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表面活性剂胶束形成的机制。

Mechanism of surfactant micelle formation.

作者信息

Cui Xiaohong, Mao Shizhen, Liu Maili, Yuan Hanzhen, Du Youru

机构信息

State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences, Wuhan 430071, P. R. China.

出版信息

Langmuir. 2008 Oct 7;24(19):10771-5. doi: 10.1021/la801705y. Epub 2008 Aug 26.

Abstract

The mechanism of micelle formation of surfactants sodium dodecyl sulfate (SDS), n-hexyldecyltrimethylammonium bromide (CTAB) and Triton X-100 (TX-100) in heavy water solutions was studied by 1H NMR (chemical shift and line shape) and NMR self-diffusion experiments. 1H NMR and self-diffusion experiments of these three surfactants show that their chemical shifts (delta) begin to change and resonance peaks begins to broaden with the increase in concentration significantly below their critical micelle concentrations (cmc's). At the same time, self-diffusion coefficients ( D) of the surfactant molecules decrease simultaneously as their concentrations increase. These indicate that when the concentrations are near and lower than their cmc's, there are oligomers (premicelles) formed in these three surfactant systems. Carefully examining the dependence of chemical shift and self-diffusion coefficient on concentration in the region just slightly above their cmc's, one finds that the pseudophase transition model is not applicable to the variation of physical properties (chemical shift and self-diffusion coefficient) with concentration of these systems. This indicates that premicelles still exist in this concentration region along with the formation of micelles. The curved dependence of chemical shift and self-diffusion coefficient on the increase in concentration suggests that the premicelles grow as the concentration increases until a definite value when the size of the premicelle reaches that of the micelle, i.e., the system is likely dominated by the monomers and micelles. Additionally, the approximate values of premicelle coming forth concentration (pmc) and cmc were obtained by again fitting chemical shifts to reciprocals of concentrations at a different perspective, and are in good accordant with experimental results and literature values and prove the former conclusion.

摘要

通过¹H NMR(化学位移和线形)以及NMR自扩散实验,研究了表面活性剂十二烷基硫酸钠(SDS)、正十六烷基三甲基溴化铵(CTAB)和 Triton X - 100(TX - 100)在重水溶液中形成胶束的机制。这三种表面活性剂的¹H NMR和自扩散实验表明,在其临界胶束浓度(cmc)以下,随着浓度的增加,它们的化学位移(δ)开始变化,共振峰开始变宽。同时,表面活性剂分子的自扩散系数(D)随着浓度的增加而同时降低。这些表明,当浓度接近并低于其cmc时,这三种表面活性剂体系中形成了低聚物(前胶束)。仔细研究化学位移和自扩散系数在略高于其cmc区域对浓度的依赖性,发现伪相转变模型不适用于这些体系物理性质(化学位移和自扩散系数)随浓度的变化。这表明在该浓度区域,前胶束与胶束的形成同时存在。化学位移和自扩散系数对浓度增加的曲线依赖性表明,前胶束随着浓度的增加而生长,直到前胶束的大小达到胶束的大小时达到一个确定值,即该体系可能由单体和胶束主导。此外,通过从不同角度再次将化学位移拟合到浓度的倒数,获得了前胶束出现浓度(pmc)和cmc的近似值,这些值与实验结果和文献值吻合良好,证明了先前的结论。

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