The accumulation of radioactive contaminants in drinking water distribution systems

被引:39
|
作者
Lytle, Darren A. [1 ]
Sorg, Thomas [1 ]
Wang, Lili [2 ]
Chen, Abe [3 ]
机构
[1] US EPA, ORD, NRMRL, WSWRD, Cincinnati, OH 45268 USA
[2] US EPA, OW, GWDW, SRMD, Washington, DC 20460 USA
[3] ALSA Tech LLC, Powell, OH 43065 USA
关键词
Distribution system; Radium; Radioactivity; Thorium; Water; RELEASE; DEPOSITS; SCALES; IRON;
D O I
10.1016/j.watres.2013.10.050
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The accumulation of trace contaminants in drinking water distribution system sediment and scales has been documented, raising concerns that the subsequent release of the contaminants back to the water is a potential human exposure pathway. Radioactive contaminants are of concern because of their known health effects and because of their persistence within associated distribution system materials. The objective of this work was to measure the amount of a number of radioactive contaminants (radium, thorium, and uranium isotopes, and gross alpha and beta activity) in distribution solids collected from water systems in four states (Wisconsin, Illinois, Minnesota, and Texas). The water utilities chosen had measurable levels of radium in their source waters. In addition, 19 other elements in the solids were quantified. Water systems provided solids primarily collected during routine fire hydrant flushing. Iron was the dominant element in nearly all of the solids and was followed by calcium, phosphorus, magnesium, manganese, silicon, aluminum and barium in descending order. Gross alpha and beta radiation averaged 255 and 181 pCi/g, and were as high as 1602 and 1169 pCi/g, respectively. Total radium, thorium and uranium averaged 143,40 and 6.4 pCi/g, respectively. Radium-226 and -228 averaged 74 and 69 pCi/g, and were as high as 250 and 351 pCi/g, respectively. Published by Elsevier Ltd.
引用
收藏
页码:396 / 407
页数:12
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