Dai Huiwang, Miao Xiaozeng, Zhu Jianxi, Chen Jianxin
School of Resources, Environmental and Chemical Engineering, Nanchang University, Nanchang, 330031, Jiangxi, China; The Key Laboratory of Poyang Lake Environment and Resource Utilization, Ministry of Education, Nanchang, 330031, Jiangxi, China.
Guangzhou Institute of Geochemistry, Chinese Academy of Sciences (CAS) Guangzhou, 510640, Guangdong, China; Guangdong Provincial Key Laboratory of Mineral Physics and Materials, Guangzhou, 510640, Guangdong, China.
Chemosphere. 2022 Jul;298:134240. doi: 10.1016/j.chemosphere.2022.134240. Epub 2022 Mar 9.
The redox cycle of iron is a well-known rate-determining step for hydroxyl radical generation in photo-Fenton system. In this study, oxalate was employed as regulator to enhance the degradation of Orange II in FeO magnetic nanoparticles (NPs)-catalyzed heterogeneous UV-Fenton system. Results showed that the oxalate could interact with the surface ≡Fe species of catalyst, which weakened the bond of ≡Fe-O and promoted the leaching of iron ions. Then the redox cycle of iron and generation of HO· would be accelerated via the homogeneous UV-Fenton reaction. The degradation rate constant of Orange II reached 0.220 min when additional oxalate concentration was 0.4 mM, which was 2.5 times as high as that without oxalate in heterogeneous UV-Fenton system. In this case, the removal efficiencies of color and TOC were 99.3% and 92.0% after 30 and 120 min treatment, respectively. In addition, based on the results of XRD and XPS characterization, it could be deduced that the crystal structure and elemental configuration of FeO magnetic nanoparticles could be maintained after reaction. Besides, the results of FTIR and magnetization characterization indicated that the CO on surface of catalyst could be degraded and the catalyst could be easily separated from aqueous by applying an external magnetic field. The FeO magnetic nanoparticles showed high catalytic stability and reusability under the regulation of oxalate due to the fact that the leached iron ions could be re-adsorbed on the catalyst after treatment.
铁的氧化还原循环是光芬顿体系中羟基自由基生成的一个众所周知的速率决定步骤。在本研究中,草酸盐被用作调节剂以增强FeO磁性纳米颗粒(NPs)催化的非均相紫外光芬顿体系中对橙黄II的降解。结果表明,草酸盐可与催化剂表面的≡Fe物种相互作用,削弱≡Fe-O键并促进铁离子的浸出。然后,通过均相紫外光芬顿反应可加速铁的氧化还原循环和·OH的生成。当额外的草酸盐浓度为0.4 mM时,橙黄II的降解速率常数达到0.220 min⁻¹,这是在非均相紫外光芬顿体系中无草酸盐时的2.5倍。在此情况下,经过30和120分钟处理后,颜色和TOC的去除效率分别为99.3%和92.0%。此外,基于XRD和XPS表征结果,可以推断FeO磁性纳米颗粒的晶体结构和元素构型在反应后能够保持。此外,FTIR和磁化表征结果表明,催化剂表面的CO可被降解,并且通过施加外部磁场可轻松地将催化剂与水相分离。由于浸出的铁离子在处理后可重新吸附在催化剂上,FeO磁性纳米颗粒在草酸盐的调节下表现出高催化稳定性和可重复使用性。