4.6 Article

Contrasting effect of 1-butanol and 1,4-butanediol on the triggered micellar self-assemblies of C16-type cationic surfactants

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 23, Issue 35, Pages 19680-19692

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cp01666k

Keywords

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Funding

  1. National Science Foundation [CHE-1665157, EPS-0903806]
  2. National Institute of General Medical Sciences from the National Institutes of Health [P20 GM103418]
  3. Wichita State University Department of Chemistry
  4. Wichita State University Fairmount College of Liberal Arts and Sciences

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The study investigated the self-assembly of three quaternary salt-based cationic surfactants with different polar head groups in aqueous solutions. The presence of BuOH promoted mixed micelle formation, while BTD interfered with micellization. Analyzing the micellar characteristics using various techniques provided insights into micelle size/shape and aggregation number, as well as the morphology transition induced by alcohol addition.
The self-assembly in aqueous solutions of three quaternary salt-based C-16-type cationic surfactants with different polar head groups and identical carbon alkyl chain viz., cetylpyridinium bromide (CPB), cetyltrimethylammonium tosylate (CTAT), and cetyltriphenylphosphonium bromide (CTPPB) in the presence of 1-butanol (BuOH) and 1,4-butanediol (BTD) was investigated using tensiometry, 2D-nuclear Overhauser enhancement spectroscopy (2D-NOESY) and small angle neutron scattering (SANS) techniques. The adsorption parameters and micellar characteristics evaluated at 303.15 K distinctly showed that BuOH promotes the mixed micelle formation while BTD interfered with the micellization phenomenon. The SANS data fitted using an ellipsoid (as derived by Hayter and Penfold using the Ornstein-Zernike equation and the mean spherical approximation) and wormlike micellar models offered an insight into the micelle size/shape and aggregation number (N-agg) in the examined systems. The evaluated descriptors presented a clear indication of the morphology transition in cationic micelles as induced by the addition of the two alcohols. We also offer an investigation into the acceptable molecular interactions governing the differences in micelle morphologies, using the non-invasive 2D-NOESY technique and molecular modeling. The experimental observations elucidated from computational simulation add novelty to this work. Giving an account to the structural complexity in the three cationic surfactants, the molecular dynamics (MD) simulation was performed for CPB micelles in an aqueous solution of alcohols that highlighted the micelle solvation and structural transition, which is further complemented in terms of critical packing parameter (PP) for the examined systems.

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