Sato Yukiko, Nakahara Hiromichi, Moroi Yoshikiyo, Shibata Osamu
Division of Biointerfacial Science, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Fukuoka 812-8582, Japan.
Langmuir. 2007 Jul 3;23(14):7505-9. doi: 10.1021/la700612x. Epub 2007 Jun 5.
Solubilization of benzene, toluene, ethylbenzene, n-propylbenzene, n-butylbenzene, and n-pentylbenzene into the micelles of octaethylene glycol monotetradecyl ether (C(14)E(8)) was studied, where equilibrium concentrations of all the solubilizates were determined spectrophotometrically at 298.2, 303.2, and 308.2 K. The concentration of the above solubilizates except benzene remained constant below the critical micelle concentration (cmc) and increased linearly with an increase in C(14)E(8) concentration above the cmc, whereas benzene concentration was found to remain constant over the whole concentration range of C(14)E(8). The Gibbs energy change (DeltaG(0)) for their solubilization was evaluated by the partitioning of the solubilizates between the aqueous phase and the micellar phase because of the large aggregation number of the C(14)E(8) micelle. Furthermore, enthalpy and entropy changes for their solubilization were evaluated from the temperature dependence of the DeltaG(0) values. From these thermodynamical parameters and the change in absorption spectra of the solubilizates due to their incorporation into the micelles, the solubilization site was found to move into the inner core of the micelle with increasing alkyl chain length of the solubilizates.
研究了苯、甲苯、乙苯、正丙苯、正丁苯和正戊苯在八甘醇单十四烷基醚(C(14)E(8))胶束中的增溶情况,在298.2、303.2和308.2 K下通过分光光度法测定了所有增溶物的平衡浓度。除苯外,上述增溶物的浓度在临界胶束浓度(cmc)以下保持恒定,在cmc以上随C(14)E(8)浓度的增加呈线性增加,而苯的浓度在C(14)E(8)的整个浓度范围内保持恒定。由于C(14)E(8)胶束的聚集数较大,通过增溶物在水相和胶束相之间的分配来评估其增溶的吉布斯自由能变化(ΔG(0))。此外,根据ΔG(0)值对温度的依赖性评估了其增溶的焓变和熵变。根据这些热力学参数以及增溶物因掺入胶束而导致的吸收光谱变化,发现增溶位点随着增溶物烷基链长度的增加而移入胶束的内核。