Clathrate Adhesion Induced by Quasi-Liquid Layer

被引:22
|
作者
Nguyen, Ngoc N. [1 ,2 ]
Berger, Ruediger [1 ]
Kappl, Michael [1 ]
Butt, Hans-Juergen [1 ]
机构
[1] Max Planck Inst Polymer Res, Phys Interfaces, D-55128 Mainz, Germany
[2] Hanoi Univ Sci & Technol, Sch Chem Engn, Hanoi 100000, Vietnam
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2021年 / 125卷 / 38期
基金
欧洲研究理事会;
关键词
CYCLOPENTANE HYDRATE; SURFACE; FORCE; PARTICLES; DYNAMICS; STORAGE; SIZE;
D O I
10.1021/acs.jpcc.1c06997
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The adhesive force of clathrates to surfaces is a centuryold problem of pipeline blockage for the energy industry. Here, we provide new physical insight into the origin of this force by accounting for the existence of a quasi-liquid layer (QLL) on clathrate surfaces. To gain this insight, we measure the adhesive force between a tetrahydrofuran clathrate and a solid sphere. We detect a strong adhesion, which originates from a capillary bridge that is formed from a nanometer-thick QLL on the clathrate surface. The curvature of this capillary bridge is nanoscaled, causes a large negative Laplace pressure, and leads to a strong capillary attraction. The microscopic capillary bridge expands and consolidates over time. This dynamic behavior explains the time-dependent increase of measured capillary forces. The adhesive force decreases greatly upon increasing the roughness and the hydrophobicity of the sphere, which founds the fundamental basics for reducing clathrate adhesion by using surface coating.
引用
收藏
页码:21293 / 21300
页数:8
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