表面张力
吸附
吉布斯等温线
肺表面活性物质
扩散
化学
离子键合
热力学
最大气泡压力法
化学工程
物理化学
材料科学
化学物理
离子
有机化学
物理
工程类
生物化学
作者
Julian Eastoe,James S. Dalton
标识
DOI:10.1016/s0001-8686(99)00017-2
摘要
Recent advances in understanding dynamic surface tensions (DSTs) of surfactant solutions are discussed. For pre-CMC solutions of non-ionic surfactants, theoretical models and experimental evidence for a mixed diffusion-kinetic adsorption mechanism are covered. For micellar solutions of non-ionics, up to approximately 100 x CMC, the DST behaviour can also be accounted for using a mixed mechanism model. Finally, the first reported measurements of the dynamic surface excess Gamma(t), using the overflowing cylinder in conjunction with neutron reflection, are described.
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