“A Computational Study of how Solutes Load into a Surfactant Bilayer Using Monte Carlo Techniques.”
Friday, February 16th, 2018 at 3:30 p.m. / OMH 103
Dr. Minkara is a Postdoctoral Researcher at the University of Minnesota Chemistry Department.
Understanding solute uptake into soft micro-structured materials, such as bilayers and worm-like and spherical micelles, is of interest in the pharmaceutical, agricultural, and personal care industries. To obtain molecular-level insight on the effects of solutes loading into a lamellar phase, we utilize the Shinoda-Devane-Klein (SDK) coarse-grain force field in conjunction with configurational-bias Monte Carlo (CBMC) simulations in the osmotic Gibbs ensemble. The lamellar phase is comprised of a bilayer formed by triethylene glycol mono-n-decyl ether (C10E3) surfactants surrounded by water with a 50/50 surfactant/water weight ratio. We study both the unary adsorption isotherm and the effects on bilayer structure and stability caused by n-nonane, 1-hexanol, and ethyl butyrate at several different reduced reservoir pressures. The non-polar n-nonane molecules load near the center of the bilayer with no preferred orientation. In contrast, the polar 1-hexanol and ethyl butyrate molecules both load with their polar bead close to the surfactant head groups with a preferred orientation (more pronounced for 1-hexanol) perpendicular to the interface. Loading of n-nonane leads to an increase of the bilayer thickness, but does not affect the surface area per surfactant. Loading of polar additives leads to both lateral and transverse swelling. The reduced Henry’s law constants of adsorption are 0.23, 1.4, and 14 for n-nonane, 1-hexanol, and ethyl butyrate and it appears that the SDK force field significantly overestimates the ethyl butyrate – surfactant interactions.