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In 2012, the molecular structure of a new, broad class of ice-binding proteins, classified as "domain of unknown function" (DUF) 3494, was described for the first time. These proteins have a common tertiary structure and are characterized by a very wide spectrum of antifreeze activity (from weakly active to hyperactive). The ice-binding surface (IBS) region of these molecules differs significantly in its structure from the IBS of previously known antifreeze proteins (AFPs), showing a complete lack of regularity and high hydrophilicity. The presence of a regular, repeating structural motif in the IBS region of hitherto known AFP molecules, combined with the hydrophobic nature of this surface, promotes the formation of an ice-like ordering of the solvation water layer and, as a result, facilitates the process of transformation of this water layer into ice. It is, therefore, surprising that the newly discovered DUF3494 class of proteins clearly breaks out of this characteristic. In this paper, using molecular dynamics simulations, we analyze the solvation water structure of the IBS region of both DUF3494 family molecules and AFPs. As we show, although the IBS of DUF3494 molecules does not form an ice-like water structure in the solvation layer, this is compensated by the formation of the equivalent of "anchored clathrate water," in the form of a relatively large number of water molecules bound to the surface of the protein molecule and providing potential binding sites for it to the ice surface. [ABSTRACT FROM AUTHOR]

Thermophoresis, or thermodiffusion, is becoming a more popular method for investigating the interactions between proteins and ligands due to its high sensitivity to the interactions between solutes and water. Despite its growing use, the intricate mechanisms behind thermodiffusion remain unclear. This gap in knowledge stems from the complexities of thermodiffusion in solvents that have specific interactions as well as the intricate nature of systems that include many components with both non-ionic and ionic groups. To deepen our understanding, we reduce complexity by conducting systematic studies on aqueous salt solutions. In this work, we focused on how guanidinium salt solutions behave in a temperature gradient, using thermal diffusion forced Rayleigh scattering experiments at temperatures ranging from 15 to 35 °C. We looked at the thermodiffusive behavior of four guanidinium salts (thiocyanate, iodide, chloride, and carbonate) in solutions with concentrations ranging from 1 to 3 mol/kg. The guanidinium cation is disk-shaped and is characterized by flat hydrophobic surfaces and three amine groups, which enable directional hydrogen bonding along the edges. We compare our results to the behavior of salts with spherical cations, such as sodium, potassium, and lithium. Our discussions are framed around how different salts are solvated, specifically in the context of the Hofmeister series, which ranks ions based on their effects on the solvation of proteins. [ABSTRACT FROM AUTHOR]

Amyloidosis is characterized by the deposition of fibrillar aggregates, with a specific peptide or protein as the primary component, in affected tissues or organs. Excessive proliferation and deposition of amyloid fibrils can cause organismal dysfunction and lethal pathological outcomes associated with amyloidosis. In this study, a nanochaperone (nChap-NA) was developed to inhibit protein misfolding and fibrillation by simulating the function of natural molecular chaperones. The nanochaperone was prepared by self-assembly of two block copolymers PEG-b-PCL and PCL-b-P(NIPAM-co-AANTA), which had a phase-separated surface consisting of hydrophobic PNIPAM microdomains with coordinative NTA(Zn) moieties and hydrophilic PEG chains. The hydrophobic interaction of the PNIPAM microdomain and the coordination of NTA(Zn) synergistically work together to effectively trap the amyloid monomer and block its fibrillation site. Insulin and human islet amyloid polypeptide (hIAPP) were used as model proteins to investigate the nanochaperone's inhibition of amyloid misfolding and fibrillation. It was proved that the nanochaperone could stabilize the natural conformation of the trapped insulin and hIAPP, and effectively inhibit their fibrillation. In vivo study demonstrated that the nanochaperone could effectively preserve the bioactivity of insulin and reduce the cytotoxicity caused by hIAPP aggregation. This study may provide a promising strategy for the prophylactic treatment of amyloidosis. [ABSTRACT FROM AUTHOR]

With the inherent demand for hydrophobic materials in processes such as membrane distillation and unidirectional moisture conduction, the preparation and application development of profiles such as modified cellulose acetate membranes that have both hydrophobic functions and biological properties have become a research hotspot. Compared with the petrochemical polymer materials used in conventional hydrophobic membrane preparation, cellulose acetate, as the most important cellulose derivative, exhibits many advantages, such as a high natural abundance, good film forming, and easy modification and biodegradability, and it is a promising polymer raw material for environmental purification. This paper focuses on the research progress of the hydrophobic cellulose acetate preparation process and its current application in the water-treatment and resource-utilization fields. It provides a detailed introduction and comparison of the technical characteristics, existing problems, and development trends of micro- and nanostructure and chemical functional surface construction in the hydrophobic modification of cellulose acetate. Further review was conducted and elaborated on the applications of hydrophobic cellulose acetate membranes and other profiles in oil–water separation, brine desalination, water-repellent protective materials, and other separation/filtration fields. Based on the analysis of the technological and performance advantages of profile products such as hydrophobic cellulose acetate membranes, it is noted that key issues need to be addressed and urgently resolved for the further development of hydrophobic cellulose acetate membranes. This will provide a reference basis for the expansion and application of high-performance cellulose acetate membrane products in the environmental field. [ABSTRACT FROM AUTHOR]

In the last decade, the task of developing environmentally friendly and cost-effective methods for obtaining stable superhydrophobic coatings has become topical. In this study, we examined the effect of the concentrations of filler and polymer binder on the hydrophobic properties and surface roughness of composite coatings made from organic–aqueous compositions based on hexyl methacrylate (HMA) and glycidyl methacrylate (GMA) copolymers. Silicon dioxide nanoparticles were used as a filler. A single-stage "all-in-one" aerosol application method was used to form the coatings without additional intermediate steps for attaching the adhesive layer or texturing the substrate surface, as well as pre-modification of the surface of filler nanoparticles. As the ratio of the mass fraction of polymer binder (Wn) to filler (Wp) increases, the coatings show the lowest roll-off angles among the whole range of samples studied. Coatings with an optimal mass fraction ratio (Wn/Wp = 1.2 ÷ 1.6) of the filler to polymer binder maintained superhydrophobic properties for 24 h in contact with a drop of water in a chamber saturated with water vapor and exhibited roll-off angles of 6.1° ± 1°. [ABSTRACT FROM AUTHOR]

The acrylic polymer composites in this study are made up of various weight ratios of cement or silica nanoparticles (1, 3, 5, and 10 wt%) using the casting method. The effects of doping ratio/type on mechanical, dielectric, thermal, and hydrophobic properties were investigated. Acrylic polymer composites containing 5 wt% cement or silica nanoparticles had the lowest abrasion wear rates and the highest shore-D hardness and impact strength. The increase in the inclusion of cement or silica nanoparticles enhanced surface roughness, water contact angle (WCA), and thermal insulation. Acrylic/cement composites demonstrated higher mechanical, electrical, and thermal insulation properties than acrylic/silica composites because of their lower particle size and their low thermal/electrical conductivity. Furthermore, to improve the surface hydrophobic characteristics of acrylic composites, the surface was treated with a dielectric barrier discharge (DBD) plasma jet. The DBD plasma jet treatment significantly enhanced the hydrophobicity of acrylic polymer composites. For example, the WCA of acrylic composites containing 5 wt% silica or cement nanoparticles increased from 35.3° to 55° and 44.7° to 73°, respectively, by plasma treatment performed at an Ar flow rate of 5 L/min and for an exposure interval of 25 s. The DBD plasma jet treatment is an excellent and inexpensive technique for improving the hydrophobic properties of acrylic polymer composites. These findings offer important perspectives on the development of materials coating for technical applications. [ABSTRACT FROM AUTHOR]

The process of osteointegration depends significantly on the surface roughness, structure, chemical composition, and mechanical characteristics of the coating. In this regard, an important direction in the development of medical materials is the development of new techniques of surface modification and the creation of bioactive ceramic coatings. Calcium-phosphate materials based on hydroxyapatite have been proposed as bioactive ceramic coatings on titanium implants for the effective acceleration of bone tissue healing. To obtain bioactive ceramic coatings, pulse power sources are best suited, namely detonation spraying, in which the energy of the explosion of gas mixtures is used as a source of pulse action. The pulse mode of operation in the detonation spraying method is preferable for the formation of bioactive ceramic coatings. It provides a high velocity of hydroxyapatite particles, which promotes their effective fixation on the titanium substrate, while minimizing the heating of the material. This approach preserves the substrate structure and improves the coating adhesion. Four different types of coatings with varying O2/C2H2 molar ratios, ranging from 2.6 to 3.7, were obtained using detonation spraying. Powders and obtained coatings of hydroxyapatite were studied by Raman spectroscopy and XRD structural analysis. The results of XRD phase analysis showed the partial conversion of the hydroxyapatite phase to the α-tricalcium phosphate (α-TCP) phase during the detonation spraying process. The results obtained by Raman spectroscopy indicate that hydroxyapatite is the main phase in coatings. All hydroxyapatite-based coatings exhibited hydrophobic properties, which was confirmed by contact-angle values above 90° in wettability tests, characteristic of hydrophobic surfaces. The adhesive strength of the coatings was measured by the scratch test method. Tribological tests were conducted using the ball-on-disk method under both dry conditions and in Ringer's solution. This approach enabled the evaluation of wear resistance and friction coefficient of the coatings in different environments, simulating both lubrication-free conditions and those resembling physiological environments. [ABSTRACT FROM AUTHOR]

Surface engineering is one of the most extensive industries. Virtually all areas of the economy benefit from the achievements of surface engineering. Surface quality affects the quality of finished products as well as the quality of manufactured parts. It affects both functional qualities and esthetics. Surface quality affects the image and reputation of a brand. This is particularly true for cars and household appliances. Surface modification of products is also aimed at improving their functional and protective properties. This applies to surfaces for producing hydrophobic surfaces, anti-wear protection of friction pairs, corrosion protection, and others. Metal technologies and 3D printing benefit from surface technologies that improve their functionality and facilitate the operation of products. Surface engineering offers a range of different coating and layering methods from varnishing and painting to sophisticated nanometric coatings. This paper presents an overview of selected surface engineering issues pertaining to metal products, with a particular focus on surface modification of products manufactured by 3D printing technology. It evaluates the impact of the surface quality of products on their functional and performance qualities. [ABSTRACT FROM AUTHOR]

The carbon dioxide emissions caused by heat transfer have become one of the largest sources of carbon dioxide emissions. Reducing greenhouse gas emissions caused by heat conduction have become an urgent problem to be solved. In this paper, we are committed to the preparation and evaluation of the properties of the wood-based oxidized cellulose microtube thermal insulation foam materials inspired by natural microtubule insulation structure. The oxidized cellulose microtube can be uniformly dispersed in water due to the introduction of active carboxyl functional groups. The introduction of active carboxyl functional groups can improve the flexibility and dispersibility of the oxidized cellulose microtubules in water. The oxidized cellulose microtube (HOCM-X) foam can be prepared through strong electrostatic force between Ca2 + and carboxylic acid groups and MTMS surface hydrophobic treatment. The property of the wood-based oxidized cellulose microtube thermal insulation foam materials can be effectively tuned by the concentration of the oxidized cellulose microtubule. The water contact angle of the HOCM-X foam was about 135°. As the oxidized cellulose microtubules content increases, the mechanical strength of the HOCM-X foam gradually increases. The HOCM-2.5 foam exhibits the best thermal insulation properties with the thermal conductivity as low as 47 mW·m−1·k−1. [ABSTRACT FROM AUTHOR]

We describe the design and performance of a portable closed electrowetting-on-dielectric (EWOD) system for digital microfluidics applications. The system is cost-effective and is capable of controlling the motion of one or more droplets under the influence of an asymmetric electric field. Using polypropylene (commercial cello tape) as a dielectric layer with Glaco™ spray to create a hydrophobic surface lowers device fabrication cost. For the first time, a superhydrophobic Glaco™ layer (equilibrium contact angle ~ 150°) is used for the EWOD device fabrication. The device has four modules that are designed to provide a high actuation voltage in the range of 5–300 VDC over the array of electrode pads. Given a large enough electrode array over the lower surface, the effect of the applied potential of the top electrode on droplet motion is studied via numerical simulation and is shown to be insignificant. This result further helps in simplifying the fabrication process. The user-friendly interface that defines droplet motion is designed using Qt, a cross-platform framework that is used as a graphical toolkit and an open-source image processing software in Raspberry Pi. Two types of closed EWOD configurations are developed to demonstrate their features in terms of moving and merging multiple droplets. For the designs implemented, the greatest speed of droplet movement at 295 VDC was measured to be 60 mm/s. Additional features of the device include calculation of the real-time mixing index and a thermal management module for temperature control. The simplicity of design and low-cost makes the device attractive for studying electrically induced drop motion on one end to a biomedical diagnostic test kit, on the other. [ABSTRACT FROM AUTHOR]

The effect of a hydrophobic surface on photocatalytic hydrogen evolution was investigated, which inhibited the hydrogen dissociation reaction. [Display omitted] Covalent organic frameworks (COFs) have gained considerable interest as candidate photocatalysts for hydrogen evolution. In this work, we synthesized β-keto-enamine-based COFs (TpPa-X, TpDB, and TpDTP) to explore the relations between structures and photocatalytic hydrogen evolution. COFs were divided into two groups: (1) TpPa-X with different substituents attached to the TpPa backbone and (2) COFs featuring diamine linkers of varied lengths (TpDB and TpDTP). Experiments and density functional theory (DFT) calculations show that moderate hydrophobicity is favorable for the photocatalytic hydrogen evolution process, and acceptable contact angles are anticipated to range from 65° to 80°. Naturally, there are comprehensive factors that affect photocatalytic reactions, and the regulation of different backbones and substituents can considerably affect the performance of COFs for photocatalytic hydrogen evolution in terms of electronic structure, specific surface area, surface wettability, carrier separation efficiency, and hydrogen dissociation energy. Results show that TpPa-Cl 2 (TpPa-X, X = Cl 2) demonstrates the highest photocatalytic activity, approximately 14.51 mmol g-1h−1, with an apparent quantum efficiency of 4.62 % at 420 nm. This work provides guidance for designing efficient COF-based photocatalysts. [ABSTRACT FROM AUTHOR]

[Display omitted] Hypothesis: In the interfacial wetting boundary, the superhydrophobic surface is often damaged, and the anisotropic wettability of its surface has attracted many researchers' attention. The "petal effect" surface has typical anisotropic wettability. We predict that under the dual conditions of structural defects and high impact velocity, the "petal effect" becomes more adhesive on the surface. Experiments: This study refers to the droplet state on rose petals, structural defects were constructed on the superhydrophobic surface. This paper studies the influence of macro-structural defects on the wettability change from natural to bionic "lotus effect" to "petal effect" in both static and dynamic angles. Findings: Macro defects significantly change the static contact angle of the superhydrophobic surface. The higher the impact velocity of the droplet, the higher the energy dissipation of the "petal effect" surface (DSHS), which improves the adhesion of the surface to the droplet and prolongs the contact time. It is found that the defect structure and high impact velocity will directly affect the deposition and desorption of droplets on the superhydrophobic surface, and they are both essential. This wetting dynamic law is very likely to be helpful in the quantitative design of defect structure scale for dynamic desorption of droplets on superhydrophobic surfaces. [ABSTRACT FROM AUTHOR]

Interfacial solar-driven evaporation technology shows great potential in the field of industrial seawater desalination, and the development of efficient and low-cost evaporation materials is key to achieving large-scale applications. Hydrogels are considered to be promising candidates; however, conventional hydrogel-based interfacial solar evaporators have difficulty in simultaneously meeting multiple requirements, including a high evaporation rate, salt resistance, and good mechanical properties. In this study, a Janus sponge-like hydrogel solar evaporator (CPAS) with excellent comprehensive performance was successfully constructed. The introduction of biomass agar (AG) into the polyvinyl alcohol (PVA) hydrogel backbone reduced the enthalpy of water evaporation, optimized the pore structure, and improved the mechanical properties. Meanwhile, by introducing hydrophobic fumed nano-silica aerogel (SA) and a synergistic foaming-crosslinking process, the hydrogel spontaneously formed a Janus structure with a hydrophobic surface and hydrophilic bottom properties. Based on the reduction of the evaporation enthalpy and the modulation of the pore structure, the CPAS evaporation rate reached 3.56 kg m-2 h-1 under one sun illumination. Most importantly, owing to the hydrophobic top surface and 3D-interconnected porous channels, the evaporator could work stably in high concentrations of salt-water (25 wt% NaCl), showing strong salt resistance. Efficient water evaporation, excellent salt resistance, scalable preparation processes, and low-cost raw materials make CPAS extremely promising for practical applications. [ABSTRACT FROM AUTHOR]

AbstractThe effects of corona-discharged atmospheric plasma treatment on the surfaces of polyvinyl chloride (PVC) were studied for their application in adhesively joining PVC with AA 6061 aluminium alloy. Although no alteration has been observed in the topography of the treated PVC surfaces, ATR-FTIR analysis reveals the incorporation of –OH functional groups. Therefore, the untreated hydrophobic surface of PVC changes to a hydrophilic nature after corona treatment. Single lap shear (SLS) specimens were prepared using treated PVC and Al bonded with a room temperature cure epoxy adhesive. The obtained SLS strength of the joint between 20-second treated PVC and etched Al is found to be 15 times larger than that of untreated PVC with as-received Al. [ABSTRACT FROM AUTHOR]

SUMMARY Land plants have evolved a hydrophobic cuticle on the surface of aerial organs as an adaptation to ensure survival in terrestrial environments. Cuticle is mainly composed of lipids, namely cutin and intracuticular wax, with epicuticular wax deposited on plant surface. The composition and permeability of cuticle have a large influence on its ability to protect plants against drought stress. However, the regulatory mechanisms underlying cuticular wax biosynthesis in response to drought stress have not been fully elucidated. Here, we identified three AP2/ERF transcription factors (DREB26/ERF12, ERF13 and ERF14) involved in the regulation of water permeability of the plant surface. Transmission electron microscopy revealed thicker cuticle on the leaves of DREB26‐overexpressing (DREB26OX) plants, and thinner cuticle on the leaves of transgenic plants expressing SRDX repression domain‐fused DREB26 (DREB26SR). Genes involved in cuticular wax formation were upregulated in DREB26OX and downregulated in DREB26SR. The levels of very‐long chain (VLC) alkanes, which are a major wax component, increased in DREB26OX leaves and decreased in DREB26SR leaves. Under dehydration stress, water loss was reduced in DREB26OX and increased in DREB26SR. The erf12/13/14 triple mutant showed delayed growth, decreased leaf water content, and reduced drought‐inducible VLC alkane accumulation. Taken together, our results indicate that the DREB26/ERF12 and its closed family members, ERF13 and ERF14, play an important role in cuticular wax biosynthesis in response to drought stress. The complex transcriptional cascade involved in the regulation of cuticular wax biosynthesis under drought stress conditions is discussed. [ABSTRACT FROM AUTHOR]

SUMMARY Lipid droplets (LDs) are unusual organelles that have a phospholipid monolayer surface and a hydrophobic matrix. In oilseeds, this matrix is nearly always composed of triacylglycerols (TGs) for efficient storage of carbon and energy. Various proteins play a role in their assembly, stability and turnover, and even though the major structural oleosin proteins in seed LDs have been known for decades, the factors influencing LD formation and dynamics are still being uncovered mostly in the “model oilseed” Arabidopsis. Here we identified several key LD biogenesis proteins in the seeds of pennycress, a potential biofuel crop, that were correlated previously with seed oil content and characterized here for their participation in LD formation in transient expression assays and stable transgenics. One pennycress protein, the lipid droplet associated protein‐interacting protein (LDIP), was able to functionally complement the Arabidopsis ldip mutant, emphasizing the close conservation of lipid storage among these two Brassicas. Moreover, loss‐of‐function ldip mutants in pennycress exhibited increased seed oil content without compromising plant growth, raising the possibility that LDIP or other LD biogenesis factors may be suitable targets for improving yields in oilseed crops more broadly. [ABSTRACT FROM AUTHOR]

AbstractThe high viscosity and poor fluidity of heavy oil challenge its extraction, leading to the widespread use of surfactant emulsification to reduce viscosity and enhance recovery. This study evaluated three surfactants—sodium dodecyl sulfate (SDS), sodium oleate (SO), and APG0810—for their suitability and effectiveness in the X reservoir. The solution properties of these surfactants were analyzed and their micro-mechanisms investigated using MD calculations. The effects of surfactant concentration and additives on emulsification and viscosity reduction were elucidated. Ultimately, a system for emulsification and viscosity reduction was selected for physical simulation research. The experimental findings show that SO reduces interfacial tension from 52.4 mN/m to 0.0027 mN/m, transforming lipophilic surfaces into hydrophilic. MD analyses reveal SO’s optimal interfacial properties, with the lowest interfacial energy of −6423.4 kcal/mol, maximum interfacial thickness of 2.56 nm, and minimal diffusion coefficient of 0.4087 Å2/ps at the oil-water interface. These findings align with experimental results, confirming SO’s superior interfacial properties. Combining 0.3% SO with 0.5% n-pentanol results in a 98% viscosity reduction. The emulsion shows excellent stability, with no water separation in the first 30 min and only 8.3% after 2 h. Physical simulation results show that in high(low) permeability core displacement experiments, system flooding and subsequent water flooding can increase recovery rates by 15.39%(36.91%), indicating the system’s potential for enhancing oil recovery in Reservoir X. The findings suggest that the implementation of this system not only boosts the crude oil recovery rate but also carries economic significance in the industry. [ABSTRACT FROM AUTHOR]

Fluorescence polarization (FP) assays are widely used to quantify biomolecules, and their combination with microfluidic devices has the potential for application in onsite analysis. However, the hydrophobic surface of polydimethylsiloxane (PDMS)-based microfluidic devices and the amphiphilicity of the blocking agents can cause the nonspecific adsorption of biomolecules, which in turn reduces the sensitivity of the FP assay. To address this, we demonstrated an FP assay with improved sensitivity in microfluidic devices using a polyethylene glycol-based surface modification to avoid the use of blocking agents. We evaluated the effectiveness of the modification in inhibiting nonspecific protein adsorption and demonstrated the improved sensitivity of the FP immunoassay (FPIA). Our study addressed the lack of sensitivity of FP assays in microfluidic devices, particularly for the quantification of low-abundance analytes. [ABSTRACT FROM AUTHOR]

Removal of confined space carbon dioxide (CO2) that is in low concentration and with coexisting water is necessary but challenging by physical adsorption method. To make the removal process effective, rendering the nanopore surface hydrophobic to resist water is the popular way. Instead of preventing water from occupying the nanopores, in this work, we propose to utilize the guest water for the spatially selective formation of local surface bound water and further induce the preferential CO2 capture. We observe an anomalous enhancement of CO2 capture performance under humid conditions over carbon nanopores with spatially selective polar sites. It is evidenced that the surface bound water is formed at non-CO2-selective areas of polar carbon nanopores, thus creating additional CO2 trapping sites. This work may inspire the design of environment tolerable materials for molecular separation and purification under harsh conditions. The removal of low-concentration humid CO2 from confined space is necessary but challenging. Here, the authors propose a strategy to boost the humid CO2 removal performance by dynamically optimizing polar carbon nanopores with the formation of local surface bound water. [ABSTRACT FROM AUTHOR]

Fungi (Neolentinus lepideus, Nl, and Trametes versicolor, Tv) impart wood rot, leading to economic and environmental issues. To overcome this issue, toxic chemicals are commonly employed for wood preservation, impacting the environment and human health. Surface coatings based on antimicrobial chitosan (CS) of high molar mass (145 × 105 Da) were tested as wood preservation agents using an innovative strategy involving ultra-pressurizing CS solutions to deposit organic coatings on wood samples. Before coating deposition, the antifungal activity of CS in diluted acetic acid (AcOOH) solutions was evaluated against the rot fungi models Neolentinus lepideus (Nl) and Trametes versicolor (Tv). CS effectively inhibited fungal growth, particularly in solutions with concentrations equal to or higher than 0.125 mg/mL. Wood samples (Eucalyptus sp. and Pinus sp.) were then coated with CS under ultra-pressurization at 70 bar. The polymeric coating deposition on wood was confirmed through X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM) images, and water contact angle measurements. Infrared spectroscopy (FTIR) spectra of the uncoated and coated samples suggested that CS does not penetrate the bulk of the wood samples due to its high molar mass but penetrates in the surface pores, leading to its impregnation in wood samples. Coated and uncoated wood samples were exposed to fungi (Tv and Nl) for 12 weeks. In vivo testing revealed that Tv and Nl fungi did not grow on wood samples coated with CS, whereas the fungi proliferated on uncoated samples. CS of high molar mass has film-forming properties, leading to a thin hydrophobic film on the wood surface (water contact angle of 118°). This effect is mainly attributed to the high molar mass of CS and the hydrogen bonding interactions established between CS chains and cellulose. This hydrophobic film prevents water interaction, resulting in a stable coating with insignificant leaching of CS after the stability test. The CS coating can offer a sustainable strategy to prevent wood degradation, overcoming the disadvantages of toxic chemicals often used as wood preservative agents. [ABSTRACT FROM AUTHOR]

In specific applications like ice-repellent coatings or membrane separation technology, wettability is a key parameter affecting the applicability of commodity polymers. This study presents a technique to fine-control the wetting properties of a hierarchically structured polypropylene surface, enabling the transition between superhydrophobic and superhydrophilic states. To demonstrate the tunability of the wetting properties of polypropylene (PP) substrate, we prepared in a consecutive way superhydrophobic (advancing contact angle (CAadv) of 152°) and superhydrophilic (CAadv of 0°) material by solvent-treatment and mild air plasma treatment. The optimal plasma treatment parameters to achieve superhydrophilic wetting behaviour, which is stable for at least one week of storage in air was also explored. Water contact angle measurement and X-ray photoelectron spectroscopy were used to monitor the time dependency of hydrophobic recovery on a hierarchically structured PP surface. With a simple model considering structural and wetting parameters, we characterized the droplet spreading behaviour of plasma-treated roughened surfaces, which exhibited superhydrophilic wetting behaviour with equilibrium CAadv of nearly 0°. The proposed model, which aligns well with experimental data, can be used to compare the droplet spreading behaviour of plasma-treated roughened surfaces. [ABSTRACT FROM AUTHOR]

In the last two decades, a great interest has been focused on the creation and study of superhydrophobic nanomaterials based on the "lotus effect." This effect is caused by the heterogeneous wetting of rough surfaces, when the grooves of a rough surface are filled with air (vapor) and water contacts only with the tops of the protrusions. A drop forms a sphere on the surface and rolls down picking up dirt particles when the surface is slightly tilted. Diverse methods have been developed for producing such materials, and the potential of the ion-track technology (ITT) is being investigated. The goal of this work is to study the wettability of surface microtextures by the examples of two materials with different initial degrees of hydrophobicity. The ITT has been employed to obtain samples with maximum water contact angles of 140 ± 5° and 151 ± 5° by modifying the surfaces of polycarbonate and polypropylene films, respectively. It has been shown that such angles are characteristic of microtextures, for which surface fraction f that is in contact with a droplet is decreased to a range of 0 < f < 0.3. Materials with tilted microtextures have been obtained in order to increase the probability of droplet rolling down a material surface in a certain direction. In this case, the wettability becomes anisotropic. A droplet loses its spherical shape and is deformed in the direction of the tilt of needle-like surface elements. It has been found that the anisotropy of wettability is higher at a tilt angle of the texture elements of 45° than that at 30° (relative to the flat surface). [ABSTRACT FROM AUTHOR]

Doping is a critical method for enhancing the electrical properties of semiconducting polymers, with ongoing innovations in dopant molecules and doping techniques. However, introducing dopants can disrupt the conjugated backbone of polymers like poly[(2,5-bis(3-tetradecylthiophen-2-yl)thieno[3,2-b]thiophene)] (PBTTT) and indendithiophene-benzothiadiazole (IDTBT), accelerating the degradation of electronic properties, particularly under air exposure. Cytop, as a cross-linked fluorine-rich polymer material, can form amorphous, smooth hydrophobic surfaces that are isolated from air. However, there is a lack of research on Cytop to inhibit the degradation of electrical properties of polymers in air. This study employed ion-exchange and immersion doping techniques on these polymers and explored the protective effects of the crosslinked polymer Cytop as a barrier layer. We measured the electrical properties of doped films both with and without the Cytop layer under various conditions to determine its impact on the polymers' stability. The findings demonstrate that Cytop significantly enhances the films' stability, offering insights into the long-term performance and reliability of doped semiconducting polymers. [ABSTRACT FROM AUTHOR]

The flow and heat transfer processes of liquid argon within nanochannels with random roughness are investigated using the molecular dynamics method. This study explores the effects of surface roughness and wettability on flow and heat transfer performance. The results indicate that both surface roughness and wettability significantly influence temperature jumps, velocity slip, flow resistance, and temperature distribution. Specifically, hydrophilic surfaces can reduce temperature jumps and velocity slip due to their enhanced ability to adsorb liquid atoms, which effectively improves heat transfer while simultaneously increasing flow resistance. The fractal dimension D characterizes the surface roughness, which decreases as D increases. Additionally, both the Nusselt number and drag coefficient decrease with increasing D. In this study, we investigate cases where D ranges from 2.5 to 2.9, with D = 2.5 representing the highest roughness, and the smooth channel corresponding to the lowest roughness. For hydrophilic nanochannels at D = 2.5, the Nusselt number and drag coefficient increased by factor of 2.2 times and 5.2 times compared to smooth channels, respectively. For hydrophobic nanochannels at D = 2.5, the Nusselt number and drag coefficient increased by a factor of 4.5 times and 29.1 times compared to smooth surface channels, respectively. Considering both flow and heat transfer performances, the best comprehensive performance is achieved with D = 2.8 for channels with hydrophilic surfaces and D = 2.6 for channels with hydrophobic surfaces. This work systematically investigates the coupled effects of random roughness and wettability on the flow and heat transfer characteristics in nanochannels, providing new theoretical insights for optimizing nanochannel design. [ABSTRACT FROM AUTHOR]

Liquid droplet impact on dry surfaces often results in bouncing or breakup beyond a certain threshold. Surface contact angles, especially dynamic ones present during impact, significantly affect this process. Our experimental study underscores that advancing and receding contact angles influence droplet behaviors like rebounding and different types of breakup. This discovery provides new insights and criteria for understanding liquid droplet impact on surfaces. Special characteristics were found in the breakup on microstructured surfaces: the size of fractured droplets notably decreases, and the spreading–breakup occurs more easily and earlier. Additionally, microstructured surfaces reduce contact time to some extent. Furthermore, the uniqueness of oblique impacts is mainly reflected in how they lower the threshold of the receding contact angle for rebound. Studying the correlations and differences in droplet rebound and breakup related to these surface characteristics will contribute to improving research on liquid–solid interactions and the design of hydrophobic surfaces, including microstructured surfaces. [ABSTRACT FROM AUTHOR]

In this study, the dynamic behaviors of non-Newtonian fluid droplets with shear-thinning properties eccentrically impacting hydrophobic particle surfaces are investigated through a combination of numerical simulations and experiments. The simulation integrates the dynamic contact angle and a non-Newtonian fluid power-law model within the volume of fluid model framework. The effects of apparent viscosity (η), impact velocity (v0), and dimensionless eccentricity parameter (B) on the dynamic behaviors of non-Newtonian droplets are analyzed. Furthermore, the study offers insight into the progression of pressure distribution, kinetic energy, and liquid viscosity across droplets during the entire impact process. An energy balance analysis, which includes kinetic energy, surface energy, potential energy, and viscous dissipation, is employed to elucidate the fundamental physical mechanisms that govern the dynamics of eccentric impacts of non-Newtonian droplets. Finally, a model (Recr D* = −95.7 + 11 450.6e−B/0.18) is proposed to predict the adhesion or detachment of shear-thinning droplets eccentrically impacting hydrophobic particle surfaces. [ABSTRACT FROM AUTHOR]

A stable attachment between bubbles and solid particles is essential for flotation. Therefore, it is particularly necessary to study the dynamic process that occur in the attachment of bubbles to a solid surface. In this paper, Teflon and plexiglass plates were used as hydrophobic and hydrophilic solid surfaces, respectively, and solid surfaces with roughness of 0.018 μm to 5.33 μm were prepared by polishing with sandpaper. The influence of roughness on the dynamic process in bubble attachment to solid surfaces with different hydrophobicity was studied via a high-speed camera (750 frames per second). It was found that roughness played a positive role in the attachment to the hydrophobic Teflon surface while a negative role in the attachment to the hydrophilic plexiglass surface in terms of the bubble's attachment to the solid plates. For a smooth Teflon surface, the formation of three–phase contact (i.e., the drainage of wetting film) took up to 95 ms, whereas for a very rough Teflon surface it took only 5 milliseconds. On the contrary, the high roughness prevented the bubble from attaching to the hydrophilic plexiglass surface. It was concluded that the increased roughness of Teflon plates was conductive to air entrapment in surface irregularities, inducing the rapid rupture of the wetting film on a very rough Teflon surface, while the increased roughness of the plexiglass plates resulted in "water pockets" in surface grooves, making the wetting film on the plexiglass surface stable. [ABSTRACT FROM AUTHOR]

This work aims to serve as a comprehensive guide to properly characterize solid-contact ion-selective electrodes (SC-ISEs) for long-term use as they advance toward calibration-free sensors. The lack of well-defined SC-ISE performance criteria limits the ability to compare results and track progress in the field. Laser-induced graphene (LIG) is a rapid and scalable method that, by adjusting the CO2 laser parameters, can create LIG substrates with tunable surface properties, including wettability, surface chemistry, and morphology. Herein, we fabricate laser-induced graphene (LIG) solid-contact electrodes using different laser settings and subsequently convert them into ion-selective sensors using a potassium-selective membrane. We measure the aforementioned tunable surface properties and correlate them with resultant low-frequency capacitance and water layer formation in an effort to pinpoint their effects on the sensitivity (Nernstian response), reproducibility (E°' variation), and potential stability of the LIG-based SC-ISEs. More specifically, we demonstrate that the surface wettability of the LIG substrate, which can be tuned by controlling the lasing parameters, can be modified to exhibit hydrophobic (contact angle > 90°) and even highly hydrophobic surfaces (contact angle ≈ 130°) to help reduce sensor drift. Recommendations are also provided to ensure proper and robust characterization of SC-ISEs for long-term and continuous measurements. Ultimately, we believe that a comprehensive understanding of the correlation between LIG tunable surface properties and SC-ISE performance can be used to improve the electrochemical behavior and stability of SC-ISEs designed with a wide range of materials beyond LIG. [ABSTRACT FROM AUTHOR]

For dropwise condensation of water over a textured surface, the condensation rate is limited by the conduction resistance of the droplet. Conduction models with varying levels of approximation have been reported in the literature. In the present study, the conduction resistance of a spherical-cap droplet is derived by regression analysis of data generated by 3D numerical simulation. Results show that conduction resistance is sensitive to the choice of contact angle and droplet radius. The proposed model has significant differences from reported models which are based on 1-D and 2-D approximations. An important source of discrepancy is traced to additional heat flux localized at the three-phase contact line. Equivalently, high local heat flux serves to lower thermal resistance between the vapor-liquid interface and the condensing wall. The prediction of the droplet growth rate using the proposed conduction model is in good agreement with the experiments reported in the literature. The improved conduction resistance correlation is incorporated in the model for a space- and time-resolved dropwise condensation cycle for vapor condensing from moist air. Simulations with the improved condensation model show close agreement with experimental data, justifying the utility of an improved correlation for conduction resistance. [ABSTRACT FROM AUTHOR]

An experimental apparatus was designed to study the impacts of wettability on evaporation of water from Ottawa sand. Evaporation rates were measured for: (1) a 5.7-cm-thick layer of hydrophilic Ottawa sand; (2) a 5.7-cm-thick layer with 12% hydrophobic content, consisting of a 0.7-cm-layer of n-Octyltriethoxysilane-coated hydrophobic sand buried 1.8 cm below the surface of hydrophilic sand; and (3) a 5.7-cm-thick layer with mixed wettabilities, consisting of 12% n-Octyltriethoxysilane-coated hydrophobic sand mixed into hydrophilic sand. The sand-water mixtures experienced forced convection above and through the sand layer, while a simulated solar flux (i.e., 112±20 W/m²) was applied. Evaporation from homogeneous porous media is classified into the constant-rate, falling-rate, and slow-rate periods. Wettability affected the observed evaporation mechanisms, including the transition from constant-rate to falling-rate periods. Evaporation entered the falling-rate period at 12%, 20%, and 24% saturations for the all hydrophilic sand, hydrophobic layer, and hydrophobic mixture, respectively. Wettability affected the duration of the experiments, as the all hydrophilic sand, hydrophobic layer, and hydrophobic mixture lasted 17, 20, and 26 trials, respectively. Both experiments with hydrophobic particles lasted longer than the all hydrophilic experiment and had shorter constant-rate evaporation periods, suggesting hydrophobic material interrupts capillary action of water to the soil surface and reduces evaporation. Sand temperatures suggest more evaporation occurred near the test section inlet for higher saturations and the hydrophobic layer experienced more evaporation occur near the outlet. Evaporation fluxes were up to 12× higher than the vapor diffusion flux due to enhanced vapor diffusion and forced convection. [ABSTRACT FROM AUTHOR]

The surface modification of SnO 2 electron transporting layer (ETL) is investigated for the performance and stability improvement of perovskite solar cells by adding citric acid (SnO 2 -citric) and graphene quantum dots (SnO 2 -GQDs) in SnO 2 ETL precursors for carboxyl group and GQDs, respectively. As a result, the hydrophobic surface of SnO 2 -GQDs is obtained by adding GQDs to the SnO 2 precursor, forming SnO 2 -GQDs ETL. In addition, the hydrophobic surface of SnO 2 ETL is significant in increasing grain size crystallinity of perovskite obtained by this modification process. Also, the charge trap density and recombination carriers between ETL and perovskite interface were advanced. Thus, the surface modification of SnO 2 -GQDs ETL can enhance the power conversion efficiency (PCE) of PSCs at the highest value of 17.81% from 15.52% with a decrease of the hysteresis effect. The enhancement is due to the combining effect of carboxyl groups and GQDs interface engineering between ETL and perovskites layers. Also, the stability of perovskite solar cells without encapsulation for 28 days is achieved. These suggest that the combining effect can be used in surface modification and for efficiency enhancement of PSCs. [ABSTRACT FROM AUTHOR]

Challenges exist regarding the bonding efficiency of polyaryletherketone (PAEK), a high-performance thermoplastic, attributed to its chemical inertness and hydrophobic surface, hindering effective bonding with resin-matrix cement. This research explored the impact of handheld nonthermal plasma (HNP), under varying operational parameters, on PAEK surface wettability and changes in bonding performance with cement. Three types of disc-shaped PEAK specimens were prepared, with surface treatments categorized as grinding, airborne-particle abrasion (APB), and HNP. Surface wettability was analyzed using a contact angle analyzer (n = 10). Specimens were bonded with resin cement and subjected to artificial aging tests: distilled water bath (NA), thermocycling, and highly accelerated stress tests (n = 10 for each test). Shear bond strength (SBS) was measured, failure modes were analyzed, and statistical analyses were conducted. The HNP markedly improved PAEK surface wettability, achieving superhydrophilicity (P < 0.05). This effect intensified with extended operation times (30 or 60 s) and reduced elapsed times (<30 s). HNP-treated PAEK exhibited higher SBS than APB (P < 0.05) and maintained bonding durability after artificial aging, particularly in ketone-enriched variants. Failure analysis revealed predominantly adhesive failure under APB–NA treatment, mixture failures under HNP–NA treatment and postaging, but no cohesive failure. The HNP device benefits dental settings by transforming the PAEK surface into superhydrophilic properties, thereby improving PAEK–cement bonding. It significantly enhances bond durability within 30 s of operation and after a 30 s elapsed period. It is noteworthy that ketone-enriched PAEK demonstrates markedly improved bonding performance. [ABSTRACT FROM AUTHOR]

Porous Zn scaffold, as a novel biodegradable metallic material, has emerged as a promising candidate for biomedical applications. In this paper, by using carbamide particles as the pore-making agent and Zn and Mg powders as the starting materials, porous Zn-Mg alloy scaffolds were fabricated via the low-temperature sintering route. A so-called one-step hydrothermal method was applied to form a hydrophobic film on surface of the porous Zn alloy scaffolds. The degradability of the porous Zn alloy scaffolds coated with/without hydrophobic film in the simulated body fluid (SBF) was investigated, and the results show that the hydrophobic film, which can adhere well to the metal substrate with thickness around 50 μm, can effectively delay the degradation of porous Zn alloy scaffolds; the degradation rates of porous Zn alloy scaffolds coated by the hydrophobic film are 26–57% lower than those of porous scaffolds without coating; especially the degradation rate of the porous Zn-5 wt.%Mg scaffold with the coating in SBF, which is 0.32 mg/(cm2 day), is at the same level as that of pure Zn. [ABSTRACT FROM AUTHOR]

Polyurethane (PU) stands out as a crucial category of polymers which have become indispensable in improving our quality of life, revolutionizing various aspects of human existence. However, this convenience comes with a dark side – the environmental impact associated with its disposal. Nevertheless, recycling presents a promising solution, aligning with the principles of a circular economy by transforming polymer waste into new materials. A notable focus within this realm is the utilization of dicarboxylic acids (DA) as depolymerization agents, achieved through a process known as acidolysis. This method has proven to be an exceptional solution, primarily explored for recycling PU foams and subsequently employed in the production of new foams. The resulting recycled polyol finds successful applications in various PU products, including rigid and flexible foams, adhesives, and coatings. Analyzing the impact of recycled polyol on the properties of new PU products reveals interesting insights. While it slightly affects the morphology and color of foams, there is no significant impact on density or thermal conductivity. Notably, flexible foams exhibit increased stiffness when produced using recycled polyol. Additionally, the strength of PU adhesives and the surface hardness of PU coatings are enhanced with the incorporation of recycled polyol, albeit with a reduction in gloss. The recycled PU coatings also display a more hydrophobic surface. Considering both environmental and economic benefits, the advantages of this approach are evident. With the aim of catering to the needs of both the academic and industrial sectors, this review delves into the subject of PU recycling via acidolysis, subsequently exploring the utilization of recycled materials in the creation of new PU products. The review offers an in-depth explanation of the acidolysis process and thoroughly examines the degradation mechanisms involved. Additionally, it scrutinizes the impact of reaction conditions on the properties of the recycled materials and investigates their applicability in the production of novel materials. Moreover, the review presents an analysis of the environmental and economic implications associated with these processes. In summary, this review overviews the current status of acidolysis of PU and prospects for its future. [ABSTRACT FROM AUTHOR]

This study explores the use of cellulose nanofiber (CNF)-stabilized Pickering emulsions for paper coatings, focusing on their rheological properties and effects on hydrophilicity and water vapor transmission rate (WVTR). Two types of Pickering emulsions, oil-in-water (O/W), were stabilized with 1 wt% CNF extracted from fique by-products. The oily phases of the emulsions were composed of poly(lactic acid) (PLA) and cocoa butter (CB). The physical stability, viscosity, and viscoelasticity of the emulsions were characterized. The emulsions were applied to the surfaces of Bond and Kraft papers using the rod-coating method. The coating process involved first applying a layer of the PLA emulsion followed by a layer of the CB emulsion. The coated papers were then evaluated by FE-SEM, contact angle, adhesion work, and water vapor transmission rate (WVTR). The results indicated that the coatings effectively produced a slightly hydrophobic surface on the papers, with contact angles approaching 90°. Initially, Kraft paper exhibited a WVTR value of 29.20 ± 1.13 g/m2·h, which significantly decreased to 7.06 ± 2.80 g/m2·h after coating, representing a reduction of 75.82%. Similarly, natural Bond paper showed a WVTR value of 30.56 ± 0.34 g/m2·h, which decreased to 14.37 ± 5.91 g/m2·h after coating, indicating a reduction of 47.02%. These findings demonstrate the potential of CNF-stabilized Pickering emulsions for enhancing the performance of paper coatings in terms of hydrophobicity and moisture barrier properties. The approach of this study aligns with global sustainability goals in packaging materials combining the use of PLA and CB to develop a waterborne coating to enhance the moisture barrier properties, demonstrated by a substantial reduction in water vapor transmission rates, and an improved hydrophobicity of coated papers. [ABSTRACT FROM AUTHOR]

Dust deposition poses a significant challenge in the implementation of photovoltaic panels (PV) especially in hot and dusty environments, such as the Middle East and North Africa (MENA) region. This issue leads to progressive degradation of PV efficiency and output power. In this context, this research work aims to improve PV performance by developing self-cleaning sprays as a preventative solution. Different concentrations of SnO2 and TiO2 nanoceramics were dispersed in isopropyl alcohol solvent to reduce the mixture's viscosity and facilitate smooth spraying on solar panels, whose efficiency was continually assessed in outdoor conditions. Although less commonly used for this application, the nano-SnO2 was selected for the purpose of enhancing the surface hydrophobicity, whereas nano-TiO2 was included for its favorable photocatalytic properties. Polydimethylsiloxane (PDMS) oil, known for its self-cleaning characteristic, was served as the base material in the developed sprays. The described blend of materials represents a novel combination. The results indicated that 2.5% nano-SnO2 and 2.5% nano-TiO2 in PDMS oil enhanced efficiency by 5.4% compared to a non-sprayed panel after five weeks of outdoor exposure. This efficiency gain was experimentally justified and attributed to the spray's ability to achieve a water contact angle (WCA) of 100.6°, forming a hydrophobic surface conducive to self-cleaning. Further characterization results, including photocatalysis and zeta potential have been gathered and analyzed. [ABSTRACT FROM AUTHOR]

Polymer electrolyte membrane fuel cell durability is still a major challenge. To overcome time‐consuming durability tests, so‐called accelerated durability tests (ADTs) are of urgent need. This work presents our recent results in developing ADT protocols in the context of realistic operating conditions, especially voltage clipping at 0.85 V. A 5500 h long‐term test was carried out as a reference applying a realistic automotive drive cycle. Focusing on different stressors such as temperature, relative humidity (RH), and load profile four different ADT protocols of 1200 h duration were derived. Seven‐cell short stacks with 240 cm2 active area were used. Comparing cell voltage as a key indicator, an acceleration factor of 3–7 could be achieved. In‐situ characterization techniques such as spatially resolved current measurement, cyclic voltammetry, and electrochemical impedance spectra were employed to investigate the influences of individual stressors on specific degradation mechanisms and components. The highest acceleration was observed in the mass transport region of ADTs addressing RH as a stressor, suggesting that RH cycling leads to increased degradation of hydrophobic surfaces. Increased temperature was found to accelerate primarily carbon support degradation. Accelerated catalyst aging seems to be low, demonstrating the effectiveness of voltage‐clipping conditions. Our most promising ADT shows quite a homogeneous acceleration of voltage degradation across all current regions. [ABSTRACT FROM AUTHOR]

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In this study, inorganic-organic coatings composed of titanium dioxide (TiO 2) as the ceramic component and poly(vinylidene fluoride- co -hexafluoropropylene) (PVDF-HFP) as the polymer matrix, hybridized with nano-TiO 2 particles, were developed for protecting mild steel (MS) from corrosion. Prior to TiO 2 coating deposition, the MS substrates were pretreated with a bioinspired sub-layer of polydopamine to improve the surface coating adhesion, followed by uniform co-deposition of PVDF-HFP with varying concentrations of embedded nano-TiO 2. The inclusion of nano-TiO 2 further reinforces and densifies PVDF-HFP, providing added corrosion protection. The fabricated coatings were characterized by microscopy, spectroscopy, and diffraction technique, while the corrosion protection properties were evaluated by impedance, potentiodynamic polarization, salt spray, and cyclic corrosion tests. Results showed that both the PVDF-HFP matrix and TiO 2 contents had substantial effects on the coatings' thermal stability, hydrophobicity, and surface mechanical properties. The coatings also exhibited satisfactory corrosion resistance, with increased impedance modulus to roughly sixteen orders of magnitude for the TiO 2 -PVDF-HFP coating containing 0.5 g/L TiO 2 , relative to the untreated MS substrate. This result can be attributed to the low surface energy of PVDF-HFP, coupled with the dense structure and added physical barrier of nano-TiO 2. Overall, these hybrid polymer/ceramic coatings are poised to help design other highly resilient and hydrophobic surface coatings with durable protection against corrosion. [ABSTRACT FROM AUTHOR]

Highlights In the present work, the impact of corona aging on the dielectric, thermal, and surface properties of silicone rubber filled with different nanofillers such as alumina (Al2O3), aluminum trihydrate (ATH), boron nitride (BN), and titania (TiO2) are studied. The surface degradation of the silicone rubber nanocomposites after corona aging is evaluated through contact angle measurement, atomic force microscopy (AFM) studies, and by water droplet‐initiated corona inception voltage studies. Alumina filled silicone rubber shows less reduction in surface and hydrophobic properties after corona aging. Water droplet initiated corona inception voltage (CIV) under negative DC voltage is much higher than under positive DC and AC voltages. Al2O3/TiO2‐ filled silicone rubber samples show better CIV performance. The Dielectric Response Spectroscopy (DRS) indicates that TiO2 filled silicone rubber insulating material possesses higher permittivity at lower frequencies. Boron nitride added composites have high thermal conductivity whereas ATH filled silicone rubber composites shows higher decay rate, as observed through laser‐induced thermography studies. A significantly high surface leakage current is observed in all samples after corona aging. The Space Charge Limited Current (SCLC) studies clearly indicate that inclusion of nano‐fillers resulted in an increase in crossover voltage and trap density values compared to base silicone rubber. Al2O3 filled silicone rubber exhibits lower surface roughness even after corona aging. High thermal conductive composites show better performance even after corona aging. ATH, and BN filled silicone rubber have improved thermal conductivity by 35.2% and 76.3%. TiO2 filler added silicone rubber exhibits high permittivity with low tan δ. Al2O3 filled silicone rubber has minimal surface and volume leakage current Crossover voltage and the trap density get enhanced on addition of fillers to the base polymer. [ABSTRACT FROM AUTHOR]

A durable and efficient hydrophobic/superoleophilic MIL-88A(Fe)@sponge (MS) with high throughput was fabricated via the dip-coating technique. Its adsorption capacities for pump oil, peanut oil, and CCl4 were 32.13 g g−1, 34.85 g g−1, and 34.25 g g−1, respectively. The hydrophobic surface of MS has excellent chemical resistance and physical stability in harsh environments. [ABSTRACT FROM AUTHOR]

\nHIGHLIGHTSPolymer nanocomposites are increasingly used in insulation applications for enhanced electrical properties. However, there are intricate parameters that control the properties of the polymer, and hence investigations are required. This paper attempts to correlate the electrical properties of Epoxy/Organically modified montmorillonite clay composites with the free volume resulting from the incorporation of the Organically modified montmorillonite clay filler of 2, 5, and 7 weight per cent (wt.%). Positron annihilation spectroscopy has been used to compute the fractional free volume and free volume. The free volume percentage is observed to increase with the incorporation of 2 and 5 wt.% and reduces at 7 wt.%. A similar trend is observed in the average size of free volume. The filler increases the AC electric breakdown strength by 20%, arc resistance by 5%, and comparative tracking index by 10% at 5 wt.%. Thermal conductivity is seen to increase marginally with the filler. The surfaces of the composites are hydrophilic at 2 and 7 wt.%, and at 5 wt.%, it is hydrophobic. Longer durations of water diffusion render the surfaces of the nanocomposites hydrophobic. Fourier transform infrared spectroscopy investigations reveal broadening of peak, increase in peak intensity and stretching of Si–O–Si bonds at 5 wt.% of filler due to exfoliation. An attempt has been made to understand the results of electrical parameters based on the results of positron annihilation lifetime spectroscopy and thermal conductivity. Water diffusion is minimal at 5 wt.% of OMMT.Highest CTI of 588 is achieved at 5 wt.%.Arc resistance of 400 s is achieved at 5 wt.%. OMMT.Proof tracking is higher at 5 wt.% of OMMT.Surface is hydrophobic at 5 wt.% OMMT.Water diffusion is minimal at 5 wt.% of OMMT.Highest CTI of 588 is achieved at 5 wt.%.Arc resistance of 400 s is achieved at 5 wt.%. OMMT.Proof tracking is higher at 5 wt.% of OMMT.Surface is hydrophobic at 5 wt.% OMMT. [ABSTRACT FROM AUTHOR]

Laboratory sciences and disease diagnostics need accelerated medical tests, ease of testing for patients, and lower diagnostic costs. In this respect, one of the most innovative methods is paper-based microfluidic analysis tools, called micro-PAD. Since the chemical-based micro-PADs need sufficient blood to show an accurate blood test, the shape of the micro-PADs, the blood quantity, and the droplet flow to reach the end of the microchannels are important. Therefore, this research showed the liquid droplet motion on a heterogeneous (hydrophobic and hydrophilic) surface using the lattice Boltzmann method, and two star-shaped micro-PADs were modeled to investigate the effect of the droplet size and the droplet deflection from the center of the micro-PAD on liquid flow in microchannels. Based on the obtained results, fluid behavior was similar in two patterns (ten-pointed pattern and four-pointed pattern). This study compared the effects of parallel, convergent, and divergent channels in a four-pointed pattern on fluid velocity. The off-center error of the droplet was considered at the initial moment. The obtained results confirmed the direct relationship between the increased deviation of the center and the lack of uniformity in the fluid penetration. The present simulation results were validated against the laboratory data. [ABSTRACT FROM AUTHOR]

To solve the frost failure problem on super-hydrophobic surfaces in low temperature and high humidity environment, the slippery surface was fabricated by coating with lubricant oil on the rough super-hydrophobic surface. The wettability and microstructures of slippery surfaces were determined. The experimental platforms of frost prevention system and vertical defrosting test system were designed and constructed to investigate the dynamic behavior of frosting and defrosting on slippery surface, super- hydrophobic surface and pure copper surface. The results show that on the slippery surface, the dynamic lubricant film can be generated in the porous and rough structures of the substrate, which can effectively reduce the frost crystal nucleation and prevent the formation of "ice bridge". The frost mass and propagation speed wave on slippery surface are significantly lower than those on super-hydrophobic surface and pure copper surface, which shows better frost inhibition performance. During the process of vertical defrosting and drainage, the defrosting efficiency on cach surface is proportional to the frosting mass. The mass and surface coverage of residual water upon defrosting on slippery surfaces are slightly higher than that on super-hydrophobic surface and lower than that on pure copper surface, which exhibits good defrosting and drainage performance. [ABSTRACT FROM AUTHOR]

Chitosan (CHT) and propolis (P) are natural materials with antiseptic, anti-inflammatory, antimicrobial, and mucoadhesive properties with many applications in orthopaedia dentistry. The objective of this study was to develop a low molecular weight (LMW) and medium molecular weight (MMW) chitosan polymeric system with propolis at different concentrations (0.31%, 0.62%, 1.25%, 2.5%, and 5%) and to evaluate the effect in terms of their cell interaction with dental pulp fibroblasts. FTIR spectra of both molecular weights CHT's films with propolis show increased transmittance bands at 1730–1720 cm−1 and 1460 cm−1, indicating the presence of propolis ethanolic extract in the organic matrix. Contact angles test to determine hydrophobicity CHT films functionalized with propolis exhibit a more hydrophobic surface as propolis concentration increases. Cytotoxicity showed synergy between chitosan and propolis; the highest proliferation was observed in LMW CHT with 0.31% of propolis. Membranes made with CHT of both molecular weights plus propolis in an inflammatory stage (cells previously treated with LPS) can inhibit the expression of NF-k-B, MAPK, and VEGF. A polymeric system based on chitosan/ethanolic extract propolis could be a future alternative treatment for oral ulcers. [ABSTRACT FROM AUTHOR]

Hydrophobic surfaces exhibit unique surface effects and hold broad potential across numerous domains, including anti-icing, condensation, and self-cleaning. Conventionally, droplets on hydrophobic surfaces have been conceptualized as spherical segments to predict contact angles. However, a droplet deposited on hydrophobic surfaces tends to be flattened at the bottom due to gravity, leading to a discrepancy between the experimental observation and prediction derived from the Cassie–Baxter equation. Here, we propose an approximation that divides the distorted droplet into upper and lower segments, i.e., simplifying its morphology into a double-radius contour. This approach leads to a more accurate prediction of the contact angle on hydrophobic structured surfaces. The deviation between experiment and our model is less than 1.7%. Further water evaporation was conducted to investigate the transition condition from the Cassie–Baxter state to the Wenzel state, and we show that the critical transition radius for substrates with varied microstructural geometry parameters consistently falls slightly below the theoretical prediction, which is attributed to an inaccurate assessment of the structure angle. Finally, we demonstrate that the stability of the Cassie–Baxter state can be enhanced by employing hierarchical micro-/nanostructures on the surface. This research advances our foundational comprehension of wetting phenomenon and the stability of the Cassie–Baxter state. [ABSTRACT FROM AUTHOR]

Droplet impact on surfaces integrated with the electrowetting effect has been recently explored to control droplet spreading and recoiling behavior on hydrophobic surfaces. With the integration of electrowetting, the spreading of the impacting droplet on hydrophobic surfaces increases, whereas the rebound tendency is suppressed. The present work numerically investigates the droplet impact on hydrophobic surfaces under partial electrowetting (EW) effects. In partial EW, the electrowetting effect is immediately cut off once the droplet attains the maximum spreading diameter. In addition, based on the energy conservation principle, a mathematical model is developed to predict the maximum spreading diameter of the droplet and its kinetic energy during bouncing for different parameters. The partial EW technique enhances the maximum spreading diameter and reduces the recoiling time compared to full EW and no EW effect. The recoiling time decreases with the increase in voltage amplitude, frequency, Weber number, and surface wettability. [ABSTRACT FROM AUTHOR]

The impact of droplets on solid surfaces is a crucial fluid phenomenon in the additive industry, biotechnology, and chemistry, where controlling impact dynamics and duration is essential. While extensive research has focused on flat substrates, our understanding of impact dynamics on curved surfaces remains limited. This study seeks to establish phase diagrams for the process of droplet impact on solid spheres and further quantitatively describe the effect of curvature through theoretical analysis. It aims to determine the critical conditions between different impact outcomes and also establish a scaling relationship for the contact time. Here, the post-impact outcome regimes occurring for a wide range of Weber numbers (We) from 1.2 to 173.8, diameter ratio (λ) of solid spheres to nanodroplets from 0.25 to 2, and surface wettability (θ) from 21° to 160°, through the molecular dynamics simulation method (MD) and theoretical analysis. The MD simulations reveal that the phase diagrams of droplet impacts on hydrophilic, hydrophobic, and superhydrophobic spheres differ, with specific distinctions focusing on rebound and three different forms of dripping. Furthermore, a theoretical model based on the principle of energy conservation during impact on superhydrophobic surfaces has been developed to predict the critical conditions between rebound and dripping states, showing good agreement with simulation results. Additionally, a new scaling relationship of contact time for droplet impact on superhydrophobic spherical surfaces has also been established by extending and modifying the existing models, which also agrees well with the simulated results. These insights provide a foundational understanding for designing surface structures. [ABSTRACT FROM AUTHOR]