Adsorption of ionic surfactants at the air-solution interface

Citation
J. Eastoe et al., Adsorption of ionic surfactants at the air-solution interface, LANGMUIR, 16(10), 2000, pp. 4511-4518
Citations number
33
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
LANGMUIR
ISSN journal
07437463 → ACNP
Volume
16
Issue
10
Year of publication
2000
Pages
4511 - 4518
Database
ISI
SICI code
0743-7463(20000516)16:10<4511:AOISAT>2.0.ZU;2-5
Abstract
Neutron reflection (NR) and surface tension methods were compared for acces sing the equilibrium adsorption isotherm of various ionic surfactants at th e air-water interface. Four custom-synthesized anionics we,re investigated in detail: sodium dihexyl sulfosuccinate (di-C6SS), bis(1H,1H-perfluoro-n-p entyl)sodium sulfosuccinate (di-CF4), bis(1H,1H,5H-octafluoro-n-pentyl)sodi um sulfosuccinate (di-HCF4), and bis(1H, 3H,5H-octafluoropentyl)-2-sulfoglu taconate (di-HCF4GLU). Commercial n-alkyltrimethylammonium bromide (Cn-TAB) cationic surfactants with C12, C14, and C16 chain lengths were also studie d. The experiments examined the validity of the Gibbs equation, and the pre factor 2, for these seven compounds. Effects of contaminants, trace levels of polyvalent metal ions, and hydrophobic impurities were assessed for the anionics. When added at low levels, tetrasodium ethylenediaminetetraacetate (EDTA) was effective for eliminating effects of metallic impurities, and f oam fractionation was used to remove hydrophobic contaminants. The effects of these treatments on the apparent surface excess and procedures for obtai ning agreement between the neutronic and tensiometric isotherms are describ ed. Finally, it was confirmed that the Gibbs prefactor of 2 applies for all these 1:1 ionic surfactants.