Xue Yunfei, Sui Qian, Brusseau Mark L, Zhou Wei, Qiu Zhaofu, Lyu Shuguang
State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237, China.
Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, China.
Chem Eng J. 2019 Apr 1;361:919-928. doi: 10.1016/j.cej.2018.12.121. Epub 2018 Dec 21.
This study conducted a comparison of the CaO-based Fenton (CaO/Fe(II)) and Fenton-like (CaO/Fe(III)) systems on their benzene degradation performance. The HO, Fe(II), Fe(III), and HO variations were investigated during the benzene degradation. Although benzene has been totally removed in the two systems, the variation patterns of the investigated parameters were different, leading to the different benzene degradation patterns. In terms of the Fe(II)/Fe(III) conversion, the CaO/Fe(II) and CaO/Fe(III) systems were actually inseparable and had the inherent mechanism relationships. For the CaO/Fe(III) system, the initial Fe(III) must be converted to Fe(II), and then the consequent Fenton reaction could be later developed with the regenerated Fe(II). Moreover, some benzene degradation intermediates could have the ability to facilitate the transformation of the Fe(III) to Fe(II) without the classic HO-associated propagation reactions. By varying the Fe(II) dosing method, an effective degradation strategy has been developed to take advantage of the two CaO-based oxidation systems. The proposed strategy was further successfully tested in TCE degradation, therefore extending the potential for the application of this technique.
本研究对基于CaO的芬顿(CaO/Fe(II))体系和类芬顿(CaO/Fe(III))体系的苯降解性能进行了比较。在苯降解过程中研究了·OH、Fe(II)、Fe(III)和·OOH的变化情况。尽管在这两个体系中苯已被完全去除,但所研究参数的变化模式不同,导致苯的降解模式也不同。就Fe(II)/Fe(III)转化而言,CaO/Fe(II)体系和CaO/Fe(III)体系实际上是不可分割的,且具有内在的机理关系。对于CaO/Fe(III)体系,初始的Fe(III)必须先转化为Fe(II),随后再生的Fe(II)才能引发后续的芬顿反应。此外,一些苯降解中间体能够在没有经典的与·OH相关的传播反应的情况下促进Fe(III)向Fe(II)的转化。通过改变Fe(II)的投加方式,开发了一种有效的降解策略,以利用这两种基于CaO的氧化体系。所提出的策略在三氯乙烯降解中进一步得到成功验证,从而扩展了该技术的应用潜力。