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Journal ArticleDOI

Competitive Sorption of Arsenate and Phosphate on Different Clay Minerals and Soils

Antonio Violante, +1 more
- 01 Nov 2002 - 
- Vol. 66, Iss: 6, pp 1788-1796
TLDR
In this article, the competitive sorption of PO 4 and AsO 4 on selected phyllosilicates, metal oxides, synthetic organo-mineral complexes, and soil samples as affected by pH (4.0-8.0), ligands concentration, surface coverage of the oxyanions on the samples and the residence time.
Abstract
Sorption and desorption of AsO 4 on or from different soil components may have a dominant role in regulating As mobility in soils. The objectives of this work were to provide information on the factors that influence the competitive sorption of AsO 4 and PO 4 in soil. We studied the competitive sorption of PO 4 and AsO 4 on selected phyllosilicates, metal oxides, synthetic organo-mineral complexes, and soil samples as affected by pH (4.0-8.0), ligands concentration, surface coverage of the oxyanions on the samples and the residence time. We found that Mn, Fe, and Ti oxides and phyllosilicates particularly rich in Fe (nontronite, ferruginous smectites) were more effective in sorbing AsO 4 than PO 4 . In fact, by adding AsO 4 and PO 4 as a mixture (AsO 4 /PO 4 molar ratio of 1) more AsO 4 , than PO 4 was usually sorbed on birnessite, pyrolusite, goethite, nontronite, and ferruginous smectite, but more PO 4 than AsO 4 was sorbed on noncrystalline Al precipitation products, gibbsite, boehmite, allophane, and kaolinite. For example, at pH 5.0 the sorbed AsO 4 /sorbed PO 4 molar ratio (rf) was 1.81 for bimessite, 1.05 for nontronite, but was only 0.45 for kaolinite and 0.14 for allophane. For montmorillonite, illite, and vermiculite the rf values were slightly <1. For soil samples, particularly rich in kaolinite, halloysite, allophane, and containing relatively large amounts of organic C, the rf values were usually much <1. For all the samples, the rf values increased by decreasing the pH and with the residence time of the oxyanions. The sorption of AsO 4 (or PO 4 ) on goethite and gibbsite decreased by increasing the initial PO 4 /AsO 4 (or ASO 4 / PO 4 molar ratio) up to 2.0. However, PO 4 inhibited AsO 4 sorption more on gibbsite than on goethite, whereas AsO 4 prevented PO 4 sorption more on goethite than on gibbsite. The data reported in this paper suggest that the mobility, the bioavailability, and the toxicity of As in soil environments may be greatly affected by the nature of soil components, pH, presence of anions (PO 4 ), and residence time.

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Book ChapterDOI

Biogeochemical processes controlling the fate and transport of arsenic: implications for South and Southeast Asia.

TL;DR: Arsenic is a ubiquitous toxin present in soils and waters resulting from both natural and anthropogenic sources as discussed by the authors, and the key biogeochemical step leading to human exposure of arsenic via drinking water is a result of arsenic release from soil/sediment solids into pore water.
Journal ArticleDOI

Adsorption of arsenate on soils. Part 1: laboratory batch experiments using 16 Chinese soils with different physiochemical properties.

TL;DR: The Jiangxi and Hubei soils were more effective sorbents for arsenate than other soils, and the Langmuir two-surface equation generally provided a better fit to the arsenate adsorption data.
Journal ArticleDOI

Effect of Competing Anions on Arsenate Adsorption onto Maghemite Nanoparticles

TL;DR: In this paper, the effect of several competing anions on arsenate adsorption with maghemite nanoparticles was investigated and the combined effect of ions and other water characteristics were examined with a natural groundwater sample which was spiked with a certain amount of arsenate.
Journal ArticleDOI

Potential bioavailability of lead, arsenic, and polycyclic aromatic hydrocarbons in compost-amended urban soils.

TL;DR: Assessment of the effectiveness of adding different compost types to reduce both direct and indirect exposure of Pb, As, and PAHs to humans found them to be low or nondetectable in vegetables grown at this site.
Journal ArticleDOI

Effect of ionic strength on adsorption of As(III) and As(V) on variable charge soils

TL;DR: Results indicated that the amount of As(III) adsorbed by these two soils increased with increasing solution pH, whereas it decreased with increasing ionic strength under the acidic condition, which supported the hypothesis of the adsorption model that the potential in the Adsorption plane changes with ionicstrength with an opposite trend to surface charge of the soils.
References
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Journal ArticleDOI

Arsenite and Arsenate Adsorption on Ferrihydrite: Kinetics, Equilibrium, and Adsorption Envelopes

TL;DR: In this paper, the authors compared the adsorption behavior of arsenite and arsenate on ferrihydrite, under carefully controlled conditions, with regard to adaption kinetics and the influence of pH.
Journal ArticleDOI

Surface chemistry of ferrihydrite: Part 1. EXAFS studies of the geometry of coprecipitated and adsorbed arsenate

TL;DR: In this article, the As and Fe K-edges were collected from samples of two-line ferrihydrite with adsorbed (ADS) and coprecipitated (CPT) arsenate prepared over a range of conditions and arsenate surface coverages.
Journal ArticleDOI

Arsenic contamination of groundwater and drinking water in Vietnam: a human health threat.

TL;DR: The high arsenic concentrations found in the tubewells indicate that several million people consuming untreated groundwater might be at a considerable risk of chronic arsenic poisoning.
Journal ArticleDOI

Arsenate and Chromate Retention Mechanisms on Goethite. 1. Surface Structure

TL;DR: In this paper, the authors used Extended X-ray absorption fine structure (EXAFS) spectroscopy to deduce the local coordination environment of two environmental contaminants, arsenate and chromate, on the mineral goethite (α-FeOOH).
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