Sliding behavior of water droplets on line-patterned hydrophobic surfaces

We prepared line-patterned hydrophobic surfaces using fluoroalkylsilane (FAS) and octadecyltrimethoxysilane (ODS) then investigated the effect of line direction on sliding behavior of water droplets by direct observation of the actual droplet motion during sliding. Water droplets slide down with a periodic large deformation of the contact line and sliding velocity fluctuation that occurred when they crossed over the 500-μm ODS line regions in FAS regions on a Si surface tilted at 35°. These behaviors are less marked for motion on a 100-μm line surface, or on lines oriented parallel to the slope direction. Smaller droplets slide down with greater displacement in the line direction on 500-μm line patterning when the lines were rotated at 13° in-plane for the slope direction. This sliding behavior depended on the droplet size and rotation angle, and is accountable by the balance between gravitational and retentive forces.     

Dynamic hydrophobicity of water droplets on the line-patterned hydrophobic surfaces

Static and dynamic hydrophobicities of water droplet on a patterned surface prepared using fluoroalkylsilanes with different molecular chain lengths were investigated. Contact angles on the patterned surfaces well agreed with values predicted using Cassie’s theory. On the same line width ratio, total retention force was governed by the fluoroalkylsilane with slow-sliding acceleration. The total retention force decreased with the decreasing width ratio of silane with slow-sliding acceleration on the surface. These results imply that the sliding acceleration of water droplets on a hydrophobic surface depends both on chemical composition and patterning structure.     

疏水薄膜上水滴滑行加速度的观测(英文)

Weevaluatedslidingaccelerationofawater dropletonasiliconsurfacetreatedwithoctadecyl trichlorosilanebychangingthedropletweight. Theslopeoftheslidingaccelerationagainstthe dropletweightwaschangedat20mg,suggesting thatthedominantslidingmodewasshiftedfrom sl…     

Room temperature synthesis of water repellent silica coatings by the dip coat technique

The present paper describes the room temperature synthesis of dip coated water repellent silica coatings onto stainless steel substrates using 1,1,1,3,3,3-hexamethyldisilazane as a surface modifying agent. The hydrophobic property of the silica coating was enhanced by increasing its surface roughness, which was achieved by a proper control over the MeOH/TMOS molar ratio (S) during the synthesis. The contact angle of a water droplet (10 μl) increased from 72° to 145° with an increase in the S value from 9.1 to 36.4. The silica coating showed a minimum sliding angle of 15° for a water droplet of 10 μl. The water repellent silica coatings are thermally stable up to a temperature of 340 °C. The results have been discussed by taking into consideration the contact angle measurements, surface morphology and sol-gel parameters.     

Relationship between sliding acceleration of water droplets and dynamic contact angles on hydrophobic surfaces

This study measured sliding acceleration of water droplets on hydrophobic solid surfaces and used expanding and contracting method to compare that value with dynamic contact angles. Sliding action of the droplet was classified into three motion categories: constant accelerated motion, constant velocity and stasis. Differences exist in the dependencies of contact radius and the injection-suction rate in dynamic contact angle hysteresis according to these categories. This method is an effective indicator of water droplets’ sliding acceleration.     

Fabrication and characterization of a cotton candy like surface with superhydrophobicity

Superhydrophobic thin films were prepared on glass by air-brushing the in situ polymerization compositions of D₅/SiO₂. The wettability and morphology were investigated by contact angle measurement and scanning electron microscopy. The most superhydrophobic samples prepared had a static water contact angle of 157° for a 5 μl droplet and a sliding angle of ∼1° for 10 μl droplet. Thermal stability analysis showed that the surface maintained superhydrophobic at temperature up to 450 °C. Air trapping and capillary force on superhydrophobic behavior were evaluated.     

EHD atomization characteristics of a point-plate system with a porous point electrode

An electrohydrodynamic (EHD) atomization from a point-to-plate system, with a wet porous point as a corona electrode, has been studied. And the atomized water droplets from the wet porous point, as well as the water droplet traces, the water droplet charge-to-mass ratios, and the water droplet number concentrations, were investigated. It was observed that the wet porous point can atomize abundant amounts of water droplet, 2.8, 2.6 and 2.2 mg/min for negative, AC and positive corona, respectively. The migrated water droplet traces were observed. The positive wet porous point atomized very fine water droplets than those obtained with the negative wet porous point. Moreover, the water droplets atomized from the AC corona showed granular-like larger traces. A weak corona discharge can atomize water droplets very effectively. On the other hand, an intensive corona discharge can eject more water droplets. As a result with the wet porous point, the maximum corona-current-based and corona-power-based water droplet atomization yields of Y_C = 3.34, 3.32 and 3.25 μg/μAs and Y_P = 0.35, 0.40 and 0.27 mg/Ws have been obtained for the negative, AC and positive corona discharges.     

Fabrication and anti-frosting performance of super hydrophobic coating based on modified nano-sized calcium carbonate and ordinary polyacrylate

Nano-sized calcium carbonate (CaCO₃) particles were modified by heptadecafluorodecyl trimethoxysilane under acidic water condition. An ordinary polyacrylate prepared via radical copolymerization of methyl methacrylate, butyl acrylate, acrylic acid and β-hydroxyethyl methacrylate was used as the binder to form hydrophobic coatings with the modified CaCO₃. Super hydrophobic coating with water contact angle of 155° was obtained from modified CaCO₃ and the polyacrylate at their weight ratio of 8/2 by a simple procedure. Based on surface analysis by scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS), the super hydrophobicity can be attributed to both the surface microstructure and surface enrichment of fluoroalkyl chains. Due to a low water sliding angle, carbon black powder on super hydrophobic surface was easily removed by rolling water droplet. Furthermore, the anti-frosting performance of different surfaces was investigated, which indicated that the frost formed on superhydrophobic surface was greatly retarded compared with that on bare copper surface. The surface kept super hydrophobicity even after freezing-thawing treatment for 10 times.     

Physical and chemical characteristics of ultrasonically-prepared water-in-diesel fuel: Effects of ultrasonic horn position and water content

An ultrasonic technique was applied to preparation of two-phase water-in-oil (W/O) emulsified fuel of water/diesel oil/surfactant. In this study, an ultrasonic apparatus with a 28 kHz rod horn was used. The influence of the horn tip position during ultrasonic treatment, sonication time and water content (5 or 10 vol%) on the emulsion stability, viscosity, water droplet size and water surface area of emulsion fuels prepared by ultrasonication was investigated. The emulsion stability of ultrasonically-prepared fuel significantly depended on the horn tip position during ultrasonic irradiation. It was found that the change in the stability with the horn tip position was partly related to that in the ultrasonic power estimated by calorimetry. Emulsion stability, viscosity and sum of water droplets surface area increased and water droplet size decreased with an increase in sonication time, and they approached each limiting value in the longer time. The maximum values of the viscosity and water surface area increased with water content, while the limiting values of the emulsion stability and water droplet size were almost independent of water content. During ultrasonication of water/diesel oil mixture, the hydrogen and methane were identified and the cracking of hydrocarbon components in the diesel oil occurred. The combustion characteristics of ultrasonically-prepared emulsion fuel were studied and compared with those of diesel oil. The soot and NOx emissions during combustion of the emulsified fuel with higher water contents were significantly reduced compared with those during combustion of diesel oil.     

Transparent water repellent silica films by sol-gel process

Non-wettable surfaces with high contact angles and facile sliding angle of water droplets have received tremendous attention in recent years. The present paper describes the room temperature (∼27 °C) synthesis of dip coated water repellent silica coatings on glass substrates using iso-butyltrimethoxysilane (iso-BTMS) as a co-precursor. Emphasis is given to the influence of the hydrophobic reagent (iso-BTMS) on the water repellent properties of the silica films. Silica sol was prepared by keeping the molar ratio of tetraethoxysilane (TEOS) precursor, methanol (MeOH) solvent, water (H₂O) constant at 1:16.53:8.26 respectively, with 0.01 M NH₄F throughout the experiment and the molar ratio of iso-BTMS/TEOS (M) was varied from 0 to 0.965. The effect of M on the surface structure and hydrophobicity has been researched. The static water contact angle values of the silica films increased from 65° to 140° and water sliding angle values decreased from 42° to 16° with an increase in the M value from 0 to 0.965. The water repellent silica films are thermally stable up to a temperature of 280 °C and above this temperature the film shows hydrophilic behavior. The water repellent silica films were characterized by the Fourier Transform Infrared (FT-IR) Spectroscopy, Scanning Electron Microscopy (SEM), Atomic Force Microscopy (AFM), % of optical transmission, thermal and chemical aging tests, humidity tests, static and dynamic water contact angle measurements.     

Microexplosion of an emulsion droplet during Leidenfrost burning

An experimental study has been made of the microexplosion of an emulsion droplet on a hot surface during Leidenfrost burning. Photographic observation is used to study how the emulsion droplet behaves and what happens inside the droplet and to measure the waiting time for the onset of microexplosion. Weibull analysis was used to obtain the distribution function of the waiting time for the onset of microexplosion and to derive the formula for the rate of microexplosion as a function of water volume and emulsion temperature. The base fuels employed were n-decane, n-dodecane, n-tetradecane, and n-hexadecane. The results show that the increase in emulsion temperature with lapse of time results in the agglomeration and coalescence of microdroplets of base fuel dispersed in the continuous phase of water inside the emulsion droplet, terminated by the complete separation of the two phases. At the end of the phase separation process, an opaque water droplet is formed in the central core and is enveloped by the transparent shell of base fuel. Preferential evaporation of the base fuel occurs after the phase separation. The volume of the base fuel decreases while the water volume remains constant. The onset of the microexplosion of an emulsion droplet burning on the hot surface is classified by the wearout type of the Weibull distribution. The waiting time for the onset of the microexplosion decreases with increases in the normal boiling point of base fuel, initial water content, ambient pressure, and test surface temperature. The rate of microexplosion increases with the lapse of time and with increased normal boiling point of the base fuel. The rate of microexplosion increases linearly with increasing water volume in the emulsion droplet and decreases exponentially with the inverse of emulsion temperature.     

壁面温度对疏水表面上水滴冻结的影响

本文研究了冷壁面温度对疏水表面(θ=108.8°)上单个水滴冻结过程的影响,比较了水滴的冻结时间及冻结前后的形态变化。结果表明,水滴冻结所需要的时间随冷表面温度的降低而减小,冷表面温度越低,水滴冻结后其顶端越容易出现树枝状霜晶生长。最后,根据能量守恒原理建立了冷表面上水滴冻结的数学模型,给出了相应的表达式,进而分析了壁面温度对水滴冻结时长的影响,计算结果与实验结果一致。     

Characterization of fluoroalkylsilane monolayer on polystyrene sphere arrays after plasma treatment

Polystyrene (PS) colloidal crystal films with well-ordered arrays of PS spheres treated with argon plasma and coated with fluoroalkylsilane (FAS) were characterized by means of spectroscopy ellipsometry, X-ray photoelectron spectroscopy (XPS) and time of flight secondary ion mass spectrometry (ToF-SIMS). The XPS analysis indicated that the FAS film on the plasma treated PS surface was a monolayer with an orderly packed CF₃ group pointing outwards from the surface. The chemical composition of the PS surface changed immediately after a very short period of argon plasma treatment, while the subsequent coating of FAS on the plasma treated PS surface further modified the surface chemistry. The untreated PS surface exhibited poor interaction with FAS molecules. XPS and ToF-SIMS analyses showed the plasma treatment involved the oxidation of PS surface, where oxygen functional groups -O and O were generated, promoting FAS deposition on the plasma treated surface with strong secondary ion fragments originating from the FAS. The overall results indicated that plasma treatment was beneficial to the deposition of the FAS monolayer.     

Sliding behavior of oil droplets on nanosphere stacking layers with different surface textures

Two facile coating techniques, gravitational sediment and spin coating, were applied for the creation of silica sphere stacking layers with different textures onto glass substrates that display various sliding abilities toward liquid drops with different surface tensions, ranged from 25.6 to 72.3 mN/m. The resulting silica surface exhibits oil repellency, long-period durability > 30 days, and oil sliding capability. The two-tier texture offers a better roll-off ability toward liquid drops with a wide range of γ_L, ranged from 30.2 to 72.3 mN/m, i.e., when the sliding angle (SA) < 15°, the oil droplet start to roll off the surface. This improvement of sliding ability can be ascribed to the fact that the two-tier texture allows for air pockets (i.e., referred to as the Cassie state), thus favoring the self-cleaning ability. Taking Young-Duprè equation into account, a linearity relationship between sine SA and work of adhesion (W_ad) appears to describe the sliding behavior within the W_ad region: 2.20-3.03 mN/m. The smaller W_ad, the easier drop sliding (i.e., the smaller SA value) takes place on the surfaces. The W_ad value ∼3.03 mN/m shows a critical kinetic barrier for drop sliding on the silica surfaces from stationary to movement states. This work proposes a mathematical model to simulate the sliding behavior of oil drops on a nanosphere stacking layer, confirming the anti-oil contamination capability.     

Visualization of aggregation process of dispersed water droplets and the effect of aggregation on secondary atomization of emulsified fuel droplets

The effect of aggregation of dispersed water droplets on secondary atomization of emulsified fuel droplets in a heating process was investigated. Secondary atomization was observed using a single droplet experiment in which a water-in-oil (W/O) emulsified fuel droplet prepared using colored water was heated by a halogen heater. The initial diameter of dispersed water droplets before heating was controlled, and the change in the diameter of dispersed water droplets was measured by image analysis. As a result, the aggregation process of dispersed water droplets in the heating process was successfully visualized. The dispersed water droplet diameter increased with an increase in W/O emulsified fuel droplet temperature. The occurrence probability of micro-explosion increased with an increase in the dispersed water droplet diameter in emulsified fuel droplets. It is suggested that the occurrence probability of micro-explosion can be increased by accelerating the aggregation and coalescence of dispersed water droplets below 430 K, which is the average temperature of the starting point of puffing.     

Ultrasonic emulsification of food-grade nanoemulsion formulation and evaluation of its bactericidal activity

Basil oil (Ocimum basilicum) nanoemulsion was formulated using non-ionic surfactant Tween80 and water by ultrasonic emulsification method. Process of nanoemulsion development was optimized for parameters such as surfactant concentration and emulsification time to achieve minimum droplet diameter with high physical stability. Surfactant concentration was found to have a negative correlation with droplet diameter, whereas emulsification time had a positive correlation with droplet diameter and also with intrinsic stability of the emulsion. Stable basil oil nanoemulsion with droplet diameter 29.3 nm was formulated by ultrasonic emulsification for 15 min. Formulated nanoemulsion was evaluated for antibacterial activity against Escherichia coli by kinetics of killing experiment. Fluorescence microscopy and FT-IR results showed that nanoemulsion treatment resulted alteration in permeability and surface features of bacterial cell membrane.     

Differential friction force spectroscopy of micropatterned organosilane self-assembled monolayers

Frictional properties of organosilane self-assembled monolayers (SAMs) and hydrated silicon oxide (SiOH) surfaces on a single sample substrate were studied; the frictional force difference between the surfaces was measured by employing one as a standard. Using a lateral force microscope (LFM), differential frictional force microscopic data were obtained by measuring the difference in the friction forces of the two surfaces with respect to the vertical load force applied to the LFM probe. The SAMs were prepared from n-octadecyltrimethoxysilane [ODS, H₃C(CH₂)₁₇Si(OCH₃)₃], n-(6-aminohexyl) aminopropyltrimethoxysilane [AHAPS, H₂N(CH₂)₆NH(CH₂)₃Si(OCH₃)₃], 3,3,3-trifluoropropyltrimethoxysilane [FAS3, F₃C(CH₂)₂Si(OCH₃)₃] and heptadecafluoro-1,1,2,2-tetrahydro-decyl-1-trimethoxysilane [FAS17, F₃C(CF₂)₇(CH₂)₂Si(OCH₃)₃] by chemical vapor deposition. In the vertical force range of 0 to 600 nN, the SAMs showed no damage at all, and frictional force on the SAM surfaces increased linearly with the vertical force. The order of the frictional force magnitudes determined with the SiOH-terminated probe was SiOH > AHAPS > FAS3 > FAS17 > ODS. In addition, the frictional force difference did not become zero even at a vertical force of 0 nN, that is, the frictional differences could even be imaged by LFM through probe-sample adhesion.     

Sliding behavior of water drops on sol-gel derived hydrophobic silica films

Control on the wettability of solid state materials is a classical and key issue in surface engineering. Optically transparent methyltriethoxysilane (MTES)-based silica films with water sliding angle as low as 9° were successfully prepared by two-step sol-gel co-precursor method. The emphasis is given to the effect of trimethylethoxysilane (TMES) as a co-precursor on water sliding behavior of silica films. The coating sol was prepared with molar ratio of methyltriethoxysilane (MTES), methanol (MeOH), acidic water (0.01 M, oxalic acid) and basic water (12 M, NH₄OH) kept constant at 1:12.73:3.58:3.58 respectively, and the molar ratio of TMES/MTES (M) was varied from 0 to 0.22. The static water contact angle as high as 120° and the water sliding angle as low as 9° was obtained by keeping the molar ratio (M) of TMES/MTES at 0.22. When the modified films were cured at temperature higher than 280 °C, the films became superhydrophilic. Further, the humidity study was carried out at a relative humidity of 90% at 30 °C over 60 days. We characterized the water repellent silica films by Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), atomic force microscopy (AFM), % of optical transmission, humidity tests and static and dynamic water contact angle (CA) measurements.     

Tailoring the wettability of nanocrystalline TiO2 films

The water contact angle (WCA) of nanocrystalline TiO₂ films was adjusted by fluoroalkylsilane (FAS) modification and photocatalytic lithography. FAS modification made the surface hydrophobic with the WCA up to ∼156°, while ultraviolet (UV) irradiation changed surface to hydrophilic with the WCA down to ∼0°. Both the hydrophobicity and hydrophilicity were enhanced by surface roughness. The wettability can be tailored by varying the concentration of FAS solution and soaking time, as well as the UV light intensity and irradiation time. Additionally, with the help of photomasks, hydrophobic-hydrophilic micropatterns can be fabricated and manifested via area-selective deposition of polystyrene particles.     

Wetting characteristics of ZnO smooth film and nanowire structure with and without OTS coating

ZnO is an important material that is used in a variety of technologies including optical devices, sensors, and other microsystems. In many of these technologies, wettability is of great concern because of its implications in numerous surface related interactions. In this work, the effects of surface morphology and surface energy on the wetting characteristics of ZnO were investigated. ZnO specimens were prepared in both smooth film and nanowire structure in order to investigate the effects of surface morphology. Also, a hydrophobic octadecyltrichlorosilane (OTS) coating was used to chemically modify the surface energy of the ZnO surface. Wettability of the surfaces was assessed by measuring the water contact angle. The results showed that the water contact angle varied significantly with surface morphology as well as surface energy. OTS coated ZnO nanowire specimen had the highest contact angle of 150°, which corresponded to a superhydrophobic surface. This was a drastic difference from the contact angle of 87° obtained for the smooth ZnO film specimen. In addition to the initial contact angle, the evolution of the water droplet with respect to time was investigated. The wetting state of water droplet was analyzed with both Wenzel and Cassie-Baxter models. Spontaneous and gradual spreading, together with evaporation phenomenon contributed to the changing shape, and hence the varying contact angle, of the water droplet over time.