Zn isotopic fractionation caused by sorption on goethite and 2-Lines ferrihydrite

被引:186
作者
Juillot, F. [1 ]
Marechal, C. [2 ]
Ponthieu, M. [3 ]
Cacaly, S. [1 ]
Morin, G. [1 ]
Benedetti, M. [3 ]
Hazemann, J. L. [4 ]
Proux, O. [4 ]
Guyot, F. [1 ]
机构
[1] Univ Paris Diderot, IMPMC, Univ Paris 06, IPGP,CNRS,UMR 7590, F-75015 Paris, France
[2] Univ Lyon 1, CNRS, PEPS, UMR 5125, F-69622 Villeurbanne, France
[3] Univ Paris Diderot, LGE, IPGP, CNRS,UMR 7047, F-75252 Paris, France
[4] European Synchrotron Radiat Facil, FAME Beamline, F-38043 Grenoble, France
关键词
D O I
10.1016/j.gca.2008.07.007
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Zn isotopic fractionation caused by sorption on 2-Lines ferrihydrite (Fh2L) and goethite was investigated to assess the role of reactions at the Fe-oxyhydroxide/water interface in changes of the isotopic distribution of Zn. Since sorption reactions are ubiquitous in Earth's surface environments, it is important to evaluate their influence on the isotopic distribution of Zn before it can be used to track and quantify contributions of various sources and/or biogeochemical processes involving this element. Our results show that Zn isotopes are fractionated upon sorption on Fe-oxyhydroxides with an enrichment of the heavy isotopes present on the solid's surface. This fractionation appears to proceed through an equilibrium mechanism and yields different (Delta(66)/Zn-64)(sorbed-aqueous) values for Zn sorption on goethite [(Delta(66)/Zn-64)-(sorbed-aqueous) around +0.29 parts per thousand] and Fh2L [(Delta(66)/Zn-64)(sorbed-aqueous) around +0.53 parts per thousand]. These different magnitudes of Zn fractionation are related to structural differences between Zn complexes existing on the surface of goethite (octahedrally coordinated Zn by oxygen atoms) and Fh2L (tetrahedrally coordinated Zn by oxygen atoms), as evidenced by Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy and CD-MUSIC modeling. These results show the importance of accounting for reactions at the Fe-oxyhydroxide/water interface when dealing with the isotopic distribution of Zn at the Earth's surface. Considering the large range of other possible sorbents (Mn or Al oxides, phyllosilicates, carbonates, biologic surfaces, etc.) and the importance of reactions at sorbent/water interfaces for other non-traditional stable isotopes (i.e. Cr, Fe, Ni and Cu) that are increasingly used in environmental Studies, these results emphasize the need for further experimental studies that are needed to quantify the isotopic fractionation of these elements possibly accompanying their sorption. (C) 2008 Elsevier Ltd. All riiihts reserved.
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收藏
页码:4886 / 4900
页数:15
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