Structural Studies of TeO2–SeO2–Na2O Glass System

Glass Physics and Chemistry - The growth of nanocrystalization in TeO2–SeO2–Na2O glasses is achieved by the conventional heat treatment method. The influence of Na2O concentration on...     

Grafting of a liquid crystal polymer on carbon fibers

Covalent grafting of mesogenic chains on carbon fiber surfaces was attempted as part of a study on composite materials containing liquid crystal polymer matrices. Grafting in these composite systems is viewed not only as a mechanism to achieve interfacial bonding but also as an approach to modify the interphase physical structure. The synthetic approach to grafting involved the in-situ polymerization of monomers in the presence of functionalized fibers in order to grow chains covalently attached to the fibers. The chemical mechanism may be viewed as the “transesterification of car boxy lated fibers” with acetylated monomers. The monomers used were pimelic acid, p-acetoxybenzoic acid and diacetoxy hydroquinone which are known to yield upon condensation a chemically aperiodic nematic polymer. Evidence for grafting was obtained from X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) analysis on fibers retrieved from composite samples. Interestingly, SEM micrographs of fractured composite specimens containing the mesogen-grafted fibers reveal excellent wetting and interfacial bonding of a liquid crystalline matrix on the carbon surfaces. Based on theoretical considerations for end-adsorbed macromolecules and the nematogenic nature of the grafted chains we infer that dense layers of adsorbed polymer may form at the interfaces studied. From a materials point of view the in situ growth of liquid crystal polymer chains on fibers may offer mechanisms to control composite properties through both bonding and molecular orientation in interfacial regions.     

Color Subspaces as Photometric Invariants

Complex reflectance phenomena such as specular reflections confound many vision problems since they produce image ‘features’ that do not correspond directly to intrinsic surface properties such as shape and spectral reflectance. A common approach to mitigate these effects is to explore functions of an image that are invariant to these photometric events. In this paper we describe a class of such invariants that result from exploiting color information in images of dichromatic surfaces. These invariants are derived from illuminant-dependent ‘subspaces’ of RGB color space, and they enable the application of Lambertian-based vision techniques to a broad class of specular, non-Lambertian scenes. Using implementations of recent algorithms taken from the literature, we demonstrate the practical utility of these invariants for a wide variety of applications, including stereo, shape from shading, photometric stereo, material-based segmentation, and motion estimation.     

Mechanochemically assisted room temperature solid state metathesis reaction for the synthesis of MMoO4 (M = Ca, Sr and Ba)

This communication reports a novel mechanochemically assisted room temperature solid state metathesis reaction for the synthesis of submicron-size alkaline-earth molybdates crystallizing in a tetragonal Scheelite structure. The solids were characterized by powder XRD, FTIR, TGA, DTA, SEM, EDAX and TEM to ascertain their composition, phase homogeneity and morphology.     

Stokes flow past a swarm of porous circular cylinders with Happel and Kuwabara boundary conditions

The problem of creeping flow past a swarm of porous circular cylinders with Happel and Kuwabara boundary conditions is investigated. The Brinkman equation for the flow inside the porous cylinder and the Stokes equation outside the porous cylinder in their stream function formulations are used. The force experienced by each porous circular cylinder in a cell is evaluated. Explicit expressions of stream functions are obtained for both the inside and outside flow fields. The earlier results reported by Happel and Kuwabara for flow past a solid cylinder in Happel’s and Kuwabara’s cell model, have been deduced. Analytical expressions for the velocity components, pressure, vorticity and stresstensor are also obtained     

Designing fault-tolerant real-time computer systems with diversified bus architecture for nuclear power plants

Fault-tolerant real-time computer (FT-RTC) systems are widely used to perform safe operation of nuclear power plants (NPP) and safe shutdown in the event of any untoward situation. Design requirements for such systems need high reliability, availability, computational ability for measurement via sensors, control action via actuators, data communication and human interface via keyboard or display. All these attributes of FT-RTC systems are required to be implemented using best known methods such as redundant system design using diversified bus architecture to avoid common cause failure, fail-safe design to avoid unsafe failure and diagnostic features to validate system operation. In this context, the system designer must select efficient as well as highly reliable diversified bus architecture in order to realize fault-tolerant system design. This paper presents a comparative study between CompactPCI bus and Versa Module Eurocard (VME) bus architecture for designing FT-RTC systems with switch over logic system (SOLS) for NPP.     

Compaction and Sintering Behavior of Niobium Powder for Making Consumable Electrodes

Niobium consumable electrodes of 10?mm dia?×?50?mm length were prepared by cold isostaic pressing with compaction pressure of 125?C250?MPa. The compacts were sintered under vacuum at different temperatures in the range of 1000?C1800?oC. The CIPed and sintered electrodes were characterized with respect to chemical analysis, density, microstructure and bend strength. The results showed that there is a marginal improvement in density at a sintering temperature in the range of 1000?C1400?oC, while a significant improvement in density was observed at sintering temperature in the range of 1600?C1800?oC. The bend strength of sintered electrode was found to increase with increasing sintering temperature and that attains a highest value at a sintering temperature in the range of 1600?C1800?oC. Sintering at a temperature higher than 1400?oC leads to decrease in oxygen content of the electrodes. The oxygen content was decreased from 2000 to 500?ppm when electrode was sintered at 1800?oC.     

A Novel Highly Sensitive Humidity Sensor Based on ZnO/SBA‐15 Hybrid Nanocomposite

This work deals with the study of hydrothermally synthesized zinc oxide (ZnO) loaded mesoporous SBA‐15 hybrid nanocomposite for relative humidity sensing (RH) at room temperature. The sensor exhibits an excellent ~5 orders impedance change along with excellent linearity, quick response time (17 s), rapid recovery time (18 s), negligible hysteresis (1.2%), good repeatability, and stability (1.8%) in 11%–98% RH range. In addition, complex impedance spectra of the sensor at different RHs were analyzed to understand the humidity sensing mechanism. Our study can open a new way for realizing ZnO/SBA‐15 hybrid nanocomposite for fabrication of high‐performance RH sensors.     

Exploring the Bioactive Potentials of C60-AgNPs Nano-Composites against Malignancies and Microbial Infections

At present, the potential role of the AgNPs/endo-fullerene molecule metal nano-composite has been evaluated over the biosystems in-vitro. The intra-atomic configuration of the fullerene molecule (C₆₀) has been studied in-vitro for the anti-proliferative activity of human breast adenocarcinoma (MDA-MB-231) cell lines and antimicrobial activity against a few human pathogens that have been augmented with the pristine surface plasmonic electrons and antibiotic activity of AgNPs. Furthermore, FTIR revealed the basic vibrational signatures at ~3300 cm⁻¹, 1023 cm⁻¹, 1400 cm⁻¹ for O-H, C-O, and C-H groups, respectively, for the carbon and oxygen atoms of the C₆₀ molecule. NMR studies exhibited the different footprints and magnetic moments at ~7.285 ppm, explaining the unique underlying electrochemical attributes of the fullerene molecule. Such unique electronic and physico-chemical properties of the caged carbon structure raise hope for applications into the drug delivery domain. The in-vitro dose-dependent application of C₆₀ elicits a toxic response against both the breast adenocarcinoma cell lines and pathogenic microbes. That enables the use of AgNPs decorated C₆₀ endo fullerene molecules to design an effective anti-cancerous drug delivery and antimicrobial agent in the future, bringing a revolutionary change in the perspective of a treatment regime.     

Ratiometric Interactions of Anionic Surfactants with Calf Thymus DNA Bound Cationic Surfactants: Study II

Cationic surfactant cetyltrimethylammonium bromide (CTAB) and cetylpyridinium bromide (CPB) bind to the calf thymus DNA (ct‐DNA) like anionic biopolymers electrostatically, and establish equilibrium in aqueous medium at pH 7. At low concentration, ct‐DNA does not interact with anionic surfactants, sodium dodecylsulfate (SDS) and sodium dodecylbenzylsulfonate (SDBS). However, in the ground state, anionic surfactant is found to clearly establish equilibrium with ct‐DNA‐bound cationic surfactant whereby the same surfactant–DNA isosbestic point reappears. We herein report a detail ratiometric binding of CPB with ct‐DNA, and interaction of anionic SDBS with DNA‐bound CPB in comparison with the combined ct‐DNA–CTAB–SDS system. Compaction of ct‐DNA in presence of CPB and its decompaction using anionic SDBS is also studied in comparison with CTAB–SDS combination. The techniques used are tensiometry, spectrophotometry, viscometry, cyclic voltammetry, circular dichroism, isothermal titration calorimetry, and density functional theory (DFT)‐based computational calculations. The size and surface charge density of the surfactant headgroups and the phosphate group in DNA have a contributing role in the DNA compaction–decompaction phenomenon.