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131I Sorption by Thermally Treated Hydrotalcites

Published online by Cambridge University Press:  28 February 2024

María Teresa Olguín
Affiliation:
Instituto Nacional de Investigaciones Nucleates, A.P. 18-1027, Col. Escandón, Delegación Miguel Hidalgo, C.P. 11801, México, D.F.
Pedro Bosch
Affiliation:
Universidad Autónoma Metropolitana, Iztapalapa, Michoacán y Purísima, A.P. 55-532, Iztapalapa, C.P. 09340, México, D.F.
Dwight Acosta
Affiliation:
Universidad Nacional Autónoma de México, Instituto de Física de la UNAM, Ciudad Universitaria A.P. 70-360, C.P. 04510, México, D.F.
Silvia Bulbulian
Affiliation:
Instituto Nacional de Investigaciones Nucleates, A.P. 18-1027, Col. Escandón, Delegación Miguel Hidalgo, C.P. 11801, México, D.F.

Abstract

The sorption capacity of hydrotalcite (HT) and its calcined product (CHT) was evaluated for 131I sorption from water solution and it was determined as a function of the calcining temperature. The radionuclide content was determined by γ-spectrometry. Solids were characterized by thermal analysis, X-ray diffraction (XRD), electron microscopy and Brunauer-Emmett-Teller (BET) analysis. For 0.1 M Na I solution, labeled with 131I, sorption capacity was found to be 0.24 meq g−1 (7.2% of the anion exchange capacity, AEC). But, if the sample was previously calcined at 773 K and the HT structure destroyed, the sorption of I increased considerably, up to 2.08 meq g−1 (63% of the AEC) and the HT structure was reconstructed. The 131I sorption at very low concentrations (10−14M) was 0.04 × 10−14 meq of 131I g−1 in the noncalcined HT, but for calcined samples at 773 K, the sorption increased to circa 0.97 × 10−14 meq g−1. Calcination temperature determines the surface area of the resulting mixed oxides, and that property seems to be the most important factor controlling the I sorption. If the calcination temperature was increased to 873 K, the specific surface area of the oxide mixture increased and I sorption increased as well, whereas calcination of HT at 973–1073 K resulted in a low surface area and a low I retention.

Type
Research Article
Copyright
Copyright © 1998, The Clay Minerals Society

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