Positive solutions and pattern formation in a diffusive tritrophic system with Crowley–Martin functional response

Nonlinear Dynamics - In the present work, we have studied a diffusive tritrophic food chain model in which the species at each trophic level interact in accordance with Crowley–Martin...     

Hydromagnetic instability of streaming fluids in porous medium

The instability of the plane interface between two uniform, superposed, electrically conducting and counter-streaming fluids through a porous medium is considered in the presence of a horizontal magnetic field. In the absence of surface tension, perturbations transverse to the direction of streaming are found to be unaffected by the presence of streaming if perturbations in the direction of streaming are ignored. For perturbations in all other directions there exists instability for a certain wavenumber range. The instability of this system is postponed by the presence of magnetic field. The magnetic field and surface tension are able to suppress this Kelvin-Helmholtz instability for small wavelength perturbations and the medium porosity reduces the stability range given in terms of a difference between the streaming velocities and the Alfvén velocity.This research forms a part of the research project awarded to the first author (R.C.S.) by the University Grants Commission.     

Sorption and concentration of51Cr(VI) traces on TiO2 and ZrO2 by radioindicator study

The carrier technique has been used to concentrate Cr(VI) radiometrically by studying the carrying efficiency as a function of pH of aqueous medium, added ions, carrying capacity, amount of carrier and subsequent desorption of the activity adsorbed under optimum experimental conditions. The study shows that under optimum experimental conditions, 0.15 g of ZrO₂ and 0.25 g of TiO₂ carry 0.01 mg and 0.001 mg of chromium respectively. Further, the activity carried under the specified conditions can be recovered more or less quantitatively by leaching the carrier.     

Search for a precursor crystal-to-crystal phase transition to amorphization in α-GeO2 and α-AlPO4 under pressure

Recent X-ray diffraction studies on α-quartz (SiO₂) by Kingmaet al [1], have shown the occurrence of a reversible, crystalline-to-crystalline, phase transition just prior to amorphization at ≈ 21 GPa. This precursor transition has also been confirmed by our recent molecular dynamics simulation study [2]. In order to investigate the possibility of a similar behaviour in other isostructural compounds, which also undergo pressure induced amorphization, α-GeO₂ and α-AlPO₄ (berlinite form) were studied using energy dispersive X-ray diffraction. In either of these materials, no such phase transition is detected prior to amorphization. The onset of amorphization and its reversal is found to be time dependent in GeO₂.     

Antimicorbial effects of newly synthesized organotin(IV) and organolead(IV) derivatives

Triorganotin(IV) and triorganolead(IV) derivatives of the types Me₃Sn(SCZ) and Ph₃Pb(SCZ) (where SCZ^? is the anion of a semicarbanzone ligand) have been synthesized by substitution reactions of trimethyltin chloride and triphenyl-lead chloride with semicarbazones derived from heterocyclic ketones. The resulting complexes have been characterized by elemental analyses, molecualr weight determinations and conductivity measurements. The mode of bonding has been established on the basis of infrared and ¹H, ¹³C and ¹¹⁹Sn NMR spectroscopic studies. Some respresentative complexes have also been evaluated for their antimicrobial effects on different species of pathogenic fungi and bacteria; the results of these investigations have been reported in the present paper.     

PHOTOREACTIVATION OF THYMINE-STARVED ESCHERICHIA COLIBs-1

Abstract —Thymine starvation prior to 254 nm ultraviolet light (UV) exposures has been found to decrease the level of maximum photoreactivation in Escherichia coli B _s-1. The dark equilibrium level of photoreactivating enzyme-substrate complexes was determined from the levels of photoreactivation obtained with exposures to single flashes of high-intensity light. The kinetics indicate that photoreactivating enzyme concentration does not decrease as a result of thymine starvation. The UV sensitivities of normal and thymine-starved cells are found to be the same. Photoreactivation by sequential flashes shows a lesser number of total photorepairable lesions in starved cells. It is concluded that thymine starvation renders a portion of the dimers inaccessible to the photoreactivating enzyme, thus lowering the level of maximum photoreactivation.     

Formatation of pore structure in tape-cast alumina membranes – effects of binder content and firing temperature

Disc type ceramic aluminium oxide membrane has been prepared by tape casting technique. Thickness of this single layer membrane is in the range 200–300 μm. Porosity and pore size distribution have been determined by mercury porosimetry. Polymeric binder content of the green tape and the firing temperature are found to have strong influence on the average pore size, pore size distribution and overall porosity. Higher binder content promotes agglomeration of the ceramic particles, which on firing leads to wider pore size distribution and formation of closed pores. Pore coarsening is observed with increasing firing temperature.     

Photochemical C–N bond forming reactions for the synthesis of five-membered fused N-heterocycles

Abstract

Few conversions cannot take place with ground-state reactions even with the help of a catalyst, therefore they are made to occur under photochemical conditions. The transfer of electrons took place even with the photochemical excitement of one molecule where redox reaction cannot occur at the ground state. The ground-state reactions resulted in the formation of side products. The substrates did not require any sort of chemical activation for C–N bond construction in the course of photochemical reactions. The source of energy; light has always been the interest of researchers in order to induce chemical reactions ever since the starting of scientific chemistry. The present review encloses the chemistry of photochemical transformations with a focus on their synthetic uses. The organic photochemical reactions prevent the polluting or harmful reagents thus, provides a possibility for sustainable procedures as well as green chemistry. This review article displays the formation of numerous of five-membered fused nitrogen-heterocyclic compounds.     

Solid-state synthesis, structural variants and transformation of three-dimensional sulfides, AGaSnS4 (A=Na, K, Rb, Cs, Tl) and Na1.263Ga1.263Sn0.737S4

New cubic-AGaSnS₄ (A=Na, K, Rb, Cs, Tl) and orthorhombic-NaGaSnS₄ compounds were synthesized by solid-state reactions and characterized by X-ray diffraction and diffuse reflectance spectroscopy. Single crystals of orthorhombic-Na_1.263Ga_1.263Sn_0.737S₄ were obtained in the crystal growth attempts of sodium compound. All six new compounds have orthorhombic AgGaGeS₄ and cubic BaGa₂S₄ structures, as determined from single crystal X-ray structures of Na_1.263Ga_1.263Sn_0.737S₄ and cubic-AGaSnS₄ (A=Na, K, Rb). Orthorhombic-NaGaSnS₄ and known layered-KGaSnS₄ undergo structural transformation to thermodynamically stable cubic form.     

Spin density distributions in some fluorinated radical cations

A theoretical study of π-electron spin density distributions has been made for a series of fluoro-substituted hydrocarbon radical cations using unrestricted Hartree-Fock theory. Although some of the predicted proton splittings are not in very good agreement with experiment, the overall agreement with experiment can be passed as fairly satisfactory considering the approximate nature of the theory used. The experimental fluorine splittings can be well predicted by using a one-parameter relationship between the isotropic fluorine splitting (a_F) and the π-electron spin density (ρ_CC) on the attached carbon. It has been further shown that both ρ_CC and the proportionality constant (Q_eff) in the linear relation, are fairly insensitive to the parameter choice.