Penfold J, Tucker I, Thomas R K, Zhang J
ISIS, Rutherford Appleton Laboratory, CCLRC, Chilton, Didcot, OXON OX11 0QX, United Kingdom.
Langmuir. 2005 Oct 25;21(22):10061-73. doi: 10.1021/la0505014.
Neutron reflectivity and surface tension have been used to characterize the adsorption of the polyelectrolyte/ionic surfactant mixture of poly(ethyleneimine) (PEI) and sodium dodecyl sulfate (SDS) at the air-water interface. The surface tension behavior and adsorption patterns show a strong dependence upon the solution pH. However, the SDS adsorption at the interface is unexpectedly most pronounced when the pH is high (when the polymer is essentially a neutral polymer) and when the polymer architecture is branched rather than linear. For both the branched and the linear PEI polymer/surfactant complex formation results in a significant enhancement of the amount of SDS at the interface, down to surfactant concentrations approximately 10(-6) M. For the branched PEI a transition from a monolayer to a multilayer adsorption is observed, which depends on surfactant concentration and pH. In contrast, for the linear polymer, only monolayer adsorption is observed. This substantial increase in the surface activity of SDS by complexation with PEI results in spontaneous emulsification of hexadecane in water and the efficient wetting of hydrophobic substrates such as Teflon. In regions close to charge neutralization the multilayer adsorption is accentuated, and more extensively ordered structures, giving rise to Bragg peaks in the reflectivity data, are evident.
中子反射率和表面张力已被用于表征聚(乙烯亚胺)(PEI)和十二烷基硫酸钠(SDS)的聚电解质/离子表面活性剂混合物在空气-水界面的吸附情况。表面张力行为和吸附模式显示出对溶液pH值的强烈依赖性。然而,当pH值较高时(此时聚合物基本上是中性聚合物)以及聚合物结构为支链而非线性时,SDS在界面处的吸附出乎意料地最为明显。对于支链和线性PEI聚合物,聚合物/表面活性剂复合物的形成都会导致界面处SDS量的显著增加,直至表面活性剂浓度约为10^(-6) M。对于支链PEI,观察到从单层吸附到多层吸附的转变,这取决于表面活性剂浓度和pH值。相比之下,对于线性聚合物,仅观察到单层吸附。SDS与PEI络合导致其表面活性大幅增加,从而使十六烷在水中自发乳化,并有效润湿诸如聚四氟乙烯等疏水基材。在接近电荷中和的区域,多层吸附加剧,并且在反射率数据中出现更广泛有序的结构,从而产生布拉格峰。