Flame temperature determination by dual laser ionization

A dual laser ionization (DLI) apparatus was used to determine ionic diffusion and mobility coefficients for sodium and lithium in a stoichiometric H₂/O₂/Ar flame. The flame temperature was calculated using the Einstein relation. The sodium and lithium DLI temperature estimates are in agreement with each other and with temperatures measured by the line-reversal technique in similar flames.     

Scale dependence of branching in arterial and bronchial trees

Although models of branching in arterial and bronchial trees often predict a dependence of bifurcation parameters on the scale of the bifurcating vessels, direct verification of this dependence by comparison with data is uncommon. We compare measurements of bifurcation parameters of airways and arterial trees of different mammals as a function of scale to general features predicted by theoretical models based on minimization of pumping power and network volume. We find that the size dependence is more complex than existing theories based solely on energy and volume minimization explain, and suggest additional factors that may govern the branching at different scales.     

A fluorescence polarisation molecular imprint sorbent assay for 2,4-D: a non-separation pseudo-immunoassay

The first pseudo-immunoassay which employs a molecularly imprinted receptor and a fluorescent probe, and quantifies the bound analyte directly using the fluorescence anisotropy of the polymer-probe-analyte suspension, is described.     

Infrared spectral changes with crystallization in poly(vinylchloride): Correlations with X-ray and density data

The influence of crystallinity and stereoregularity on the infrared (IR) spectrum of atactic PVC in the solid state has been studied by many researchers [1-12]. Although the molecules in commercial PVC consist of both syndiotactic and isotactic sequences, the bulk polymer is not highly stereoregular, having approximately 50% syndiotacticity. Its infrared spectrum is different from that of highly syndiotactic PVC [3,5,7,9,10-12], particularly in the carbon-to-chlorine stretching region where there are three bands located at 610(615), 635, and 690 cm^?1. These three bands are known to be of complex origin, since each band consists of more than one absorption frequency and its relative intensity depends on the physical state or history of the specimen [3,5,7,9,10-12]. The spectrum in this region is most rigorously interpreted in terms of chain conformational structure, the spatial arrangement of the atoms around the C-C1 bond. Thus, while changes in absorbance intensities for the bands with history do not necessarily reflect changes in crystallinity, their history dependence renders these bands potentially useful as crystallinity indicators.     

Raman Scattering Tensors in Biological Molecules and Their Assemblies

INTRODUCTION

The tensor associated with a Raman band plays an important role in determining the band intensity and its structural significance. Each Raman tensor interrelates two electric vectors, that of the exciting radiation (i.e. laser photon) and that of the Raman scattered radiation (i.e. the inelastically scattered photon which results from the exchange of a vibrational quantum between the exciting photon and the molecule). The Raman tensor is obtained formally as the first derivative of the molecular polarizability tensor, the derivative being taken with respect to the vibrational normal coordinate. In other words, the Raman tensor associated with a vibrational Raman band is an indicator of how the polarizability of the molecule oscillates with the molecular normal mode of vibration.     

Investigating the mechanisms of diamond polishing using Raman spectroscopy

Recent research has shown that a phase transformation of diamond to a different form of carbon is involved when diamonds are polished in the traditional fashion. The question as to how this phase transformation is activated and maintained to produce high wear rates is of great technological interest since it may radically change the way we view the processing of diamond. This paper describes the use of Raman spectroscopy to examine debris produced on the diamond polishing wheel, both during its preparation and during polishing. In addition, polished diamond surfaces were examined for the possible existence of non-diamond surface layers in an attempt to identify material removal mechanisms. Raman spectroscopy proves ideal for these analyses because its relatively high spatial resolution is well suited to the analysis of small wear features and debris particles, and because of the wealth of information it reveals about chemical structure. This level of structural information has been lacking in previous analyses of diamond polishing debris. In addition to the non-diamond carbon found in the wear debris, significant quantities of two iron oxides, magnetite (Fe₃O₄) and haematite (α-Fe₂O₃), were also found. An interesting observation was that a transformation from magnetite to haematite could be induced either by using high power laser excitation or by frictional heating during polishing. It is suggested that some of the Raman peaks previously attributed to lonsdaleite might better be explained by the presence of these oxides.     

Distribution of hydraulic conductivity in single scale anisotropy

The cluster statistics of percolation theory are used to find the distributions of hydraulic conductivity, K, of anisotropic (truncated) random fractal media. Rescaling of variables to transform anisotropic to isotropic media also produces deformations of, for example experimental volumes, and the resulting non-equidimensional shapes may generate interesting size effects on K. Previously, the most likely value of K was obtained by comparing the correlation length from percolation theory with system dimensions, a procedure analogous to those developed for hopping conduction in disordered systems to calculate the longitudinal conductivity of thin films. The result probably explains the frequent tendencies of measurements of K in anisotropic fracture networks and agricultural soils to increase with the scale of measurement, similarly to how the longitudinal conductivity of a thick film would be larger than the corresponding conductivity of a thin film (three- rather than two-dimensional conduction). However, the same procedure applied to the conductivity in the perpendicular direction (analogous to the transverse electrical conductivity of a thin film) shows a diminishing function of spatial scale. Collectively, these ‘scale effects’ disappear if the shape of the experimental volume is selected to maintain the relationships of conduction in the various directions as the scale of the experiment is increased analogously to equidimensional volumes in isotropic media. The increase in K is, thus, merely due to an increase in the dimensionality of conduction from one to three with increasing system size. The paper, thus, provides a solid argument against a common assumption in the porous media communities that the connectivity of highly conducting regions of a medium should increase with increasing scale of measurement.     

Longitudinal dispersion of solutes in porous media solely by advection

The purpose of this work is to predict the transport of non-sorbing solutes through water flow in the subsurface. We derive what we consider to be the first reliable calculations of the entire distribution of arrival times, W(t), for non-sorbing solutes in advective flow in strongly disordered porous media. Solutes treated can be contaminant plumes from any source or radioactive tracers, both experimentally and naturally generated. Our approach is microscopic and based on effects of disorder. It generates longitudinal dispersion (in the direction of flow) in the absence of diffusion. Effects on dispersion from a single capillary tube velocity distribution, known to produce long-tailed arrival time distributions, are also neglected. On the other hand, our calculations are based on effects generated from real porous media, such as wide pore-size distributions and complex connectivity. In particular, the calculation of the distribution of arrival times is based on a distribution of conserved fluxes and the known tortuosity of the associated geometrical paths. The results are found to be predictive when compared with simulations of two-dimensional flow on percolation structures, and appear to have relevance for experiments as well.