Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
Plenarvorträge - DPG-Tagungen
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Chemische Physik und Polymerphysik Dienstag<br />
Wir berechnen z.B. die mittlere radiale Dichteverteilung in einer Mikrodomäne.<br />
Ferner haben wir mit Minkowskifunktionalen die Dynamik<br />
von Strukturwandlungen zwischen geordneten und ungeordneten Phasen<br />
untersucht, die wir mit dynamischer Dichtefunktionaltheorie simulieren.<br />
Wir vergleichen unsere Ergebnisse mit Fourieranalysen und Analysen von<br />
Skeletten der Mikrodomänenstrukturen.<br />
CPP 15.35 Di 17:00 B<br />
Adsorption of a heteropolymer on a structured surface —<br />
•Thorsten Bogner, Friederike Schmid, and Andreas Degenhard<br />
— Condensed Matter Theory, Fakutät für Physik, Universität<br />
Bielefeld, Postfach 100131, 33501 Bielefeld<br />
The specific adsorption of a molecule, especially of a protein, on a<br />
surface is of interest in biological processes as well as for technical applications.<br />
The specificity within such molecular recognition processes<br />
results from unspecific non-covalent interactions. For proteins in a solvent,<br />
the spatial arrangements of the single monomers is determined by<br />
the same non-covalent interactions that lead to molecular recognition. As<br />
a result, the structure and therefore the physical shape of the protein is<br />
affected by the adsorption.<br />
We have calculated the energy spectra of a single heteropolymer for<br />
both, the non adsorbed as well as the adsorbed case, considering all possible<br />
compact folds. The heterogeneity of the polymer, as well as the<br />
structure of the surface was characterised by a sequence or respectively<br />
a pattern of hydrophobic and hydrophilic (polar) sites.<br />
Our calculations allowed to identify a preference of a surface pattern<br />
and to make a first attempt to define selectivity. We found general features<br />
among sequences that are selective for a particular surface pattern.<br />
These allow to identify relevant positions on the polymer chain, that decide<br />
if a particular surface is recognised. Furthermore, we were able to<br />
find sets of sequences that can recognise all surfaces by a process similar<br />
to mutations.<br />
CPP 15.36 Di 17:00 B<br />
Brillouin-microscopy, a versatile technique to study the<br />
mechanical properties of polymers — •Ravindrakumar BAC-<br />
TAVATCHALOU 1,2 , Roland SANCTUARY 1,3 , Jan Kristian<br />
KRÜGER 1,2 , Uli MÜLLER 1,2 , and Wolfgang MANGLKA-<br />
MMER 1,2 — 1 Laboratoire Européen de Recherche Universitaire<br />
Saarland-Lorraine (LERUSL) — 2 Universität des Saarlandes, Experimentalphysik,<br />
Postfach 151150, D-66041 Saarbrücken, Germany<br />
— 3 Université du Luxembourg, Avenue de la Faïencerie, L-1511,<br />
Luxembourg<br />
Brillouin spectroscopy (BS) is a versatile method to study the elastic<br />
properties of bulk and film-like samples. In contrast to the well established<br />
micro-Raman technique such a spatial resolving technique was not<br />
yet available for BS. We propose here a new kind of Brillouin microscopy<br />
(BM) without using a standard optical microscope, instead we use a home<br />
made optical magnifier in combination with a spatial filtering and scanning<br />
set-up. We will show that this new Brillouin technique is especially<br />
valuable for the investigation of polymers. Recently, a spatial resolution<br />
about 1µm was demonstrated (J. Phys. D: Appl. Phys. 36 (2003) 2738-<br />
2742). In order to prove the capability of BM we present and discuss the<br />
mechanical properties of interphases in ’substrate-1/adhesive/substrate-<br />
2’ sandwiches.<br />
CPP 15.37 Di 17:00 B<br />
Slippage and Nanorheology of Thin Polymer Films — •Renate<br />
Konrad and Karin Jacobs — Experimental Physics, Saarland University,<br />
POB 151 150, 66041 Saarbrücken<br />
The properties of a liquid in contact with a solid interface are very<br />
important for applications involving e.g. flow through porous media or<br />
in lab-on-a-chip devices. Solving the hydrodynamic equations for a liquid<br />
flowing over a solid surface, one usually assumes the relative velocity<br />
between liquid and solid to be zero, which is the so-called ”no-slip boundary<br />
condition”. Experiments with complex fluids and, very recently, also<br />
with simple (Newtonian) fluids have shown that there can be a non-zero<br />
velocity (”slippage”) at the boundary. The sizes involved are expected to<br />
be on the nm-scale. On the same scale we therefore determine the velocity<br />
and the shape of a moving liquid front. Both are known to serve as<br />
extremely sensitive ”nano-rheometers”. It is expected from theory that<br />
slippage is enforced for smooth and low surface-energy substrates. In our<br />
experiments, we vary the substrate properties as well as the ones of the<br />
liquid like viscosity and viscoelasticity. A significant correlation between<br />
these system properties and the sliding friction can be found.<br />
CPP 15.38 Di 17:00 B<br />
Microdomain Ordering and Slippage of a Structured Liquid —<br />
•Daniel Podzimek and Karin Jacobs — Saarland University, FR<br />
7.2 Experimental Physics, D-66123 Saarbrücken<br />
In this contribution we present flow properties and flow induced microdomain<br />
ordering of a confined structured liquid that is dewetting a<br />
solid substrate. The microdomains emerge, since the two blocks of the<br />
copolymer poly(styrene-ethylene/propylene) are incompatible and phase<br />
separate. The equilibrium film structure shows lamellae which are aligned<br />
parallel to the substrate. We find that dewetting induced shear causes a<br />
structural rearrangement of the microdomains into cylinders. AFM observations<br />
furthermore show that the dewetting process can be separated<br />
into two distinct stages. The first stage is characterized by round hole formation<br />
and structural rearrangements of the domains. The second stage<br />
of dewetting is defined by an irregular hole shape and the alignment of<br />
the microdomain structure along the three phase contact line. Additional<br />
to the experiments on the polymer surface we present AFM scans of the<br />
film-substrate interface. Effects due to slippage of the melt are apparent.<br />
CPP 15.39 Di 17:00 B<br />
Characterisation of plasma treated fluorinated copolymers —<br />
•Thorsten Meyer, Manfred ap. Prof. Neumann, Markus<br />
Bach, and Andreas Selinger — Universität Osnabrück, FB Physik,<br />
Barbarastrasse 7, 49069 Osnabrück<br />
The functionalisation of polymer surfaces with plasma is established<br />
for many fields and has several advantages compared to other chemical<br />
modification methods.<br />
For many industrial applications a rapid switching from hydrophobic to<br />
hydrophilic surfaces is required. With plasma treatments chemical modifications<br />
can be obtained, not reachable by simple wet chemical treatment.<br />
In order to study and optimize the inner parameters of the plasma<br />
treatment, the processing was studied under ultra clean conditions. The<br />
plasma treated surfaces were investigated by x-ray photoelectron spectroscopy<br />
(XPS), and atomic force microscopy (AFM) in combination with<br />
contact angle measurments. The relation between the fractal dimension<br />
and the wettability of the surface was studied.<br />
CPP 15.40 Di 17:00 B<br />
Zum Glaszustand dünner adsorbierter Polymerschichten —<br />
•Richard Hofmann und Dietmar Göritz — Fakultät für Physik,<br />
Universität Regensburg, 93040 Regensburg<br />
Die Frage der Beweglichkeit von Polymerketten dünner adsorbierter<br />
Schichten konnte bisher experimentell und theoretisch nicht widerspruchsfrei<br />
geklärt werden. Insbesondere besteht Uneinigkeit über den<br />
Einfluss des Trägermaterials auf die Glastemperatur und die kinetischen<br />
Vorgänge in dessen Umgebung. Ziel unserer Untersuchungen ist es, den<br />
Zustand der adsorbierten Polymerschicht durch die Messung der mechanischen<br />
Eigenschaften des Adsorbats auf einem Füllstoff zu erfassen.<br />
Die Experimente wurden an dem Modellsystem Hochorientierter Graphit<br />
(HOPG) und Polymer mit Hilfe der AFM durchgeführt.<br />
CPP 15.41 Di 17:00 B<br />
Influence of preparation conditions on the piezoelectric activity<br />
of ferroelectric polyamide 11 — •Alexander Kremmer1 , Peter<br />
Fruebing1 , Michael Wegener1 , Werner Wirges1 , Reimund<br />
Gerhard-Multhaupt1 , and Harald Goering2 — 1Department of<br />
Physics, University of Potsdam, Am Neuen Palais 10, 14469 Potsdam —<br />
2Federal Institute for Materials Research and Testing, Unter den Eichen<br />
87, 12205 Berlin<br />
The piezoelectric d33 coefficient of electrically poled commercial<br />
polyamide-11 films as well as of ferroelectric films, prepared by melting<br />
the powder in a hot press at 210◦C, quenching in ice-water, uniaxially<br />
stretching with a ratio of 3:1 and subsequent electrical poling above the<br />
coercive field (75 MV/m) is studied by use of dynamic piezoelectrical<br />
measurements where a force acts on the film periodically and the piezoelectric<br />
voltage across the film is measured. The influence of processing<br />
conditions (particularly stretching and annealing temperatures) on the<br />
piezoelectric activity and the temperature dependence of the piezoelectric<br />
coefficient is investigated in detail. The aim is the enhancement of<br />
the piezoelectric coefficient of the film material without losing its excellent<br />
thermal stability up to temperatures just below the melting region.