Surface Structures and Stability of Arsenic(III) on Goethite:  Spectroscopic Evidence for Inner-Sphere Complexes

The adsorption and stability of arsenite [As(III)] on goethite (α-FeOOH) was investigated using a combination of standard batch techniques and X-ray absorption spectroscopy (XAS). The reactivity of As(III) with α-FeOOH at varying pH and As(III) concentration provided macroscopic evidence for strong...

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Veröffentlicht in:Environmental Science and Technology 1998-08, Vol.32 (16), p.2383-2388
Hauptverfasser: Manning, Bruce A, Fendorf, Scott E, Goldberg, Sabine
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Fendorf, Scott E
Goldberg, Sabine
description The adsorption and stability of arsenite [As(III)] on goethite (α-FeOOH) was investigated using a combination of standard batch techniques and X-ray absorption spectroscopy (XAS). The reactivity of As(III) with α-FeOOH at varying pH and As(III) concentration provided macroscopic evidence for strong complexation on the α-FeOOH surface. Extended X-ray absorption fine structure (EXAFS) spectroscopy gave an average As(III)−Fe interatomic distance of 3.378 ± 0.014 Å, which is indicative of bidentate binuclear bridging As(III) complexes on the α-FeOOH surface and which is similar to other oxyanions which adsorb on α-FeOOH by an inner-sphere mechanism. X-ray absorption near-edge structure (XANES) analysis indicated that the As(III)−α-FeOOH surface complex is stable toward heterogeneous oxidation to As(V), as determined by the energy position of the X-ray absorption edge. The structural information from EXAFS was included in the description of As(III) adsorption on the α-FeOOH surface using a surface complexation model (the constant capacitance model). These results suggest that As(III) surface complex formation on iron(III) oxides may play an important role in the environmental behavior of arsenic.
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The reactivity of As(III) with α-FeOOH at varying pH and As(III) concentration provided macroscopic evidence for strong complexation on the α-FeOOH surface. Extended X-ray absorption fine structure (EXAFS) spectroscopy gave an average As(III)−Fe interatomic distance of 3.378 ± 0.014 Å, which is indicative of bidentate binuclear bridging As(III) complexes on the α-FeOOH surface and which is similar to other oxyanions which adsorb on α-FeOOH by an inner-sphere mechanism. X-ray absorption near-edge structure (XANES) analysis indicated that the As(III)−α-FeOOH surface complex is stable toward heterogeneous oxidation to As(V), as determined by the energy position of the X-ray absorption edge. The structural information from EXAFS was included in the description of As(III) adsorption on the α-FeOOH surface using a surface complexation model (the constant capacitance model). 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Sci. Technol</addtitle><description>The adsorption and stability of arsenite [As(III)] on goethite (α-FeOOH) was investigated using a combination of standard batch techniques and X-ray absorption spectroscopy (XAS). The reactivity of As(III) with α-FeOOH at varying pH and As(III) concentration provided macroscopic evidence for strong complexation on the α-FeOOH surface. Extended X-ray absorption fine structure (EXAFS) spectroscopy gave an average As(III)−Fe interatomic distance of 3.378 ± 0.014 Å, which is indicative of bidentate binuclear bridging As(III) complexes on the α-FeOOH surface and which is similar to other oxyanions which adsorb on α-FeOOH by an inner-sphere mechanism. X-ray absorption near-edge structure (XANES) analysis indicated that the As(III)−α-FeOOH surface complex is stable toward heterogeneous oxidation to As(V), as determined by the energy position of the X-ray absorption edge. The structural information from EXAFS was included in the description of As(III) adsorption on the α-FeOOH surface using a surface complexation model (the constant capacitance model). 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Sci. Technol</addtitle><date>1998-08-15</date><risdate>1998</risdate><volume>32</volume><issue>16</issue><spage>2383</spage><epage>2388</epage><pages>2383-2388</pages><issn>0013-936X</issn><issn>1520-5851</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>The adsorption and stability of arsenite [As(III)] on goethite (α-FeOOH) was investigated using a combination of standard batch techniques and X-ray absorption spectroscopy (XAS). The reactivity of As(III) with α-FeOOH at varying pH and As(III) concentration provided macroscopic evidence for strong complexation on the α-FeOOH surface. Extended X-ray absorption fine structure (EXAFS) spectroscopy gave an average As(III)−Fe interatomic distance of 3.378 ± 0.014 Å, which is indicative of bidentate binuclear bridging As(III) complexes on the α-FeOOH surface and which is similar to other oxyanions which adsorb on α-FeOOH by an inner-sphere mechanism. X-ray absorption near-edge structure (XANES) analysis indicated that the As(III)−α-FeOOH surface complex is stable toward heterogeneous oxidation to As(V), as determined by the energy position of the X-ray absorption edge. The structural information from EXAFS was included in the description of As(III) adsorption on the α-FeOOH surface using a surface complexation model (the constant capacitance model). These results suggest that As(III) surface complex formation on iron(III) oxides may play an important role in the environmental behavior of arsenic.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/es9802201</doi><tpages>6</tpages></addata></record>
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1520-5851
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subjects ADSORPTION
ARSENIC
CHEMICAL REACTION KINETICS
Chemistry
Earth sciences
Earth, ocean, space
Environment
ENVIRONMENTAL SCIENCES
ENVIRONMENTAL TRANSPORT
Exact sciences and technology
GOETHITE
GROUND WATER
iron oxides
Mineralogy
Non silicates
pollutants
SOILS
spectroscopy
surfaces
X-RAY SPECTROSCOPY
X-rays
title Surface Structures and Stability of Arsenic(III) on Goethite:  Spectroscopic Evidence for Inner-Sphere Complexes
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