Increase In Contact Angle Research Articles

Experimental and theoretical study on the ceasing motion of a droplet manipulated by air-blowing nozzle

In this study, the dynamic process of a droplet moving with a substrate until blocked by air flow is investigated experimentally and theoretically. A sequence of experiments has been conducted to investigate the impacts of wetting properties, droplet volumes, air flow velocities, and droplet velocities. The substrate is driven by a linear motion motor to ensure the droplet moves at a certain velocity alongside the substrate. The air flow that is vertically injected from the nozzles toward the substrate is known as an impinging jet. After the air flow impacts the substrate, it will blow horizontally. When the direction of air flow is opposite to that of the droplet movement, a force will be exerted on the surface of the droplet. This action incurs the deformation of the droplet and the cessation of its movement, eventually resulting in an equilibrium state. The droplet shape and motion processes are recorded by a high-speed camera. A mathematical model considering the effect of droplet contact angle, droplet size, droplet moving velocity, and air flow velocity is established in the state of equilibrium. Correlation factors are used in the model for the drag coefficient and air average velocity acting on the droplet. It is found that the air flow rate required to stop the motion of the droplet increases with the droplet moving velocity and the droplet size but reduces with the increase in the static contact angle. The mathematical model, when equipped with suitable correlation factors, exhibits good agreement with experimental data and could potentially be utilized as a predictor of critical velocity for the cessation of the droplet motion.

Phase-field-based lattice Boltzmann method for containerless freezing.

In this paper we first propose a phase-field model for the containerless freezing problems, in which the volume expansion or shrinkage of the liquid caused by the density change during the phase change process is considered by adding a mass source term to the continuum equation. Then a phase-field-based lattice Boltzmann (LB) method is further developed to simulate solid-liquid phase change phenomena in multiphase systems. We test the developed LB method by the problem of conduction-induced freezing in a semi-infinite space, the three-phase Stefan problem, and the droplet solidification on a cold surface, and the numerical results are in agreement with the analytical and experimental solutions. In addition, the LB method is also used to study the rising bubbles with solidification. The results of the present method not only accurately capture the effect of bubbles on the solidification process, but also are in agreement with the previous work. Finally, a parametric study is carried out to examine the influences of some physical parameters on the sessile droplet solidification, and it is found that the time of droplet solidification increases with the increase of droplet volume and contact angle.

Intensive coagulation of secondary effluent to mitigate reverse osmosis membrane fouling at low temperatures: Strategies of pre-oxidation and coagulant aids addition

Conventional coagulation-sedimentation, typically used as a pretreatment for ultrafiltration-reverse osmosis, is ineffective in solving the problem of reverse osmosis membrane fouling at low temperatures. In this study, the coagulation enhancement effect of pre-oxidation and the addition of coagulant aids on conventional coagulation with polyaluminum chloride as a coagulant was investigated. The results showed that the addition of fly ash, powdered activated carbon, or diatomite as coagulant aids improved the reduction of turbidity, dissolved organic carbon (DOC), and ultraviolet absorbance at 254 nm (UV254), and also reduced the residual content of dissolved aluminum ions. Among them, diatomite was superior. Pre-oxidation before conventional coagulation increased the reduction of turbidity and UV254 by about 50 % and doubled the removal of proteins, polysaccharides, and DOC compared to conventional coagulation. Ozone was superior to sodium hypochlorite. The combination of ozone pre-oxidation and diatomite addition with conventional coagulation further increased the pollutant removal rate, with the removal rates of turbidity, UV254, polysaccharides, proteins, and DOC reaching 82.20 %, 52.35 %, 26.34 %, 24.89 %, and 26.38 %, respectively. In addition, the residual content of dissolved aluminum ions decreased to 0.84 mg/L. The reverse osmosis filtration simulation test showed that pretreating the feed water with the enhanced coagulation by the combination of ozone pre-oxidation and diatomite addition resulted in a slower decrease in membrane flux, reduced foulant content on the membrane surface, and the smallest increase in contact angle. The results of this research may offer a viable pretreatment method to reduce fouling in reverse osmosis membranes operating at low temperatures.

Theoretical analysis of the initial nucleation characteristics of trace water vapor frosting on a cryogenic surface

In certain extreme conditions characterized by ultra-low water vapor content and ultra-low temperatures (e.g. cryogenic wind tunnel), trace water vapor frosting can also pose significant hazards. Considering the crucial role of initial nucleation on subsequent frosting processes, this study firstly investigated and compared the nucleation characteristics of frosting at different water vapor contents (0.1−1000 ppmv) from humid air to trace water vapor based on classical nucleation theory. The preferred nucleation phase diagrams and critical nucleation conditions were analyzed. Sensitivity of the nucleation mass transfer rate, as well as the frosting pathways were further identified. Results show that the nucleation characteristics of trace water vapor frosting (<100 ppmv) is significantly different from that of humid air frosting (>1000 ppmv). Trace water vapor frosting is more inclined towards desublimation nucleation due to its lower nucleation temperature and larger critical contact angle. The critical contact angles for 1000 ppmv, 100 ppmv and 0.1 ppmv are 49°, 75° and 120°, respectively. Furthermore, trace water vapor nucleation requires a greater subcooling degree, has a smaller critical nucleation radius, and is highly sensitive to surface contact angle and further-subcooling degree. At a surface contact angle of 120°, the nucleation subcooling degree of 0.1 ppmv is 2.9 K greater than that of 1000 ppmv. This study helps understanding the nucleation characteristics under different water vapor content conditions, which indicates that reducing subcooling degree and increasing contact angle are more effective anti-frosting methods than reducing water vapor content for trace water vapor frosting.

Fabrication of biocomposite materials with polycaprolactone and activated carbon extracted from agricultural waste

In this study, activated carbon was extracted from a source of agricultural waste (wheat straw) through a chemical activation process and blended with polycaprolactone (PCL) to fabricate new biocomposite materials. Three distinct types of activated carbon, designated as C1, C2, and C3 were obtained by varying the ratio of the activation agent and wheat straw and different drying conditions. Through a comprehensive array of analytical techniques, including FTIR, XRD, BET, EDS, and FE-SEM, we determined the optimal experimental method for extracting activated carbon from wheat straw and identified the most effective type of activated carbon (C3). Based on these analyses, C3 exhibits the highest carbon content, the greatest specific surface area (386.47 m2/g), and the highest total pore volume (0.2596 cm3/g). By blending polycaprolactone with the optimal activated carbon (at concentrations of 1, 3, and 5 wt%), biocomposite samples were fabricated. The results of FTIR indicate that the biocomposite materials containing 1, 3, and 5 wt% of activated carbon exhibit no disturbing peaks. However, the sample PCL-C,1 wt%, shows significant increases in the intensity of observed peaks. XRD analyses of the fabricated biocomposite samples illustrate that the sample containing 1 wt% of activated carbon has a greater tendency for crystallization compared to the other samples. Morphological analysis of the biocomposites and the dispersion of carbon particles within them demonstrate the least amount of agglomeration in the sample with an activated carbon concentration of 1 wt%. Upon assessing the mechanical properties of biocomposites, the same sample (1 wt% of C3) demonstrates more favorable characteristics than the other samples. Furthermore, a contact angle test was conducted to gauge the biocomposite hydrophilicity, revealing a 7 degree increase in contact angle for the sample with an activated carbon concentration of 1 wt% compared to the pure PCL sample. Thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) were used to examine the weight loss, degradation temperature, melting temperature, and glass transition temperature of the synthesized materials. These analyses indicate a marginal augmentation in both melting and glass transition temperatures for the sample with an activated carbon concentration of 1 wt%.

Drop Retention and Departure in Adiabatic Shear Flow on Structured Superhydrophobic Surfaces.

Drops are retained or held on surfaces due to a retention force exerted on the drop by the surface. This retention force is a function of the surface tension of the liquid, drop geometry, and the contact angle between the drop and the surface. When external or body forces exceed the retention force, the drop begins to move. This work explores the conditions for which drop departure occurs on structured superhydrophobic surfaces in the presence of an applied shear flow. Drop departure is explored for five microstructured superhydrophobic surfaces, one nanostructured carbon nanotube surface and one smooth hydrophobic surface. Surface solid fractions range from 0.05 to 1.00, and measured static contact angles range from 121° to 161°. Droplet volumes of 5, 10, 20, 30, 40, and 50 μL are tested on each surface. For each experiment, increasing air velocity is applied to a droplet placed on a surface until the droplet departs. High-speed imaging is used to track droplet base length, height, cross-section area (as viewed from the side) and advancing/receding contact angles. Measurements of drop advancing and receding contact angles are reported at the point of departure, with increasing contact angle hysteresis observed prior to departure. Contact angle hysteresis is observed to be a good indicator of droplet mobility. Measurements of the average air velocity over the height of the droplet are determined at the point of departure for all conditions. The measured air velocity shows strong dependence on the surface solid fraction, and the required shear flow velocity decreases as the surface solid fraction decreases. This is most pronounced at very low solid fractions. A coefficient of drag for the departing drops in shear flow is calculated and is shown to decrease with increasing Reynolds number.

Development of superhydrophobic PVA/CNC nanofibrous membranes for enhanced oil-water separation

Effective oil–water separation is crucial for environmental purification and the remediation of oil pollution, yet current methods face limitations in efficiency, durability, and environmental impact. In this study, we aimed a green nanofibrous membrane with excellent oil–water separation efficiency, addressing the significant environmental challenge of separating oil from water in various states. For this purpose, polyvinyl alcohol (PVA)-based nanofibers were prepared by aqueous electrospinning. The mechanical strength of the nanofibers was reinforced by adding cellulose nanocrystals (CNCs). The surface of the nanofibers was modified with hexadecyltrimethoxysilane (HDTMS) to induce hydrophobicity, evidenced by the increase in contact angle from 44.41° to 133.19°, facilitating effective oil separation from various states, including dispersed, suspended, and emulsified states. The prepared PVA/CNC-HDTMS nanofiber showed 194 %, 539 %, and 407 % higher tensile strength, yield strength, and Young’s modulus than PVA nanofibers, respectively. The oil sorption capacity of the nanofibers varied widely from 17.01-113.76 g/g, which is strongly influenced by the viscosity and volatility of the oil species. The durability and reusability of the nanofibers were well maintained, even after being reused more than 10 times without morphological deterioration. In separating oil–water mixtures, the nanofibers maintained a high flux of 40,039 L/m2h and a separation efficiency of 99.2 % under pressurized conditions. Additionally, the nanofibers achieved a separation efficiency of 98.5 % in oil–water emulsion states.

Development of Hematite Nano Ellipsoids/Pectin Composite Films for Green Packaging Applications.

Synthetic packaging materials are known to cause serious environmental and human health problems. Among the eco-friendly biopolymers from nonfood sources that are suitable for packaging applications, pectin is a promising candidate. However, native pectin films (NPF) exhibit poor mechanical strength, high hydrophilicity, and poor gas diffusion barrier properties. These shortcomings offset the advantages of pectin as a potential packaging material. To address these limitations, in this study, hematite nano ellipsoids (HNEs) were incorporated as fillers to reinforce native pectin films. This reinforcement resulted in substantial improvements in the mechanical properties, hydrophobicity, thermal stability, barrier properties, and optical attributes of pectin films. Compared to NPF, the pectin-hematite composite film exhibited a 35% increase in tensile strength, a 30° increase in contact angle, a 6-fold increase in the oxygen diffusion barrier properties, and a 20% increase in the water vapor barrier properties. This study presents a sustainable, biocompatible, and biodegradable packaging solution by capitalizing on eco-friendly biopolymer and nanoparticle engineering.

Azoles as corrosion inhibitors in alkaline medium for ruthenium chemical mechanical planarization applications:Electrochemical and theoretical analysis

The adsorption performance and inhibition mechanism of azoles; Imidazole (IMD), 1, 2, 4-Triazole (TAZ), and 1, 2, 3-Benzotriazole (BTAH) inhibitors on ruthenium (Ru) at 9 pH, were investigated in this study using electrochemical techniques and density functional theory (DFT) simulations. The electrochemical data demonstrate that the three azole compounds being investigated are mixed type corrosion inhibitors with anodic predominance, and the order of corrosion inhibition efficiency for Ru is BTAH > TAZ > IMD. The azole compounds suppress the metal dissolution reaction rate by adhering on to the Ru surface and nature of adsorption (combined physisorption and chemisorption) is explained via Langmuir adsorption isotherm model. The increase in contact angle on the Ru surface verified the successful adsorption of the three organic inhibitors on the Ru surface. Furthermore, the suppression of corrosion reaction kinetics is validated with field emission scanning electron microscopy (FESEM) images. The results of quantum chemistry calculations indicate that the corrosion inhibition effect of BTAH is superior to that of IMD and TAZ. Further, using molecular dynamics modelling, the reliable configuration of the organic inhibitor molecules on the Ru (001) surface in aqueous medium was investigated and the total adsorption energy was computed.

Effects of low-molecular-weight organic acids on the transport of polystyrene nanoplastics: An insight at the structure of organic acids

Plastic nanoparticles are extensively used in various products, leading to inevitable pollution in soil. Understanding their transport in soils where various organic substances exist is crucial. This study examined the impact of low-molecular-weight organic acids (LMWOAs) on the transport of polystyrene nanoplastics (PS-NPs) through saturated quartz sand. The experiments involved three dibasic acids—malonic acid (MA1), malic acid (MA2) and tartaric acid (TA) — and four monobasic acids— formic acid (FA), acetic acid (AA), propanoic acid (PA) and glycolic acid (GA) —under different pH levels (4.0, 5.5, 7.0) and in the presence of cations (Na+, Ca2+). The results demonstrated that in the presence of Na+, dibasic acids significantly enhanced PS-NPs transport, with TA being the most effective, followed by MA2 and MA1. This enhancement is attributed to the adsorption of LMWOAs onto the nanoparticles and sand, creating a more negative ζ-potential, which increases the electrostatic repulsion and decreases the PS-NPs deposition, thereby facilitating the transport. Applying the Derjaguin-Landau-Verwey-Overbeek theory, higher pH levels increased the energy barrier and secondary energy minimum, decreasing PS-NPs deposition. Moreover, dibasic acids significantly enhanced the hydrophilicity of PS-NPs. Conversely, monobasic acids, except for GA, slightly reduced the hydrophilicity of PS-NPs, as indicated by a small increase in the water contact angle, hereby minimally affecting PS-NPs transport. As for GA, although it is a monobasic acid, the additional -OH group in its molecular structure promoted PS-NPs transport, similar to dibasic acids. For example, GA also significantly enhanced the hydrophilicity of PS-NPs. In the presence of Ca2+, the enhancement of PS-NPs transport by LMWOAs was comparable to that with Na+, primarily due to the complex-forming and bridging effects of Ca2+ with the organic acids and PS-NPs. These findings provide important insights into predicting and analyzing the transport behaviors of PS-NPs.

Experimental Investigation of Runback Water Flow Behavior on Aero-Engine Rotating Spinners with Different Wettabilities

The accumulation of ice on the aero-engine inlet compromises engine safety. Traditional hot air anti-icing systems, which utilize bleed air, require substantial energy, decreasing engine performance and increasing emissions. Superhydrophobic materials have shown potential in reducing energy consumption when combined with these systems. Research indicates that superhydrophobic surfaces on stationary components significantly reduce anti-icing energy consumption by altering runback water flow behavior. However, for rotating aero-engine components, the effectiveness of superhydrophobic surfaces and the influence of surface wettability on runback water flow remain unclear due to centrifugal and Coriolis forces. This study investigates the runback water flow behavior on aero-engine rotating spinner surfaces with varying wettabilities in a straight-flow spray wind tunnel. The results demonstrated that centrifugal force reduces the amount of runback water on the rotating spinner compared to the stationary surface, forming rivulet flows deflected opposite to the direction of rotation. Furthermore, wettability significantly affects the flow characteristics of runback water on rotating surfaces. As the contact angle increases, the liquid water on the rotating spinner transitions from continuous film flow to rivulet and bead-like flows. Notably, the superhydrophobic surface prevents water adhesion, indicating its potential for anti-icing on rotating components. In addition, the interaction between rotational speed and surface wettability enhances the effects, with both increased rotational speed and larger contact angles contributing to higher liquid water flow velocities, promoting the rapid formation and detachment of rivulet and bead-like flows.

Capillary sealing capability alteration of shale caprock induced by CO2-brine-rock interaction: Implication for CO2 geological storage

The capillary sealing mechanism plays a pivotal role in the sealing capability of caprock in CO2 geological storage. The interactions between CO2, brine, and rock induced by CO2 injection may potentially impact the capillary sealing capability of the caprock. To characterize the capillary sealing capability of Yanchang shale, breakthrough pressure (Pb) tests were conducted before and after CO2-brine-rock interaction while analyzing the contributions of pore structure and wettability to Pb alteration. The results revealed that Pb of Yanchang shale samples decreased by 7.14%–22.22% after CO2-brine-rock interaction, indicating a deterioration in their capillary sealing capability. This degradation can be attributed to changes in pore structure and wettability, as they collectively influence the capillary sealing capability of shale caprock. The increase of small-pore (<200 nm) porosity and contact angle promoted the reduction of Pb. The alteration of shale caprock's capillary sealing capability due to CO2-brine-rock interaction significantly impacts CO2 storage potential and long-term safety, which should be considered prior to large-scale CO2 injection.

Investigation of canopy interception characteristics in slope protection grasses: A laboratory experiment

Canopy interception significantly affects hydrological processes such as infiltration, runoff and evapotranspiration. Research on grass canopy interception remains limited, and the experimental methods employed differ substantially. To thoroughly investigate the canopy interception characteristics of grass and clarify the methodological differences, five commonly utilized slope protection grass species in temperate regions were cultivated in a laboratory setting, and their canopy interception characteristics were experimentally investigated using the water-balance method (WBM), the water-wiping method (WWM) and the water-immersion method (WIM), respectively. The results showed that the WBM is more accurate for measuring canopy interception in grass, whereas both the WWM and the WIM underestimate grass canopy interception capacity. The canopy interception capacity measured by the WBM was 1.61–2.09 times higher than that of the WWM and 1.93–3.47 times higher than that of the WIM. Grey correlation analysis of the eight evaluated factors indicated that leaf area is the most influential factor affecting canopy interception in grass, followed by rainfall amount, dry mass, rainfall intensity, canopy projection area, leaf contact angle, fresh weight, and average height. There is a negative power function relationship between the interception ratio and the rainfall amount. With increasing rainfall intensity, the canopy interception capacity initially increases and then decreases, peaking at rainfall intensities of 15 to 20 mm/h. Leaf contact angle is a key quantifiable parameter that explains the differences in canopy interception among different grass species, and the canopy interception per unit leaf area decreases as the leaf contact angle increases. This study demonstrates that the WBM provides the most accurate measurements of grass canopy interception compared to the WWM and WIM, and highlights the leaf contact angle as a key factor in explaining interspecies differences. These findings could enhance the understanding of grass canopy interception and guide the selection of experimental methods.

Separation of the topographical and chemical components of the wettability of textured surfaces by femtosecond laser

Contrary to what is usually found in the literature, we show in this work that the contribution of ripples (LSFL LIPSS) to the increase in hydrophobicity of femtosecond laser-textured metal surfaces is negligible. Following the demonstration of wettability according to the Wenzel regime, a methodology for decorrelating the chemical and the topographical components of wettability is implemented. This makes it possible to quantify the respective responsibilities of the chemical and topographical contributions to the increase in contact angle. For femtosecond laser-textured 304L steel, it is shown that the topographical contribution made by ripples is around 6% of the increase in hydrophobicity. In contrast, the chemical contribution accounts for 94% of the increase in contact angle after texturing. The chemistry/topography decorrelation approach is validated by comparing wettability results on PDMS as test-materials.

Mikrostruktur dan Karakteristik Permukaan Kayu Pinus Scots (Pinus sylvestris L.) Termodifikasi Gliserol dan Asam Sitrat

Scots pine (Pinus sylvestris L.) wood is one of the most popular timber export products. However, its low durability can reduce the potential and utilization of the wood. Chemical modification is one of the solutions to overcome this drawback. Chemical modification using non-biocide materials such as glycerol and citric acid was carried out to improve the inferior properties of wood. The study aimed to observe the microstructure and evaluate the surface characteristics of glycerol and citric acid-modified scots pine wood. Scots pine wood was modified using glycerol and citric acid with weight percent gain (WPG) values of 20% and 46%. Surface characteristics were measured, including surface roughness, surface free energy (SFE), wettability, and bonding quality. The results show that chemical modification using glycerol and citric acid resulted in the structure of the pine wood being more filled and denser. The modification could also reduce the roughness of the wood surface, resulting in decreased SFE value, increased contact angle, and decreased wettability on the wood surface. It might cause a decrease in the bonding quality because the wood did not have the strength to mechanically lock with the paint. Glycerol and citric acid modified-scots pine wood can be considered for exterior application. Keywords: citric acid, glycerol, microstructure, scots pine, surface characteristics

Can pulsed laser treatment reduce microbial adhesion on the surface of resin denture base materials?

Objectives. The present work investigates the influence of pulsed nanosecond laser patterning of two commercial heat cure poly (methyl methacrylate) denture base materials, Trevalon and DPI heat cure, on their surface characteristics such as roughness, hydrophobicity, and microbial adhesion. Methods. A Q-switched Nd:YAG solid state nanosecond pulsed laser at a wavelength of 532 nm with a fluence of 2.55 × 1010 W cm−2 having a pulse frequency of 10 Hz was used at varying translation stage speed and vertical spacing for the surface patterning of denture base materials. The surface properties of control and patterned materials were characterized by measuring the compositional changes, wettability, and roughness. Microbial adhesion was assessed by incubating the specimens in Candida albicans suspension at 37 °C for 2 h followed by estimating the number of adherent Candida cells. Results. The micro-Raman spectroscopic studies indicated no chemical changes in the materials due to laser patterning. However, laser patterning increased the average surface roughness from 0.02 ± 0.005 and 0.04 ± 0.003 μm to 3.85 ± 0.20 μm and 3.70 ± 0.12 μm respectively for Trevalon and DPI heat cure materials. In addition, a reduction in the surface wettability was evident as manifested by an increase in water contact angle from 76 ± 2° to 105 ± 1° for Trevalon and from 72 ± 1° to 97 ± 1° for DPI heat cure. Finally, the microbial adhesion studies clearly indicated that the surfaces with higher hydrophobicity and roughness following laser patterning exhibited reduced microbial adhesion. Significance. Laser patterning can be utilized to tune the surface features of denture base materials and thus offer a promising method to create microbial adhesion resistant surfaces. Clinically, such surfaces help in reducing the incidence of denture stomatitis, especially in immunocompromised patients, without altering the composition and bulk properties of denture base materials.

Changes in the properties of the corn starch glycerol film in a time-dependent manner during gelatinization

This study aimed to investigate the fundamental properties, solubility, mechanical properties, barrier performance, and microstructural features of films composed of corn starch and glycerol. Changes in the microstructure were analyzed to understand how they relate to the physical and chemical properties of these films. Specifically, we found that increasing the gelatinization time decreased the film thickness, solubility, water vapor permeability, and maximum degradation temperature and increased the water content. A gradual increase in the water contact angle of the corn starch–glycerol films was observed with increasing gelatinization time. This trend is likely due to the disruptive effect of gelatinization on the crystalline and amorphous structures inherent in corn starch, resulting in reduced film crystallinity, degree of order (DO) and degree of double helix (DD).

Contact Angle Modulation: In Situ Polymer Deposition during Sessile Drop Evaporation.

The drying kinetics of a sessile drop on a solid surface are a widely studied phenomenon because of their relevance to various fields such as coating, printing, medical diagnostics, sensing, and microfluidic technology. Typically, the drop undergoes drying either at a constant contact radius (R) with a decrease in the three-phase contact angle or at a constant contact angle (θ) with a reduction in the radius with time. These two drying modes are referred to as CCR and CCA, respectively. It is not uncommon where both R and θ may decrease during drying, especially in the penultimate stage of drying. In this work, we report a scenario wherein the θ increases while R decreases during the drying process of an aqueous polymer solution on a high surface energy substrate. This behavior is observed across different polymer systems (such as poly(ethylene oxide) and polyvinyl pyrrolidine), varying molecular weights, and polymer concentrations. As the drop dries, the polymer gets deposited at the three-phase contact line, thus reducing the surface energy of the substrate and leading to an increase in the contact angle. The drop responds by attempting to reach a new equilibrium contact angle through slipping. The temporal increase in contact angle follows a power law scaling behavior. This study demonstrates an in situ modulation of contact angle facilitated by evaporation and polymer deposition, showcasing unconventional drying dynamics.

Transition of Liquid Drops on Microstructured Hygrophobic Surfaces from the Impaled Wenzel State to the "Fakir" Cassie-Baxter State.

Low adhesion of liquids on solid surfaces can be achieved with protrusions that minimize the contact area between the liquid and the solid. The wetting state where an air cushion forms under the drop is known as the Cassie-Baxter state. Surfaces where liquids form macroscopic contact angles above 150° are called superhydrophobic and superhygrophobic, if we refer to water or any liquid, respectively. The Cassie state is desirable for applications, but it is usually unstable compared to the Wenzel state, where the drop is in direct contact with the rough surface. The Cassie-to-Wenzel transition can be triggered by an increase in pressure and vibrations, but the inverse Wenzel-to-Cassie is much more difficult to observe. Here, we examine under what conditions the Wenzel-to-Cassie transition is triggered when the microscopic contact angle changes abruptly. For this, we applied a lubricant of low surface tension around drops that were in the Wenzel state on microstructured surfaces. The increase of the microscopic contact angle lifted the drop from the rough surface, when the pillar height and spacing are large and small, respectively. Numerical calculations for the drop-lubricant interface showed that the surface geometry requirements for the Wenzel-to-Cassie transition are stricter than the ones for the stability of the Cassie state. A surface geometry where the Cassie state is more stable than the Wenzel for a given Laplace pressure of the drop may not always allow the Wenzel-to-Cassie transition to take place. Therefore, the stability of the Cassie state is a necessary but insufficient condition for the inverse transition.

Cold plasma-assisted pretreatment for fabrication and characterization of rice starch-stearic acid complexes

The present study explored the modification of rice starch via dielectric barrier discharge cold plasma (DBD-CP) employing air and argon as the input gas, followed by complexation with stearic acid to yield modified rice starch-stearic acid complexes. The complexes were characterized by a V-type crystalline structure, exhibiting enhanced thermal stability and hydrophobicity compared to conventional rice starch-stearic acid complexes. Utilization of argon as the input gas markedly improved the modification effects on complexes over air, as evidenced by a further increase in the water contact angle to 78.99°, an ergosterol encapsulation rate of 50.91%, and an in vitro digestive release rate of 70.84% within the prepared Pickering emulsion. These findings indicate the significant potential of DBD-CP pretreatment with argon for enhancing the physicochemical properties of starch-fatty acid complexes, particularly in the formulation of Pickering emulsions with improved emulsifying capacities.