Effect mechanism of metal cations on the interface interaction of cell-collector-bubble for microalgal foam flotation.

Foam flotation is generally recognized as a low-cost and efficient technology for the harvesting of microalgae for food, feed and fuel production, as well as environmental remediation. However, the harvesting efficiency of microalgae using foam flotation is restricted by the residual metal cations in the medium, and the corresponding inhibition mechanism has not yet been revealed. This study investigated the effects of metal cations in the medium on the harvesting efficiency and concentration factor during the foam flotation of Scenedesmus acuminatus. The interface interaction of cell-collector-bubble effected by metal cations was revealed by quantifying the amount of collector (cetyl trimethylammonium bromide, CTAB) between cells and bubbles, as well as the response of bubble interface characteristics. Results showed that the harvesting efficiency dropped linearly as the increase of cationic concentrations. Under the CTAB dose of 20 mg L-1, the harvesting efficiency decreased from 98.65% to 56.77% with a decrease of concentration factor from 25.41 to 9.05 in the presence of metal cations. The Na+ and Mg2+ in the medium were the major inhibitors. The inhibitory mechanisms revealed that metal cations obviously impeded the adsorption of CTAB onto the cells by competing adsorption site, resulting in a low harvesting efficiency. The presence of metal cations also inhibited the bubble coalescence and slowed down drainage velocity in the plateau channel of foam layer, forming foam with higher water content, thus reducing the concentration factor. A schematic illustration is proposed to better understand the effect mechanism of metal cations on microalgal foam flotation. This study might facilitate the process development in an effort to overcome the inhibition of cations during microalgal foam flotation.

Flotation mechanism and performance of air/condensate bubbles for removing oil droplets in the presence of acetic acid.

Flotation technology is widely utilized to remove emulsified oil droplets from Produced water. Organic acid adsorption on the oil droplet surface affects bubble attachment, reducing oil removal efficiency. This investigation exploited the principle of similar dissolution to synthesize condensate bubbles (CB). The surface properties of oil droplets and CB and air bubbles (AB) were appraised using FTIR, zeta potential, interfacial tension, and contact angle measurements. The research also investigated the effects of acetic acids (AA) on the adhesion of oil droplets to AB and CB along with the underlying mechanism via the Extended Derjaguin-Landau-Verwey-Overbeek (EDLVO) interaction theory and the Stefan-Reynolds model of liquid film thinning, integrated with adhesion times. Flotation efficiency and kinetic dissimilarities between AB and CB were also examined. The results indicated that CB exhibits superior lipophilic hydrophobicity compared to AB, reduced induction and spreading times upon oil droplet attachment, and maximized oil removal efficiency. Furthermore, CB could mitigate the impact of AA on adhesion. The interaction barriers between CB and oil droplets were minimal, and the thinning rate of the hydration film was quicker than in AB. The conventional first-order model proved effective in fitting the AB flotation, whereas a delay constant was applied to the model of the CB flotation rate.

Molecular Dynamics Simulation of the Synergistic Effect of Alkali/Surfactant/Polymer on the Formation and Stabilization of Water-Based Foam Systems.

The stable maintenance effect of a chemical oil displacement agent on a foam liquid film usually creates problems with the oilfields surface system. To achieve comprehensive insights into the influence mechanism of these chemical agent components on the foam liquid film, an "SDBS/HPAM/OH-" water-based foam simulation system and corresponding control systems were constructed by adjusting the categories and quantities of component molecules by molecular dynamics (MD) simulation. The simulated results indicated that the foam stability follows the order of "SDBS/HPAM/OH-" system > "SDBS/HPAM" system > "SDBS" system. The smaller the inclination angle of the SDBS molecular tail chain, the greater the tendency of the SDBS molecular configuration to be "upright" at the gas-liquid interface, which is not conducive to preventing the aggregation and penetration of gas molecules at the gas-liquid interface. Although the presence of HPAM molecules can significantly enhance the stability of the liquid film by restricting the liquid film's drainage and the diffusion of gas molecules, the addition of HPAM molecules would weaken the formation ability of the foam liquid film. Through decreasing the aggregation of cations around the co-adsorption layer, OH- not only enhances the interfacial activity of SDBS molecules, but also reduces the electrostatic repulsion between -COO- groups on the HPAM molecular chain, which makes the foam more stable. With an increase in the pH, SDBS concentration, and HPAM concentration, the stability of foam liquid film was strengthened. These results are helpful in facilitating new insights into the formation and stabilization mechanism of water-based foams. In particular, they provide support for the development and application of new defoaming technologies.

Endoscopic Vacuum Therapy for Staple Line Leaks after Sleeve Gastrectomy.

PURPOSE: Management of staple line leaks (SLL) after sleeve gastrectomy (SG) is challenging. The aim of this study was to evaluate the effectiveness of a novel endoscopic vacuum therapy (EVT) modality in the management of sleeve leaks. MATERIALS AND METHODS: Eight patients were treated with EVT for SLL. Therapy data and outcome measures including duration of therapy, therapy success, and change of treatment strategy were collected and analyzed. RESULTS: During the study period, SLL occurred in 1.6% of patients who underwent SG. After 9.8 ± 8.6 days of EVT, 3.3 ± 2.2 endoscopies, and 19 ± 15.1 days of hospitalization, endoscopic treatment using EVT was successful in seven out of eight patients (87.5%). CONCLUSIONS: EVT is an effective method for the management of staple line leaks after sleeve gastrectomy. The use of the intraluminal open-pore film drainage (OFD) could be considered as an advantageous modality of EVT, regarding placement and complications.

The influence of pH on the interfacial behaviour of Quillaja bark saponin at the air-solution interface.

The interfacial behavior of surfactants present in a natural extract from Quillaja saponaria Molina bark at the air-solution interface is studied by measurements of interfacial tension, interfacial elasticity, and interfacial reflectance FTIR spectroscopy. The active molecule, saponin, is observed directly at the air-solution interface (via reflectance FTIR spectroscopy) above and below the pKa of the molecule, and spectra confirm the altered charge of the interfacial layer at the two solution conditions. For all concentrations of saponin studied, and at pH values below and above pKa (i.e. pH 3 and 7), a reduction in interfacial tension as a function of time is observed, with some differences in early time-scale adsorption and with lower values of quasi-equilibrium interfacial tension for pH 3. The interfacial layer is seen to be elastic, as determined from measurements of hydrostatic expansion, with some variation at the two pH values, and as a function of concentration. In addition to interfacial layer characterisation, the interaction between two air-solution interfaces is probed using bubble collisions with an air-solution interface. This experiment allows for observation of thin film drainage kinetics and determination of the final foam film thickness for the case when one of the interfaces is at equilibrium while the dynamic adsorption layer is being established at the other. This is the first time when the interactions between such interfaces (i.e. only one being at equilibrium) have been studied. This is of particular importance for the formation stage of foams, during which time many of the interfaces are not at equilibrium. When two interfaces interact across a thin liquid film, pH is seen to significantly influence foam film thickness.

Linking aggregation and interfacial properties in monoclonal antibody-surfactant formulations.

Monoclonal antibodies (mAbs) are therapeutic proteins used in the treatment of many diseases due to their specificity in binding targets. Aggregation of these molecules is a major challenge in their formulation development. MAbs spontaneously adsorb onto air-solution interfaces and experience interfacial stresses, which is one of the major causes of aggregation. This work studies the effect of pharmaceutically relevant surfactants like polysorbate-20, poloxamer-188 and polyethylene glycol in controlling the aggregation and interfacial behavior of a mAb prone to interfacial aggregation. Agitation-induced aggregation was characterized using size-exclusion chromatography, flow cytometry and light obscuration. The addition of surfactants reduced the formation of aggregates. In the presence of surfactants competitively adsorbing to the interface, the number of soluble aggregates (size < 100 nm) depended on the amount of mAb adsorbed. On the other hand, the number of insoluble aggregates was governed not by the surface concentration, but by the ability of the adsorbed mAbs to interact and form a cohesive network. To correlate the aggregation in these mAb-surfactant mixtures with their interfacial behavior, studies on the drainage of a fluid film sandwiched between two mAb-surfactant laden interfaces were performed. The amount of fluid entrained depended on different governing mechanisms - interfacial rheology, surface tension and surface tension gradients for different surfactants. The surface tension gradients further resulted in an instability and local thickening in the sandwiched fluid film, which was affected by the presence of mAbs. Understanding the aggregation propensities of different mAb-surfactant mixtures and linking them to the interfacial behavior will greatly aid in understanding the aggregation mechanism and in mitigating aggregate formation by optimizing surfactant type and concentration in the formulation.

Recent experimental advances for understanding bubble-particle attachment in flotation.

Bubble-particle interaction is of great theoretical and practical importance in flotation. Significant progress has been achieved over the past years and the process of bubble-particle collision is reasonably well understood. This, however, is not the case for bubble-particle attachment leading to three-phase contact line formation due to the difficulty in both theoretical analysis and experimental verification. For attachment, surface forces play a major role. They control the thinning and rupture of the liquid film between the bubble and the particle. The coupling between force, bubble deformation and film drainage is critical to understand the underlying mechanism responsible for bubble-particle attachment. In this review we first discuss the advances in macroscopic experimental methods for characterizing bubble-particle attachment such as induction timer and high speed visualization. Then we focus on advances in measuring the force and drainage of thin liquid films between an air bubble and a solid surface at a nanometer scale. Advances, limits, challenges, and future research opportunities are discussed. By combining atomic force microscopy and reflection interference contrast microscopy, the force, bubble deformation, and liquid film drainage can be measured simultaneously. The simultaneous measurement of the interaction force and the spatiotemporal evolution of the confined liquid film hold great promise to shed new light on flotation.

The suppression of droplet-droplet coalescence in a sheared yield stress fluid.

Efforts to stabilize emulsions against coalescence in flow have often focused on modifying properties of the interface between the continuous and dispersed phases, to create a repulsive barrier against coalescence. But prior to experiencing any interaction force, the liquid film between two colliding drops has to drain, and if this drainage process is arrested, coalescence will be suppressed. In this work, scaling analyses and thin-film lubrication simulations are used to study the hydrodynamic drainage properties of thin films of a Bingham fluid (a yield stress fluid, which flows only when a critical stress is exceeded) created between two drops colliding under the action of a constant force. Our study shows that the hydrodynamic drainage process can be arrested completely when the film reaches a critical thickness, before attractive forces result in the rupture of the film, provided that the film shape is in the dimpled configuration. This critical thickness is hf=6τ02R3/γ2, where τ0 is the yield stress of the suspending medium, R is the drop radius and γ is the interfacial tension between the fluids. The yield stress can thus serve as an independent tuning parameter that sets an upper bound on the drop size beyond which coalescence is turned off in sheared emulsions.

The hydrodynamics of bubble rise and impact with solid surfaces.

A bubble smaller than 1mm in radius rises along a straight path in water and attains a constant speed due to the balance between buoyancy and drag force. Depending on the purity of the system, within the two extreme limits of tangentially immobile or mobile boundary conditions at the air-water interface considerably different terminal speeds are possible. When such a bubble impacts on a horizontal solid surface and bounces, interesting physics can be observed. We study this physical phenomenon in terms of forces, which can be of colloidal, inertial, elastic, surface tension and viscous origins. Recent advances in high-speed photography allow for the observation of phenomena on the millisecond scale. Simultaneous use of such cameras to visualize both rise/deformation and the dynamics of the thin film drainage through interferometry are now possible. These experiments confirm that the drainage process obeys lubrication theory for the spectrum of micrometre to millimetre-sized bubbles that are covered in this review. We aim to bridge the colloidal perspective at low Reynolds numbers where surface forces are important to high Reynolds number fluid dynamics where the effect of the surrounding flow becomes important. A model that combines a force balance with lubrication theory allows for the quantitative comparison with experimental data under different conditions without any fitting parameter.

Coalescence behavior of oil droplets coated in irreversibly-adsorbed surfactant layers.

Coalescence between oil caps with irreversibly adsorbed layers of nonionic surfactant is characterized in deionized water and electrolyte solution. The coalescence is characterized using a modified capillary tensiometer allowing for accurate measurement of the coalescence time. Results suggest two types of coalescence behavior, fast coalescence at low surface coverages that are independent of ionic strength and slow coalescence at high coverage. These slow coalescence events (orders of magnitude slower) are argued to be due to electric double layer forces or more complicated stabilization mechanisms arising from interfacial deformation and surface forces. A simple film drainage model is used in combination with measured values for interfacial properties to quantify the interaction potential between the two interfaces. Since this approach allows the two caps to have the same history, interfacial coverage and curvature, the results offer a tool to better understand a mechanism that is important to emulsion stability.

Hydrodynamics of thin liquid films: Retrospective and perspectives.

This review presents a summary of the results in the domain of microscopic liquid film hydrodynamics for several decades of experimental and theoretical research. It mainly focuses on the validation, application and further development of the Stefan-Reynolds theory on the liquid drainage, based on the accumulated knowledge of surface forces, surface tension caused by the surfactant adsorption, and diffusion of surfactants. Liquid films are of primary significance for colloidal disperse systems, and diverse industrial processes. The transient stability of the froth phase and the froth drainage is a function of the drainage and rupture of liquid films between air bubbles. In flotation, the bubble-particle attachment is controlled by the thinning and rupture of the intervening liquid film between an air bubble and a mineral particle. Both the experimental and theoretical results are mostly related to the foam liquid films between two bubbles, but can be principally generalized for emulsion films, formed in another liquid, as well as wetting films between a bubble and a solid surface.

Review and perspectives of AFM application on the study of deformable drop/bubble interactions.

The applications of Atomic Force Microscopy (AFM) on the study of dynamic interactions and film drainage between deformable bodies dispersed in aqueous solutions are reviewed in this article. Novel experimental designs and recent advances in experimental methodologies are presented, which show the advantage of using AFM as a tool for probing colloidal interactions. The effects of both DLVO and non-DLVO forces on the colloid stabilization mechanism are discussed. Good agreement is found between the force - drop/bubble deformation behaviour revealed by AFM measurements and the theoretical modeling of film drainage process, giving a convincing explanation of the occurrence of certain phenomenon. However, the behaviour and shape of deformable drops as they approach or retract is still not well resolved. In addition, when surfactants are present further research is needed on the absorption of surfactant molecules into the interfaces, their mobility and the effects on interfacial film properties.

Measuring forces and spatiotemporal evolution of thin water films between an air bubble and solid surfaces of different hydrophobicity.

A combination of atomic force microscopy (AFM) and reflection interference contrast microscopy (RICM) was used to measure simultaneously the interaction force and the spatiotemporal evolution of the thin water film between a bubble in water and mica surfaces with varying degrees of hydrophobicity. Stable films, supported by the repulsive van der Waals-Casimir-Lifshitz force were always observed between air bubble and hydrophilic mica surfaces (water contact angle, θ(w) < 5°) whereas bubble attachment occurred on hydrophobized mica surfaces. A theoretical model, based on the Reynolds lubrication theory and the augmented Young-Laplace equation including the effects of disjoining pressure, provided excellent agreement with experiment results, indicating the essential physics involved in the interaction between air bubble and solid surfaces can be elucidated. A hydrophobic interaction free energy per unit area of the form: WH(h) = -γ(1 - cos θ(w))exp(-h/D(H)) can be used to quantify the attraction between bubble and hydrophobized solid substrate at separation, h, with γ being the surface tension of water. For surfaces with water contact angle in the range 45° < θ(w) < 90°, the decay length DH varied between 0.8 and 1.0 nm. This study quantified the hydrophobic interaction in asymmetric system between air bubble and hydrophobic surfaces, and provided a feasible method for synchronous measurements of the interaction forces with sub-nN resolution and the drainage dynamics of thin films down to nm thickness.

Ion-specific effects in foams.

We present a critical review on ion-specific effects in foams in the presence of added salts. We show the theoretical basis developed for understanding experimental data in systems with ionic surfactants, as well as the nascent approaches to modeling the much more difficult systems with non-ionic surfactants, starting with the most recent models of the air-water interface. Even in the case of ionic surfactant systems, we show methods for improving the theoretical understanding and apply them for interpretation of surprising experimental results we have obtained on ion-specific effects in these systems. We report unexpectedly strong ion-specific effects of counter-ions on the stability and the rate of drainage of planar foam films from solutions of 0.5mM sodium dodecyl sulfate (SDS) as a function of concentration of a series of inorganic salts (MCl, M=Li, Na, K). We found that the counter-ions can either stabilize the foam films (up to a critical concentration) or destabilize them beyond it. The ordering for destabilization is in the same order as the Hofmeister series, while for stabilization it is the reverse Therefore, the strongest foam stabilizer (K(+)), becomes the strongest foam destabilizer at and beyond its critical concentration, and vice versa. Though the critical concentration is different for different salts, calculating the critical surfactant adsorption level one could simplify the analysis, with all the critical concentrations occurring at the same surfactant adsorption level. Beyond this level, the foam lifetime decreases and films suddenly start draining faster, which may indicate salt-induced surfactant precipitation. Alternatively, formation of pre-micellar structures may result in slower equilibration and fewer surfactant molecules at the surface, thus leading to unstable foams and films.

Influence of acoustic pressure and bubble sizes on the coalescence of two contacting bubbles in an acoustic field.

In this study, the coalescence time between two contacting sub-resonance size bubbles was measured experimentally under an acoustic pressure ranging from 10kPa to 120kPa, driven at a frequency of 22.4kHz. The coalescence time obtained under sonication was much longer compared to that calculated by the film drainage theory for a free bubble surface without surfactants. It was found that under the influence of an acoustic field, the coalescence time could be probabilistic in nature, exhibiting upper and lower limits of coalescence times which are prolonged when both the maximum surface approach velocity and secondary Bjerknes force increases. The size of the two contacting bubbles is also important. For a given acoustic pressure, bubbles having a larger average size and size difference were observed to exhibit longer coalescence times. This could be caused by the phase difference between the volume oscillations of the two bubbles, which in turn affects the minimum film thickness reached between the bubbles and the film drainage time. These results will have important implications for developing film drainage theory to account for the effect of bubble translational and volumetric oscillations, bubble surface fluctuations and microstreaming.

Measurement and modeling on hydrodynamic forces and deformation of an air bubble approaching a solid sphere in liquids.

The interaction between bubbles and solid surfaces is central to a broad range of industrial and biological processes. Various experimental techniques have been developed to measure the interactions of bubbles approaching solids in a liquid. A main challenge is to accurately and reliably control the relative motion over a wide range of hydrodynamic conditions and at the same time to determine the interaction forces, bubble-solid separation and bubble deformation. Existing experimental methods are able to focus only on one of the aspects of this problem, mostly for bubbles and particles with characteristic dimensions either below 100 µm or above 1 cm. As a result, either the interfacial deformations are measured directly with the forces being inferred from a model, or the forces are measured directly with the deformations to be deduced from the theory. The recently developed integrated thin film drainage apparatus (ITFDA) filled the gap of intermediate bubble/particle size ranges that are commonly encountered in mineral and oil recovery applications. Equipped with side-view digital cameras along with a bimorph cantilever as force sensor and speaker diaphragm as the driver for bubble to approach a solid sphere, the ITFDA has the capacity to measure simultaneously and independently the forces and interfacial deformations as a bubble approaches a solid sphere in a liquid. Coupled with the thin liquid film drainage modeling, the ITFDA measurement allows the critical role of surface tension, fluid viscosity and bubble approach speed in determining bubble deformation (profile) and hydrodynamic forces to be elucidated. Here we compare the available methods of studying bubble-solid interactions and demonstrate unique features and advantages of the ITFDA for measuring both forces and bubble deformations in systems of Reynolds numbers as high as 10. The consistency and accuracy of such measurement are tested against the well established Stokes-Reynolds-Young-Laplace model. The potential to use the design principles of the ITFDA for fundamental and developmental research is demonstrated.