Investigation of the Thermodynamic Properties of the Cationic Surfactant CTAC in EG + Water Binary Mixtures

被引:1
作者
Jie Yan
Dong Wang
Fang Bu
Fei Fei Yang
机构
[1] Dalian University of Technology,School of Environmental Science and Technology
[2] Liaoning Normal University,School of Chemistry and Chemical Engineering
来源
Journal of Solution Chemistry | 2010年 / 39卷
关键词
Thermodynamic properties; Critical micelle concentration; CTAC; EG;
D O I
暂无
中图分类号
学科分类号
摘要
To understand the thermodynamic characteristics of cationic surfactants in binary mixtures, the aggregation behavior of hexadecyltrimethylammonium chloride (CTAC) has been investigated in ethylene glycol (EG) + water solvent mixtures at different temperatures and EG to water ratios. The critical micelle concentration (CMC) and degree of counter ion bonding (β) were calculated from electrical conductivity measurements. An equilibrium model for micelle formation was applied to obtain the thermodynamic parameters for micellization, including the standard Gibbs energies of micellization (\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$\Delta G_{\mathrm{mic}}^{\mathrm{o}})$\end{document}, standard enthalpies of micelle formation (\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$\Delta H_{\mathrm{mic}}^{\mathrm{o}})$\end{document} and standard entropies of micellization (\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$\Delta S_{\mathrm{mic}}^{\mathrm{o}})$\end{document}. Our results show that \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$\Delta G_{\mathrm{mic}}^{\mathrm{o}}$\end{document} is always negative and slightly dependent on temperature. The process of micellization is entropy driven in pure water, whereas in EG + water mixtures the micellization is enthalpy driven.
引用
收藏
页码:1501 / 1508
页数:7
相关论文
共 39 条
  • [1] Abbott L.N.(1999)Surfactant Applications Curr. Opin Colloid Interface Sci. 4 322-324
  • [2] MacKay A.R.(2002)Thermal parameters associated to micellization of dodecylpyridinium bromide and chloride in aqueous solution J. Therm. Anal. Calorim. 70 229-234
  • [3] Galan J.J.(2007)Thermodynamics of micelle formation of alkyltrimethylammonium chlorides from high performance electric conductivity measurements J. Colloid Interface Sci. 313 288-295
  • [4] Gonzalez-Perez A.(2000)Aggregation of ionic surfactants in formamide J. Colloids Surf. A, Physicochem. Eng. Aspects 173 95-100
  • [5] Del Castillo J.L.(2005)Critical micelle concentrations and interaction parameters of aqueous binary surfactant: ionic surfactant mixtures J. Colloid Interface Sci. 288 238-246
  • [6] Rodriguez J.R.(1996)Solution behavior of surfactant in ethylene glycol: Probing the existence of a CMC and of micellar aggregates J. Colloid Interface Sci. 178 471-482
  • [7] Perger T.-M.(2009)Spectral characterization and colloidal properties of 1-hexadecylpyridinium chloride in aqueous binary mixtures of different glycols J. Colloid Interface Sci. 333 646-654
  • [8] Bester-Rogac M.(1998)Effect of hydrophobic chain length of surfactants on enthalpy-entropy compensation of micellization J. Phys. Chem. B 102 4350-4356
  • [9] Akhter M.S.(1999)Thermodynamics of micellization of tetradecyltrimethylammonium bromide in ethylene glycol-water binary mixture J. Colloid Polym. Sci. 277 701-707
  • [10] Alawi S.M.(1997)Micelle formation of dodecylammonium surfactant with mixed counterions: perfluorocarboxylate and alkanesulfonate ions J. Colloid Interface Sci. 187 435-442