Occurrence of Zn/Al hydrotalcite in smelter-impacted soils from northern France: Evidence from EXAFS spectroscopy and chemical extractions

Farid Juillot 1 , Guillaume Morin 1 , Philippe Ildefonse 1 , Thomas P. Trainor 2 , Marc Benedetti 3 , Laurence Galoisy 1 , Georges Calas 1  and Gordon E. Brown Jr. 2 , 4
  • 1 Laboratoire de Minéralogie-Cristallographie, UMR CNRS 7590, Universités Paris 6 et 7, 4 Place Jussieu 75252 Paris Cedex 05 France
  • 2 Department of Geological and Environmental Sciences, Stanford University, Stanford, California 94305-2115 U.S.A.
  • 3 Laboratoire de Géochimie et Métallogénie, UMR CNRS 7047, Université Paris 6, 4 Place Jussieu 75252 Paris Cedex 05 France
  • 4 Stanford Synchrotron Radiation Laboratory, SLAC, 2575 Sand Hill Road, MS 99, Menlo Park, California 94025 U.S.A.


Zinc speciation was studied by EXAFS spectroscopy, μ-SXRF elemental mapping, XRD, and chemical extraction methods in two smelter-impacted soils sampled near one of the largest Pb and Zn processing plants in Europe, which is located in northern France about 50 km south of Lille. The tilled and wooded soils chosen for study differ in Zn concentration (≈600 and 1400 mg/kg, respectively), soil pH (7.5 and 5.5, respectively), and organic matter content (1.5 and 6.4 wt% TOC, respectively). In both soils, the occurrence of Fe- and Zn-rich (up to 10 wt% Zn) slag particles ranging in size from a few micrometers to a few millimeters, was shown by m-SXRF elemental mapping of soil thin sections as well as by SEM and chemical analysis of different soil size fractions. For both soils, XRD analysis of the dense coarse fraction, which contains up to 10 wt% Zn, revealed the presence of a minor amount (1-1.5 wt%) of crystalline ZnS (sphalerite and wurtzite). In this fraction, EXAFS data show that Zn is mainly incorporated in the tetrahedral sites of a magnetite- franklinite solid solution.

The clay fraction (<2 μm) represents the largest pool of Zn in both soils, with 77 and 62% of the total Zn in the tilled and wooded soils, respectively. However, XRD was not able to detect any Znbearing phases in this fraction. Comparison of Zn K-EXAFS data of untreated and chemically treated samples from the bulk (<2 μm) and the clay (<2 μm) soil fractions with Zn K-EXAFS data from more than 30 model compounds suggests that Zn is present in the following chemical forms: (1) Zn outer-sphere complexes, (2) Zn-organic matter inner-sphere complexes, (3) Zn/Al-hydrotalcite (Zn/ Al-HTLC), (4) phyllosilicates in which Zn is present in the dioctahedral layer at dilute levels, and (5) magnetite-franklinite solid solutions inherited from the smelting process. The presence of exchangeable Zn outer-sphere complexes and of Zn inner-sphere complexes on organic matter is indicated by the relative increase of second-neighbor contributions in the EXAFS RDFs after chemical treatments with 0.01 M CaCl2 and 0.1 M Na4P4O7. The occurrence of Zn/Al-HTLC is demonstrated by the persistence of a Zn-Zn pair correlation at 3.10 ± 0.04 Å (i.e., edge sharing ZnO6 octahedra in the trioctahedral layer structure) in EXAFS data of Na4P2O7 treated soil samples and its disappearance after treatment with 0.45 M HNO3. This latter treatment also revealed the occurrence of Znbearing phyllosilicate minerals, as shown by two Zn-Mg/Al/Si pair correlations at 3.05 ± 0.04 Å and 3.26 ± 0.04 Å, and of magnetite-franklinite solid solutions, as indicated by a Zn-Mn/Fe/Zn pair correlation at 3.50 ± 0.04 Å. Significant changes in the relative proportions of the different forms of Zn between the two soils explain their different responses to chemical treatments and emphasizes the relationships between solid state speciation and mobility of Zn in soils.

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