A phosphate glass‐ceramic wasteform incorporating cerium monazite was synthesized through a two‐step solid phase sintering methodology, aimed at immobilizing waste salts derived from the pyrochemical reprocessing of spent nuclear fuel. The initial phase involved the synthesis of cerium monazite powder, employing a stoichiometric mixture of CeF 3 and NH 4 H 2 PO 4 in a molar ratio of mol(Ce:PO 4 ) = 1:1.4, which was subjected to a thermal treatment at 900°C. Subsequently, the glass‐ceramic matrix was fabricated by sintering a composite mixture of the synthesized cerium monazite and iron phosphate glass (IPG) powder at a temperature of 1000°C for a duration of 2 h, resulting in a cerium incorporation exceeding 36.5 wt%. Microstructural analysis and structural characterization of the glass‐ceramic sample elucidated the presence of monazite crystallites (CePO 4 ) with dimensions ranging from .2 to 5.5 µm. The chemical durability of the wasteform was assessed through modified ASTM C1308 tests conducted in deionized water over a period of 28 days, revealing a total elemental leaching rate of 2.58 × 10 −7 g m −2 min −1 .
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Liu et al. (2024) studied this question.
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