A NEW SOLID-LIQUID EXTRACTION SAMPLING TECHNIQUE FOR DIRECT DETERMINATION OF TRACE-ELEMENTS IN BIOLOGICAL-MATERIALS BY GRAPHITE-FURNACE ATOMIC-ABSORPTION SPECTROMETRY

Citation
H. Minami et al., A NEW SOLID-LIQUID EXTRACTION SAMPLING TECHNIQUE FOR DIRECT DETERMINATION OF TRACE-ELEMENTS IN BIOLOGICAL-MATERIALS BY GRAPHITE-FURNACE ATOMIC-ABSORPTION SPECTROMETRY, Spectrochimica acta, Part B: Atomic spectroscopy, 51(2), 1996, pp. 211-220
Citations number
25
Categorie Soggetti
Spectroscopy
ISSN journal
05848547
Volume
51
Issue
2
Year of publication
1996
Pages
211 - 220
Database
ISI
SICI code
0584-8547(1996)51:2<211:ANSEST>2.0.ZU;2-9
Abstract
A new solid-liquid extraction sampling technique with graphite furnace atomic absorption spectrometry is based on the quantitative extractio n of the element of interest from the biological powdered samples into a liquid phase of 1 mol l(-1) nitric acid solution. Examinations of t he conditions for sample preparation using solid-liquid extraction (i. e. the effect of concentration of nitric acid, sample mass and ultraso nication time on the extraction) have been carried out in order to obt ain 100% extraction of cadmium, copper, lead and manganese from powder ed biological samples to the liquid phase. 100% of extraction of these metals is successfully carried out using 1 mol l(-1) nitric acid, and separation of solid phase and liquid phase is done by using a centrif uge (20 min, 4000 rev min(-1)). The proposed method is applied to the determination of cadmium and lead at 0.1 mu g g(-1) levels and of copp er and manganese at 10 mu g g(-1) levels in powdered biological sample s. These analytical results are ascertained by microwave induced nitro gen plasma-mass spectrometry. Detection limits for cadmium, copper, le ad and manganese are, respectively, 0.012 mu g g(-1), 0.829 mu g g(-1) , 0.082 mu g g(-1) and 0.125 mu g g(-1) in solid samples, when 50 mg o f powdered biological samples is extracted in 5 ml of 1 mol l(-1) nitr ic acid and then 10 mu l of extracted solution is measured. Precisions of the determination (relative standard deviation at five determinati ons) of cadmium, copper, lead and manganese are 3.4%, 3.1%, 3.9% and 3 .1%, respectively.