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胶束生长的分析模型。5. 两性离子表面活性剂胶束的分子热力学。

Analytical modeling of micelle growth. 5. Molecular thermodynamics of micelles from zwitterionic surfactants.

机构信息

Department of Chemical & Pharmaceutical Engineering, Faculty of Chemistry & Pharmacy, Sofia University, 1164 Sofia, Bulgaria.

Department of Chemical & Pharmaceutical Engineering, Faculty of Chemistry & Pharmacy, Sofia University, 1164 Sofia, Bulgaria.

出版信息

J Colloid Interface Sci. 2022 Dec;627:469-482. doi: 10.1016/j.jcis.2022.07.087. Epub 2022 Jul 16.

Abstract

HYPOTHESIS

The critical micelle concentration, aggregation number, shape and length of spherocylindrical micelles in solutions of zwitterionic surfactants can be predicted by knowing the molecular parameters and surfactant concentrations. This can be achieved by upgrading the quantitative molecular thermodynamic model with expressions for the electrostatic interaction energy between the zwitterionic dipoles and micellar hydrophobic cores of spherical and cylindrical shapes.

THEORY

The correct prediction of the mean micellar aggregation numbers requires precise calculations of the free energy per molecule in the micelles. New analytical expressions for the dipole electrostatic interaction energy are derived based on the exact solutions of the electrostatic problem for a single charge close to a boundary of spherical and cylindrical dielectric media. The obtained general theory is valid for arbitrary ratios between dielectric constants, radii of spheres and cylinders, positions, and orientations of dipoles.

FINDINGS

The detailed numerical results show quantitatively the effects of the micelle curvature and dielectric properties of the continuum media on the decrease of the dipole electrostatic interaction energy. Excellent agreement was achieved between the theoretical predictions and experimental data for the critical micelle concentration, size and aggregation number of zwitterionic surfactant micelles. This study can be extended to mixed micelles of zwitterionic and ionic surfactants in the presence of salt to interpret and predict the synergistic effect on the rheology of solutions.

摘要

假设

通过了解分子参数和表面活性剂浓度,可以预测两性离子表面活性剂溶液中胶束的临界胶束浓度、聚集数、形状和长度。这可以通过升级定量分子热力学模型来实现,该模型包含了球形和圆柱形胶束疏水性核心与两性离子偶极子之间的静电相互作用能的表达式。

理论

正确预测平均胶束聚集数需要精确计算胶束中每个分子的自由能。基于单个电荷靠近球形和圆柱形介电介质边界的静电问题的精确解,推导出了新的偶极子静电相互作用能的解析表达式。所得到的普遍理论适用于介电常数、球体和圆柱体半径、位置和偶极子取向之间的任意比值。

发现

详细的数值结果定量地显示了胶束曲率和连续介质介电性能对偶极子静电相互作用能降低的影响。理论预测与两性离子表面活性剂胶束的临界胶束浓度、尺寸和聚集数的实验数据之间具有极好的一致性。这项研究可以扩展到存在盐的两性离子和离子表面活性剂的混合胶束中,以解释和预测对溶液流变性的协同效应。

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