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Surfactant desorption and scission free energies for cylindrical and spherical micelles from umbrella-sampling
Boyao Wen1, Bofeng Bai2, Ronald G Larson3
1Department of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109, United States; State Key Laboratory of Multiphase Flow in Power Engineering, Xi'an Jiaotong University, Xi'an, Shaanxi 710049, China.
Hypothesis:
The free energies associated with adsorption/desorption of individual surfactants from micelles and the fusion/scission of long micelles can be used to estimate the rate constants for micellar kinetics as functions of surfactant and salt concentration.
Experiments:
We compute the escape free energies △Gesc of surfactant from micelles and the scission free energies △Gsciss of long micelles from coarse-grained molecular dynamics simulations coupled with umbrella sampling, for micelles of both sodium dodecylsulfate (SDS) in sodium chloride (NaCl) and cetyltrimethylammonium chloride (CTAC) in sodium salicylate (NaSal).
Findings:
For spherical micelles, △Gesc values have maxima at certain aggregation numbers, and at salt-to-surfactant molar concentration ratios R near unity, consistent with experiments. For cylindrical micelles, SDS/NaCl shows a minimum, and CTAC/NaSal a maximum in △Gesc, both at R ~ 0.7, while △Gsciss of CTAC micelles also peaks at around R ~ 0.7 and that of SDS micelles increases monotonically with R. We explain the non-monotonic dependence of escape and scission free energies on R by a combination of electrostatic screening and the decrease of micelle radius with increasing R. Transitions from predominantly spherical to cylindrical micelles, and between adsorption/desorption and fusion/scission kinetics with changing salt concentration can be inferred from the free energies for CTAC/NaSal.
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