Browsing by Author "Whitby CP"

Now showing 1 - 5 of 5
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    Dual-network hydrogel capsules for controlled molecular transport via pH and temperature responsiveness
    (Elsevier Inc, 2025-01) Yang H; Whitby CP; Travas-Sejdic J
    We have developed innovative core-shell hydrogel capsules with a dual-network shell structure designed for precise control of molecular transport in response to external stimuli such as pH and temperature. The capsules were fabricated using a combination of microfluidic electrospray techniques and water-in-water (w/w) core-shell droplets templating. The primary network of the shell, calcium alginate (Ca-Alg), with a pKa around 3.4, exhibits sensitivity to pH. The secondary network of the shell, poly(ethylene glycol) methyl ether methacrylate (PEGMA), undergoes a volume phase transition near 60 °C. These properties enable precise molecular transport control in/out of the capsules by modulating the surface charges through varying pH and modifying pore size through temperature changes. Moreover, the dual-network shell structure not only significantly enhances the mechanical strength of the capsules but also improves their stability under external stimulus, ensuring structural integrity during the transport of molecules. This research lays the groundwork for further investigations into the multimodal stimuli-responsive hydrogel systems to control molecular transport, important in applications such as sensors and reactors for chemical cascade reactions.
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    Interfacial colloidal assembly guided by optical tweezers and tuned via surface charge
    (Elsevier Inc, 2022-09) Pradhan S; Whitby CP; Williams MAK; Chen JLY; Avci E
    HYPOTHESIS: The size, shape and dynamics of assemblies of colloidal particles optically-trapped at an air-water interface can be tuned by controlling the optical potential, particle concentration, surface charge density and wettability of the particles and the surface tension of the solution. EXPERIMENTS: The assembly dynamics of different colloidal particle types (silica, polystyrene and carboxyl coated polystyrene particles) at an air-water interface in an optical potential were systematically explored allowing the effect of surface charge on assembly dynamics to be investigated. Additionally, the pH of the solutions were varied in order to modulate surface charge in a controllable fashion. The effect of surface tension on these assemblies was also explored by reducing the surface tension of the supporting solution by mixing ethanol with water. FINDINGS: Silica, polystyrene and carboxyl coated polystyrene particles showed distinct assembly behaviours at the air-water interface that could be rationalised taking into account changes in surface charge (which in addition to being different between the particles could be modified systematically by changing the solution pH). Additionally, this is the first report showing that wettability of the colloidal particles and the surface tension of the solution are critical in determining the resulting assembly at the solution surface.
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    Investigating hydrodynamic cavitation as an efficient means for removal of per- and polyfluoroalkyl substances from solution
    (Elsevier BV, 2024-11-11) Kabiri S; Jafarian M; Navarro DA; Whitby CP; McLaughlin MJ
    With nearly five decades of per- and polyfluoroalkyl substances (PFASs) being associated with firefighting and industrial activities, these compounds inevitably accumulate in both ground and surface water. PFAS contamination in water has emerged as a significant environmental and public health concern, particularly perfluorooctanesulfonic acid (PFOS), which is often found in higher concentrations compared to other PFAS and has more pronounced adverse health effects. Addressing PFAS contamination requires treating large volumes of water, making technologies that rapidly separate and concentrate PFASs highly favoured. The strong surface activity of PFAS, such as PFOS, enables them to generate colloidal gas aphrons (CGAs) during high shear mixing of their aqueous solutions, where PFASs can be separated and collected as foam. This study aims to evaluate the effectiveness of high shear mixing in separating PFOS from solution, leveraging its accumulation at air–water interfaces. High shear-assisted PFOS separation was tested by varying parameters like rotational speed (4000 to 10,000 rpm), mixing time (30 s to 30 min), and the effect of electrolytes. Results showed greater PFOS separation in the presence of electrolytes, particularly monovalent cations like Na+, compared to divalent cations such as Ca2+, due to the creation of more stable CGAs with smaller sizes. At a mixing rate of 6000 rpm, 85 % of PFOS was removed in 30 s from a highly contaminated PFOS solution (10 mg/L), with over 95 % separation after 5 mixing cycles. While high-shear mixing was efficient in PFOS separation from highly contaminated solutions it was less efficient for low-level contaminated solutions (less than 1 mg/L). These results suggest that hydrodynamic cavitation induced by high-shear mixing seems promising for enhancing the separation of PFOS from heavily contaminated solutions. This technique could serve as a standalone method or be integrated with other PFAS removal technologies to enhance the overall efficiency of PFAS removal from polluted water sources.
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    Nanoprecipitation to produce hydrophobic cellulose nanospheres for water-in-oil Pickering emulsions
    (Springer Nature B V, 2024-07) Tiban Anrango BA; Naiya MM; Van Dongen J; Matich O; Whitby CP; Chen JL-Y
    In recent years, there has been growing interest in replacing petroleum-based water-in-oil (W/O) emulsifiers with sustainable and less toxic natural materials. Pickering emulsifiers are considered well-suited candidates due to their high interfacial activity and the ability to form emulsions with long-term stability. However, only sporadic examples of natural materials have been considered as inverse Pickering emulsifiers. This study describes the synthesis of a series of hydrophobic cellulose nanospheres by bulk modification with acyl groups of different chain lengths followed by nanoprecipitation, and their application as inverse emulsifiers. Modification with acyl groups of longer chain length (C16, C18) afforded lower degrees of substitution, but resulted in greater thermal stability than groups with shorter acyl chains (C12, C14). Formation of nanospheres with low aspect ratios and narrow size distributions required low initial cellulose concentrations (< 1% w/v), high volumetric ratios of antisolvent to solvent (> 10:1), and slow addition rates (< 20 mL/h). The modified cellulose nanospheres were able to reduce the interfacial tension between water and hexane from 45.8 mN/m to 31.1 mN/m, with an effect that increased with the number of carbons in the added acyl chains. The stearate-modified nanospheres exhibited superhydrophobic behavior, showing a contact angle of 156° ± 4° with water, and demonstrated emulsification performance comparable to the commonly used molecular surfactant sorbitan stearate. Our findings suggest that hydrophobically modified cellulose nanospheres have the potential to be a bio-derived alternative to traditional molecular W/O emulsifiers.
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    Phenolic compounds from macadamia husk: An updated focused review of extraction methodologies and antioxidant activities
    (Elsevier Ltd on behalf of the Institution of Chemical Engineers, 2024-12) Ahmed MF; Popovich DG; Whitby CP; Rashidinejad A
    This review explores the potential of agri-food waste materials, with a particular focus on macadamia nut by-products. Industrial processing of macadamia nuts yields a significant volume of by-products, including green husk and woody shell. Recent research has highlighted these by-products as readily available, cost-effective rich sources of phenolic compounds, renowned for their potent antioxidant and antibacterial properties. This paper emphasizes the importance of selecting an optimal extraction method to fully harness the bioactive potential of these phenolic compounds. In this work, we provide a comprehensive overview of conventional and advanced extraction techniques that are used to extract phenolic compounds from macadamia by-products, with a particular focus on the methods applied to macadamia green husk. Among the various techniques, it appears that ultrasound-assisted extraction, especially when combined with aqueous organic solvents, is more efficient than other methods for this purpose. This review also addresses the challenges in phenolic compound recovery, primarily due to the lack of a standardized extraction process. This often results in the extensive use of extraction solvents to achieve an extract that is rich in phenolic compounds. Overall, this research offers a valuable understanding of the most effective methods for the extraction and recovery of phenolic compounds from macadamia by-products and discusses the potential for scaling up these extraction processes. Hence, it can serve as a useful resource for researchers and industry professionals interested in sustainable and efficient utilization of by-products of the nut industry.