Open AccessMicrowave dissolution of plant tissue and the subsequent determination of trace lanthanide and actinide elements by inductively coupled plasma-mass spectrometry
Author(s) -
Jorge Alvarado,
Teresa J. Neal,
L.L. Smith,
Erickson
Publication year - 1997
Language(s) - English
Resource type - Reports
DOI - 10.2172/513544
Subject(s) - inductively coupled plasma mass spectrometry , microwave digestion , chemistry , actinide , nitric acid , inductively coupled plasma , lanthanide , detection limit , mass spectrometry , uranium , analytical chemistry (journal) , cerium , radiochemistry , environmental chemistry , nuclear chemistry , chromatography , materials science , metallurgy , inorganic chemistry , plasma , ion , physics , organic chemistry , quantum mechanics
Recently there has been much concern with the ability of plants to uptake heavy metals from their surroundings. With the development of instrumental techniques with low detection limits such as inductively coupled plasma-mass spectrometry (ICP-MS), attention is shifting toward achieving faster and more elegant ways of oxidizing the organic material inherent in environmental samples. Closed-vessel microwave dissolution was compared with conventional methods for the determination of concentrations of cerium, samarium, europium, terbium, uranium and thorium in a series of samples from the National Institute of Standards and Technology and from fields in Idaho. The ICP-MS technique exhibited detection limits in parts-per-trillion and linear calibration plots over three orders of magnitude for the elements under study. The results obtained by using nitric acid and hydrogen peroxide in a microwave digestion system for the analysis of reference materials showed close agreement with the accepted values. These values were compared with results obtained from dry- and wet-ashing procedures. The findings from an experiment comparing radiometric techniques for the determination of actinide elements to ICP-MS are reported