Static Contact Angle Measurements Research Articles

Stearic Acid Modified Nano-ZnO Superhydrophobic Coating for Steel Mesh

Abstract To mitigate the detrimental effects of water on metal textiles, hydrophobic modification of such materials has garnered significant attention. However, traditional approaches often rely on complex procedures or costly materials, limiting their widespread application. Herein, we present a facile method for fabricating a superhydrophobic coating on steel mesh, and characterize the properties of the modified material. Initially, the surface of the dry steel mesh is uniformly coated with nano-ZnO crystals using a liquid deposition technique at room temperature. Subsequently, stearic acid is employed to hydrophobically modify the ZnO crystals, yielding a ZnO-based superhydrophobic coating. The influence of ZnO concentration and deposition duration on the surface crystal structure, hydrophobicity, and abrasion resistance is investigated. X-ray diffraction (XRD) analysis is performed to study the surface groups before and after hydrophobic modification, while static contact angle measurements are used to assess the hydrophobic properties of the coated surface. Remarkably, even after abrasion with 1000-mesh sandpaper, the superhydrophobic properties of the steel mesh with an optimized ZnO concentration decrease by only 4%. This simple, cost-effective, and highly efficient preparation method holds promising potential for applications in related fields.

Synthesis of mesoporous niobium phosphosilicate with high catalytic activity in the conversion of glucose to 5‐hydroxymethylfurfural in water solvent

AbstractMesoporous niobium‐based solid acid catalysts were successfully synthesized using the soft template method with sodium lignosulfonate (SLS) as the template. In most studies the template is calcined to form mesopores after hydrothermal synthesis; however, in this study SLS was retained to produce niobium‐carbon composite catalysts. The catalysts obtained were characterized by X‐ray diffraction, nitrogen adsorption–desorption, Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, and static contact angle measurements. The catalytic activity of the solids was also investigated in the conversion of glucose to 5‐hydroxymethylfurfural (HMF) using pure water as the solvent. Under optimal conditions, niobium‐carbon composite catalyst achieved a glucose conversion yield of 65.1% and an HMF yield of 42.1%. The enhanced catalytic activity was attributed to the timely extraction of the HMF by the carbonized SLS.

Accurate and Robust Static Hydrophobic Contact Angle Measurements Using Machine Learning.

We present a machine learning (ML) approach to static contact angle measurement, trained on a large data set (>7.2 million) of half drop contours based on solutions to the Young-Laplace equation where the contact angle is known a priori (removing all sources of error from human input). The data set included the effects of surface roughness, gravity, the size of drop relative to the image, and reflections of the drop on the surface. The presented ML model (valid for contact angles >110°), in combination with a new automated image and contour processing approach, is shown to be more accurate than other methods when benchmarked against an experimental data set, with an estimated error of 1°. The ML model is also 2 orders of magnitude faster at predicting contact angles than Young-Laplace fitting (the current best practice approach). The accuracy and speed of the presented approach provides a viable pathway toward robust and reproducible high-throughput contact angle analysis. This approach, Conan-ML, is open-source and provided for the use and development of new approaches to goniometry.

Fabrication of a salivary amylase electrochemical sensor based on surface confined MWCNTs/β-cyclodextrin/starch architect for dental caries in clinical samples

Salivary α-amylase (α-ALS) has drawn attention as a possible bioindicator for dental caries. Herein, combining the synergistic properties of multi-walled carbon nanotubes (MWCNTs), β-cyclodextrin (β-CD) and starch, an electrochemical sensor is constructed employing ferrocene (FCN) as an electrochemical indicator to oversee the progression of the enzymatic catalysis of α-ALS. The method involves a two-step chemical reaction sequence on a screen-printed carbon electrode (SPCE). X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Field emission scanning electron microscope (FE-SEM), and Dynamic light scattering (DLS) were used to characterize the synthesized material, while Static water Contact angle measurements, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) were performed to monitor each step of sensor fabrication. The electrochemical sensor permitted to detect α-ALS within the linear range of 0.5–280 U mL−1, revealing detection (LOD), and quantification (LOQ) values of 0.041 U mL−1, and 0.159 U mL−1, respectively. Remarkably, the sensor demonstrated exceptional specificity and selectivity, effectively discriminating against other interfering substances in saliva. Validation of the method involved analyzing α-ALS levels in artificial saliva with an accuracy range of 97 % to 103 %, as well as in real clinical saliva samples across various age groups.

Surface properties of laser-woven magnesium alloys based on dot-matrix processing

Abstract This paper investigates the enhancement of surface properties of magnesium alloys through infrared nanosecond laser processing with a focus on creating hydrophobic and wear-resistant surfaces. By manipulating dot-matrix microgroove sizes on the magnesium alloy surfaces, the research evaluates the influence on hydrophobicity and mechanical durability. The experimental results reveal that larger microgrooves contribute to increased hydrophobicity due to decreased liquid-solid contact, confirmed by static contact angle measurements which align with predictions from the Cassie-Baxter model. Mechanical durability tests, involving sandpaper abrasion, demonstrate that the surface integrity is maintained despite wear, attributed to the effective laser-texturing approach. The hydrophobic surfaces were achieved through a low-surface-energy modification using fluorosilanes, followed by a thermal treatment to ensure durability. The findings highlight the potential of this processing method in applications requiring robust, hydrophobic materials such as biomedical and engineering materials, offering a cost-effective and efficient solution for industry-scale problems. This work not only extends the understanding of surface engineering via laser texturing but also provides a novel approach for optimizing surface properties crucial for advanced material applications.

Analysing the surface morphology of annealed FTO/ZnS bilayer films: stereometric, fractal, and wettability approaches

The surface micromorphology and roughening of the thermal evaporation-coated FTO/ZnS bilayer thin films annealed at 300, 400, 500, and 550∘C\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$550\\,^\\circ{\ ext{C}}$$\\end{document} for 1 h have been studied. AFM images of the prepared samples were analysed by the MountainsMap software, and the effects of the annealing temperature on the surface texture of the FTO/ZnS thin film’s surface were investigated. Stereometric and advanced fractal analyses showed that the sample annealed at 500∘C\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$500\\,^\\circ{\ ext{C}}$$\\end{document} exhibited greater surface roughness and greater skewness and kurtosis. This film also has the most isotropic surface and exhibits the highest degree of heterogeneity. Also, despite the decrease in surface roughness with increasing temperature from 500 to 550∘C\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$550 \\,^\\circ{\ ext{C}}$$\\end{document}, the fractal dimension tends to increase. The static water contact angle measurements indicate that the film annealed at 500∘C\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$500 \\,^\\circ{\ ext{C}}$$\\end{document} exhibits higher hydrophobicity, which can be attributed to its greater topographic roughness. Our research indicates that the surface morphology of FTO/ZnS bilayer thin films is influenced by the annealing temperature. Changing factors such as roughness, fractality, and wettability parameters to help improve surface performance make the FTO/ZnS bilayer suitable for application in electronic and solar systems.

Regulating material wettability through surface plastic deformation post-processing via friction modification

The wettability of engineering materials significantly influences their cleaning and antifreeze properties, making it a key consideration in aerospace applications. Methods for controlling surface plastic deformation can alter the wettability of materials and contribute to a certain level of strengthening effect, thereby presenting significant application potential. This study aimed to modify the wetting characteristics of aviation titanium alloys in harsh environments through adjustments in surface roughness via peening treatments (such as laser shock peening with coating and mechanical shot peening). The impact of various peening processes on wetting characteristics was investigated through comprehensive surface energy, macro, and nano morphology analyses. Static contact angle measurements were quantified, followed by evaluating other properties, such as surface free energy. Through adjustments in post-treatment processes and control of surface roughness, tailored acquisition of wetting characteristics was achieved. This study elucidates the beneficial effect of surface plastic deformation post-processing on controlling material wettability and introducing strengthening effects. Additionally, the study indicates the importance of accurately determining the sampling range for precise characterization of material wettability.

Gallium-doped zirconia coatings modulate microbiological outcomes in dental implant surfaces.

Despite the significant recent advances in manufacturing materials supporting advanced dental therapies, peri-implantitis still represents a severe complication in dental implantology. Herein, a sol-gel process is proposed to easily deposit antibacterial zirconia coatings onto bulk zirconia, material, which is becoming very popular for the manufacturing of abutments. The coatings' physicochemical properties were analyzed through x-ray diffraction and scanning electron microscopy-energy-dispersive x-ray spectroscopy investigations, while their stability and wettability were assessed by microscratch testing and static contact angle measurements. Uniform gallium-doped tetragonal zirconia coatings were obtained, featuring optimal mechanical stability and a hydrophilic behavior. The biological investigations pointed out that gallium-doped zirconia coatings: (i) displayed full cytocompatibility toward human gingival fibroblasts; (ii) exhibited significant antimicrobial activity against the Aggregatibacter actinomycetemcomitans pathogen; (iii) were able to preserve the commensal Streptococcus salivarius. Furthermore, the proteomic analyses revealed that the presence of Ga did not impair the normal oral microbiota. Still, interestingly, it decreased by 17% the presence of Fusobacterium nucleatum, a gram-negative, strictly anaerobic bacteria that is naturally present in the gastrointestinal tract. Therefore, this work can provide a valuable starting point for the development of coatings aimed at easily improving zirconia dental implants' performance.

Reshapable bio-based thiol-ene vitrimers for nanoimprint lithography: Advanced covalent adaptability for tunable surface properties

Taking inspiration from natural surfaces known for their ability to adaptively remodel their shape, we fabricated stimuli-responsive microstructures by using UV-induced nanoimprint lithography. For this, a fully bio-based dynamic thiol-ene photopolymer was synthetized by the radical mediated addition of a trifunctional eugenol-based thiol (SH3E) crosslinker across an allylated linseed oil (ALELO). To catalyze the bond exchange reactions between the hydroxyl and ester groups within the network, a bio-based eugenol phosphate ester was introduced as a transesterification catalyst. Pure eugenol was further added as a reactive diluent to increase the number of hydroxyl groups and thus, accelerate the thermo-activated bond exchange reactions. Once cured by UV exposure, the dynamic photopolymer is thermally stable up to 250 °C and is able to relax 63% of the original stress within 62 min at 160 °C. Subsequently, films with micropillars, having an aspect ratio of 1:2.5 were prepared by using nanoimprint lithography. The macroscopic reflow capability of the dynamic network enabled a reorientation of the imprinted structures during a thermal reshaping step. The imprints were characterized by 2D/3D optical microscopy, μCT imaging and static water contact angle measurements. Based on the orientation of the micropillars, the water contact angle was varied between 118° and 95°, giving rise to a possible application in microfluidic devices.

Session 18. Oral Presentation for: Static contact angle, interfacial tension, and column height measurements for underground hydrogen storage

Session 18. Oral Presentation for: Static contact angle, interfacial tension, and column height measurements for underground hydrogen storage

Effect of Process Parameters on the Roughness and Wetting Characteristics of SS304 Surfaces Using Electrolytic and Plasma Electrolytic Polishing Techniques

Metallic parts manufactured by conventional machining and additive manufacturing techniques possess poor surface quality and require post-processing operations before their end-use. Many methods exist for the post-processing of parts with free-form surfaces. In this study, two of the most used polishing techniques, electrolytic polishing (EP) and plasma electrolytic polishing (PeP), were investigated to understand the morphology of the resultant surface after both techniques. Pilot experiments suggested that an aqueous solution of ammonium sulphate is the most effective electrolyte for both the polishing techniques in terms of the lowest achievable value of average surface roughness ( Ra ). A systematic investigation of the electrolyte concentration, applied voltage, and polishing time revealed an identical dependence on all these process parameters: First, a decrease and then an increase in Ra. A minimum Ra of 0.63 μm and 0.49 μm were achieved with EP and PeP, respectively. Samples polished by PeP possess high gloss with negligible changes to the shape and form of the samples. Furthermore, static contact angle measurements with water revealed that surfaces treated with PeP showed higher hydrophilicity compared to those polished with EP. This can be attributed to the lower Ra value achieved with PeP.

Fabrication of three‐dimensional micropatterned hydrophobic surfaces by fused filament fabrication printing technology

AbstractIn recent years, the interest in structured hydrophobic surfaces has considerably grown, finding applications in many industrial fields, including aerospace, automotive, and biomedical. Three‐dimensional (3D) printing technology is a simple, rapid, and economic process to fabricate structured surfaces based on neat polymers and composite materials, allowing working with a wide variety of plastic materials. The manufactured surfaces show a roughness depending on the printing design and the printing resolution: this characteristic is ideal to achieve superhydrophobic properties. Furthermore, patterned surface structures can be printed by fused filament fabrication (FFF), so increasing the hydrophobic character of the samples; indeed, micro‐ and nanosurface structures are required to make a hydrophobic surface. In this study, 3D micropatterned textures of pillars were printed by FFF using polylactide (PLA) and polypropylene (PP) as polymer filaments and PLA/carbon nanotubes (PLA/CNTs) and PP/carbon fibers (PP/CF) as composite filaments. Morphologies of printed specimens were analyzed by optical microscopy and scanning electron microscopy. Good correspondence was found between pillar dimensions and edge‐edge pillars distance of computer aided design (CAD) and composites 3D‐printed samples. Their wettability was evaluated by static contact angle (CA) measurements. Results clearly show a significant increase of water CA values up to 50% in all micropatterned samples with respect to flat surfaces. This improvement was achieved by surface microstructuring without the use of nanoparticles and/or chemical treatment.

Static and impact performance of engineered cementitious composites with hybrid graphite nano platelets modified PVA and shape memory alloy fibres

Polyvinyl alcohol (PVA) fibre has been widely adopted to produce engineered cementitious composites (ECC), the overall performance of which is highly dependent on the fibre surface characteristics. The traditional approach to improve PVA fibre bridging ability is to tailor the surrounding matrix properties. However, this common practice need to do a lot of laborious experimental works, and thus it has limited efficiency and practicality. Therefore, special surface treatments on PVA fibres are required to create synergistic interactions between fibre and surrounding matrix to retain excellent tensile ductility and better mechanical performance. This paper proposes a novel treatment method for PVA fibres using nano graphite platelets to modify the PVA fibre surface and improve the mechanical properties of PVA fibre reinforced ECC. To evaluate the effectiveness of such treatment, a systematic experimental study was performed. Firstly, static contact angle measurements, scanning electron microscopy and atomic force microscopy were employed to monitor the wettability and physical changes on the fibre surface. Then, the static and dynamic mechanical properties as well as microstructural characteristics of ECC with hybrid modified PVA fibres (2 vol%) and shape memory alloy (SMA) fibres (0.25 vol%, 0.50 vol% and 1 vol%) were examined. The results indicate that the graphite nanoplatelets treated PVA fibres (GPVA) exhibit high hydrophobicity and surface roughness providing steady-state crack propagation, which is a necessary condition to ensure multiple cracking and improving the higher fibre bridging complementary energy. This is evidenced by significantly densified the transition zone between the graphite treated PVA fibres and the matrix, and improved the flexural tensile strength and the toughness. The calculated surface roughness of 28.86 μm and lots of peaks and valleys on the 3D topographical micrographs of the cracking faces confirmed that 1 SMA-2 GPVA specimen efficiently participated in transferring stress through the composite, leading to a greater vertical impact reaction force. Finally, the structure-property relation for flexural versus fracture behaviour and the effectiveness of SMA fibres on the crack-healing feature of the composites were studied by using digitized fractal analysis and through the heat treatment. The disseminated fracture energy (Ws/Gf) value reached 130 and the crack sizes the crack size decreased by 34 %, which were much better than that of the reference composites. The nano treatment of PVA fibres in ECC provides an innovative and sustainable solution for engineering structures with requirement of high tensile ductility and high impact resistance, e.g., military infrastructure and industrial floors.

Phenyl-Substituted Cage Silsesquioxane-Based Star-Shaped Giant Molecular Clusters: Synthesis, Properties, and Surface Segregation Behavior.

The crystallinity, solubility, and physical properties of polyhedral oligomeric silsesquioxane (POSS) compounds are highly dependent on their organic substituents. We previously synthesized a series of isobutyl-substituted star-shaped POSS derivatives with aliphatic chain linkers of different length. In this study, we prepared C3- and C6-linked phenyl-substituted star-shaped POSS derivatives (3Ph-C3 and 3Ph-C6) by the hydrosilylation of heptaphenylallyl- and hexenyl-POSS (1a and 1b) and octadimethylsiloxy-Q8-silsesquioxane (Q8M8H) (2), respectively, and their properties were compared with those of the corresponding isobutyl-substituted derivatives (5iBu-C3 and 5iBu-C6). Although 3Ph-C6 was only soluble in chloroform and insoluble in tetrahydrofuran (THF) and toluene, 3Ph-C3 was soluble even in THF and toluene, suggesting that the shorter linkers of the derivative afford a wider range of solvents for dissolution. Differential scanning calorimetry analysis showed that 3Ph-C3 exhibited a baseline shift at 190 °C and an endothermic peak at 316 °C. However, no clear baseline shift was observed for 3Ph-C6. Thermogravimetric analysis showed that the shorter linker in the phenyl-substituted star-shaped POSS derivative significantly increased the decomposition temperature compared with the longer linker. The annealed cast film of 3Ph-C3 at 340 °C above its melting temperature formed a transparent film even after cooling to room temperature. However, an opaque whitish film was formed in the case of 3Ph-C6. Poly(methyl methacrylate) (PMMA) films containing 2 wt % 3Ph-C3 and 3Ph-C6 were prepared by casting their chloroform solutions onto glass substrates overnight at room temperature. The static water contact angle measurements and XPS analysis for the castings film containing 3Ph-C3 and 3Ph-C6 suggested that degree of the segregation amount of 3Ph-C3 was larger than that of 3Ph-C6. The shorter linker length in the phenyl-substituted star-shaped POSS derivative, 3Ph-C3, with its greater predicted solubility in PMMA, exhibited entropy-driven surface segregation.

Static contact angle, interfacial tension, and column height measurements for underground hydrogen storage

Geological porous media are key for large-scale hydrogen (H2) storage and production, where fluid interactions at interfaces and within rock formations are vital for effective gas containment. Although advancements have been achieved in comprehending structural trapping for estimating column height (CH), additional insights are required regarding how pore size impacts this estimation. Currently, CH estimates often consider seal rock potential, without including the capillary contribution from reservoir rock pore for structural trapping capacity assessment. This study measures the static contact angle (CA) on Wolfcamp (WC) Shale and interfacial tension (IFT) under modified drainage and imbibition conditions at temperatures of 30 and 50°C, pressures ranging from 500 to 3000 psia, and a salinity of 10 wt% sodium chloride. Subsequently, the static gas CH was calculated, accounting for contributions from the caprock pores alone and both the caprock and reservoir, to assess the structural sealing capacity of the caprock layer. The experimental procedures are comprehensively detailed in this paper. The outcome indicates that the static CA after drainage for H2)/brine/WC shale rises with pressure as the static CA after imbibition decreases. Both CAs decrease with increasing temperatures. For H2/brine systems, both drainage and imbibition IFTs decline with increasing pressure and temperature. Calculated CHs reveal that lower CAs substantially impact the gas trapping capacity beneath the caprock. In summary, this study highlights the preference for the drainage method in measuring IFT and CA to evaluate the potential structural trapping capacity of injected gas by the overlying caprock.

Antibacterial Zirconia Surfaces from Organocatalyzed Atom-Transfer Radical Polymerization.

Antibacterial coatings are becoming increasingly attractive for application in the field of biomaterials. In this framework, we developed polymer coating zirconia with antibacterial activity using the "grafting from" methodology. First, 1-(4-vinylbenzyl)-3-butylimidazolium chloride monomer was synthesized. Then, the surface modification of zirconia substrates was performed with this monomer via surface-initiated photo atom transfer radical polymerization for antibacterial activity. X-ray photoelectron spectroscopy, ellipsometry, static contact angle measurements, and an atomic force microscope were used to characterize the films for each step of the surface modification. The results revealed that cationic polymers could be successfully deposited on the zirconia surfaces, and the thickness of the grafted layer steadily increased with polymerization time. Finally, the antibacterial adhesion test was used to evaluate the antibacterial activity of the modified zirconia substrates, and we successfully showed the antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa strains.

Bioinspired Superhydrophobic Nanocoating Based on Polydopamine and Nanodiamonds to Mitigate Bacterial Attachment to Polyvinyl Chloride Surfaces in Food Industry Environments.

Polyvinyl chloride (PVC) is commonly utilized as a food-contact surface by the food industry for processing and storage purposes due to its durability, ease of fabrication, and cost-effectiveness. Herein, we report a composite coating for the superhydrophobization of PVC without the use of polyfluoroalkyl chemistry. This coating rendered the PVC superhydrophobic, exhibiting a static water contact angle of 151.9 ± 0.7° and a contact angle hysteresis of only 3.1 ± 1.0°. The structure of this composite coating, consisting of polydopamine, nanodiamonds, and an alkyl silane, was investigated by utilizing both scanning electron microscopy and atomic force microscopy. Surface chemistry was probed using attenuated total reflectance-Fourier transform infrared, and the surface wetting behavior was thoroughly characterized using both static and dynamic water contact angle measurements. It was demonstrated that the superhydrophobic PVC was cleanable using a food-grade surfactant, becoming wet in contact with high concentration surfactant solutions, but regaining its nonwetting property upon rinsing with water. It was demonstrated that the coating produced a 2.1 ± 0.1 log10 reduction (99.2%) in the number of Escherichia coli O157:H7 cells and a 2.2 ± 0.1 log10 reduction (99.3%) in the number of Salmonella enterica Typhimurium cells that were able to adsorb onto PVC surfaces over a 24 h period. The use of this fluorine-free superhydrophobic coating on PVC equipment, such as conveyor belts within food production facilities, may help to mitigate bacterial cross-contamination and curb the spread of foodborne illnesses.

Gravimetric and electrochemical evaluation of environmentally novel nanopyrazole derivatives for 304 SS in acidic solution: AFM, SEM/EDX, contact angle, and DFT/MDs simulations

Influence of two novel corrosion inhibitors of bis(chromeno[4,3‐c]pyrazol‐4‐oxo‐2‐yl)phosphineoxide (CPO) and bis(4‐formyl‐3‐phenyl‐1H‐pyrazol‐1‐yl)phosphineoxide (FPO) on the localized corrosion protection of 304 stainless steel (304 SS) in a 1.0 M HCl solution was investigated at different concentrations (10−13−10−5 M) and at different temperatures (298–343 K). Weight loss and electrochemical measurements indicated that the pyrazole derivatives are efficient inhibitors for corrosion of 304 SS, and the inhibition efficiency was increased with inhibitor concentrations up to 73.18 and 98.50 % for CPO and FPO, respectively. Langmuir adsorption isotherm was found to be the more fitted model for the adsorption process description with mixed adsorption mechanisms. UV–visible and XRD measurements showed the formation of a protective film formed by corrosion inhibitors. The scanning electron microscope (SEM) images, energy dispersive X-ray spectroscopy (EDX), atomic force microscopy (AFM), and static contact angle measurement corroborated the protection provided by CPO and FPO inhibitors on the surface of 304 SS immersed in a 1.0 M HCl solution. FPO exhibits antibacterial activity, and CPO has antifungal activity. The relationships between the corrosion protection performance of the pyrazole derivatives, their structural properties, and the adsorption type were determined by density functional theory (DFT), natural bond orbital (NBO), and molecular dynamics (MD), which confirmed that FPO has a higher corrosion protection efficiency than CPO. The theoretical parameters were in good agreement with the experimental results.

Effect of Camera Parallax Angle on the Accuracy of Static Contact Angle Measurements.

Measuring the contact angle at the solid/liquid/vapor triple point in sessile drop experiments is one of the most popular and simple ways to quantify the wettability of surfaces and determine the surface free energy. Despite decades of technical advancements in contact angle measurements, which allowed for improving the precision of sessile drop measurements below ±1°, an often overlooked source of experimental error in these measurements originates from the camera's parallax angle (PA) - the angle between the camera optical axis and the sample stage surface. Here, we quantified the systematic errors in the measurement of contact angles due to the acquisition of drop images at finite PA values by simulating sessile drop experiments in which synthetic drops were created using the Young-Laplace equation. The absolute contact angle error induced by imaging drops at nonzero PAs was found to increase as the true contact angle (TCA) deviates from 90° and resulted in an overestimation (underestimation) of the contact angle for drops having TCAs lower (higher) than 90°. The computed absolute contact angle error reaches values as high as -20° (+12.2°) for drops having a TCA of 175° (5°) when imaged with a PA of 10°, thus indicating the importance of considering the PA when accurately quantifying contact angles in sessile drop experiments. The shape and, by extension, volume of the sessile drop was also found to affect the magnitude of the absolute contact angle error as sessile drops with higher apex curvatures exhibited lower absolute error than those with lower curvatures at any given PA. The outcomes of this work provide guidelines for minimizing systematic errors in sessile drop measurements due to the collection of drop images at nonzero PAs.

Hydrothermally synthetized WO3 coated stainless steel mesh for oil–water separation purposes

To separate oil–water mixtures especially in oil field operations, new energy-efficient methods are urgently required. Conventional separation techniques using demulsifiers for separation of oil–water mixtures or even use of membranes usually suffered from high cost and energy consumption, composition dependency of demulsifiers and fouling or inability of a single membrane to separate all types of oil–water mixtures. This research aimed to synthesize tungsten oxide-coated stainless steel mesh using the hydrothermal method, with a focus on evaluating its effectiveness in oil–water separation. The coating procedure was carried out using hydrothermal techniques, with an emphasis on investigating the impact of precursor concentration, pH levels, reaction temperature and duration, on the separation efficiency of the optimal coating solution. The hydrothermally coated stainless steel mesh was created within a polytetrafluoroethylene reaction vessel, submerged in a 150 ml aqueous solution containing 0.0094 mol of sodium tungstate di-hydrate at pH 3.0, achieved through the addition of hydrochloric acid. Additionally, 1 g of oxalic acid, acting as a chelating agent, was introduced. Subsequently, the mesh underwent a 4 h reaction at 220 °C and was subsequently annealed for 30 min in a 350 °C furnace. Remarkably, the resultant mesh exhibited an exceptional water separation flux of 9870 ± 15 L/hr/m2 when exposed to 1:1 v/v oil–water mixtures. This performance significantly outperformed previous filters designed for similar oil–water separation tasks. The mesh efficiently facilitated the passage of water through the oil–water mixture, achieving an efficiency rate exceeding 98 ± 1%. To gauge its wetting behavior, the hydrophilic/underwater oleophobic filter underwent static contact angle measurements. The filter's wetting mechanism was primarily attributed to its hierarchical surface structure, which enhanced surface hydrophilicity and roughness. Analytical techniques such as XRD, FTIR, and FE-SEM were employed to scrutinize the fabricated filter's composition. These analyses confirmed the successful creation of a nanostructured WO3 coating on both sides of the stainless steel mesh. Moreover, the utilization of commercially available chemicals and straightforward fabrication techniques underscores the promising potential of this approach for large-scale applications.