34 research outputs found

    Hiding in Plain View: Colloidal Self-Assembly from Polydisperse Populations

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    We report small-angle x-ray scattering experiments on aqueous dispersions of colloidal silica with a broad monomodal size distribution (polydispersity, 14%; size, 8 nm). Over a range of volume fractions, the silica particles segregate to build first one, then two distinct sets of colloidal crystals. These dispersions thus demonstrate fractional crystallization and multiple-phase (bcc, Laves AB2, liquid) coexistence. Their remarkable ability to build complex crystal structures from a polydisperse population originates from the intermediate-range nature of interparticle forces, and it suggests routes for designing self-assembling colloidal crystals from the bottom up

    Packing polydisperse colloids into crystals: when charge-dispersity matters

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    Monte Carlo simulations, fully constrained by experimental parameters, are found to agree well with a measured phase diagram of aqueous dispersions of nanoparticles with a moderate size polydispersity over a broad range of salt concentrations and volume fractions. Upon increasing volume fraction the colloids freeze first into coexisting compact solids then into a body centered cubic phase (bcc) before they melt into a glass forming liquid. The surprising stability of the bcc solid at high volume fractions and salt concentrations is explained by the interaction (charge) polydispersity and vibrational entropy

    Assessment of electrophoresis and electroosmosis in construction materials: effect of enhancing electrolytes and heavy metals contamination

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    Electrokinetic effects are those that take place by application of an electric field to porous materials, with the zeta potential as the key parameter. Specifically, in the case of contaminated construction materials, the generation of an electroosmotic flux, with the corresponding dragging due to water transport, is a crucial mechanism to succeed in the treatment of decontamination. Therefore, it is of great interest trying to optimize the treatment by the addition of specific electrolytes enhancing the electrokinetic phenomena. Most of the data of zeta potential found in literature for construction materials are based in micro-electrophoresis measurements, which are quite far of the real conditions of application of the remediation treatments. In this paper, electrophoretic and electroosmotic experiments, with monolithic and powdered material respectively, have been carried out for mortar, brick and granite clean and contaminated with Cs, Sr, Co, Cd, Cu and Pb. The electrolytes tested have been distilled water (DW), Na2–EDTA, oxalic acid, acetic acid and citric acid. The zeta potential values have been determined through the two different techniques and the results compared and critically analysed

    The growth of charged platelets

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    Controlling the cohesion of cement paste

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    The main source of cohesion in cement paste is the nanoparticles of calcium silicate hydrate (C-S-H), which are formed upon the dissolution of the original tricalcium silicate (C3S). The interaction between highly charged C-S-H particles in the presence of divalent calcium counterions is strongly attractive because of ion-ion correlations and a negligible entropic repulsion. Traditional double layer theory based on the Poisson-Boltzmann equation becomes qualitatively incorrect in these systems. Monte Carlo (MC) simulations in the framework of the primitive model of electrolyte solutions is then an alternative, where ion-ion correlations are properly included. In addition to divalent calcium counterions, commercial Portland cement contains a variety of other ions (sodium, potassium, sulfate, etc.). The influence of high concentrations of these ionic additives as well as pH on the stability of the final concrete construction is investigated through MC simulations in a grand canonical ensemble. The results show that calcium ions have a strong physical affinity (in opposition to chemical adsorption) to the negatively charged silicate particles of interest (C-S-H, C3S). This gives concrete surprisingly robust properties, and the cement cohesion is unaffected by the addition of a large variety of additives provided that the calcium concentration and the C-S-H surface charge are high enough. This general phenomenon is also semiquantitatively reproduced from a simple analytical model. The simulations also predict that the affinity of divalent counterions for a highly and oppositely charged surface sometimes is high enough to cause a “charge reversal” of the apparent surface charge in agreement with electrophoretic measurements on both C3S and C-S-H particles
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