Please use this identifier to cite or link to this item:
|Title:||Salt effect on the interactions between gemini surfactant and oppositely charged polyelectrolyte in aqueous solution||Authors:||Pi, Y.
|Issue Date:||15-Feb-2007||Citation:||Pi, Y., Shang, Y., Liu, H., Hu, Y., Jiang, J. (2007-02-15). Salt effect on the interactions between gemini surfactant and oppositely charged polyelectrolyte in aqueous solution. Journal of Colloid and Interface Science 306 (2) : 405-410. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jcis.2006.10.020||Abstract:||The effect of alkali halides (NaBr, NaCl, KCl) on the interactions between the cationic gemini surfactant hexylene-1,6-bis(dodecyldimethylammonium bromide) (12-6-12) and the anionic polyelectrolyte sodium polyacrylate (NaPAA) in aqueous solution has been investigated by fluorescence emission spectroscopy, UV transmittance, zeta potential, and transmission electron microscopy (TEM). With increased addition of NaBr, a counterbalancing salt effect on the critical aggregation concentration (CAC) is observed. At low concentrations, NaBr facilitates the formation of micelle-like structures between surfactant and polyelectrolyte and results in a smaller CAC. At high concentrations, NaBr screens the electrostatic attraction between surfactant and polyelectrolyte and leads to a larger CAC. Upon the formation of micelle-like structures at high surfactant concentrations, the addition of NaBr is favorable for larger aggregates. The microstructure detected by TEM show that a global structure is generally formed in the presence of NaBr. The interactions also depend on ion species. Compared to NaBr, the addition of NaCl or KCl yields a smaller CAC. © 2006 Elsevier Inc. All rights reserved.||Source Title:||Journal of Colloid and Interface Science||URI:||http://scholarbank.nus.edu.sg/handle/10635/64541||ISSN:||00219797||DOI:||10.1016/j.jcis.2006.10.020|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.