Assessment of thermal expansion coefficient of methylsilsesquioxane thin film

For the methylsilsesquioxane film whose optical birefringence is almost zero, it was recently reported that its vertical thermal expansion coefficient (CTE) was approximately one order of magnitude larger than the lateral CTE. Though the birefringence is not an absolute predictor of anisotropic behavior, the discrepancy in both the CTEs was so remarkable that it was essential to investigate whether the anisotropy was intrinsic property or not. If the effect of Poisson's ratio is considered in the calculation of the vertical CTE and when elastic modulus measured by surface acoustic wave spectroscopy is used in the assessment of the lateral CTE, both the CTEs are coincident with each other. Therefore, it can be concluded that the discrepancy in the CTEs can be attributed to a higher in‐plane polymer chain orientation but it can also arise from the misleadingly assumed modulus and Poisson's ratio. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 3109–3120, 2006     

Mutual coupling of elements in finite microstrip antennas

The mutual coupling of the radiating elements in microstrip antennas is studied using a rigorous electrodynamic approach in which the field singularities at the radiator edges are taken into account with analytic accuracy. A spectral method is employed in combination with a method of semi-inversion by extraction of the Green-function singularity. The degree of interaction of the elements of microstrip structures at the fundamental and higher current harmonicsis determined, and the applicability of various approximations is assessed.Radio-Astronomy Institute, Academy of Sciences of Ukraine. Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Radiofizika, Vol. 35, No. 8, pp. 688–701, August, 1992.     

Research problem

This section appears from time to time. Contributions are invited, and should be submitted to R C. Thompson, Mathematics Department. University of California, Santa Barbara, CA93106-3080, USA.     

Deuterium NMR studies of inositol liquid crystals [1]

Deuterium NMR investigations are presented on members of two new mesogenic series derived from the naturally occurring stereoisomers myo- and scW/o-inositol. Tetraethers of these two series exhibit thermotropic columnar phases in which the columns are apparently formed by stacked hydrogen bonded dimers of these molecules which chemically are vicinal diols. Deuterium NMR measurements were performed on the tetraoctyl homologues 2e (a cis diol) and 3e (a trans diol) of these series. We have investigated mixtures of these diols with small amounts of benzene-d₆ as probe molecules as well as samples of the neat diol compounds deuteriated at their hydroxyl groups. The results obtained show that the mesophases of both compounds are uniaxial and align partially in a magnetic field upon slow cooling from their isotropic liquids. The alignment is with the director parallel to the field direction indicating that the anisotropic magnetic susceptibility of this mesophase is positive. The deuterium quadrupole splitting of the benzene-d₆ probe in both systems is temperature dependent and in the trans diol 3e it even changes sign. This is interpreted in terms of a model in which the benzene-d₆ probe equilibrates rapidly between two (or more) solvation sites with quadrupole splittings of opposite signs The deuterium spectra of the neat deuterium labelled cis diol 2e exhibit two different signals due to the two deuterons which are located at the axial and equatorial hydroxyl groups. This indicates that there is no fast intra- or intermolecular exchange of the hydroxyl hydrogens. The overall quadrupole splittings of the hydroxyl deuterons in this compound are highly reduced compared to their static values and this is interpreted in terms of motional modes involving both reorientation of the hydroxyl deuterons about their C-O axis and overall reorientation of the molecules (or pairs of molecules) around the columnar axes. The corresponding spectra of the neat deuteriated trans diol 3e exhibit a single spectrum indicating that both hydroxyl deuterons in this compound are equivalent, or very nearly so. Within the mesophase region the spectrum undergoes gradual changes due to the increase in the molecular mobility, but the overall motional narrowing is less than in the cis isomer 2e. Apparently due to stronger hydrogen bonding in the trans isomer 3e the precession of the hydroxyl groups is hindered and a fast molecular reorientation is only possible at high temperatures.     

Differential determination of arsenic(III) and total arsenic using flow injection on-line separation and preconcentration for graphite furnace atomic absorption spectrometry

Arsenic(III) can be quantitatively extracted using sodium diethyldithiocarbamate (NaDDTC) as the complexing agent and C18 reversed phase packing as the column material for solid phase extraction. Arsenic(V) must be reduced to its trivalent oxidation state prior to extraction. A mixture of sodium sulphite, hydrochloric acid, sodium thiosulphate and potassium iodide was found to be optimum for on-line reduction. When the sorbent extraction is carried out without and with the addition of the reduction mixture, arsenic(III) and total arsenic can be determined sequentially by graphite furnace atomic absorption spectrometry with detection limits (3 σ) of 0.32 ng for As(III) and 0.43 ng for total arsenic. A 7.6-fold enhancement in peak area compared to direct injection of 40 μl samples was obtained after 60 s preconcentration. Results obtained for sea water standard reference materials, using aqueous standards for calibration, agree well with certified values. A precision of 5.5% RSD was obtained for total arsenic in a sea water sample (1.65 As). Results obtained for synthetic mixtures of trivalent and pentavalent arsenic agreed well with expected values.     

Transport properties of a side-chain liquid-crystalline polymer. Poly(4-acryloyloxy biphenyl)

The transport properties of a side-chain liquid-crystalline polymer forming a smectic A phase have been investigated using dichloromethane as a permeant. Samples differing in the isotropization enthaoly were analyzed. A. Correlation between this thermal parameter and sorption has been found, while the diffusion coefficient is substantially the same in all samples. The results obtained can be explained in terms of a biphasis model in which a disordered permeable phase is present within the liquid-crystalline phase, which is impermeable to the diffusant molecules.     

Mixing mechanisms of vortex ring formed by gravity slumping motion

 This paper is concerned with an experimental investigation of the mixing inside the vortex ring formed by the gravity slumping motion of a dense cloud in a less dense atmosphere. The dynamics of the spreading and instantaneous structures of the turbulent flow were examined by visualization, single and multi-point measurements of velocity and concentration for two heavy gases, carbondioxide (CO₂) and dichlorodifluoromethane (CCl₂F₂), in a configuration in that heavy gas, initially trapped in a reservoir, was released with the rise of a shutter into calm air of a sector-shaped dispersion channel. Visualization of the cloud as a whole showed a spreading motion in which an advancing frontal structure was followed by a stratified flow with a layer of dense fluid of higher velocities near the wall and, on top of it, a layer of dilute fluid whose concentration is controlled by the mixing mechanisms within the head. During the course of spreading, there was always a phase in which the head attained to a constant speed of advance, which occurred as 0.13 m/s for CO₂ and 0.48 m/s for CCl₂F₂. It was interesting to observe for CO₂ that the phase of constant speed took place in between two acceleration phases; the former was due to the initial slumping of the cloud at the exit of the reservoir, and the latter was attributed to the collapse of the head on the transition to the passive dispersion phase. Instantaneous two-dimensional velocity field, measured with particle image velocimeter (PIV), showed that the cloud overran the ambient air which caused the approaching dense fluid deflected away from the wall with significant vertical velocities and downstream-moving separation, and the air trapped under the head resulted in the density inversion which introduced further intricacy to the turbulent structure of the head. Instabilities at the upper free shear layer due to density and velocity discontinuity rolled into periodic array of vortices which engulfed a considerable amount of air as they were convected backwards over the head, but the incorporation of heavy and light fluids was completed with the appearance of microscales after the collapse on the stratified layer. Analyses of the cloud head at different downstream locations also revealed that its size remained unchanged when the speed of advance was constant, allowing the rate of change of the cloud volume being modeled with the rate of spreading. Contours of concentration obtained from digitized PIV pictures confirmed the kinematic features of the mixing revealed by the velocity field and that the concentration values within the large structures were higher than those at the upper part of the stratified layer. Motivated by the experimental observations, a semi-empirical analysis was presented to describe the results and based on local values of the Richardson and Reynolds numbers. Received: 4 October 1995 / Accepted: 4 July 1996     

Inertia-preserving secant updates

Corrections to the last two equations of Ref. 1 are given.     

New synthesis of 2',3'-didehydro-2',3'-dideoxynucleosides.

The 3'-iodonucleoside 4 and the 3'-O-methylsulfonylthymidine 9 have been synthesized by condensation of silylated uracils 2 with methyl 5-O-tert-butyldiphensilyl-2,3-dideoxy-3-iodo-D-threo-pentofuran oside (3) and methyl 5-O-tert-butyldiphenylsilyl-2-deoxy-3-methylsulfonyl-D-erythro- pentofuranoside (8), respectively. The nucleoside 4 and 9 produced the corresponding 2',3'-didehydro-2',3'-dideoxynucleosides 5 in an elimination reaction on treatment with sodium methoxide. The compounds 5b showed no antiviral activity against HIV-1.     

Analysis of atmospheric particular matter and water using atomic emission spectrometry with inductively-coupled plasma and two-jet plasmatron

Summary A method for the atomic emission spectrometric analysis of air and water with inductively coupled and two-jet direct current plasmas has been developed. The method has been applied to the determination of impurity contents with good accuracy and sensitivity.