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Aqueous and solid-phase speciation of arsenic in Cornish soils

Published online by Cambridge University Press:  05 July 2018

C. Hutton*
Affiliation:
Camborne School of Mines, School of Geography Archaeology and Earth Resources, University of Exeter, Tremough Campus, Penryn, Cornwall TR10 9EZ, UK
D. W. Bryce
Affiliation:
PS Analytical, Arthur House, Crayfields Industrial Estate, Main Road, Orpington, Kent BR5 3HP, UK
W. Russeau
Affiliation:
University of Greenwich, Medway Sciences, Central Avenue, Chatham Maritime, Kent ME4 4TB, UK
H. J. Glass
Affiliation:
Camborne School of Mines, School of Geography Archaeology and Earth Resources, University of Exeter, Tremough Campus, Penryn, Cornwall TR10 9EZ, UK
L. E. T. Jenkin
Affiliation:
Camborne School of Mines, School of Geography Archaeology and Earth Resources, University of Exeter, Tremough Campus, Penryn, Cornwall TR10 9EZ, UK
W. T. Corns
Affiliation:
PS Analytical, Arthur House, Crayfields Industrial Estate, Main Road, Orpington, Kent BR5 3HP, UK
P. B. Stockwell
Affiliation:
PS Analytical, Arthur House, Crayfields Industrial Estate, Main Road, Orpington, Kent BR5 3HP, UK
*

Abstract

Cornwall (UK) has suffered extensive arsenic contamination due to the historic mining and processing of mineral ores. Standard procedures for contaminated land risk assessment (DEFRA and Environment Agency, 2002a) are probably unworkable in Cornwall, with a very large number of sites classified as contaminated by arsenic. Methods of measuring the speciation and mobility of arsenic are essential for effective and rapid risk assessments of arsenic contamination.

Three clusters of lysimeters were installed in three different areas of an arsenic-contaminated Cornish site. A novel phosphoric acid microwave extraction technique was applied to the soils removed from the lysimeter holes; HPLC-HG-AFS analysis showed the majority of solid-phase arsenic to be arsenate (AsV). Pore waters obtained from the lysimeters showed variable, relatively low levels of arsenite (AsIII) and arsenate (AsV) to be present (<1–129 μg l–1). Less toxic arsenate predominated in most pore waters, with the presence of minor amounts of arsenite suggesting heterogeneous redox conditions. Pore-water arsenic concentrations were strongly positively related to solid-phase arsenate concentrations.

The use of techniques that assess the speciation of arsenic both in the solid and aqueous phases of a soil provides important information about the mobility of arsenic. The methodology presented in this paper may offer a novel basis for risk assessments of other contaminated sites.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2005

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