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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

Heavy metals in soils : trace metals and metalloids in soils and their bioavailability

B. J. Alloway
TL;DR: In this article, the authors defined the sources of heavy metals and metalloids in Soils and derived methods for the determination of Heavy Metals and Metalloids in soil.
Journal ArticleDOI

Mobility and bioavailability of heavy metals and metalloids in soil environments

TL;DR: In this paper, the impact of physical, chemical, and biological interfacial interactions on bioavailability and mobility of metals and metalloids in soil is highlighted, focusing on the sorption/desorption processes of metals on/from soil components and soils.
Book ChapterDOI

The geochemistry of acid mine drainage

TL;DR: In this article, the authors developed and applied molecular tools to determine the activity and role of microorganisms in sulfide-mineral-bearing systems and developed tools for assessing the toxicity of mine-waste effluent.
Journal ArticleDOI

Arsenic and chromium removal by mixed magnetite-maghemite nanoparticles and the effect of phosphate on removal.

TL;DR: Magnetite-maghemite nanoparticles can readily adsorb arsenic and chromium in an acidic pH range, and it is anticipated that an optimum design with magnetite- maghemites nanoparticles may achieve high arsenic uptake in field applications.
Journal ArticleDOI

Effect of magnetite particle size on adsorption and desorption of arsenite and arsenate

TL;DR: In this paper, the effect of magnetite particle size on the adsorption and desorption behavior of arsenite and arsenate was evaluated, and a substantial decrease in arsenic sorption to magnetite nanoparticles was observed.
References
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Journal ArticleDOI

Modeling arsenate competitive adsorption on kaolinite, montmorillonite and illite

TL;DR: The adsorption of arsenate (As(V)) on kaolinite, montmorillonite and illite was investigated at varying pH and competing anion concentration while holding As(V) concentration (6.7 X lo-' M), clay suspension density (2.5 g L-') and ionic strength (0.1 M NaCl) constant as mentioned in this paper.
Journal ArticleDOI

Residence time effects on arsenate adsorption/desorption mechanisms on goethite

TL;DR: In this paper, the effects of aging or residence time on the kinetics of arsenate sorption and desorption on goethite, and to combine spectroscopic x-ray absorption fine structure (XAFS) and macroscopic studies in order to determine arsenate's behavior over time at pH 4 and 6.

Adsorption of arsenate by soils and its relation to selected chemical properties and anions.

N. T. Livesey, +1 more
TL;DR: In this paper, the retention of arsenate by four soils of Saskatchewan, Canada, and its relation to selected soil properties and anionic environments were studied, and the data indicate that As retention by the soils at the dilute, As concentration range studied does not proceed through the precipitation of sparingly soluble arsenate compounds.
Journal ArticleDOI

Arsenic(iii) and Arsenic(v) Adsorption on Three California Soils

Bruce A. Manning, +1 more
- 01 Dec 1997 - 
TL;DR: Inorganic arsenite (As(III)) and arsenate (As (V)) are toxic pollutants that are transported in surface and ground waters and can adsorb on soil and sediment mineral surfaces as mentioned in this paper.
Journal ArticleDOI

Adsorption of arsenate by soils and its relation to selected chemical properties and anions

N. T. Livesey, +1 more
- 01 Feb 1981 - 
TL;DR: In this paper, the retention of arsenate by four soils of Saskatchewan, Canada, and its relation to selected soil properties and anionic environments were studied, and the data indicate that As retention by the soils at the dilute, As concentration range studied does not proceed through the precipitation of sparingly soluble arsenate compounds.
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