5 research outputs found
Tuning particle–particle interactions to control Pickering emulsions constituents separation
We demonstrate that the separation and recovery of solid-stabilized (Pickering) emulsion constituents are significantly improved via a simple filtration approach – without any additional chemical agent – by initially grafting sodium alginate (SA), a natural polysaccharide, onto silane-modified sub-micrometer silica particles. The combination of surface-grafted trimethoxy(propyl)silane (TMPS) and (3-aminopropyl)trimethoxysilane (APTMS) controls particle wettability, verified via zeta potential and contact angle measurements. Rheometry and filtration experiments reveal that further grafting of SA via APTMS enhances particle–particle and droplet–droplet interactions. This work provides an approach towards the design of environmentally friendly Pickering emulsion based chemical engineering processes with easy-to-separate and reusable particles, allowing waste reduction and reduced toxicity advantages
One-step processing of highly viscous multiple Pickering emulsions
ABSTRACT: Hypothesis Solid-stabilized Pickering emulsions have attracted a lot of attention recently due to their surfactant-free character, and exceptional stability. At the moment, how the viscosities of the liquid phases impact the processing of Pickering emulsions remain to be clearly understood – it is however an important parameter to consider when developing chemical engineering processes employing these multiphase liquids. Our first assumption was that the amount of emulsified dispersed phase would drastically decrease as viscosity increases. Experiments and findings In this work, we demonstrate that double water-in-oil-in-water (W/O/W) Pickering emulsions are obtained in a single processing step when using very high viscosity silicone oils (≥10,000 cSt) and a single type of sub-μm silica particles modified with two grafted silanes and sodium alginate. The formation of water sub-inclusions proceeds via a phase-inversion mechanism. These sub-inclusions are subsequently stabilized and retained in the oil phase due to its viscosity, limiting sub-inclusions mobility, and the presence of adsorbed particles forming dense layers at oil-water interfaces, acting as barriers. The process we present is simple, requires a minimum number of components, and allows the preparation of multiple emulsions which could then be used to efficiently protect and/or transport a variety of sensitive encapsulated compounds
Sodium alginate-grafted submicrometer particles display enhanced reversible aggregation/disaggregation properties
In this article, we demonstrate that submicrometer particles with surface-grafted sodium alginate (SA) display enhanced and reversible aggregation/disaggregation properties in aqueous solution. 300 nm silica particles were first functionalized with an aminosilane coupling agent, followed by the grafting of pH-sensitive SA, as confirmed by zeta potential, XPS and FTIR analyses. The SA-modified particles show enhanced aggregation properties at acidic pH compared to unmodified silica, with a 10 times increase in average aggregate diameter. The process is reversible, as the aggregates can be broken and dispersed again when the pH is increased back to 7.0. As a result, the sedimentation rate of SA-modified particles at pH 3.0 is both significantly faster and complete compared to the unmodified particles. This enhanced aggregation is most likely due to the formation of intermolecular hydrogen bonds between neighboring SA-modified particles. This work illustrates how surface-grafted macromolecules of natural origins can be used to tune interparticle interactions, in order to improve separation processes