The cellulose nanofibers of bacterial cellulose aerogel (BCA) are modified only on their surfaces using a trimethylsilylation reaction with trimethyichlorosilane in liquid phase followed by freeze-drying. The obtained hydrophobic bacterial cellulose aerogels (HBCAs) exhibit low density (≤6.77 mg/cm(3)), high surface area (≥169.1 m(2)/g), and high porosity (≈ 99.6%), which are nearly the same as those of BCA owing to the low degrees of substitution (≤0.132). Because the surface energy of cellulose nanofibers decreased and the three-dimensional web-like microstructure, which was comprised of ultrathin (20-80 nm) cellulose nanofibers, is maintained during the trimethylsilylation process, the HBCAs have hydrophobic and oleophilic properties (water/air contact angle as high as 146.5°) that endow them with excellent selectivity for oil adsorption from water. The HBCAs are able to collect a wide range of organic solvents and oils with absorption capacities up to 185 g/g, which depends on the density of the liquids. Hence, the HBCAs are wonderful candidates for oil absorbents to clean oil spills in the marine environment. This work provides a different way to multifunctionalize cellulose aerogel blocks in addition to chemical vapor deposition method.

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Aerogels are nanoporous materials with excellent properties, especially super thermal insulation. However, owing to their serious high brittleness, the macroscopic forms of aerogels are not sufficiently rich for the application in some fields, such as thermal insulation clothing fabric. Recently, freeze spinning and wet spinning have been attempted for the synthesis of aerogel fibers. In this study, robust fibrous silica-bacterial cellulose (BC) composite aerogels with high performance were synthesized in a novel way. Silica sol was diffused into a fiber-like matrix, which was obtained by cutting the BC hydrogel and followed by secondary shaping to form a composite wet gel fiber with a nanoscale interpenetrating network structure. The tensile strength of the resulting aerogel fibers reached up to 5.4 MPa because the quantity of BC nanofibers in the unit volume of the matrix was improved significantly by the secondary shaping process. In addition, the composite aerogel fibers had a high specific area (up to 606.9 m2/g), low density (less than 0.164 g/cm3), and outstanding hydrophobicity. Most notably, they exhibited excellent thermal insulation performance in high-temperature (210 °C) or low-temperature (−72 °C) environments. Moreover, the thermal stability of CAFs (decomposition temperature was about 330 °C) was higher than that of natural polymer fiber. A novel method was proposed herein to prepare aerogel fibers with excellent performance to meet the requirements of wearable applications.

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