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Meeting Materials Science & Technology 2020
Symposium Ceramics in the Nuclear Fuel Cycle
Presentation Title Multi-scale Cs Sorbents Easily Transformable into Waste Confinement Matrices
Author(s) Agnes Grandjean, Micheal Maloney, Clément Cabaud, N. Massoni, Scott Misture
On-Site Speaker (Planned) Scott Misture
Abstract Scope We demonstrate multimodal materials with the ability to selectively entrap Cs+ from a radioactive multi-ion liquid phase, after which they are easily transformable into the final waste form using a simple thermal treatment. we focus on K-containing copper (II) hexacyanoferrate (II) nanoparticles. Selectivity to Cs ions was studied, and we show that insertion of Cs+ into the structure leads to a weakening of the local bonds and a decrease in Jahn-Teller distortions around the metal centers. By anchoring the HCF sorption centers into porous silica, it become feasible to directly calcine (no additives) Cu-HCF functionalized silica after Cs-exchange at 1000°C without Cs loss. We attribute this desirable performance to in-situ formation of an alkali silicate glass zone that that immobilize by-products of decomposed HCF (Cs, K, Cu, Fe ) and Si coming from the siliceous matrix.


A First-principles Database Approach to Predicting Trans-Uranic Waste Forms
Evaluation of the Corrosion of High Purity CVD SiC in Light Water Reactor Environments
First-principles Study on the Trapping and Recombination of Tritium in Lithium Vacancy of the γ-LiAlO2 (100) Surface
Multi-scale Cs Sorbents Easily Transformable into Waste Confinement Matrices
Nb and Ti Alloying Effects on the Phase and Oxidation of U3Si2
Radiolytic Damage and Hydrogen Generation at Carbide – Water Interfaces
Thermophysical Properties of Sintered Yttrium Dihydride

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