165 research outputs found

    Self-diffusion and Cooperative Diffusion in Semidilute Polymer Solutions as measured by Fluorescence Correlation Spectroscopy

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    We present a comprehensive investigation of polymer diffusion in the semidilute regime by fluorescence correlation spectroscopy (FCS) and dynamic light scattering (DLS). Using single-labeled polystyrene chains, FCS leads to the self-diffusion coefficient while DLS gives the cooperative diffusion coefficient for exactly the same molecular weights and concentrations. Using FCS we observe a new fast mode in the semidilute entangled concentration regime beyond the slower mode which is due to self-diffusion. Comparison of FCS data with data obtained by DLS on the same polymers shows that the second mode observed in FCS is identical to the cooperative diffusion coefficient measured with DLS. An in-depth analysis and a comparison with current theoretical models demonstrates that the new cooperative mode observed in FCS is due to the effective long-range interaction of the chains through the transient entanglement network

    Universitäres Selbstbewusstsein

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    Scanning probe microscopy with 'chemical sensitivity'

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    We discuss recent developments in scanning probe microscopy aiming to combine ultra-high lateral resolution with the potential of “chemical sensitivity”. Particular attention is given to techniques beyond the well-established scanning tunneling microscopy (STM) and atomic force microscopy (AFM), which allow surface imaging with atomic resolution, however, do hardly allow chemical identification of the structures under study. Starting with “nanomechanical” imaging using a modified AFM capable of local friction and elasticity measurements, we demonstrate that scanning probe microscopy can well be combined with a kind of materials recognition capability. We then turn to scanning near-field optical microscopy and spectroscopy (SNOM), a technique that combines high lateral resolution with nearly all the information accessible by optical techniques. In both cases, the present spatial resolution limits are discussed

    Dewetting at the interface between two immiscible polymers

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    We review the recent theoretical and experimental efforts that have been made in studying the dynamics of dewetting at the interface between two liquids. While detailed theoretical predictions are already available, the experimental studies are still at an early stage. The first experiments using high-molecular-weight homopolymers not only enable a study of the dewetting dynamics to be made, but also allow a detailed analysis of the deformed liquid/liquid interface around the growing holes to be undertaken. The experimental results are compared with theoretical predictions

    Wetting at polymer surfaces and interfaces

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    Experimental research on wetting in polymer films is a subject that is reaching maturity. We review progress from the past few years in research into the influence of a boundary in polymer blends, concentrating largely on the wetting transition, and the growth of wetting layers, where we pay particular attention to blends in which hydrodynamic flow plays a dominant role. A summary of work over the same period concerning the dewetting of polymer films is also included, along with a discussion of the role of pattern formation caused by dewetting and topographically and chemically patterned substrates. We conclude by summarising some experiments that we believe may inspire future research
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