Reaction Engineering, Kinetics, and Catalysis
Low-temperature conversion of spent adsorbent to iodine sodalite by a mechanochemical route
Article first published online: 11 OCT 2011
DOI: 10.1002/aic.12756
Copyright © 2011 American Institute of Chemical Engineers (AIChE)
Additional Information
How to Cite
Hirabayashi, D., Tanada, Y., Sugiyama, T., Enokida, Y. and Sawada, K. (2012), Low-temperature conversion of spent adsorbent to iodine sodalite by a mechanochemical route. AIChE J., 58: 2441–2447. doi: 10.1002/aic.12756
Publication History
- Issue published online: 5 JUL 2012
- Article first published online: 11 OCT 2011
- Accepted manuscript online: 18 AUG 2011 10:15AM EST
- Manuscript Revised: 8 AUG 2011
- Manuscript Received: 2 JUN 2011
Funded by
- JSPS, KAKENHI “Grant-in-Aid for Exploratory Research”. Grant Number: 23656588
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Keywords:
- radioactive iodine;
- spent adsorbent;
- iodine sodalite;
- mechanochemical conversion;
- immobilization
Abstract
The focus on a ball milling induced conversion as a possible synthesis route of iodine sodalite (Na8Al6Si6O24I2) from zeolite-based iodine adsorbents in order to treat a radioactive iodine filter for the off-gas cleaning during nuclear facilities is presented. A mixture of silver iodide and zeolite 13X as a simulated adsorbent was mechanochemically milled using a laboratory-scale planetary ball mill. The obtained powders were characterized by X-ray diffraction to determine the effect of milling time on the conversion of the iodine sodalite. The crystal grain size and the lattice strain of the grounded phases were evaluated. After the ball milling, the milled samples were hydrothermally crystallized to form a sodalite phase with a sodium hydroxide solution for 48 h in an autoclave maintained at 150°C. The iodine sodalite was successfully obtained after hydrothermal crystallization. A leaching test was carried out for the assessment of the order of iodine leachability and chemical durability under reducing conditions. The leaching amount was found to be low on the orders of 10−4 ∼10−5 mol dm−3 in sodium thiosulfate solution. © 2011 American Institute of Chemical Engineers AIChE J, 58: 2441–2447, 2012

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