Large-area Si-doped graphene (SiG) is controllably synthesized for the first time. A much-enhanced molecular-sensing performance is achieved when SiG is used as a probing surface. This will open up opportunities for developing high-performance sensors that are able to detect trace amounts of organic and fluorescent molecules. Furthermore, many fascinating properties predicted by theoretical calculations can be tested based on the as-synthesized SiG.
Macroporous separators are critical components in liquid electrolyte batteries. Besides preventing physical contact between electrodes, they enable free ionic transport, electronic isolation and thermal shutdown. Nevertheless, separators also increase electrical resistance and takes up limited space inside the battery, affecting ionic conductivity. Widely used in lithium-ion batteries, commercial polyolefinbased separators operate in a limited temperature range, mainly ranging from À20 C to +60 C. The purpose of this contribution is to assess the possibility to use these separators in lithium-ion batteries operating at extended temperatures, i.e. between À20 C and 120 C. For this purpose, four commercially available macroporous separators based on polyethylene and polypropylene, were investigated. To determine the effect of temperature on their performance, they were aged for one week at 120 C. Evolution of their morphology and thermomechanical behavior was investigated using XRD, SEM, DSC, TGA and DMA. The thermal aging impact on the ionic conductivity was also investigated using LP30 1 as reference electrolyte. Thermal aging, i.e. partial clogging of the porosity, was found to have significant effects mainly on mechanical strength, morphology and conductivity.
Local glass transition temperatures (T g ) have been measured in the interfaces of solution blended silica/poly(methyl methacrylate) (PMMA) nanocomposites using florescence spectroscopy and compared with T g measured by differential scanning calorimetry (DSC). It was found that the two types of measurements yielded significantly different information. Combinations of silanes and poly(propylene glycol)-based molecular spacers bound to fluorophores were covalently linked to the surface of the nanoparticles, allowing for variation of the fluorophore response with respect to the distance from the nanofiller surface. Increases in the bulk T g from the neat PMMA value were found upon the addition of nanofillers, but were independent of the nanofiller concentration when the filler concentration was above 2% by weight. Furthermore, as the size of the grafted molecular spacer was increased, T g values were found to decrease and approach T g of the neat PMMA.Owing to variable conformations of the spacers, an effective distribution of fluorophore-silica distances exists, which influences the fluorophores' response to the transition.
Fluorescence labeling was used as a tool for the interfacial characterization of nanocom-posites. The solvatochromic probe dansyl chloride was employed as interfacial reporter in epoxy/silica nanocomposites. Molecular spacers (organosiloxanes and polyetheramines) of different lengths were used to vary the location of the chromophore at the interface. The steady state and time resolved fluorescent responses reflect a rigid polar interface. Fluores-cence changes during heating at a constant rate were analyzed for determining the local glass transition (T g ) at the interface region. The fluorescence results were then compared to the T g obtained from differential scanning calorimetry and the results showed the existence of a gradient interface of a few nanometers thick having different properties than the bulk matrix. The thickness of this interface is small but its altered dynamics due to strong interactions with the nanofiller spreads its influence throughout the whole matrix.
Millimeter‐size beads of gelatin are manufactured by dripping process to give enzyme supports qualified for micropollutants biodegradation in alternative wastewater treatment. The bead diameter is dependent on the tip diameter, the gelatin solution viscosity and the swelling of polymer chains in the collecting bath. Chemical crosslinking was performed with glutaraldehyde using optimal concentration to give mechanical and thermal properties suitable for application in stirred reactor in aqueous medium. Laccases from Trametes versicolor are grafted on the gelatin beads with glutaraldehyde. Sixty percentage of the initial enzymatic activity, evaluated by the oxidation of 2′‐Azino‐bis(3‐ethylbenzothiazoline‐6‐sulfonic acid)diammonium salt (ABTS) is maintained after 10 successive cycles of reaction. Thermal stability at 60°C of immobilized biocatalysts is improved when compared to free enzymes (45% vs 10% of relative activity after 6 h of incubation). The simplicity of the procedure to form gelatin beads and their properties make them promising bio‐based and biodegradable support for enzyme immobilization.
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