23Na relaxation in SDS and SDES–polymer systems

• Published in: Colloids and surfaces. A, Physicochemical and engineering aspects Physicochemical and engineering aspects, 2004-09, Vol.245 (1-3), p.127-132
• Main Authors: Asaro, Fioretta, Feruglio, Luigi, Pellizer, Giorgio
• Format: Article
• Language: English
• Subjects: 13C NMR; 23Na NMR relaxation; Polymer–surfactant association; Sodium decylsulfate; Sodium dodecylsulfate
• ISSN: 0927-7757; 1873-4359
• DOI: 10.1016/j.colsurfa.2004.03.032

23Na NMR longitudinal relaxation rates (R1 = 1/T1) measurements were carried out, at a magnetic field of 9.4T, on surfactant and surfactant–polymer solutions (surfactant: sodium dodecylsulfate (SDS), sodium decylsulfate (SDES); polymer: poly(ethylene oxide) (PEO) MW 20,000, poly(vinyl pyrrolidone) (PVP) MW 24,000). The sharp increase of R1 on aggregation allows to determine the CMCs in pure surfactant solutions and the critical aggregation concentrations (CACs) in the presence of polymer. Sodium relaxes at the same rate in the vicinity both of pure surfactant micelles and of the mixed aggregates. The observed R1 are different because of the different ionization degrees. A peculiar feature of the SDS–PEO system is the strong increase of sodium relaxation rate at concentrations higher than 8mmolkg−1. This is not due to the saturation of the polymer, but rather indicates an abrupt change in the aggregates. The 23Na relaxation has been complemented by 13C NMR spectra, in particular for the SDS–PEO system. They support the view that, in the range between the CAC and the polymer saturation, modifications of the mixed polymer–surfactant aggregates occur.