College of Environmental Science and Engineering, Yangzhou University, Jiangsu, 225127, China.
Jiangsu Collaborative Innovation Center for Solid Organic Waste Resource Utilization, Nanjing, 210095, China.
Sci Rep. 2017 Jul 20;7(1):6070. doi: 10.1038/s41598-017-06398-3.
Magnetic attapulgite-FeO nanocomposites (ATP-FeO) were prepared by coprecipitation of FeO on ATP. The composites were characterized by scanning electron microscopey, X-ray diffractometry, Brunauer-Emmett-Teller analysis, X-ray photoelectron spectroscopy, energy dispersive spectrometer and transmission electron microscopy. Surface characterization showed that FeO particles with an average size of approximately 15 nm were successfully embedded in matrix of ATP. The capacity of the FeO-activated ATP (A-ATP@FeO) composites for catalytic degradation of ethidium bromide (EtBr, 80 mg/L) at different pH values, hydrogen peroxide (HO) concentrations, temperatures, and catalyst dosages was investigated. EtBr degradation kinetics studies indicated that the pseudo-first-order kinetic constant was 2.445 min at T = 323 K and pH 2.0 with 30 mM HO, and 1.5 g/L of A-ATP@FeO. Moreover, a regeneration study suggested that A-ATP@FeO maintained over 80% of its maximal EtBr degradation ability after five successive cycles. The effects of the iron concentrations and free radical scavengers on EtBr degradation were studied to reveal possible catalytic mechanisms of the A-ATP@FeO nanocomposites. Electron Paramagnetic Resonance revealed both hydroxyl (∙OH) and superoxide anion (∙O) radicals were involved in EtBr degradation. Radical scavenging experiment suggested EtBr degradation was mainly ascribed to ∙OH radicals, which was generated by reaction between Fe and HO on the surface of A-ATP@FeO.
磁性凹凸棒石-FeO 纳米复合材料(ATP-FeO)是通过 FeO 在 ATP 上共沉淀制备的。通过扫描电子显微镜、X 射线衍射仪、Brunauer-Emmett-Teller 分析、X 射线光电子能谱、能量色散光谱仪和透射电子显微镜对复合材料进行了表征。表面特性表明,成功地将平均粒径约为 15nm 的 FeO 颗粒嵌入到 ATP 基体中。研究了不同 pH 值、过氧化氢(HO)浓度、温度和催化剂用量下 FeO 激活的 ATP(A-ATP@FeO)复合材料对溴化乙锭(EtBr,80mg/L)催化降解的性能。EtBr 降解动力学研究表明,在 T=323K 和 pH2.0 条件下,HO 浓度为 30mM,A-ATP@FeO 用量为 1.5g/L 时,准一级动力学常数为 2.445min。此外,再生研究表明,A-ATP@FeO 在连续五次循环后仍保持超过 80%的最大 EtBr 降解能力。研究了铁浓度和自由基清除剂对 EtBr 降解的影响,以揭示 A-ATP@FeO 纳米复合材料的可能催化机制。电子顺磁共振(EPR)表明,羟基(∙OH)和超氧阴离子(∙O)自由基均参与了 EtBr 的降解。自由基清除实验表明,EtBr 的降解主要归因于 ∙OH 自由基,它是 A-ATP@FeO 表面的 Fe 和 HO 之间的反应生成的。