4.8 Article

Zinc coordination to multiple ligand atoms in organic-rich surface soils

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 40, Issue 18, Pages 5688-5695

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/es0608343

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We report on the solid-phase speciation of naturally occurring Zn in metalliferous organic-matter-rich surface soils. Synchrotron-based studies were used to probe elemental distribution and associations in soil particles (mu-XRF) together with the mineralogy (mu-XRD) and Zn bonding environment (Zn-mu-XANES) at the micrometer-scale level. The average bonding environment of Zn was also probed for bulk soils using XANES. We found the distribution of elements within soil particles to be heterogeneous; however, some elements are consistently co-located. While conventional XRD analyses of whole soils did not identify any Zn mineral phase, synchrotron-based-mu-XRD analyses indicated that sphalerite (ZnS) is present in a particle from a wetland soil (soil labeled G3). Linear combination fit (LCF) analyses of XANES spectra collected for bulk soils (Zn-XANES) and mu m-regions (Zn-mu-XANES) within soil particles suggest Zn bonds to oxygen-, nitrogen-, and sulfur-functional groups in these sulfur-, nitrogen-, and zinc-rich organic surface soils. The XANES spectra of all bulk soils and of all mu m-regions except for the wetland soil (G3), where ZnS was the most significant constituent, were best fitted by the Zn-arginine reference compound and therefore seems to indicate Zn bonding to nitrogen. Thus, these results provide compelling evidence of the formation of highly covalent Zn-organic bonds in the organic-rich surface soils that were studied. This may explain in part why metal partition coefficients (K-d) are generally higher in organic soils, and why the toxic thresholds for total metal concentrations are higher in organic than in mineral soils.

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