Structure Insides at the Reaction Interface Between Pyrochlore Glass-Ceramics and Stainless Steel Canister Under Hot Isostatic Pressing Conditions

Yingjie Zhang, Tao Wei, A. Xu, P. Dayal, D.J. Gregg
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Abstract

As potential waste forms for immobilizing actinide-rich radioactive wastes, Eu2Ti2O7 pyrochlore glass-ceramics were fabricated via hot isostatic pressing (HIPing) at 1200 oC. The structure at the reaction interface between the glass-ceramic waste form and the stainless steel (SS) canister under HIPing conditions were carefully investigated with SEM, TEM and synchrotron single crystal X-ray diffraction (SC-XRD). The interactions at the reaction interface led to the formations of a ∼10 µm thick Cr2O3 layer as the oxidation front of the SS and a layer of a mixed oxide phase (Eu1.25SiCr0.8Ti1.2O7.5) on the glass-ceramic side of the reaction interface. The crystal structure of such a unique mixed oxide phase was revealed indubitably with a combination of synchrotron SC-XRD and TEM assisted with a FIB-SEM system. The improved structural understanding of the reaction interface will help to support the utilization of HIPing as a versatile hot consolidation process for the treatment of radioactive wastes.
热等静压条件下焦绿玻璃陶瓷与不锈钢罐反应界面的内部结构
采用热等静压法(HIPing)在1200℃下制备了Eu2Ti2O7焦绿玻璃陶瓷,作为固定化富锕系放射性废物的潜在废物形式。采用扫描电子显微镜(SEM)、透射电子显微镜(TEM)和同步单晶x射线衍射仪(SC-XRD)研究了在高温条件下玻璃陶瓷废料与不锈钢(SS)罐反应界面的结构。反应界面处的相互作用导致SS的氧化面形成了~ 10µm厚的Cr2O3层,在反应界面的玻璃陶瓷侧形成了一层混合氧化相(eu1.25 sicr0.8 ti1.2 2o7.5)。利用同步加速器SC-XRD和TEM结合FIB-SEM系统,对这种独特的混合氧化物相的晶体结构进行了分析。对反应界面结构的进一步了解将有助于支持HIPing作为处理放射性废物的通用热固结工艺的利用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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