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