TY - JOUR
T1 - A possible way to extract the dynamic contact angle at the molecular scale from that measured experimentally
AU - Blake, T. D.
AU - Fernández-Toledano, J. C.
AU - De Coninck, J.
N1 - Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2023/1
Y1 - 2023/1
N2 - Hypothesis: The maximum velocity of dewetting encodes sufficient information on the hydrodynamics of the wetting process to enable the local dynamic contact angle at the molecular scale, θ, to be determined from the apparent contact angle measured experimentally at much larger scales, θapp. Methods: Effective models of wetting dynamics need to account for differing channels of dissipation. One such model was recently verified by large-scale molecular dynamics (MD). It combines the 2-parameter molecular-kinetic theory of dynamic wetting (MKT), which attributes the velocity-dependence of θ to dissipation at the contact line, with the Cox-Voinov hydrodynamic (HD) model. The latter attributes the difference between θ and θapp to viscous bending of the interface and contains an additional, non-predictable, logarithmic parameter. Crucially, the MD simulations indicated that viscous bending may play a minor role during wetting, but dominates dewetting. This observation suggested that by applying the MKT to the advancing contact angle only and combining the results with the maximum velocity of dewetting, it might be possible to extract the value of the logarithmic parameter and so determine θ and, hence, the relative significance of the two channels of dissipation. A simple iterative procedure has been developed to achieve this. Findings: Data available to test the procedure are sparce, but comparisons with the MD results and those from three experimental studies are encouraging. Near perfect agreement is achieved with the simulations, where both θ and θapp are known, and plausible results are obtained for the experimental systems. Moreover, the procedure appears to be more effective than simply fitting θapp to the 3-parameter model.
AB - Hypothesis: The maximum velocity of dewetting encodes sufficient information on the hydrodynamics of the wetting process to enable the local dynamic contact angle at the molecular scale, θ, to be determined from the apparent contact angle measured experimentally at much larger scales, θapp. Methods: Effective models of wetting dynamics need to account for differing channels of dissipation. One such model was recently verified by large-scale molecular dynamics (MD). It combines the 2-parameter molecular-kinetic theory of dynamic wetting (MKT), which attributes the velocity-dependence of θ to dissipation at the contact line, with the Cox-Voinov hydrodynamic (HD) model. The latter attributes the difference between θ and θapp to viscous bending of the interface and contains an additional, non-predictable, logarithmic parameter. Crucially, the MD simulations indicated that viscous bending may play a minor role during wetting, but dominates dewetting. This observation suggested that by applying the MKT to the advancing contact angle only and combining the results with the maximum velocity of dewetting, it might be possible to extract the value of the logarithmic parameter and so determine θ and, hence, the relative significance of the two channels of dissipation. A simple iterative procedure has been developed to achieve this. Findings: Data available to test the procedure are sparce, but comparisons with the MD results and those from three experimental studies are encouraging. Near perfect agreement is achieved with the simulations, where both θ and θapp are known, and plausible results are obtained for the experimental systems. Moreover, the procedure appears to be more effective than simply fitting θapp to the 3-parameter model.
KW - Apparent contact angle
KW - Combined theory of dynamic wetting
KW - Cox-Voinov equation
KW - Local, microscopic contact angle
KW - Maximum velocity of dewetting
KW - Molecular-kinetic theory of dynamic wetting (MKT)
UR - http://www.scopus.com/inward/record.url?scp=85137347779&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2022.08.170
DO - 10.1016/j.jcis.2022.08.170
M3 - Article
C2 - 36088708
AN - SCOPUS:85137347779
SN - 0021-9797
VL - 629
SP - 660
EP - 669
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -