Experimental verification of an interpolation algorithm for improved estimates of animal position

This article presents experimental verification of an interpolation algorithm that was previously proposed in Jaffe [J. Acoust. Soc. Am. 105, 3168-3175 (1999)]. The goal of the algorithm is to improve estimates of both target position and target strength by minimizing a least-squares residual between noise-corrupted target measurement data and the output of a model of the sonar's amplitude response to a target at a set of known locations. Although this positional estimator was shown to be a maximum likelihood estimator, in principle, experimental verification was desired because of interest in understanding its true performance. Here, the accuracy of the algorithm is investigated by analyzing the correspondence between a target's true position and the algorithm's estimate. True target position was measured by precise translation of a small test target (bead) or from the analysis of images of fish from a coregistered optical imaging system. Results with the stationary spherical test bead in a high signal-to-noise environment indicate that a large increase in resolution is possible, while results with commercial aquarium fish indicate a smaller increase is obtainable. However, in both experiments the algorithm provides improved estimates of target position over those obtained by simply accepting the angular positions of the sonar beam with maximum output as target position. In addition, increased accuracy in target strength estimation is possible by considering the effects of the sonar beam patterns relative to the interpolated position. A benefit of the algorithm is that it can be applied "ex post facto" to existing data sets from commercial multibeam sonar systems when only the beam intensities have been stored after suitable calibration.     

Raman Spectrum of Vanadium-Zirconia Yellow Pigment

Monoclinic vanadium-zirconia yellow pigments were prepared by gelling mixtures of zirconium n-propoxide and vanadyl acetylacetone. The nature of interactions between the host ion and the foreign cation in the vanadium-zirconia pigment was investigated in order to contribute to a better understanding of the origin of this pigmenting system using Raman scattering measurements. The Raman spectra of powdered samples of the vanadium-zirconia pigment recorded between 100 and 1400 cm^?1 show the peaks at 991, 701, and 403 cm^?1 assigned to the asymmetric and symmetric stretching and bending vibrations of the V⁴⁺ = O bonds, respectively. The assignment of these peaks was discussed by comparison with Raman spectra of vanadium oxides and on the basis of V-O bond distances deduced from the Hardcastle and Wachs equation and from the valence state of the vanadium cation calculated by Brown in the valence sum rule. This suggests that the V⁴⁺ cations replace Zr⁴⁺ in sevenfold coordinated site in the monoclinic zirconia structure. The V⁴⁺ cation allowing the d-d electronic transition is related to the origin of the lemon yellow coloration.     

Synthesis of rhenium chelated MAG3 functionalized rosette nanotubes

Rosette nanotubes (RNTs) are discrete nanostructures self-assembled from a guanine–cytosine hybrid motif (G∧C) under aqueous conditions. These materials have substantial design flexibility and a range of applications, which are partly attributed to their diverse surface functionalization. Given the potential for interesting properties resulting from a metal-RNT construct, here we describe an oxorhenium-functionalized RNT. More specifically, we present the synthesis of a twin G∧C motif expressing the mercaptoacetyl triglycine (MAG₃) ligand. We then examine the chelation reaction of the MAG₃ with ReOCl₃(PPh₃)₂ and self-assemble the resulting ReO-MAG₃-G∧C conjugate into RNTs under DMSO and aqueous conditions.     

Mesophase behaviour and thermal stability of octa-alkoxy substituted phthalocyaninatocobalt (II) complexes

Cobalt (II) phthalocyanines substituted with eight alkoxy chains in the peripheral (2, 3, 9, 10, 16, 17, 23, 24) positions were prepared. The alkoxy chain length was varied between n-butyloxy (C₄H₉O) and n-octadecyloxy (C₁₈H₃₇O). Studies by polarizing optical microscopy and high temperature X-ray diffraction revealed that all the complexes are liquid crystalline and that they exhibit a hexagonal columnar mesophase (Col_h). Transition enthalpies were determined by differential scanning calorimetry. The clearing point could only be observed for compounds with a chain length longer than C₁₃H₂₇O. Both the melting and clearing points decrease with increasing chain length. The transition temperatures of these discotic metallomesogens are higher than those of the corresponding metal-free phthalocyanines, but are comparable with those of the corresponding copper (II) compounds. The thermal decomposition of the compounds was studied by thermogravimetry.     

Pumping power of nanofluids in a flowing system

Nanofluids have the potential to increase thermal conductivities and heat transfer coefficients compared to their base fluids. However, the addition of nanoparticles to a fluid also increases the viscosity and therefore increases the power required to pump the fluid through the system. When the benefit of the increased heat transfer is larger than the penalty of the increased pumping power, the nanofluid has the potential for commercial viability. The pumping power for nanofluids has been considered previously for flow in straight tubes. In this study, the pumping power was measured for nanofluids flowing in a complete system including straight tubing, elbows, and expansions. The objective was to determine the significance of two-phase flow effects on system performance. Two types of nanofluids were used in this study: a water-based nanofluid containing 2.0–8.0 vol% of 40-nm alumina nanoparticles, and a 50/50 ethylene glycol/water mixture-based nanofluid containing 2.2 vol% of 29-nm SiC nanoparticles. All experiments were performed in the turbulent flow region in the entire test system simulating features typically found in heat exchanger systems. Experimental results were compared to the pumping power calculated from a mathematical model of the system to evaluate the system effects. The pumping power results were also combined with the heat transfer enhancement to evaluate the viability of the two nanofluids.     

Estimating fish orientation from broadband, limited-angle, multiview, acoustic reflections

This article demonstrates that multiview, broadband (635-935 kHz), nearly monostatic, acoustic reflections recorded from lateral views of juvenile fish can be used to infer animal orientation. Calibrated acoustic data were recorded from live fish in a laboratory, while orientation was measured simultaneously via optical images. Using eight animals, two-dimensional data sets of target strength as a function of frequency and orientation were obtained. Fish length, lateral thickness, and dorsoventral thickness ranged from 24 to 48 mm, 3 to 7 mm and 10 to 20 mm, respectively. Preliminary estimates of orientation were computed from the direction of the gradient of the local autocorrelation function in the target strength image. These local estimates were then median-filtered over the full system bandwidth (but still limited-angle) to improve accuracy. Angular estimates were then corrected for systematic bias via a simple, one-dimensional model that approximated the animals' reflection by that of a bar target. Taken over all orientations, the average absolute error in orientation estimation is 5.6° to 17°, dependent on the data set. Results indicate, for most sets of views, reasonable estimates of lateral orientation can be obtained from broadband, multiview data over a set of limited angular reflections.     

Molecular Lanthanide Switches for Magnetism and Photoluminescence

Solvation of [(CNT)Ln(η⁸-COT)] (Ln=La, Ce, Nd, Tb, Er; CNT=cyclononatetraenyl, i.e., C₉H₉⁻; COT=cyclooctatetraendiid, i.e., C₈H₈²⁻) complexes with tetrahydrofuran (THF) gives rise to neutral [(η⁴-CNT)Ln(thf)₂(η⁸-COT)] (Ln=La, Ce) and ionic [Ln(thf)_x(η⁸-COT)][CNT] (x=4 (Ce, Nd, Tb), 3 (Er)) species in a solid-to-solid transformation. Due to the severe distortion of the ligand sphere upon solvation, these species act as switchable luminophores and single-molecule magnets. The desolvation of the coordinated solvents can be triggered by applying a dynamic vacuum, as well as a temperature gradient stimulus. Raman spectroscopic investigations revealed fast and fully reversible solvation and desolvation processes. Moreover, we also show that a Nd:YAG laser can induce the necessary temperature gradient for a self-sufficient switching process of the Ce(III) analogue in a spatially resolved manner.     

Multicomponent adsorption modeling: isotherms for ABE model solutions using activated carbon F-400

Biobutanol has attracted significant interest in recent decades and is seriously considered as a potential biofuel to partly replace gasoline. However, some production challenges must be addressed to make butanol economically viable such as the low product concentration and product toxicity inhibiting the microorganism. To alleviate these limitations, several in situ or ex situ separation techniques have been investigated in view of their integration to the biobutanol production process to enhance its economic viability. One of these techniques is adsorption which is one of the most energy-efficient techniques used for biobutanol separation. Considering the number of chemical species present in the ABE fermentation broth, it is essential to develop multicomponent adsorption isotherms for all components as a first step to design a high performance adsorption process. Few multicomponent isotherm models have been proposed such as multicomponent Langmuir and Freundlich. In this study, these two models as well as artificial neural networks were used to model the isotherms of each component in an ABE fermentation broth as a function of the equilibrium concentrations of all components for activated carbon F-400. Results showed that the multicomponent Langmuir model was not accurate due to the many simplifying assumptions. The multicomponent Freundlich and feedforward neural network (FFNN) isotherm models were able to predict the behavior of multicomponent systems very well. Indeed, the predictive model of the experimental data had a coefficient of determination (R²) of 0.97 and 0.99, for multicomponent Freundlich and FFNN isotherm models, respectively.     

Low-frequency dilational elasticity of the nematic 4'-pentyl-4-biphenylcarbonitrile (5CB)/water interface

Axisymmetric oscillating pendant drop shape analysis has been used to study the interfacial rheology of the liquid crystal 4'-pentyl-4-biphenylcarbonitrile (5CB) in water with homeotropic anchoring. Nearly spherical 5CB droplets were subjected to low frequency (1-5 mHz) volume oscillations, and the increase in tension with surface dilation was used to calculate the complex modulus. The droplet interface response is completely elastic, with no relaxations occurring on the experimental time scale. This surprising result is attributed to droplet storage of elastic energy in the form of distorted orientational distributions within the bulk (Frank elasticity) and on the surface (anchoring elasticity).     

Determination of ubidecarenone (coenzyme Q10, ubiquinol-10) in raw materials and dietary supplements by high-performance liquid chromatography with ultraviolet detection: single-laboratory validation

A method based on high-performance liquid chromatography with ultraviolet detection has been developed to quantify ubidecarenone [coenzyme Q10 (CoQ10)] in raw materials and dietary supplements. Single-laboratory validation has been performed on the method to determine repeatability, accuracy, selectivity, limits of detection and quantification (LOQ), ruggedness, and linearity for CoQ10. As CoQ10 can exist as the biologically active reduced form, the application of an oxidizing agent, ferric chloride, drives the equilibrium mechanics to the fully oxidized state and allows for exact quantification of total CoQ10 in the sample. This method was found to be fit and linear for the testing of materials containing CoQ10 in the range of approximately equal 50-1000 mg/g. Repeatability precision for CoQ10 was between 2.15 and 5.00% relative standard deviation. Observed recovery of CoQ10 was found to be between 93.8 and 100.9%. LOQ was found to be 9 microg/mL. Further, limited studies showed that some adulterants and degraded material could be satisfactorily separated from CoQ10 and identified.