Arsenic Speciation: Reduction of Arsenic(V) to Arsenic(III) by Fulvic Acid

2006 ◽  
Vol 3 (2) ◽  
pp. 137 ◽  
Author(s):  
Tsanangurayi Tongesayi ◽  
Ronald B. Smart

Environmental Context.Most technologies for arsenic removal from water are based on the oxidation of the more toxic and more mobile arsenic(iii) to the less toxic and less mobile arsenic(v). As a result, research effort has been focussed on the oxidation of arsenic(iii) to arsenic(v). It is equally important to explore environmental factors that enhance the reduction of arsenic(v) to arsenic(iii). An understanding of the redox cycling of arsenic could result in the development of cheaper and more efficient arsenic removal technologies, especially for impoverished communities severely threatened by arsenic contamination. Abstract.The objective of this study was to investigate the reduction of inorganic arsenic(v) with Suwannee River fulvic acid (FA) in aqueous solutions where pH, [FA], [As(v)], [As(iii)], and [Fe(iii)] were independently varied. Samples of inorganic As(v) were incubated with FA in both light and dark at constant temperature. Sterilisation techniques were employed to ensure abiotic conditions. Aliquots from the incubated samples were taken at various time intervals and analysed for As(iii) using square-wave cathodic-stripping voltammetry at a hanging mercury drop electrode. The study demonstrated the following important aspects of As speciation: (1) FA can significantly reduce As(v) to As(iii); (2) reduction of As(v) to As(iii) is a function of time; (3) both dark and light conditions promote reduction of As(v) to As(iii); (4) Fe(iii) speeds up the reduction reaction; and (5) oxidation of As(iii) to As(v) is promoted at pH 2 more than at pH 6.

2008 ◽  
Vol 20 (7) ◽  
pp. 776-781 ◽  
Author(s):  
Leandro M. de Carvalho ◽  
Paulo C. do Nascimento ◽  
Denise Bohrer ◽  
Raquel Stefanello ◽  
Eduardo J. Pilau ◽  
...  

2010 ◽  
Vol 7 (4) ◽  
pp. 386 ◽  
Author(s):  
L. Haffert ◽  
S. G. Sander ◽  
K. A. Hunter ◽  
D. Craw

Environmental context.The speciation of the toxic element arsenic directly controls its environmental mobility and toxicity. The current study took place on site in an historic mine processing environment that is extremely arsenic-rich and comparatively sulfur-deficient. When arsenic is one of the major chemical components, redox state and pH of the chemical system are closely linked to arsenic speciation. Abstract.This study investigates the chemistry of the AsIII–AsV redox couple in association with As-rich processing residues (up to 40 wt%) from a historic gold mine in New Zealand. The site provides a unique natural laboratory of a sulfide-free chemical system driven by arsenolite dissolution. Field based cathodic stripping voltammetry, which circumvents post-sampling preservation issues, was successfully applied to analyse the AsIII to the microgram level. The AsIII–AsV redox couple, in particular the oxidation of AsIII, was found to have a noticeable influence on system pH and EH. The As redox pair itself is controlled by a range of processes, which were identified for the varying aqueous environments present on the studied site.


2010 ◽  
Vol 662 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Kristoff Gibbon-Walsh ◽  
Pascal Salaün ◽  
Constant M.G. van den Berg

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