Multielement analysis of polyethylene using solid sampling electrothermal vaporization ICP mass spectrometry

Citation
F. Vanhaecke et al., Multielement analysis of polyethylene using solid sampling electrothermal vaporization ICP mass spectrometry, ANALYT CHEM, 72(18), 2000, pp. 4310-4316
Citations number
37
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
ANALYTICAL CHEMISTRY
ISSN journal
00032700 → ACNP
Volume
72
Issue
18
Year of publication
2000
Pages
4310 - 4316
Database
ISI
SICI code
0003-2700(20000915)72:18<4310:MAOPUS>2.0.ZU;2-Z
Abstract
Next to laser ablation (LA) also electrothermal vaporization (ETV) from a g raphite furnace as a means of sample introduction opens possibilities for d irect analysis of solid samples using inductively coupled plasma mass spect rometry (ICPMS). In this paper, it is demonstrated that solid sampling ETV- ICPMS is very web suited for the determination of metal traces in polyethyl ene. A limited multielement capability is often cited as an important drawb ack of ETV-ICPMS. However, by studying the effect of monitoring an increasi ng number of mass-to-charge ratios on the signal profile (integrated signal intensity and repeatability) of selected analyte elements, the multielemen t capability of (solid sampling) ETV-ICPMS was systematically evaluated, an d the results obtained suggest that,with a quadrupole-based ICPMS instrumen t, at least 11 elements can be determined "simultaneously" (from the same v aporization step), in essence without compromising the sensitivity or the p recision of the results obtained. In this work, the "simultaneous" determin ation of Al, Ba, Cd, Cu, Mn, Pb, and Ti in a polyethylene candidate referen ce material. has been accomplished, despite the large variation in analyte concentration (from 5 ng/g for Mn to 500 mu g/g for Ti) and in furnace beha vior (volatility) they exhibit. To avoid premature losses of Cd during ther mal pretreatment of the samples, Pd was used as a chemical modifier. Two di fferent calibration methods external calibration using an aqueous standard solution and single standard additon-were studied and the results obtained were compared with those obtained using neutron activation analysis (NAA) a nd/or with the corresponding (candidate) certified values (if available). S ingle standard addition was shown to be preferable (average deviation betwe en ICPMS result and reference value < 3%), although-except for Ba-acceptabl e results could also be obtained with external calibration.