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Measurement of Forces between Supported Cationic Bilayers by Colloid Probe Atomic Force Microscopy: Electrolyte Concentration and Composition
Author(s) -
Matthew Leivers,
John M. Seddon,
Marc Declercq,
Eric S. J. Robles,
Paul F. Luckham
Publication year - 2018
Publication title -
langmuir
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.042
H-Index - 333
eISSN - 1520-5827
pISSN - 0743-7463
DOI - 10.1021/acs.langmuir.8b03555
Subject(s) - dlvo theory , chemistry , bilayer , van der waals force , colloid , mica , analytical chemistry (journal) , electrolyte , halide , muscovite , chemical physics , crystallography , inorganic chemistry , membrane , chromatography , molecule , materials science , organic chemistry , biochemistry , quartz , electrode , composite material
The interactions between supported cationic surfactant bilayers were measured by colloidal probe atomic force spectroscopy, and the effect of different halide salts was investigated. Di(alkylisopropylester)dimethylammonium methylsulfate (DIPEDMAMS) bilayers were fabricated by the vesicle fusion technique on muscovite mica. The interactions between the bilayers were measured in increasing concentrations of NaCl, NaBr, NaI, and CaCl 2 . In NaCl, the bilayer interactions were repulsive at all concentrations investigated, and the Debye length and surface potential were observed to decrease with increasing concentration. The interactions were found to follow the electrical double layer (EDL) component of DLVO theory well. However, van der Waals forces were not detected; instead, a strong hydration repulsion was observed at short separations. CaCl 2 had a similar effect on the interactions as NaCl. NaBr and NaI were observed to be more efficient at decreasing surface potential than the chloride salts, with the efficacy increasing with the ionic radius.

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