Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

On Micelle Formation and Degree of Counterion Binding of α-Sulfonatomyristic Acid Ethyl Ester in Water : a Study Performed by Comparing with α-Sulfonatomyristic Acid Methyl Ester


Affiliations
1 Fukuoka University, Faculty of Science, Department of Chemistry, Jonan-ku, Fukuoka 814-0180, Japan
2 Dept. Chem., Fukuoka Univ., Jonan-ku, Fukuoka 814-0180, Japan
3 Lion Co., Surfactant Science Research Center, 7-13-12 Hirai, Edogawa-ku, Tokyo 123-0035, Japan
     

   Subscribe/Renew Journal


Sodium salts of α-sulfonatomyristic acid ethyl ester (α-SMy.Et) and methyl ester (α-SMy.Me) in aqueous medium were investigated in terms of critical micellization concentration (CMC) and degree of counterion binding to micelles (β) as functions of temperature and added salt concen­tration. For the determination of CMC, the differential conductance (derived from the specific con­ductance, κ as a function of the molarity, (C), ∂κ/∂C being plotted against √C) was applied to the systems with and without added NaCl. The β values were determined from the Corrin-Harkins plot By using the data of CMC and β as a function of temperature, the standard Gibbs energy change (ΔG0m, ) was evaluated on the basis of phase separation model, and from the van’t Hoff plot the standard enthalpy and entropy changes (ΔH0m, and ΔS0m) were evaluated. The enthalpy-entropy com­pensation relation, empirically expressed as ΔS0m = (1/300) ΔH0m + σ, was found to completely hold for both the surfactants and also for other surfactants. The degree of micellar dissociation (α) was examined in terms of the conductivity data and compared with the empirically estimated values (αEX) assuming αEX = 1-β.

Keywords

Critical Micelle Concentration (CMC), Degree of Counterion Binding, Differential Conductivity, α-Sulfonatomyristic Acid Ethyl and Methyl Esters.
Subscription Login to verify subscription
User
Notifications
Font Size


Abstract Views: 210

PDF Views: 0




  • On Micelle Formation and Degree of Counterion Binding of α-Sulfonatomyristic Acid Ethyl Ester in Water : a Study Performed by Comparing with α-Sulfonatomyristic Acid Methyl Ester

Abstract Views: 210  |  PDF Views: 0

Authors

A. A. Nakamura
Fukuoka University, Faculty of Science, Department of Chemistry, Jonan-ku, Fukuoka 814-0180, Japan
M. Hisatomi
Fukuoka University, Faculty of Science, Department of Chemistry, Jonan-ku, Fukuoka 814-0180, Japan
G. Sugihara
Dept. Chem., Fukuoka Univ., Jonan-ku, Fukuoka 814-0180, Japan
M. Fujiwara
Lion Co., Surfactant Science Research Center, 7-13-12 Hirai, Edogawa-ku, Tokyo 123-0035, Japan
T. Okano
Lion Co., Surfactant Science Research Center, 7-13-12 Hirai, Edogawa-ku, Tokyo 123-0035, Japan

Abstract


Sodium salts of α-sulfonatomyristic acid ethyl ester (α-SMy.Et) and methyl ester (α-SMy.Me) in aqueous medium were investigated in terms of critical micellization concentration (CMC) and degree of counterion binding to micelles (β) as functions of temperature and added salt concen­tration. For the determination of CMC, the differential conductance (derived from the specific con­ductance, κ as a function of the molarity, (C), ∂κ/∂C being plotted against √C) was applied to the systems with and without added NaCl. The β values were determined from the Corrin-Harkins plot By using the data of CMC and β as a function of temperature, the standard Gibbs energy change (ΔG0m, ) was evaluated on the basis of phase separation model, and from the van’t Hoff plot the standard enthalpy and entropy changes (ΔH0m, and ΔS0m) were evaluated. The enthalpy-entropy com­pensation relation, empirically expressed as ΔS0m = (1/300) ΔH0m + σ, was found to completely hold for both the surfactants and also for other surfactants. The degree of micellar dissociation (α) was examined in terms of the conductivity data and compared with the empirically estimated values (αEX) assuming αEX = 1-β.

Keywords


Critical Micelle Concentration (CMC), Degree of Counterion Binding, Differential Conductivity, α-Sulfonatomyristic Acid Ethyl and Methyl Esters.