On Totally Ordered Rings Whose Positive Cones are Finitely Generated

This paper is mainly dealt with the structure of totally ordered rings (t.o. rings) whose positive cones are finitely generated as multiplicative right ideals.AMS Subject Classification (1991): 16W80, 13J25     

Electronegativities in the calculation of diatomic molecular parameters (Hydrides of some transition elements)

The force constants for diatomic molecules and isolated bonds may be expressed by using equalized electro-negativities, bond orders, bond strengths and interatomicdistances. We have studied Mn¹H, Mn²H, Co²H, Ni¹H, Ni²H, Cu¹H, Cu²H, Ag¹H, and Ag²H and have determined the proportionality constant d, as well as the Lennard-Jones parameters a and b, for the potential energy functions used by Szöke and calculated the anharmonicity ω_eξ_e and the rotational-vibrational coupling constant α_e. The relation between electronegativity and ionization potential has been verified and the variations of molecular parameters with atomic number Z have been studied.     

Preparation and characterization of (PVP + NaClO4) electrolytes for battery applications

A sodium ion-conducting polymer electrolyte based on polyvinyl pyrrolidone (PVP) complexed with NaClO₄ was prepared using the solution-cast technique. The cathode film of V₂O₅ xerogel modified with polyvinyl pyrrolidone was prepared using the sol-gel method. Investigations were conducted using X-ray diffractometry (XRD), Fourier transformation infrared (FT-IR) spectroscopy. The ionic conductivity and transference number measurements were performed to characterize the polymer electrolyte for battery applications. The transference number data indicated that the conducting species in these electrolytes are the anions. Using the electrolyte, electrochemical cells with a configuration Na/(PVP + NaClO₄)/V₂O₅ modified by (PVP) were fabricated and their discharge profiles studied.     

Spectroscopic and magnetic studies of manganese ions in ZnO-Sb2O3-B2O3 glass system

ZnO-Sb₂O₃-B₂O₃ glasses containing different concentrations of MnO ranging from 0 to 1.0 mol% were prepared. A number of studies, viz. optical absorption, infrared and ESR spectra and magnetic susceptibility, were carried out as a function of manganese ion concentration. The analysis of the results indicate that manganese ions mostly exist in Mn²⁺ state in these glasses when the concentration of MnO≤0.6 mol% and above this concentration, these ions seem to exist in Mn³⁺ state in the glass network.     

Carbon Sphere@Nickel sulfide core-shell nanocomposite for high performance supercapacitor application

The Carbon sphere@Nickel sulfide core-shell nanocomposites for different mole ratios of Carbon sphere (0:1; 0.5:1 and 1:1) have been synthesized by a facile low temperature water-bath method without any further calcination. XRD studies on the core-shell nanocomposites show that characteristic peaks associated with rhombohedral phase structure of nickel sulfide have been retained. TEM morphology presents the interlinked core-shell of Carbon sphere@Nickel sulfide composite with grass-leaf dexterity for better ionic diffusion. BET study confirms the formation of mesoporous structure with high surface area. The existence of elements and its electronic configuration is noted through XPS. The electrochemical studies on pristine nickel sulfide and its Carbon sphere@Nickel sulfide core-shell composites reveal that Carbon sphere@Nickel sulfide (0.5:1) exhibits high specific capacitance of 1022?F?g^?1 at a current density of 1?A?g^?1. It shows good cyclic performance even beyond 4000 consecutive charge/discharge cycles at a relatively high current density of 20?A?g^?1 with the ～83% of retention.     

Temperature-dependent chemical shift and relaxation times of (23)Na in Na(4)HTm[DOTP

We describe the characterization of a (23)Na temperature-dependent chemical shift and relaxation rates in the complex, Na(4)HTm[DOTP]. This is the first characterization of a (23)Na temperature-dependent chemical shift in a nonmetallic sample. The (23)Na temperature-dependent chemical shift coefficient is approximately -0. 5 PPM/ degrees C for both an aqueous solution and a 6% agarose gel of this compound. This is 50 times the magnitude of the temperature-dependent chemical shift coefficient of water protons. The relaxation times, T(1), T(2f), and T(2s) increased by 0.1, 0.01, and 0.05 ms/ degrees C, respectively. Applications of these unique properties for designing an MRI technique for monitoring heat deposition in tissue and tissue phantoms are discussed.     

Electron Spin Resonance study of gamma irradiated MA-AMPS copolymer

Electron Spin Resonance (ESR) spectra of gamma irradiated methylacrylamide-2-acrylamido-2-methyl-propanesulphonic acid (MA-AMPS) are recorded to identify the radical species formed during the irradiation of the copolymer. The ESR spectrum observed for irradiated MA-AMPS copolymer at liquid nitrogen temperature (LNT) (77 r K) is an asymmetric triplet; while the spectrum observed at room temperature (RT) is a quintet. The intensity distribution of both the spectra deviated appreciably from the expected theoretical values. Computer simulations are employed to analyze the ESR spectra observed at different temperatures. The triplet spectrum observed at LNT is simulated to be a superposition of component spectra arising from macroradicals of the type～CH 2 - \dot {\rm C} H-CH 2 ～ (I), radicals of the type \dot {\rm C} H 2 SO 3 H (II), and peroxy radicals (III). In contrast, the RT spectrum is simulated to be a superposition of component spectra arising due to radicals I, II, III together with the component quartet assigned to methyl radicals ( \dot {\rm C} H 3 ). The formation of such free radicals in irradiated copolymer is discussed.     

The effect of the location of stage-I fatigue crack across the persistent slip band on its growth rate – A 3D dislocation dynamics study

Abstract

A 3D dislocation dynamics study to ascertain the probable path of stage-I fatigue crack propagation across the persistent slip band (PSB) in austenitic stainless steel is presented. Cyclic plasticity and the resulting crack tip slip displacement (CTSD) are evaluated for cracks of varying length introduced at PSB-center and at two PSB-matrix interfaces. CTSD attains high value at either of the two interfaces irrespective of the proximity of crack front to the grain boundary. Further, a difference in microcrack propagation rate is also observed among the two interfaces. The present results assert microcrack propagation preferrentially along one of the two PSB-matrix interfaces rather than at the PSB-center. A pre-existing PSB dislocation structure localises the cyclic slip for crack lengths up to approximately half of the grain depth for an applied strain range of 2 × 10^?4.     

Magnetic-field-induced valence transition in rare-earth systems

The magnetic-field-induced valence transition in rare-earth systems has been investigated using the periodic Anderson model supplemented by the Falicov-Kimball term. This model has been solved by first decoupling the Falicov-Kimball term as proposed by Khomskii and Koharjan and then taking the limit of infinite intra-site Coulomb repulsion. The valence transition both in the absence and in the presence of magnetic field as a function of temperature is studied. It has been found that the system makes transition from non-magnetic to magnetic state when the magnetic field increases beyond a critical value H _c. The phase boundary defined in terms of reduced field H _c(T)/H _c(0) and reduced temperature T/T _v (T _v being the valence transition temperature in the absence of field) is almost independent of the position of the localized level. The results are in qualitative agreement with experimental observations in Yb- and Eu-compounds.