88 search hits
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Jahresbericht Universitätsbibliothek Bayreuth
(2011)
- Jahresbericht der Universitätsbibliothek Bayreuth - Berichtsjahr 2009
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Jahresbericht Universitätsbibliothek Bayreuth
(2011)
- Jahresbericht der Universitätsbibliothek Bayreuth - Berichtsjahr 2010
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Jahresbericht 2010 - Universität Bayreuth Rechenzentrum
(2011)
- Jahresbericht
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Gesprochene Sprache im Deutsch-als-Fremdsprache-Unterricht. Eigenschaften der gesprochenen Sprache in Lehrwerkdialogen
(2011)
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Mohammed Al-Nasser
- Gegenstand der hier vorgestellten Arbeit ist der Lehrwerkdialog, der als Grundlage des Fremdsprachenunterrichts dient. Ihr Ziel ist es, die Eigenschaften der gesprochenen Sprache in den Lehrwerkdialogen zu untersuchen. Im ersten Kapitel wird die Kommunikative Wende, die den fremdsprachlichen Deutschunterricht beeinflusst hat, dargestellt. Das zweite Kapitel beschäftigt sich mit der Fertigkeit des Sprechens. Im dritten Kapitel werden die Gesprochene-Sprache-Forschung und die Gesprächsanalyse mit einigen ihrer Merkmale vorgestellt. Im vierten Kapitel werden Methodik und Auswahlverfahren der Arbeit erklärt. Das fünfte Kapitel führt eine Analyse der Dialoge und ihrer Übungen in fremdsprachlichen Lehrwerken hinsichtlich dreier Eigenschaften der gesprochenen Sprache und Interaktion vor: die Prosodie, die Operator-Skopus-Struktur und der Sprecherwechsel. Es geht darum, zu untersuchen, ob die Lehrwerkdialoge die oben erwähnten Merkmale enthalten und inwieweit sie im Fremdsprachenunterricht eingeübt werden. Kapitel sechs widmet sich der Zusammenfassung und der Diskussion der Analyseergebnisse und der Schlussbetrachtung. Mit der vorliegenden Untersuchung der aufgenommenen Modelldialoge der fremdsprachlichen Lehrwerke mit dem Instrument der Gesprächsanalyse wird insofern eine Forschungslücke geschlossen, als bisher nur die Texte der Muster-Dialoge, die in Lehrbüchern vorhanden sind, untersucht wurden.
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Active and Passive Transport at Interfaces
(2011)
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Saeedeh Aliaskarisohi
- In this thesis we studied different forms of transport at interfaces. Four different interfacial transport mechanisms have been investigated. In each of them one physical aspect of active and passive transport is discussed. The four systems are arranged and discussed in four separate chapters. In chapter 3 and 4 we study the effect of static or hydrodynamic interactions on the cross over from individual diffusion towards collective diffusion. In chapter 3 the diffusion of circular domains on a giant unilamellar vesicle is measured. By tracking the motion of hydrodynamic interacting domains on a curved membrane we determined whether it is possible to extract rheological properties of the bilayer membrane. A similar two dimensional system interacting via static dipole interactions is studied in chapter 4. A mixture of paramagnetic and nonmagnetic colloidal particles immersed into a diluted ferrofluid is self assembled into colloidal flowers. In this experiment the effect of static interactions on the modes of diffusion of the petals of the colloidal flower is investigated in a one dimensional system. The results are compared with the single file diffusion of a hard core interacting one dimensional system. In chapter 5, the effect of actively directing particles with fluctuating active forces in a symmetry broken environment is studied. We address the question how to competing symmetry breaking effects decide on the direction of motion. The system consists of paramagnetic colloidal particles placed into an aqueous solution above the liquid-solid interface of a magnetic garnet film. An external modulated field supplies the fluctuations and the symmetry is broken by tilting the external field with respect to the magnetic film and/or by a magnetic symmetry broken pattern of the magnetic film. The direction of motion of the paramagnetic colloids is measured and we give a theoretical explanation of why which symmetry breaking wins. The fluidization of a two dimensional solid to a two dimensional liquid via the yielding of the monolayer is studied in chapter 6. The monolayer is locally yielded with thermo capillary interactions by focusing a laser onto it. We investigate the yielding as a function of the chemical nature of the monolayer and determine the thermodynamic requirements necessary for thermo capillary yielding.
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Holographic Investigation of Azobenzene-Containing Low-Molecular-Weight Compounds
(2011)
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Hubert Audorff
- In the present thesis, holographic volume and surface relief gratings in azobenzene-containing low-molecular-weight compounds are investigated to obtain a broader understanding of this new class of material. Azobenzene chromophores undergo light-induced trans-cis-trans isomerization cycles leading to a reorientation of the long axis of the chromophores. If linearly polarized light is incident on the sample, these isomerizations result in a reorientation of this axis perpendicular to the light polarization. A holographic light grating, which can be formed by the interference of two coherent laser beams, leads to the inscription of a refractive-index modulation in the material. The azobenzene-containing low-molecular-weight compounds studied in this thesis consist of different building blocks: the core unit, the azobenzene chromophores with substituents, and the spacer and the linkage group between chromophore and core unit. These components can be used in a modular-design principle to synthesize a large library of low-molecular-weight compounds. Surprisingly, some of the investigated low-molecular-weight compounds form also a liquid-crystalline phase besides the amorphous phase as evidenced by polarized microscopy. If these liquid-crystalline compounds are prepared as solid films, however, they are quenched to an amorphous state. Upon reorientation of the azobenzene chromophores by illumination with a holographic light grating, a phase transition from the amorphous to an ordered state can be induced. This phase change in the latent liquid-crystalline low-molecular-weight compounds is very interesting for applications. The latent liquid-crystalline low-molecular-weight compounds show a post-development of the refractive-index modulation after the writing process. The holographic gratings are even stable at temperatures higher than the glass transition temperature, which further proves the light-induced formation of an ordered domain. In contrast to their polymeric counterparts, molecular materials are expected to show a faster response to light because of the absence of polymer chain entanglements. Therefore, molecular glasses can be used as blending material for photo-addressable polymers to improve the photo-sensitivity of the blend as compared to the pure polymer. The influence of the core and the substituent was investigated in low-molecular-weight compounds which do not form liquid-crystalline phases. An azobenzene-containing diblock copolymer for holographic data storage consists of an inert majority block and a minority block containing the covalently bound photo-sensitive azobenzene chromophores. Blending a few weight percent of the optimized molecular glass to the diblock copolymer leads to an increase of sensitivity with increasing content of the molecular glass, mainly because the writing time to the maximum of the refractive-index modulation decreased. The increase of the sensitivity is much larger than the observed rise of the refractive-index modulation due to the higher concentration of azobenzene chromophores. It was demonstrated that the shorter writing times are not caused by thermal effects, the molecules of the molecular glass in the inert block, or by changes of the free volume or the morphology, but that they are due to the azobenzene chromophores of the molecular glass in the minority block. They reorient faster than the chromophores attached to the polymer backbone and, thereby create free volume. Additionally, they can assist the reorientation of the azobenzene chromophores bound to the polymer by cooperative effects, i.e. dipolar and steric interactions. Both effects result in shorter writing time and higher sensitivity of the system. In a blend containing two weight percent of the molecular glass, the inscribed gratings are still long-term stable and the sensitivity increases by a factor of 1.7 as compared to the pure diblock copolymer. Upon illumination of an azobenzene-containing material with a holographic light grating, besides the volume grating, also a surface relief grating can develop. Surface modulations with heights of up to 600 nm were achieved in molecular glasses. It was found that the build-up of the surface relief grating depends on the electrical susceptibility of the material at the optical frequency of the laser and the polarization of the laser beams. These experimental findings are in agreement with the gradient force model. According to this theory, the macroscopic material transport results from the forces on the polarized material in the electrical field gradient caused by the holographic light grating. For many applications it is important that the holographically produced surface relief gratings can be transferred to polymer surfaces. Replica molding can be used to easily copy the surface modulations to e.g. polycarbonate.
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Towards the Governance of Open Distributed Grids - A Case Study in Wireless Mobile Grids
(2011)
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Tina Balke
- New networking technologies such as wireless mobile grids and peer-to-peer middleware are examples of a growing class of open distributed systems whose strength is the absence of a central controlling instance and which function through the cooperation of autonomous entities that voluntarily commit resources to a common pool. The social dilemma in such systems is that it is advantageous for rational users to access the common pool resources without making any commitment of their own. This is commonly known as “free-riding”. However, if a substantial number of users followed this selfish strategy, the system itself would fail, depriving all users of its benefits. In this dissertation, we demonstrate how governance decisions can induce cooperation in such systems and how normative frameworks in combination with multi-agent system simulations can be successfully employed to analyse their effects, even at an early development stage. We show that our approach is not only practical and powerful, but also easily accessible. We demonstrate its functionality by implementing a prototype to explore the impact of enforcement mechanisms on wireless mobile grids, a concept which has been proposed to address the energy issues arising in the next generation of mobile phones and the networks that connect them. We also infer lessons from this example for open distributed systems in general. Simulation experiments quantify the benefits of enforcement mechanisms for wireless mobile grids. We analyse these results with respect to the costs of enforcement as well as further criteria that reflect the interests of the multiple stakeholders in the system. We conclude with some observations on how the lessons learned from both process and outcomes may be applicable to the broader context of open distributed systems. In particular, we highlight (i) the use of simulation using intelligent agents and a normative framework as a means for in silico exploration of complex systems for both business and technological objectives, and (ii) the insight offered into a range of enforcement mechanisms and a better understanding of the conditions and constraints under which they are applicable.
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Dynamics and statistics of hydrodynamically interacting particles in laminar flows
(2011)
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Jochen Bammert
- The subject of this thesis is the investigation of the dynamics and statistics of hydrodynamically interacting particles in low Reynolds number flows, which is discussed in three interrelated themes. The first theme focuses on polymer fractionation. With our basic model we explore the possibility to sort dumbbells with respect to their size using a two dimensional periodic potential. It turns out that the purely diffusive behavior of a dumbbell in this structured landscape is dominated by the ratio of two characteristic length scales, namely the wavelength of the potential l and the size of the dumbbell b. We explain why the diffusion constant in the potential plane shows a pronounced local maximum around l/b equal 3/2. Furthermore, the influence of the spring rigidity and the hydrodynamic interaction on the diffusive motion are examined as well as the dumbbell statistics. If the dumbbell is driven by an external flow through the periodic landscape two different kinds of motion occur: transport along a potential valley and a stair-like motion oblique to the trenches. In the latter case, the dumbbell jumps regularly to a neighboring valley which results in an effective deflection. The onset of the oblique movement as well as the deflection angle beta depend on the hydrodynamic interaction, on the ratio l/b, and on the Brownian motion of the beads. Especially the significant dependence of beta on l/b enables particle sorting. The results are published. The second theme deals with the Brownian dynamics in shear flows. Here, we investigate the correlations of particle fluctuations in order to characterize the direct interplay between thermal motion, hydrodynamic interactions, and non-uniform flows.With respect to the experimental implementation the particles are caught by harmonic potentials. First, we consider one trapped Brownian bead in linear shear and Poiseuille flows. The correlation functions of the particle’s position and velocity fluctuations are calculated analytically. The main result is the occurrence of shear-induced cross-correlations between orthogonal fluctuations in the shear plane which are asymmetric in time. Moreover, the positional probability distribution, P(r), of a single bead in both types of flow is determined. In Poiseuille flow, where no analytical solutions can be obtained, we use perturbation expansions to derive formulas for P(r) that are valuable for the analysis of experimental data. In the case of a linear shear flow, a connection between the static correlations and the distribution functions is derived which allows a consistency check between independent measurements. Considering a system with several Brownian particles it is obvious that hydrodynamic interactions influence the correlations. In order to investigate this effect, we calculate the positional correlation functions for a setup of two trapped Brownian beads which are exposed to a linear shear flow. As expected, the one-particle correlations change compared to the single particle case described above. They depend on the distance between the two beads. In addition, we find inter-particle correlations between orthogonal positional fluctuations of different particles. The structure of these new cross-correlations depends significantly on the relative orientation of the two beads in the shear flow. They can have zero, one, or two local extrema as a function of time. In collaboration with Prof. Wagner from Saarbrücken some of our predictions are already confirmed by experiments, where polystyrene beads are caught by optical traps and simultaneously exposed to linear shear flows in a special microfluidic device. The results are published and further investigations are in progress.The third theme concentrates on the rheology of colloidal suspensions. Our deterministic model system consists of Hookean dumbbells suspended in a confined Newtonian fluid under constant shear. We perform a numerical study using fluid particle dynamics simulations, where the effective viscosity of the suspension, eta, and the dumbbell statistics are determined. The investigations on the tumbling motion of a single dumbbell reveals that eta is influenced by three different contributions: the volume fraction occupied by the dumbbell, the hydrodynamic interaction between the beads, and elastic correlation effects. For a suspension of independent spheres we observe in our simulations that the viscosity, as a function of the volume fraction Phi, differs from the prediction of Einstein, Batchelor and Green if Phi becomes larger than 8%. Replacing the beads by dumbbells leads to an increase of eta , which depends significantly on the length of the springs connecting the two beads. The distribution function for the orientation angle of the dumbbells indicates the complex motion of the individual objects in the suspension, which may lead to the so-called elastic turbulence, as experimentally discovered by Groisman and Steinberg.
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Halogens and trace elements in subduction zones
(2011)
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Diego Bernini
- This thesis concentrates on solubilities and incorporation mechanisms of halogens and trace elements in minerals and aqueous fluids at high temperatures and pressures. The solubility of fluorine and chlorine in upper mantle minerals (forsterite, enstatite and pyrope) and halogen partitioning between aqueous fluids and these minerals were investigated by piston-cylinder experiments at 1100 °C and 2.6 GPa. Chlorine solubility in forsterite, enstatite and pyrope is below the ppm level, and it is independent of fluid salinity. The fluid-mineral partition coefficient of chlorine is 103-106, indicating extreme incompatibility of chlorine in nominally anhydrous silicates. The fluorine solubility in enstatite and pyrope is two orders of magnitude higher than for Cl, with no dependence on fluid salinity. Forsterite dissolves 246-267 ppm up to a fluid salinity of 1.6 wt. % F. At higher fluorine contents in the system, forsterite is replaced by the minerals of the humite group, which host fluorine in the hydroxyl site. The fluid-mineral partition coefficient of fluorine ranges from 101 to 103. Due to the extreme incompatibility of Cl in a peridotite mineral assemblage, fluid flow from a subducting slab through the mantle wedge will lead to more efficient sequestration of H2O (when compared to Cl) into minerals, thus inducing a gradual increase in the fluid salinity. Mass balance calculations reveal that rock-fluid ratios of (1.3-4)∙103 are required to produce the characteristic Cl/H2O signature of primitive arc magmas. This indicates that fluid flow from subducting slabs into the melting regions in the overlying mantle is not confined to narrow channels but it is sufficient to pervasively metasomatize the bulk wedge. Energetics of fluorine incorporation in forsterite and forsterite-humite chemical equilibria were explored in the system Mg2SiO4-MgF2 by first principles computations. The pressure-volume equations of state and ground-state energies were determined for orthorhombic Mg2SiO4-Mg2F4 solutions, fluorine-bearing end-members of the humite group, and sellaite (MgF2). Humite group minerals and sellaite are energetically more stable than their equivalent solid solution compounds, hence they can act as buffers of fluorine solubility in forsterite. Compressibility increases systematically with the F content for both solid solution compounds and stable minerals. Nevertheless, end member solids are systematically less compressible than the respective solid solution compounds. The pressure-volume equations of state, internal energies, configurational and excess properties were used to set up a thermodynamic model of fluorine solubility in forsterite buffered by humite-group minerals up to 1900 K and 12 GPa. Humite is the stable F buffer in the investigated pressure and temperature range. The fluorine solubility in forsterite increases with temperature, from 0.01 ppm F at 500 K up to 0.33 wt. % F at 1900 K and 0 GPa. By contrast, the effect of pressure on the fluorine solubility is small, leading to its minor decrease as pressure rises to 12 GPa. These results demonstrate that partition coefficients of fluorine between forsterite and aqueous fluid (or silicate melt) are expected to increase with increasing temperature and decreasing pressure. When fluids or melts pass through the mantle wedge, fluorine will most efficiently be stored in the high-temperature portions of the wedge, promoting mantle metasomatism beneath the arc, and it will be released when the metasomatized mantle is advected to colder regions or to higher pressures. The mobility of high field strength elements in aqueous fluids in subduction zones was addressed by in-situ zircon solubility measurements in a hydrothermal diamond anvil cell. The zircon solubilities in aqueous fluids at 865-1025 oC and 6-20 kbar buffered by quartz are very low, ranging from 1.0 to 3.3 ppm Zr, and solubilities weakly increase with temperature and pressure. Experimental results were fitted to a density model: , where c is the Zr concentration in the fluid (ppm), T is temperature (K) and rho is the fluid density (g cm-3). Additional experiments have shown that Zr solubility increases with a decrease in silica activity and with the presence of NaCl and albite due to Zr-Cl or alkali-Zr complexing but it still remains very low. Therefore, the low Zr content observed in arc magmas is due to a very low mobility of Zr in aqueous fluid.
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Tibet Plateau Atmosphere-Ecology-Glaciology Cluster Joint Kobresia Ecosystem Experiment: Documentation of the first Intensive Observation Period Summer 2010 in Kema, Tibet
(2011)
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Tobias Biermann
Thomas Leipold
- no abstract
