School of Environmental Science and Engineering, Sun Yat-Sen (Zhongshan) University, Guangzhou, 510275, PR China.
Environ Technol. 2010 Feb;31(2):145-54. doi: 10.1080/09593330903397755.
Iron tetrapolyvanadate (Fe2V4O13) was prepared and characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) measurement and scanning electron microscopy (SEM). It was found that Fe2V4O13 could effectively catalyse H2O2 to generate active OH; therefore, Fe2V4O13 was employed as a new two-metal heterogeneous Fenton-like catalyst. The decomposition of H2O2 and the degradation of Acid Orange II catalysed by Fe2V4O13 could be well described with a simple pseudo-first-order rate equation between the reaction temperatures of 15 degrees C and 30 degreesC. It was inferred from the reaction activation energy data that the generation of the hydroxyl radical was a control step in a series of reactions for the oxidation of Acid Orange II in the presence of H2O2 and Fe2V4O13. The catalytic activity of Fe2V4O13 towards degradation of Acid Orange II was not only much higher than that of alpha-Fe2O3, V2O5 and FeVO4 but also than that of their mixtures with an identical ratio of Fe and V, such as 2FeVO4 + V2O5 and Fe2O3 + 2V2O5. The high catalytic activity possibly involved a special two-way Fenton-like mechanism and the synergistic activation of Fe(III) and V(V) in Fe2V4O13 towards H2O2.
四聚铁钒酸(Fe2V4O13)通过 X 射线衍射(XRD)、BET 测量和扫描电子显微镜(SEM)进行了制备和表征。结果发现,Fe2V4O13 能够有效地催化 H2O2 生成活性 OH;因此,Fe2V4O13 被用作新型双金属非均相类 Fenton 催化剂。在 15°C 至 30°C 的反应温度范围内,H2O2 的分解和酸性橙 II 的降解可以用简单的拟一级速率方程很好地描述。从反应活化能数据推断,在 H2O2 和 Fe2V4O13 的存在下,羟基自由基的生成是一系列氧化酸性橙 II 反应的控制步骤。Fe2V4O13 对酸性橙 II 降解的催化活性不仅明显高于α-Fe2O3、V2O5 和 FeVO4,而且也明显高于具有相同 Fe 和 V 比例的混合物,如 2FeVO4 + V2O5 和 Fe2O3 + 2V2O5。高催化活性可能涉及一种特殊的双向类 Fenton 机制,以及 Fe2V4O13 中 Fe(III)和 V(V)对 H2O2 的协同活化。