Thermal conductivity and interfacial energy of solid Bi solution in the Bi–Al–Zn eutectic system

The equilibrated grain boundary groove shapes for solid Bi solution (Bi–6.1 at.%Zn–0.38 at.%Al) in equilibrium with the Bi–Al–Zn eutectic liquid have been observed from quenched sample with a radial heat flow apparatus. The Gibbs–Thomson coefficient, solid–liquid interfacial energy and grain boundary energy of solid Bi solution have been determined from the observed grain boundary groove shapes. The variations of thermal conductivity with temperature for solid Bi solution (Bi–6.1 at.%Zn–0.38 at.%Al) has been measured up to five degree below the melting temperature by using radial heat flow technique. The ratio of thermal conductivity of equilibrated Bi–Al–Zn eutectic liquid phase to solid Bi solution (Bi–6.1 at.%Zn–0.38 at.%Al) phase has also been measured with a Bridgman type growth apparatus at the melting temperature.     

Refractive index enhancement with vanishing absorption in an atomic vapor

We report a proof-of-principle experiment where the refractive index of an atomic vapor is enhanced while maintaining vanishing absorption of the beam. The key idea is to drive alkali atoms in a vapor with appropriate control lasers and induce a gain resonance and an absorption resonance for a probe beam in a two-photon Raman configuration. The strength and the position of these two resonances can be manipulated by changing the parameters of the control lasers. By using the interference between these two resonances, we obtain an enhanced refractive index without an increase in the absorption.     

Modeling primary substrate controlled biotransformation and transport of halogenated aliphatics in porous media

In situ biorestoration is a groundwater remediation technique in which the indigenous aquifer bacteria are stimulated by injecting compounds to provide carbon source and energy. Stimulated bacteria may transform the target contaminants such as tetrachloroethylene (PCE) and trichloroethylene (TCE) into intermediate products. In this study, we developed a model to simulate the substrate-limited biotransformation of the halogenated solvents present in anoxic groundwater by sequential reductive dehalogenation under methanogenic conditions. The model consists of conservation of mass equations for the primary substrate, immobile indigenous biomass, organic solvents such as PCE and TCE, and their intermediate products trichloroethylene, dichloroethylene, and vinyl chloride. The utilization of primary substrate and the biotransformation of organic solvents are assumed to follow Monod kinetics. The limiting factor on bacterial growth is assumed to be the primary substrate. The microbial yield coefficient is determined from the stoichiometric equation describing the anaerobic process. The model is solved by using a finite difference technique. Results are presented for three different case studies: continuous injection of primary substrate (acetate), single-pulse injection, and double-pulse injection. The single-pulse or double-pulse injection techniques were found to be more effective than continuous injection of primary substrate. Double-pulse technique reduces the clogging of injection wells caused by excessive microbial growth around boreholes and achieves a more uniform distribution of microbial growth in the subsurface. In all cases target compounds were effectively removed. The results, however, indicate substantial levels of intermediate product accumulation. Numerical results of a simplified model which assumes an abundance of primary substrate and a constant population of biomass, compare favorably with experimental data reported in the literature.     

Wave propagation in fractured porous media

A theory of wave propagation in fractured porous media is presented based on the double-porosity concept. The macroscopic constitutive relations and mass and momentum balance equations are obtained by volume averaging the microscale balance and constitutive equations and assuming small deformations. In microscale, the grains are assumed to be linearly elastic and the fluids are Newtonian. Momentum transfer terms are expressed in terms of intrinsic and relative permeabilities assuming the validity of Darcy's law in fractured porous media. The macroscopic constitutive relations of elastic porous media saturated by one or two fluids and saturated fractured porous media can be obtained from the constitutive relations developed in the paper. In the simplest case, the final set of governing equations reduce to Biot's equations containing the same parameters as of Biot and Willis.Now at Izmir Institute of Technology, Anafartalar Cad. 904, Basmane 35230, Izmir, Turkey.     

Systematic Investigation of the Effect of Polymerization Routes on the Gas‐Sorption Properties of Nanoporous Azobenzene Polymers

Functional‐group‐oriented polymerization strategies have contributed significantly to the initial development of porous polymers and have led to the utilization of several well‐known organic transformations in the synthesis of these polymers. Because there are multiple polymerization routes that can be used to introduce the same chemical functionality, it is very important to demonstrate the effect of different polymerization routes on the gas‐sorption properties of these chemically similar polymers. Herein, we have studied the rich chemistry of azobenzenes and synthesized four chemically similar nanoporous azobenzene polymers (NABs) with surface areas of up to 1021 m² g^?1. The polymerization routes have a significant impact on the pore‐size distributions of the NABs, which directly affects the temperature dependence of the CO₂/N₂ selectivity. A pore‐width maximum of 6–8 Å, narrow pore‐size distribution, and small particle size (20–30 nm) were very critical for high CO₂/N₂ selectivity and N₂ phobicity, which is associated with azo linkages and realized at warm temperatures. Our findings collectively suggest that an investigation of different polymerization routes for the same chemical functionalization is critical to understand fully the combined effect of textural properties, local environment, and chemical functionalization on the gas‐sorption properties of nanoporous polymers.     

Invariant Subspaces for Banach Space Operators with a Multiply Connected Spectrum

We consider a multiply connected domain where denotes the unit disk and denotes the closed disk centered at with radius r _j for j = 1, . . . , n. We show that if T is a bounded linear operator on a Banach space X whose spectrum contains ∂Ω and does not contain the points λ₁, λ₂, . . . , λ _n , and the operators T and r _j (T − λ _j I)⁻¹ are polynomially bounded, then there exists a nontrivial common invariant subspace for T ^* and (T − λ _j I)^*-1.     

The syntheses of some novel (naphthalen-1-yl-selenyl)acetic acid derivatives

Some new (naphthalen-1-yl-selenyl)acetic acids derivatives 7a-d have been synthesized by two different methods, using naphthylselenols or naphthylselenocyanates. The structures of the products were investigated by spectroscopic methods.     

Reactions of pentachloro-2-nitrobutadiene with some aliphatic and heterocyclic thiols and a crystallographic study

In this study, S-, S,S- and S,O-substituted novel nitrodiene compounds were synthesized. Cyclization products were formed when difunctional nucleophiles were used. The stereoisomerism of a heterocyclic nitrodiene is discussed with the help of XRD studies. The structures of all compounds were characterized by spectroscopic methods (FT-IR, ¹H NMR, ¹³C NMR, ¹⁹F NMR, MS) and microanalysis.     

Synthesis of novel 5‐aryl‐1H‐tetrazoles

In this study phenylselenocyanate and some of its derivatives (o‐Cl, p‐Cl, p‐Br, o‐NO₂, p‐NO₂, o‐CH₃, p‐CH₃, o‐COOH, p‐COOH, p‐OCH₃ substituted) were synthesized ( 3a–3j ). The synthesized compounds were converted to 5‐aryl‐1H‐tetrazole ( 4a–4j ), by Et₃N ċ HCl‐NaN₃ in toluene, which are a new series of phenylselanyl‐1H‐tetrazoles. The structure of all the presently synthesized compounds were confirmed using spectroscopic methods (FTIR, ¹H NMR, MS). © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:255–258, 2007; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20293     

Comparison of Kinetic and Hybrid-Equilibrium Models Simulating Colloid-Facilitated Contaminant Transport in Porous Media

The presence of colloidal particles in groundwater can enhance contaminant transport by reducing retardation effects and carrying them to distances further than predicted by a conventional advective/dispersive equation with normal retardation values. When colloids exist in porous media and affect contaminant migration, the system can best be simulated as a three-phase medium. Mechanisms of mass transfer from one phase to another by colloids and contaminants can be kinetic or equilibrium-based, depending on the sorption–desorption reaction rate between the aqueous and solid phases. When the rate of sorption between the water phase and the solid phase(s) is not much greater than the rate of change in contaminant concentration in the water phase, kinetic sorption models may better describe the phenomenon. In some cases of modeling one or more mass transfer processes, a useful simplification may be to introduce the local equilibrium assumption. In this study, the local equilibrium assumption for sorption processes on colloidal surfaces (hybrid equilibrium model) was compared with kinetic-based models. Sensitivity analyses were conducted to deduce the effect of major parameters on contaminant transport. The results obtained from the hybrid equilibrium model in predicting the transport of colloid-facilitated groundwater contaminant are very similar to those of the kinetic model, when the point of interest is not at contaminant and colloid source vicinities and the time of interest is sufficiently long for imposed sources.