Molecular Investigation of Contact Line Movement in Electrowetted Nanodroplets

Langmuir ◽  
2020 ◽  
Vol 36 (42) ◽  
pp. 12580-12589
Author(s):  
Dipayan Chakraborty ◽  
Shakul Pathak ◽  
Monojit Chakraborty
2019 ◽  
Vol 553 ◽  
pp. 557-566 ◽  
Author(s):  
G.V. Kuznetsov ◽  
D.V. Feoktistov ◽  
E.G. Orlova ◽  
I.Y. Zykov ◽  
A.G. Islamova

2016 ◽  
Vol 91 ◽  
pp. 01026
Author(s):  
Dmitry V. Feoktistov ◽  
Evgeniya G. Orlova ◽  
Anastasia G. Islamova

Author(s):  
Payam Delgoshaei ◽  
Jungho Kim

Measurements of space and time resolved heat transfer during lateral bubble merger during subcooled pool boiling of pentane in earth gravity environments were obtained using a microscale heater array. Data from individual heater elements in the array were synchronized with bottom and side view images from two high-speed cameras. The heat transfer due to the lateral merger was found to be closely related to the contact line movement on the heater.


Polymers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 2081
Author(s):  
Wenxiu Zheng ◽  
Chengzhen Sun ◽  
Boyao Wen ◽  
Bofeng Bai ◽  
Eric Lichtfouse

The movement of the contact line in liquid-liquid-solid systems is a major phenomenon in natural and industrial processes. In particular, n-alkanes are widely occurring in the oil, soil pollution, and chemical industries, yet there is little knowledge on the effects of molecular chain length on the contact line movement. Here, we studied the effects of molecular chain length on the contact line movement in water/n-alkane/solid systems with different surface wettabilities. We used n-heptane (C7), n-decane (C10), and n-hexadecane (C16) as alkanes and α-quartz as the solid surface. We calculated the time-variation contact line moving velocity and also analyzed the jump frequency and the mean distance of the molecular displacement occurring within the contact line zone by molecular-kinetic theory. Molecular dynamics simulation results show that the contact line velocity decreases with increasing the chain length, originally caused by the decreasing the jump frequency and mean distance. These variations with the molecular chain length are related to the more torsions and deformations of the molecules with a longer chain length. In addition, the moving mechanism of the contact line on the same solid surface does not change at different molecular chain lengths, implying that the moving mechanism mainly depends on the three-phase wettability.


2018 ◽  
Vol 844 ◽  
pp. 1026-1037 ◽  
Author(s):  
Jian Qin ◽  
Peng Gao

When a contact line moves with a sufficiently large speed, liquid or gas films can be entrained on a solid depending on the direction of contact-line movement. In this work, the contact-line dynamics in the situation of a generic two-fluid system is investigated. We demonstrate that the hydrodynamics of a contact line, no matter whether advancing or receding, can formally reduce to that of a receding one with small interfacial slopes. Since the latter can be well treated under the classical lubrication approximation, this analogy allows us to derive an asymptotic solution of the interfacial profiles for arbitrary values of contact angle and viscosity ratio. For the dip-coating geometry, we obtain, with no adjustable parameters, an analytical formula for the critical speed of wetting transition, which in particular predicts the onset of both liquid and gas entrainment. Moreover, the present analysis also builds a novel connection between the Cox–Voinov law and classical lubrication theory for moving contact lines.


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