Comparison of two non-specific flow-through sequential extraction approaches to identify the physico-chemical partitioning of potentially harmful elements in a certified reference material

Balarabe S. Sagagi, Christine M. Davidson*, Mark R. Cave, Joanne Wragg

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Two non-specific sequential extraction methods utilising chemometric data processing (chemometric identification of substrates and element distribution, CISED) have been developed and used to determine the physico-chemical partitioning of potentially harmful elements (PHE) in certified reference material BCR CRM 701 (lake sediment). A miniaturized centrifugation method in which the sample was extracted on a filter insert in a polypropylene centrifuging tube, and a quasi-flow through method in which the sample was supported on a TX40
filter in a 47 mm in-line polycarbonate filter holder, gave similar results. The CISED data processing identified nine components. Seven of these were of geochemical origin – two carbonate components, an Al/Fe oxide/hy
droxide component, three Fe-dominated components and one Si-dominated component – while the others represented the TX40 filter blank. The overall extraction capabilities of the methods were similar to that of the well-established BCR sequential extraction (Σsteps 1–3). However, whilst the BCR extraction is operationally defined, the CISED provides information on associations between PHE and the geochemical components identified. The flow through CISED procedure has potential applications in investigating the chemical speciation of PHE associated with urban airborne particular matter.
Original languageEnglish
Article number121685
Number of pages10
JournalTalanta
Volume223
Issue numberPt. 1
Early online date5 Oct 2020
DOIs
Publication statusPublished - 1 Feb 2021

Keywords

  • sequential extraction
  • CISED
  • chemometrics
  • BCR CRM 701
  • airborne particulate matter
  • inductively coupled plasma mass spectrometry

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