Carbon-13 NMR spectra of kauranoid diterpenes

Carbon-13 NMR spectra of a number of (?)-ent-kauranoids have been studied. An unambiguous selfconsistent assignment of resonances has been made by considering the changes in chemical shifts produced by the change of substituent(s).     

Carbon-13 NMR spectroscopy of some pentacyclic triterpenoids

Carbon-13 NMR signal assignment of a number of polyoxygenated triterpenes of the olean-12-ene and urs-12-ene series, carried out by considering the changes in chemical shift produced by the change of oxygenation pattern(s), and using methyl oleanolate as a model, are reported.     

Preparation and photoluminescence properties of Y2SiO5:Eu3+ nanocrystals

The sol-emulsion-gel method is used for the preparation of about 5-7 nm size Eu2O3 doped and coated Y2SiO5 nanoparticles at 1300 degrees C. Here, we report the role of surface coating, dopant concentration and temperature of heating on the modification of crystal structure and the photoluminescence properties of Y2SiO5:Eu3+ nanocrystals. It is found that photoluminescence properties are sensitive to the crystal structure which is again controlled by surface coating, concentration and heating temperature. The decay times are 0.76, 1.14, 1.23 and 1.40 ms for 0.25, 0.5, 1.0 and 2.5 mol% Eu2O3 doped Y2SiO5 nanocrystals prepared at 1100 degrees C (X1-Y2SiO5). However, in X2-Y2SiO5 crystal phase (at 1300 degrees C) the average decay times are 1.05, 1.35, 1.55 and 1.60 ms for 0.25, 0.5, 1.0 and 2.5 mol% Eu2O3 doped Y2SiO5 nanocrystals, indicating the photoluminescence properties depend on both the crystal structure and the concentration of ions. The emission intensity of the peak at 612 nm (5D0-->7F2) of the Eu3+-ions is found to be sensitive to the doping and surface coating of Y2SiO5 nanocrystals. The decay times are 1.55 and 1.70 ms for 1300 degrees C heated 1.0 mol% Eu2O3 doped and coated Y2SiO5 nanocrystals, respectively. Our analysis suggests that the site symmetry of ions plays a most important role in the modification of radiative relaxation mechanisms and as a result on the overall photoluminescence properties.     

Role of dopant concentration and surface coating on photophysical properties of CdS: Eu3+ nanocrystals

Here, we report the role of dopant concentration and surface coating of CdS: Eu3+ nanocrystals on the modification of crystal structure and their photoluminescence properties by steady-state and time resolved fluorescence studies. It is found that photoluminescence properties are sensitive to the crystal structure which is controlled by surface coating and dopant concentration. The emission intensity of the peak at 614 nm (5D0 --> 7F2) of the Eu3+-ions is found to be sensitive to the doping and surface coating of CdS nanocrystals. It is found that the average decay times tau are 248, 353 and 499 micros for 0.25, 0.5 and 1.0 mol% Eu ions doped into CdS nanocrystals, respectively. From the decay time measurements, it is evident that the energy transfer occurs from CdS nanoparticles to Eu3+ ions and the calculated energy transfer efficiency from CdS nanoparticles to Eu3+ ions is 9.2 and 35% for Eu3+ ions coated and doped CdS nanoparticles, respectively. Our analysis suggests that site symmetry of ions plays a very important role in the modifications of radiative and nonradiative relaxation mechanisms.     

Similarity analytical solutions for the Schrӧdinger equation with the Riesz fractional derivative in quantum mechanics

The present article deals with the similarity method to tackle the fractional Schrӧdinger equation where the derivative is defined in the Riesz sense. Moreover, the procedure of reducing a fractional partial differential equation (FPDE) into an ordinary differential equation (ODE) has been efficiently displayed by means of suitable scaled transform to the proposed fractional equation. Furthermore, the ODEs are treated effectively via the Fourier transform. The graphical solutions are also depicted for different fractional derivatives α .     

J/ψ gluonic dissociation revisited: III. Effects of transverse hydrodynamic flow

In a recent paper [B.K. Patra, V.J. Menon, Eur. Phys. J. C 44, 567 (2005)] we developed a very general formulation to take into account explicitly the effects of the hydrodynamic flow profile on the gluonic breakup of J/ψs produced in an equilibrating quark–gluon plasma. Here we apply that formulation to the case when the medium is undergoing a cylindrically symmetric transverse expansion starting from RHIC or LHC initial conditions. Our algebraic and numerical estimates demonstrate that the transverse expansion causes enhancement of the local gluon number density n_g, affects the p_T-dependence of the average dissociation rate through a partial-wave interference mechanism and makes the survival probability S(p_T) to change with p_T very slowly. Compared to the previous case of a longitudinal expansion the new graph of S(p_T) is pushed up at LHC but develops a rich structure at RHIC, due to a competition between the transverse catch-up time and the plasma lifetime.PACS 12.38.Mh     

Bionomic exploitation of a ratio-dependent predator–prey system

The present article deals with the problem of combined harvesting of a Michaelis–Menten-type ratio-dependent predator–prey system. The problem of determining the optimal harvest policy is solved by invoking Pontryagin's Maximum Principle. Dynamic optimization of the harvest policy is studied by taking the combined harvest effort as a dynamic variable. Computer simulations are carried out to illustrate our analytical findings. Biological and bioeconomical interpretations of the results are explained critically.     

Crystal plasticity-based constitutive modelling of irradiated bcc structures

A constitutive crystal plasticity model is proposed and developed for the inelastic deformation of irradiated bcc ferritic/martensitic steels. Defects found in these irradiated materials are used as substructure variables in the model. Insights from lower length- and time-scale simulations are used to frame the kinematic and substructure evolution relations of the governing deformation mechanisms. Models for evolution of mobile and immobile dislocations, as well as interstitial loops (formed due to irradiation), are developed. A rate theory-based approach is used to model the evolution of point defects generated during irradiation. The model is used to simulate the quasi-static tensile and creep response of a martensitic steel over a range of loading histories.     

Crystal plasticity modeling of irradiation growth in Zircaloy-2

Abstract

A physically based reaction-diffusion model is implemented in the visco-plastic self-consistent (VPSC) crystal plasticity framework to simulate irradiation growth in hcp Zr and its alloys. The reaction-diffusion model accounts for the defects produced by the cascade of displaced atoms, their diffusion to lattice sinks and the contribution to crystallographic strain at the level of single crystals. The VPSC framework accounts for intergranular interactions and irradiation creep, and calculates the strain in the polycrystalline ensemble. A novel scheme is proposed to model the simultaneous evolution of both, number density and radius, of irradiation-induced dislocation loops directly from experimental data of dislocation density evolution during irradiation. This framework is used to predict the irradiation growth behaviour of cold-worked Zircaloy-2 and trends compared to available experimental data. The role of internal stresses in inducing irradiation creep is discussed. Effects of grain size, texture and external stress on the coupled irradiation growth and creep behaviour are also studied and compared with available experimental data.