Charge tunable thin-film composite membranes by gamma-ray triggered surface polymerization

Thin-film composite poly(amide) (PA) membranes have greatly diversified water supplies and food products. However, users would benefit from a control of the electrostatic interactions between the liquid and the net surface charge interface in order to benefit wider application. The ionic selectivity of the 100 nm PA semi-permeable layer is significantly affected by the pH of the solution. In this work, for the first time, a convenient route is presented to configure the surface charge of PA membranes by gamma ray induced surface grafting. This rapid and up-scalable method offers a versatile route for surface grafting by adjusting the irradiation total dose and the monomer concentration. Specifically, thin coatings obtained at low irradiation doses between 1 and 10 kGy and at low monomer concentration of 1 v/v% in methanol/water (1:1) solutions, dramatically altered the net surface charge of the pristine membranes from-25 mV to +45 mV, whilst the isoelectric point of the materials shifted from pH 3 to pH 7. This modification resulted in an improved water flux by over 55%, from 45.9 to up 70 L.m -2 .h -1 , whilst NaCl rejection was found to drop by only 1% compared to pristine membranes

Mapping coalescence of micron-sized drops and bubbles

Emulsion formulation, solvent extraction and multiphase microfluidics are all examples of processes that require precise control of drop or bubble collision stability. We use a previously validated numerical model to map the exact conditions under which micron-sized drops or bubbles undergo coalescence in the presence of colloidal forces and hydrodynamic effects relevant to Brownian motion and low Reynolds number flows. We demonstrate that detailed understanding of how the equilibrium surface forces vary with film thickness can be applied to make accurate predictions of the outcome of a drop or bubble collision when hydrodynamic effects are negligible. In addition, we illuminate the parameter space (i.e. interaction velocity, drop deformation, interfacial tension, etc.) at which hydrodynamic effects can stabilise collisions that are unstable at equilibrium. Further, we determine conditions for which drop or bubble collisions become unstable upon separation, caused by negative hydrodynamic pressure in the film. Lastly, we show that scaling analyses are not applicable for constant force collisions where the approach timescale is comparable to the coalescence timescale, and demonstrate that initial conditions under these circumstances cannot be ignored

Effect of Orientation and Wetting Properties on the Behavior of Janus Particles at the Air-Water Interface.

The adhesion force and contact angle of gold-capped silica Janus particles and plain silica particles at an air-water interface are studied via colloidal atomic force microscopy. Particles are attached to cantilevers at various orientations, and wetting properties of the gold surface are varied through modification with dodecanethiol. Thiol modification increases the hydrophobicity of the gold surface, thereby increasing the difference between the contact angles of the gold hemisphere and the silica hemisphere and, thus, increasing the degree of amphiphilicity of the Janus particle. Subsequently, the colloidal probe is pushed into a stationary bubble from the water phase followed by retraction back into the water phase. Adhesion force is found to be higher for Janus particles than isotropic silica particles, regardless of orientation of the anisotropic hemisphere. Particles with their polar half oriented toward the water and apolar half facing the air show an increase in adhesion force and contact angle as the degree of amphiphilicity of the particles increases. For particles of the reverse orientation, no significant difference is observed as wetting properties change. Both adhesion force and contact angle display an inverse relationship with a cap angle for particles with a higher degree of amphiphilicity. These results are of importance for using Janus particles to stabilize interfaces as well as for understanding the equilibrium height of Janus particles at the interface, which will impact capillary interactions and thus self-assembly

Precise measurements of capsule mechanical properties using indentation

Application of elastic theory to experimental data of capsule and particle compression under-predicts the value of material properties such as the Young's modulus by up to 100% when the effect of the rigid substrate is neglected, as is commonly done in the literature. Results of numerical simulations, spanning the range from thin-shelled capsules to solid particles, are presented in terms of correction factors that account for the substrate. In addition, the scaling relationship between indentation force and displacement is characterised for arbitrary shell thicknesses and indenter radii

Dynamic forces between emulsified water drops coated with Poly-Glycerol-Poly-Ricinoleate (PGPR) in canola oil

The dynamic collision of emulsified water drops in the presence of non-ionic surfactants plays a crucial role in many practical applications. Interaction force between water drops coated with non-ionic food grade surfactants is expected to exhibit rich dynamic behavior that is not yet explored. The collision forces between immobilized water drops in canola oil in the presence of a well-known food grade surfactant polyglycerol polyricinoleate (PGPR) are measured at concentrations well below typically used to form stable emulsions. An extension or kink, attributed to a short-range attractive interaction due to PGPR bridging between the drops, was observed in the retract portion of the force curves at higher applied forces or slower collision velocities. The Stokes-Reynolds-Young-Laplace (SRYL) model was used to calculate theoretical force curves. For higher collisions velocities, the agreement between the calculated and experiment data was acceptable, but the SRYL model failed to describe the extension or kink feature observed at slower velocities below. Both the AFM data and the comparison to the model calculation indicated the presence of a short-range attractive force, not of a hydrodynamic origin, attributed to the bridging and extension of PGPR molecules on the surface of water drops below saturation of the interface

Charge and Film Drainage of Colliding Oil Drops Coated with the Nonionic Surfactant C12E5

The interaction forces between colliding tetradecane drops were measured in the presence of the nonionic surfactant pentaethylene glycol monododecyl ether (C12E5). The force behavior was measured in the range of premicellar compositions of the nonionic surfactant in various salt solutions and was consistent with the presence of a surface charge even though the surfactant was nonionic in nature. The surface potential of oil drops was found to decrease with an increase in C12E5 concentration. The measured electrophoretic mobilities and ζ potentials of emulsified tetradecane drops also decreased with an increase in the C12E5 concentration. The surface potential decreased with an increase in the electrolyte at a constant C12E5 concentration, further confirming the presence of a charged oil-water interface. In addition to the charging behavior, the nonequilibrium film drainage between the tetradecane drops coated with C12E5 was also measured. In contrast to some existing experiments in the literature, it was found that oil drops coated with the nonionic surfactant were stable against coalescence, even when the drops were deformed on the order of their radii. These findings have significant implications on the stability of emulsions in food, personal care, and detergent industries

Changes in morphological and nano-mechanical properties of the milk fat globule membrane during processing

C1 - Journal Articles Referee

Forces between oil drops in polymer-surfactant systems: Linking direct force measurements to microfluidic observations

Hypothesis Linking atomic force microscopy and microfluidics opens up the possibility of probing adhesive interactions between drops in a high-throughput context. A microfluidic device designed to form, and subsequently break-up, chains of drops, where the drop break-up is sensitive to the underlying surface forces between drops, not hydrodynamic drainage forces, would play a key role in developing this link. Experiments Both techniques have been used to quantify the forces between oil drops in the presence of complexes formed with anionic surfactant, sodium dodecylsulphate, and neutral, water soluble polymer, poly(vinylpyrrolidone). Measurement and modelling of the interaction forces between both rigid and deformable surfaces demonstrated that the attraction between the drops is due to depletion forces, whereas the repulsive force is a combination of electrical double layer and steric forces, indicating complexes exist both in the bulk and at the drop interface. Findings The interaction behaviour between the force measurements and the microfluidic observations showed a strong correlation, where the observed adhesion between drops in the microfluidics is sensitive to the drop deformation and Laplace pressure. Correlation between the two techniques provides insight into the surface forces between drops in flowing systems and has potential utility in the formulation of emulsions

Measurement and analysis of forces in bubble and droplet systems using AFM

C1 - Journal Articles RefereedThe use of atomic force microscopy to measure and understand the interactions between deformable colloids - particularly bubbles and drops - has grown to prominence over the last decade. Insight into surface and structural forces, hydrodynamic drainage and coalescence events has been obtained, aiding in the understanding of emulsions, foams and other soft matter systems. This article provides information on experimental techniques and considerations unique to performing such measurements. The theoretical modelling frameworks which have proven crucial to quantitative analysis are presented briefly, along with a summary of the most significant results from drop and bubble AFM measurements. The advantages and limitations of such measurements are noted in the context of other experimental force measurement techniques