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We report results of direct measurements of velocity profiles in a microchannel with hydrophobic and hydrophilic walls, using a new high precision method of double-focus spacial fluorescence cross-correlation under a confocal microscope. In the vicinity of both walls the measured velocity profiles do not turn to zero by giving a plateau of constant velocity. This apparent slip is proven to be due to a Taylor dispersion, an augmented by shear diffusion of nanotracers in the direction of flow. Comparing the velocity profiles near the hydrophobic and hydrophilic walls for various conditions shows that there is a true slip length due to hydrophobicity. This length, of the order of several tens of nanometers, is independent on electrolyte concentration and shear rate.
Inspired by recent publications doubtful of the FCS technique, we scrutinize how irreversible (static) and reversible (dynamic) quenching can influence the interpretation of such data. We consider intermediate cases where the assessment of photophysi
Cross-correlation signals are recorded from fluorescence photons scattered in free space off a trapped ion structure. The analysis of the signal allows for unambiguously revealing the spatial frequency, thus the distance, as well as the spatial align
We discuss the manner in which the dynamics of tracer polystyrene chains varies with the concentration of matrix polystyrene chains dissolved in toluene. Using fluorescence correlation spectroscopy and theory, it is shown that the cooperative diffusi
Direct correlation functions (DCFs), linked to the second functional derivative of the free energy with respect to the one-particle density, play a fundamental role in a statistical mechanics description of matter. This holds in particular for the or
Hydrogen bonding is modeled in terms of virtual exchange of protons between water molecules. A simple lattice model is analyzed, using ideas and techniques from the theory of correlated electrons in metals. Reasonable parameters reproduce observed ma