An efficient meshless computational technique to simulate nonlinear anomalous reaction–diffusion process in two-dimensional space

Nonlinear Dynamics - In this paper, a numerical simulation of an anomalous reaction–diffusion process in two-dimensional space with a nonlinear source term is presented. An efficient and...     

Highly Sensitive Nanostructured Electrochemical Sensor Based on Carbon Nanotubes-Pt Nanoparticles Paste Electrode for Simultaneous Determination of Levodopa and Tyramine

A multicomponent electrochemical sensor, with two nanometer-scale components in sensing matrix/electrode, was used to simultaneous determination of levodopa (LD) and tyramine (TR) in pharmaceutical and diet samples. Multiwall carbon nanotubes (MWCNTs) were used as carbonaceous materials in the electrode construction. 5-amino-3',4'-dimethoxy-biphenyl-2-ol (5ADMB) was used as electron mediator and Pt nanoparticles (nPt) as a catalyst. The 5ADMB catalyzes the oxidation of LD to the corresponding catecholamine, which is electrochemically reduced back to LD. Preparation of this electrode was very simple and modified electrode showed good properties at electrocatalytic oxidization of LD and TR. Using differential pulse voltammetry (DPV), a highly selective and simultaneous determination of LD and TR has been explored at the modified electrode. Differential pulse voltammetry peak currents of LD and TR increased linearly with their concentrations at the ranges of 0.50–100.0 μM and 0.60–100.0 μM, respectively. Also, the detection limits for LD and TR were 0.31 and 0.52 μM, respectively. The electrode exhibited an efficient catalytic response with good reproducibility and stability.     

Sensitive and selective fluorescence detection of aqueous uranyl ions using water-soluble CdTe quantum dots

Herein we report a fluorescent method for sensitive and selective detection of uranyl ions using CdTe quantum dots functionalized with mercaptopropionic acid, which the fluorescence of the quantum dots could be quantitatively quenched through electron transfer mechanism. The detection limit of the method was estimated to be 4 nM, less than the maximum allowed content of 130 nM for uranyl in drinking water defined by the U.S. Environmental Protection Agency. Furthermore, the probe was successfully applied in detection of uranyl ions in real samples, demonstrating its potential practical applications for monitoring of uranyl ions in environment.     

Improve Corrosion Resistance of Zircaloy by Copper–Graphene Nanocomposite Coatings

In this study, the corrosion behavior of Zircaloy was investigated in the presence and absence of copper–graphene nanocomposites coating. The coating was prepared employing Hummers’ and electrochemical reduction methods. The morphology of copper–graphene nanocomposites coating was studied using scanning electron microscopy (SEM). Corrosion behavior was investigated employing dynamic polarization and electrochemical impedance spectroscopy (EIS) tests in a solution containing lithium hydroxide (LiOH), boric acid (H₃BO₃), and deionized water. The results showed that corrosion resistance of Zircaloy increased with introduction of copper–graphene nanocomposites coatings. The lowest corrosion rate was attained in the Zircaloy with copper–graphene nanocomposites coating (corrosion rate: 0.040 mm/year). An approximately 20 times decrease in the corrosion rate was observed in the Zircaloy with copper–graphene nanocomposites coating when compared to the un-coated Zircaloy (corrosion rate: 0.831 mm/year).

     

Low‐Cost Self‐Assembled Oxide Separator for Rechargeable Batteries

Rechargeable battery cells having a liquid electrolyte require a separator permeable to the electrolyte between the two electrodes. Because the electrodes change their volume during charge and discharge, the porous separators are flexible polymers with an electronic energy gap E_g large enough for the Fermi levels of the two electrodes to be within it. In this work, a porous film of self‐assembled SiO₂ nanoparticles is developed as the separator for a Li‐ion battery with a liquid electrolyte. This coating does not require the plasticity of a polymer membrane and has the required large E_g. If adsorbed water is removed from the SiO₂ surface, the nanoparticles bond to one another and to an oxide cathode to form a plastic self‐assembling porous layer into which the liquid electrolyte can penetrate. The Li‐ion batteries with a LiCoO₂ cathode coated with SiO₂ as a separator show similar performance to cells with a traditional polypropylene separator and improved cyclability with a reduced volume of liquid electrolyte owing to the electrolyte wetting properties of the SiO₂ nanoparticles. The SiO₂ nanoparticles are easy to prepare, cheap, and environmentally friendly.     

Photonic crystal-based permutation switch for optical networks

We present, for the first time, the design of a low-cross talk scalable permutation switch employing photonic crystal ring resonators in an optical network. Through this novel approach, the transition between different states of the \(2 \times 2\) optical switch, as the basic element, is achieved by applying different operating wavelengths. Subsequently, the shuffling mechanisms in \(3 \times 3\) and \(4 \times 4\) optical networks are realized by controlling the position of photonics crystal ring resonators. Lowest cross talk levels of 6 and 5% are obtained for “bar” and “cross” switching states, respectively.     

Comparison of Performance of Packet Scheduling Algorithms in LTE-A HetNets

The concept of usage of heterogeneous networks (HetNets) is about improving the LTE system performance by increasing the capacity and coverage of the Macro cell. In this paper, a performance comparison of various packet scheduling algorithms such as Proportional Fair, Maximum Largest Weighted Delay First and Exponential/Proportional Fair is studied in detail in the HetNets environment. The key performance indicators such as throughput, packet loss ratio, delay and fairness are considered to judge the performance of the scheduling algorithms. Various strategies such as increasing the number of Pico cells in the cell edge were used in the simulation for the performance evaluation study. The results achieved through various simulations show that adding Pico cells to the existing Macros enhances the overall system performance in addition to the various scheduling algorithms implemented in Macros. For reader’s convenience, various types of graphs have been used to represent the simulation results to better understand the performance metrics of various scheduling algorithms. Simulation results shows that overall system gain has increased because of adding Picos and thereby providing better coverage in the cell edge areas and thereby increasing the capacity of the network to provide better quality of service.     

Theoretical study of N–H· · ·O hydrogen bonding properties and cooperativity effects in linear acetamide clusters

We investigated geometry, energy, ${\nu_{{\text{N--H}}}}$ harmonic frequencies, ¹⁴N nuclear quadrupole coupling tensors, and ${n_{\rm O}\to \sigma _{{\text{N--H}}}^\ast}$ charge transfer properties of (acetamide) _n clusters, with n = 1 ? 7, by means of second-order Møller-Plesset perturbation theory (MP2) and DFT method. Dependency of dimer stabilization energies and equilibrium geometries on various levels of theory was examined. B3LYP/6-311++G** calculations revealed that for acetamide clusters, the average hydrogen-bonding energy per monomer increases from ?26.85 kJ mol^?1 in dimer to ?35.12 kJ mol^?1 in heptamer; i.e., 31% cooperativity enhancement. The n-dependent trend of ${\nu_{{\text{N--H}}}\,{and}\,^{14}}$ N nuclear quadrupole coupling values were reasonably correlated with cooperative effects in ${r_{{\text{N--H}}}}$ bond distance. It was also found that intermolecular ${n_{\rm O}\to \sigma_{{\text{N--H}}}^\ast}$ charge transfer plays a key role in cooperative changes of geometry, binding energy, ${\nu_{{\text{N--H}}}}$ harmonic frequencies, and ¹⁴N electric field gradient tensors of acetamide clusters. There is a good linear correlation between ¹⁴N quadrupole coupling constants, C _Q (¹⁴N), and the strength of Fock matrix elements (F _ij ). Regarding the ${n_{\rm O}\to \sigma_{{\text{N--H}}}^\ast}$ interaction, the capability of the acetamide clusters for electron localization, at the N–H· · ·O bond critical point, depends on the cluster size and thereby leads to cooperative changes in the N–H· · ·O length and strength, N–H stretching frequencies, and ¹⁴N quadrupole coupling tensors.