Pumice is a porous volcanic rock containing a significant proportion of silica and alumina, and which has a low iron content. This natural, silica-rich material attracts wide attention because of its applications in adsorption processes, heterogeneous catalysis and nanotechnology. In this contribution, the white amorphous silica nanoparticles were extracted using an optimized alkaline treatment and an acid-precipitation process using grey pumice powder. The isolated amorphous silica SiO2 was characterized via X-Ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Transmission Electronic Microscopy (TEM-EDS), N2 adsorption/desorption measurements and simultaneous Thermal Gravimetry/Differential Thermal Analysis (TG/DTA). The obtained results indicated that the nanosilica powder was successfully prepared via the acid-base route with a predominantly amorphous mesoporous structure having a high surface area (422m2/g). The TEM images exhibited relatively homogeneous dispersed nanosilica particles with small sizes about 5–15 nm, in accordance with XRD data. Thermal analysis of the silica powder under air atmosphere showed total mass losses of 6.5%, with endothermic effects corresponding to the removal of water molecules and the OH of silanol groups contained in the material. The investigations performed in this work have indicated that there is great scope for pumice exploitation as a raw material in the production of amorphous silica nanopowder on large scale.

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Two-dimensional nanosilicate particles (NS) have shown promise for the prolonged release of small-molecule therapeutics while minimizing burst release. When incorporated in a hydrogel, the high surface area and charge of NS enable electrostatic adsorption and/or intercalation of therapeutics, providing a lever to localize and control release. However, little is known about the physio-chemical interplay between the hydrogel, NS, and encapsulated small molecules. Here, we fabricated polyethylene glycol (PEG)-NS hydrogels for the release of model small molecules such as acridine orange (AO). We then elucidated the effect of NS concentration, NS/AO incubation time, and the ability of NS to freely associate with AO on hydrogel properties and AO release profiles. Overall, NS incorporation increased the hydrogel stiffness and decreased swelling and mesh size. When individual NS particles were embedded within the hydrogel, a 70-fold decrease in AO release was observed compared to PEG-only hydrogels, due to adsorption of AO onto NS surfaces. When NS was pre-incubated and complexed with AO prior to hydrogel encapsulation, a >9000-fold decrease in AO release was observed due to intercalation of AO between NS layers. Similar results were observed for other small molecules. Our results show the potential for use of these nanocomposite hydrogels for the tunable, long-term release of small molecules.

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