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小分子表面活性剂在高动态气-水界面的组装。

Assembly of small molecule surfactants at highly dynamic air-water interfaces.

机构信息

Faculty of Engineering and Science, University of Greenwich, Medway Campus, Central Avenue, Chatham Maritime, Kent, ME4 4TB, UK.

出版信息

Soft Matter. 2017 Nov 29;13(46):8807-8815. doi: 10.1039/c7sm01914a.

Abstract

Small-angle neutron scattering has been used to probe the interfacial structure of foams stabilised by small molecule surfactants at concentrations well below their critical micelle concentration. The data for wet foams showed a pronounced Q dependence at low Q and noticeable inflexions over the mid Q range. These features were found to be dependent on the surfactant structure (mainly the alkyl chain length) with various inflexions across the measured Q range as a function of the chain length but independent of factors such as concentration and foam age/height. By contrast, foam stability (for C < CMC) was significantly different at this experimental range. Drained foams showed different yet equally characteristic features, including additional peaks attributed to the formation of classical micellar structures. Together, these features suggest the dynamic air-water interface is not as simple as often depicted, indeed the data have been successfully described by a model consisting paracrystalline stacks (multilayer) of adsorbed surfactant layers; a structure that we believe is induced by the dynamic nature of the air-water interface in a foam.

摘要

小角中子散射已被用于探测小分子表面活性剂稳定的泡沫的界面结构,其浓度远低于临界胶束浓度。湿泡沫的数据在低 Q 值时表现出明显的 Q 依赖性,在中 Q 值范围内有明显的拐点。这些特征与表面活性剂结构(主要是烷基链长度)有关,在测量的 Q 值范围内,各种拐点随链长而变化,但与浓度和泡沫龄期/高度等因素无关。相比之下,在这个实验范围内,泡沫稳定性(C < CMC)有显著差异。排水泡沫表现出不同但同样具有特征的特征,包括归因于形成经典胶束结构的附加峰。这些特征表明,动态气-水界面并不像通常描述的那样简单,实际上,这些数据已经被一个由吸附表面活性剂层的准晶堆(多层)组成的模型成功地描述了;我们相信这种结构是由泡沫中气-水界面的动态性质引起的。

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