Patrickchandler4440

Copyright © 2020 American Chemical Society.Reliable hardware connectivity is vital in heterogeneous integrated systems. For example, in digital microfluidics lab-on-a-chip systems, there are hundreds of physical connections required between a microelectromechanical fabricated device and the driving system that can be remotely located on a printed circuit board. Unfortunately, the connection reliability cannot be checked or monitored by vision-based detection methods that are commonly used in the semiconductor industry. Therefore, a sensing platform that can be seamlessly integrated into existing digital microfluidics systems and provide real-time monitoring of multiconnectivity is highly desired. Here, we report an impedance sensing platform that can provide fast detection of a single physical connection in timescales of milliseconds. Once connectivity is established, the same setup can be used to determine the droplet location. The sensing system can be scaled up to support multiple channels or applied to other heterogeneously integrated systems that require real-time monitoring and diagnostics of multiconnectivity systems. Copyright © 2020 American Chemical Society.The main objective of this study is to evaluate the effect of the textural properties and surface chemical nature of silica nanoparticles obtained from different synthesis routes and silicon precursors, on their interactions with asphaltenes and further viscosity reduction of heavy crude oil (HO). Four different SiO2 nanoparticles were used, namely, commercial fumed silica nanoparticles (CSNs) and three in-house-synthesized nanoparticles (named based on the silicon source) modifying the silicon precursor sodium silicate (SNSS), tetraethylorthosilicate (TEOS) (SNT), and rice husk (SNRH). The nanomaterials were characterized through dynamic light scattering (DLS), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, N2 physisorption (S BET), atomic force microscopy (AFM), and X-ray photoelectron (XP) spectroscopy (XPS). Actidione The adsorption of asphaltenes over the different nanoparticles was evaluated at a concentration of 1000 mg·L-1 in toluene. The asphaltene-nanoparticle interact, the oxygen amount related to silanol groups, estimated by the XPS analysis, showed a direct relation regarding adsorption capacity and further HO viscosity reduction. link2 Copyright © 2020 American Chemical Society.Efficient structured catalysts of partial methane oxidation into synthesis gas were obtained by electrochemical modification of the surface of sintered FeCrAl alloy fibers in an ionic liquid BMIM-NTf2 with further introduction of platinum nanoparticles. It was shown that etching and electrochemical modification of sintered FeCrAl alloy fibers result in a decrease of the surface aluminum content. With an increase of the reaction temperature to 900 °C, the methane conversion reaches 90% and the selectivity to CO increases significantly to achieve 98%. The catalysts with a Pt loading of 1 × 10-4 wt % demonstrate high activity and selectivity as well as TOF in synthesis gas production by the CH4 + O2 reaction at 850-900 °C. To trace the composition and structure evolution of the catalysts, XRD and SEM methods were used. Copyright © 2020 American Chemical Society.Mass transfer processes are one of the most important operations in chemical, biochemical, and food industries worldwide. In the processes that are controlled by the gas-liquid mass transfer rate, the volumetric mass transfer coefficient k L a becomes a crucial quantity. The dataset was measured with the aim to create a correlation for k L a prediction in a non-coalescent batch under the wide range of experimental conditions. The dynamic pressure method, which was reported as physically correct in the past, was chosen to be the method for experimental determination of k L a. Our previous work targeted the k L a dependencies in viscous and coalescent batches resulting in correlations that are viable for the broad range of process conditions. We reported that the best-fit correlation is based on the hydrodynamic parameter circumferential velocity of impeller blades in the case of non-coalescent liquids in the vessel equipped by single or multiple impellers at a constant D/T ratio (diameter of the impeller to the inner diameter of the tank). Now, we focus on the influence of various impeller diameters on transport characteristics (mainly k L a) in a non-coalescent batch. The experiments are carried out in a multiple-impeller vessel equipped with Rushton turbines (of four diameters) and in both laboratory and pilot-plant scales. Various impeller frequencies and gas flow rates are used. We examine the suitability of the hydrodynamic description, which was reported in the past, to predict k L a also when the D/T ratio changes. We show that the correlation based on the energy dissipation rate better fits the experimental data and predicts k L a values more accurately in the case of varying D/T values. This correlation could be adopted in the design and scale-up of agitated devices operating with non-coalescent batches. Copyright © 2020 American Chemical Society.Methyl palmitate (or triglyceride) was converted into C15 olefin with remarkable selectivity using nickel-molybdenum oxides on the mesoporous titanosilicate support. The olefin has one carbon atom less than the acid portion of the ester. A new catalyst NiMoK/TS-1 was synthesized in which the effect of acidity of supports and molybdenum loading on the decarboxylation conversion along with product selectivity was investigated in methyl palmitate conversion into C15 olefin. The prepared catalysts were analyzed using ammonia-temperature-programmed desorption (NH3-TPD), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) techniques. The reaction was carried out using a vapor-phase fixed-bed downflow reactor system at atmospheric pressure. The NiMoK/TS-1 catalyst at a weight hourly space velocity (WHSV) of 5.6/h was found to be selective toward C15 olefin. The catalyst was stable up to 15 h, and it can be regenerated with no considerable decrease in the activity even after fourth reuse. Beyond 653 K, the conversion of methyl palmitate increased but the selectivity for C15 products and C15 olefin was decreased. Copyright © 2020 American Chemical Society.Shale gas has attracted increasing attention as a potential alternative gas in recent years. Because a large fraction of gas in shale formation is in an adsorbed state, knowledge of the supercritical methane adsorption behavior on shales is fundamental for gas-in-place predictions and optimum gas recovery. A practical model with rigorous physical significance is necessary to describe the methane adsorption behavior at high pressures and high temperatures on shales. In this study, methane adsorption experiments were carried out on three Lower Silurian Longmaxi shale samples from the Sichuan Basin, South China, at pressures of up to 30 MPa and temperatures of 40, 60, 80, and 100 °C. The simplified local density/Elliott-Suresh-Donohue model was adopted to fit the experimental data in this study and the published methane adsorption data. The results demonstrate that this model is suitable to represent the adsorption data from the experiments and literature for a wide range of temperatures and pressures, and the average absolute deviation is within 10%. The methane adsorption capacity of the Longmaxi shale exhibited a strong linear positive correlation with the total organic carbon content and a linear negative correlation with increasing temperature. The rate of decrease in the methane adsorption capacity with swing temperature increased with the total organic carbon content, indicating that the organic matter is sensitive to temperature. Copyright © 2020 American Chemical Society.Graphene oxide-silver nanocomposite (GO-Ag) was fabricated via the sonochemical method, which shows unique physiochemical properties. Graphene oxide (GO) and silver nanoparticles (AgNPs) were synthesized by modified Hummer's and Chemical reduction methods, respectively. The synthesized nanocomposite was characterized using powder X-ray diffraction, Raman spectroscopy, and Fourier-transform infrared spectroscopy. link3 The surface morphology of synthesized nanoparticles was studied using scanning electron microscopy and transmission electron microscopy. The thermoluminescence property of the nanocomposite was analyzed by irradiating the samples in gamma radiation at 1 kGy. Electrochemical reversibility of the GO-Ag nanocomposite was examined by cyclic voltammetry. The photocatalytic application of the nanocomposite was studied using degradation of methylene blue dye. Results reveal that doping of AgNPs on the GO surface not only improves its dye degradation property but also enhances its thermoluminescence property. This knowledge will be helpful in determining the antibacterial property of the GO-Ag nanocomposite in the future. Copyright © 2020 American Chemical Society.The reaction mechanism involved in the decomposition of ammonium nitrate (AN) in the presence of CaCO3 and CaSO4, commonly used for stabilization and the reduction of explosivity properties of AN, was theoretically investigated using a computational approach based on density functional theory. The presented computational results suggest that both carbonate and sulfate anions can intercept an acid proton from nitric acid issued from the first step of decomposition of AN, thus inhibiting its runaway decomposition and the generation of reactive species (radicals). The reaction then leads to the production of stable products, as experimentally observed. Our modeling outcomes allow for tracing a relationship between the capability of proton acceptance of both carbonate and sulfate anions and the macroscopic behavior of these two additives as inhibitor or inert in the AN mixture. Copyright © 2020 American Chemical Society.This study aimed to develop a highly efficient nanofilter for capturing fine particles using electrostatic forces. Poly(vinyl alcohol) (PVA), a water-soluble synthetic polymer, was selected as the main component of the filter because it can be easily fabricated by electrospinning. Titanium dioxide (TiO2) nanopowder with an anatase structure was applied to the nanofilters as it has the highest photocatalytic activity among the existing photocatalysts. PVA nanofilters fabricated by electrospinning could still be dissolved in water by hydrolysis. Therefore, heat treatment was performed to make the nanofilters stable, thereby forming C=O bonds by keto-enol tautomerization. Structural changes in the PVA nanofilter before and after heat treatment were investigated by X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) analysis. As the TiO2 concentration increased, the fiber diameter of the PVA nanofilter decreased and a homogeneous fiber was obtained. The filtration efficiency and pressure drop also improved significantly, compared to those of the PVA-only nanofilter. Moreover, we observed eco-friendly decomposition of the PVA/TiO2 nanofilter into water and carbon dioxide by a photocatalytic reaction under UV irradiation. Copyright © 2020 American Chemical Society.