可渗透反应墙
菱铁矿
含水层
化学
环境修复
铁质
沉积物
环境化学
脱氯作用
地下水修复
连二亚硫酸钠
零价铁
氧化还原
氧化铁
吸附
无机化学
地下水
矿物学
地质学
黄铁矿
生物降解
污染
岩土工程
有机化学
古生物学
生物
生态学
作者
Jim E. Szecsody,J.S. Fruchter,Mark D. Williams,Vince R. Vermeul,Debbie S. Sklarew
摘要
In situ chemical reduction of aquifer sediments is currently being used for chromate and TCE remediation by forming a permeable reactive barrier. The chemical and physical processes that occur during abiotic reduction of natural sediments during flow by sodium dithionite were investigated. In different aquifer sediments, 10-22% of amorphous and crystalline FeIII-oxides were dissolved/reduced, which produced primarily adsorbed FeII, and some siderite. Sediment oxidation showed predominantly one FeII phase, with a second phase being oxidized more slowly. The sediment reduction rate (3.3 h batch half-life) was chemically controlled (58 kJ mol(-1)), with some additional diffusion control during reduction in sediment columns (8.0 h half-life). It was necessary to maintain neutral to high pH to maintain reduction efficiency and prevent iron mobilization, as reduction generated H+. Sequential extractions on reduced sediment showed that adsorbed ferrous iron controlled TCE reactivity. The mass and rate of field-scale reduction of aquifer sediments were generally predicted with laboratory data using a single reduction reaction.
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