Johnstone E V, Bailey D J, Lawson S, Stennett M C, Corkhill C L, Kim M, Heo J, Matsumura D, Hyatt N C
University of Sheffield, Materials Science and Engineering Department Sheffield S1 3JD UK
Department of Materials Science and Engineering, Pohang University of Science and Technology (POSTECH) Pohang Gyeongbuk 790-784 South Korea.
RSC Adv. 2020 Jul 2;10(42):25116-25124. doi: 10.1039/d0ra04114a. eCollection 2020 Jun 29.
The synthesis of a palladium-containing iodovanadinite derivative, hypothetically "PdPb(VO)I", was attempted using PdI as a source of iodine in searching for a novel waste form for radioiodine. Stoichiometric amounts of Pb(VO) and PdI were batched and reacted at elevated temperatures in sealed vessels. Batched material was also subjected to high-energy ball-milling (HEBM) in order to reduce reaction time and the potential for iodine volatilization during subsequent reaction at 200-500 °C. The resulting products were characterized using X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray analysis, IR spectroscopy, thermal analysis and Pd K XANES. Results showed that PdI can function as a sacrificial iodine source for the formation of iodovanadinite, prototypically Pb(VO)I, however, the incorporation of Pd into this phase was not definitively observed. The sacrificial reaction mechanism involved the decomposition of PdI to Pd metal and nascent I, with the latter incorporated into the iodovanadinite Pb(VO)I phase. In comparison to processing using standard solid state reaction techniques, the use of HEBM prior to high temperature reaction generates a more homogeneous end-product with better iodine retention for this system. Overall, the key novelty and importance of this work is in demonstrating a method for direct immobilisation of undissolved PdI from nuclear fuel reprocessing, in a composite wasteform in which I-129 is immobilised within a durable iodovandinite ceramic, encapsulating Pd metal.
为寻找放射性碘的新型固化体,尝试以碘化钯(PdI)作为碘源来合成一种含钯碘钒铅矿衍生物,假定其化学式为“PdPb(VO)I”。将化学计量比的Pb(VO)和PdI配料,并在密封容器中于高温下反应。为缩短反应时间并降低后续200 - 500°C反应过程中碘挥发的可能性,配料还进行了高能球磨(HEBM)处理。使用X射线衍射、扫描电子显微镜、能量色散X射线分析、红外光谱、热分析和钯K边X射线吸收近边结构(Pd K XANES)对所得产物进行表征。结果表明,PdI可作为形成碘钒铅矿(典型的Pb(VO)I)的牺牲碘源,然而,并未明确观察到钯进入该物相。牺牲反应机理涉及PdI分解为钯金属和新生碘,后者进入碘钒铅矿Pb(VO)I相。与使用标准固态反应技术的处理方法相比,在高温反应之前使用HEBM能生成更均匀的最终产物,且该体系的碘保留效果更好。总体而言,这项工作的关键新颖之处和重要性在于展示了一种将核燃料后处理中未溶解的PdI直接固定在复合固化体中的方法,在这种复合固化体中,I - 129固定在耐用的碘钒铅矿陶瓷内,包裹着钯金属。