958 research outputs found
Phase behavior of weakly polydisperse sticky hard spheres: Perturbation theory for the Percus-Yevick solution
We study the effects of size polydispersity on the gas-liquid phase behaviour
of mixtures of sticky hard spheres. To achieve this, the system of coupled
quadratic equations for the contact values of the partial cavity functions of
the Percus-Yevick solution is solved within a perturbation expansion in the
polydispersity, i.e. the normalized width of the size distribution. This allows
us to make predictions for various thermodynamic quantities which can be tested
against numerical simulations and experiments. In particular, we determine the
leading-order effects of size polydispersity on the cloud curve delimiting the
region of two-phase coexistence and on the associated shadow curve; we also
study the extent of size fractionation between the coexisting phases. Different
choices for the size-dependence of the adhesion strengths are examined
carefully; the Asakura-Oosawa model of a mixture of polydisperse colloids and
small polymers is studied as a specific example.Comment: 43 pages, 12 figures, and 1 tabl
The Lyotropic Sequence in the Stability of Hydrophobic Colloids
The nature of the counterion, among other parameters, has
a pronounced influence on the flocculation values for hydrophobic
sols. A discussion of the lyotropic sequence, i. e. of the increase of
the flocculation values for a typical, negatively charged silver
iodide sol, in the series Rb+, K•, Na•, and Li+, is given in terms
of the Deryagin-Landau-Verwey-Overbeek theory of colloidal
stability. More recent data on adsorption of alkali metal ions on
the surface of a-hematite indicate a reversal of the lyotropic series.
Interpretation is sought in the predominance of steric factors
The Electrical Double Layer on Oxides
The properties of the electrical double layer at the interface
between oxides and aqueous electrolyte solutions have been studied
on the basis of apparent surface charge - pH curves. It appears
that all oxides studied so far can bear very high surface charges
without giving rise to particularly high electrokinetic potentials.
The trend is that this charge is the higher, the more porous is the
surface layer. These results are discussed in terms of a quantitative
theory, based on the concept that potential-determining as
well as counter ions can penetr;:ite into the solid, to an extent
depending on the porosity of the surface for that ion. The theory
and experiments are also applied to the glass-solution interface.
The results seem to support the idea that glass-electrode potentials
are diffusion potentials
Charge Inversion of Divalent Ionic Solutions in Silica Channels
Recent experiments (F.H.J. Van Der Heyden et al., PRL 96, 224502 (2006)) of
streaming currents in silica nanochannels with divalent ions report charge
inversion, i.e. interfacial charges attracting counterions in excess of their
own nominal charge, in conflict with existing theoretical and simulation
results. We reveal the mechanism of charge inversion by using all-atomic
molecular dynamics simulations. Our results show excellent agreement with
experiments, both qualitatively and quantitatively. We further discuss the
implications of our study for the general problem of ionic correlations in
solutions as well as in regards of the properties of silica-water interfaces.Comment: 5 pages, 5 figure
First-order phase transition during displacement of amphiphilic biomacromolecules from interfaces by surfactant molecules
The adsorption of surfactants onto a hydrophobic interface, already laden with a fixed number of amphiphilic macromolecules, is studied using the self consistent field calculation method of Scheutjens and Fleer. For biopolymers having unfavourable interactions with the surfactant molecules, the adsorption isotherms show an abrupt jump at a certain value of surfactant bulk concentration. Alternatively, the same behaviour is exhibited when the number of amphiphilic chains on the interface is decreased. We show that this sudden jump is associated with a first-order phase transition, by calculating the free energy values for the stable and the metastable states at both sides of the transition point. We also observe that the transition can occur for two approaching surfaces, from a high surfactant coverage phase to a low surfactant coverage one, at sufficiently close separation distances. The consequence of this finding for the steric colloidal interactions, induced by the overlap of two biopolymer + surfactant films, is explored. In particular, a significantly different interaction, in terms of its magnitude and range, is predicted for these two phases. We also consider the relevance of the current study to problems involving the competitive displacement of proteins by surfactants in food colloid systems
Electro-osmosis on anisotropic super-hydrophobic surfaces
We give a general theoretical description of electro-osmotic flow at striped
super-hydrophobic surfaces in a thin double layer limit, and derive a relation
between the electro-osmotic mobility and hydrodynamic slip-length tensors. Our
analysis demonstrates that electro-osmotic flow shows a very rich behavior
controlled by slip length and charge at the gas sectors. In case of uncharged
liquid-gas interface, the flow is the same or inhibited relative to flow in
homogeneous channel with zero interfacial slip. By contrast, it can be
amplified by several orders of magnitude provided slip regions are uniformly
charged. When gas and solid regions are oppositely charged, we predict a flow
reversal, which suggests a possibility of huge electro-osmotic slip even for
electro-neutral surfaces. On the basis of these observations we suggest
strategies for practical microfluidic mixing devices. These results provide a
framework for the rational design of super-hydrophobic surfaces.Comment: 4 pages, 4 figures; submitted to PRL Revised version: several
references added, typos corrected. Supplementary file was restructured, the
second part of the original EPAPS was removed and is supposed to be published
as a separate pape
Can a Protein Adsorb on its Own? The Thermodynamics of Ion Participation
We present a general thermodynamic method to obtain information about co-adsorption and oo-partitioniiug of low molecular weight ions upon adsorption or partitioning of proteins between two phases. Esin-Markov coefficients are central quantities. By this procedure useful additional information is obtained that, in turn, can be used in mechanistic interpretations. Applications are presented for (1) ion binding to free BSA, (2) charge adjustments in the protein and on the surface upon adsorption of BSA on silver iodide and (3) ion co-participation upon solubilization of cytoohrome-C into micro-emulsdon .droplets
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