scispace - formally typeset
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.

read more

Citations
More filters
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
More filters
Journal ArticleDOI

The adsorption of molybdenum on oxide surfaces

RM McKenzie
- 01 Jan 1983 - 
TL;DR: In this paper, the Bowden adsorption model was used to measure the adaption of molybdenum on 12 oxides with zero points of charge (ZPC) ranging from pH 2 to 7.6.
Journal ArticleDOI

Arsenate-73 uptake by components of several acidic soils and Its Implications for phosphate retention

AW Fordham, +1 more
- 01 Jan 1979 - 
TL;DR: The arsenate and phosphate sorbing properties of the various components in the clay fractions of several acidic soils were assessed by autoradiography using radioactive arsenate-73 as discussed by the authors, which was recognized by localization of silver grains upon soil particles dispersed on electron microscope grids.
Journal ArticleDOI

The nature of soil particles particularly those reacting with arsenate in a series of chemically treated samples

AW Fordham, +1 more
- 01 Jan 1983 - 
TL;DR: In this article, it was shown that arsenate uptake by a surface sample of a lateritic podzol was controlled mainly by iron oxide particles in a very finely divided state of about 50 A in diameter, which had semi-regular appearance; had limited solubility in ammonium oxalate (in darkness) and in sodium pyrophosphate; and sometimes gave ring-type electron diffraction patterns identifiable as goethite.
Journal ArticleDOI

Interactions of humic substances with allophanic compounds

TL;DR: In this paper, organic matter from two Chilean Andisols, Vilcun and Osorno soils, were extracted and fractionated into humic (HA) and fulvic acids (FA).
Journal ArticleDOI

Displacement of adsorbed anions from soil. 2. Displacement of phosphate by arsenate

N. J. Barrow
- 01 Jan 1974 - 
TL;DR: In this article, the ability of solutions of arsenate to displace previously adsorbed phosphate from soil was investigated, and it was argued that conversion does not involve diffusion of phosphate from one site to another through the solution phase.
Related Papers (5)