Physico-chemical studies on polymethyl methacrylate alite composite

The influence of methyl metharcylate and gamma exposure dose on the physico-chemical and mechanical properties of polymer-alite composite have been investigated. The hardened alite samples were impregnated with a methyl methacrylate monomer and then subjected to γ irradiation doses from 10–50 KGy. The effect of polymer loading (%), compressive strength, bulk density and the microstructure (scanning electron microscopy SEM), in addition IR spectra were studied. The results indicate that, polymer loading, compressive strength and bulk density increase with increasing absorbed dose. This is attributed to the deposition of the polymer in the pores of the samples. SEM showed the voids between the particles in the samples before the impregnation, whereas, the formation of new products in the pores appeared after impregnation.     

Evaluation of linear and nonlinear convection schemes on multidimensional non‐orthogonal grids with applications to KVLCC2 tanker

Almost all evaluations of convection schemes reported in the literature are conducted using simple problems on uniform orthogonal grids; thus, having limited contribution when solving industrial computational fluid dynamics (CFD), where the grids are usually non‐orthogonal with distortions. Herein, several convection schemes are assessed in uniform and distorted non‐orthogonal grids with emphasis on industrial applications. Linear and nonlinear (TVD) convection schemes are assessed on analytical benchmarks in both uniform and distorted grids. To evaluate the performance of the schemes, four error metrics are used: dissipation, phase and L₁ errors, and the schemes' effective order of accuracy. Qualitative and quantitative deterioration of these error metrics as a function of the grid distortion metrics are investigated, and rigorous verifications are performed. Recommendations for effective use of the convection schemes based on the range of grid aspect ratio (AR), expansion ratio (ER) and skewness (Q) are included. A ship hydrodynamics case is studied, involving a Reynolds averaged Navier–Stokes simulation of a bare‐hull KVLCC2 tanker using linear and nonlinear convection schemes coupled with isotropic and anisotropic Reynolds‐stress (ARS) turbulence models using CFDShip‐Iowa v4. Predictions of local velocities and turbulent quantities from the midships to the nominal wake plane are compared with experimental fluid dynamics (EFD), and rigorous verification and validation analyses for integral forces and moments are performed for 0° and 12° drift angles. Best predictions are observed when coupling a second‐order TVD scheme with the anisotropic turbulence model. Further improvements are observed in terms of prediction of the vortical structures for 30° drift when using TVD2S‐ARS coupled with DES. Copyright © 2009 John Wiley & Sons, Ltd.     

Characterization of fe bearing compounds in environmental samples

Using⁵⁷Mössbauer spectroscopy and neutron activation analysis, various kinds of environmental samples have been studied, in order to demonstrate that the combination of a phase sensitive and a multi-element technique is a powerful tool for studying environmental problems.     

A scale model investigation of sound reflection from building façades

A simple model for predicting the sound reflected from a building façade is developed based upon the assumption that the scattering coefficient is small. This model is then used as the basis of an experimental attempt to measure the scattering properties of scale model façades featuring a similar degree of surface irregularity to that found on real buildings. A series of measurements made on a simple scale model are described and the effect of a non-uniform distribution of façade scattering is examined. The measured value of the scattering coefficient is found to be small and not very sensitive to the degree of surface irregularity. A progression of energy from a specular reflection field to a diffuse reflection field for successive orders of reflections is observed. It is suggested that the dominant mechanism of sound propagation for higher order reflections is via random scattering and that the development of propagation models based upon purely random scattering is a valid approach.     

Synthesis and characterization of novel antimicrobial cationic polyelectrolytes

Cationic polyelectrolytes containing quaternary nitrogen atoms within the main chain were prepared via condensation polymerization of epichlorhydrin (ECH) with benzyl amine (BA). Polyelectrolytes having different molecular weights were obtained by varying the ECH/BA mole ratio. Cationic polymers were characterized by ¹H-NMR and gel permeation chromatography. The antimicrobial activity of the polymers was tested against bacteria, yeast, and fungi.     

On formulas of Ramanujan and Evans

We give short elementary proofs of a formula of Ramanujan as interpreted by Bradley, and a companion formula originally proved by W. Chu. We also give an elementary proof of a generalization of an identity originally proved using modular functions and used to study a generating function for the number of partitions with specified crank. Research partially supported by NSF grant DMS 99-70865. 2000 Mathematics Subject Classification Primary—39A70, 11P83; Secondary—33C20     

Preparation and Characterization of Chitosan Thin Films on Mixed-Matrix Membranes for Complete Removal of Chromium

Herein we present a new approach for the complete removal of Cr^VI species, through reduction of Cr^VI to Cr^III, followed by adsorption of Cr^III. Reduction of chromium from water is an important challenge, as Cr^IV is one of the most toxic substances emitted from industrial processes. Chitosan (CS) thin films were developed on plain polysulfone (PSf) and PSf/TiO₂ membrane substrates by a temperature-induced technique using polyvinyl alcohol as a binder. Structure property elucidation was carried out by X-ray diffraction, microscopy, spectroscopy, contact angle measurement, and water uptake studies. The increase in hydrophilicity followed the order: PSf < PSf/TiO₂ < PSf/TiO₂/CS membranes. Use of this thin-film composite membrane for chromium removal was investigated with regards to the effects of light and pH. The observations reveal 100 % reduction of Cr^VI to Cr^III through electrons and protons donated from OH and NH₂ groups of the CS layer; the reduced Cr^III species are adsorbed onto the CS layer via complexation to give chromium-free water.     

Trapping Nanostructures on Surfaces through Weak Interactions

The assembly of imidazole‐functionalized phenanthroline‐strapped zinc porphyrins (ZnPorphen) with alkyl or polyethylene glycol (PEG) side chains was studied in solution and by AFM after casting on highly oriented pyrolytic graphite (HOPG) or mica. The nature of the solvent and its evaporation time influenced the morphology of the objects observed. On HOPG, short rods of about 100 nm were observed after fast evaporation of solutions of the alkyl derivatives in CHCl₃, THF, or pyridine, whereas islands of aligned rows of longer wires were obtained from methylcyclohexane (MCH). Slow evaporation of MCH led to a three‐dimensional assembly. The PEG porphyrin assembled into short wires on HOPG or fibers on mica after slow evaporation of solutions in THF. This study shows the role of surface–molecule interactions in the interfacial assembly of ZnPorphen derivatives and contributes to understanding the parameters that control their noncovalent assembly into molecular wires on a surface.     

Dissolution kinetics of fluorapatite in the hydrochloric acid solution

A thermochemical study of hydrochloric acid attack of synthetic fluorapatite was performed by a DRC. The calculated thermogenesis curves show one peak. The plot of the heat quantity as a function of the dissolved mass undergoes only one straight segment, and the thermogenesis curves present a single peak, suggesting the occurrence of a one-step dissolution process. The dissolution kinetics was examined according to the heterogeneous reaction models and showed that the dissolution is controlled by the product layer diffusion process with a reaction rate expressed by the following semiempirical equation; \(\left[ {1 + 2(1 - X) - 3(1 - X)^{{\frac{2}{3}}} } \right] = 3195 \times 10^{ - 2} C^{0.145} \left( {\frac{S}{L}} \right)^{ - 0.628} e^{{ - \frac{2600}{\text T}}} t\). The activation energy was determined as 21.6 ± 1.5 kJ mol^?1