Departamento de Química Física , Universidad Complutense de Madrid, Ciudad Universitaria s/n , 28040 Madrid , Spain.
Instituto Pluridisciplinar, Universidad Complutense de Madrid , Paseo Juan XXIII, 1 , 28040 Madrid , Spain.
Langmuir. 2018 Jun 26;34(25):7455-7464. doi: 10.1021/acs.langmuir.8b01343. Epub 2018 Jun 13.
The adsorption of concentrated poly(diallyldimethylammonium chloride) (PDADMAC)-sodium lauryl ether sulfate (SLES) mixtures at the water/vapor interface has been studied by different surface tension techniques and dilational viscoelasticity measurements. This work tries to shed light on the way in which the formation of polyelectrolyte-surfactant complexes in the bulk affects the interfacial properties of mixtures formed by a polycation and an oppositely charged surfactant. The results are discussed in terms of a two-step adsorption-equilibration of PDADMAC-SLES complexes at the interface, with the initial stages involving the diffusion of kinetically trapped aggregates formed in the bulk to the interface followed by the dissociation and spreading of such aggregates at the interface. This latter process becomes the main contribution to the surface tension decrease. This work aids our understanding of the most fundamental basis of the physicochemical behavior of concentrated polyelectrolyte-surfactant mixtures which present complex bulk and interfacial interactions with interest in both basic and applied sciences.
已通过不同的表面张力技术和扩张粘弹性测量研究了在水/蒸汽界面处浓缩聚二烯丙基二甲基氯化铵(PDADMAC)-十二烷基醚硫酸钠(SLES)混合物的吸附。这项工作试图阐明在本体中形成聚电解质-表面活性剂配合物的方式如何影响由阳离子聚合物和带相反电荷的表面活性剂形成的混合物的界面性质。根据 PDADMAC-SLES 配合物在界面上的两步吸附平衡,讨论了结果,初始阶段涉及在本体中形成的动力学捕获的聚集体扩散到界面,然后在界面上解离和展开这些聚集体。后一过程成为表面张力降低的主要贡献。这项工作有助于我们理解具有复杂本体和界面相互作用的浓缩聚电解质-表面活性剂混合物的物理化学行为的最基本基础,这些相互作用在基础科学和应用科学中都具有重要意义。