Modified Eu3+ doped Y2O3 Nanoparticles as Turn-on Fluorescence Sensor for Sensitive Determination of Methamphetamine

Journal of Analytical Chemistry - In this article, a new spectrofluorometric method was developed for the determination of methamphetamine based on a turn-on luminescence response of captopril...     

The peridynamic differential operator for solving time-fractional partial differential equations

Nonlinear Dynamics - In this paper, the numerical solution of time-fractional convection diffusion equations (TF-CDEs) is considered as a generalization of classical ones, nonexponential relaxation...     

Definition and detection of data-based uniqueness in evaluating bilinear (two-way) chemical measurements

Multivariate curve resolution methods, frequently used in analyzing bilinear data sets, result in ambiguous decomposition in general. Implementing the adequate constraints may lead to reduce the so-called rotational ambiguity drastically, and in the most favorable cases to the unique solution. However, in some special cases, non-negativity constraint as minimal information of the system is a sufficient condition to resolve profiles uniquely. Although, several studies on exploring the uniqueness of the bilinear non-negatively constrained multivariate curve resolution methods have been made in the literature, it has still remained a mysterious question. In 1995, Manne published his profile-based theorems giving the necessary and sufficient conditions of the unique resolution. In this study, a new term, i.e., data-based uniqueness is defined and investigated in details, and a general procedure is suggested for detection of uniquely recovered profile(s) on the basis of data set structure in the abstract space. Close inspection of Borgen plots of these data sets leads to realize the comprehensive information of local rank, and these argumentations furnish a basis for data-based uniqueness theorem. The reported phenomenon and its exploration is a new stage (it can be said fundament) in understanding and describing the bilinear (matrix-type) chemical data in general.     

Dissolution optimization and kinetics of nickel and cobalt from iron-rich laterite ore,using sulfuric acid at atmospheric pressure

More than 70% of the world's nickel reserves are found in laterite ores. In this research, a laterite ore sample, containing Ni, Co, and Fe, was employed to study the recovery of nickel and cobalt. Thus, the effect of calcination, acid concentration, percent solids, and stirring rate on nickel and cobalt recoveries from an iron-rich laterite sample was investigated. Optimization with response surface methodology and kinetic studies were performed. The calcination of the sample prior to leaching at 500°C for 2 h provided condition for better nickel and cobalt dissolutions. At optimal conditions, the concentration of sulfuric acid, solid-to-liquid ratio, stirring speed, temperature, and time test were equal to 5 M, 0.1, 370 rpm, 90°C, and 2 h, respectively. The highest recoveries of nickel and cobalt were 65.9% and 63.1%, respectively. Solids content had a negative effect on Ni and Co recovery, whereas acid concentration was positively affected. Addition of 10% (w/v) NaCl in the presence of 5 M acid concentration, 60°C, 370 rpm, and leaching time of 2 h increased the nickel and cobalt recoveries, 15.3% and 21.4%, respectively. The high dependence of process on temperature indicates chemical control; the activation energies E_a = 59.54 and E_a = 45.74 kJ/mol, respectively, for nickel and cobalt, were also consistent with this conclusion.     

On using mesh-based and mesh-free methods in problems defined by Eringen’s non-local integral model: issues and remedies

With the recent success of nonlocal theories in modeling of engineering problems involving small intrinsic length scales, such as modeling of crack propagation, this paper addresses issues pertaining to cost-ineffectiveness of Eringen’s integral model. The cost effectiveness of the computation may be considered as a twofold issue; one pertaining to the non-local model and another pertaining to the numerical tool. First of all, we shall show that during the solution of problems with Eringen’s non-local integral model, there is no need to consider the integral model for the whole computational domain. In fact, the problems may be solved by just using the integral model close to the boundaries, i.e. a boundary layer effect, or around the points with singularities. In this paper we propose a partitioning strategy to remarkably reduce the computational cost. This may be considered as a gateway for solving some types of two-scale problems, e.g. those with macro/micro and nano scales, in which the small scale effects are localized just at parts of the domain. To demonstrate the efficiency of the numerical tools, we examine the performance of the finite element method (FEM), the element free Galerkin method (EFG) and the finite point method (FPM). This paves the way for using mesh-free methods in the solution of problems with non-local integral models. Examples with smooth and non-smooth solutions are considered for examining the efficiency of the methods. It will be shown that, by considering the boundary layer effect, the FEM and FPM will be efficient enough for being used in problems defined by Eringen’s non-local integral model.

     

Distance-regular Cayley graphs with least eigenvalue $$$$

We classify the distance-regular Cayley graphs with least eigenvalue \(-2\) and diameter at most three. Besides sporadic examples, these comprise of the lattice graphs, certain triangular graphs, and line graphs of incidence graphs of certain projective planes. In addition, we classify the possible connection sets for the lattice graphs and obtain some results on the structure of distance-regular Cayley line graphs of incidence graphs of generalized polygons.     

Energy and exergy analysis of a novel turbo-compounding system for supercharging and mild hybridization of a gasoline engine

Journal of Thermal Analysis and Calorimetry - Number of hybrid vehicles has increased around the world significantly. Automotive industry is utilizing the hybridization of the powertrain system to...     

Torsional vibration of functionally graded nano-rod under magnetic field supported by a generalized torsional foundation based on nonlocal elasticity theory

Abstract

This article contains the nonlocal elasticity theory to capture size effects in functionally graded (FG) nano-rod under magnetic field supported by a torsional foundation. Torque effect of an axial magnetic field on an FG nano-rod has been defined using Maxwell’s relation. The material properties were assumed to vary according to the power law in radial direction. The Navier equation and boundary conditions of the size-dependent FG nano-rod were derived by the Hamilton’s principle. These equations were solved by employing the generalized differential quadrature method (GDQM). Presented model has the ability to turn into the classical model if the material length scale parameter is taken to be zero. The effects of some parameters, such as inhomogeneity constant, magnetic field and small-scale parameter, were studied. As an important result of this study can be stated that an FG nano-rod model based on the nonlocal elasticity theory behaves softer and has smaller natural frequency.     

Influence of counter-anion on the coordination geometry of manganese(II) complexes with methyl-2-pyrazinecarboximidate ligand

Two new complexes of [Mn(2-MPyzCI)₂Cl₂].H²O (1) and [Mn(2-MPyzCI)₂(H₂O)₂](NO₃)₂ (2) were synthesized from the reaction of MnX₂.4H₂O (X=Cl^? and NO₃^?) with 2-cyanopyrazine in methanolic solution. The chelating methyl pyrazine-2-carboximidate (2-MPyzCI) ligand is formed via the methanolysis of 2-cyanopyrazine. Although coordination environment around manganes(II) ions is similar, but these complexes are different in geometrical position of 2-MPyzCI ligands. As both compounds are synthesized under the same reaction conditions, the only difference between these two complexes are counter ions and changing of geometrical position of ligands can be considered as a result of influence of the counter-anions on the molecular structures.