Abstract
Praseodymium was used as the surrogate for trivalent minor actinide neptunium, and a complete series of pure monazite-type Ce1−xPrxPO4 (x=0–1) solid solutions were successfully prepared by the solid state reaction. The effects of calcining temperature, holding time and Pr content on the structure of Ce1−xPrxPO4 solid solutions were investigated. The results show that although Pr6O11 (Pr23+Pr44+O11) exists two stabilized oxidation states, there has been no tetravalent praseodymium phosphate during the synthesis process. The optimized temperature for the synthesis of Ce0.8Pr0.2PO4 solid solution is more than 1100°C, and a hypothetical reaction mechanism is also proposed. Besides, the crystalline grains coarsen as the increasing of holding time. The linear variation of unit cell parameters and a gradual hypsochromic shift in the Raman spectra are observed with the increase of Pr content, indicating that cerium is progressively replaced by praseodymium and Ce1−xPrxPO4 solid solutions were prepared.
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