Calorimetric determination of the thermodynamics of alcohol-surfactant mixed micelle formation: Temperature and concentration effects

被引:6
|
作者
MacDonald, Stephanie [1 ]
MacLennan, Shannon [1 ]
Marangoni, D. Gerrard [1 ]
机构
[1] St FX Univ, Dept Chem, Antigonish, NS B2G 2W5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Enthalpy of micellization; Entropy of micellization; Calorimetry; Mixed micelles; Hydrophobic effects; Thermodynamic compensation; ENTHALPY-ENTROPY COMPENSATION; SODIUM DODECYL-SULFATE; COUNTERION BINDING; CHAIN-LENGTH; THERMOMETRIC TITRATION; POLY(ETHYLENE OXIDE); ETHOXYLATED ALCOHOLS; AGGREGATION BEHAVIOR; ANIONIC SURFACTANT; TRIBLOCK POLYMER;
D O I
10.1016/j.molliq.2020.112531
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The thermodynamic parameters of surfactant/alcohol mixed micelles were determined in mixtures of sodium dodecyl sulfate (SDS) and dodecyltrimethylammonium bromide (DTAB) in a series of solvents composed of varying concentrations of n-propanol (C3OH), n-butanol (C4OH), and n-pentanol (C5OH). Conductivity studies were used to determine CMC values and the degrees of counterion binding. Isoperibol solution calorimetry was used to directly determine CMC values and enthalpy of micellization (Delta H-mic). From these experimentally determined values, the Gibbs energy and entropy of micellization were calculated as a function of temperature and alcohol concentration. In general, CMC values decreased with increasing alcohol carbon chain length and concentration but increased with temperature. The effects of temperature, alcohol carbon chain length, and alcohol concentration on the energetics of these mixed micellar systems are explained in terms of the relative contributions to Delta H-mic by alkyl chain interactions, hydrophobic effects, and electrostatic contributions. (C) 2020 Elsevier B.V. All rights reserved.
引用
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页数:12
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