Abstract
Searching for cationic extended materials with a capacity for anion exchange resulted in a unique thorium molybdate chloride (TMC) with the formula of [Th(MoO4)(H2O)4Cl]Cl·H2O. The structure of TMC is composed of zigzagging cationic layers [Th(MoO4)(H2O)4Cl]+ with Cl- as interlamellar charge-balancing anions. Instead of performing ion exchange, alkali thorium fluorides were formed after soaking TMC in AF (A = Na, K, and Cs) solutions. The mechanism of AF immobilization is elucidated by the combination of SEM-EDS, PXRD, FTIR, and EXAFS spectroscopy. It was observed that four water molecules coordinating with the Th4+ center in TMC are vulnerable to competition with F-, due to the formation of more favorable Th-F bonds compared to Th-OH2. This leads to a single crystal-to-polycrystalline transformation via a pathway of recrystallization to form alkali thorium fluorides.
| Original language | English |
|---|---|
| Pages (from-to) | 6778-6782 |
| Number of pages | 5 |
| Journal | Inorganic Chemistry |
| Volume | 57 |
| Issue number | 12 |
| DOIs | |
| State | Published - 18 Jun 2018 |
| Externally published | Yes |
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