Comparative study of electron conduction in azulene and naphthalene

We have studied the feasibility of electron conduction in azulene molecule and compared with that in its isomer naphthalene. We have used non-equilibrium Green’s function formalism to measure the current in our systems as a response of the external electric field. Parallely we have performed the Gaussian calculations with electric field in the same bias window to observe the impact of external bias on the wave functions of the systems. We have found that the conduction of azulene is higher than that of naphthalene inspite of its intrinsic donor-acceptor property, which leads a system to more insulating state. Due to stabilization through charge transfer the azulene system can be fabricated as a very effective molecular wire. Our calculations show the possibility of huge device application of azulene in nano-scale instruments.     

Thermal and electronic properties of Bi1 − xSbx alloys

Polycrystalline Bi_1 ? xSb_x (x = 0.10, 0.12 and 0.15) semiconducting alloys were synthesized by mechanical alloying in order to achieve homogeneous thermoelectric materials with improved mechanical strength. The homogeneity of the powder samples were repeatedly checked by X-ray diffraction and scanning electron microscopy to standardize the milling conditions. The best possible homogenized material was developed with the milling conditions of BPR 30:1, ball diameter 30 mm, 400 rpm and milling time of 15 h. The electrical resistivity, thermoelectric power and thermal conductivity were measured in the temperature range 300–500 K. It was found through these experiments that the composition with x = 0.12 behaved in a normal semiconducting way, whereas the other two compositions (x = 0.10 and 0.15) showed degenerate semiconductor behaviour. These features have been qualitatively explained from the band structure and interband scattering mechanisms.     

Single-parameter controlled-variable amplitude change function for digital filtering

A single-parameter controlled-variable amplitude change function has been constructed for digital filtering using multiple units of a prototype filter. The limits of variation are discussed. The technique is shown to be useful not only for the reduction of errors in either the pass band or the stop band of the overall filter, but also for varying the cutoff frequency of the overall filter over a wide range. Hardware implementation problems resulting from a wide variation are shown to be overcome by a modular approach.     

Locking range and stability of injection locked 1.54 µm InGaAsp semiconductor lasers

Measurements of the intensity of an injection locked 1.54 μm InGaAsP laser are reported. The change in intensity of the locked laser across the locking range is quite asymmetric, with a shape that agrees well with the theory of Lang. A linewidth parameter ofalpha = 6 pm 1was determined from the magnitude of the locking range. The injection locked laser was found to be unstable on the high frequency end of the locking range. The physical origin of this instability is explained in terms of a laser intensity change altering the phase of the laser field relative to that of the injected field.     

High-speed target tracking by fuzzy hostility-induced segmentation of optical flow field

A time efficient technique for real-time tracking of high-speed objects in a video sequence is presented in this article. The technique is primarily based on the segmentation of the optical flow field computed between the successive image frames of a video sequence, followed by the tracking of a detected point of interest (POI) within the segmented flow field. In the initial phase of the technique, the optical flow field between the first two successive image frames acquired from a video sequence, is computed. A fuzzy hostility index indicative of the degree of coherence of the moving objects in the image frames, is used to segment the optical flow field. This yields different coherent regions of interest (ROIs) in the segmented flow field. A POI is then detected in the different ROIs obtained. Tracking of the moving object is then carried out by computing the flow fields between predefined ROIs in the neighborhood of the detected POI in the subsequent image frames.Since the selected ROIs are smaller than the image frames, a fair amount of reduction in the time required for the computation of the optical flow field is achieved, thereby facilitating real-time operation. An application of the proposed technique is demonstrated on three video sequences of high-speed flying fighter aircrafts.     

Benzene physical and chemical organogels: Effect of network scaffolding on the thermodynamic behavior of entrapped solvent molecules

This paper presents a thermodynamic investigation of the benzene physical and chemical organogels, using differential scanning calorimetry (DSC) and intends to draw an appropriate relationship between the gel network structure and the properties. Physical gels, formed by an aluminium soap of fatty acid, and chemical gels, created by in situ cross‐linking of a siloxane copolymer are investigated. The effects of the type and quantity of the gelators and their corresponding network mesh size distribution in the gels on crystallization, melting, and their kinetics are examined. It appears that the kinetics of crystallization of the entrapped solvent is significantly affected by the quality of the gel network scaffolding and can be treated successfully by the Avrami equation of crystallization. From the melting behavior of the entrapped solvent crystallites, quantitative information about the number of solvent molecules bound per molecule of the gelator has been extracted. DSC proves to be a reliable technique to evaluate the population distribution of solvent molecules trapped in the physical and chemical organogel network scaffolding. The state of the solvent may be treated as a probe to understand the structure of the gels. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1253–1264, 2004     

Electrochemical sulfide removal and recovery from paper mill anaerobic treatment effluent

Sulfide can be removed from wastewater and recovered as elemental sulfur using an electrochemical process. Recently, we demonstrated this principle of product recovery on synthetic feeds. Here, we present a lab scale electrochemical reactor continuously removing sulfide from the effluent of an anaerobic treatment process operated on paper mill wastewater. The effluent contained 44 ± 7 mg of sulfide-S L⁻¹. Sulfide was reduced to 8 ± 2 mg-S L⁻¹, at a removal rate of 0.845 ± 0.133 kg-S m⁻³ of total anodic compartment (TAC) d⁻¹. The removed sulfide was recovered (75 ± 4% recovery) as pure concentrated alkaline sulfide/polysulfide solution, from which solid elemental sulfur was obtained. The electrochemical sulfide removal was not affected by different soluble constituents or particulate materials present in the wastewater. However, over time sulfide removal decreased due to biological sulfur reduction using the organics present in the wastewater. Therefore, a periodic switching strategy between anode and cathode was developed. Biofilm formation was avoided as the pH of the cathode solution increased to inhibitory levels during cathodic operation, while still allowing full recovery of the sulfur as end product.     

Physicochemical Properties of Garden Cress (<Emphasis Type="Italic">Lepidium sativum</Emphasis> L.) Seed Oil

Garden cress (Lepidium sativum L.) is an edible, underutilised herb, grown mainly for its seeds in India. Physicochemical properties, minor components (unsaponifiable matter, tocopherols, carotenoids), fatty acid composition and storage stability of garden cress seed oil (GCO) were studied. Cold press, solvent and supercritical CO₂ extraction methods were employed to extract the oil. The total oil content of garden cress (GC) seeds was 21.54, 18.15 and 12.60% respectively by solvent, supercritical CO₂ and cold press methods. The physical properties of GCO extracted by the above methods were similar in terms of refractive index, specific gravity and viscosity. However, cold pressed oil showed low PV and FFA compared to the oil extracted by other methods. α-Linolenic acid (34%) was the major fatty acid in GCO followed by oleic (22%), linoleic (11.8%), eicosanoic (12%), palmitic (10.1%) erucic (4.4%), arachidic (3.4%) and stearic acids (2.9%). Oleic acid (39.9%) and α-linolenic acid (42.1%) were the predominant fatty acids at the sn-2 position. The total tocopherol and carotenoid content of GCO was 327.42 and 1.0 μmol/100 g oil, respectively. The oil was stable up to 4 months at 4 °C. Tocopherol and BHT offered the least protection, while ascorbyl palmitate (200 ppm) offered the maximum protection to the oil, when subjected to the accelerated oxidative stability test. Thus GCO can be considered as a fairly stable oil with a high content of α-linolenic acid.     

Hydroformylation of 1-octene using rhodium–phosphite catalyst in a thermomorphic solvent system

The use of a liquid–liquid biphasic thermomorphic or temperature-dependent multicomponent solvent (TMS) system, in which the catalyst accumulates in one of the liquid phases and the product goes preferably to the other liquid phase, can be an enabling strategy of commercial hydroformylation processes with high selectivity, efficiency and ease of product separation and catalyst recovery. This paper describes the synthesis of n-nonanal, a commercially important fine chemical, by the hydroformylation reaction of 1-octene using a homogeneous catalyst consisting of HRh(PPh₃)₃(CO) and P(OPh)₃ in a TMS-system consisting of propylene carbonate (PC), dodecane and 1,4-dioxane. At a reaction temperature of 363 K, syngas pressure of 1.5 MPa and 0.68 mM concentration of the catalyst, HRh(CO)(PPh₃)₃, the conversion of 1-octene and the yield of total aldehyde were 97% and 95%, respectively. With a reaction time of 2 h and a selectivity of 89.3%, this catalytic system can be considered as highly reactive and selective compared to conventional ones. The resulting total turnover number was 600, while the turnover frequency was 400 h^?1. The effects of increasing the concentration of 1-octene, catalyst loading, partial pressure of CO and H₂ and temperature on the rate of reaction have been studied at 353, 363 and 373 K. The rate was found to be first order with respect to concentrations of the catalyst and 1-octene, and the partial pressure of H₂. The dependence of the reaction rate on the partial pressure of CO showed typical substrate inhibited kinetics. The kinetic behavior differs significantly from the kinetics of conventional systems employing HRh(CO)(PPh₃)₃ in organic solvents. Most notable are the lack of olefin inhibition and the absence of a critical catalyst concentration. A mechanistic rate equation has been proposed and the kinetic parameters evaluated with an average error of 5.5%. The activation energy was found to be 69.8 kJ/mol.     

Polymeric organogel as an effective approach for eradication of heavy metal ions As,Pb, Cd,and Cr from the surface of groundwater through adsorption stratagem

Excess metal pollutant has affected and caused serious havoc in the lives of terrestrial as well as aquatic beings. The core of this work revolves around eradicating highly toxic heavy metal ions from underground water systems using a cost-effective, high removal efficiency polymeric adsorbent capable of adsorbing and removing ionic metals whose backbone is composed of a bio-degradable polymer, polyvinyl alcohol. The obtained adsorbent was characterized using FT-IR, HNMR, and P-XRD. Morphological studies were carried out using SEM. Detection and adsorption of metal ions were performed using SEM–EDX and AAS; wherein the adsorbent was found to remove nearly 80% of arsenic ions, 70.5% and 70.7% for lead and chromium ions while 60.7% for cadmium ions, respectively. Further, the kinetics of adsorption along with intraparticle diffusion studies were also performed to determine the mechanism alongside observing the isothermal influence of the sorbent. The adsorption capacity was seen to be highest in arsenic at around 570.42 mg g⁻¹ thus acting as a potential and effective adsorbent for the removal of heavy metal ions from groundwater.