Zhang Shu, Williams Paul N, Zhou Chun-Yang, Ma Lena Q, Luo Jun
State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, Jiangsu 210023, PR China.
Institute for Global Food Security, School of Biological Sciences, Queen's University Belfast, Belfast BT9 7BL, United Kingdom.
Chemosphere. 2017 Oct;184:812-819. doi: 10.1016/j.chemosphere.2017.06.062. Epub 2017 Jun 18.
The monitoring of oxyanions in waters, presents significant challenges due to their relatively low concentrations, and a characteristically changeable/unstable/reactive geochemistry with high spatial and temporal turnover. This results in a very heterogeneous pattern of mobility and bioavailability, which is difficult to capture reliably and in a cost effective manner. The diffusive gradients in thin-films (DGT) technique is a popular analytical tool for testing water quality, primarily because it provides a time-integrated measurement. However, to date, the most widely used DGT configuration for oxyanion sampling, the slurry ferrihydrite binding layer (SF-DGT) has only been fully characterized for phosphate. Confirmatory testing of the functional range of ionic strengths, pH, deployment times and ionic competition effects, that the SF-DGT's operates within has not been carried out, but is addressed in this study for V, As, Sb, and Mo. In this study SF-DGT Sb measurements functioned over the largest range of conditions (ionic strength, 0.1-500 mM; pH 3.86-9.90), while ionic strengths above 100 and 500 mM were found to be problematic for As and Mo, respectively. Low pH (below 4) caused inferences with V, conversely As and Mo determination faltered/deviated from predicted responses in pH conditions of ∼9. SF-DGT measurements adequately predicted up to weeklong averaged in situ metal oxyanion concentrations in a freshwater river. This study concludes that the SF-DGT configuration is highly suitable for pollution monitoring applications in freshwater systems for key oxyanion species.
由于水中含氧阴离子浓度相对较低,且具有典型的可变/不稳定/活性地球化学特征,其在空间和时间上的周转率很高,因此对水中含氧阴离子的监测面临重大挑战。这导致了迁移率和生物有效性的非常不均匀的模式,难以以可靠且经济高效的方式捕捉。薄膜扩散梯度(DGT)技术是一种常用的水质检测分析工具,主要是因为它提供了一种时间积分测量方法。然而,迄今为止,用于含氧阴离子采样的最广泛使用的DGT配置,即浆液水铁矿结合层(SF-DGT),仅针对磷酸盐进行了全面表征。尚未对SF-DGT运行所涉及的离子强度、pH值、部署时间和离子竞争效应的功能范围进行验证测试,但本研究针对V、As、Sb和Mo进行了此项研究。在本研究中,SF-DGT对Sb的测量在最大条件范围内(离子强度为0.1 - 500 mM;pH值为3.86 - 9.90)有效,而发现离子强度高于100 mM和500 mM分别对As和Mo存在问题。低pH值(低于4)会干扰V的测量,相反,在pH值约为9的条件下,As和Mo的测定结果出现偏差/偏离预测响应。SF-DGT测量能够充分预测淡水河中长达一周的原位金属含氧阴离子平均浓度。本研究得出结论,SF-DGT配置非常适合淡水系统中关键含氧阴离子物种的污染监测应用。