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Colloid-polymer mixtures are an archetype for modeling phase transition processes, as they exhibit a low-density gas phase, high-density crystalline phase and an intervening liquid phase. While their equilibrium behavior has been studied extensively, the role of hydrodynamics in driving their phase separation is not yet understood. We present a theoretical model that describes hydrodynamic interactions in colloid-polymer mixtures in a microgravity environment. Our phase-field model consists of the Cahn-Hilliard equation, which describes phase separation processes in multicomponent mixtures, coupled with the Stokes equation for viscous fluid flow. We account for the dependence of the suspension viscosity on the colloid concentration, and the so-called Korteweg stresses that arise at the interfaces of colloidal phases. We process video microscopy images from NASA's Binary Colloid Alloy Test (BCAT) experiments, which were performed on the International Space Station. While terrestrial experiments would be dominated by gravitational forces and buoyancy-driven flows, the microgravity environment of the BCAT experiments allows for the visualization of phase separation by low interfacial tension, and thus enables a quantitative comparison between experiment and our model predictions.
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http://dx.doi.org/10.1038/s41526-025-00500-0 | DOI Listing |
NPJ Microgravity
September 2025
Department of Mathematical Sciences & Center for Applied Mathematics and Statistics, New Jersey Institute of Technology, Newark, NJ, USA.
Colloid-polymer mixtures are an archetype for modeling phase transition processes, as they exhibit a low-density gas phase, high-density crystalline phase and an intervening liquid phase. While their equilibrium behavior has been studied extensively, the role of hydrodynamics in driving their phase separation is not yet understood. We present a theoretical model that describes hydrodynamic interactions in colloid-polymer mixtures in a microgravity environment.
View Article and Find Full Text PDFJ Chem Phys
June 2025
Soft Condensed Matter and Biophysics, Debye Institute for Nanomaterials Science, Utrecht University, Utrecht, The Netherlands.
Machine learning (ML) strategies are opening the door to faster computer simulations, allowing us to simulate more realistic colloidal systems. Since the interactions in colloidal systems are often highly many-body, stemming from, e.g.
View Article and Find Full Text PDFJ Chem Theory Comput
June 2025
Korea Institute for Advanced Study, Seoul 02455, Korea.
Depletion forces are relevant in a variety of contexts such as the phase behavior of colloid-polymer or colloid-depletant mixtures and clustering of inclusions in mobile brushes. They arise from the tendency to minimize the volume of the depletion zone formed around colloidal particles or inclusions. In comparison to depletion interactions widely studied for colloidal particles or polymers in a suspension of spherical depletants, depletion interactions between nonspherical inclusions in mobile polymer brushes display complex behaviors.
View Article and Find Full Text PDFPhys Rev Lett
May 2025
Sezione INFN, Padova, University of Padova, Department of Physics and Astronomy, Via Marzolo 8, I-35131 Padova, Italy.
We study a spherically confined mixture of polymers and colloidal rings. Unlike in standard colloid-polymer mixtures, the polymers interact topologically with the rings by threading them. We find that, above a critical value of the ring radius, threading yields a topological transition from a fluid to a gel-like phase characterized by a space-spanning network of interlocked polymers and rings, which we refer to as a bicomponent gel, or bigel.
View Article and Find Full Text PDFLangmuir
May 2025
Beijing National Laboratory for Molecular Sciences, Laboratory of Polymer Physics and Chemistry, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Polymers are often used to modulate interactions and, consequently, the stability of colloids, which depends on a range of parameters such as concentration, the nature of the polymer (adsorbing/nonadsorbing, molecular weight, charged/neutral, etc.), temperature, and so on, as has been well studied before. However, the effect of colloid concentration on the stability of colloid-polymer mixtures at high polymer concentrations has been little addressed.
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