ABSTRACT
With the rapid development of industry and the acceleration of urbanization, oil pollution has caused serious damage to water, and its treatment has always been a research hotspot. Compared with traditional adsorption materials, aerogel has the advantages of light weight, large adsorption capacity and high selective adsorption, features that render it ideal as a high-performance sorbent for water treatment. The objective of this research was to develop novel hydrophobic polymer-reinforced silica aerogel microspheres (RSAMs) with water glass as the precursor, aminopropyltriethoxysilane as the modifier, and styrene as the crosslinker for oil removal from water. The effects of drying method and polymerization time on the structure and oil adsorption capacity were investigated. The drying method influenced the microstructure and pore structure in a noteworthy manner, and it also significantly depended on the polymerization time. More crosslinking time led to more volume shrinkage, thus resulting in a larger apparent density, lower pore volume, narrower pore size distribution and more compact network. Notably, the hydrophobicity increased with the increase in crosslinking time. After polymerization for 24 h, the RSAMs possessed the highest water contact angle of 126°. Owing to their excellent hydrophobicity, the RSAMs via supercritical CO2 drying exhibited significant oil and organic liquid adsorption capabilities ranging from 6.3 to 18.6 g/g, higher than their state-of-the-art counterparts. Moreover, their robust mechanical properties ensured excellent reusability and recyclability, allowing for multiple adsorption-desorption cycles without significant degradation in performance. The novel sorbent preparation method is facile and inspiring, and the resulting RSAMs are exceptional in capacity, efficiency, stability and regenerability.
ABSTRACT
An acidified SnO2/rGO aerogel (ASGA) is an attractive contributor in ethanol gas sensing under ultralow concentration because of the sufficient active sites and adsorption pores in SnO2 and the rGA, respectively. Furthermore, a p-n heterojunction is successfully constructed by the high electron mobility between ASP and rGA to establish a brand-new bandgap of 2.72 eV, where more electrons are released and the surface energy is decreased, to improve the gas sensitivity. The ASGA owns a specific surface area of 256.1 m2/g, far higher than SnO2 powder (68.7 m2/g), indicating an excellent adsorption performance, so it can acquire more ethanol gas for a redox reaction. For gas-sensing ability, the ASGA exhibits an excellent response of Ra/Rg = 137.4 to 20 ppm of ethanol at the optimum temperature of 210 °C and can reach a response of 1.2 even at the limit detection concentration of 0.25 ppm. After the concentration gradient change test, a nonlinear increase between concentration and sensitivity (S-C curve) is observed, and it indirectly proves the chemical adsorption between ethanol and ASGA, which exhibits charge transfer and improves electron mobility. In addition, a detailed energy band diagram and sensor response diagram jointly depict the gas-sensitive mechanism. Finally, a conversed calculation explains the feasibility of the nonlinear S-C curve from the atomic level, which further verifies the chemical adsorption during the sensing process.