Using isotopic dilution to assess chemical extraction of labile Ni, Cu, Zn, Cd and Pb in soils. (July 2016)
- Record Type:
- Journal Article
- Title:
- Using isotopic dilution to assess chemical extraction of labile Ni, Cu, Zn, Cd and Pb in soils. (July 2016)
- Main Title:
- Using isotopic dilution to assess chemical extraction of labile Ni, Cu, Zn, Cd and Pb in soils
- Authors:
- Garforth, J.M.
Bailey, E.H.
Tye, A.M.
Young, S.D.
Lofts, S. - Abstract:
- Abstract: Chemical extractants used to measure labile soil metal must ideally select for and solubilise the labile fraction, with minimal solubilisation of non-labile metal. We assessed four extractants (0.43 M HNO3, 0.43 M CH3 COOH, 0.05 M Na2 H2 EDTA and 1 M CaCl2 ) against these requirements. For soils contaminated by contrasting sources, we compared isotopically exchangeable Ni, Cu, Zn, Cd and Pb (EValue, mg kg −1 ), with the concentrations of metal solubilised by the chemical extractants (MExt, mg kg −1 ). Crucially, we also determined isotopically exchangeable metal in the soil–extractant systems (EExt, mg kg −1 ). Thus 'EExt – EValue ' quantifies the concentration of mobilised non-labile metal, while 'EExt – MExt ' represents adsorbed labile metal in the presence of the extractant. Extraction with CaCl2 consistently underestimated EValue for Ni, Cu, Zn and Pb, while providing a reasonable estimate of EValue for Cd. In contrast, extraction with HNO3 both consistently mobilised non-labile metal and overestimated the EValue . Extraction with CH3 COOH appeared to provide a good estimate of EValue for Cd; however, this was the net outcome of incomplete solubilisation of labile metal, and concurrent mobilisation of non-labile metal by the extractant (MExt < EExt > EValue ). The Na2 H2 EDTA extractant mobilised some non-labile metal in three of the four soils, but consistently solubilised the entire labile fraction for all soil-metal combinations (MExt ≈ EExt ).Abstract: Chemical extractants used to measure labile soil metal must ideally select for and solubilise the labile fraction, with minimal solubilisation of non-labile metal. We assessed four extractants (0.43 M HNO3, 0.43 M CH3 COOH, 0.05 M Na2 H2 EDTA and 1 M CaCl2 ) against these requirements. For soils contaminated by contrasting sources, we compared isotopically exchangeable Ni, Cu, Zn, Cd and Pb (EValue, mg kg −1 ), with the concentrations of metal solubilised by the chemical extractants (MExt, mg kg −1 ). Crucially, we also determined isotopically exchangeable metal in the soil–extractant systems (EExt, mg kg −1 ). Thus 'EExt – EValue ' quantifies the concentration of mobilised non-labile metal, while 'EExt – MExt ' represents adsorbed labile metal in the presence of the extractant. Extraction with CaCl2 consistently underestimated EValue for Ni, Cu, Zn and Pb, while providing a reasonable estimate of EValue for Cd. In contrast, extraction with HNO3 both consistently mobilised non-labile metal and overestimated the EValue . Extraction with CH3 COOH appeared to provide a good estimate of EValue for Cd; however, this was the net outcome of incomplete solubilisation of labile metal, and concurrent mobilisation of non-labile metal by the extractant (MExt < EExt > EValue ). The Na2 H2 EDTA extractant mobilised some non-labile metal in three of the four soils, but consistently solubilised the entire labile fraction for all soil-metal combinations (MExt ≈ EExt ). Comparison of EValue, MExt and EExt provides a rigorous means of assessing the underlying action of soil chemical extraction methods and could be used to refine long-standing soil extraction methodologies. Highlights: Stable isotope dilution can inform underlying mechanisms during chemical extraction. Agreement between extracted metal and E values is sometimes fortuitous. Powerful extractants (0.05 M EDTA and 0.43 M Nitric acid) solubilise non-labile metal. Weaker extractants (0.43 M CH3 COOH and 1 M CaCl2 ) fail to solubilise all labile metal. E values measured within on the soil extraction reveal non-labile metal mobilisation. … (more)
- Is Part Of:
- Chemosphere. Volume 155(2016)
- Journal:
- Chemosphere
- Issue:
- Volume 155(2016)
- Issue Display:
- Volume 155, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 155
- Issue:
- 2016
- Issue Sort Value:
- 2016-0155-2016-0000
- Page Start:
- 534
- Page End:
- 541
- Publication Date:
- 2016-07
- Subjects:
- Soil chemical extraction -- Stable isotope dilution
Pollution -- Periodicals
Pollution -- Physiological effect -- Periodicals
Environmental sciences -- Periodicals
Atmospheric chemistry -- Periodicals
551.511 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00456535/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.chemosphere.2016.04.096 ↗
- Languages:
- English
- ISSNs:
- 0045-6535
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.280000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 7892.xml