吸附
铁
化学
铁质
水合氧化铁
氧化物
曝气
离子
氧化铁
降级(电信)
过氧化氢
无机化学
核化学
赤铁矿
氧化还原
氧化剂
氧气
催化作用
氧化法
化学工程
有机化学
工程类
电信
吸附
计算机科学
作者
Bharat Lodha,Sanjeev Chaudhari
出处
期刊:Journal of Hazardous, Toxic, and Radioactive Waste
[American Society of Civil Engineers]
日期:2016-10-20
卷期号:21 (3)
被引量:1
标识
DOI:10.1061/(asce)hz.2153-5515.0000347
摘要
The major limitations of the Fenton process are the working pH range (2–5) and the high cost of H2O2. These limitations were unraveled using the Fe2+-air oxidation process, in which ferrous ions were used with continuous aeration without H2O2 at a higher pH (pH = 10). This paper studies the effect of the initial hydrous ferric oxide (HFO) concentration on the Fe2+-air process. The enhancement in degradation of the dye [Reactive Black 5 (RB5)] was observed using the Fe2+-air process in the presence of initial HFO, as compared to the Fe2+-air process in the absence of initial HFO. The enhancement is possibly attributable to the adsorption of ferrous ions, dye, and oxygen onto the HFO surface and leading to effective utilization of reactive oxidizing species. The oxidizing entities appear to be generated during oxidation of adsorbed ferrous ions under oxic conditions—probably on the surface of HFO. Furthermore, the Fe2+-air process in the presence of HFO reduces the concentration of ferrous ions required for decolorization of RB5 compared to the Fe2+-air process without HFO and hence resulting in an overall-economical process for the pretreatment or degradation of recalcitrant compounds.
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