胶束
肺表面活性物质
化学
十二烷基硫酸钠
聚合数
环氧乙烷
水溶液
小角中子散射
胶体
混合(物理)
中子散射
临界胶束浓度
化学工程
结晶学
色谱法
有机化学
散射
共聚物
工程类
物理
光学
量子力学
聚合物
生物化学
作者
Michael Ludwig,Ramsia Geisler,Sylvain Prévost,Regine von Klitzing
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2021-07-07
卷期号:26 (14): 4136-4136
被引量:23
标识
DOI:10.3390/molecules26144136
摘要
Aqueous solutions of a nonionic surfactant (either Tween20 or BrijL23) and an anionic surfactant (sodium dodecyl sulfate, SDS) are investigated, using small-angle neutron scattering (SANS). SANS spectra are analysed by using a core-shell model to describe the form factor of self-assembled surfactant micelles; the intermicellar interactions are modelled by using a hard-sphere Percus–Yevick (HS-PY) or a rescaled mean spherical approximation (RMSA) structure factor. Choosing these specific nonionic surfactants allows for comparison of the effect of branched (Tween20) and linear (BrijL23) surfactant headgroups, both constituted of poly-ethylene oxide (PEO) groups. The nonionic–anionic surfactant mixtures are studied at various concentrations up to highly concentrated samples (ϕ ≲ 0.45) and various mixing ratios, from pure nonionic to pure anionic surfactant solutions. The scattering data reveal the formation of mixed micelles already at concentrations below the critical micelle concentration of SDS. At higher volume fractions, excluded volume effects dominate the intermicellar structuring, even for charged micelles. In consequence, at high volume fractions, the intermicellar structuring is the same for charged and uncharged micelles. At all mixing ratios, almost spherical mixed micelles form. This offers the opportunity to create a system of colloidal particles with a variable surface charge. This excludes only roughly equimolar mixing ratios (X≈ 0.4–0.6) at which the micelles significantly increase in size and ellipticity due to specific sulfate–EO interactions.
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