SOLID SAMPLING ELECTROTHERMAL VAPORIZATION INDUCTIVELY-COUPLED PLASMA-MASS SPECTROMETRY FOR THE DETERMINATION OF ARSENIC IN STANDARD REFERENCE MATERIALS OF PLANT-ORIGIN
F. Vanhaecke et al., SOLID SAMPLING ELECTROTHERMAL VAPORIZATION INDUCTIVELY-COUPLED PLASMA-MASS SPECTROMETRY FOR THE DETERMINATION OF ARSENIC IN STANDARD REFERENCE MATERIALS OF PLANT-ORIGIN, Journal of analytical atomic spectrometry, 10(2), 1995, pp. 81-87
The direct determination of As in solid samples of plant origin using
electrothermal vaporization inductively coupled plasma mass spectromet
ry (ETV-ICP-MS) is reported. The first phase of the work consisted of
an optimization of the carrier gas bow rate and the heating cycle of t
he modified graphite furnace lashing and vaporization temperatures). A
systematic study of the signal profiles (signal intensity as a functi
on of time) showed that As coming from the solid samples and As coming
from Liquid standards added to the solid material, only showed an ana
logous behaviour on condition that these liquid spikes were previously
dried before the solid sample was introduced into the sample boat. Th
e potential of the technique was assessed by establishing figures of m
erit and analysing some standard reference materials for As, An absolu
te limit of detection of approximately 1 pg was established for As, co
rresponding to a relative limit of detection of approximately 1 ng g(-
1) for a typical sample mass of 1 mg. Results obtained for the As cont
ent in the samples analysed were not deteriorated by the presence of C
l, as even on addition of amounts of Cl exceeding the Cl content of th
e samples no (ArCl+)-Ar-40-Cl-35 interference on the As-75(+) signal c
ould be established. For the determination of As in these reference ma
terials of plant origin, several methods of calibration were investiga
ted, including external calibration using both liquid and solid standa
rds and single standard addition. The use of an internal standard (Sb)
was studied and its requirement was assessed as being from advisable
to imperative, depending on the calibration method used. Although seve
ral methods offered possibilities for accurate determination (mean dev
iation between ETV-ICP-MS results and certified values < 10%), single
standard addition was assessed to be the most practicable and straight
forward method.