A group of continuous self-maps on a topological groupoid

The group of bisections of groupoids plays an important role in the study of Lie groupoids. In this paper another construction is introduced. Indeed, for a topological groupoid G, the set of all continuous self-maps f on G such that (x, f(x)) is a composable pair for every \(x\in G\), is denoted by \(S_G\). We show that \(S_G\) by a natural binary operation is a monoid. \(S_G(\alpha )\), the group of units in \(S_G\) precisely consists of those \(f\in S_G\) such that the map \(x\mapsto xf(x)\) is a bijection on G. Similar to the group of bisections, \(S_G(\alpha )\) acts on G from the right and on the space of continuous self-maps on G from the left. It is proved that \(S_G(\alpha )\) with the compact- open topology inherited from C(G, G) is a left topological group. For a compact Hausdorff groupoid G it is proved that the group of bisections of \(G^2\) is isomorphic to the group \(S_G(\alpha )\) and the group of transitive bisections of G, \(Bis_T(G)\), is embedded in \(S_G(\alpha )\), where \(G^2\) is the groupoid of all composable pairs.     

Existence Result for a Superlinear Fractional Navier Boundary Value Problems

In this paper, we study the following fractional Navier boundary value problem

$$\begin{aligned} \left\{ \begin{array}{lllc} D^{\beta }(D^{\alpha }u)(x)=u(x)g(u(x)),\quad x\in (0,1), \\ \displaystyle \lim _{x\longrightarrow 0}x^{1-\beta }D^{\alpha }u(x)=-a,\quad \,\,u(1)=b, \end{array} \right. \end{aligned}$$

where \(\alpha ,\beta \in (0,1]\) such that \(\alpha +\beta >1\), \(D^{\beta }\) and \(D^{\alpha }\) stand for the standard Riemann–Liouville fractional derivatives and a, b are nonnegative constants such that \(a+b>0\). The function g is a nonnegative continuous function in \([0,\infty )\) that is required to satisfy some suitable integrability condition. Using estimates on the Green’s function and a perturbation argument, we prove the existence of a unique positive continuous solution, which behaves like the unique solution of the homogeneous problem.

     

A Hybrid Particle Swarm Optimization Algorithm for the Redundancy Allocation Problem

The Redundancy Allocation Problem generally involves the selection of components with multiple choices and redundancy levels that produce maximum system reliability given various system level constraints as cost and weight. In this paper we investigate the series–parallel redundant reliability problems, when a mixing of components was considered. In this type of problem both the number of redundancy components and the corresponding component reliability in each subsystem are to be decided simultaneously so as to maximise the reliability of system. A hybrid algorithm is based on particle swarm optimization and local search algorithm. In addition, we propose an adaptive penalty function which encourages our algorithm to explore within the feasible region and near feasible region, and discourage search beyond that threshold. The effectiveness of our proposed hybrid PSO algorithm is proved on numerous variations of three different problems and compared to Tabu Search and Multiple Weighted Objectives solutions.     

Reconstruction of Thin Conductivity Imperfections

We consider the case of a uniform plane conductor containing a thin curve-like inhomogeneity of finite conductivity. In this article we prove that the imperfection can be uniquely determined from the boundary measurements of the first order correction term in the asymptotic expansion of the steady state voltage potential as the thickness goes to zero.     

Uniformly Classical Primary Submodules

We shall introduce the notion of uniformly classical primary submodule that generalizes the concept of uniformly primary ideal as given by J. A. Cox and A. J. Hetzel. We also advance the companion concepts of fully uniformly classical primary module and uniformly primary compatible module. Along these lines, we present a characterization of Noetherian rings R for which every R-module is fully uniformly classical primary and we present a characterization of rings R for which every finitely generated R-module is uniformly primary compatible. Results illustrating connections among the notions of uniformly classical primary submodule, uniformly primary ideal, and uniformly primary submodule as given by R. Ebrahimi-Atani and S. Ebrahimi-Atani are also provided.     

Computational singular perturbation with non-parametric tabulation of slow manifolds for time integration of stiff chemical kinetics

This paper presents a novel tabulation strategy for the adaptive numerical integration of chemical kinetics using the computational singular perturbation (CSP) method. The strategy stores and reuses CSP quantities required to filter out fast dissipative processes, resulting in a non-stiff chemical source term. In particular, non-parametric regression on low-dimensional slow invariant manifolds (SIMs) in the chemical state space is used to approximate the CSP vectors spanning the fast chemical subspace and the associated fast chemical time-scales. The relevant manifold and its dimension varies depending on the local number of exhausted modes at every location in the chemical state space. Multiple manifolds are therefore tabulated, corresponding to different numbers of exhausted modes (dimensions) and associated radical species. Non-parametric representations are inherently adaptive, and rely on efficient approximate-nearest-neighbor queries. As the CSP information is only a function of the non-radical species in the system and has relatively small gradients in the chemical state space, tabulation occurs in a lower-dimensional state space and at a relatively coarse level, thereby improving scalability to larger chemical mechanisms. The approach is demonstrated on the simulation of homogeneous constant pressure H₂–air and CH₄–air ignition, over a range of initial conditions. For CH₄–air, results are shown that outperform direct implicit integration of the stiff chemical kinetics while maintaining good accuracy.     

The Arboreal Jump Number of an Order

Let ${\mathcal P}$ be a partial order and ${\mathcal A}$ an arboreal extension of it (i.e. the Hasse diagram of ${\mathcal A}$ is a rooted tree with a unique minimal element). A jump of ${\mathcal A}$ is a relation contained in the Hasse diagram of ${\mathcal A}$ , but not in the order ${\mathcal P}$ . The arboreal jump number of ${\mathcal A}$ is the number of jumps contained in it. We study the problem of finding the arboreal extension of ${\mathcal P}$ having minimum arboreal jump number—a problem related to the well-known (linear) jump number problem. We describe several results for this problem, including NP-completeness, polynomial time solvable cases and bounds. We also discuss the concept of a minimal arboreal extension, namely an arboreal extension whose removal of one jump makes it no longer arboreal.     

Effect of ring substitution on synthesis of benzimidazolium salts and their silver(I) complexes: characterization,electrochemical studies and evaluation of anticancer potential

Transition Metal Chemistry - A series of bidendate 5,6-dimethyl benzimidazolium-based N-heterocyclic carbene (NHC) proligands and their silver complexes were synthesized. The synthetic approaches...     

Unsymmetrically substituted benzimidazolium based Silver(I)-N-heterocyclic carbene complexes: Synthesis,characterization and in vitro anticancer study against human breast cancer and colon cancer

The promising biomedical applications of silver complexes stimulated the researchers to test these compounds against cancer. The present research work was designed to achieve this goal. In this work, a series of 5-methyl benzimidazole based N-Heterocyclic carbene ligands and respective silver(I) complexes were synthesized and tested on cancer cell lines to assess their anticancer activity. Unsymmetrically substituted benzimidazole was found unique in its reactivity and generation of a single product during NHC ligand formation was only possible after two successive alkylations with same alkyl halide. The corresponding Ag(I)-NHC adducts were obtained by in situ deprotonation of the NHC ligands. Synthesized compounds were characterized by various physcio-chemical and spectroscopic methods. Single crystal X-ray diffraction study of complex 7 revealed its mononuclear structure. Preliminary in vitro anticancer study of azolium salts and respective Ag(I)-NHC complexes against human breast cancer (MDA-MB-231), colon cancer (HCT-116) and normal endothelial cells (EA.hy926) cells revealed that all the compounds are more cytotoxic to cancer cells than normal cells and the complexes are relatively more potent compared to the corresponding NHC ligands. It was found that increased chain length and presence of methyl substituent on benzimidazole ring enhance the biopotency of Ag(I)-NHC complexes. The synthesized compounds were further studied for pro-apoptotic mechanism of action via Rhodamine 123 test. The tested compounds were found to induce apoptosis via extrinsic mitochondrial pathway.