Montmorillonite / Uranium / Sorption / EXAFSSummary. Extended X-ray absorption fine structure (EXAFS) spectroscopy at the uranium L III -edge was used for determining the structural environment of aqueous uranyl sorbed onto montmorillonite. The study reveals that uranyl uptake at pH ∼ 5-∼ 7 and at an initial uranyl concentration of 5 × 10 −5 M takes place at amphoteric surface hydroxyl sites as inner-sphere complex. The measured bond distances between uranium and the equatorial oxygen atoms are in the range of 2.34 Å and 2.37 Å indicating an inner-sphere coordination. At ∼ 3.4 Å the presence of a U−Al backscattering pair was determined. This backscattering pair indicates that the binding of the uranyl unit to amphoteric surface hydroxyl sites occurs preferred as a bidentate inner-sphere complex on aluminol groups.

Iron is an important redox-active element that is ubiquitous in both engineered and natural environments. In this study, the retention mechanism of Fe(II) on clay minerals was investigated using macroscopic sorption experiments combined with Mössbauer and extended X-ray absorption fine structure (EXAFS) spectroscopy. Sorption edges and isotherms were measured under anoxic conditions on natural Fe-bearing montmorillonites (STx, SWy, and SWa) having different structural Fe contents ranging from 0.5 to 15.4 wt % and different initial Fe redox states. Batch experiments indicated that, in the case of low Fe-bearing (STx) and dithionite-reduced clays, the Fe(II) uptake follows the sorption behavior of other divalent transition metals, whereas Fe(II) sorption increased by up to 2 orders of magnitude on the unreduced, Fe(III)-rich montmorillonites (SWy and SWa). Mössbauer spectroscopy analysis revealed that nearly all the sorbed Fe(II) was oxidized to surface-bound Fe(III) and secondary Fe(III) precipitates were formed on the Fe(III)-rich montmorillonite, while sorbed Fe is predominantly present as Fe(II) on Fe-low and dithionite-reduced clays. The results provide compelling evidence that Fe(II) uptake characteristics on clay minerals are strongly correlated to the redox properties of the structural Fe(III). The improved understanding of the interfacial redox interactions between sorbed Fe(II) and clay minerals gained in this study is essential for future studies developing Fe(II) sorption models on natural montmorillonites.

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Extended X-ray absorption fine structure (EXAFS) and Mössbauer spectroscopy combined with macroscopic sorption experiments were employed to investigate the sorption mechanism of Fe(II) on an iron-free synthetic montmorillonite (Na-IFM). Batch sorption experiments were performed to measure the Fe(II) uptake on Na-IFM at trace concentrations as a function of pH and as a function of sorbate concentration at pH 6.2 and 6.7 under anoxic conditions (O2 < 0.1 ppm). A two-site protolysis nonelectrostatic surface complexation and cation exchange sorption model was used to quantitatively describe the uptake of Fe(II) on Na-IFM. Two types of clay surface binding sites were required to model the Fe(II) sorption, the so-called strong (≡S(S)OH) and weak (≡S(W)OH) sites. EXAFS data show spectroscopic differences between Fe sorbed at low and medium absorber concentrations that were chosen to be characteristic for sorption on strong and weak sites, respectively. Data analysis indicates that Fe is located in the continuity of the octahedral sheet at trans-symmetric sites. Mössbauer spectroscopy measurements confirmed that iron sorbed on the weak edge sites is predominantly present as Fe(II), whereas a significant part of surface-bound Fe(III) was produced on the strong sites (∼12% vs ∼37% Fe(III) species to total sorbed Fe).

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X-ray absorption fine structure (XAFS) spectroscopy and diffuse reflectance spectroscopy (DRS) were applied to assess the solubility-limiting phase of Ni in cement systems.The study provides first direct spectroscopic evidence for the formation of Ni-and Al-containing hydrotalcite-like layered double hydroxides (Ni-Al LDHs) when cement material (a complex mixture of mainly CaO, SiO 2 , Al 2 O 3 , Fe 2 O 3 , MgO, and SO 3 ) was treated with Ni in artificial cement pore water under highly alkaline conditions (pH ) 13.3). The study shows that Ni-Al LDHs were formed in cement suspensions oversaturated with respect to β-Ni(OH) 2 and aged at room temperature for 150 days. This finding indicates that Ni-Al LDHs and not Ni-hydroxides may determine the solubility of Ni in cement materials.

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