A. Seubert et R. Meinke, ONLINE COUPLED ION CHROMATOGRAPHY-ICP-(AES, MS) AND ELECTROTHERMAL VAPORIZATION-ICP-MS IN USE FOR ULTRA-TRACE ANALYSIS OF HIGH-PURITY RHENIUM, Fresenius' journal of analytical chemistry, 348(8-9), 1994, pp. 510-519
This work presents the benefits of coupling techniques such as Electro
Thermal Vaporisation (ETV)-ICP-MS and Ion Chromatography (IC)-ICP-(AE
S, MS) for ultra trace analysis in a high purity rhenium powder sample
. Direct analysis using ICP-AES suffers from poor detection limits and
allows trace analysis only above 1 mug/g for most analytes. ICP-MS an
alysis of trace elements is more sensitive, but signal depression caus
ed by the heavy Re-ions limits trace analysis to concentrations of 50
- 100 ng/g analyte in the solid sample. Coupling Ion Chromatography wi
th ICP-spectrometers, combined with time resolved measurement (IC-ICP-
TRM) of the elution signals, was used to enhance the sensitivity of bo
th ICP-AES and ICP-MS. Resulting detection limits are in the very low
ng/g to pg/g range. Coupling of ETV and ICP-MS offers the possibility
of eliminating the volatile Re2O7 matrix by thermal pretreatment and a
llows ICP-MS measurements without matrix interferences caused by Re. R
esults from these methods are compared with Glow Discharge Mass Spectr
ometry (GDMS) analysis, a semiquantitative solid state technique. The
results are also compared with the manufacturers' specifications to sh
ow the power of modern routine analysis using ICP-AES or FAAS.