Effects of Surface Topography and Colloid Particles on the Evaporation Kinetics of Sessile Droplets on Superhydrophobic Surfaces

2012 ◽  
Vol 134 (5) ◽  
Author(s):  
Wei Xu ◽  
Chang-Hwan Choi

In this paper, the evaporation kinetics of microliter-sized sessile droplets of gold colloids (∼250 nm in particle diameters) was experimentally studied on micropatterned superhydrophobic surfaces, compared with those of pure water on a planar hydrophobic surface. The structural microtopography of superhydrophobic surfaces was designed to have a constant air fraction (∼0.8) but varying array patterns including pillars, lines, and wells. During evaporation in a room condition, the superhydrophobic surfaces exhibited a stronger pinning effect than a planar surface, especially in the initial evaporation stage, with significant variations by the surface topographies. Compared to a pure water droplet, colloids exhibited further promoted pinning effects, mainly in the later stage of evaporation. While the well-known evaporative mass transport law of sessile droplets (i.e., linear law of “V2/3∝t”) was generally applicable to the superhydrophobic surfaces, much smaller evaporation rate constants were measured on the patterned superhydrophobic surfaces than on a planar hydrophobic surface. A colloidal droplet further showed lower evaporation rate constants than a pure water droplet as the concentration of particles in the droplets increased over the evaporation. Such transition was more dramatic on a planar surface than on the micropatterned surfaces. Whereas there was no clear correlation between evaporation mode and the evaporation rate observed on the superhydrophobic surfaces, the prominent decrease of the evaporation rate on the planar hydrophobic surface was accompanied with the onset of a second pinning mode.

Author(s):  
Wei Xu ◽  
Chang-Hwan Choi

In this paper, we experimentally studied the evaporation kinetics of sessile droplets of nanofluids with systematically varying particle sizes on superhydrophobic surfaces of well-defined micro-post structures. The superhydrophobic surface patterns were fabricated on a silicon wafer by photolithography and deep reactive ion etching (DRIE) at cryogenic temperature followed by Teflon coating. The 0.01 wt% suspensions of gold (Au) nanoparticles with varying sizes (5, 50, and 250 nm in diameter) were tested as nanofluids for the evaporation kinetics including the contact angle, base diameter, height, volume and evaporation rate by using a goniometer. The dryout patterns were investigated by using scanning electron microscopy (SEM). The results show that the surface topography and nanoparticle sizes have significant effects on the initial contact angle, profile evolution, wetting transition, evaporation rate, and dryout deposition pattern of the nanofluid droplets.


2012 ◽  
Vol 610-613 ◽  
pp. 296-299
Author(s):  
Xin Jie Li ◽  
Dan Nan Jiang ◽  
Yue Jun Zhang

In order to learn the ClO2 decay behaviour in tap water, the kinetics of ClO2 decay in pure water was studied. Under the conditions of tap water treatment and keeping away from light, the effects of temperature and pH on ClO2 degradation were investigated. The results show that the ClO2 decay reaction in pure water is the first-order with respect to ClO2, the decay rate constants increase with increase in temperature or pH. At pH=6.87, the rate constants are 0.012h-1(15°C), 0.017h-1(25°C), 0.023h-1(35°C), and 0.029h-1(45°C), respectively. At 25°C, the rate constants are 0.0083h-1(pH=4.5), 0.0111h-1(pH=5.5), 0.0143h-1(pH=6.5), 0.0222h-1(pH=7.5), and 0.0351h-1(pH=8.5), respectively. The experimental data prove that ClO2 is more stable in acidic or lower temperature water than in neutral, alkalescent, or higher temperature water.


Langmuir ◽  
2013 ◽  
Vol 29 (20) ◽  
pp. 6032-6041 ◽  
Author(s):  
Wei Xu ◽  
Rajesh Leeladhar ◽  
Yong Tae Kang ◽  
Chang-Hwan Choi

2013 ◽  
Vol 58 (1) ◽  
pp. 197-201 ◽  
Author(s):  
L. Blacha ◽  
R. Burdzik ◽  
A. Smalcerz ◽  
T. Matuła

In the paper, results of the study on manganese evaporation from the OT4 alloy are presented. In the experiments, the effects of pressure on the manganese evaporation kinetics and the stages that limit the evaporation rate were investigated. It was demonstrated that the rate of manganese evaporation from the alloy increased with pressure reduction in the system. When the pressure decreases from 1000 Pa to 10 Pa, the value of overall mass transfer kMn increases from 3.9*10-6 ms-1 to 208.4*10-6 ms-1. At the same time, the manganese fraction in the alloy decreased from 1.49% mass to 0.045% mass. Within the whole pressure range, the analysed evaporation process is diffusion-controlled. For pressures above 50 Pa, the determining stage is transfer in the gaseous phase, while for pressures below 50 Pa, it is transfer in the liquid phase.


Langmuir ◽  
2017 ◽  
Vol 33 (23) ◽  
pp. 5666-5674 ◽  
Author(s):  
Alexandros Askounis ◽  
Yutaku Kita ◽  
Masamichi Kohno ◽  
Yasuyuki Takata ◽  
Vasileios Koutsos ◽  
...  

1990 ◽  
Vol 45 (7) ◽  
pp. 1032-1036 ◽  
Author(s):  
Derek P. N. Satchell ◽  
Rosemary S. Satchell ◽  
Wasfy N. Wassef

The second order-rate constants for the addition of water and ethanol to p-nitrophenyl isothiocyanate are larger in dimethyl sulphoxide solution than in pure water or ethanol. The detailed behaviour over a wide composition range suggests that H-bonding by the hydroxylic reactant to the solvent favours reaction, whereas H-bonding to this reactant retards reaction. The behaviour and relative reactivities of isocyanates and isothiocyanates suggest that protontransfer concurrent with nucleophilic attack at carbon, is less important in additions of hydroxylic compounds to isothiocyanates than to isocyanates. Branched-chain alcohols react more slowly with isothiocyanates than do primary alcohols. An excess of ethoxide ions reacts relatively rapidly with p-nitrophenyl isothiocyanate in ethanol to give the ionized thiourethane. The kinetics of this process, and the equilibrium constant for proton transfer between thiourethane and ethoxide ions, have been determined.


2018 ◽  
Vol 20 (36) ◽  
pp. 23453-23466 ◽  
Author(s):  
Yong-yang Su ◽  
Rachael E. H. Miles ◽  
Zhi-ming Li ◽  
Jonathan P. Reid ◽  
Jiang Xu

Numerous analytical models have been applied to describe the evaporation/condensation kinetics of volatile components from aerosol particles for use in many applications.


Author(s):  
Wei Xu ◽  
Chang-Hwan Choi

In this paper, we experimentally studied the evaporation kinetics and wetting dynamics of nanofluid sessile droplets on microstructured superhydrophobic surfaces of a constant air fraction but different structural topographies including arrays of pillars, lines, and wells. The dissimilar superhydrophobic surface patterns were fabricated on a silicon substrate by photolithography and deep reactive ion etching (DRIE) followed by Teflon coating. The 0.01wt% suspensions of gold (Au) nanoparticles of 250 nm in diameter were tested as nanofluids. The change of contact angle, base diameter, height, volume, and evaporation rate of the evaporating nanofluid droplet was measured in a room condition by using a goniometer. The results show that the change of structural topographies, despite the same air fraction on the surface, make significant difference in the droplet profile evolution during sequential evaporation phases. Compared to pure water tested as control, the distinctive influence of nanoparticles was especially observed in the final pinning phase with the tested nanofluid condition. This paper demonstrates that the evaporation kinetics and wetting dynamics of liquid droplets are significantly affected by the structural topography and the presences of nanoparticulates, which should be considered in the design and applications of superhydrophobic surfaces for droplet-based heat and mass transfer systems.


2018 ◽  
Vol 98 (5) ◽  
Author(s):  
Tejaswi Josyula ◽  
Zhenying Wang ◽  
Alexandros Askounis ◽  
Daniel Orejon ◽  
Sivasankaran Harish ◽  
...  

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