Inverse Probleme in der Elektrotechnik

Ohne Zusammenfassung     

Particle Propagation in Cosmological Backgrounds

We analyse the quantum propagation of interacting particles in cosmological backgrounds. The model we use consists of a doublet of massive scalar fields propagating in an expanding universe filled with massless radiation. The masses are much larger than the Hubble expansion rate, so that the number of massive particles is preserved and the fields adequately described within the adiabatic approximation. We focus on the dissipative effects related to the expansion rate by computing the imaginary part of the self-energy. In the quasi static approximation, we recover the expected result that instantaneous decay rate is governed by the local temperature. We then analyse the long time behavior of the propagator to unravel the secular effects induced by the self-energy. We show that these effects can be expressed in terms of integrals of local quantities. Applications to the trans-Planckian question are briefly discussed.     

Extending the applicability of the discrete dipole approximation for multi-scale features on surface

Many problems in science and engineering involve significant physical entities and processes that span a substantial range of dimensions. In the case of characterization of bacteria on growth media using light scattering the length scales of interest can be classified as micro-scale (single bacterium), macro-scale (bacterial colonies of more than 10¹² bacterium that have passed through the exponential growth phase and reached mm size), and the intermediate or meso-scale of several tens of hundreds of bacteria. Light scattering approaches, to be effective in determining physical properties such as morphology and material composition, must comprehend this spectrum of length scales. The discrete dipole approximation (DDA), a powerful modeling tool for rigorous 3-D vector scattering, has shown its capability to predict the light scattering from micro-scale objects. To be able to accommodate meso-scale objects, we need to extend the computational limits of the DDA method such that it could compute object sizes of 10λ-30λ characteristic dimension (i.e. volumes of 10³-10⁴ cubic wavelengths). To accomplish this, an analysis of the DDA method was performed for meso-scale cases of interest especially in biological applications. Based on this study, we propose new Sommerfeld integration paths and a revised iterative algorithm that combine to provide substantial improvements in the size of the computational domain that can be modeled for a given convergence criterion.     

Tropospheric OH and HO(2) radicals: field measurements and model comparisons

The hydroxyl radical, OH, initiates the removal of the majority of trace gases in the atmosphere, and together with the closely coupled species, the hydroperoxy radical, HO(2), is intimately involved in the oxidation chemistry of the atmosphere. This critical review discusses field measurements of local concentrations of OH and HO(2) radicals in the troposphere, and in particular the comparisons that have been made with numerical model calculations containing a detailed chemical mechanism. The level of agreement between field measurements of OH and HO(2) concentrations and model calculations for a given location provides an indication of the degree of understanding of the underlying oxidation chemistry. We review the measurement-model comparisons for a range of different environments sampled from the ground and from aircraft, including the marine boundary layer, continental low-NO(x) regions influenced by biogenic emissions, the polluted urban boundary layer, and polar regions. Although good agreement is found for some environments, there are significant discrepancies which remain unexplained, a notable example being unpolluted, forested regions. OH and HO(2) radicals are difficult species to measure in the troposphere, and we also review changes in detection methodology, quality assurance procedures such as instrument intercomparisons, and potential interferences.     

Coexistence of ferro- and antiferromagnetic interactions in a metal-organic radical-based (6,3)-helical network with large channels

A metal-organic open-framework with an unprecedented (6,3)-helical topology, large channels and mixed ferro- and antiferromagnetic interactions has been synthesized using a three-connecting tricarboxylic polychlorotriphenylmethyl radical and Co(ii) ions.     

Molecular assemblies of perylene bisimide dyes in water

Perylene bisimides are among the most valuable functional dyes and have numerous potential applications. As a result of their chemical robustness, photostability, and outstanding optical and electronic properties, these dyes have been applied as pigments, fluorescence sensors, and n‐semiconductors in organic electronics and photovoltaics. Moreover, the extended quadrupolar π system of this class of dyes has facilitated the construction of numerous supramolecular architectures with fascinating photophysical properties. However, the supramolecular approach to the formation of perylene bisimide aggregates has been restricted mostly to organic media. Pleasingly, considerable progress has been made in the last few years in developing water‐soluble perylene bisimides and their application in aqueous media. This Review provides an up‐to‐date overview on the self‐assembly of perylene bisimides through π–π interactions in aqueous media. Synthetic strategies for the preparation of water‐soluble perylene bisimides and the influence of water on the π–π stacking of perylene bisimides as well as the resulting applications are discussed.     

Enantioseparation of citalopram analogues with sulfated β‐cyclodextrin by capillary electrophoresis

Capillary electrophoresis methods were developed for the enantiomeric separation of 27 citalopram analogues. Sulfated β‐cyclodextrin was the most broadly selective and useful chiral selector. The separations of most of the citalopram analogue compounds reported in this work have not been reported previously. Excellent enantiomeric separations were obtained for 26 out of 27 compounds, and most of the separations were achieved within 10 min. The effects of chemical parameters such as chiral selector types, buffer types, chiral selector and buffer concentrations, buffer pH and organic modifiers on the separation were investigated. The influence of analyte structure on separation also was examined and discussed.     

Morphological regimes of poly(ε-caprolactone)/octaisobutyl polyhedral oligosilsesquioxane composite films in relation to film composition and thickness

The morphological evolution of poly(ε-caprolactone) (PCL)/octaisobutyl polyhedral oligomeric silsesquioxane (IBUPOSS) films was analyzed using scanning electron microscopy (SEM) and polarized optical microscopy (POM). The morphologies of the blend films with PCL/IBUPOSS mass ratios of 95:5 to 50:50 were discussed according to decomposition mechanism in relation to film composition and thickness. In addition to the morphological regime for films with lower IBUPOSS loadings, in which the growth of PCL spherulites was nearly independent on the presence of fine IBUPOSS aggregates, two new morphological regimes were observed for the films with higher IBUPOSS loadings: (1) thicker blend films exhibited a rich dynamics, giving rise to a trilayer structure and (2) the decomposition of thinner films was induced by the kinetically controlled growth of IBUPOSS aggregates. By varying the thickness and the composition of the blend films, the current study provides important new insight into the rich phase behavior of nanoparticle-filled polymer films.