Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
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