 cm-1. Copyright © 2020 American Chemical Society.