Thermoreversible crystallization of charged colloids due to adsorption/desorption of ionic surfactants.

J Colloid Interface Sci

Faculty of Pharmaceutical Sciences, Graduate School of Nagoya City University, 3-1 Tanabe, Mizuho, Nagoya City, Aichi 467-8603, Japan. Electronic address:

Published: March 2016

AI Article Synopsis

  • Charged colloids undergo thermoreversible crystallization as ionic surfactants adsorb onto their surfaces, causing them to crystallize when cooled and melt when heated.
  • The study used polystyrene particles in mixtures of ethylene glycol and water, allowing for modulation of surfactant adsorption by adjusting the ethylene glycol concentration.
  • Changes in ionic strength due to the temperature-dependent concentration of non-adsorbed surfactants were found to drive this crystallization and melting behavior, with implications for controlling colloidal materials in lower permittivity environments.

Article Abstract

We report that charged colloids exhibit thermoreversible crystallization via the adsorption of ionic surfactants onto particle surfaces. Due to the temperature dependence of the adsorption quantity, the colloids crystallized upon cooling and melted upon heating. To clarify the influences of surfactant adsorption on the crystallization, polystyrene (PS) particles dispersed in ethylene glycol (EG)/water mixtures were employed, enabling continuous tuning of the adsorption quantity by changing the EG concentration. The thermoreversible crystallization/melting behavior was found to be mainly attributable to changes in the ionic strength of the medium resulting from variation in the concentration of the non-adsorbed ionic surfactant molecules with temperature. We expect that the present findings will be useful for fine control of colloidal crystallization and the further study of colloidal crystallization in low permittivity media.

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http://dx.doi.org/10.1016/j.jcis.2015.11.064DOI Listing

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