TY - THES A1 - Leiendecker, Mai-Thi T1 - Physikalische Hydrogele auf Polyurethan-Basis T1 - Physical hydrogels based on polyurethanes N2 - Physical hydrogels have gained recent attention as cell substrates, since viscoelasticity or stress relaxation is a powerful parameter in mechanotransduction, which has long been neglected. We designed multi-functional polyurethanes to form physical hydrogels via a unique tunable gelation mechanism. The anionic polyurethanes spontaneously form aggregates in water that are kept in a soluble state through electrostatic repulsion. Fast subsequent gelation can be triggered by charge shielding which allows the aggregation and network building to proceed. This can be induced by adding either acids or salts, resulting in acidic (pH 4-5) or pH-neutral hydrogels, respectively. Whereas conventional polyurethane-based hydrogels are commonly prepared from toxic isocyanate precursors, the physical hydrogelation mechanism described here does not involve chemically reactive species which is ideal for in situ applications in sensitive environments. Both stiffness and stress relaxation can be tuned independently over a broad range and the gels exhibit excellent stress recovery behavior. N2 - Physikalische Hydrogele gewinnen derzeit als Zellsubstrate zunehmend an Interesse, da Viskoelastizität oder Stressrelaxation ein bedeutender Parameter in der Mechanotransduktion ist, der bisher vernachlässigt wurde. In dieser Arbeit wurden multi-funktionelle Polyurethane entworfen, die über einen neuartigen Gelierungsmechanismus physikalische Hydrogele bilden. In Wasser bilden die anionischen Polyurethane spontan Aggregate, welche durch elektrostatische Abstoßung in Lösung gehalten werden. Eine schnelle Gelierung kann von hier aus durch Ladungsabschirmung erreicht werden, wodurch die Aggregation voranschreitet und ein Netzwerk ausgebildet wird. Dies kann durch die Zugabe von verschiedenen Säuren oder Salzen geschehen, sodass sowohl saure (pH 4 - 5) als auch pH-neutrale Hydrogele erhalten werden können. Während konventionelle Hydrogele auf Polyurethan-Basis in der Regel durch toxische isocyanat-haltige Präpolymere hergestellt werden, eignet sich der hier beschriebene physikalische Gelierungsmechanismus für in situ Anwendungen in sensitiven Umgebungen. Sowohl Härte als auch Stressrelaxation der Hydrogele können unabhängig voneinander über einen breiten Bereich eingestellt werden. Darüberhinaus zeichnen sich die Hydrogele durch exzellente Stressregeneration aus. KW - Polyurethane KW - Hydrogele KW - physikalische Hydrogele KW - Kolloidchemie KW - Viskoelastizität KW - Stressrelaxation KW - Stressrelaxierung KW - Bulkgele KW - Mikrogele KW - Mechanotransduktion KW - polyurethanes KW - hydrogels KW - physical hydrogels KW - colloidal chemistry KW - viscoelasticity KW - stress-relaxation KW - stress relaxation KW - bulk gels KW - microgels KW - mechanotransduction Y1 - 2016 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-103917 ER - TY - GEN A1 - Goychuk, Igor A1 - Kharchenko, Vasyl O. T1 - Rocking subdiffusive ratchets BT - origin, optimization and efficiency T2 - Mathematical Modelling of Natural Phenomena N2 - We study origin, parameter optimization, and thermodynamic efficiency of isothermal rocking ratchets based on fractional subdiffusion within a generalized non-Markovian Langevin equation approach. A corresponding multi-dimensional Markovian embedding dynamics is realized using a set of auxiliary Brownian particles elastically coupled to the central Brownian particle (see video on the journal web site). We show that anomalous subdiffusive transport emerges due to an interplay of nonlinear response and viscoelastic effects for fractional Brownian motion in periodic potentials with broken space-inversion symmetry and driven by a time-periodic field. The anomalous transport becomes optimal for a subthreshold driving when the driving period matches a characteristic time scale of interwell transitions. It can also be optimized by varying temperature, amplitude of periodic potential and driving strength. The useful work done against a load shows a parabolic dependence on the load strength. It grows sublinearly with time and the corresponding thermodynamic efficiency decays algebraically in time because the energy supplied by the driving field scales with time linearly. However, it compares well with the efficiency of normal diffusion rocking ratchets on an appreciably long time scale. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 622 KW - anomalous Brownian motion KW - generalized Langevin equation KW - memory effects KW - viscoelasticity KW - ratchet transport KW - stochastic Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-416138 SN - 1866-8372 IS - 622 ER -