Rapid identification and analysis of airborne plutonium using a combination of alpha spectroscopy and inductively coupled plasma mass spectrometry

被引:14
|
作者
Farmer, DE
Steed, AC
Sobus, J
Stetzenbach, K
Lindley, K
Hodge, VF
机构
[1] US EPA, Radiat & Indoor Environm Natl Lab, Las Vegas, NV 89119 USA
[2] Univ Nevada, Groundwater Chem Div, Harry Reid Ctr Environm Studies, Las Vegas, NV 89154 USA
[3] Univ Nevada, Dept Chem, Las Vegas, NV 89154 USA
来源
HEALTH PHYSICS | 2003年 / 85卷 / 04期
关键词
air sampling; plutonium; spectroscopy; alpha; emergency planning;
D O I
10.1097/00004032-200310000-00009
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Recent wildland fires near two U.S. nuclear facilities point to a need to rapidly identify the presence of airborne plutonium during incidents involving the potential release of radioactive materials. Laboratory turn-around times also need to be shortened for critical samples collected in the earliest stages of radiological emergencies. This note discusses preliminary investigations designed to address both these problems. The methods under review are same day high-resolution alpha spectroscopy to screen air filter samples for the presence of plutonium and inductively coupled plasma mass spectrometry to perform sensitive plutonium analyses. Thus far, using modified alpha spectroscopy techniques, it has been possible to reliably identify the similar to5.2 MeV emission of Pu-239 on surrogate samples (air filters artificially spiked with plutonium after collection) even though the primary alpha-particle emissions of plutonium are, as expected, superimposed against a natural alpha radiation background dominated by short-lived radon and thoron progeny (similar to6-9 MeV). Several processing methods were tested to prepare samples for analysis and shorten laboratory turn-around time. The most promising technique was acid-leaching of air filter samples using a commercial open-vessel microwave digestion system. Samples prepared in this way were analyzed by both alpha spectroscopy (as a thin-layer iron hydroxide co-precipitate) and inductively coupled plasma mass spectrometry. The detection levels achieved for Pu-239-approximately 1 mBq m(-3) for alpha spectroscopy screening, and, < 0.1 mBq m(-3) for inductively coupled plasma mass spectrometry analysis-are consistent with derived emergency response levels based on EPA's Protective Action Guides, and samples can be evaluated in 36 to 72 h. Further, if samples can be returned to a fixed-laboratory and processed immediately, results from mass spectrometry could be available in as little as 24 h. When fully implemented, these techniques have the potential to provide useful information and improved operational flexibility to emergency planners and first-responders during radiological emergencies.
引用
收藏
页码:457 / 465
页数:9
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