Search results for "scattering"
showing 10 items of 8332 documents
Self-Diffusion in Concentrated Colloid Suspensions Studied by Digital Video Microscopy of Core−Shell Tracer Particles
1998
Optical video microscopy and digital image processing have been used to study the self-diffusion of colloidal particles with a hard-sphere potential. The colloid particles consist of cross-linked polymers and are dispersed in a good solvent to avoid aggregation. To investigate single particle motion in highly concentrated dispersions, a host−tracer system, consisting of two different kinds of polymer particles, has been designed: the host particles are made of poly-t-butylacrylate (with ethanedioldiacrylate as cross-linker) and have the same refractive index as the employed solvent, 4-fluorotoluene. The tracer particles have a core−shell structure with a polystyrene core (cross-linked with…
Interaction between a water-in-oil microemulsion and a linear-dendritic poly(propylene oxide)–polyglycerol block copolymer
2011
We present small angle scattering and dielectric spectroscopy results on the influence of an amphiphilic diblock copolymer on the structure and dynamics of a microemulsion. We use a water-in-oil (w/o) droplet microemulsion based on the anionic surfactant AOT (sodium bis(2-ethylhexyl) sulfosuccinate), that forms spherical water droplets coated by a monolayer of AOT dispersed in the continuous oil matrix. The studied polymer consists of a hydrophobic poly(propylene oxide) (PPO) block and a hydrophilic hyperbranched polyglycerol with 74 glycerol units (NG74). Combining small angle neutron scattering (SANS) and small angle X-ray scattering (SAXS) we find that the droplet structure is preserved …
Industrial applications of the aggregation of block copolymers in supercritical CO 2 : a SANS study
2002
Industrial applications of supercritical carbon dioxide (scCO2) rely upon the rather selective and easily adjustable solvent ability of CO2. CO2 near the critical point is a poor solvent for high molecular weight (HMW) hydrocarbon polymers, while it is a very good solvent for amorphous fluorinated polymers. By increasing the pressure, CO2 becomes a good solvent even for HMW hydrogenated chains. Specially engineered amphiphilic di-block copolymers, with CO2-philic and CO2-phobic portions, are expected to undergo trough a monomer–aggregate transition when the solvent density of the scCO2 changes. Here small-angle neutron scattering (SANS) results are reported for a block copolymer dissolved i…
Unusual crystallization kinetics in a hard sphere colloid-polymer mixture.
2008
We investigated the crystallization kinetics of a hard sphere colloid-polymer mixture at conditions where about 95% of solid coexists with about 5% of fluid. From time resolved Bragg and small angle light scattering, we find that the crystallite size increases with a power law of exponent alpha approximately 1/3 during both the conversion and the coarsening stage. This observation points to a single conserved order parameter for both stages and cannot be explained if the mixture is regarded as an effective one-component system. We alternatively suggest that--based on local geometric demixing--the polymer density takes the role of the conserved order parameter.
1987
X-ray scattering experiments on oriented polysiloxanes with paired mesogens and different distances between these swallow-tailed side groups show a remarkable dependence of the smectic monolayer thickness on the degree of dilution, whereas the interplanar distance of the side groups remain nearly constant. Due to the dominating interaction of the mesogenic moieties, the flexible main chain is forced to take part in the layer formation. A packing model is proposed to explain the results of the X-ray studies. For polymers with five or more dimethylsiloxane copolymer segments, a diffuse scattering appears in the smectic as well as in the isotropic phase. This scattering is independent of the o…
Quasielastic neutron scattering study of dynamics at the crossover from dilute to semidilute behavior in polymer solutions
1982
Re-entrant glass transition in a colloid-polymer mixture with depletion attractions.
2002
Performing light scattering experiments we show that introducing short-ranged attraction to a colloidal suspension of nearly hard spheres by addition of free polymer produces new glass transition phenomena. We observe a dramatic acceleration of the density fluctuations amounting to the melting of a colloidal glass. Increasing the strength of the attractions the system freezes into another nonergodic state sharing some qualitative features with gel states occurring at lower colloid packing fractions. This reentrant glass transition is in qualitative agreement with recent theoretical predictions.
Glassy dynamics of simulated polymer melts: Coherent scattering and van Hove correlation functions
2001
Whereas the first part of this paper dealt with the relaxation in the β-regime, this part investigates the final relaxation (α-relaxation) of a simulated polymer melt consisting of short non-entangled chains in the supercooled state above the critical temperature of ideal mode-coupling theory (MCT). The temperature range covers the onset of a two-step relaxation behaviour down to a temperature merely 2% above . We monitor the incoherent intermediate scattering function as well as the coherent intermediate scattering function of both a single chain and the melt over a wide range of wave numbers q. Upon approaching the coherent α-relaxation time of the melt increases strongly close to the max…
Dynamics-based assessment of nanoscopic polymer-network mesh structures and their defects.
2018
Polymer-network gels often exhibit complex nanoscopic architectures. First, the polymer-network mesh topology on scales of 1–10 nm is usually not uniform and regular, but disordered and irregular. Second, on top of that, many swollen polymer networks display spatial inhomogeneity of their polymer segmental density and crosslinking density on scales of 10–100 nm. This multi-scale structural complexity affects the permeability, mechanical strength, and optical clarity of the polymer gels, which is of central relevance for their performance in popular applications. As a result, there is a need to characterize the polymer network structures on multiple scales. On the scale of the spatial inhomo…
Mesoscopic gel at low agarose concentration in water: a dynamic light scattering study
1995
Previous work in our laboratory has shown that at very low agarose concentration in water gelation still occurs within mutually disconnected, high concentration regions generated by spinodal demixing. The freely diffusing particles obtained in these conditions are studied in the present work by depolarized dynamic light scattering and probe diffusion experiments. These particles are found to behave as large (in fact, mesoscopic) polymer fibers entangled in a continuously rearranged mesh with scaling parameters typical of partially flexible, neutral chains. The present results allow specifying the notion of mesoscopic gelation. They also reveal that the same symmetry-breaking mechanism that …