Interplay between surfactant self-assembly and adsorption at hydrophobic surfaces: insights from dissipative particle dynamics.

0545827 - ÚCHP 2022 RIV GB eng J - Journal Article
Šindelka, Karel - Lísal, Martin
Interplay between surfactant self-assembly and adsorption at hydrophobic surfaces: insights from dissipative particle dynamics.
Molecular Physics. Roč. 119, č. 15-16 (2021), č. článku e1857863. ISSN 0026-8976. E-ISSN 1362-3028
EU Projects: European Commission(XE) 760907 - VIMPP
Institutional support: RVO:67985858
Keywords : critical micelle concentration * generic mesoscopic force field * hemispheres
OECD category: Physical chemistry
Impact factor: 1.937, year: 2021
Method of publishing: Limited access

We study the self-organisation of aqueous surfactants in bulk phase, and the adsorption and selforganisation of the aqueous surfactants at a planar hydrophobic surface by dissipative particle dynamics. Nonionic surfactants, n-alkyl poly(ethylene oxide) CnEm, and water are coarse-grained into mesoscopic beads comprising 1–3 heavy atoms and two water molecules, respectively. The size of the mesoscopic beads is related to the molar volume of the underlying molecular fragments while the bead–bead interaction parameters are calibrated against the water-octanol partition coefficients.
Wefocus on theC6E3, C6E4, C8E3, andC8E4 surfactants in water that form spherical micelles in the bulk. The bulk micellization is primarily affected by the alkyl tail length which is demonstrated by an order of magnitude decrease in the critical micelle concentration when going from the aqueous C6Em to aqueous C8Em solutions. Surfactants strongly adsorb on the hydrophobic surface, adopting lying-down configurations and forming hemispheres which are in equilibrium with the spherical micelles in the bulk. In contrast to the bulk phase, the surfactant adsorption behaviour is influenced by both the alkyl tail and head chain lengths.
Permanent Link: http://hdl.handle.net/11104/0322472