Involving a succession of oil refining stages for edible oil production, a notable constraint lies in the necessity to employ diverse adsorbents at various steps within these processes. This study investigates the synthesis of mesoporous silica aerogels from rice husk ash, comparing their efficacy in physical sunflower oil refining with earth clay (Bentonite) and commercial silica (Trisyl). Tetraethyl orthosilicate (TEOS) impact during aging was analyzed using scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), and N₂ adsorption-desorption analyzer to examine alterations in the structure of silica aerogels. The surface areas of TEOS-doped silica aerogel (TSA) and non-TEOS-doped silica aerogel (NTSA) were 296.18 and 267.06 m²/g. Mesoporous silica aerogels were evaluated for their ability to reduce free fatty acids (FFA), peroxide value (PV), phosphorus, and color pigments in sunflower oil. TSA and NTSA demonstrated significant FFA removal, with TSA at 3 wt.% achieving the highest performance of 32.2%. TSA also effectively reduced PV and phosphorus compared to NTSA, Bentonite and Trisyl, exhibiting performance similar to Bentonite in the bleaching process. TEOS-doped silica aerogels have shown promise as adsorbents for impurity removal in sunflower oil and has emerged as the potential adsorbent that can comprehensively and effectively meet the requirements of many edible oil physical refining applications in a singular step. Graphical Abstract

Several therapeutic approaches have been developed to promote bone regeneration, including guided bone regeneration (GBR), where barrier membranes play a crucial role in segregating soft tissue and facilitating bone growth. This study emphasizes the importance of considering specific tissue requirements in the design of materials for tissue regeneration, with a focus on the development of a double-layered membrane to mimic both soft and hard tissues within the context of GBR. The hard tissue-facing layer comprises collagen and zinc-doped bioactive glass to support bone tissue regeneration, while the soft tissue-facing layer combines collagen and chitosan. The electrospinning technique was employed to achieve the production of nanofibers resembling extracellular matrix fibers. The production of nano-sized (~116 nm) bioactive glasses was achieved by microemulsion assisted sol-gel method. The bioactive glass-containing layers developed hydroxyapatite on their surfaces starting from the first week of simulated body fluid (SBF) immersion, demonstrating that the membranes possessed favorable bioactivity properties. Moreover, all membranes exhibited distinct degradation behaviors in various mediums. However, weight loss exceeding 50% was observed in all tested samples after four weeks in both SBF and phosphate-buffered saline (PBS). The double-layered membranes were also subjected to mechanical testing, revealing a tensile strength of approximately 4 MPa. The double-layered membranes containing zinc-doped bioactive glass demonstrated cell viability of over 70% across all tested concentrations (0.2, 0.1, and 0.02 g/mL), confirming the excellent biocompatibility of the membranes. The fabricated polymer bioactive glass composite double-layered membranes are strong candidates with the potential to be utilized in tissue engineering applications.