Cetylpyridinium chloride plus tetradecyltrimethylammonium bromide mixed micelles in polyethylene glycol 1000+water mixtures

Authors
Citation
Ms. Bakshi, Cetylpyridinium chloride plus tetradecyltrimethylammonium bromide mixed micelles in polyethylene glycol 1000+water mixtures, J MACR S PU, A36(5-6), 1999, pp. 879-892
Citations number
31
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY
ISSN journal
10601325 → ACNP
Volume
A36
Issue
5-6
Year of publication
1999
Pages
879 - 892
Database
ISI
SICI code
1060-1325(1999)A36:5-6<879:CCPTBM>2.0.ZU;2-X
Abstract
The conductances of cetylpyridinium chloride (CPyCl) + tetradecyltrimethyla mmonium bromide (TTAB) mixtures over the entire mole fraction range of CPyC l (x(CPyCl)) were measured in aqueous binary mixtures of polyethylene glyco l 1000 (PEG 1000) containing 0.5, 1, 2, 5 and 10 wt% of PEG 1000 at 30 degr ees C. From the conductivity data, the critical micellar concentration (cmc ), degree of counter ion association (chi) and the standard free energy of micelle formation (Delta(GM)(o)) of CPyCl and TTAB were computed. The Delta G(M)(o) value is further divided into the hydrophobic contribution of free energy of transfer of the surfactant hydrocarbon chain from the medium to the micelle (Delta G(HP)(o)), and the energy associated with the surface co ntributions (Delta G(S)(o)) consisting of electrostatic interactions betwee n the head groups and counter ions. Both contributions show a linear depend ence on the amount of PEG additive. These results have been explained on th e basis of the medium effects of aqueous PEG. The mixed micelle formation by CPyCl+TTAB show non-ideal behavior which is quite similar in the absence, as well as in the presence, of PEG additive a s evaluated by using the regular solution theory. The interaction parameter , b, is always negative and remains almost constant with respect to the amo unt of PEG additive. This indicates that the mixed micelle formation occurs mainly due to the synergistic interactions between the unlike surfactant m onomers only.