首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >The impact of multivalent counterions, Al~(3+), on the surface adsorption and self-assembly of the anionic surfactant alkyloxyethylene sulfate and anioniconionic surfactant mixtures
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The impact of multivalent counterions, Al~(3+), on the surface adsorption and self-assembly of the anionic surfactant alkyloxyethylene sulfate and anioniconionic surfactant mixtures

机译:多价抗衡离子Al〜(3+)对阴离子表面活性剂烷氧基亚硫酸乙烯酯和阴离子/非离子表面活性剂混合物的表面吸附和自组装的影响

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The impact of multivalent counterions, Al~(3+), on the surface adsorption and self-assembly of the anionic surfactant sodium dodecyl dioxyethylene sulfate, SLES, and the anioniconionic surfactant mixtures of SLES and monododecyl dodecaethylene glycol, C_(12)E_(12), has been investigated using neutron reflectivity, NR, and small angle neutron scattering, SANS. The addition of relatively low concentrations of Al ~(3+) counterions induces a transition from a monolayer to welldefined surface bilayer, trilayer, and multilayer structures in the adsorption of SLES at the air-water interface. The addition of the nonionic cosurfactant, C _(12)E_(12), partially inhibits the evolution in the surface structure from monolayer to multilayer interfacial structures. This surface phase behavior is strongly dependent upon the surfactant concentration, solution composition, and concentration of Al~(3+) counterions. In solution, the addition of relatively low concentrations of Al~(3+) ions promotes significant micellar growth in SLES and SLES/C_(12)E_(12) mixtures. At the higher counterion concentrations, there is a transition to lamellar structures and ultimately precipitation. The presence of the C _(12)E_(12) nonionic cosurfactant partially suppresses the aggregate growth. The surface and solution behaviors can be explained in terms of the strong binding of the Al~(3+) ions to the SLES headgroup to form surfactant-ion complexes (trimers). These results provide direct evidence of the role of the nonionic cosurfactant in manipulating both the surface and solution behavior. The larger EO_(12) headgroup of the C_(12)E _(12) provides a steric hindrance which disrupts and ultimately prevents the formation of the surfactant-ion complexes. The results provide an important insight into how multivalent counterions can be used to manipulate both solution self-assembly and surface properties.
机译:多价抗衡离子Al〜(3+)对阴离子表面活性剂十二烷基二氧乙烯磺酸钠SLES以及SLES和十二烷基十二烷基乙二醇的阴离子/非离子表面活性剂混合物C_(12)的表面吸附和自组装的影响E_(12)已使用中子反射率NR和小角中子散射SANS进行了研究。相对较低浓度的Al〜(3+)抗衡离子的加入会导致SLES在空气-水界面上的吸附从单层过渡到轮廓分明的表面双层,三层和多层结构。加入非离子表面活性剂C _(12)E_(12)会部分抑制表面结构从单层到多层界面结构的演变。这种表面相行为在很大程度上取决于表面活性剂的浓度,溶液的组成以及Al〜(3+)抗衡离子的浓度。在溶液中,添加相对较低浓度的Al〜(3+)离子可促进SLES和SLES / C_(12)E_(12)混合物中明显的胶束生长。在较高的抗衡离子浓度下,过渡到层状结构并最终沉淀。 C _(12)E_(12)非离子型辅助表面活性剂的存在会部分抑制聚集体的生长。表面和溶液的行为可以用Al〜(3+)离子与SLES头基形成表面活性剂-离子配合物(三聚体)的牢固结合来解释。这些结果提供了非离子表面活性剂在操纵表面和溶液行为中的作用的直接证据。 C_(12)E_(12)的较大的EO_(12)头基提供空间位阻,该空间位阻会破坏并最终阻止表面活性剂离子络合物的形成。结果提供了关于如何使用多价抗衡离子来操纵溶液自组装和表面性质的重要见解。

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