Influence of Hydrolytic and Chemical Treatment on the Mechanical Properties of Aramid and Copolyaramid Fibers

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.Commercial PPTA fibers ( Kevlar 49® and Twaron 1055®) and copolyaramid fibers (Trevar®) are subjected to various hydrolytic and chemical treatments. Tensile mod ulus, tensile strength, and elongation at break are measured, and mechanical property deterioration is compared. Copolyaramid fibers show improved hydrolytic stability and chemical resistance compared to PPTA fibers. The time dependence of degradation pro cesses can be described by two decreasing exponential functions. WAXS measurements detect only slight differences in the crystalline structure and superstructure of the treated fibers. Thus, the main origin of mechanical degradation is the destruction of intercrys talline links such as tie molecules or tie crystallites

The Ingalls-Thomas Bijections

Given a finite acyclic quiver Q with path algebra kQ, Ingalls and Thomas have exhibited a bijection between the set of Morita equivalence classes of support-tilting modules and the set of thick subcategories of mod kQ and they have collected a large number of further bijections with these sets. We add some additional bijections and show that all these bijections hold for arbitrary hereditary artin algebras. The proofs presented here seem to be of interest also in the special case of the path algebra of a quiver.Comment: This is a modified version of an appendix which was written for the paper "The numbers of support-tilting modules for a Dynkin algebra" (see arXiv:1403.5827v1

Stability of Virus Infection Models with Antibodies and Chronically Infected Cells

Two virus infection models with antibody immune response and chronically infected cells are proposed and analyzed. Bilinear incidence rate is considered in the first model, while the incidence rate is given by a saturated functional response in the second one. One main feature of these models is that it includes both short-lived infected cells and chronically infected cells. The chronically infected cells produce much smaller amounts of virus than the short-lived infected cells and die at a much slower rate. Our mathematical analysis establishes that the global dynamics of the two models are determined by two threshold parameters R0 and R1. By constructing Lyapunov functions and using LaSalle's invariance principle, we have established the global asymptotic stability of all steady states of the models. We have proven that, the uninfected steady state is globally asymptotically stable (GAS) if R0<1, the infected steady state without antibody immune response exists and it is GAS if R11. We check our theorems with numerical simulation in the end

RCS of Chiral Elliptic Cylinder Embedded in Infinite Chiral Medium

This paper presents an analytic solution to the scattering properties of chiral elliptic cylinder embedded in infinite chiral medium due to incident plane wave. The external electromagnetic fields as well as the internal electromagnetic fields are written in terms Mathieu functions and expansion coefficients. In order to obtain both the internal and external unknown field expansion coefficients, the boundary conditions are applied rigorously at the surface of different chiral/chiral material. Results are plotted graphically for the normalized scattering widths for elliptic cylinders of different sizes and chiral materials to show the effects of these parameters on scattering cross widths. It is shown numerically by adding the external chiral material to elliptic cylinder provides more parameters to control the RCS

Fast solvers and efficient numerical cfd techniques for dynamic porous media problems

We present a fully implicit, monolithic finite element solution scheme to efficiently solve the governing set of differential algebraic equations of incompressible poroelastodynamics. Thereby, we proceed from a two-dimensional, biphasic, saturated porous medium model with intrinsically coupled and incompressible solid and fluid constituents. Our approach, motivated by well-accepted CFD techniques and originally developed for the efficient simulation of incompressible flow problems, is characterized by the following aspects: (1) a special treatment of the algebraically coupled volume balance equation leading to a reduced form of the boundary conditions; (2) usage of a higher-order accurate mixed LBB-stable finite element pair with piecewise discontinuous pressure for the spatial discretization; (3) application of the fully implicit 2nd-order Crank-Nicolson scheme for the time discretization; (4) use of a special fast multigrid solver for the resulting discrete linear equation system. For the purpose of validation and to expose the merits and benefits of our new solution strategy in comparison to other established approaches, canonical one- and two-dimensional wave propagation problems are solved. Finally, a large-scale, dynamic soil-structure interaction problem serves to reveal the efficiency of the special multigrid solver in combination with the chosen finite element discretization

Design and Implementation of Educational Data Warehouse Using OLAP

Educational Data Mining (EDM) is a method to support learning and teaching processes. Educational Intelligence (EI) is not wide spreading like a business Intelligence (BI). Data Warehouse (DW) technology aims to collect historical data from different kinds of Database (DB) and unifies them under single schema by using the most powerful tool as OLAP which helps the decision maker to make a right decision. Educational Intelligence system combines Educational records of students from two different sources in a single DW. The inputs of educational data warehouse can be in any format (such as reports...). Since the quantities are huge, they are almost meaningless, on the other hand the outputs mainly consist of reports and flowcharts and KPIs with meaning and effective factor for decision maker. The proposed DW is implemented based on two simulated databases of Computer Science Department in the College of Science, University of Basra for the last ten years and AL_IRAQ University for the last 4 years implemented by SQL Server 2014 and SQL Server Data Tool (SSDT) 2012

Spectrodensitometric and ultra-performance liquid chromatographic quantification of dapagliflozin and saxagliptin in their dosage form and human plasma

Purpose: To simultaneously quantify dapagliflozin (DAPA) and saxagliptin (SAX) in a pharmaceutical product and human plasma. Methods: Separation and quantification of DAPA and SAX were performed on pre-coated TLC plates in TLC-densitometric method using a solvent system of chloroform, ethyl acetate and methanol at a volume ratio of 8:1:1 as the mobile phase. The developed spots were scanned at 225 and 210 nm in absorbance mode. Moreover, the studied drugs were concurrently determined in human plasma using ultra-performance liquid chromatography (UPLC). The separation process was carried out in WatersTM Acquity C18 BEH column using a solvent system of 0.02 M KH2PO4 buffer, pH 4; MeOH and acetonitrile (2:1:1, v:v:v) isocratically at a flow speed of 0.5 mL/min. The absorbance of each eluent was read at 220 nm. Results: Concurrent evaluation of DAPA and SAX was carried without separation using TLC-densitometric method, and it was successful in determination of DAPA and SAX in concentration ranges of 10 – 70 μg/band and 5 – 60 μg/band, respectively. In addition, retardation factor (Rf) values for SAX and DAPA were 0.17 and 0.31, respectively. Furthermore, the studied drugs were concurrently determined in human plasma using UPLC, which was sensitive enough to quantify DAPA and SAX in concentration ranges of 100 – 1000 and 20 – 200 ng/mL, respectively. Conclusion: These methods can be utilized for sensitive monitoring of DAPA and SAX in pharmacokinetic and bioequivalence studies