An experimental design based strategy to optimize a capillary electrophoresis method for the separation of 19 polycyclic aromatic hydrocarbons

Because of their high toxicity, international regulatory institutions recommend monitoring specific polycyclic aromatic hydrocarbons (PAHs) in environmental and food samples. A fast, selective and sensitive method is therefore required for their quantitation in such complex samples. This article deals with the optimization, based on an experimental design strategy, of a cyclodextrin (CD) modified capillary zone electrophoresis separation method for the simultaneous separation of 19 PAHs listed as priority pollutants. First, using a central composite design, the normalized peak-start and peak-end times were modelled as functions of the factors that most affect PAH electrophoretic behavior: the concentrations of the anionic sulfobutylether-β-CD and neutral methyl-β-CD, and the percentage of MeOH in the background electrolyte. Then, to circumvent computational difficulties resulting from the changes in migration order likely to occur while varying experimental conditions, an original approach based on the systematic evaluation of the time intervals between all the possible pairs of peaks was used. Finally, a desirability analysis based on the smallest time interval between two consecutive peaks and on the overall analysis time, allowed us to achieve, for the first time in CE, full resolution of all 19 PAHs in less than 18 min. Using this optimized capillary electrophoresis method, a vegetable oil was successfully analyzed, proving its suitability for real complex sample analysis.     

Independent components analysis coupled with 3D-front-face fluorescence spectroscopy to study the interaction between plastic food packaging and olive oil

Olive oil is one of the most valued sources of fats in the Mediterranean diet. Its storage was generally done using glass or metallic packaging materials. Nowadays, plastic packaging has gained worldwide spread for the storage of olive oil. However, plastics are not inert and interaction phenomena may occur between packaging materials and olive oil. In this study, extra virgin olive oil samples were submitted to accelerated interaction conditions, in contact with polypropylene (PP) and polylactide (PLA) plastic packaging materials. 3D-front-face fluorescence spectroscopy, being a simple, fast and non destructive analytical technique, was used to study this interaction. Independent components analysis (ICA) was used to analyze raw 3D-front-face fluorescence spectra of olive oil. ICA was able to highlight a probable effect of a migration of substances with antioxidant activity. The signals extracted by ICA corresponded to natural olive oil fluorophores (tocopherols and polyphenols) as well as newly formed ones which were tentatively identified as fluorescent oxidation products. Based on the extracted fluorescent signals, olive oil in contact with plastics had slower aging rates in comparison with reference oils. Peroxide and free acidity values validated the results obtained by ICA, related to olive oil oxidation rates. Sorbed olive oil in plastic was also quantified given that this sorption could induce a swelling of the polymer thus promoting migration.     

Direct simulation of turbulent flow and heat transfer in a channel. Part I: Smooth walls

Interest in the use of supercomputers for the direct numerical calculation of turbulence prompts the development of efficient numerical techniques so that calculation at higher Reynolds numbers might be made. This paper presents an efficient pseudo-spectral technique, similar to but different from others that have recently appeared, for the calculation of momentum and heat transfer to a constant-property, turbulent fluid in a two-dimensional channel with walls at different, uniform temperature. The code uses no empiricism, although periodic boundary conditions are used for fluctuating quantities in the streamwise and spanwise directions. Calculations were made for a Prandtl number of 0·72 and Reynolds number based on friction velocity and channel half-height of 180 or 2800 based on channel half-height and average velocity. Calculations of mean velocity profile, turbulence intensities, skewness, flatness, Reynolds stress and eddy diffusivity of heat near a wall compare favourably with experimental results. Representative contour plots of the temperature field near the wall and of the spanwise and streamwise two-point velocity correlations are given. Deficiencies are that the calculation requires many hours on a fast computer with a large high-speed memory and that the grid size in each direction for appropriate resolution is approximately proportional to the square of the Reynolds number and to the Prandtl number raised to some power greater than one.     

A polystyrene cap for matching a silicon lens at millimeter wavelengths

A polystyrene cap for a silicon lens has been fabricated by thermal molding. The cap is 0.5mm thick, and it acts as a quarter-wave matching layer at 94GHz. The measured performance from 75GHz to 170GHz agrees with theory. The reflection loss at 94GHz is reduced by 1.5dB. This is an economical way to make a millimeter-wave anti-reflection coating. This makes a monolithic circuit with a gallium-arsenide substrate and a silicon lens much more attractive than before. The total absorption and reflection loss for a linch diameter lens with the cap should be 1.1dB.     

Far-infrared microbolometer detectors

The bismuth microbolometer is a simple, easily made detector suitable for use throughout the far-infrared, which has been integrated with a variety of planar antennas. The general thermal properties of these devices and some of the constraints on bolometer materials are discussed. The fabrication and performance of several different types of microbolometers and microthermocouples are described.Supported by the Department of Energy contract DE-AM03-765F-00010 Task IIA; Army Research Office contract DAAG29-82-K-0165; and the Jet Propulsion Laboratory through Dr. M. Litvak.     

Grid oscillators

Loading a two-dimensional grid with active devices offers a means of combining the power of solid-state oscillators in the microwave and millimeter-wave range. The grid structure allows a large number of negative resistance devices to be combined. This approach is attractive because the active devices do not require an external locking signal, and the combining is done in free space. In addition, the loaded grid is a planar structure amenable to monolithic integration. Measurements on a 25-MESFET grid at 9.7 GHz show power-combining and frequencylocking without an external locking signal, with an ERP of 37 W. Experimental far-field patterns agree with theoretical results obtained using reciprocity.     

yDNA versus xDNA pyrimidine nucleobases: computational evidence for dependence of duplex stability on spacer location

The structural and binding properties of the natural and x- and y-pyrimidines were compared using computational methods. Our calculations show that although the x-pyrimidines favor different orientations about the glycosidic bond compared to the natural pyrimidines, which could have implications for the formation and resulting stability of xDNA duplexes and jeopardize the selectivity of expanded nucleobases, y-pyrimidines have rotational profiles more similar to the natural bases. Increasing the pyrimidine size using a benzene spacer leads to relatively minor changes in the hydrogen-bond strength of isolated Watson-Crick base pairs. However, differences in the anomeric carbon distances in pairs composed of x- or y-pyrimidines suggest yDNA may yield a more optimal expanded structure. By stacking two monomers via their centers of mass, we find that the expanded nucleobases stack much stronger than the natural bases. Additionally, although replacing xT by yT changes the stacking energy by less than 5 kJ mol (-1), replacing xC by yC significantly strengthens complexes with the natural nucleobases (by up to 30%). Calculations on larger duplex models composed of four nucleobases reveal that x- and y-pyrimidines can increase duplex stability of natural helices by strengthening both the intra and interstrand stacking interactions. Furthermore, when the total stability (sum of all hydrogen-bonding and (intrastrand and interstrand) stacking interactions) of the larger models is considered, y-pyrimidines lead to more stable complexes than x-pyrimidines for all but three duplex sequences. Thus, through analysis of a variety of properties, our calculations suggest that the location of the benzene spacer affects the properties of expanded nucleobases and the stability of expanded duplexes, and therefore should be carefully considered when designing future expanded analogues.     

Molecular dynamics simulation of thermomechanical properties of montmorillonite crystal. 1. Isolated clay nanoplate

The structure and mechanical properties of clay nanoparticles is a subject of growing interest because of their numerous applications in engineering. We present the results of molecular dynamics simulation for a single nanoplate of pyrophyllite - a 2:1 clay mineral consisting of two tetrahedral sheets of SiO4 and an intervening octahedral AlO6 sheet. Simulations were performed in the temperature interval from 5 to 750 K using the ionic-type potentials of Cygan et al. On this basis the temperature dependences of structural parameters, characterizing both tetrahedral and octahedral sheets as well as single lamella, have been studied. Two slightly different structures were observed in this wide temperature interval. The mechanical properties of the nanoplate were calculated from stress-strain diagrams, which have been obtained at relatively slow rates of deformation (for molecular simulations). Using different types of loading, we calculated the full elasticity tensor and estimated the influence of temperature on its components. We estimated also the bending and torsion stiffnesses of the nanoplate as specific characteristics of this type of particle. Because the nanoplate is atomically thin, a reasonable determination of the thickness is a nontrivial problem, both in the modeling of mechanical properties and in physical interpretation of the obtained data. We propose a procedure for its calculation.     

Mixtures of interacting particles with well-defined composition field coupling chi parameters

This article proposes a systematic, quantitative treatment of the problem of associating a scalar Flory-Huggins-like chi parameter directly with the interaction potentials in a binary mixture of point particles. This work fulfills the need for a general, quantitative way to compare chi values in explicitly simulated ensembles of lattice and off-lattice polymer models with field theoretic calculations. Emphasis is placed on constructing particle models where chi is relatively well defined. In general, chi is defined through pair correlation functions, whose thermal fluctuations are coupled to local average composition and composition gradients. This implies that chi is composition dependent even in the simplest particle models. At the same time, by quantifying this effect, it is found that composition-independent chi may be defined to within a few percent for cases where the range of the potential is large relative to the interparticle distance. An explicit formula for chi in terms of interaction potentials is given.