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In situ chemical reduction of aquifer sediments: Enhancement of reactive iron phases and TCE dechlorination

机译:原位化学还原含水层沉积物:增强反应性铁相和TCE脱氯

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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 Fe-III-oxides were dissolved/reduced, which produced primarily adsorbed Fe-II, and some siderite. Sediment oxidation showed predominantly one Fell 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.
机译:通过形成可渗透的反应性屏障,目前将含水层沉积物的原位化学还原用于铬酸盐和三氯乙烯的修复。研究了连二亚硫酸钠在流动过程中非生物还原天然沉积物过程中发生的化学和物理过程。在不同的含水层沉积物中,溶解/还原了10-22%的非晶态和结晶态的Fe-III-氧化物,主要生成了吸附的Fe-II和一些菱铁矿。沉积物的氧化主要表现为一个倒相,而第二相的氧化速度更慢。化学沉积(58 kJ mol(-1))控制了沉积物减少速率(3.3 h批半衰期),在沉积物柱减少(8.0 h半衰期)期间进行了一些额外的扩散控制。由于还原会生成H +,因此必须保持中性至高pH值以保持还原效率并防止铁迁移。对减少的沉积物进行连续萃取表明,吸附的亚铁可控制TCE反应性。通常使用单个还原反应通过实验室数据预测含水层沉积物的现场规模减少的质量和速率。

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