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Microstructure evolution and weathering reactions of Synroc samples crystallized form CaZrTi_2O_7 melts: TEM/AEM investigation and geochemical modeling

机译:Synroc样品的微观结构演化和耐候反应结晶形式Cazrti_2O_7 Melts:TEM / AEM调查和地球化学建模

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Scanning electron microscopy (SEM), transmission electron microscopy (TEM), and analytical electron microscopy (AEM) studies have been conducted on samples crystallized from a melt with a composition of zirconolite {Ca_(0.9)Gd_(0.1))Zr(Ti_(1.9)Al_(0.1))_2O_7}. The formation of a whole suite of Synroc minerals (zirconia, ZrTiO_4, zirconolite, perovskite, and rutile) has been observed. The formation of these minerals follows the crystallization sequence of Ti-bearing zirconia ->ZrTiO_4 phase ->Zr-rich zirconolite ->Zr-poor zirconolite -> rutile/perovskite. This sequence is induced by a fractional crystallization process, in which Zr-rich mineral phases tend to crystallize first, resulting in continuous depletion of Zr in melt. Consistent with this melt compositional evolution, Zr content in the zirconolite decreases from the area next to ZrTiO_4 phase to the area next to rutile or perovskite. High-resolution TEM images show that there are no glassy phases at the grain boundary between zirconolite and perovskite. The fractional crystallization-induced textural heterogeneity may have a significant impact on the incorporation of radionuclides into crystalline phases and the resistance of radioniclides to leaching proesses. Exsolution lamellae and multiple twining result from the phase transition from tetragonal zirconia to monoclinic zirconia may decrease durability of the Synroc. Fast cooling of melt may produce more zirconolite phase and relatively uniform texture. In general, however, a Synroc prepared by a through-melt method is less uniform in texture than that prepared by a through-sol-gel method. The reaction path calculation for the alteration of U-bearing zirconolite in al oxidizing fluid shows that zirconolite is first altered into a perovskite-like phase (CaZrO_3), followed by rutile (TiO_2), and U~(6+) -bearing phases of soddyite [UO_2)_2SiO_42H_2O] and haiweeite [Ca(UO_2)_2Si_6O_(15)5H_2O].
机译:扫描电子显微镜(SEM),透射电子显微镜(TEM)和分析电子显微镜(AEM)研究已经在用氧化锆组合物中结晶的样品上进行了研究(0.9)Gd_(0.1))Zr(Ti_( 1.9)AL_(0.1))_ 2O_7}。已经观察到形成整体Synroc矿物质(氧化锆,ZrTiO_4,锆石,钙钛矿和金红石)。这些矿物的形成遵循Ti轴承氧化锆的结晶序列 - > ZrTiO_4相 - >富锆锆 - > Zr-差锆石 - >金红石/钙钛矿。该序列由分数结晶过程引起的,其中富含Zr的矿物相倾向于首先结晶,导致熔体中连续耗尽Zr。与该熔体组成的演进一致,锆醇中的Zr含量从ZrTiO_4相旁边的区域降低到金红石或钙钛矿旁边的区域。高分辨率TEM图像表明,锆龙与钙钛矿之间的晶界中没有玻璃阶段。分数结晶诱导的纹理异质性可能对辐射核素掺入结晶相和辐射硅酸酯的抗浸出工艺的抗性产生显着影响。来自四边形氧化锆到单斜氧化锆的相转变的eX展开薄片和多个缠绕结果可能降低Synroc的耐久性。熔体的快速冷却可以产生更多的锆石相和相对均匀的质地。然而,通常,通过熔融方法制备的Synroc在质地上的均匀性比通过溶胶 - 凝胶法制备的均匀。用于在Al氧化流体中改变U轴承锆沸石的反应路径计算表明,锆醇首先将钙钛矿状相(Cazro_3)改变为金红石(TiO_2),以及u〜(6+)的阶段SODDDYITE [UO_2)_2SIO_42H_2O]和HAIWEATE [CA(UO_2)_2SI_6O_(15)5H_2O]。

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