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  • Banchio, Adolfo J.  (5)
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  • 1
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 134, No. 12 ( 2011-03-28)
    Type of Medium: Online Resource
    ISSN: 0021-9606 , 1089-7690
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2011
    detail.hit.zdb_id: 3113-6
    detail.hit.zdb_id: 1473050-9
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  • 2
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 134, No. 4 ( 2011-01-28)
    Abstract: We present a comprehensive study of the equilibrium pair structure in fluids of nonoverlapping spheres interacting by a repulsive Yukawa-like pair potential, with special focus on suspensions of charged colloidal particles. The accuracy of several integral equation schemes for the static structure factor, S(q), and radial distribution function, g(r), is investigated in comparison to computer simulation results and static light scattering data on charge-stabilized silica spheres. In particular, we show that an improved version of the so-called penetrating-background corrected rescaled mean spherical approximation (PB-RMSA) by Snook and Hayter [Langmuir 8, 2880 (1992)], referred to as the modified PB-RMSA (MPB-RMSA), gives pair structure functions which are in general in very good agreement with Monte Carlo simulations and results from the accurate but nonanalytical and therefore computationally more expensive Rogers-Young integral equation scheme. The MPB-RMSA preserves the analytic simplicity of the standard rescaled mean spherical (RMSA) solution. The combination of high accuracy and fast evaluation makes the MPB-RMSA ideally suited for extensive parameter scans and experimental data evaluation, and for providing the static input to dynamic theories. We discuss the results of extensive parameter scans probing the concentration scaling of the pair structure of strongly correlated Yukawa particles, and we determine the liquid-solid coexistence line using the Hansen-Verlet freezing rule.
    Type of Medium: Online Resource
    ISSN: 0021-9606 , 1089-7690
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2011
    detail.hit.zdb_id: 3113-6
    detail.hit.zdb_id: 1473050-9
    Location Call Number Limitation Availability
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  • 3
    Online Resource
    Online Resource
    AIP Publishing ; 2011
    In:  The Journal of Chemical Physics Vol. 135, No. 15 ( 2011-10-21)
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 135, No. 15 ( 2011-10-21)
    Abstract: A comprehensive study is presented on the short-time dynamics in suspensions of charged colloidal spheres. The explored parameter space covers the major part of the fluid-state regime, with colloid concentrations extending up to the freezing transition. The particles are assumed to interact directly by a hard-core plus screened Coulomb potential, and indirectly by solvent-mediated hydrodynamic interactions. By comparison with accurate accelerated Stokesian Dynamics (ASD) simulations of the hydrodynamic function H(q), and the high-frequency viscosity η∞, we investigate the accuracy of two fast and easy-to-implement analytical schemes. The first scheme, referred to as the pairwise additive (PA) scheme, uses exact two-body hydrodynamic mobility tensors. It is in good agreement with the ASD simulations of H(q) and η∞, for smaller volume fractions up to about 10% and 20%, respectively. The second scheme is a hybrid method combining the virtues of the δγ scheme by Beenakker and Mazur with those of the PA scheme. It leads to predictions in good agreement with the simulation data, for all considered concentrations, combining thus precision with computational efficiency. The hybrid method is used to test the accuracy of a generalized Stokes-Einstein (GSE) relation proposed by Kholodenko and Douglas, showing its severe violation in low salinity systems. For hard spheres, however, this GSE relation applies decently well.
    Type of Medium: Online Resource
    ISSN: 0021-9606 , 1089-7690
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2011
    detail.hit.zdb_id: 3113-6
    detail.hit.zdb_id: 1473050-9
    Location Call Number Limitation Availability
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  • 4
    Online Resource
    Online Resource
    AIP Publishing ; 2018
    In:  The Journal of Chemical Physics Vol. 148, No. 13 ( 2018-04-07)
    In: The Journal of Chemical Physics, AIP Publishing, Vol. 148, No. 13 ( 2018-04-07)
    Abstract: We report on a comprehensive theory-simulation-experimental study of collective and self-diffusion in concentrated suspensions of charge-stabilized colloidal spheres. In theory and simulation, the spheres are assumed to interact directly by a hard-core plus screened Coulomb effective pair potential. The intermediate scattering function, fc(q, t), is calculated by elaborate accelerated Stokesian dynamics (ASD) simulations for Brownian systems where many-particle hydrodynamic interactions (HIs) are fully accounted for, using a novel extrapolation scheme to a macroscopically large system size valid for all correlation times. The study spans the correlation time range from the colloidal short-time to the long-time regime. Additionally, Brownian Dynamics (BD) simulation and mode-coupling theory (MCT) results of fc(q, t) are generated where HIs are neglected. Using these results, the influence of HIs on collective and self-diffusion and the accuracy of the MCT method are quantified. It is shown that HIs enhance collective and self-diffusion at intermediate and long times. At short times self-diffusion, and for wavenumbers outside the structure factor peak region also collective diffusion, are slowed down by HIs. MCT significantly overestimates the slowing influence of dynamic particle caging. The dynamic scattering functions obtained in the ASD simulations are in overall good agreement with our dynamic light scattering (DLS) results for a concentration series of charged silica spheres in an organic solvent mixture, in the experimental time window and wavenumber range. From the simulation data for the time derivative of the width function associated with fc(q, t), there is indication of long-time exponential decay of fc(q, t), for wavenumbers around the location of the static structure factor principal peak. The experimental scattering functions in the probed time range are consistent with a time-wavenumber factorization scaling behavior of fc(q, t) that was first reported by Segrè and Pusey [Phys. Rev. Lett. 77, 771 (1996)] for suspensions of hard spheres. Our BD simulation and MCT results predict a significant violation of exact factorization scaling which, however, is approximately restored according to the ASD results when HIs are accounted for, consistent with the experimental findings for fc(q, t). Our study of collective diffusion is amended by simulation and theoretical results for the self-intermediate scattering function, fs(q, t), and its non-Gaussian parameter α2(t) and for the particle mean squared displacement W(t) and its time derivative. Since self-diffusion properties are not assessed in standard DLS measurements, a method to deduce W(t) approximately from fc(q, t) is theoretically validated.
    Type of Medium: Online Resource
    ISSN: 0021-9606 , 1089-7690
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2018
    detail.hit.zdb_id: 3113-6
    detail.hit.zdb_id: 1473050-9
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  • 5
    Online Resource
    Online Resource
    International Union of Crystallography (IUCr) ; 2010
    In:  Journal of Applied Crystallography Vol. 43, No. 5 ( 2010-10-01), p. 970-980
    In: Journal of Applied Crystallography, International Union of Crystallography (IUCr), Vol. 43, No. 5 ( 2010-10-01), p. 970-980
    Abstract: Analytical theory and Stokesian dynamics simulations are used in conjunction with dynamic light scattering to investigate the role of hydrodynamic interactions in short-time diffusion in suspensions of charge-stabilized colloidal particles. The particles are modeled as solvent-impermeable charged spheres, repelling each other via a screened Coulomb potential. Numerical results for self-diffusion and sedimentation coefficients, as well as hydrodynamic and short-time diffusion functions, are compared with experimental data for a wide range of volume fractions. The theoretical predictions for the generic behavior of short-time properties obtained from this model are shown to be in full accord with experimental data. In addition, the effects of microion kinetics, nonzero particle porosity and residual attractive forces on the form of the hydrodynamic function are estimated. This serves to rule out possible causes for the strikingly small hydrodynamic function values determined in certain synchrotron radiation experiments.
    Type of Medium: Online Resource
    ISSN: 0021-8898
    RVK:
    Language: Unknown
    Publisher: International Union of Crystallography (IUCr)
    Publication Date: 2010
    detail.hit.zdb_id: 2020879-0
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