| The aim of this work is to synthesize WO3, WO3-SiO2, WO3-SiO2-TiO2compositeaerogel via an ambient pressure drying process. The composite aerogels would to be capcityof visible light photocatalytic activity of WO3, UV photocatalytic activity of TiO2andadsorption properties of porous materials, so as to overcome the pore strength of WO3andTiO3aerogels network and low photocatlysis efficiency of pure TiO3aerogel under visiblelight.The WO3, WO3-SiO2, WO3-SiO2-TiO2wet gels were prepared by sol-gel method withsodium tungsten, titanium tetrachloride and water glass as raw materials. Hexamethyldisilazane (HMDS)/hexamethyldisiloxane (HMDSO)/hexane (Hexane) mixed solution wasused as modifcation of WO3, WO3-SiO2wet gel. Trimethylchlorosilane (TMCS)/ethanol(EtOH)/hexane(Hexane) mixed solution were used as modification of WO3-SiO2-TiO2wet gel. The WO3, WO3-SiO2, WO3-SiO2-TiO2composite aerogels were prepared via anambient pressure drying process. The morphology and pore properties of WO3, WO3-SiO2andWO3-SiO2-TiO2composite aerogels were studied by SEM, XRD, FTIR, and BET. Theproperties of adsorption and photocatalytic degradation of rhodamine B were analyzed byspectrophotometer. The results indicate that the obtained WO3aerogels dried at150℃havethe specific surface area of433to566m2/g and pore volume of0.29to0.77cm3/g. WO3-SiO2aerogels dried at150℃have the specific surface area of519to719m2/g and pore volume of1.2to1.9cm3/g. WO3-SiO2-TiO2composite aerogels dried at150℃have the specific surfacearea of565to601m2/g and pore volume1.5to2.9cm3/g. The synergistic adsorption/photocatalysis activity of WO3-SiO2, WO3-SiO2-TiO2composite aerogels are excellent. Theirperformances of adsorption and photocatalytic degradation of Rhodamine B were better thanpure SiO2and pure WO3aerogels, achieving85%even more. |