Contact Angle Research Articles

SIMPLIFIED METHOD FOR ESTIMATING A DYNAMIC LOADRATING FOR ROLLING BEARINGS

The method for calculating the dynamic load ratings of rolling bearings is described in the ISO 281 standard.The calculation procedure presented there requires reading appropriate values from many tables, dependingon the geometry of the bearing components. This approach makes numerical calculations and quick estimationof the dynamic load ratings for various bearing design variants difficult. Moreover, the tables are discrete(they provide selected values, e.g. for nominal bearing contact angles every 15), and intermediate values,in accordance with the commentary included in the ISO 281 standard, should be calculated using linearinterpolation. However, in reality, the parameters given in the tables are not linearly dependent on each other,which makes this interpolation inaccurate. In the context of the mentioned imperfections of the ISO 281standard, the aim of the work is to simplify the calculation procedure, adapt it to numerical applications,and replace linear interpolation with an appropriate non-linear function. The difference between the valuescalculated according to the proposed formula and the value calculated according to the ISO 281 standard is onaverage less than 0.5%.

Efficient Separation of Oil/Water by a Biodegradable and Superhydrophobic Composite Based on Loofah and Rice Straw

Membrane filtration is one of the preferred choices for petroleum wastewater disposal due to its simplicity and low energy consumption. In this paper, a biodegradable superhydrophobic membrane based on loofah and rice straw (LF-RS) was prepared and modified with dodecyltriethoxysilane to improve its stability, morphology, and performance. The membrane showed an efficiency of 99.06% for oil/water separation with an average water flux of 2057.37 Lm−2h−1 and a tensile strength of 11.19 MPa. The tensile strength of the LF-RS membrane was 322.47% higher than that of the PVDF membrane and 126.58% higher than that of the commercially available nitrocellulose membrane. Through molecular simulations, we showed a 96.3% reduction in interaction energy between water and membrane post-modification, which is beneficial for increasing the contact angle and separation performance. This study provides an option for the large-scale, cost-effective fabrication of eco-friendly membranes for pollutant removal.

A Review of the Mineral Contact Angle Measurements and Applications in the Froth Flotation Process: Techniques and Influential Parameters, Part II

A Review of the Mineral Contact Angle Measurements and Applications in the Froth Flotation Process: Techniques and Influential Parameters, Part II

A Universal Interfacial Reconstruction Strategy Based on Converting Residual Alkali for Sodium Layered Oxide Cathodes: Marvelous Air Stability, Reversible Anion Redox, and Practical Full Cell.

Mn-based layered oxide cathodes have attracted widespread attention due to high capacity and low cost, however, poor air stability, irreversible phase transitions, and slow kinetics inhibit their practical application. Here, we propose a universal interfacial reconstruction strategy based on converting residual alkali to tunnel phase Na0.44MnO2 for addressing the above mentioned issue simultaneously, using O3 NaNi0.4Fe0.2Mn0.4O2@2 mol % Na0.44MnO2 (NaNFM@NMO) as the prototype material. The optimized material exhibits an initial capacity and energy density comparable with lithium-ion batteries. The reversible anionic redox behavior and charge compensation mechanism of NaNFM@NMO were analyzed and verified by soft X-ray absorption spectrum and in situ X-ray absorption spectrum. Due to the intrinsic stability of the tunnel structure, excellent air stability and highly reversible structure evolution of the NaNFM@NMO cathode material are achieved, which are confirmed by contact angle test, rigorous aging test, and in situ X-ray diffraction. More importantly, the NaNFM@NMO cathode demonstrates a great match with the nonpresodiated hard carbon anode and shows excellent electrochemical performance of the full cell. Additionally, such a strategy could be also applied to modify P2-type cathodes, showing superior universality and good prospects in industrialized production. Overall, the proposed strategy could improve air stability while remaining interfacial and bulk stable simultaneously and will open up a whole new field for the optimization of other electrode materials.

Fabrication of superhydrophobic transparent coatings prepared by spraying dual-sized silica particles

Abstract Photovoltaic modules exposed to severe wind and sand conditions over extended periods often accumulate dust, significantly impacting their power generation efficiency. Superhydrophobic self-cleaning coatings present a promising solution to mitigate this issue. In this study, a SiO2/PU coating was applied to glass substrates using a combined sol-gel spraying technique. The sol system comprised a mixture of SiO2 particles with diameters of 20 nm and 200 nm, enabling the construction of a micro-nano structure that enhances surface hydrophobicity. The SiO2/PU coatings prepared with mixed particle sizes demonstrated significant improvements in contact angle, rolling angle, self-cleaning, and antifouling properties compared to those made with a single particle size, achieving a water contact angle of 164.52°. Furthermore, the prepared SiO2/PU coatings possess excellent stability and transmittance. It is anticipated that this superhydrophobic SiO2/PU coating will be a candidate for anti- dust applications in photovoltaic modules.

Enhancement of surfactant performance via titanium dioxide nanoparticles: implication for oil recovery in sandstone

The application of titanium dioxide nanoparticles in the petroleum research area has received ample attention in recent years owing to its impact on wettability-altering agents. Further, employing a surfactant injection to improve oil production in sandstone formations on an industrial scale has become an alternative solution, particularly for mature fields. However, the existing literature on the combination of alkyl ethoxy carboxylate (AEC) surfactant with titanium dioxide nanoparticles on the application of enhanced oil recovery in sandstone formations remains underreported. This study explores the impact of combining AEC surfactant with titanium dioxide nanoparticles on recovering trapped oil in sandstone by examining the interfacial tension, contact angle, zeta potential, and core flooding with various concentrations of added titanium dioxide nanoparticles (0, 0.01, 0.025, and 0.05 wt%) on AEC surfactant. Although the addition of 0.05 wt% TiO2 to AEC surfactant can significantly reduce the interfacial tension to the lowest value of 5.85 × 10−5 mN/m, our results show that the highest oil recovery in Berea sandstone (59.52% recovery factor) is achieved at the concentration of 0.025 wt% added TiO2 to AEC surfactant. We find that the stability of TiO2 nanoparticles on AEC surfactant plays a significant role in getting maximum oil recovery. These important findings from this study contribute to improving our understanding on the application of TiO2 combined with AEC surfactant to achieve more efficient and sustainable enhanced oil recovery in sandstone.

Development of photoactive biomaterial using modified fullerene nanoparticles

Medical device-associated biofilm infections continue to pose a significant challenge for public health. These infections arise from biofilm accumulation on the device, hampering the antimicrobial treatment. In response, significant efforts have been made to design functional polymeric devices that possess antimicrobial properties, limiting or preventing biofilm formation. However, until now none of the strategies showed a promissory effect. Thus, antimicrobial photodynamic therapy (aPDT) has been shown as a promising candidate to overcome this problem. Photosensitizers (PS) are the main key component for aPDT and fullerenes have been chosen as PS due to their good quantum yields and lifetimes spans. In this study, polylactic acid (PLA) surface was modified with fullerene (C60) and reaction was proven by XPS analysis. The biopolymer surface was characterized by AFM, SEM, and water contact angle measurements. The obtained results imply that the highest fullerene precipitation was attained when PLA was modified with ethylenediamine (EDA) before the reaction with C60, as the highest carbon increase was identified using XPS following reaction with C60. While samples’ hydrophobicity decreased after PLA modification with EDA, it increased after fullerene precipitation. Which implies that bacteria have a lower propensity to attach. Although the surface of the samples became smoother following PLA modification with EDA and reaction with 0.1% C60 precipitation, with 1% C60 precipitation the surface roughness was comparable to unmodified PLA, according to AFM and SEM analyses. Fullerene-based biopolymers could potentially be used in aPDT to make antimicrobial surfaces or medical devices.

Wettability of saliva substitutes across various denture base fabrication techniques.

The present study evaluated the contact angles (CAs) of four denture base materials subjected to different surface treatments using deionized water and saliva substitutes. A total of 32 rectangular specimens were manufactured using four different denture base materials: heat-cured compression molded Lucitone 199 (C), milled Lucitone 199 (M), Formlabs Denture Base RP (P), and SR Ivocap High Impact (I). The CA of the surface of the unaltered, mechanically polished, and sandblasted surface specimens was evaluated after the application of five saliva substitutes: Biotene, VEGA, Spry, Moi-Stir, Dentilube, and ionized water. Ten droplet measurements were obtained for each group, with each droplet analyzed for advancing contact angle (ACA), receding contact angle (RCA), and the contact angle hysteresis (CAH) was calculated. The data of the experiment was analyzed using 2-way ANOVA, (α=0.05) with Tukey's test. CAH was demonstrated to have statistically significant differences among the denture bases (p<0.05), with unaltered 3D printed exhibiting the largest CAH, followed by unaltered milled. The unaltered denture bases exhibited higher CAH than the polished, and there were no significant differences in CAH among the polished denture bases (p>0.05). Sandblasting increased the ACA of the milled and conventional bases. The saliva substitutes exhibited differences in ACA, with Spry and VEGA having the highest ACA, and Biotene had the lowest CA of all the saliva substitutes evaluated. The manufacturing methods of denture bases influences the CAH, while the chemical composition of the denture base specimens does not appear to affect CAH. Sandblasting increases the ACA for the milled and conventional groups. Saliva substitutes do impact the ACA. Drawing from previous research, it is hypothesized that a 3D-printed denture base or sandblasting a milled denture base may offer greater resistance to dislodgement.

Optimizing Carbon Structures in Laser-Induced Graphene Electrodes Using Design of Experiments for Enhanced Electrochemical Sensing Characteristics.

In this study, we explored the morphological and electrochemical properties of carbon-based electrodes derived from laser-induced graphene (LIG) and compared them to commercially available graphene-sheet screen-printed electrodes (GS-SPEs). By optimizing the laser parameters (average laser power, speed, and focus) using a design of experiments response surface (DoE-RS) approach, binder-free LIG electrodes were achieved in a single-step process. Traditional trial-and-error methods can be time-consuming and may not capture the interactions between all variables effectively. To address this, we focused on linear resistance and substrate delamination to streamline the DoE-RS optimization process. Two LIGs, designated LIG A and LIG B, were fabricated using distinct and optimized laser settings, which resulted in a sheet resistance of 25 ± 2 Ω/sq and 21 ± 1 Ω/sq, respectively. These LIGs, characterized by scanning electron microscopy, Raman spectroscopy, and contact angle analysis, exhibited a highly porous morphology with 13% pore coverage and a contact angle <50°, which significantly increased their hydrophilicity when compared to the GS-SPE. For the electrochemical studies, the oxidation of NO2- ion by the graphene-based working electrodes was investigated, as it allowed for the direct comparison of the LIGs to the GS-SPE. These included cyclic voltammetry, electrochemical impedance spectroscopy, and differential pulsed voltammetry studies, which revealed that LIG electrodes displayed a remarkable 500% increase in peak current during NO2- oxidation compared to the GS-SPE. The LIGs also demonstrated improved stability and sensitivity (420 ± 30 and 570 ± 10 nAμM-1 cm-2) compared to the GS-SPE (73 ± 4 nAμM-1 cm-2) in the oxidation of NO2- ions; however, LIG B was more susceptible to ionic interference than LIG A. These findings highlight the value of applying statistical approaches such as DoE-RS to systematically improve the LIG fabrication process, enabling the rapid production of optimized LIGs that outperform conventional carbon-based electrodes.

All-natural, hydrophobic, biodegradable cellulose-based straws through simultaneous esterification and filling with stearic acid for cold beverages.

Disposable plastic straws have caused severe environmental pollution because microplastics produced in the degradation process harm human health and marine ecosystems. Paper straws as substitutes need to be incorporated into hydrophobic agents and other chemicals to achieve hydrophobicity, which may be harmful to human health. In this study, a novel and purely natural hydrophobic cellulose-based straw was made from bleached bamboo fibers (BBF) and stearic acid (SA). The prepared straw (BBF/SA@straw) exhibited improved hydrophobicity, biodegradability, and applicability. The water absorption rate was maintained at 58.66 % using single-factor analysis and response surface methodology and the maximum water contact angle was up to 133o. Additionally, the paper straw was almost completely degraded after 50 days in soil. Moreover, it could be used normally in water at 0 °C and 25 °C and was suitable for various beverages (tea, coffee, coke, and milk), demonstrating an extensive application prospect. This work supplies a promising and green alternative to plastic straws, alleviating the burden of white pollution in the environment.

Introducing the SNW-1 Covalent Organic Framework to the Polyamide Layer of the TFC-RO Membrane with Enhanced Permeability and Desalination Performance.

This study investigates the synthesis and characterization of Schiff base network-1 (SNW-1) covalent organic framework (COF) nanomaterials and their application in the fabrication of thin-film nanocomposite (TFN) membranes. The embedding of SNW-1 COF in reverse osmosis (RO) membranes with a polysulfone (PSf) substrate was done using the interfacial polymerization method. The result of the study demonstrated that the porous and hydrophilic structure of the COF increased the hydrophilic properties of the produced RO membranes. When the COF was embedded with a concentration of 0.02 wt %, the hydrophilicity of the RO membrane was higher than that of the other membranes, with a contact angle value of 45.2°. Pure water flux, saline solution flux, and humic acid (HA)/sodium chloride (NaCl) foulant solution flux were measured to determine the membrane performance, and it was found that as the COF ratio increased, the fluxes increased up to a certain concentration rate. The RO membrane with a SNW-1 concentration of 0.005 wt % had the highest values of pure water flux and saline solution flux with high salt rejection (34.2 and 32.2 LMH, 97.1%, respectively) and was the most resistant membrane against fouling. This study presents the potential of the SNW-1 COF with precise design capabilities and controlled unique properties as an additive for desalination applications.

Role of surface grain refinement in AZ31 Mg alloy by shot peening on surface energy, biomineralization and degradation behavior

Grain refinement of magnesium (Mg) alloys to improve their performance as potential candidates for degradable implant applications is a promising strategy in the field of materials engineering. Surface properties play an important role in promoting higher implant tissue interactions which dictate the healing rate of the fractured bone. In the present work, AZ31 Mg alloy was subjected to shot peening by using steel balls of 2 mm diameter. From the microstructural studies carried out at the cross section, fine grain structure was observed up to 50 μm depth from the surface. Grain refinement up to ∼1.5 μm was achieved at the surface of shot peened AZ31. X-ray diffraction analysis confirms the development of non-basal texture at the surface. Increased surface energy was measured by contact angle measurements for the shot peened AZ31. Higher hardness was measured from the surface in the thickness direction of the AZ31 after shot peening. Corrosion behavior assessed by potentiodynamic polarization tests indicated marginally increased corrosion resistance for shot peened AZ31. In vitro bioactivity studies carried out in simulated body fluids demonstrated higher mineral depositions and lower weight loss for the surface grain refined AZ31. The results demonstrate the potential of shot peening to promote higher biomineralization and to control the degradation in improving the performance of biodegradable AZ31 Mg alloy.

Membranes fouling propensity of PSF/GO hollow fiber mixed matrix membranes for water treatment ultrafiltration application.

The study investigated the fouling propensity of polysulfone (PSF) hollow fiber (HF) mixed matrix membranes modified with 1.0 wt.% graphene oxide (GO). Using scanning electron microscopy (SEM), atomic force microscopy (AFM), water contact angle (WCA), and mechanical assessments, the structural characteristics of both untreated and GO-modified PSF HF membranes were examined. Filtration experiments included pure water and model contaminants such as bovine serum albumin (BSA), humic acid (HA), E. coli, and oil-in-water emulsion. The GO-modified membranes demonstrated a significant enhancement in antifouling performance, recovering over 90% of their initial pure water flux with HA and oil, indicating high resistance to irreversible fouling. Additionally, the GO-modified membranes showed superior oil separation efficiency. However, fouling parameters for BSA were similar for both membrane types, suggesting that GO does not significantly affect membrane-BSA interactions. Both types of membranes displayed high retention capabilities for E. coli, with no noticeable improvement due to GO addition. This study highlights the potential of GO-modified PSF HF membranes in enhancing antifouling performance and oil separation efficiency.

Fabrication, characterization, and 3D printing of high-internal phase Pickering emulsion stabilized by heat-treated copra protein and calcium composite.

HCP-Ca nanoparticles were prepared by incorporating varying concentrations of CaCl2 into heated copra protein (HCP). The results showed a positive correlation between Ca2+ concentration and turbidity, indicating greater HCP aggregation with increasing Ca2+ levels. Microscopy analysis revealed that HCP-Ca nanoparticles had a rough surface morphology. Intermolecular forces such as disulfide bonds, hydrophobic interactions, and hydrogen bonds were key in the conformation of HCP aggregates, with calcium ions enhancing stability by forming salt bridges. HCP-Ca nanoparticle-based high internal phase Pickering emulsions (HIPPEs) were also fabricated using homogenization-centrifugation treatment. The nanoparticles showed contact angles of 87.8° to 98.3°, particle sizes between 80.42 and 80.95 nm, and the HIPPEs had zeta potentials ranging from -23 to -39 mV. The addition of Ca2+ enhanced stability by forming salt bridges, reducing particle size, and altering size distributions. Rheological and texture analysis showed that Ca2+ addition significantly improved the viscoelasticity of HCP-Ca nanoparticle-based HIPPEs, as well as increasing hardness and adhesiveness. Optical microscopy and magnetic imaging techniques revealed details about emulsion formation and oil-water distribution in HCP-Ca nanoparticle-based HIPPEs. The excellent printing stability and structural versatility of HCP-Ca nanoparticle-based HIPPEs allowed the formation of complex 3D structures, offering a valuable approach for fabricating processable and editable HIPPEs from waste materials. This paper aims to develop a food-grade copra protein-based Pickering HIPPE and explore differences in fabrication methods, providing new insights into the design of innovative Pickering stabilizers.

Preparation and performance study of heparinized multi‐walled carbon nanotube/cellulose acetate hemodialysis membrane

AbstractCurrently, the incidence of kidney failure is increasing worldwide. Hemodialysis is the main method for the treatment of kidney diseases, and the continuous development of new hemodialysis membranes is the key to improve the treatment effect and the quality of life of patients. In this study, heparinized multi‐walled carbon nanotube/cellulose acetate (Hep/MWCNTs@CA) membranes were prepared by non‐solvent induced phase separation (NIPS). The morphology and pore structure of Hep/MWCNTs@CA membranes were characterized by scanning electron microscopy (SEM). The elongation at break and tensile strength of the membranes were characterized by a mechanical property universal tester. The results showed that mechanical properties of 0.1 wt% MWCNTs enhanced the membrane is best. The water contact angle test confirmed that MWCNTs can improve the membrane hydrophilicity, and combined with the adsorption test results for proteins, it was found that the hydrophilicity can reduce the adsorption of proteins to the composite membrane and improve the blood compatibility of the material. The dialysis performance of urea and lysozyme was tested by a self‐made simulated hemodialysis device, and the clearance rates of urea and lysozyme were 84% and 47.2%, respectively, which showed that the interfacial gap between MWCNTs and CA matrix can make the composite membrane retain a high retention rate of macromolecular proteins (92.3%) and further improved the clearance rate of small and medium molecular toxins. In addition, the good blood compatibility and biocompatible properties of the materials were confirmed by hemolysis, recalcification and cytotoxicity tests on Hep/MWCNTs@CA membranes. In conclusion, the prepared Hep/MWCNTs@CA holds great potential for application in the field of hemodialysis.

Bioinspired Antireflective and Antifogging Surface for Highly Efficient and Stable Inverted Solar Cells.

Photovoltaic devices are essentially solar energy collectors that convert incident photons into charge carriers. However, light reflection losses and external factors (e.g., fog) can lead to an inefficient utilization of incident photons. Therefore, the development of antifogging surface materials that can efficiently reduce reflection is a critical issue in the upgradation of photovoltaic devices. Herein, inspired by the wing scale structures of butterfly Trogonoptera brookiana, an antireflective and antifogging surface (BRFS) was prepared by a method combining biotemplate and sol-gel. Remarkably, the BRFS possesses a relatively large surface roughness and exhibits superhydrophilic property (static water contact angle of 0°), which can quickly split fog droplet film within 6.6 s to realize the antifogging effect. In addition, the final transmittance of BRFS is as high as 90.25%. Furthermore, as an application demonstration, BRFS was applied to the surface of the reverse organic solar cells. Without compromising the inherent performance of the panels, the BRFS enhances the electrical performance of the inverted solar panels by 18%. This work provides a simple and effective strategy for designing surfaces with superior antifogging and antireflective properties and offers significant potential value for the practical application of photoelectric devices.

Mimicking Osteoid 3D Porous Dense Microfiber Silk Fibroin Embedded Poly(vinyl alcohol) Scaffold for Alveolar Ridge Preservation

Abstract Alveolar ridge loss presents difficulties for implant placement and stability. To address this, alveolar ridge preservation (ARP) is required to maintain bone and avoid the need for ridge augmentation using socket grafting. In this study, a scaffold for ARP was created by fabricating a 3D porous dense microfiber silk fibroin (mSF) embedded in poly(vinyl alcohol) (PVA), which mimics the osteoid template. The research utilized a freeze-thawing technique to create a mimicked osteoid 3D porous scaffold by incorporating different amounts of mSF into the PVA, namely, 1%, 3%, 5%, and 7%. Subsequently, a 3D profilometer machine and a scanning electron microscope (SEM) were employed to examine the morphology and size of the mSF and the mimicked osteoid 3D porous scaffold in all groups. Thermal characteristics and crystalline structure were analyzed before assessing the water contact angle, swelling behavior, degradation, and mechanical properties. The experiment evaluated the biological performance of the mimicked osteoid 3D porous scaffold by examining the efficacy of osteoblast cell adhesion, proliferation, viability, protein synthesis, alkaline phosphatase (ALP) activity, and calcium synthesis. Finally, the ability of osteoblast cells to regulate the osteoid matrix deposition on the osteoid 3D porous scaffold was assessed by mimicking the dynamic bone environment using rat mesenchymal stem cells (RMSC). The findings suggest that incorporating mSF into PVA enhances the interconnective pore size, crystalline structure, and thermal behavior of the mimicked osteoid 3D porous scaffold. The hydrophilicity of PVA decreased with an increase in the proportion of mSF, while a higher proportion of mSF resulted in increased swelling and mechanical characteristics. Incorporating a greater proportion of mSF, specifically 5% and 7%, led to a reduced rate of degradation. The addition of 5% mSF to the PVA 3D porous scaffold resulted in remarkable biological properties and excellent osteoconductive activity.

Enhancing green polyethylene composites with filler heat treatment: Pecan nutshells and Pinus sawdust impact

The aim of the present study was to produce sustainable composites using green low-density polyethylene (LDPE) reinforced with heat-treated lignocellulosic residues. The transformation processes were employed to enhance the chemical compatibility of lignocellulosic wastes with the polymer matrices of the composite materials. Sawdust from pine wood (PW) and milled pecan nutshells (NS) were subjected to a thermal treatment at 180°C for 2 h. These heat-treated residues were then homogenized with the polymer matrix and molded through hot compression. The resulting wood polymer composites (WPCs) were subjected to various characterization tests, including density, mechanical properties, infrared spectroscopy, thermal stability, hygroscopic behavior, and morphology. Comparing the composites, the inclusion of heat-treated fillers led to reductions in water absorption and thickness swelling, especially for the NS. Furthermore, the composites didn’t exhibit increased flexural strength and/or tensile strength after the bio-components treatment. The insertion of thermally treated lignocelluloses also resulted in slight decreases in equilibrium moisture content and apparent contact angles.

Orthogonal Agent Comprising a Nitrile N-Oxide and a Phenylcarbamate for Facile Molecular Integration on Styrne-Butadiene Resin.

The covalent attachment of poly(ethylene glycol) (PEGylation) to materials minimizes non-specific fouling of the material surface with biocomponents. While the PEGylation reaction on polar surfaces is widely used and regarded as a common technique, the PEGylation on less polar polymers and elastomers is extremely difficult due to the absence of reactive points with PEG terminus. Herein, the design and synthesis of an orthogonal agent with a nitrile N-oxide and a phenyl carbamate that can mediate between an alkene and an amine are reported. The ligation capacity of the orthogonal agent is demonstrated through the model reaction to connect between 1-hexene and 4-methoxybenzylamine and the grafting reaction of PEG onto poly(styrene-co-butadiene) (SB) resin. The surface characteristics of PEGylated SB film are evaluated by X-ray photoelectron spectroscopy (XPS) and contact angle measurements. Because SB resin is frequently used as a 3D-printing polymer, the present study indicates that the orthogonal agent can be applicable to the surface modification of 3D-printed objects precisely manufactured by using a computer-aided design (CAD) file in the future.

Droplet impact dynamics on the surface of super-hydrophobic BNNTs stainless steel mesh.

The 'gas‒liquid‒solid' mechanism annealing method was used to create a superhydrophobic boron nitride nanotube (BNNT) stainless steel mesh in a tube furnace at 1250°C in an NH3 environment. Fe powder was used as a catalyst, and B:B2O3 = 4:1 was used as the raw material. The water droplets on the surface of the superhydrophobic material had a contact angle of approximately 150° and a slide angle of approximately 3°. By using molecular dynamics (MD) simulation technology, a three-dimensional braided physical model of nanodroplets and superhydrophobic BNNT mesh surfaces with the same contact angle and rolling angle was prepared via the function weaving method. The Weber number (We) was used as the entrance point to establish the relationship between macroscale experimental studies and nanoscale MD simulation analysis on the basis of these efforts. A study was conducted on the dynamic behaviour of droplets impacting a superhydrophobic BNNT filter surface. We suggest that the wettability, substrate structure, and impact velocity are connected to the impact dynamic behaviour of droplets on the basis of the data obtained at various scales. The findings demonstrate that when the droplet impact velocity increases, several droplet phenomena-such as impact-rebound, impact-spread-rebound, and impact-spread-breaking-polymerisation-spatter-appear on the substrate surface sequentially. The mechanism of impact behaviour at various scales is explained in light of these events. Furthermore, a better theoretical model is proposed to assess the droplet wetting transition at the nanoscale. This model accurately predicts the boundary Weber number that starts the wetting transition. Moreover, the connections among the impact velocity, spreading diameter, and contact time (or We) are examined. The tendencies found via MD simulations match the outcomes of the experiments. Our discoveries and outcomes broaden our understanding of how droplet impact affects the dynamic behaviour of superhydrophobic surfaces. A scientific foundation for examining the dynamic behaviour of droplets is provided by combining simulations and experiments.