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Plenarvorträge - DPG-Tagungen

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Chemische Physik und Polymerphysik Montag<br />

CPP 8.2 Mo 16:00 H 37<br />

Hypersonic relaxation in glass-formers: Thermodynamic theory<br />

and experimental studies using Brillouin spectroscopy — •Jörg<br />

Baller 1,2 , Jan Kristian Krüger 1,2 , Thomas Britz 1,2 , Wulff<br />

Possart 1,3 , Wolfgang Manglkammer 1,2 , and Roland Sanctuary<br />

1,4 — 1 Laboratoire Européen de Recherche Universitaire Saarland-<br />

Lorraine (LERUSL) — 2 Universität des Saarlandes, Fakultät für Physik<br />

und Elektrotechnik 7.2, Geb. 38, D-66041 Saarbrücken, Germany —<br />

3 Universität des Saarlandes, Fakultät für Chemie, Pharmazie und Werkstoffwissenschaften<br />

8.15, Geb. 22, D-66041 Saarbrücken, Germany —<br />

4 Universitaire du Luxembourg, 162a av. de la Faïencerie, L-1511 Luxembourg,<br />

Luxembourg<br />

The presented work gives a theoretical framework for the relaxation<br />

behaviour of the elastic moduli of glass-formers near the glass transition<br />

temperature. Using linear irreversible thermodynamics, an expression for<br />

the temporal evolution of the elastic moduli (measured at hypersonic frequencies)<br />

after a step-like change of temperature is calculated. These theoretical<br />

results are compared to measurements of the hypersonic elastic<br />

modulus by Brillouin Light Scattering (BLS). Three different materials<br />

- an oligomer, an epoxy resin and a classical polymer - have been examined<br />

by measuring the relaxation behaviour of the hypersound velocity<br />

after a temperature pertubation. A discussion of the importance and the<br />

influence of thermodynamic equilibrium during accomplishment of an<br />

relaxation experiment is given by comparison to the theoretical results.<br />

CPP 8.3 Mo 16:15 H 37<br />

Breakup of droplets in PS/PMMA blends after equibiaxial elongation<br />

— •Ulrich A. Handge — Institute of Polymers, Department<br />

of Materials, ETH Zürich, Switzerland<br />

The breakup of liquid droplets in emulsions and molten blends of immiscible<br />

polymers has attracted much attention since many decades. The<br />

intensive research is motivated by the fundamentally oriented interest in<br />

understanding the deformation of drops in definable fields of flow and<br />

the technological relevance of dispersion processes. In this study, we investigated<br />

the breakup of equibiaxially deformed PS droplets in molten<br />

polystyrene (PS)/poly(methyl methacrylate) (PMMA) blends using a<br />

multiaxial elongational rheometer [1]. In equibiaxial deformation, the PS<br />

drop is deformed into a flat circular disc. During subsequent relaxation,<br />

the PS drop can retract to one single drop or breakup into many smaller<br />

drops. The driving force for this phenomenon is the interfacial tension at<br />

the interphase between the PS phase and the PMMA phase. During relaxation,<br />

the interfacial tension attempts to minimize the surface area of<br />

the PS drop. Using light microscopy, we observed the formation of fingers<br />

and holes in the elongated PS drop which finally results in a breakup of<br />

the extended drop into many smaller drops.<br />

[1] P. Hachmann and J. Meissner, Rheometer for equibiaxial and planar<br />

elongations of polymer melts, J. Rheol. 47, 989 (2003).<br />

CPP 8.4 Mo 16:30 H 37<br />

Microtribological Properties of Fluorine-Based Polymers Deposited<br />

by Sol-Gel — •Phani Ayalasomayajula, Guiseppe Breliozzi,<br />

Imad Ahmed, and Henry Haefke — CSEM Swiss Center<br />

for Electronics and Microtechnology, Inc., Rue Jacquet-Droz 1, CH-2007<br />

Neuchatel, Switzerland<br />

The versatility of sol-gel processing makes this technology relevant to a<br />

wide range of industries. Applications include high-performance, protective<br />

coatings against scratch and corrosion, optical fibers and waveguides,<br />

filters and membranes, etc. Compared to other deposition techniques, solgel<br />

has many advantages, such as easy composition control, fabrication<br />

of thin films on large surfaces area, film homogeneity, cost effectiveness<br />

and simple operation cycles. In the present investigation, sol-gel deposition<br />

has been applied to coat three fluorine-based polymer layers with a<br />

maximum thickness of 50 nm onto silicon substrates. Prior to deposition,<br />

the silicon substrates were etched using HF to remove the native oxide<br />

layer. Adhesion, friction and wear were analyzed in the microNewton<br />

load regime using a precision microtribometer and compared with the<br />

properties of the native oxide covered silicon surface. Film composition,<br />

wetting behavior and surface topography were characterized by Rutherford<br />

backscattering spectroscopy, contact angle testing and atomic force<br />

microscopy, respectively. The obtained structural data has been correlated<br />

with the tribological results. It was also found that the degree of<br />

hydrophobicity of the coating results in a decrease of the pull-off force.<br />

Furthermore, an increase in the molecular weight of the polymer results<br />

in a reduction of wear.<br />

CPP 8.5 Mo 16:45 H 37<br />

Strain-dependent localization, microscopic deformations, andmacroscopic<br />

normal tensions in model polymer networks —<br />

•Carsten Svaneborg 1 , Gary S. Grest 2 , and Ralf Everaers 1<br />

— 1 Max-Planck-Institut für Physik komplexer Systeme, Nöthnitzerstr.<br />

38, 01187 Dresden, Germany — 2 Sandia National Laboratories, Albuquerque,<br />

New Mexico 87185, USA<br />

We use Molecular Dynamics simulations to characterize the microscopic<br />

and macroscopic response of a polymer network to an imposed<br />

macroscopic strain. Our motivation is to provide a framework for the<br />

quantitative test and the controlled development of statistical mechanical<br />

theories of rubber elasticity as well as for the validation of critical<br />

steps in the data analysis of experiments addressing these issues. We<br />

present a quantitative test of various tube models of rubber elasticity<br />

and show that recent theory by Mergell and Everaers is quite successful<br />

in rationalizing the observed behavior. By accounting for localization<br />

effects due to chemical crosslinks and entanglements, the theory is able<br />

to describe the length scale dependent microscopic deformations and to<br />

predict the elastic response of the network. We also discuss the interpretation<br />

of neutron scattering data for labelled paths through model polymer<br />

networks.<br />

CPP 8.6 Mo 17:00 H 37<br />

Infrared ellipsometric study of miscibility in thin double layers<br />

of two polymers — •K. Hinrichs 1 , A. Röseler 1 , E.H. Korte 1 ,<br />

N. Nikonenko 2 , J. Pionteck 3 , and K.-J. Eichhorn 3 — 1 Institut<br />

für Spektrochemie und Angewandte Spektroskopie - Institutsteil Berlin,<br />

— 2 B.I. Stepanov Institute of Physics, National Academy of Sciences<br />

of Belarus, F. Scaryna Ave. 68, 220072 Minsk, Belarus — 3 Institut für<br />

Polymerforschung Dresden e.V., Hohe Str. 6, D-01069 Dresden<br />

Mid infrared spectroscopic ellipsometry [1] has been applied for the<br />

investigation of poly-(n-butyl methacrylate) / poly(vinyl chloride) double<br />

layers (100 nm each) on gold substrates and to analyze the process<br />

of mixing caused by interdiffusion during annealing [2]. Interpretation of<br />

the ellipsometric spectra in optical layer models allows the determination<br />

of the thickness, the high frequency refractive index and the parameters<br />

of molecular vibrations of the different polymer compounds. For a more<br />

detailed evaluation infrared ellipsometry is used in combination with a<br />

regularized deconvolution method [3]. The deconvolution method allowed<br />

to determine positions of overlapping vibrational bands and to investigate<br />

the shape of their profile. Annealing induced spectral changes were<br />

discussed with respect to the miscibility and conformational changes in<br />

the polymer film. [1] Hinrichs, K., Tsankov, D., Korte, E.H., Röseler, A.,<br />

Sahre, K., Eichhorn, K.-J. Appl. Spectrosc. 2002, 56, 737. [2] Dlubek G.,<br />

Bondarenko, V., Pompe G., Taesler Ch., Petters K., Krause-Rehberg R.,<br />

Macromolecules 2002, 35, 6313; Dlubek G., Pompe G., Pionteck J., Janke,<br />

A., Kilburn, D. Macromol. Chem. Phys. 2003, 204, 1234. [3] Buslov, D.<br />

K., Nikonenko, N. A. Appl. Spectrosc. 1997, 51, 666.<br />

CPP 8.7 Mo 17:15 H 37<br />

Generalized Cauchy-Relation and its Implications for Amorphous<br />

and Nano-Structured Materials — •Jan Kristian<br />

Krüger, Thomas Britz, Jörg Baller, Andrä le Coutre,<br />

Wulff Possart, Patrick Alnot, and Roland Sanctuary —<br />

Laboratoire Européen de Recherche Universitaire Saarland-Lorraine<br />

(LERUSL). Universität des Saarlandes, Fakultät für Physik und<br />

Elektrotechnik 7.2, Geb. 38, D-66041 Saarbrücken, Germany<br />

The generalized Cauchy-Relation (GCR) shows an unexpected linear<br />

transformation (LT) between the elastic stiffness constants c11 and c44<br />

in materials with effective isotropic symmetry. The slope B of this LT is<br />

identical to that of the classical Cauchy-relation (B=3) but the additive<br />

constant A is far from beeing zero. The magnitude of A will be discussed<br />

as a measure of nanostructuration. Astonishingly, the GCR holds true<br />

during irreversible processes like the curing process of adhesives.<br />

The thermal glass transition, on the other hand shows two different<br />

behaviors of the GCR: on slow cooling, the glass transition is completely<br />

hidden in the GCR whereas on fast cooling the parameter B deviates significantly<br />

from its classical value. Thus, the GCR is able to distinguish<br />

between two states of glasses. Aging drives the broken GCR towards the<br />

undisturbed GCR

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