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P Falus

Publications and source records attributed to P Falus.

7 recordsLinked to original sources

Crossover from stretched to compressed exponential relaxations in a polymer-based sponge phase.

X-ray photon correlation spectroscopy was used to characterize the wave vector- and temperature-dependent dynamics of spontaneous thermal fluctuations in a sponge (L3) phase that occurs in a blend of a symmetric poly(styrene-ethylene/butylene-styrene) triblock copolymer with a polystyrene homopolymer. Measurements of the intermediate scattering function reveal a crossover from stretched- to compressed-exponential relaxations as the temperature is lowered from 180 to 120 degrees C.

Journal Article↗

Optimizing the signal-to-noise ratio for X-ray photon correlation spectroscopy.

An analysis is presented of how to optimize the experimental beamline configuration for achieving the best possible signal-to-noise ratio (SNR) in X-ray photon correlation spectroscopy experiments using area detectors. It is shown that there exists an optimum detector distance; namely, the highest SNR is achieved by matching the angular pixel size with the angular source size. Binning several pixels together can increase the SNR by permitting to match the shape of a detector pixel to the shape of the source. It is also shown that collimating slits several times wider than the effective transverse coherence length are optimal; further, it is demonstrated that the energy dependence of the SNR is dictated by the energy dependence of detector efficiency and source brilliance. Ultimately the effects of focusing and low longitudinal coherence are discussed.

Algorithms↗

Fluctuation dynamics of block copolymer vesicles.

X-ray photon correlation spectroscopy was used to characterize the wave-vector- and temperature-dependent dynamics of spontaneous thermal fluctuations in a vesicle (L4) phase that occurs in a blend of a symmetric poly(styrene-ethylene/butylene-styrene) triblock copolymer with a polystyrene homopolymer. Measurements of the intermediate scattering function reveal stretched-exponential behavior versus time, with a stretching exponent slightly larger than 2/3. The corresponding relaxation rates show an approximate q(3) dependence versus wave vector. Overall, the experimental measurements are well described by theories that treat the dynamics of independent membrane plaquettes.

Computer Simulation↗

Symmetric-to-asymmetric transition in triblock copolymer-homopolymer blends.

In blends of a symmetric poly(styrene-ethylene/butylene-styrene) tri-block-copolymer with a polystyrene homopolymer, small-angle x-ray scattering and cryotransmission electron microscopy measurements reveal a microstructure consisting of a disordered arrangement of poly(ethylene/butylene) membranes suspended in polystyrene. For triblock volume fractions less than 0.22, the membranes form an asymmetric sponge or L4 phase, consisting predominantly of equilibrium vesicles. For volume fractions greater than 0.22, they form a symmetric sponge-phase (L3 phase), separated from the L4 phase by a first-order transition.

Journal Article↗

Equilibrium dynamics in the nondiffusive regime of an entangled polymer blend.

The dynamics of compositional fluctuations in a miscible, entangled homopolymer blend of poly(ethylene oxide) and poly(methyl methacrylate) were studied on length scales smaller than the polymer radii of gyration, and for times comparable to the polymers' disentanglement time. The measured relaxation rates are consistent with predictions of the reptation model, as expressed via the dynamic random-phase approximation. Moreover, the observed mode amplitudes allow for an estimate of the entanglement length in the blend.

Journal Article↗

Absence of scaling for the intermediate scattering function of a hard-sphere suspension: static and dynamic x-ray scattering from concentrated polystyrene latex spheres.

X-ray photon correlation spectroscopy and small-angle scattering measurements are presented of the dynamics and structure of concentrated suspensions of charge-stabilized polystyrene latex spheres dispersed in glycerol, for volume fractions from 3% to 52%. The static structures of the suspensions show essentially hard-sphere behavior, and the short-time dynamics shows good agreement with predictions for the wave-vector-dependent collective diffusion coefficient. However, the intermediate scattering function is found to violate a scaling behavior found previously for a sterically stabilized hard-sphere suspension.

Journal Article↗

Structure and dynamics of concentrated dispersions of polystyrene latex spheres in glycerol: static and dynamic x-ray scattering

X-ray photon correlation spectroscopy and small-angle x-ray scattering measurements are applied to characterize the dynamics and structure of concentrated suspensions of charge-stabilized polystyrene latex spheres dispersed in glycerol, for volume fractions between 2.7% and 52%. The static structures of the suspensions show essentially hard-sphere behavior. The short-time dynamics shows good agreement with predictions for the wave-vector-dependent collective diffusion coefficient, which are based on a hard-sphere model [C. W. J. Beenakker and P. Mazur, Physica A 126, 349 (1984)]. However, the intermediate scattering function is found to violate a scaling behavior found previously for a sterically stabilized hard-sphere suspension [P. N. Segre and P. N. Pusey, Phys. Rev. Lett. 77, 771 (1996)]. Our measurements are parametrized in terms of a viscoelastic model for the intermediate scattering function [W. Hess and R. Klein, Adv. Phys. 32, 173 (1983)]. Within this framework, two relaxation modes are predicted to contribute to the decay of the dynamic structure factor, with mode amplitudes depending on both wave vector and volume fraction. Our measurements indicate that, for particle volume fractions smaller than about 0.30, the intermediate scattering function is well described in terms of single-exponential decays, whereas a double-mode structure becomes apparent for more concentrated systems.

Journal Article↗