Ion population fraction calculations using improved screened hydrogenic model with l-splitting

Ion population fraction(IPF) calculations are very important to understand the radiative spectrum emitted from the hot dense matter. IPF calculations require detailed knowledge of all the ions and correlation interactions between the electrons of an ion which are present in a plasma environment. The average atom models, e.g., screened hydrogenic model with l-splitting(SHML), now have the capabilities for such calculations and are becoming more popular for in line plasma calculations. In our previous work [Ali A, Shabbir Naz G, Shahzad M S, Kouser R, Rehman A and Nasim M H 2018 High Energy Density Phys. 26 48], we have improved the continuum lowering model and included the exchange and correlation effects in SHML. This study presents the calculation of IPF using classical theory of fluctuation for our improved screened hydrogenic model with l-splitting(I-SHML) under local thermodynamic equilibrium conditions for iron and aluminum plasma over a wide range of densities and temperatures. We have compared our results with other models and have found a very good agreement among them.     

Automatic Debye–Scherrer elliptical ring extraction via a computer vision approach

The accurate calibration of powder diffraction data acquired from area detectors using calibration standards is a crucial step in the data reduction process to attain high‐quality one‐dimensional patterns. A novel algorithm has been developed for extracting Debye–Scherrer rings automatically using an approach based on computer vision and pattern recognition techniques. The presented technique requires no human intervention and, unlike previous approaches, makes no restrictive assumptions on the diffraction setup and/or rings. It can detect complete rings as well as portions of them, and works on several types of diffraction images with various degrees of ring graininess, textured diffraction patterns and detector tilt with respect to the incoming beam.     

Hydrodynamics of viscous fluid through porous slit with linear absorption

The exact solutions for the viscous fluid through a porous slit with linear ab-sorption are obtained. The Stokes equation with non-homogeneous boundary conditions is solved to get the expressions for the velocity components, pressure distribution, wall shear stress, fractional absorption, and leakage flux. The volume flow rate and mean flow rate are found to be useful in obtaining a convenient form of the longitudinal velocity component and pressure difference. The points of the maximum velocity components for a fixed axial distance are identified. The value of the linear absorption parameter is ran-domly chosen, and the rest available data of the rat kidney to the tabulate pressure drop and fractional absorption are incorporated. The effects of the linear absorption, uniform absorption, and flow rate parameters on the flow properties are discussed by graphs. It is found that forward flow occurs only if the volume flux per unit width is greater than the absorption velocity throughout the length of the slit, otherwise back flow may occur. The leakage flux increases with the increase in the linear absorption parameter. Streamlines are drawn to help the analysis of the flow behaviors during the absorption of the fluid flow through the renal tubule and purification of blood through an artificial kidney.     

Study of projectile fragmentation in the reaction (158 A GeV) Pb + Pb using CR-39

The fragmentation of Pb ions at 158 A GeV energy produced in the interaction with Pb target has been studied using a CR-39 track detector. A stack comprising of 64 detectors was prepared such that a target of 1 cm thickness was sandwiched between the sheets of CR-39. The purpose of this exposure geometry was to calibrate CR-39 with respect to relativistic heavy ions as well as to study the fragmentation of Pb ions at 158 A GeV energy. The exposure was carried out at the SPS beam facility of CERN at normal incidence with a fluence of . Two detectors from the exposed stack have been selected for this study: one before and the other after the target material. After etching, the detectors were scanned using an optical microscope and the etched track lengths and the diameters of the track openings were measured manually. Considering that the lengths of tracks provide the best charge resolution for Z>65, we have measured track lengths for a sufficiently large number of fragments to identify individual charge states for 65<Z<83. The total charge-changing cross section has also been determined.     

Neighbourhood-Perfect Line Graphs

We show that the line graph of any balanced hypergraph is neighbourhood-perfect. This result is a hypergraphic extension of a recent theorem in [GKLM] saying that the line graphs of bipartite graphs are neighbourhood-perfect. The note contains also a graphical extension of the same theorem: the characterization of all graphs with neighbourhood-perfect line graph. The proof relies on a characterization of neighbourhood-perfect graphs among line graphs in terms of forbidden induced subgraphs.     

Structural Properties of Cubic Sets in Regular LA-semihypergroups

In this article we characterize the regular LA-semihypergroups in terms of $({\in }_{\Gamma },{\in }_{\Gamma }\vee q_{\Delta })$-cubic (left, right, two sided, bi, generalized bi, interior, quasi)-hyperideals of LA-semihypergroups. Meanwhile, some illustrative examples are given to show the rationality of the definitions popularized in the present paper.     

Schiff base tantalum(V) complexes

Summary Complexes of pentachlorotantalum with the Schiff bases: bis(vanillin)benzidine, bis(vanillin)-o-dianisidine, bis(acetylacetone)benzidine, bis(p-dimethylaminobenzaldehyde)-o-dianisidine, bis(anisaldehyde)-1, 3-propanediamine and bis(p-dimethylaminobenzaldehyde)-o-phenylenediamine have been prepared and characterized by molar conductance, decomposition temperature, elemental and t.g. analyses and i.r. spectral measurements. The conductances reveal that pentachlorotantalum (1 mole) interacts with all the ligands (1 mole), all five chloride ions thus forming simple adducts. A comparative study of the i.r. spectra of the parent ligands and their complexes allows the coordination sites to be ascertained. The studies show that tantalum(V) chloride prefers to form complexes of high coordination number.