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水热合成(Zr,U)SiO:将铀掺入锆石的有效途径。

Hydrothermal synthesis of (Zr,U)SiO: an efficient pathway to incorporate uranium into zircon.

作者信息

Estevenon Paul, Barral Thomas, Avallone Arthur, Jeffredo Mateo, De La Hos Alexis, Strzelecki Andrew, Le Goff Xavier, Szenknect Stephanie, Kvashnina Kristina, Moisy Philippe, Podor Renaud, Guo Xiaofeng, Dacheux Nicolas

机构信息

CEA, DES, ISEC, DMRC, Univ Montpellier, Marcoule, France.

ICSM, Univ Montpellier, CNRS, CEA, ENSCM, Bagnols-sur-Cèze, France.

出版信息

Dalton Trans. 2024 Aug 20;53(33):13782-13794. doi: 10.1039/d4dt01604a.

DOI:10.1039/d4dt01604a
PMID:39101436
Abstract

The preparation of synthetic (Zr,U)SiO solid solution is challenging, as the conventional high-temperature solid-state method limits the solubility of uranium (4 ± 1 mol%) in the orthosilicate phase due to its thermodynamic instability. However, these compounds are of great interest as a result of (Zr,U)SiO solid solutions, with uranium contents exceeding this concentration, being observed as corium phases formed during nuclear accidents. It has been identified that hydrothermal synthesis pathways can be used for the formation of the metastable phase, such as USiO. The investigation carried out in this study has indeed led to the confirmation of metastable (Zr,U)SiO compounds with high uranium contents being formed. It was found that (Zr,U)SiO forms a close-to-ideal solid solution with uranium loading of up to 60 mol% by means of hydrothermal treatment for 7 days at 250 °C, at pH = 3 and starting from an equimolar reactant concentration equal to 0.2 mol L. A purification procedure was developed to obtain pure silicate compounds. After purification, these compounds were found to be stable up to 1000 °C under an inert atmosphere (argon). The characterisation methods used to explore the synthesis and thermal stability included powder X-ray diffraction (PXRD), Fourier transform infrared (FTIR) and Raman spectroscopies, scanning electron microscopy (SEM) and thermogravimetric analysis (TGA).

摘要

合成(Zr,U)SiO固溶体具有挑战性,因为传统的高温固态方法由于其热力学不稳定性,限制了铀在正硅酸盐相中的溶解度(4±1摩尔%)。然而,由于在核事故中形成的熔岩层相中观察到铀含量超过该浓度的(Zr,U)SiO固溶体,这些化合物备受关注。已经确定水热合成途径可用于形成亚稳相,如USiO。本研究进行的调查确实证实了高铀含量的亚稳(Zr,U)SiO化合物的形成。结果发现,通过在250°C、pH = 3的条件下进行7天水热处理,且起始反应物浓度为0.2 mol L的等摩尔浓度,(Zr,U)SiO能形成铀负载量高达60摩尔%的接近理想的固溶体。开发了一种纯化程序以获得纯硅酸盐化合物。纯化后,发现这些化合物在惰性气氛(氩气)下直至1000°C都是稳定的。用于探索合成和热稳定性的表征方法包括粉末X射线衍射(PXRD)、傅里叶变换红外光谱(FTIR)和拉曼光谱、扫描电子显微镜(SEM)和热重分析(TGA)。

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