Structure extraction by stochastic estimation with adaptive events

Various aspects of turbulence structure can be found by a new class of stochasticestimation methods in which the conditional events that define the stochastic estimate are systematically varied. Methods are presented to find the length scale of large periodic structures, the form of structures that have specified geometric constraints such as two-dimensionality, and the structure of small-scale motions embedded in large-scale motions. These methodologies are demonstrated in high Rayleigh number turbulent convection by extracting both the large-scale roll-cell and coherent thermal plumes. A method of compressed representation using a stochastic estimate given data on optimally chosen points is also demonstrated.This work was supported by AFOSR Grant 90-0169, ONR Grant N000-14-90-J-1415, and NSF Grant ATM 89-20605.     

Alignment of plate-like particles in a colloidal dispersion under flow in a uniform pipe studied by high-energy X-ray diffraction

High-energy angle-dispersive X-ray diffraction has been used to study the alignment of colloidal suspension of kaolinite particles in water as they flow along a pipe. X-rays with energies above 25 keV have a major advantage, as they can penetrate through thick samples and walls of containers and permit investigation of samples under realistic flow conditions. As an example of the method, flow through a circular cross-section pipe with an internal diameter of 5 mm has been studied: this is typical of industrial applications. The angular distribution of intensities of peaks in the diffraction pattern as a function of the location of the pipe in the X-ray beam provides information about the alignment of particles under flow. Order parameters have been calculated to describe the alignment and direction of orientation. It is observed that the particles align in the direction of flow with their flat faces parallel to the flow. The experimental results are compared with the calculations of the local strain rate that help to explain the onset of alignment of the particles.     

Preparation of Fe2O3-exfoliated graphite composite and its electrochemical properties investigated in alkaline solution

In the present work, a simple method of preparation of FeCl₄⁻- graphite intercalation compounds from HCl/FeCl₃ solution with the aid of chemical oxidant is presented. Based on X-ray diffraction measurements it was concluded, that stages 8, 6, and 5 FeCl₄⁻-graphite intercalation compounds were obtained. The compounds thus obtained were thermally treated to obtain Fe₂O₃-exfoliated graphite composites. The dispersion of Fe₂O₃ in the exfoliated graphite flakes was examined with the aid of the energy dispersive X-ray analysis combined with a scanning electron microscopy. Electrochemical behavior of electrodes was investigated in 6 M KOH solution. Electrochemical investigations proved the formation of FeOOH on the surface of exfoliated graphite during the anodic process. Besides, electrochemical investigations showed that the lower limit potential strongly affects the redox behavior of the Fe₂O₃-EG electrode.     

Involvement of cyan and ester groups in surface interactions of aerosil–cyanophenyl alkyl benzoate systems with high silica density: Infrared investigations

Composites prepared from aerosil A380 and liquid crystals (LCs) of 4-n-alkyl-4′-cyanophenyl benzoate type, with four to six carbon atoms in the alkyl chain were investigated by infrared spectroscopy. Their high silica content (of 2–7 g aerosil/1 g of LC) was given by thermogravimetric investigations and allows the observation of a rather thin LC layer on the silica particles. Several surface species onto the external surface of the grains were demonstrated. Arguments are given that monomer and dimer species are present in the bulk cyanophenyl benzoate materials while bulk-like species along with hydrogen-bonded ones coexist in the so-called surface layer of the composites. The main interaction of LC molecules with the aerosil surface is by hydrogen bonding taking place with the involvement of the cyan group. There is a contribution of ester carbonyl group to these surface interactions but this cannot be well quantified.     

New N-aryloxy-phthalimide derivatives. Synthesis,physico-chemical properties,and QSPR studies

Starting from N-hydroxyphthalimide 1 and the reactive fluoro- or chloro-nitroaryl derivatives 2, 3 and 4a-e (2-chloro-3,5-dinitropyridine; 3, NBD-chloride; 4a, 1-fluoro-2,4-dinitrobenzene; 4b, picryl chloride; 4c, 4-chloro-3,5-dinitrobenzotrifluoride; 4d, 2-chloro-3,5- dinitrobenzotrifluoride; 4e, 4-chloro-3,5-dinitrobenzoic acid) the corresponding N-(2-nitroaryloxy)-phthalimide derivatives 5a-e, or 6 and 7 were obtained and characterized by IR, UV-Vis ¹H-NMR and ¹³C-NMR spectroscopy. The TLC behavior and the hydrophobicity of these derivatives have been experimentally evaluated by R_M0 parameters (using RP-TLC). The experimental R_M0 parameters were compared with the calculated partition coefficient, log P. A QSPR study was also performed to establish possible correlations between the structure and physical properties (λ_max and R_M0) of compounds 5a-e, 6, and 7.      

Arsenic speciation by gradient anion exchange narrow bore ion chromatography and high resolution inductively coupled plasma mass spectrometry detection

Based on gradient anion exchange chromatography (AEC), a new strategy in As-speciation was evaluated. A narrow bore chromatographic system with lower flow rates (≤300 μL) well suitable for the low flow requirements of higher efficiency nebulizers was splitless coupled to a high resolution sector field ICP MS. The AEC system takes full advantage of the detector sensitivity allowing more diluted samples (50–100 times) to be injected, delivering substantially less sample matrix to the column and a lower eluent load to the plasma. The unique plasma compatibility of the NH₄NO₃-eluent salt used in this study enabled high linear salt ramps in gradient applications, highly reproducible retention times (±1%) and detection limits in the low ng/L range. The separation conditions were applied on two different polymeric anion-exchangers: a low capacity, weakly hydrophobic material (AS11, Dionex) and a more frequently used higher capacity, higher hydrophobic material (AS7, Dionex). On both columns, As-species (As(III/V), MMA, DMA, AsB) and Cl⁻ were separated in less than nine minutes and co-elution was circumvented by adapting the separation pH to the optimal column selectivity. The key-advantage of the NH₄NO₃-eluent is that it can adopt any separation pH without compromising the eluent strength which is not possible with all other eluents used so far. The influences of chloride and methanol were investigated and found not to affect the chromatographic performance. Column deposits caused strong reversible As(v) adsorption which reduced As(v) to As(III). A corresponding phosphate excess in the injected sample eliminated the adsorption and prevented artefacts in As(v)/As(III) ratios. The method applied to ground water samples provided robust separations and is compatible with any sample preservation procedure.     

Isomer ratios for products of photonuclear reactions with middle-weight nuclei

The isomer ratios for nuclei ^104m,g Ag, ^110m,g In, ^108m,g In as products of the photonuclear reactions ¹⁰⁷Ag(γ, 3n)^104m,g Ag, ¹¹³In(γ, 3n)^110m,g In, ¹⁰⁹Ag(γ, 5n)^104m,g Ag, ¹¹⁵In)(γ, 5n)^110m,g In, ¹¹⁵In(γ, 7n)^108m,g In are obtained. The Bremsstrahlung of electrons with energies within 32–84 MeV from the LU-40 linear accelerator was used for the irradiation of targets. The energy resolution and mean current of the electron beam were ～1% and 5 μA, respectively. The induced activity was used to obtain experimental isomer ratios. An HPGe spectrometer with an energy resolution of 1.9 keV for ⁶⁰Co γ-line 1332 keV was used to acquire the instrumental γ-ray spectra of the activation products. A set of serial measurements with various acquisition times was performed. The cooling times varied from 5 seconds to several hours for Ag and up to tens of hours for In specimens. The obtained experimental isomer ratios are compared with the results from theoretical calculations.     

Extending reference scan drift correction to high-magnification high-cone-angle tomography

The reference scan method is a simple yet powerful method for measuring spatial drift of the x-ray spot during a low-cone-angle μ-CT experiment. As long as the drift is smooth, and occurring on a time scale that is long compared to the acquisition time of each projection, this method provides a way to compensate for the drift by applying 2D in-plane translations to the radiographs. Here we show that this compensation may be extended to the regime of high-magnification, high-cone-angle CT experiments where source drift perpendicular to the detector plane can cause significant magnification changes throughout the acquisition.     

Dual-core ytterbium fiber amplifier for high-power 1060 nm swept source multichannel optical coherence tomography imaging

A novel (to our knowledge) dual-core ytterbium (Yb(3+)) doped fiber, as an optically pumped amplifier, boosts the output power from a 1060 nm swept source laser beyond 250 mW, while providing a wavelength tuning range of 93 nm, for optical coherence tomography (OCT) imaging. The design of the dual-core Yb-doped fiber amplifier and its multiple wavelength optical pumping scheme to optimize output bandwidth are discussed. Use of the dual-core fiber amplifier showed no appreciable degradation to the coherence length of the seed laser. The signal intensity improvement of this amplifier is demonstrated on a multichannel in vivo OCT imaging system at 1060 nm.