Ground Water and Ecosystems Restoration Division, National Risk Management Research Laboratory, Office of Research and Development, United States Environmental Protection Agency, 919 Kerr Research Drive, Ada, OK 74820, USA.
Water Res. 2013 Aug 1;47(12):4095-106. doi: 10.1016/j.watres.2012.12.042. Epub 2013 Mar 21.
Nanoscale zerovalent iron (NZVI) such as Toda Kogyo RNIP-10DS has been used for site remediation, yet information is lacking regarding how far injected NZVI can travel, how long it lasts, and how it transforms to other minerals in a groundwater system. Previously we reported effective mass destruction of chlorinated ethenes dominated by tetrachloroethene (PCE) using emulsified zerovalent iron (EZVI) nanoparticles of RNIP-10DS in a shallow aquifer (1-6 m below ground surface, BGS) at Site 45, Marine Corps Recruit Depot, Parris Island, South Carolina, USA. Here we report test results on transport and transformation of injected EZVI in the subsurface. We employed two EZVI delivery methods: pneumatic injection and direct injection. Effective delivery of EZVI to the targeted zone was achieved with pneumatic injection showing a travel distance from injection points of up to 2.1 m and direct injection showing a travel distance up to 0.89 m. X-ray diffraction and scanning electron microscopy studies on particles harvested from well purge waters indicated that injected black colored NZVI (α-Fe(0)) was transformed largely to black colored cube-like and plate-like magnetites (Fe3O4, 0.1-1 μm, 0-9 months), then to orange colored irregularly shaped lepidocrocite (γ-FeOOH, 0.1-1 μm, 9 months to 2.5 years), then to yellowish lath-like goethite (α-FeOOH, 2-5 μm, 2.5 years) and ferrihydrite-like spherical particles (0.05-0.1 μm) in the top portion of the aquifer (1-2 m BGS). No α-Fe(0) was found in most monitoring wells three months after injection. The formed iron oxides appeared to have a wider range of particle size (submicron to 5 μm) than the pristine NZVI (35-140 nm). Injected NZVI was largely transformed to magnetite (0.1-1 μm) during two and half years in the lower portion of the aquifer (3-6 m).
纳米零价铁(NZVI),如 Toda Kogyo RNIP-10DS,已被用于现场修复,但关于注入的 NZVI 能传播多远、持续多长时间以及在地下水系统中如何转化为其他矿物质的信息还很缺乏。此前,我们曾报道过在南卡罗来纳州帕里斯岛美国海军陆战队新兵训练营第 45 号场地的浅层含水层(地面以下 1-6 米)中,使用 RNIP-10DS 乳化零价铁(EZVI)纳米颗粒有效降解了以四氯乙烯(PCE)为主的氯代烯烃。在这里,我们报告了在地下注入 EZVI 的传输和转化的测试结果。我们采用了两种 EZVI 输送方法:气动注射和直接注射。气动注射可有效将 EZVI 输送到目标区域,其注射点的传播距离可达 2.1 米,而直接注射的传播距离可达 0.89 米。从井中清除水收集的颗粒的 X 射线衍射和扫描电子显微镜研究表明,注入的黑色 NZVI(α-Fe(0))主要转化为黑色立方体形和板形磁铁矿(Fe3O4,0.1-1 μm,0-9 个月),然后转化为橙色不规则形状的纤铁矿(γ-FeOOH,0.1-1 μm,9 个月至 2.5 年),然后转化为黄棕色板状针铁矿(α-FeOOH,2-5 μm,2.5 年)和类水铁矿的球形颗粒(0.05-0.1 μm)在含水层的顶部(地面以下 1-2 米)。在注入后三个月,大多数监测井中均未发现α-Fe(0)。形成的氧化铁颗粒的粒径范围似乎比原始 NZVI(35-140nm)更宽(亚微米至 5μm)。在含水层的下部(3-6m),注入的 NZVI 在两年半的时间内主要转化为磁铁矿(0.1-1μm)。