Synthesis and performance study of cobalt-substituted lithium iron phosphate

LiCo_0.2Fe_0.8PO₄ cathode material was prepared by succinic assisted soft combustion technique. This method of synthesis ensures homogeneity of the precursor material, improved activity and crystal grain size. Calcinations at high temperature confirm the purity of the cathode material. The aim of this work is to investigate the effects of cobalt substitution in LiFePO₄. The structural characterization of the products was analysed by the X-ray powder diffraction. Conductivity measurements were made to characterize the transport property of the cathode material. Fourier transform infrared spectroscopy and differential scanning calorimeter and thermogravimetry analysis have been studied to investigate the functional group present and the phase transition involved in the sample, respectively.     

Attenuation of Sommerfeld effect in an internally damped eccentric shaft-disk system via active magnetic bearings

Meccanica - Eccentric shaft-disk system with internal damping driven by a non-ideal power source exhibits Sommerfeld effect characterized by nonlinear jump phenomena of amplitude and rotor speed...     

Kinetics of ruthenium(III) catalyzed and uncatalyzed oxidation of monoethanolamine by <Emphasis Type="Italic">N</Emphasis>-bromosuccinimide

Kinetics of uncatalyzed and ruthenium(III) catalyzed oxidation of monoethanolamine by N-bromosuccinimide (NBS) has been studied in an aqueous acetic acid medium in the presence of sodium acetate and perchloric acid, respectively. In the uncatalyzed oxidation the kinetic orders are: the first order in NBS, a fractional order in the substrate. The rate of the reaction increased with an increase in the sodium acetate concentration and decreased with an increase in the perchloric acid concentration. This indicates that free amine molecules are the reactive species. Addition of halide ions results in a decrease in the kinetic rate, which is noteworthy. Both in absence and presence of a catalyst, a decrease in the dielectric constant of the medium decreases the kinetic rate pointing out that these are dipole—dipole reactions. A relatively higher oxidation state of ruthenium i.e., Ru(V) was found to be the active species in Ru(III) catalyzed reactions. A suitable mechanism consistent with the observations has been proposed and a rate law has been derived to explain the kinetic orders.     

Development of nano-catalyzed membrane for PEM fuel cell applications

Nano-catalyzed membrane with different platinum (Pt) catalyst loadings (0.25 to 1 mg cm^?2) was investigated for proton exchange membrane fuel cell applications, and the Pt loading on the Nafion membrane was prepared by non-equilibrium impregnation reduction method. The prepared catalyzed membranes were subjected to various characterisations, namely, X-ray diffraction, high-resolution scanning electron microscopy (HRSEM) with energy-dispersive X-ray, cyclic voltammetry, polarisation and electrochemical impedance spectroscopy. The polycrystalline fcc cubic structure and the particle size of Pt catalyst were estimated by X-ray diffraction analysis. The membrane with 0.4 mg cm^?2 of Pt loading exhibits a favourable surface morphology which is confirmed by HRSEM image. Electrochemical investigations were clearly evident that the uniform distributions of Pt particles with fine pores on Nafion membrane facilitated the three-phase boundary which leads to a better cell performance. Electrochemical impedance spectroscopy demonstrated that the cell constructed using 0.4 mg cm^?2 of platinum-loaded membrane has lower resistance than the other Pt loading.     

Nanomaterial-based functional scaffolds for amperometric sensing of bioanalytes

Functional nanomaterials have emerged as promising candidates in the development of an amperometric sensing platform for the detection and quantification of bioanalytes. The remarkable characteristics of nanomaterials based on metal and metal oxide nanoparticles, carbon nanotubes, and graphene ensure enhanced performance of the sensors in terms of sensitivity, selectivity, detection limit, response time, and multiplexing capability. The electrocatalytic properties of these functional materials can be combined with the biocatalytic activity of redox enzymes to develop integrated biosensing platforms. Highly sensitive and stable miniaturized amperometric sensors have been developed by integrating the nanomaterials and biocatalyst with the transducers. This review provides an update on recent progress in the development of amperometric sensors/biosensors using functional nanomaterials for the sensing of clinically important metabolites such as glucose, cholesterol, lactate, and glutamate, immunosensing of cancer biomarkers, and genosensing.     

Synthesis and characterization of poly(epoxy‐imide) crosslinked networks

Poly(epoxy imide)s were prepared by a reaction between a hydroxyl‐group‐containing soluble copolyimide and commercial epoxy resins at 220 °C for 2 h. Poly(epoxy imide) thin films exhibited higher thermal stability and lower dielectric constants than a commercial flip‐chip package material (U300). The thermal stabilities of the poly(epoxy imide)s were 1.4–2.0 times higher than that of U300. The thermal stability increased with increasing crosslink density and with decreasing bulky CF₃ groups (which were easily decomposable). The dielectric constants of the poly(epoxy imide)s were 1.1–1.3 times lower than that of U300, and this is highly desirable for the microelectronic packaging industry. The dielectric constant dramatically decreased when bulky CF₃ groups were added and when the functionalities of epoxy resins decreased. The residual stresses, slopes in the cooling curves, and glass‐transition temperatures of the poly(epoxy imide)s were measured with a thin‐film stress analyzer. Low residual stresses and slopes in the cooling curves were achieved with a higher crosslink density. However, in the presence of bulky CF₃ groups, the copolyimide backbone structure did not affect the residual stress values. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 4293–4302, 2004     

Randomized online graph coloring

We study the problem of coloring graphs in an online manner. The only known deterministic online graph coloring algorithm with a sublinear performance function was found by [9.], 319–325). Their algorithm colors graphs of chromatic number χ with no more than (2χn)/log^* n colors, where n is the number of vertices. They point out that the performance can be improved slightly for graphs with bounded chromatic number. For three-chromatic graphs the number of colors used, for example, is O(n log log log n/log log n). We show that randomization helps in coloring graphs online. We present a simple randomized online algorithm to color graphs with expected number of colors O(2^χχ²n^{(χ−2)/(χ−1)}(log n)^1/(χ−1)). For three-colorable graphs the expected number of colors our algorithm uses is . All our algorithms run in polynomial time. It is interesting to note that our algorithm compares well with the best known polynomial time offline algorithms. For instance, the best polynomial time algorithm known for three-colorable graphs, due to [4.] pp. 554–562). We also prove a lower bound of Ω((1/(χ − 1))((log n/(12(χ + 1))) − 1)^χ−1) for the randomized model. No lower bound for the randomized model was previously known. For bounded χ, our result improves even the best known lower bound for the deterministic case: Ω((log n/log log n)^χ−1), due to Noga Alon (personal communication, September 1989).