Contact Angles Of Air Bubbles Research Articles

High-performance porous 3D Ni skeleton electrodes for the oxygen evolution reaction

A key component of green hydrogen production technologies is the fabrication of large-scale porous transport layer (PTL) for use in anion electrolyte membrane water electrolysers (AEMWEs). One strategy to achieve that goal is to manufacture Ni-based 3D electrode skeletons that can be further catalyzed to achieve high current densities at low overpotentials. In the present work, shock-wave induced spray (SWIS) and cold spray (CS) deposition techniques were used to prepare 20 cm2 Ni-based electrode skeletons. In our experimental conditions, the porosity of coatings prepared using the SWIS deposition system and Ni powders with particle sizes D50 = 32 and 75 μm never exceeded 28%. Higher porosity could only be achieved using the CS deposition system and a spheroidal Ni–Al powder, whose particles consist of an aluminum core encapsulated in a nickel shell. After Al leaching in an alkaline solution, the resulting electrodes showed good mechanical and structural integrity with up to 41% porosity. The electrochemical active surface area of the most porous electrodes is a factor of 2100 larger than a polished Ni plate, and it has superaerophobic properties with a captive air bubble contact angle of 151°. During 1 h of electrolysis, the overpotential at 100 mA cm−2 of the most active leached Ni–Al cold spray deposited electrode was 330 mV, compared to 380 mV for a Ni foam electrode.

The orbital hoods of snapping shrimp have surface features that may represent tradeoffs between vision and protection

Snapping shrimp (Alpheidae) are decapod crustaceans named for the snapping claws with which they produce cavitation bubbles. Snapping shrimp use the shock waves released by collapsing cavitation bubbles as weapons. Along with their distinctive claws, snapping shrimp have orbital hoods, extensions of their carapace that cover their heads and eyes. Snapping shrimp view the world through their orbital hoods, so we asked if the surfaces of the orbital hoods of the snapping shrimp Alpheus heterochaelis have features that minimize the scattering of light. Using SEM, we found that surface features, primarily microbial epibionts, covered less space on the surfaces of the orbital hoods of A. heterochaelis (∼18%) than they do elsewhere on the carapace (∼50%). Next, we asked if these surface features influence aerophobicity. By measuring the contact angles of air bubbles, we found the orbital hoods of A. heterochaelis are less aerophobic than other regions of the carapace. Surfaces that are less aerophobic are more likely to have cavitation bubbles adhere to them and are more likely to have shock waves cause new cavitation bubbles to nucleate upon them. Computational modeling indicates the orbital hoods of A. heterochaelis face a functional trade-off: fewer surface features, such as less extensive communities of microbial epibionts, may minimize the scattering of light at the cost of making the adhesion and nucleation of cavitation bubbles more likely.

Flexible coatings with microphase separation structure attained by copolymers and ultra-fine nanoparticles for endurable antifouling

Incorporating antibacterial agent into biomimetic coating inspired by natural organisms with micro-nano structure surface has generated more interest for antifouling applications. In this work, poly(dimethylsiloxane) (PDMS)-based triblock copolymers and sub-20 nm nanoparticles Ag and heterogeneous Fe3O4-coated Ag (Fe3O4@Ag) were used to construct microphase separation topography with oriented copolymer blocks structure. The artificial surface was verified by atomic force microscopy and scanning electron microscopy images. Meanwhile, the surface exhibited relative stable hydrophobic property, which was demonstrated by the water contact angle and dynamic air-bubble contact angle measurements. Consequently, after immersed in BSA solution 24 h and 720 h, the actual BSA absorption amount of the surface with Fe3O4@Ag nanoparticles was as low as 10 % and 27 % that of the initial BSA amount, respectively. Moreover, the surface also showed remarkable antibacterial performance, which effectively suppressed the growth rate of Escherichia coli. The strategy of constructing the flexible microphase separation structure by introducing heterogeneous inorganic antibacterial nanoparticles into a block copolymer substrate opens up a new way to create an antifouling surface coating.

Contact angles and movement of air bubbles on bioinspired conical surfaces

Air bubbles are of interest in various applications. The study of their formation, interaction with underlying surfaces, and their movement is of importance. Bioinspired conical surfaces have been known to exhibit Laplace pressure gradient which facilitates the movement of liquid droplets. These conical surfaces, with various geometries and wettabilities, can be used to regulate gas bubble movement. In this study, contact angles of air bubbles and their movement on various conical surfaces were investigated. The effect of parameters including cone orientation, air bubble volume, tip angle, and wettability on air bubble movement were studied. A smaller tip angle cone with high wettability was found to be most efficient for an air bubble movement.

Wetting characteristic of bubble on micro-pillar structured surface under a water pool

In this study, the contact angle of air bubbles on a micro-structured surface under a water pool is experimentally investigated. A previous study “Kang and Jacobi, Equilibrium Contact Angles of Liquids on Ideal Rough Surfaces, Langmuir (2011)” adopted the work of adhesion as the additional work of the process of droplet contact on a textured surface, and it explained the reason for failure of the classical theoretical model (Wenzel equation) in real wetting tests. We extended the above concept to bubble interaction with the textured surface. First, the bubble contact angles on the textured surface were modeled based on the concept of the work of adhesion in the free energy calculation. Second, the contact angle of air bubbles was measured on the bottom of test surfaces under a water pool. The test-section surfaces have micro-pillars with a size of 5–40 μm prepared by the microelectromechanical systems (MEMS) technique. The bubble contact angles were compared with both the modeled bubble shape and classical prediction (Wenzel & Cassie–Baxter equations). In addition, detail wetting features which shows wetting transition and critical wetting behavior of bubble were discussed.

Effects of PEG-TMS on the stability and antifouling performances of hydrocarbon-modified amphiphilic xerogel coatings

Amphiphilic xerogel films with slight swelling were prepared by the acid-catalysed sol-gel method starting from tetraethoxysilane (TEOS), triethoxyoctylsilane (C8Si), n-octadecyl trimethoxysilane (C18Si) and poly(ethylene glycol) siloxane (PEG-TMS). In these amphiphilic xerogel films, the presence of hydrophobic chains, especially C18Si facilitated the emigration of PEG chain to the coating/air interface during the film formation/curing process, and then the PEG chains enriched at the surface of coatings further slightly emigrated to form hydration layer underwater confirmed by energy dispersive X-ray spectroscopic (EDS) analysis, captive air-bubble contact angle (CA) and CA hysteresis. Furthermore, the amphiphilic xerogel films showed the optimal water absorption ratio lower than 1.0% due to the restraint of higher crosslinked density and little network aperture of the films on PEG chains. The antifouling performances of amphiphilic xerogel films included the protein resistance for FITC-BSA, antibacterial property for Escherichia coli and the resistance for diatom Navicula, were better than those of the elastic silicone-based coatings and xerogel film without hydrophilic PEG chains. In general, the amphiphilic xerogel films containing both PEG and proper levels of C8Si and C18Si possessed excellent fouling release properties and slight swelling due to the synergistic effects.

A study on air bubble wetting: Role of surface wettability, surface tension, and ionic surfactants

Fabrication of hydrophobic/hydrophilic surfaces by biomimicking nature has attracted significant attention recently due to their potential usage in technologies, ranging from self-cleaning to DNA condensation. Despite the potential applications, compared to surfaces of tailored wettability, less attention has been paid towards development and understanding of air bubble adhesion and its dynamics on surfaces with varying wettability. In this manuscript, following the commonly used approach of oxygen plasma treatment, polydimethylsiloxane surfaces with tunable wettability are prepared. The role of plasma treatment conditions on the surface hydrophilicity and the consequent effect on adhesion dynamics of an underwater air bubble is explored for the first time. The ATR-FTIR spectroscopic analysis reveals that the change in hydrophilicity arises from the chemical modification of the surface, manifested as Si-OH vibrations in the spectra. The thickness of the formed thin liquid film at the surface responsible for the experimentally observed air bubble repellency is estimated from the augmented Young-Laplace equation. The concentration dependent studies using cationic as well as anionic surfactant elucidate that the reduced surface tension of the aqueous solution results in a stable thicker film and causes non-adherence of air bubble to the aerophilic surface. Furthermore, the study carried out to understand the combined effect of plasma treatment and surfactants reveals that even below critical micelle concentration, a negatively charged surface results in air bubble repellency for the anionic surfactant, whereas only enhanced air bubble contact angle is observed for the cationic surfactant.

Construction of a blood-compatible interface based on surface segregation in a polymer blend

The technique of surface segregation was applied to prepare a bio-inert polymer interface. A small amount, 10 wt%, of poly(2-methoxyethyl acrylate) (PMEA), which exhibits excellent bio-inertness properties, fed into a matrix polymer was able to suppress platelet adhesion sufficiently to be of practical use. PMEA was effective because it was preferentially segregated at the outermost region of the polymer blend. Combining interfacial-sensitive analyses such as the air bubble contact angle and neutron reflectivity measurements and sum-frequency generation spectroscopy with the platelet adhesion test gives a better understanding of how the bio-inert property is expressed at the water interface.

STIMULI RESPONSIVE MORPHOLOGICAL CHANGES OF PNIPA POLYMER BRUSHES SYNTHESIZED ON SILICON SUBSTRATE

High-density polymer brushes were grown from the silicon surface by atom transfer radical polymerization of Poly(N-isopropylacrylamide) (PNIPA) at different polymerization conditions. PNIPA brushes were prepared using Copper (I) Chloride/tris(2-(dimetylamino)ethyl)amine (Me6TREN) as a catalytic system in DMSO at 20°C. Free polymer formed during the brush formation was characterized by gel permeation chromatography. The grafting densities up to 0.52 chains/nm2 were obtained. The layer thickness of polymer brush increases with the increase of conversion of the monomer conversion as well as polymerization time. Atomic force microscopy and air bubble contact angle under pH solution were employed to study the surface morphology, reversible conformational changes of and stimulus-response behavior. PNIPA brushes exhibited a different nanomorphology after treatment with different pH solution. It also revealed a unique reversible wetting behavior with pH. The reversible properties of the PNIPA brushes can be used to regulate the adsorption of the sulfonated PS nanoparticles.

Thin phosphatidylcholine films as background surfaces with further possibilities of functionalization for biomedical applications

Non-specific adsorption is a crucial problem in the biomedical field. To produce surfaces avoiding this phenomenon, we functionalized thin (7–180nm) poly(methylhydrosiloxane) (PMHS) network films at room temperature (≈20°C) with phospholipids (PL) bearing a phosphorylcholine head. Regardless of their mode of preparation (casting or immersion), all surfaces appeared to be very hydrophilic with a captive air-bubble contact angle stabilized around 40°. The thin films were protein-repellent in phosphate saline buffer pH 7.4 according to analysis by normal scanning confocal fluorescence. Neither was any adsorption or spreading of l-α-phosphatidylcholine liposomes on such films observed. In addition, amino functional groups could be easily attached to the surface remaining available for further functionalization.

Reconstruction of Surfaces from Mixed Hydrocarbon and PEG Components in Water: Responsive Surfaces Aid Fouling Release

Coatings derived from surface active block copolymers (SABCs) having a combination of hydrophobic aliphatic (linear hydrocarbon or propylene oxide-derived groups) and hydrophilic poly(ethlyene glycol) (PEG) side chains have been developed. The coatings demonstrate superior performance against protein adsorption as well as resistance to biofouling, providing an alternative to coatings containing fluorinated side chains as the hydrophobe, thus reducing the potential environmental impact. The surfaces were examined using dynamic water contact angle, captive air-bubble contact angle, atomic force microscopy, X-ray photoelectron spectroscopy, and near-edge X-ray absorption fine structure analysis. The PS(8K)-b-P(E/B)(25K)-b-PI(10K) triblock copolymer precursor (K3) initially dominated the dry surface. In contrast to previous studies with mixed fluorinated/PEG surfaces, these new materials displayed significant surface changes after exposure to water that allowed fouling resistant behavior. PEG groups buried several nanometers below the surface in the dry state were able to occupy the coating surface after placement in water. The resulting surface exhibits a very low contact angle and good antifouling properties that are very different from those of K3. The surfaces are strongly resistant to protein adsorption using bovine serum albumin as a standard protein challenge. Biofouling assays with sporelings of the green alga Ulva and cells of the diatom Navicula showed the level of adhesion was significantly reduced relative to that of a PDMS standard and that of the triblock copolymer precursor of the SABCs.

Fluorinated Amphiphilic Polymers and Their Blends for Fouling-Release Applications: The Benefits of a Triblock Copolymer Surface

Surface active triblock copolymers (SABC) with mixed polyethylene glycol (PEG) and two different semifluorinated alcohol side chains, one longer than the other, were blended with a soft thermoplastic elastomer (TPE), polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SEBS). The surface composition of these blends was probed by X-ray photoelectron spectroscopy (XPS) and near edge X-ray absorption fine structure (NEXAFS) spectroscopy. The surface reconstruction of the coatings in water was monitored qualitatively by dynamic water contact angles in air as well as air bubble contact angle measurements in water. By blending the SABC with SEBS, we minimize the amount of the SABC used while achieving a surface that is not greatly different in composition from the pure SABC. The 15 wt % blends of the SABC with long fluoroalkyl side chains showed a composition close to that of the pure SABC while the SABC with shorter perfluoroakyl side chains did not. These differences in surface composition were reflected in the fouling-release performance of the blends for the algae, Ulva and Navicula.

Understanding the biocompatibility of microcapsules designed for islet cell transplantation

| 233 (score 1.02 ± 0.03). This difference in biocompatibility was significant (p < 0.001). Yet, alginate hydrophilicity was similar, as water droplets on dry films had contact angles of 38.7 ± 1.7° and 39.0 ± 1.3° for Alg I and Alg II, respectively. When PLL was added to the capsule membrane, the immune response was more severe (p < 0.01), as cell adhesion scores increased to 1.11 ± 0.11 for Alg I and to 1.55 ± 0.07 for Alg II. Similarly, the cell adhesion score increased to 0.49 ± 0.06 when PLO was added to Alg I capsules, indicating a non-significant increase in capsule immunogenicity. A comparison of contact angles of water on dry films containing polycations was not possible due to irregular surfaces and complete wetting. We are currently measuring the contact angles of air bubbles on hydrated films. conclusions: The guluronic acid content of alginate has a significant effect on its biocompatibility in vivo. Incorporating polycations into the membranes of alginate microcapsules lowers their biocompatibility. So far, these results cannot be explained by the hydrophilicity of the samples. Transplantation islet and pancreas No conflict of interest

Incidence of urinary tract infections and of genital infections in two T2DM populations cotreated with dapagliflozin and oral antidiabetics +/− insulin

| 233 (score 1.02 ± 0.03). This difference in biocompatibility was significant (p < 0.001). Yet, alginate hydrophilicity was similar, as water droplets on dry films had contact angles of 38.7 ± 1.7° and 39.0 ± 1.3° for Alg I and Alg II, respectively. When PLL was added to the capsule membrane, the immune response was more severe (p < 0.01), as cell adhesion scores increased to 1.11 ± 0.11 for Alg I and to 1.55 ± 0.07 for Alg II. Similarly, the cell adhesion score increased to 0.49 ± 0.06 when PLO was added to Alg I capsules, indicating a non-significant increase in capsule immunogenicity. A comparison of contact angles of water on dry films containing polycations was not possible due to irregular surfaces and complete wetting. We are currently measuring the contact angles of air bubbles on hydrated films. conclusions: The guluronic acid content of alginate has a significant effect on its biocompatibility in vivo. Incorporating polycations into the membranes of alginate microcapsules lowers their biocompatibility. So far, these results cannot be explained by the hydrophilicity of the samples. Transplantation islet and pancreas No conflict of interest

Efficacy of dapagliflozin in three populations of patients on different treatment regimens for various stages of T2DM

| 233 (score 1.02 ± 0.03). This difference in biocompatibility was significant (p < 0.001). Yet, alginate hydrophilicity was similar, as water droplets on dry films had contact angles of 38.7 ± 1.7° and 39.0 ± 1.3° for Alg I and Alg II, respectively. When PLL was added to the capsule membrane, the immune response was more severe (p < 0.01), as cell adhesion scores increased to 1.11 ± 0.11 for Alg I and to 1.55 ± 0.07 for Alg II. Similarly, the cell adhesion score increased to 0.49 ± 0.06 when PLO was added to Alg I capsules, indicating a non-significant increase in capsule immunogenicity. A comparison of contact angles of water on dry films containing polycations was not possible due to irregular surfaces and complete wetting. We are currently measuring the contact angles of air bubbles on hydrated films. conclusions: The guluronic acid content of alginate has a significant effect on its biocompatibility in vivo. Incorporating polycations into the membranes of alginate microcapsules lowers their biocompatibility. So far, these results cannot be explained by the hydrophilicity of the samples. Transplantation islet and pancreas No conflict of interest

Wettability of coal – a comparative study

A comparative study of the contact angles of air bubbles, hydrocarbon oils (benzene and dodecane – both in the absence and in the presence of water‐soluble dodecylamine (laurylamine) chloride), flocculants and coagulants drops on flat polished coal surfaces immersed in water was made. The effect of the hydrocarbon chain length of some n‐alkylamine chlorides on the coal‐oil‐water was also investigated. The relationship of the measured contact angles to the flocculants, coagulants and dodecylamide chloride concentrations and pH was established. Results obtained show that maximum contact angles for the coals studied occur in the alkaline pH range (pH&gt;7) for the systems investigated. Evidence is also provided to show that benzene and dodecane do not spread spontaneously on wet coal surfaces, even in the presence of a water‐soluble cationic surfactant. The results further show that the coal‐benzene water contact angles increase with an increase in the hydrocarbon chain length of the surfactant. Coagulants probably affect flotation of coal fines adversely, whereas flocculants have a remarkable effect on contact angles similar to that of surfactants.

Temperature-Responsiveness of A-B-A Block Telomers at Solid–Liquid Interfaces

Macroinitiators were prepared by coupling disuccinimidyl ester of 4,4′-azobis(cyanovaleric acid) with poly(N-isopropylacrylamide) (PIPA), which had an amino group at its end. Styrene was telomerized with the initiators in THF. When the styrene content in the A-B-A block telomer obtained (PIPA-b-PSt-b-PIPA) was high, the telomer formed an irreversible aggregation resulting in microspheres, whereas the telomer with a much shorter styrene block could be dispersed monomolecularly. The telomers dispersed in water were aggregated by raising the temperature above 32°C due to a coil–globule transition of PIPA moieties. The PIPA-b-PSt-b-PIPA could be strongly adsorbed to polystyrene (PSt) solid surfaces to form a layer, and the PSt blocks might lay on the PSt surface and the PIPA blocks might direct to the solution phase. The contact angle of air bubbles on the surface of telomer-coated PSt in the air-in-water system was dependent on temperature; that is, with the increase in temperature the contact angle of air bubbles largely decreased and leveled off above the coil–globule transition temperature (Tc). Correspondingly, the amount of protein Concanavalin A adsorbed to the telomer layer deposited on the PSt surface increased gradually with an increase in temperature and leveled off above theTc. These phenomena were attributed to the changes in hydrophobicity of the telomer layer below and above theTc. The usefulness of macroinitiators in preparing various kinds of block telomers which have responsiveness to external stimuli was strongly suggested.

Biofouling potentials of microporous polysulfone membranes containing a sulfonated polyether-ethersulfone/polyethersulfone block copolymer: correlation of membrane surface properties with bacterial attachment

Multivariate methods were used to identify relationships between bacterial attachment (biofouling potential), water transport, and the surface properties of nine modified polysulfone (MPS) membranes comprising blends of polysulfone (PS) with a sulfonated polyether-ethersulfone/polyethersulfone block copolymer. The topology of the microporous MPS membranes, including surface roughness, surface height, pore size and pore geometry were determined by atomic force microscopy (AFM) and digital image analysis. Other measurements included relative surface hydrophobicity by captive bubble contact angle, surface charge (i.e., degree of sulfonation) by uranyl cation binding, wt% solids, porosity, membrane thickness, water flux, and the affinity of membranes for a hydrophilic Flavobacterium and hydrophobic Mycobacterium species. The mycobacteria attached best to the MPS membranes, but the attachment of both organisms was inversely correlated with the mean aspect ratio of pores, suggesting that irregular or elliptic pores discouraged attachment. Multivariate regression analyses identified the pore mean aspect ratio, mean surface height, PS content, and the n-methylpyrrolidone+propionic acid (NMP–PA) solvent concentration as influential factors in Mycobacterium attachment, whereas membrane thickness, surface roughness, pore mean aspect ratio, porosity, and the mean pore area/image area ratio influenced Flavobacterium attachment. Cluster analyses revealed that Mycobacterium attachment was associated with hydrophobic determinants of the MPS membranes, including PS content, wt% solids, and air bubble contact angle. In contrast, Flavobacterium attachment was primarily associated with membrane thickness and charge (i.e., uranyl cation binding or degree of sulfonation). Membrane flux was inversely correlated with surface hydrophobicity and PS content, but (in contrast to cell attachment) positively correlated with most pore geometry parameters including the mean aspect ratio, suggesting that pore geometry can be optimized to minimize cell attachment and maximize water transport. Other variables influencing water flux included the NMP–PA solvent concentration and membrane roughness. The results should facilitate the design of novel microporous PS membranes having reduced biofouling potentials and greater water fluxes.

Contact angle of air bubbles attached to an air-water surface in foam applications

A new method is developed to measure the contact angle of air bubbles attached to an air-water interface. The measurements made from the microscopic interference pattern (Newton rings), which are obtained by viewing the bubble in reflected light, are used in conjunction with the solutions of the Laplace equations to the fluid interfaces to obtain the contact angle of the film. Measurements made from a differential microscopic interference pattern were used to check the validity of the results.

The influence of n-alcohols on the wettability of hydrophobic solids

Measurements were made of contact angles of air bubbles on the hydrophobic solid surface of sulphur, graphite and Teflon in aqueous solutions of methanol, ethanol and propanol. Special attention was given to the measurements at low alcohol concentrations. The greatest changes in contact angle values as a function of alcohol concentration were observed at small alcohol concentrations, where changes in the solution surface tension were small. On this basis it is concluded that polar interactions between alcohol molecules in solution and those already adsorbed are important in defining the wetting properties of the hydrophobic solid under these conditions. The calculations based on the equation of Good, Girifalco, Fowkes and Young and Tamai et al. seem to verify the above conclusion.