Ändra sökning
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
Calibration errors due to variations in peak characteristics in the measurement of transient signals by inductively coupled plasma-scanning mass spectrometry
Department of Chemistry, Analytical Chemistry, Umeå University.
Department of Chemistry, Analytical Chemistry, Umeå University.
2002 (Engelska)Ingår i: Journal of Analytical Atomic Spectrometry, ISSN 0267-9477, E-ISSN 1364-5544, Vol. 17, nr 12, s. 1582-1588Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The impact of variations in peak characteristics on the fidelity of transient signal measurement by inductively coupled plasma-quadrupole mass spectrometry (ICP-QMS) was investigated. Specifically, the question as to whether the multi-element capabilities or the accuracy in determined analyte amounts were deteriorated compared to what has been reported previously when not considering peak variations was addressed. The peak characteristics considered were the time of the signal maximum (tpeak), the standard deviation of the assumed Gaussian input function generated by the sample introduction system (σG), and the time constant for signal decay (τ). Investigations of simulated exponentially-modified Gaussian peaks revealed that, for variations of peak characteristics within reasonable ranges, measurement noise and variations in tpeak, σG and τ all contributed to calibration uncertainty. Electrothermal vaporisation (ETV) and flow injection (FI) systems were used to experimentally generate transient signals of varying peak characteristics. Removing data points from the raw signals simulated the monitoring of up to 100 mass-to-charge ratios, allowing calibration data and analyte amounts to be determined from the processed signals. To obtain calibration graph slopes with relative standard deviations below 1% for the ETV-ICP-QMS system, it was found necessary to acquire 7-24 data points per peak for 50-5 ms dwell times. On this basis, the maximum number of mass-to-charge ratios that could be monitored in a typical ETV-ICP-QMS analysis was 4-10 using dwell times of 50-5 ms. With the FI-ICP-QMS system, variations in the peak characteristics between calibration standards and samples meant that, to obtain less than 3% error in determined analyte amounts, at least 7 or 10 points per peak were required for external and internal standardisation, respectively. It was found that variations in peak characteristics contributed more than measurement noise to the error in determined analyte amounts. In recent studies it has been reported that 3-4 data points per peak are sufficient to accurately monitor a transient if peak variations are not considered, which, for typical ETV signals, would allow the monitoring of 20 mass-to-charge ratios during a single measurement cycle. Thus the results obtained here show that the multi-element capability of ICP-QMS when monitoring transient signals can be severely compromised by such variations

Ort, förlag, år, upplaga, sidor
2002. Vol. 17, nr 12, s. 1582-1588
Nyckelord [en]
Natural sciences - Chemistry
Nyckelord [sv]
Naturvetenskap - Kemi
Nationell ämneskategori
Fysikalisk kemi
Forskningsämne
Gränsytors kemi
Identifikatorer
URN: urn:nbn:se:ltu:diva-7282DOI: 10.1039/B208868AISI: 000179556500003Scopus ID: 2-s2.0-0036910566Lokalt ID: 59f69c10-b4c3-11de-b769-000ea68e967bOAI: oai:DiVA.org:ltu-7282DiVA, id: diva2:980171
Anmärkning
Validerad; 2002; 20091009 (andbra)Tillgänglig från: 2016-09-29 Skapad: 2016-09-29 Senast uppdaterad: 2018-07-10Bibliografiskt granskad

Open Access i DiVA

Fulltext saknas i DiVA

Övriga länkar

Förlagets fulltextScopus

Personposter BETA

Baxter, Douglas

Sök vidare i DiVA

Av författaren/redaktören
Baxter, Douglas
I samma tidskrift
Journal of Analytical Atomic Spectrometry
Fysikalisk kemi

Sök vidare utanför DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetricpoäng

doi
urn-nbn
Totalt: 99 träffar
RefereraExporteraLänk till posten
Permanent länk

Direktlänk
Referera
Referensformat
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annat format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annat språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf