Dynamic light scattering on semidilute aqueous systems of ethyl (hydroxyethyl) cellulose. Effects of temperature, surfactant concentration, and salinity

Citation
Al. Kjoniksen et al., Dynamic light scattering on semidilute aqueous systems of ethyl (hydroxyethyl) cellulose. Effects of temperature, surfactant concentration, and salinity, COLL SURF A, 149(1-3), 1999, pp. 347-354
Citations number
35
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
ISSN journal
09277757 → ACNP
Volume
149
Issue
1-3
Year of publication
1999
Pages
347 - 354
Database
ISI
SICI code
0927-7757(19990415)149:1-3<347:DLSOSA>2.0.ZU;2-M
Abstract
The effects of temperature, surfactant, and salt on the phenomena of associ ation and thermoreversible gelation of a semidilute aqueous solution of eth yl (hydroxyethyl) cellulose (EHEC) are studied by using dynamic light scatt ering. The autocorrelation functions revealed the existence of two relaxati on modes: a single exponential at short times, followed by a stretched expo nential at longer times. The fast relaxation mode is always diffusive and y ields a collective diffusion coefficient D-c, which is temperature dependen t and increases with increasing surfactant addition. The slow relaxation ti me is associated with disengagement of chains or clusters, and this quantit y increases during gelation and enhanced association. This parameter, which exhibits similar features as the dynamic viscosity, can be used to charact erise the degree of intermolecular association of EHEC systems. The general picture that emerges from this study is that gels are formed in the presen ce of low concentrations of sodium dodecyl sulphate at elevated temperature s. At high surfactant concentrations the network structure is disrupted, an d the slow relaxation time decreases. At moderate levels of surfactant addi tion, addition of salt is found to strengthen the intermolecular associatio ns. (C) 1999 Elsevier Science B.V. All rights reserved.