Tryba Beata, Morawski Antoni W, Inagaki Michio, Toyoda Masahiro
Technical University of Szczecin, ul. Pulaskiego 10, 70-322 Szczecin, Poland.
Chemosphere. 2006 Aug;64(7):1225-32. doi: 10.1016/j.chemosphere.2005.11.035. Epub 2006 Jan 3.
Fe-C-TiO(2) photocatalysts which contained the residue carbon (0.2-3.3 mass%) were prepared from a mixture of TiO(2) and FeC(2)O(4) through the heating at 673-1173 K in Ar. These photocatalysts did not show a high adsorption of phenol, but they were active in photo-Fenton reactions during decomposition of phenol under UV irradiation with addition of H(2)O(2). It was proved that Fe(2+) governed the photoactivity of Fe-C-TiO(2) photocatalysts, it decreased with heat-treatment temperature above 773 K. For comparison, Fe-TiO(2) photocatalyst was prepared by heating TiO(2) and FeC(2)O(4) at 823 K in air for 3h. Phenol decomposition was going much slower on Fe-TiO(2) photocatalyst in comparison with Fe-C-TiO(2), of which mechanism was different, on the former phenol was decomposed by the radical reaction, on the latter through a complex reaction with iron and intermediates of phenol decomposition. Therefore carbon-coating TiO(2) was found to be advantageous for mounting iron and its application for the phenol decomposition via photo-Fenton process.
通过在氩气中于673 - 1173 K加热由TiO₂和FeC₂O₄的混合物制备了含有残留碳(0.2 - 3.3质量%)的Fe - C - TiO₂光催化剂。这些光催化剂对苯酚的吸附性不高,但在添加H₂O₂的紫外光照射下分解苯酚的光芬顿反应中具有活性。结果表明,Fe²⁺决定了Fe - C - TiO₂光催化剂的光活性,在773 K以上的热处理温度下其活性降低。作为对比,通过在空气中于823 K加热TiO₂和FeC₂O₄ 3小时制备了Fe - TiO₂光催化剂。与Fe - C - TiO₂相比,Fe - TiO₂光催化剂上苯酚的分解要慢得多,其机理不同,前者苯酚通过自由基反应分解,后者通过与铁和苯酚分解中间体的复杂反应分解。因此,发现碳包覆TiO₂有利于负载铁及其在通过光芬顿过程分解苯酚中的应用。