Smaller Contact Angle Research Articles

Effect of Application of Vinyl Acetate Ethylene Emulsion Binder and Type of Pigment on the Quality of Inkjet Paper

Zeolites and precipitated calcium carbonate (PCC) were applied together with a vinyl acetate ethylene (VAE) emulsion to identify an alternative pigment for silica to improve runnability and develop the application technology for the VAE emulsion. The low shear and high shear viscosity of the coating color were decreased when zeolites were mixed with PCC. The coating color exhibited lower shear and higher shear viscosity when the emulsion contained VAE than when it containing poly(vinyl) alcohol. Silica with a large specific surface area and pore volume exhibited a small surface contact angle, and the coating color also showed a smaller contact angle with zeolites having a porous structure than with PCC. Silica with a large specific surface area and pore volume showed high print density. For each type of pigment, the print density of coated paper was higher when using zeolites than when using PCC. When the VAE emulsion binder was applied, the ink density decreased.

Evaporation and fluid flow near the boundary of a stationary dry patch.

We consider an isolated circular dry patch formed in an evaporating liquid layer and investigate local viscous flows in both liquid and air near the contact line which is the boundary of the dry patch. Flow patterns in the liquid deviate significantly from the predictions of single-phase models even when the air-to-liquid dynamic viscosity ratio is small. In particular, the separatrices in the liquid flow patterns at large contact angles disappear completely for a range of realistic viscosity ratios when the shear stress on the air side of the interface is accounted for. Experimentally observed motion of microdroplets near the contact line under combined action of gravity and moist air flow is described using our local flow model. We demonstrate that analysis of droplet trajectories leads to unambiguous determination of the local evaporative flux profile. A numerical finite-element approach for the steady diffusion equationis then used to extract the same flux profile from the global solution for concentration field in the limiting case of very thin liquid layer and small contact angle. The local evaporation rate is underpredicted by the numerical method, most likely due to the neglect of convective mass transfer in the air.

Laser hexagonal texture on surface of Ti6Al4V for the improvement of fluid spreadability and tribological properties

The joint capsule removal after artificial joint replacement surgery have led to improper lubrication, causing the pair to wear out quickly and reducing the joint lifespan. In this paper, laser processing and chemical corrosion were used to prepare a hexagonal convex texture on the surface of titanium alloy (Ti6Al4V). After etching and laser polishing, SEM images indicated the presence of secondary micro-nano textures in the grooves around the hexagonal texture, and the formation of anatase oxides on the surface, resulting in an increase of the surface energy and a very small contact angle (CA). The surfaces’ CA increases with the texture ratio, and the surface is super-hydrophilic when the texture ratio is less than 0.84. Furthermore, the effect of texture parameters and directions are studied by using UHMWPE and Ti6Al4V as friction pairs and simulated body fluid as lubricant. The COF is 0.068 with 0.84 area ratio, which is 51.4% lower than the original surface. The wear rate of UHMWPE on the textured surface decreases by 74.5% after two hours of tribological testing. In addition, high speed camera images and calculation results proved that creating grooves can promote fluid distribution on the textured surface. The surface texture on titanium alloy results in a significant COF and wear reduction, extending the service life of artificial joints.

Intrusion of liquids into liquid-infused surfaces with nanoscale roughness.

We present a theoretical study of the intrusion of an ambient liquid into the pores of a nanocorrugated wall w. The pores are prefilled with a liquid lubricant that adheres to the walls of the pores more strongly than the ambient liquid does. The two liquids are modeled as a binary liquid mixture of two species of particles, A and B. The mixture can decompose into a liquid rich in A particles, representing the ambient liquid, and another one rich in B particles, representing the liquid lubricant. The wall is taken to attract the B particles more strongly than the A particles. The ratio w-A/w-B of these interaction strengths is changed in order to tune the contact angle θ_{AB} formed by the A-rich/B-rich liquid interface between the two fluids and a planar wall, composed of the same material as the one forming the pores. We use classical density functional theory in order to capture the effects of microscopic details on the intrusion transition, which occurs as the concentration of the minority component or the pressure in the bulk of the ambient liquid is varied, moving away from bulk liquid-liquid coexistence within the single-phase domain of the A-rich bulk ambient liquid. These liquid structures have been studied as a function of the contact angle θ_{AB} and for various widths and depths of the pores. We also studied the reverse process in which a pore initially filled with the ambient liquid is refilled with the liquid lubricant. The location of the intrusion transition, with respect to its dependence on the contact angle θ_{AB} and the width of the pore, qualitatively follows the corresponding shift of the capillary-coexistence line away from the bulk liquid-liquid coexistence line, as predicted by a macroscopic capillarity model. Quantitatively, the transition found in the microscopic approach occurs somewhat closer to the bulk liquid-liquid coexistence line than predicted by the macroscopic capillarity model. The quantitative discrepancies become larger for narrower cavities. In cases in which the wall is completely wetted by the lubricant (θ_{AB}=0) and for small contact angles, the reverse transition follows the same path as for intrusion; there is no hysteresis. For larger contact angles, hysteresis is observed. The width of the hysteresis increases with increasing contact angle. A reverse transition is not found inside the domain within which the ambient liquid forms a single phase in the bulk once θ_{AB} exceeds a geometry-dependent threshold value. According to the macroscopic capillarity theory, for the considered geometry, this is the case for θ_{AB}>54.7^{∘}. Our computations show, however, that nanoscale effects shift this threshold value to much higher values. This shift increases strongly if the widths of the pores become smaller (below about ten times the diameter of the A and B particles).

Theoretical analysis of bubble nucleation in liquid film boiling

Many industrial applications such as electronic cooling and thermal desalination have adopted the heat dissipation technologies of capillary evaporation and liquid film boiling, with bubble nucleation being the transition criterion between them. In this paper, a theoretical model for bubble nucleation in liquid film boiling is developed, which mainly considers three aspects: transient heat conduction inside the liquid film supported with porous wick, evaporation at the liquid-vapor interface, and superheat requirement for the stable existence of a bubble nucleus. The criterion for the onset of nucleate boiling (ONB) in liquid film boiling is established, and size range of active microcavities for bubble nucleation is obtained, as well as comparisons being made with that during pool boiling and flow boiling. The results indicate that the size range of active microcavities in liquid film boiling is narrower with the minimum size being several times larger, and bubble nucleation in liquid film boiling is much more difficult. Although superhydrophilic surface with small contact angle is disadvantageous to bubble nucleation, it will decrease the minimum size of effective microcavities radius within the size scope of a few micrometers, which is beneficial for ONB in liquid film boiling. Moreover, critical thickness to trigger ONB in liquid film boiling is found to decrease with increasing contact angle, augmenting superheat and strengthening effective thermal conductivity of the wick, and its theoretical prediction is validated with experimental data in the literature. Our model offers a new avenue for understanding the ONB in liquid film boiling, and therefore can serve as a guideline for future enhancement design.

Water droplet bouncing on a hierarchical superhydrophobic surface fabricated by hydrothermal synthesis and ultraprecision machining

The ability of a water droplet to bounce on a superhydrophobic surface is an important indication of the surface wetting properties. In this study, a method integrating hydrothermal synthesis with ultraprecision machining (UPM) is reported for fabricating a hierarchical NiO-FAS-17 coated copper microgroove surface. Contact angles and water droplet bouncing behaviors were tested to evaluate the hydrophobicity of sample surfaces. Large contact angles over 160° and small contact angle hysteresis not exceeding 5° were recorded, showing good water repellency for the NiO-FAS-17 coating. The droplet bouncing results presented a larger first rebound height and stronger tendency of droplet break-up on the hierarchical NiO-FAS-17 coated microgroove surface in comparison with the NiO-FAS-17 coated flat surface, indicating a better hydrophobicity of the hierarchical surface. This reveals that the hydrophobicity of a surface can be enhanced by introducing UPM fabricated microgroove patterns into nanostructured surfaces that already possess good hydrophobicity.

A macroscopic Washburn approach of liquid imbibition in wood derived from X-ray tomography observations

Imbibition of water and silicone oil in poplar and spruce is investigated at the anatomical level by X-ray tomography observations and at the macroscopic level by imbibition kinetics. Imbibition mechanisms depend on both liquid and species. In poplar, oil penetrates vessels with a small contact angle, consistent with the value measured on solid wood (ca. 20^{circ }). Surprisingly, no direct penetration of water was observed in vessels. The large contact angle for water blocks the capillary rise at the scars between vessel cells. In spruce, oil and water penetrate primarily in latewood, where bordered pits remain open. Subsequently, water slowly invades the rest of the growth ring, while transversal migration is quasi-absent for oil. These 3D observations were quantified to feed a simple imbibition model that satisfactorily simulates macroscopic imbibition kinetics. A 1D approach is sufficient for oil imbibition while a 2D approach is required for water, revealing dual scale effects.

Lubricity and Rheological Properties of Highly Dispersed Graphite in Clay-Water-Based Drilling Fluids

Improving the tribological characteristics of water-based drilling fluids by adding graphene-based lubricants has garnered attention because of the potential for a range of inorganic-material-based additives at high temperature. In this study, we constructed a green and simple adsorption approach to prepare highly dispersed graphite using a cationic surfactant for graphite modification. The findings demonstrated that the prepared graphite was highly dispersed in water and had a low sedimentation rate and small contact angle in distilled water. The concentration dosage of cetyltrimethylammonium chloride (CTAC) on graphite was 0.02 g/g. We evaluated the performance of the modified graphite as a lubricated additive in water-based drilling through a rheological study and viscosity coefficient measurement. The results showed that the viscosity coefficient of drilling fluid with 0.05% modified graphite was reduced by 67% at 180 °C. We proved that the modified graphite can significantly improve the lubrication performance of drilling fluid. Furthermore, we revealed the lubrication mechanism by analyzing the chemical structural and crystalline and morphological features of graphite through a particle size test, zeta potential test, Fourier transform infrared (FTIR) spectroscopy, X-ray powder diffraction (XRD), and scanning electron microscopy (SEM) measurements. The results indicated that the modification of graphite by CTAC only occurs through physical adsorption, without changing the crystal structure. These findings provide a reference for the development of high-performance water-based drilling fluids.

Releasing the Bubbles: Nanotopographical Electrocatalyst Design for Efficient Photoelectrochemical Hydrogen Production in Microgravity Environment.

Photoelectrochemical devices integrate the processes of light absorption, charge separation, and catalysis for chemical synthesis. The monolithic design is interesting for space applications, where weight and volume constraints predominate. Hindered gas bubble desorption and the lack of macroconvection processes in reduced gravitation, however, limit its application in space. Physico‐chemical modifications of the electrode surface are required to induce gas bubble desorption and ensure continuous device operation. A detailed investigation of the electrocatalyst nanostructure design for light‐assisted hydrogen production in microgravity environment is described. p‐InP coated with a rhodium (Rh) electrocatalyst layer fabricated by shadow nanosphere lithography is used as a model device. Rh is deposited via physical vapor deposition (PVD) or photoelectrodeposition through a mask of polystyrene (PS) particles. It is observed that the PS sphere size and electrocatalyst deposition technique alter the electrode surface wettability significantly, controlling hydrogen gas bubble detachment and photocurrent–voltage characteristics. The highest, most stable current density of 37.8 mA cm−2 is achieved by depositing Rh via PVD through 784 nm sized PS particles. The increased hydrophilicity of the photoelectrode results in small gas bubble contact angles and weak frictional forces at the solid–gas interface which cause enhanced gas bubble detachment and enhanced device efficiency.

Talcum-doped composite separator with superior wettability and heatproof properties for high-rate lithium metal batteries

Separator is supposed to own outstanding thermal stability, superior wettability and electrolyte uptake, which is essential for developing high-rate and safe lithium metal batteries (LMBs). However, commercial polyolefin separators possess poor wettability and limited electrolyte uptake. For addressing this issue, we put forward a composite separator to implement above functions by doping layered-silicate (talcum) into polyvinylidene fluoride (PVDF). With significant improvement of electrolyte absorption benefiting from the strong adsorption energy values (-1.64 ∼ -1.70 eV) between talcum and the electrolyte in lithium metal batteries, PVDF/Talcum (PVDF/TM) composite separator owns a small contact angle and superior electrolyte uptake. PVDF/TM composite separator with 10 wt% talcum (T-10) owns a tiny contact angle of 8°, while those of polypropylene (PP) and PVDF are 48° and 20° with commercial electrolyte. Moreover, the addition of thermotolerant talcum endows the T-10 composite separator with great thermostability, whose thermal shrinkage is only 5.39% at 150 °C for 0.5 h. The cell with LiFeO4 cathode and the T-10 composite separator reaches 91.7 mAh/g in discharge capacity at 4.8 mA/cm2 (10 C), far superior to that with pure PVDF separator (56.3 mAh/g) and PP (51.4 mAh/g).

Spatters and spills: Spreading dynamics for partially wetting droplets

We present a solvable model inspired by dimensional analysis for the time-dependent spreading of droplets that partially wet a substrate, where the spreading eventually stops and the contact angle reaches a nonzero equilibrium value. We separately consider small droplets driven by capillarity and large droplets driven by gravity. To explore both regimes, we first measure the equilibrium radius vs a comprehensive range of droplet volumes for four household fluids, and we compare the results with predictions based on minimizing the sum of gravitational and interfacial energies. The agreement is good and gives a reliable measurement of an equilibrium contact angle that is consistent in both small and large droplet regimes. Next, we use energy considerations to develop equations of motion for the time dependence of the spreading, in both regimes, where the driving forces are balanced against viscous drag in the bulk of the droplet and by friction at the moving contact line. Our approach leads to explicit prediction of the functional form of the spreading dynamics. It successfully describes prior data for a small capillary-driven droplet, and it fits well to new data we obtain for large gravity-driven droplets with a wide range of volumes. While our prediction for the dynamics of small capillary-driven droplets assumes the case of thin nearly wetting droplets, with a small contact angle, this restriction is not otherwise invoked.

Tolerance analysis of wedge assembly considering impact force

This paper proposes a dynamic theory based tolerance analysis method for wedge assembly. Wedge is a class of contact features with a small contact angle such as cone and triangle. The impact usually applied in wedge assembly to tighten the structure. The force and times of the impact could affect the assembly dimension and must be considered in tolerance analysis. The wedge contact is formulated as the dynamic model, which the model could be solved to obtain the variation length. Then the variation could be compensated to the tolerance model or dimension chain. The proposed method is used in a case of wedge belt assembly for verification.

Simulation investigation of the spontaneous motion behaviors of underwater oil droplets on a conical surface.

A conical surface can realize the spontaneous transportation of micro-sized oil droplets in an aqueous environment without energy input, exhibiting great potential for applications in microfluidics, chemical micro-reactors, water remediation, etc. However, the precise manipulation of an oil droplet on a cone is still very challenging because the dynamic behavior of a droplet on a cone is not fully understood. Herein, the dynamic behavior of oil droplets on a cone is quantitively studied via numerical simulations, and the effects of wettability, apex angle, and droplet size on the droplet's dynamic behavior are systematically analyzed. The results show that the moving velocity and transport distance of the droplet on the cone are highly related to the droplet shape on the cone. It was found that a clamshell-shaped droplet moves faster than a barrel-shaped droplet. Besides, the clamshell-shaped droplet with a larger size, on the cone with a smaller apex angle and smaller contact angle tends to obtain a faster moving speed and a longer transportation distance. The droplet shape adopted on the cone was determined by the cone wettability and the size of the droplet relative to the local curvature of the cone. It was found that the oil droplet tends to form a barrel shape on the cone with a highly oleophilic and small apex angle, and tends to form a clamshell shape on cones with a highly oleophobic and large apex angle. In addition, the droplet might transit from a barrel shape to a clamshell shape when it moves from the cone tip to the cone base, and the trigger time of the transit is negatively correlated with the contact angle and apex angle of the cone. This work provides a microscale understanding of the dynamic behavior of an underwater oil droplet on a cone, and also offers theoretical guidance for manipulating the behavior of a droplet on a cone and for the rational design of cone surfaces for spontaneous droplet transport and droplet collection.

Modern methods of surface modification for new-generation titanium alloys

The constantly growing need for the use of implants in osteotomy is mainly due to the aging population and the need for long-term use of this type of biomaterials. Improving implant materials requires the selection of appropriate functional properties. Currently used titanium (Ti) alloys, such as Ti6Al4V and Ti6Al7Nb, are being replaced by materials with better biocompatibility, such as vanadium (V) or niobium (Nb), allowing for creation of the so-called new generation alloys. These new alloys, with the incorporation of zirconium (Zr), iron, and tantalum, possess Young’s modulus close to that of a bone, which further improves the improves the biomaterial’s. biocompatibility. This article describes the atomic layer deposition (ALD) method and its possible applications in the new generation of titanium alloys for biomedical applications. Also, the exemplary results of tin oxide (SnO2) thin coatings deposited by ALD and physical vapor deposition (PVD) methods are presented. This study aimed to evaluate the physicochemical properties of a Ti13Nb13Zr alloy used for elements in the skeletal system. As the temperature and the number of cycles vary, the results demonstrate that the surface area of the samples changes. The uncoated Ti13Nb13Zr alloy exhibits hydrophilic properties. However, all coated specimens improve in this respect and provide improved clinical results. after the applied modification, the samples have a smaller contact angle, but still remain in the range of 0–90°, which makes it possible to conclude that their nature remains hydrophilic. Coating the specimens decreased the mineralization risk of postoperative complications. As a result, the biomaterials demonstrated improved effectiveness, decreased complication indicators, and improved patient well-being

A high-density nickel-cobalt alloy embedded in nitrogen-doped carbon nanosheets for the hydrogen evolution reaction.

The development of novel non-noble electrocatalysts is critical for an efficient electrochemical hydrogen evolution reaction (HER). In this study, high-density nickel-cobalt alloy nanoparticles embedded in the bent nitrogen-doped carbon nanosheets are prepared as a high-performance catalyst. The optimized Ni7Co3/NC-500 catalyst displays quite a low overpotential of 90 mV at a current density of 10 mA cm-2, and a small Tafel slope of 64 mV dec-1 in alkaline medium, and even performs better than commercial 20% Pt/C at a high current density (η150 = 233 mV for Ni7Co3/NC-500 and η150 = 267 mV for 20% Pt/C). Specifically, the high-density nickel-cobalt alloy (with an average size of 6.2 nm and a distance of <3.0 nm) embedded in the bent carbon nanosheets provides plentiful active sites. Furthermore, in situ visualization of the produced hydrogen bubbles shows that the small size of hydrogen bubbles (d = 0.2 mm for Ni7Co3/NC-500 vs. d = 0.8 mm for 20% Pt/C) resulting from the small water contact angle and the bent nanosheet structure would inhibit the aggregation of H2 bubbles on the surface to facilitate efficient mass diffusion. Density functional theory calculations reveal that the formation of the nickel-cobalt alloy can effectively lower water dissociation energy barriers and optimize hydrogen adsorption Gibbs free energy, manifesting a high HER activity.

Aperture total internal reflection (A-TIR) for contact angle measurement

Recently, aperture total internal reflection (A-TIR) was proposed to characterize the microdroplet patterns, such as the coverage fraction of the droplet, by placing the aperture just in front of the detector in classical total internal reflection (TIR). However, the reflection from the curved liquid-air interface was simulated using simple two-dimensional modeling, causing inaccuracy in A-TIR measurement. In addition, the reflectance dependency on the aperture size and the working distance of the aperture was not investigated, hindering its applications. In this study, the simulation based on three-dimensional (3-D) ray tracing with Fresnel equation modeling was successfully developed and verified to explain the internal reflection from the curved droplet liquid-air interface. With this developed 3-D modeling, A-TIR characteristics were explored using the parameters of the aperture size and the working distance of the aperture as well as the droplet surface coverage fraction, which shows a good agreement between the experiment and the simulation. Furthermore, it was for the first time demonstrated that the droplet contact angle can be effectively determined by obtaining the droplet thickness from the analytic quadratic solution by subtracting the measured reflectance at the two different sized apertures and using the spherical profile relation. Low contact angles in the range of 1∼ 15° were determined experimentally for the micro- and macro-sized droplets with a droplet diameter of 70 ∼ 7000 µm by the measured thickness of 1 ∼ 450 µm using A-TIR and compared with Fizeau interferometry and side-view imaging to show a good agreement. The simulation shows that A-TIR can be a new optical diagnostic tool to measure the contact angles 0 ∼ 90° regardless of the droplet diameter by adjusting the aperture size and the working distance. In addition, A-TIR can effectively determine the small contact angles less than 5°, even ultrasmall contact angles less than 1° for the submicron thickness, not requiring the complicated microscope setup. Thus, we can observe a sessile droplet's drastic contact angle change during wetting phenomena from 90° to 0° on the same A-TIR setup. Additionally, A-TIR can be used for a single or an array of micro or nanodroplets with a microscope objective by reducing the laser beam size and scanning methodology.

Ultrastructural and Physicochemical Characterization of a Non-Crosslinked Type 1 Bovine Derived Collagen Membrane.

In this work, in vitro testing was used to study the properties of non-crosslinked type 1 bovine derived collagen membranes used in bone regeneration surgery. Collagen membranes were prepared, their surface roughness was quantified by interferometry, their morphology was observed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), their wettability was measured by the contact angle technique, their mechanical properties were investigated by tensile testing, their phase transformation temperatures were measured by Differential Scanning Calorimetry (DSC), and their biocompatibility was evaluated by immunological testing. The calorimetry tests showed that the membrane is formed only by type 1 collagen. The SEM observations showed that the morphology consists of layers of highly organized collagen fibers and patterns of striated fibrils typical of type 1 collagen. The small contact angle showed that the membrane is hydrophilic, with the possibility of rapid absorption of body fluids. The tensile tests showed that the membrane has enough elasticity, ductility, and mechanical strength for use in tissue regeneration. With the immunostaining technique, it was possible to confirm the membrane biocompatibility.

Experimental Study on the Heat Transfer Performance of a Stainless-Steel Heat Pipe With Sintered Fiber Wick

Abstract A kind of stainless-steel heat pipe with sintered fiber wick is investigated with the aim to improve the heat dissipation when it is used in spent fuel pools in nuclear power plants. The effects of test angle, porosity, and the filling rate on the heat transfer performance of the heat pipe are studied. At a test angle of 90 deg, the permeability plays an important role in the power limit since gravity can provide the necessary driving force. Larger porosity involves poor heat conductivity although it results in better permeability. When the test angle is zero, gravity is no longer the driving force. In this case, the evaporation section can still avoid dry burning because part of the evaporation section is dipped in deionized water. Therefore, permeability and filling ratio are two important factors influencing the power limit. Filling rate determines the vapor-flowing space. When the test angle is smaller than zero, gravity becomes a resistance force. Then, the lag tension and the filling rate exert the greatest influence on the performance of the heat pipe. Smaller porosity corresponds to a smaller contact angle.

Analysis of wetting behavior and its influencing factors of rejuvenator/old asphalt interface based on surface wetting theory

In hot recycling engineering of asphalt pavement, the fusion effect between rejuvenator and RAP binder which is closely related to the wettability will remarkably affect the regeneration effect of old material. To analyze the wetting behavior and its influencing factors of rejuvenator/old asphalt interface and further to optimize the asphalt rejuvenator, the dynamic contact angles of different rejuvenators at old asphalt surface were measured by using dynamic surface tension meter. Also, based on the surface wetting theory, the wetting parameters of rejuvenator at old asphalt surface were calculated based on the contact angle test results, so as to comprehensively evaluate the wetting behavior of rejuvenator/old asphalt interface and analyze its influencing factors. The results show that it is easier for rejuvenator to wet on the surface of aged modified asphalt than on the surface of aged matrix asphalt. The deepening of aging of asphalt makes it more difficult for rejuvenator to infiltrate on its surface spontaneously, and the thermal-oxidative aging shows the similar effect as photo-oxidation aging. The wetting effect of bio-rejuvenator is better than that of mineral oil rejuvenator, and four rejuvenators can all infiltrate but cannot spread on the surface of aged asphalt. The interfacial wettability of rejuvenator/old asphalt is affected by the interaction of environmental temperature, surface tension, contact angle, viscosity and aging degree of old asphalt, and the effect of viscosity and contact angle on the interfacial wettability is stronger than that of surface tension. Therefore, when selecting asphalt rejuvenator, it is recommended to select the rejuvenator with lower viscosity, larger surface tension and smaller contact angle with aged asphalt, and the lower viscosity is especially the primary consideration. The findings deeply reveal the wetting behavior of rejuvenator/old asphalt interface, and provide a theoretical basis for the development of efficient-performance rejuvenator.

Contact angle of modified fibrovascular bundle of salacca (Salacca sumatrana Becc.) frond by NaOH+Na2SO3 combination

The fibrovascular bundle (FVB) of the salacca frond is one of the potential raw materials in the development of bio-composite technology. The purpose of this study was to investigate the wettability of FVB using the contact angle method after the alkali modification treatment. The method of this research was to use FVB frond of Salacca sumatrana Becc. which was treated with alkaline modification of the combination of NaOH+Na2SO3 at various concentrations. The results showed that the combination of NaOH 1M+Na2SO3 0.4 M had the smallest contact angle, which means that the FVB has a good wettability value compared to the control treatment. Based on the results, it can be concluded that the modification of NaOH+Na2SO3 can increase the wettability of FVB.