聚合物
吸附
化学物理
胶体
气泡
材料科学
曲面(拓扑)
化学工程
表面力仪
疏水效应
化学
纳米技术
复合材料
物理化学
有机化学
工程类
计算机科学
并行计算
数学
几何学
作者
Kyuichi Yasui,Toru Tuziuti,Wataru Kanematsu
出处
期刊:Langmuir
[American Chemical Society]
日期:2021-01-26
卷期号:37 (5): 1674-1681
被引量:13
标识
DOI:10.1021/acs.langmuir.0c02844
摘要
The experimental results [Kanematsu, W. Chem. Eng. Sci. 2020, 219, 115594] on the temporal variations of number concentrations of bulk nanobubbles (ultrafine bubbles) in contact with polymer materials are theoretically analyzed based on the dynamic equilibrium model of bulk nanobubbles partly covered with hydrophobic materials (impurities). It is suggested that bulk nanobubbles are adsorbed on a polymer surface by attractive hydrophobic interaction between a polymer surface and a hydrophobic material partly covering the bubble surface, overcoming the repulsive double-layer interaction. There are two mysteries. One is that the maximum surface number concentration of bulk nanobubbles of about 70 nm in diameter adsorbed on a hydrophobic polymer surface is more than an order of magnitude lower than the typical value for colloid particles of a similar or larger size. The other is that the experimental adsorption rate of bulk nanobubbles on hydrophobic polymer surface is several orders of magnitude lower than the theoretically estimated one. The mysteries are resolved if many of the bulk nanobubbles adsorbed on a hydrophobic polymer surface change to surface nanobubbles with a footprint diameter of about 1 μm.
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