School of Environmental & Chemical Engineering, Nanchang University, Nanchang 330031, China.
J Hazard Mater. 2011 Jan 30;185(2-3):1477-81. doi: 10.1016/j.jhazmat.2010.10.071. Epub 2010 Oct 26.
An enhanced method of hydroxyl-Fe-pillared bentonite (H-Fe-P-B) during the degradation of Orange II was studied to provide novel insight to interactions of degradation intermediates with heterogeneous catalyst in UV-Fenton system. Based on the degradation mechanism of Orange II, oxalate enhanced mechanism of H-Fe-P-B in heterogeneous UV-Fenton system was developed. The results showed that additional oxalate could increase the Fe leaching of H-Fe-P-B during heterogeneous UV-Fenton process, which led to higher mineralization efficiency of Orange II and lower energy consumption of treatment. When the concentrations of additional sodium oxalate increased up to 0.1 mmol L(-1), 0.2 mmol L(-1) and 0.4 mmol L(-1), the rate of Orange II degradation could increase 30%, 46% and 63%, respectively. The iron ions leached from catalyst could be adsorbed back to the catalyst again after the organic intermediates were mineralized completely. Then the catalyst of H-Fe-P-B could be reused and additional pollution caused by iron ions could be avoided.
羟基化铁柱撑膨润土(H-Fe-P-B)在橙色 II 降解中的增强方法研究,旨在为 UV-Fenton 体系中降解中间体与多相催化剂的相互作用提供新的见解。基于橙色 II 的降解机制,开发了 H-Fe-P-B 在非均相 UV-Fenton 体系中的草酸盐增强机制。结果表明,外加草酸盐可以增加 H-Fe-P-B 在非均相 UV-Fenton 过程中的铁浸出,从而提高橙色 II 的矿化效率和处理的能耗。当外加草酸钠的浓度增加到 0.1 mmol·L(-1)、0.2 mmol·L(-1)和 0.4 mmol·L(-1)时,橙色 II 的降解速率分别提高了 30%、46%和 63%。当有机中间产物完全矿化后,从催化剂中浸出的铁离子可以被再次吸附回催化剂上。然后可以重复使用 H-Fe-P-B 催化剂,并避免铁离子造成的额外污染。