Publications by authors named "Hendrik Hansen-Goos"

To explore the curvature dependence of solid-fluid interfacial thermodynamics, we calculate, using Grand Canonical Monte Carlo simulation, the surface free energy for a 2d hard-disk fluid confined in a circular hard container of radius R as a function of the bulk packing fraction η and wall curvature C̄=-1/R. (The curvature is negative because the surface is concave.) Combining this with our previous data [Martin et al.

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Suspended colloids are often considered as models for molecules, which are sufficiently big so that they can be observed directly in (light) microscopes and for which the effective interaction among each other can be tailored. The Asakura-Oosawa model of ideal colloid-polymer mixtures captures the idea of tuning the interaction between the colloids via a potential, which possesses a range set by the size of the polymers and an attractive strength characterized by the (reservoir) number density of the polymers, which plays the role of an inverse temperature. The celebrated Asakura-Oosawa depletion potential allows one to recreate the bulk phase diagram of a simple fluid by employing a colloid-polymer mixture.

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In this work, we examine the surface thermodynamics of a hard-disk fluid at curved hard walls using Monte Carlo (MC) simulation and a generalized scaled particle theory (gSPT). The curved walls are modeled as hard disks of varying radii, . The surface free energy, γ, and excess surface volume, , for this system are calculated as functions of both the fluid packing fraction and the wall radius.

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For a standard model of patchy colloidal fluids with patch number M = 2, where chain formation (polymerization) occurs, we show that Wertheim theory predicts critical behavior at vanishing density and temperature. The analysis is based on determining lines in the phase diagram of maximal correlation length and compressibility. Simulation studies identify the latter line and confirm our prediction of Fisher-Widom crossover, i.

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Article Synopsis
  • The study explores how attractive and repulsive forces between particles in simple fluids affect their phase behavior and structural properties, particularly through pair correlation functions.
  • It examines the decay patterns of the total correlation function h(r) and how these patterns differ based on whether attractive forces dominate over repulsive forces.
  • A new thermodynamic criterion, which approximates the Fisher-Widom line within phase diagrams, is proposed and tested using four models of simple fluids, demonstrating its relevance in understanding fluid behavior.
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Within scaled-particle theory, we construct an equation of state (EOS) for hard-disk mixtures by making use of an additional scaled-particle variable which weighs the densities of the different components by its radii to the power . This allows us to simultaneously respect exact results pertaining to the cases of a large particle or a point particle being added to the mixture. In the limit → 2, the mixture EOS of Santos [Mol.

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A generalized scaled-particle theory for the uniform hard-disk mixture is derived in the spirit of the White Bear II free energy of the hard-sphere fluid [H. Hansen-Goos and R. Roth, J.

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Article Synopsis
  • Protein adsorption at solid-liquid interfaces is crucial in biological processes, but the detailed mechanisms behind it remain largely unexplored.! -
  • The research uses multivalent ions to control the adsorption of negatively charged proteins (like bovine serum albumin) at these interfaces, demonstrating this through various experimental techniques like ellipsometry and neutron reflectivity.! -
  • The study reveals a complex relationship between salt concentration and protein adsorption, explained by a model that connects bulk behavior to surface interactions, which may have broader implications for understanding processes like nucleation at interfaces.!
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Within the Asakura-Oosawa model, we study structural relaxation in mixtures of colloids and polymers subject to Brownian motion in the overdamped limit. We obtain the time evolution of the self and distinct parts of the van Hove distribution function G(r,t) by means of dynamical density functional theory (DDFT) using an accurate free-energy functional based on Rosenfeld's fundamental measure theory. In order to remove unphysical interactions within the self part, we extend the recently proposed quenched functional framework (Stopper et al 2015 J.

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We derive an analytical equation of state for the hard-sphere fluid that is within 0.01% of computer simulations for the whole range of the stable fluid phase. In contrast, the commonly used Carnahan-Starling equation of state deviates by up to 0.

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We introduce long-range weight functions to the framework of fundamental measure theory (FMT) of the non-uniform, single-component hard-sphere fluid. While the range of the usual weight functions is equal to the hard-sphere radius R, the modified weight functions have range 3R. Based on the augmented FMT, we calculate the radial distribution function g(r) up to second order in the density within Percus' test particle theory.

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We study structural relaxation of colloidal hard spheres undergoing Brownian motion using dynamical density functional theory. Contrary to the partial linearization route [D. Stopper et al.

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Article Synopsis
  • - We examine how hard sphere colloids behave under Brownian motion, focusing on their movement in a dense fluid (overdamped limit) using advanced theoretical techniques.
  • - Our analysis utilizes the White Bear II model of Rosenfeld's fundamental measure theory to accurately describe the fluid's free energy, but requires a complex adjustment to handle interactions in the self-part of the van Hove function.
  • - We validate our theory by comparing it to results from dynamical Monte Carlo simulations, finding consistency even at high densities (packing fractions up to 40%).
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Based on Santos' general solution for the scaled-particle differential equation [Phys. Rev. E 86, 040102(R) (2012)], we construct a free-energy functional for the hard-sphere system.

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We demonstrate that the Hadwiger form of the free energy of a fluid in contact with a wall is insufficient to describe the low-density behavior of a hard-sphere fluid. This implies that morphological thermodynamics of the hard-sphere fluid is an approximate theory if only four geometric measures are included. In order to quantify deviations from the Hadwiger form we extend standard fundamental measure theory of the bulk fluid by introducing additional scaled-particle variables which allow for the description of non-Hadwiger coefficients.

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We describe an optical scattering study of grain boundary premelting in water ice. Ubiquitous long ranged attractive polarization forces act to suppress grain boundary melting whereas repulsive forces originating in screened Coulomb interactions and classical colligative effects enhance it. The liquid enhancing effects can be manipulated by adding dopant ions to the system.

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It has recently been shown that a free energy for Baxter's sticky hard-sphere fluid is uniquely defined within the framework of fundamental measure theory (FMT) for the inhomogeneous hard-sphere fluid, provided that it obeys scaled-particle theory and the Percus-Yevick (PY) result for the direct correlation function [H. Hansen-Goos and J. S.

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In a recent publication (Hansen-Goos and Mecke 2009 Phys. Rev. Lett.

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We construct a density functional theory (DFT) for the sticky hard sphere (SHS) fluid which, like Rosenfeld's fundamental measure theory (FMT) for the hard sphere fluid [Y. Rosenfeld, Phys. Rev.

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Theory of ice premelting in porous media.

Phys Rev E Stat Nonlin Soft Matter Phys

March 2010

Premelting describes the confluence of phenomena that are responsible for the stable existence of the liquid phase of matter in the solid region of its bulk phase diagram. Here we develop a theoretical description of the premelting of water ice contained in a porous matrix, made of a material with a melting temperature substantially larger than ice itself, to predict the amount of liquid water in the matrix at temperatures below its bulk freezing point. Our theory combines the interfacial premelting of ice in contact with the matrix, grain-boundary melting in the ice, and impurity and curvature induced premelting, with the latter occurring in regions which force the ice-liquid interface into a high curvature configuration.

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Using the Gauss-Bonnet theorem we deconvolute exactly the Mayer f-function for arbitrarily shaped convex hard bodies in a series of tensorial weight functions, each depending only on the shape of a single particle. This geometric result allows the derivation of a free energy density functional for inhomogeneous hard-body fluids which reduces to Rosenfeld's fundamental measure theory [Phys. Rev.

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We calculate the solvation free energy of proteins in the tube model of Banavar and Maritan [Rev. Mod. Phys.

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In the spirit of the White Bear version of fundamental measure theory we derive a new density functional for hard-sphere mixtures which is based on a recent mixture extension of the Carnahan-Starling equation of state. In addition to the capability to predict inhomogeneous density distributions very accurately, like the original White Bear version, the new functional improves upon consistency with an exact scaled-particle theory relation in the case of the pure fluid. We examine consistency in detail within the context of morphological thermodynamics.

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We introduce an expansion of the equation of state for additive hard-sphere mixtures in powers of the total packing fraction with coefficients which depend on a set of weighted densities used in scaled particle theory and fundamental measure theory. We demand that the mixture equation of state recovers the quasiexact Carnahan-Starling [J. Chem.

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