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Determination of toxic trace impurities in titanium dioxide by solid sampling-electrothermal vaporization-inductively coupled plasma mass spectrometry

Maria Aramendia UGent, Martin Resano and Frank Vanhaecke UGent (2009) JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY. 24(1). p.41-50
abstract
This paper reports on the performance of solid sampling-electrothermal vaporization-inductively coupled plasma mass spectrometry (SS-ETV-ICPMS) for the direct multi-element determination of six toxic trace impurities (As, Cd, Hg, Pb, Sb and Zn) in three different TiO2 samples. Careful selection of the most suitable target nuclides for the different analytes and temperature program optimization permit the reliable monitoring of the analytes of interest, while avoiding the occurrence of potentially relevant spectral interferences. A pyrolysis-free program, in which simultaneous vaporization of all the analytes is carried out at a relatively low temperature (1700 degrees C), was used. In this way, sample matrix and analyte co-vaporization is avoided, considerably reducing matrix effects and allowing the determination of Zn, which would otherwise be hampered by a spectral overlap with TiO+ ions. Calibration against aqueous standards was found to be feasible. Addition of 50 ng Pd as carrier agent improved the linearity of the calibration curves. Two different internal standards (Pd-105(+) and Te-125(+)) were used to compensate for matrix effects. The method thus developed exhibits interesting features: low limits of detection (ng g(-1) range) for all of the elements, at least an order of magnitude lower than those for digestion-based procedures; high sample throughput (maximum 35 min per determination), contrasting with the 2 h required for sample digestion and subsequent analysis; low sample consumption (a few milligrams only); precision values usually in the 9-13% RSD range; and last but not least, the absence of any sample pre-treatment, with the subsequent lower risk of analyte losses, contamination or personal and instrumental harms derived from the necessity of using hazardous reagents for sample digestion. SS-ETV-ICPMS therefore seems to be a promising alternative for industrial control analysis of TiO2 samples with analyte contents ranging from a few ng g(-1) to several hundreds of mu g g(-1).
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
NEUTRON-ACTIVATION ANALYSIS, ATOMIC-ABSORPTION-SPECTROMETRY, GRAPHITE-FURNACE, ICP-MS, ISOTOPE-DILUTION, MULTIELEMENT CHARACTERIZATION, OPTICAL-EMISSION SPECTROMETRY, CALIBRATION, INTERFERENCES, SEPARATION
journal title
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY
J. Anal. At. Spectrom.
volume
24
issue
1
pages
41 - 50
Web of Science type
Article
Web of Science id
000263264100004
JCR category
SPECTROSCOPY
JCR impact factor
3.435 (2009)
JCR rank
3/39 (2009)
JCR quartile
1 (2009)
ISSN
0267-9477
DOI
10.1039/b808951e
language
English
UGent publication?
yes
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
512849
handle
http://hdl.handle.net/1854/LU-512849
date created
2009-03-03 08:37:18
date last changed
2012-11-22 12:21:32
@article{512849,
  abstract     = {This paper reports on the performance of solid sampling-electrothermal vaporization-inductively coupled plasma mass spectrometry (SS-ETV-ICPMS) for the direct multi-element determination of six toxic trace impurities (As, Cd, Hg, Pb, Sb and Zn) in three different TiO2 samples. Careful selection of the most suitable target nuclides for the different analytes and temperature program optimization permit the reliable monitoring of the analytes of interest, while avoiding the occurrence of potentially relevant spectral interferences. A pyrolysis-free program, in which simultaneous vaporization of all the analytes is carried out at a relatively low temperature (1700 degrees C), was used. In this way, sample matrix and analyte co-vaporization is avoided, considerably reducing matrix effects and allowing the determination of Zn, which would otherwise be hampered by a spectral overlap with TiO+ ions. Calibration against aqueous standards was found to be feasible. Addition of 50 ng Pd as carrier agent improved the linearity of the calibration curves. Two different internal standards (Pd-105(+) and Te-125(+)) were used to compensate for matrix effects. The method thus developed exhibits interesting features: low limits of detection (ng g(-1) range) for all of the elements, at least an order of magnitude lower than those for digestion-based procedures; high sample throughput (maximum 35 min per determination), contrasting with the 2 h required for sample digestion and subsequent analysis; low sample consumption (a few milligrams only); precision values usually in the 9-13\% RSD range; and last but not least, the absence of any sample pre-treatment, with the subsequent lower risk of analyte losses, contamination or personal and instrumental harms derived from the necessity of using hazardous reagents for sample digestion. SS-ETV-ICPMS therefore seems to be a promising alternative for industrial control analysis of TiO2 samples with analyte contents ranging from a few ng g(-1) to several hundreds of mu g g(-1).},
  author       = {Aramendia, Maria and Resano, Martin and Vanhaecke, Frank},
  issn         = {0267-9477},
  journal      = {JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY},
  keyword      = {NEUTRON-ACTIVATION ANALYSIS,ATOMIC-ABSORPTION-SPECTROMETRY,GRAPHITE-FURNACE,ICP-MS,ISOTOPE-DILUTION,MULTIELEMENT CHARACTERIZATION,OPTICAL-EMISSION SPECTROMETRY,CALIBRATION,INTERFERENCES,SEPARATION},
  language     = {eng},
  number       = {1},
  pages        = {41--50},
  title        = {Determination of toxic trace impurities in titanium dioxide by solid sampling-electrothermal vaporization-inductively coupled plasma mass spectrometry},
  url          = {http://dx.doi.org/10.1039/b808951e},
  volume       = {24},
  year         = {2009},
}

Chicago
Aramendia, Maria, Martin Resano, and Frank Vanhaecke. 2009. “Determination of Toxic Trace Impurities in Titanium Dioxide by Solid Sampling-electrothermal Vaporization-inductively Coupled Plasma Mass Spectrometry.” Journal of Analytical Atomic Spectrometry 24 (1): 41–50.
APA
Aramendia, M., Resano, M., & Vanhaecke, F. (2009). Determination of toxic trace impurities in titanium dioxide by solid sampling-electrothermal vaporization-inductively coupled plasma mass spectrometry. JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 24(1), 41–50.
Vancouver
1.
Aramendia M, Resano M, Vanhaecke F. Determination of toxic trace impurities in titanium dioxide by solid sampling-electrothermal vaporization-inductively coupled plasma mass spectrometry. JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY. 2009;24(1):41–50.
MLA
Aramendia, Maria, Martin Resano, and Frank Vanhaecke. “Determination of Toxic Trace Impurities in Titanium Dioxide by Solid Sampling-electrothermal Vaporization-inductively Coupled Plasma Mass Spectrometry.” JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY 24.1 (2009): 41–50. Print.