Relationship of quantitative X-ray diffraction measurements of geologic materials to cesium sorption

Author:

Payne Timothy E.,Bertram W. K.,Itakura T.,Raven M. D.

Abstract

SummaryThe amounts of clay minerals in geologic samples from the Australian arid zone were measured using the SIROQUANT program, which quantifies mineral abundances from X-ray diffraction patterns using the Rietveld method. The sorption of trace cesium on the same samples was investigated in batch experiments. The statistical relationships between the Cs distribution coefficients (Kdvalues) and the smectite, illite and kaolinite contents were assessed. Other characterisation data such as the BET surface area and total clay content were included in the statistical analysis. The correlation of the illite content with the Kdfor trace Cs was stronger than any other correlation that was tested. This can be attributed to the presence of frayed edge sites on illite which are highly selective for the adsorption of trace Cs. Sorption experiments were also carried out with higher Cs concentrations, which were expected to saturate the selective Cs sorption sites on illite. Under these conditions, there was no significant correlation between the illite content and the cesium Kd. However, the Kdwas related to the smectite content of the materials. There was no correlation between the kaolinite content and the Kdfor Cs sorption under any of the experimental conditions. The sorption of Cs on the samples was influenced by the BET surface areas, but normalisation of the Kddata by surface area did not fully explain the sorption results. Only the quantitative XRD data were able to explain the shapes of Cs sorption isotherms. The isotherm was distinctly different for an illite-rich sample and did not conform to the Freundlich isotherm exhibited by other samples. This study demonstrates that quantitative XRD measurements are valuable in predicting Cs sorption properties of complex geologic samples, particularly sorption data obtained with trace Cs levels where bulk measurements such as the BET surface area are less useful.

Publisher

Walter de Gruyter GmbH

Subject

Physical and Theoretical Chemistry

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