Alstonmays2535

However, low-salinity water thin-films are stable due to the repulsive electric double-layer forces, leading to less pressure drop during mobilization of the blob. The novelty of this work lies in efficiently capturing the nanoscale effects of the electric double-layer in pore-scale multiphase flow displacements. Our quantitative investigations provide fundamental insights into the efficiency of low-salinity waterflooding. Metal-organic frameworks (MOFs) with porous structures, high surface areas, diverse compositions, and functional linkers are promising materials and good carriers for building high-performance devices. In this work, uniform cobalt-doped ZnO nanoparticles (Co-doped ZnO NPs) derived from a MOF mold were synthesized, demonstrating the first example of synthesizing doped semiconductor metal oxide nanostructures using such strategy. The synthesis method produced Co-doped ZnO NPs that had a controllable doping mode, adjustable surface status, good dispensability, ferromagnetism and catalytic activity. The Co-doped ZnO NPs were evaluated as a sensing material for diabetes biomarker detection; the obtained sensors showed a high response to trace acetone (18.2 at 5 ppm), fast response/recovery times, a low detection limit (170 ppb), and long-term stability for 4 months. The enhanced sensing performance can be attributed to the increased number of active sites, additional impurity energy levels, and the catalytic ability of elemental Co. Moreover, the optimized sensor could distinguish between simulated diabetic breath and healthy human breath samples. The MOF-derived Co-doped ZnO NPs are a good candidate for the low-cost and noninvasive diagnosis of diabetes, and the proposed synthesis strategy can be extended to other types of extrinsically doped oxide materials. Currently, the synthesis of nanostructured inorganic materials with tunable morphology is still a great challenge. In this study, almond skin extract was employed for the biogenic synthesis of selenium nanoparticles with tunable morphologies such as rods and brooms. The effects of various synthesis parameters on morphologies were investigated using UV-Visible spectroscopy and scanning electron microscopy (SEM) which indicated that selenium brooms (SeBrs) were best synthesized using almond skin extract and optimized conditions of SeO2, ascorbic acid, pH, incubation temperature and time. Based on these results, the mechanism of SeBrs synthesis is proposed as having involved four stages such as nucleation, self-assembly, Ostwald ripening, and decomposition. Further, the test of antibacterial activity together with minimum inhibitory concentrations and minimum bactericidal concentrations indicated the selective, specific and good activity against B. subtilis. In addition, in situ coating of SeBrs on cotton fabric and its investigation by SEM demonstrated successful coating. Evident from plate-based assay and study of growth kinetics, coated fabric exhibited excellent anti-B. subtilis activity which demonstrated that biogenic SeBrs can be employed to coat cotton fabrics that can be used in operation theatres to reduce the episodes of Bacillus related Bacteraemia. Nitrogen (N) doping of porous carbon materials is an effective strategy for enhancing the electrochemical performance of electrode materials. Herein, we report on ex-situ (post) nitrogen-doped porous carbons prepared using a biomass waste, peanut shell (PS) as a carbon source and melamine as the nitrogen source. The synthesis method involved a two-step mechanism, initial chemical activation of the PS using KOH and post N-doping of the activated carbon. The effect of the activating agent/precursor ratio and the ex-situ N-doping on the structural, textural, electrochemical properties of the porous carbons was studied. The ex-situ N-doped porous carbon with an optimum amount of KOH to PS exhibited the best capacitance performance with a specific surface area (SSA) of 1442 m2 g-1 and an enriched nitrogen content (3.2 at %). The fabricated symmetric device exhibited a 251.2 F g-1 specific capacitance per electrode at a gravimetric current of 1 A g-1 in aqueous electrolyte (2.5 M KNO3) at a wide cell voltage of 2.0 V. A specific energy of 35 Wh kg-1 with a corresponding specific power of 1 kW kg-1 at 1 A g-1 was delivered with the device still retaining up to 22 Wh kg-1 and a 20 kW kg-1 specific power even at 20 A g-1. Moreover, long term device stability was exhibited with an 83.2% capacity retention over 20 000 charge/discharge cycles and also a good rate capability after 180 h of floating at 5 A g-1. This great performance of the symmetric supercapacitor can be correlated to the surface porosity and post nitrogen-doping effect which increased the electrochemically-active sites resulting in a remarkable charge storage capability. A multi-dimensional (1D/2D/3D) carbon/g-C3N4 composite photocatalyst (CCN) was successfully prepared by a facile method with carbon from cheap absorbent cotton wool. The activities and stabilities of CCN were evaluated by photo-degrading Rhodamine B (RhB) under visible light irradiation. The effect of carbon content in composite on the catalytic activities was investigated. The results show that a good interfacial contact can be observed between g-C3N4 and carbon materials in CCN. It reveals an enhanced photocatalytic activity in photocatalytic decomposition of RhB compared with g-C3N4. The carbon content has obvious effect on the performance of CCN, and the optimal carbon content in CCN is 1 wt% (CCN1.0). The first-order rate constant (k) of CCN1.0 is approximately 5.5 and 3.4 times those of g-C3N4 and AC1.0/g-C3N4. The CCN1.0 catalyst also shows the excellent photocatalytic stability in the recycling experiments. The enhanced catalytic performance of CCN is mainly due to an increase in electron-hole pair separation efficiency and visible light adsorption after coupling carbon. The hole and •O2- radicals are the main active species, and •O2- plays a more important role than h+. The photocatalytic mechanism over CCN1.0 was proposed. This work will provide a new insight to prepare highly-efficient g-C3N4-based photocatalysts. BAY-805 in vivo