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Integration of •SO4−-based AOP mediated by reusable iron particles and a sulfidogenic process to degrade and detoxify Orange II

Journal 2020 · IF 9.13 · 发表于 2020 年 2 月 15 日
作者: Xiaoyu Yu,Jianliang Sun,Guibiao Li,Yi Huang,Yu Li,Dehua Xia,Feng Jiang
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摘要

The sulfate radical (•SO 4 − )-based advanced oxidation processes (AOPs) for the degradation of refractory organic pollutants consume a large amount of persulfate activators and often generate toxic organic by-products. In this study, we proposed a novel iron-cycling process integrating •SO 4 − -based AOP mediated by reusable iron particles and a sulfidogenic process to degrade and detoxify Orange II completely. The rusted waste iron particles (Fe 0 @Fe x O y ), which contained Fe II /Fe III oxides (Fe x O y ) on the shell and zero-valent iron (Fe 0 ) in the core, efficiently activated persulfate to produce •SO 4 − and hydroxyl radicals (•OH) to degrade over 95% of Orange II within 120 min. Both •SO 4 − and •OH destructed Orange II through a sequence of electron transfer , electrophilic addition and hydrogen abstraction reactions to generate several organic by-products (e.g., aromatic amines and phenol), which were more toxic than the untreated Orange II. The AOP-generated organic by-products were further mineralized and detoxified in a sulfidogenic bioreactor with sewage treatment together. In a 170-d trial, the organic carbon removal efficiency was up to 90%. The inhibition of the bioreactor effluents on the growth of Chlorella pyrenoidosa became negligible, due to the complete degradation and mineralization of toxic AOP-generated by-products by aromatic-degrading bacteria (e.g., Clostridium and Dechloromonas ) and other bacteria. The sulfidogenic process also well recovered the used Fe 0 @Fe x O y particles through the reduction of surface Fe III back into Fe II by hydrogen sulfide formed and iron-reducing bacteria (e.g., Sulfurospirillum and Paracoccus ). The regenerated Fe 0 @Fe x O y particles had more reactive surface Fe II sites and exhibited much better reactivity in activating persulfate in at least 20 reuse cycles. The findings demonstrate that the integrated process is a promising solution to the remediation of toxic and refractory organic pollutants because it reduces the chemical cost of persulfate activation and also completely detoxifies the toxic by-products.

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