On the cohesion of fluids and their adhesion to solids: Young's equation at the atomic scale

被引:58
作者
Fernandez-Toledano, J. -C. [1 ]
Blake, T. D. [1 ]
Lambert, P. [2 ]
De Coninck, J. [1 ]
机构
[1] Univ Mons, Lab Surface & Interfacial Phys LPSI, B-7000 Mons, Belgium
[2] Univ Libre Bruxelles, BEAMS CP165-56,Av FD Roosevelt 50, B-1050 Brussels, Belgium
关键词
Wetting; Adhesion; Three-phase contact zone; Liquid-solid interface; Molecular-dynamics; MOLECULAR-DYNAMICS; CONTACT-ANGLE; COMPUTER-SIMULATION; INTERFACE; DERIVATION; NANOSCALE; SURFACES; TENSION; LIQUIDS; WALL;
D O I
10.1016/j.cis.2017.03.006
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
Using large-scale molecular dynamics simulations, we model a 9.2 nm liquid bridge between two solid plates having a regular hexagonal lattice and analyse the forces acting at the various interfaces for a range of liquid-solid interactions. Our objective is to study the mechanical equilibrium of the system, especially that at the three-phase contact line. We confirm previous MD studies that have shown that the internal pressure inside the liquid is given precisely by the Laplace contribution and that the solid exerts a global force at the contact line in agreement with Young's equation, validating it down to the nanometre scale, which we quantify. In addition, we confirm that the force exerted by the liquid on the solid has the expected normal component equal to gamma(lv)sin theta degrees, where gamma(lv) is the surface tension of the liquid and theta degrees is the equilibrium contact angle measured on the scale of the meniscus. Recent thermodynamic arguments predict that the tangential force exerted by the liquid on the solid should be equal to the work of adhesion expressed as Wa degrees=gamma(lv)(1+ cos theta degrees). However, we find that this is true only when any layering of the liquid molecules close to liquid-solid interface is negligible. The force significantly exceeds this value when strong layering is present. (C) 2017 Elsevier B. V. All rights reserved.
引用
收藏
页码:102 / 107
页数:6
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