Phillips D H, Watson D B, Roh Y, Mehlhorn T L, Moon J-W, Jardine P M
Environmental Engineering Research Centre, School of Planning, Architecture, and Civil Engineering, Queen's University of Belfast, Belfast BT9 5AG, Northern Ireland, UK.
J Environ Qual. 2006 Aug 9;35(5):1715-30. doi: 10.2134/jeq2005.0124. Print 2006 Sep-Oct.
The objective of this study was to determine how structure, stratigraphy, and weathering influence fate and transport of contaminants (particularly U) in the ground water and geologic material at the Department of Energy (DOE) Environmental Remediation Sciences Department (ERSD) Field Research Center (FRC). Several cores were collected near four former unlined adjoining waste disposal ponds. The cores were collected, described, analyzed for U, and compared with ground water geochemistry from surrounding multilevel wells. At some locations, acidic U-contaminated ground water was found to preferentially flow in small remnant fractures weathering the surrounding shale (nitric acid extractable U [U(NA)] usually < 50 mg kg(-1)) into thin (<25 cm) Fe oxide-rich clayey seams that retain U (U(NA) 239 to 375 mg kg(-1)). However, greatest contaminant transport occurs in a 2 to 3 m thick more permeable stratigraphic transition zone located between two less permeable, and generally less contaminated zones consisting of (i) overlying unconsolidated saprolite (U(NA) < 0.01 to 200 mg kg(-1)) and (ii) underlying less-weathered bedrock (U(NA) generally < 0.01 to 7 mg kg(-1)). In this transition zone, acidic (pH < 4) U-enriched ground water (U of 38 mg L(-1)) has weathered away calcite veins resulting in greater porosity, higher hydraulic conductivity, and higher U contamination (U(NA) 106 to 745 mg kg(-1)) of the weathered interbedded shale and sandstone. These characteristics of the transition zone produce an interval with a high flux of contaminants that could be targeted for remediation.
本研究的目的是确定结构、地层和风化作用如何影响美国能源部(DOE)环境修复科学部(ERSD)野外研究中心(FRC)的地下水和地质材料中污染物(特别是铀)的归宿和迁移。在四个相邻的 former unlined 废弃处置池塘附近采集了多个岩芯。对这些岩芯进行了采集、描述、铀含量分析,并与周围多层井的地下水地球化学数据进行了比较。在一些地点,发现酸性含铀污染地下水优先在细小的残余裂缝中流动,这些裂缝使周围的页岩(硝酸可提取铀[U(NA)]通常<50 mg kg(-1))风化形成薄(<25 cm)的富含铁氧化物的黏土层,这些黏土层能保留铀(U(NA)为239至375 mg kg(-1))。然而,最大的污染物迁移发生在一个2至3米厚、渗透性更强的地层过渡带,该过渡带位于两个渗透性较差且通常污染较轻的区域之间,这两个区域分别为:(i)上覆的未固结腐泥土(U(NA)<0.01至200 mg kg(-1))和(ii)下伏的风化程度较低的基岩(U(NA)通常<0.01至7 mg kg(-1))。在这个过渡带中,酸性(pH<4)富含铀的地下水(铀含量为38 mg L(-1))使方解石脉风化,导致风化的互层页岩和砂岩孔隙度更大、水力传导率更高且铀污染更严重(U(NA)为106至745 mg kg(-1))。过渡带的这些特征形成了一个污染物通量较高的区间,可作为修复的目标。 (注:原文中“former unlined”不太明确准确含义,暂保留原文表述)