Controlled Space Radiation concept for mesh-free semi-analytical technique to model wave fields in complex geometries

Numerical modelling of the ultrasonic wave propagation is important for Structural Heath Monitoring and System Prognosis problems. In order to develop intelligent and adaptive structures with embedded damage detector and classifier mechanisms, detailed understanding of scattered wave fields due to anomaly in the structure is inevitably required. A detailed understanding of the problem demands a good modelling of the wave propagation in the problem geometry in virtual form. Therefore, efficient analytical, semi-analytical or numerical modelling techniques are required. In recent years a semi-analytical mesh-free technique called Distributed Point Source Method (DPSM) is being used for modelling various ultrasonic, electrostatic and electromagnetic wave field problems. In the conventional DPSM approach point sources are placed along the transducer faces, problem boundaries and interfaces to model incident and scattered fields. Every point source emits energy in all directions uniformly. Source strengths of these 360° radiation sources are obtained by satisfying interface and boundary conditions of the problem. In conventional DPSM modelling approach it is assumed that the shadow zone does not require any special consideration. 360° Radiation point sources should be capable of properly modelling shadow zones because all boundary and interface conditions are satisfied. In this paper it is investigated how good this assumption is by introducing the ‘shadow zone’ concept at the point source level and comparing the results generated by the conventional DPSM and by this modified approach where the conventional 360° radiation point sources are replaced by the Controlled Space Radiation (CSR) sources.     

Mirror-Image Oligonucleotides: History and Emerging Applications

As chiral molecules, naturally occurring d -oligonucleotides have enantiomers, l -DNA and l -RNA, which are comprised of l -(deoxy)ribose sugars. These mirror-image oligonucleotides have the same physical and chemical properties as that of their native d -counterparts, yet are highly orthogonal to the stereospecific environment of biology. Consequently, l -oligonucleotides are resistant to nuclease degradation and many of the off-target interactions that plague traditional d -oligonucleotide-based technologies; thus making them ideal for biomedical applications. Despite a flurry of interest during the early 1990s, the inability of d - and l -oligonucleotides to form contiguous Watson–Crick base pairs with each other has ultimately led to the perception that l -oligonucleotides have only limited utility. Recently, however, scientists have begun to uncover novel strategies to harness the bio-orthogonality of l -oligonucleotides, while overcoming (and even exploiting) their inability to Watson–Crick base pair with the natural polymer. Herein, a brief history of l -oligonucleotide research is presented and emerging l -oligonucleotide-based technologies, as well as their applications in research and therapy, are presented.     

A DFT+U study of the catalytic activity of lanthanum nickelate

A density functional theory + Hubbard U (DFT+U) method is implemented to investigate the catalytic activity of lanthanum nickelate (LaNiO₃) for oxygen reduction reaction. Comparison of the surface energies of different LaNiO₃ surfaces shows that {001} surface has the lowest surface energy and hence maximum stability. Two possible terminations of the {001} surface namely LaO and NiO₂ are considered to carry out all our DFT calculations. Calculation of bond lengths of the atoms near the surface and adsorption energies for the reaction intermediates revealed that LaO terminated {001} surface is unstable for the process of OOH adsorption and hence not preferred for the oxygen reduction reaction. However, NiO₂ terminated {001} surface shows excellent catalytic activity for adsorption of all the reaction intermediates and hence is a favourable surface for reactions to occur. Superiority of the NiO₂ terminated {001} surface as catalyst over the LaO terminated one, is also confirmed from the total and partial density of states of the surfaces in presence of the adsorbates, which also shows that the desorption rate of the reaction intermediates is low in case of LaO terminated {001} surface compared to the NiO₂ terminated one.     

An explicit analytical expression for bed-load layer thickness based on maximum entropy principle

The present study aims to derive an analytical model on bed-load layer thickness in an open channel turbulent flow carrying sediments. Determination of the thickness of the bed-load layer is of utmost importance in the study of bed-load transport as it is required to determine the bed-load transport rate, as well as in the study of suspended load transport as it acts as reference level for the particles in suspension. Apart from the several deterministic approaches available in the literature, the work adopts probabilistic approach based on entropy theory to determine the bed-load layer thickness. The concept of entropy theory developed by Shannon is used and the method of Lagrange multipliers is employed for the maximization of entropy function to find the least biased probability distribution. To calculate the Lagrange multipliers, present in the probabilistic model of dimensionless bed-load layer thickness, two different methodologies are presented. The model of bed-load layer thickness is a function of dimensionless shear stress and also depends on three other parameters which are found to be functions of specific gravity of sediment particle and dimensionless particle diameter from a non-linear regression analysis. The proposed model is validated with wide sets of experimental data available in literature and a good agreement is achieved. Apart from comparison with data, the model is also compared with existing deterministic model and computation of relative percentage error proves the better efficiency of the present model.     

Magnesium-induced regiospecific C-silylation of suitably substituted enoates and dienoates

The β-aryl-β-silyl and β,β-disilyl propionates have been synthesized from cinnamates and β-silyl acrylates by a regiospecific reductive C-silylation using Mg/silyl chloride/DMF system at room temperature. These reductive C-silylation conditions have also been applied to δ-aryl substituted dienoates wherein silylation took place at the δ-position leading to the synthesis of single regioisomeric allylsilanes with very high stereoselectivity.     

A study of self-quenching of lyoluminescence yield from gamma-irradiated saccharides and amino acids

Tissue equivalent (TE) lyoluminescence (LL) dosimetry requires practical amount of phosphor for dissolution, typically 5-30 mg. Pronounced mass quenching effect has been observed even in the region of 5 mg, in the cases of LL of lactose-monohydrate, d-glucose, d-mannose, raffinose, sucrose and 1-glutamine. Ordinary concentration-quenching is non-existent but yield per mg falls rapidly with increasing mass of the phosphor. The curves have been fitted with a self-absorption type formula. A well-recognised dose effect is present in quenching curves. The role of free radicals at high radiation doses has been discussed in the contribution of dose effect in quenching.