Grupo de Fotocatálisis y Espectroscopía Aplicada al Medioambiente-FEAM (Unidad Asociada al Instituto de Ciencias de Materiales de Sevilla, CSIC), CIDIA-Departamento de Química, Universidad De Las Palmas De Gran Canaria, Las Palmas de Gran Canaria, Spain.
J Colloid Interface Sci. 2013 Jun 15;400:31-40. doi: 10.1016/j.jcis.2013.03.019. Epub 2013 Mar 26.
TiO2 particles were prepared by sol-gel method alone and by sol-gel method combined with hydrothermal treatment. The structural and photocatalytic properties of the two series of photocatalysts were compared. XRD studies revealed that rutilization was faster in the series of photocatalysts, which had been additionally subjected to a hydrothermal process (SG-HT). The hydrothermally treated photocatalysts also displayed a higher specific surface area than those which had only been synthesized using the sol-gel process (SG) and subjected to low calcination temperatures of up to 873 K, while this tendency was inverted at higher temperatures. In accordance with the above observation, the hydrothermally treated series of photocatalysts had a lower particle size than the SG series calcined immediately after the sol-gel process up to 873 K, with this relation being inverted for the highest two temperatures which were studied (973 K and 1023 K) and which saw the commencement of rutilization. Increases in average particle size were observed for both series, with a polyhedral morphology seen as calcination temperature rose. FTIR studies highlighted the presence of the band at 2351 cm(-1) in the SG-HT photocatalysts, characteristic of surface-adsorbed CO2. This was not seen in the SG or P25 photocatalysts. In terms of photoreactivity, the best photocatalyst in the SG-HT series was that calcined at 923 K and in the SG series at 1023 K (SG-1023). Comparing these two photocatalysts and the commercial P25 photocatalyst, SG-1023 was found to be the most photoactive in both the photodegradation and the mineralization of phenol.
TiO2 颗粒是通过溶胶-凝胶法单独制备的,也是通过溶胶-凝胶法与水热处理相结合制备的。比较了这两组光催化剂的结构和光催化性能。XRD 研究表明,在经过水热处理的光催化剂系列(SG-HT)中,锐钛矿的形成速度更快。与仅通过溶胶-凝胶法合成并在低煅烧温度下(高达 873 K)进行处理的 SG 光催化剂相比,经过水热处理的光催化剂具有更高的比表面积,但在更高的温度下则相反。根据上述观察结果,经过水热处理的光催化剂系列的粒径小于 SG 系列,SG 系列在溶胶-凝胶法后立即在 873 K 以下进行煅烧,而在研究的最高两个温度(973 K 和 1023 K)下则相反,在这两个温度下开始出现锐钛矿。随着煅烧温度的升高,两种系列的平均粒径均有所增加,并且随着煅烧温度的升高,观察到多面体形态。FTIR 研究强调了 SG-HT 光催化剂中存在 2351 cm(-1) 处的带,这是表面吸附 CO2 的特征。在 SG 或 P25 光催化剂中未观察到该带。在光反应性方面,SG-HT 系列中最好的光催化剂是在 923 K 下煅烧的,而在 SG 系列中最好的是在 1023 K 下煅烧的(SG-1023)。将这两种光催化剂与商业 P25 光催化剂进行比较,发现 SG-1023 在苯酚的光降解和矿化方面具有最高的光活性。