The silica aerogels were prepared via a sol-gel technique and ambient pressure drying by using industrial solid wastes, dislodged sludges, as raw materials. A strategy was put forward to reduce the corrosion of equipment during the drying procedure. The pore structure, hydrophobicity, and thermal insulation property of the obtained samples were investigated in detail. The results show that the corrosion can be effectively avoided by using an equimolar mixture of trimethylchlorosilane (TMCS) and hexamethyldisilazane (HMDS) as silylation agents. At a Si:TMCS:HMDS molar ratio of 1:0.375:0.375, the silica aerogels possess a desirable pore structure with a pore volume of 3.3 ± 0.1 cm³/g and a most probable pore size of 18.5 nm, a high hydrophobicity with a water contact angle of 144.2 ± 1.1°, and a low thermal conductivity of 0.031 ± 0.001 W/(m∙K).

The slag obtained in the process of pig iron smelting has been widely used, but the variational hydration activity always is a significant factor affecting its quality. In this experiment, the laboratory simulated slag was prepared by adjusting the chemical composition and cooling method. The experiment primary characterized the structure and hydration process with different types of slag by using MAS NMR, XRD, compressive strength, ICP, SEM, and hydration heat, then obtained the influence of the composition of the network former S/A (the mass ratio of SiO₂ and Al₂O₃ in chemical composition) and amorphous phase content on its structure and hydration activity. The result shows that lowering the S/A value can reduce the degree of vitreous polymerization in the slag; reducing the S/A value of the slag can make the slag hydration time advance, and consequently, the cumulative exotherm increases, the liquid phase Ca/Si and Al/Si ionic ratio increases, and the hydration product changes from C–S–H gel to C–A–S–H gel, which ultimately leads to an increase in compressive strength. In the high S/A value slag, the formation of the trace crystal phase of gehlenite is beneficial to reduce the degree of polymerization of the amorphous.

It is of great significance to separate hazardous methyl tert-butyl ether (MTBE) from water in terms of environmental protection and human health. In the present work, α-Al₂O₃-suppotred silica membranes were prepared by the sol-gel and dip-coating technique. Two fluorinated alkylsilanes (1H,1H,2H,2H-perfluorooctyltriethoxysilane (PFOTES) and trifluoropropyltriethoxysilane (TFPTES)) and two non-fluorinated alkylsilanes (octyltriethoxysilane (OTES) and propyltriethoxysilane (PTES)) were adopted to silylate the silica membrane by the post-grafting method which is used for the separation of MTBE from water by pervaporation. The results show that silylation enhances the hydrophobicity of silica membranes. The silylated silica membranes are selective towards MTBE, and the MTBE/water separation factor varies with grafting agents in the order: PFOTES > TFPTES > OTES > PTES. Membranes silylated with fluorinated carbon chains seem to be more selective towards MTBE than those with non-fluorinated carbon chains. The total flux is proportional to the pore volume of silica membranes, which depends on grafting agents in the order: PTES > PFOTES > OTES > TFPTES. Considering both total flux and selectivity, the PFOTES-SiO₂ membrane is most effective in separation, with a MTBE/water separation factor of 24.6 and a total flux of 0.35 kg m⁻² h⁻¹ under a MTBE concentration of 3.0% and a feed temperature of 30 °C.