UNSW Water Research Centre and School of Civil and Environmental Engineering, The University of New South Wales, Sydney 2052, Australia.
NSW Systems Biology Initiative, School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney 2052, Australia.
Environ Sci Technol. 2021 Jul 6;55(13):8793-8805. doi: 10.1021/acs.est.1c01604. Epub 2021 Jun 10.
Results of investigations into factors influencing contaminant mobility in a replica trench located adjacent to a legacy radioactive waste site are presented in this study. The trench was filled with nonhazardous iron- and organic matter (OM)-rich components, as well as three contaminant analogues strontium, cesium, and neodymium to examine contaminant behavior. Imposed redox/water-level oscillations, where oxygen-laden rainwater was added to the anoxic trench, resulted in marked biogeochemical changes including the removal of aqueous Fe(II) and circulation of dissolved carbon, along with shifts to microbial communities involved in cycling iron (, ) and methane generation (, ). Contaminant mobility depended upon element speciation and rainfall event intensity. Strontium remained mobile, being readily translocated under hydrological perturbations. Strong ion-exchange reactions and structural incorporation into double-layer clay minerals were likely responsible for greater retention of Cs, which, along with Sr, was unaffected by redox oscillations. Neodymium was initially immobilized within the anoxic trenches, due to either secondary mineral (phosphate) precipitation or via the chemisorption of organic- and carbonate-Nd complexes onto variably charged solid phases. Oxic rainwater intrusions altered Nd mobility via competing effects. Oxidation of Fe(II) led to partial retention of Nd within highly sorbing Fe(III)/OM phases, whereas pH decreases associated with rainwater influxes resulted in a release of adsorbed Nd to solution with both pH and OM presumed to be the key factors controlling Nd attenuation. Collectively, the behavior of simulated contaminants within this replica trench provided unique insights into trench water biogeochemistry and contaminant cycling in a redox oscillatory environment.
本研究介绍了紧邻放射性废物遗址的模拟沟渠中影响污染物迁移因素的调查结果。该沟渠中填充了无害的含铁和有机物(OM)丰富的成分,以及三种污染物类似物锶、铯和钕,以研究污染物的行为。施加的氧化还原/水位波动,即在缺氧沟渠中添加含氧雨水,导致明显的生物地球化学变化,包括去除水溶液中的 Fe(II)和溶解碳的循环,以及与铁循环( )和甲烷生成( )相关的微生物群落的转变。污染物的迁移性取决于元素形态和降雨事件强度。锶仍然具有迁移性,在水文干扰下很容易被迁移。强离子交换反应和结构整合到双层粘土矿物中可能是导致 Cs 更大保留的原因,Cs 与 Sr 一起不受氧化还原波动的影响。由于次生矿物(磷酸盐)沉淀或有机和碳酸盐-Nd 配合物化学吸附到可变电荷固相上,最初在缺氧沟渠中固定了钕。含氧雨水的侵入通过竞争效应改变了 Nd 的迁移性。Fe(II)的氧化导致 Nd 在高吸附 Fe(III)/OM 相中部分保留,而与雨水流入相关的 pH 降低导致吸附的 Nd 释放到溶液中,pH 和 OM 被认为是控制 Nd 衰减的关键因素。总的来说,这个模拟沟渠中模拟污染物的行为为了解氧化还原振荡环境中的沟渠水生物地球化学和污染物循环提供了独特的见解。