کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
610562 | 880652 | 2009 | 10 صفحه PDF | دانلود رایگان |

The constant thickness (H) of metastable free films of various non-ionic surfactant solutions was measured at surfactant concentrations less than the critical micelle concentrations or solubility limits with fixed 5 ×× 10-510-5 M sodium chloride (NaCl) serving as the background electrolyte. The surfactants include n-pentanol, n-octanol, methyl isobutyl carbinol (MIBC), polypropylene glycol (PPG-400), tetraethylene glycol monooctyl ether (C8E4), and tetraethylene glycol monodecyl ether (C10C10E4E4). H was interferometrically measured. For each surfactant in this study, the H-versus-surfactant-concentration curve finds a peak at a concentration around 5 ×× 10-610-6–1 ×× 10-510-5 M and a valley at a higher concentration. The measured H values were compared to those predicted from the Derjaguin–Landau–Verwey–Overbeek (DLVO) theory, which considers solely the contribution from electrostatic double-layer repulsion with van der Waals attraction being neglected in the present work. In determining the double-layer repulsion, the ionic strength was determined from the electrolytic conductivity measurement of the film-forming solutions and the surface potential was estimated from the ζζ-potential measurement of air bubbles. It was found that the DLVO theory failed to explain the thickness variance with surfactant concentration, implying that additional non-DLVO attractive forces might be required to explain the experimental results. Finally, the possible origins of these attractive forces were discussed.
This paper finds anomalous S-shaped thickness variation of the foam films stabilized by various non-ionic surfactants at relatively low surfactant concentrations.Figure optionsDownload as PowerPoint slide
Journal: Journal of Colloid and Interface Science - Volume 337, Issue 2, 15 September 2009, Pages 538–547