In this study a novel technique, micro-focus time-resolved laser-induced luminescence spectroscopy (µTRLFS) is presented to investigate heterogeneous systems like granite (mainly consisting of quartz, feldspar, and mica), regarding their sorption behavior. µTRLFS is a spatially-resolved upgrade of conventional TRLFS, which allows point-by-point analysis of single minerals by reducing the beam size of the analytic laser beam to below the size of mineral grains. This provides visualization of sorption capacity as well as speciation of a luminescent probe, here Eu
3+
. A thin-section of granitic rock from Eibenstock, Saxony, Germany was analyzed regarding its mineralogy with microprobe X-ray fluorescence (µXRF) and electron probe microanalysis (EPMA). Afterwards, it was reacted with 5.0 × 10
−5
mol/L Eu
3+
at pH 8.0 and uptake was quantified by autoradiography. Finally, the µTRLFS studies were conducted. The results clearly show that the materials interact differently with Eu
3+
, and often even on one mineral grain different speciations can be found. Alkali-feldspar shows very high uptake, with an inhomogeneous distribution, and intermediate sorption strength. On quartz uptake is almost 10-fold lower, while the complexation strength is higher than on feldspar. This may be indicative of adsorption only at surface defect sites, in accordance with low hydration of the observed species.
Reactive transport modeling (RTM) is an essential tool for the prediction of contaminants' behavior in the bio-and geosphere. However, RTM of sorption reactions is constrained by the reactive surface site assessment. The reactive site density variability of the crystal surface nanotopography provides an "energetic landscape", responsible for heterogeneous sorption efficiency, not covered in current RTM approaches. Here, we study the spatially heterogeneous sorption behavior of Eu(III), as an analogue to trivalent actinides, on a polycrystalline nanotopographic calcite surface and quantify the sorption efficiency as a function of surface nanoroughness. Based on experimental data from micro-focus time-resolved laser-induced luminescence spectroscopy (μTRLFS), vertical scanning interferometry, and electron backscattering diffraction (EBSD), we parameterize a surface complexation model (SCM) using surface nanotopography data. The validation of the quantitatively predicted spatial sorption heterogeneity suggests that retention reactions can be considerably influenced by nanotopographic surface features. Our study presents a way to implement heterogeneous surface reactivity into a SCM for enhanced prediction of radionuclide retention.
The
interaction of Eu(III) with thin sections of migmatized gneiss
from the Bukov Underground Research Facility (URF), Czech Republic,
was characterized by microfocus time-resolved laser-induced luminescence
spectroscopy (μTRLFS) with a spatial resolution of ∼20 μm, well below typical grain
sizes of the
material. By this approach, sorption processes can be characterized
on the molecular level while maintaining the relationship of the speciation
with mineralogy and topography. The sample mineralogy was characterized
by powder X-ray diffraction and Raman microscopy, and the sorption
was independently quantified by autoradiography using 152Eu. Representative μTRLFS studies over large areas of multiple
mm2 reveal that sorption on the heterogeneous material
is not dominated by any of the typical major constituent minerals
(quartz, feldspar, and mica). Instead, minor phases such as chlorite
and prehnite control the Eu(III) distribution, despite their low contribution
to the overall composition of the material, as well as common but
less studied phases like Mg–hornblende. In particular, prehnite
shows high a sorption uptake as well as strong binding of Eu to the
mineral surface. Sorption on prehnite and hornblende happens at the
expense of feldspar, which showed the highest sorption uptake in a
previous spatially resolved study on granitic rock. Similarly, sorption
on quartz is reduced, even though only low quantities of strongly
bound Eu(III) were found here previously. Our results illustrate how
competition of mineral surfaces for adsorbing cations drives the metal
distribution in heterogeneous systems.
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