Investigation of Reflectance Properties in 1D Ternary Annular Photonic Crystal Containing Semiconductor and High-<Emphasis Type="Italic">T</Emphasis><Subscript><Emphasis Type="Bold">c</Emphasis></Subscript> Superconductor

In this paper, we present the theoretical investigation and study of reflectance properties in a 1D ternary annular photonic crystal (TAPC) containing a semiconductor and a high-temperature superconductor. The proposed structure consists of alternate layers of indium nitride (InN), Bi₂Sr₂CaCu₃O₈ (BSCCO), and air placed in free space. A reflectance spectrum of the TAPC is obtained by employing the transfer matrix method (TMM) in the cylindrical waves for both transverse electric (TE) and transverse magnetic (TM) polarized waves. From the study of reflectance spectra, it is observed that the reflection band of the annular photonic crystal depends on the azimuthal mode number m in addition to other parameters. It is found that for azimuthal mode number m = 0, the width of the reflection band of the annular photonic crystal is the same as that of a planar photonic crystal (PPC). When the azimuthal mode number increases, the width of the reflection band increases at higher m values (m >5) for TE waves. In the case of the TM wave, it is interesting to observe that a superpolariton gap is created for a higher value of the azimuthal number (m >0). Further, we see the effect of the starting radius (ρ ₀) on the reflection band of the TAPC structure at the given m number for both TE- and TM-polarized waves. Finally, the effect of temperature on the reflectance spectra for both TE and TM waves at the given ρ ₀ and azimuthal mode has been studied.     

DF-LDA tree: a nonlinear multilevel classifier for pattern recognition

This article presents a new nonlinear classifier by arranging linear classifiers in a tree structure. The proposed classifier, called the direct fractional-step linear discriminant (DF-LDA) tree, adopts a tree structure containing a DF-LDA at each node. The structure of the tree classifier evolves as the training proceeds, so there is no need to decide any parameters as a priori. Due to the many DF-LDAs arranged in the tree structure, classification performance of the proposed classifier is improved over single-shot DF-LDA. The proposed DF-LDA tree is tested on various synthetic and real datasets. Experimental results show that the proposed classifier leads to very satisfactory results in terms of classification accuracy.     

Intelligent power management in micro grids with EV penetration

Large deployment of Electric Vehicles (EVs) adds new challenges in the operation of a microgrid. Assuming that a number of EV owners allow their batteries to charge when their cars are parked, this paper proposes an approach that aims to find suitable individual active power set-points corresponding to the hourly charging rate of each EV battery connected to the microgrid. A multi agent system based controller is designed to find these active power set points for optimal power management of EVs, distributed energy resources in the microgrid, and the loads.     

Electrochemical studies of ferrocene in a lithium ion conducting organic carbonate electrolyte

We carried out a detailed study of the kinetics of oxidation of ferrocene (Fc) to ferrocenium ion (Fc⁺) in the non-aqueous lithium ion conducting electrolyte composed of a solution of 1 M LiPF₆ in 1:1 EC:EMC solvent mixture. This study using cyclic (CV) and rotating disk electrode (RDE) voltammetry showed that the Fc⁰/Fc⁺ redox couple is reversible in this highly concentrated electrolyte. The ferrocene and ferrocenium ion diffusion coefficients (D) were calculated from these results. In addition, the electron transfer rate constant (k⁰) and the exchange current density for the oxidation of ferrocene were determined. A comparison of the kinetic data obtained from the two electrochemical techniques appears to show that the data from the RDE experiments are more reliable because they are collected under strict mass transport control. A Tafel slope of c.a. 79 mV/decade and a transfer coefficient α of 0.3 obtained from analysis of the RDE data for ferrocene oxidation suggest that the structure of the activated complex is closer to that of the oxidized specie due to strong interactions with the carbonate solvents. The experiments reported here are relevant to the study of redox reagents for the chemical overcharge protection of Li-ion batteries.     

Extractability and phytotoxicity of heavy metals present in petrochemical industry sludge

Bioavailability of heavy metals present in industrial sludges and their subsequent phytotoxicity are crucial parameters to assess the associated health hazards and suitability for land application. The present study is an effort to determine the extractability of heavy metals present in different phases of the sludges, coming out of two different operations involved in petrochemical industry viz. spent caustic treatment (SCT) and waste water treatment (WWT) following the BCR sequential extraction procedure. The maximum amount of Cd and Cu was found associated with oxidizable phase, whereas Cr and Ni were best recovered in residual fractions of both the sludges. Maximum Pb was recovered in oxidizable and residual phase in the WWT and SCT sludges, respectively. The stabilization treatment undergone by sludges strongly influenced the heavy metal distribution and the phases to which they were associated. The total metal concentration in both the sludges did not exceed the limit set out by the European Legislation and was found as Cd = 0.449, Pb = 3.340, Ni = 6.530, Cr = 21.087, & Cu = 27.129 μg g^?1 and Cd = 0.549, Pb = 5.664, Ni = 7.161, Cr = 27.096, & Cu = 35.479 μg g^?1 in the SCT and WWT sludges, respectively. Phytotoxicity of the sludges was assessed against the germination index and the relative root and shoot growth. Sludge leachates did not adversely affect the seed germination and the early seedling growth of Mung (Phaseolus mungo) and Gram (Cicer arietinum), indicating that these metals were concentrated in the non-bioavailable fractions of sludges.     

Oligoaniline intermediates in the aniline-peroxydisulfate system

Chemical oxidative polymerization of aniline using peroxydisulfate oxidant in aqueous pH 2.5–10.0 buffers yields electrically insulating brown powders that are believed to be mixtures of Michael-type adducts of benzoquinone monoimine and aniline at various stages of hydrolysis. A spectroscopically similar product is formed when solid 1,4-benzoquinone is added to an aqueous solution of aniline at room temperature in the absence of peroxydisulfate. This suggests that the peroxydisulfate oxidant in the aniline/S₂O₈^2? system provides a pathway for the formation of benzoquinone monoimine as an intermediate. Benzoquinone monoimine intermediate could be formed as a result of a Boyland–Sims rearrangement of aniline proceeding via the intermediacy of p-aminophenyl sulfate. Benzoquinone monoimine undergoes a series of conjugate 1,4-Michael-type addition/reoxidation/coupling steps with aniline or p-aminophenyl sulfate yielding the oligoaniline product. The precipitate that is isolated is also in the midst of two simultaneous pH dependent hydrolysis reactions: (i) hydrolysis of the imine groups to quinone, and (ii) hydrolysis of arylsulfates to phenols. The ratio of hydrolysis in each case was determined by the C/N ratio and sulfur elemental analysis values yielding analytical data that is consistent with experimentally determined values and also with our proposed reaction scheme. These findings offer a rationale for the high C/N ratios (>6.0) frequently observed in these systems while tracing the genesis of the residual sulfur in the product to unhydrolyzed arylsulfate. The oligoaniline product has previously been reported to have a novel poly-aza structure consisting of continuously linked –N–N–N– bonds, and alternately also reported to consist of phenazine-type linkages. This study is consistent with the latter and describes a pathway to phenazine coupling through a second and third stage hydrolysis of the arylsulfate and reoxidation with peroxydisulfate. There is no pathway for the formation of linear –N–N–N– linkages in the aniline/benzoquinone adduct and the striking similarity between its spectroscopic properties and the aniline/S₂O₈^2? adduct suggests that it is not a preferred pathway under these experimental conditions.     

Effects of various hydrocarbons on micellar growth

The effect of aliphatic and aromatic hydrocarbons on surfactant micellar growth has been investigated by viscosity measurements at 40°C. Aqueous and aqueous KBr (0.1 M) solutions of 0.1 M cetylpyridinium bromide (CPB) showed that the viscosity behavior changed substantially in the presence of KBr. This is attributed to favorable conditions produced by KBr that assist micellar growth by addition of hydrocarbons. Reasons for the effectiveness of the solubilized hydrocarbons are suggested and supported by theoretical arguments. The causes of viscosity decrease at higher aromatic hydrocarbon concentrations are also explained. Micellar growth with soluble aromatic/aliphatic hydrocarbons could also be initiated if a moderate salt concentration is present in CPB micellar solutions. The chainlength, solubilization site, and molar volume of the soluble hydrocarbons all affect the bulk viscosity of the solution. Such surfactant and hydrocarbon combinations may find use in micellar-enhanced ultrafiltration of benzene and its derivatives, but it should be kept in mind that micellar shape may change and be more curved at higher benzene derivative concentrations.     

On the solution and applicability of bivariate population balance equations for mixing in particle phase

New benchmarks are used to test two classes of discretization methods available in the literature to solve bivariate population balance equations (2-d PBEs), and the applicability of these mean-field equations to finite size systems. The new benchmarks, different from the extensions of their 1-d counterparts, relate to prediction of kinetics of mixing in particle phase under: (i) pure aggregation of particles, called aggregative mixing, and (ii) simultaneous breakup and coalescence of drops. The discretization methods for 2-d PBEs, derived from the widely used 1-d solution methods, are first classified into two classes. We choose one representative method from each class. The results show that the extensions based on minimum consistency of discretization perform quite well with respect to both the new and the old benchmarks, in comparison with the geometrical extensions of 1-d methods. We next revisit aggregative mixing using Monte-Carlo simulations. The simulations show that (i) the time variation of the extent of mixing in finite size systems has power law scaling with the system size, and (ii) the mean-field PBEs fail to capture the evolution of mixing for reduced population of particles at long times. The sum kernel limits the applicability of PBEs to substantially larger particle populations than that seen for the constant kernel. Interestingly, these populations are orders of magnitude larger than those at which the PBEs fail to capture the evolution of total particle population correctly.     

A near infrared optical reflector using one-dimensional photonic crystal structure containing chalcogenide glasses

The reflectivity of one-dimensional chalcogenide photonic crystal (CGPC) structure with the first order reflection band in near infrared (NIR) region is theoretically studied. Sb-Se and Ge-S chalcogenide glasses are used as high and low refractive index layers respectively, because these materials have zero absorption in NIR region. The transfer matrix method (TMM) is employed to calculate the reflective spectra of the proposed structure. The theoretical results of reflective spectra of bulk chalcogenide materials with the composition of Sb₄₀Se₆₀ and Ge₃₀S₇₀ for 4, 8, 12 and 15 layers and thicknesses of 117 nm and 183 nm respectively, at normal incidence, are close agreement with the experimental results. Furthermore, by increasing the number of layers of Sb₄₀Se₆₀ and Ge₃₀S₇₀, the reflection bands can be enhanced in the wider range of the NIR region for the polarization at different angles and thus the broadband omnidirectional reflector can be designed.