Iron [Fe(0)]-rich substrate based on iron–carbon micro–electrolysis for phosphorus adsorption in aqueous solutions

吸附 水溶液 电解 碳纤维 化学 基质(水族馆) 无机化学 环境化学 零价铁 化学工程 材料科学 电极 有机化学 物理化学 生态学 复合材料 工程类 复合数 生物 电解质
作者
Shihai Deng,Desheng Li,Xue Yang,Wei Xing,Jin‐Long Li,Qi Zhang
出处
期刊:Chemosphere [Elsevier BV]
卷期号:168: 1486-1493 被引量:57
标识
DOI:10.1016/j.chemosphere.2016.11.043
摘要

The phosphorus (P) adsorption properties of an iron [Fe(0)]-rich substrate (IRS) composed of iron scraps and activated carbon were investigated based on iron–carbon micro-electrolysis (IC–ME) and compared to the substrates commonly used in constructed wetlands (CWs) to provide an initial characterization of the [Fe(0)]-rich substrate. The results showed that P was precipitated by Fe(III) dissolved from the galvanic cell reactions in the IRS and the reaction was suppressed by the pH and stopped when the pH exceeded 8.90 ± 0.09. The adsorption capacity of the IRS decreased by only 4.6% in the second round of adsorption due to Fe(0) consumption in the first round. Substrates with high Ca– and Mg–oxide contents and high Fe– and Al–oxide contents had higher P adsorption capacities at high and low pH values, respectively. Substrates containing high Fe and Al concentrations and low Ca concentrations were more resistant to decreases in the P adsorption capacity resulting from organic matter (OM) accumulation. The IRS with an iron scrap to activated carbon volume ratio of 3:2 resulted in the highest P adsorption capacity (9.34 ± 0.14 g P kg−1), with minimal pH change and strong adaptability to OM accumulation. The Fe(0)–rich substrate has the considerable potential for being used as a CW substrate.
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