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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.

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