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The Influences of ECP and Metal Dopants on Radiation Field Build-up on Stainless Steel Surfaces

机译:ECP和金属掺杂剂对不锈钢表面辐射场堆积的影响

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In LWRs, water chemistry control has been effectively applied to countermeasure radiation field build-up and materials integrity issues. Numerous plant observations and laboratory examinations indicate that the radiation field build-up is very sensitive not only to the concentrations of various impurities of reactor water but also to the electrochemical corrosion potential (ECP). The mechanisms behind these observations have not been fully understood due to possibly rather complex interactions among fuel CRUD, reactor water, and material piping surfaces In Studsvik, an experimental loop system has been constructed to simulate BWR water conditions and applied Co-60 tracer technique to online measure radioactivity build-up and release on stainless steel surfaces under various controlled water chemistry conditions. We have also examined the microstructures of the oxide films formed under those conditions. In this paper, we report on radioactivity uptake on and release from stainless steel material under simulated cyclic oxidising and reducing conditions. Metal dopants of iron, nickel and zinc species in different concentrations were used to study the influence of water chemistry. The activity build-up and release were studied in different exposure intervals during a 3-month long autoclave experiment. The radioactivity uptake rate was seen to increase when shifting water chemistry from oxidising to reducing conditions. The corresponding changes from reducing to oxidising chemistry resulted in a decreased rate. Different activity uptake rates were observed with and without zinc injection in the presence of iron and nickel dopants. With zinc injection, instantaneous release of Co-60 was seen in conjugation to any water chemistry shift from oxidising to reducing or from reducing to oxidising conditions. The results of this study are compared with that obtained previously to shed some light on the possible mechanisms behind the activity build-up and the influence of water chemistry conditions.
机译:在轻水堆,水化学控制得到了有效的应用到对抗辐射场集结和材料的完整性问题。许多植物的观察和实验室检查表明,辐射场积聚是非常敏感的,不仅对的反应器水的各种杂质浓度还要电化学腐蚀电位(ECP)。这些观察背后的机制还没有由于被完全理解到燃料CRUD,反应堆水之间可能相当复杂的相互作用,以及材料管道表面在Studsvik,实验回路系统已经构造以模拟BWR水条件和施加的钴60示踪技术来在线测量放射性积累和释放在不锈钢上的各种控制水化学条件下的表面。我们还审查了这些条件下形成的氧化膜的微观结构。在本文中,我们对放射性摄取的报告,并从下模拟循环氧化和还原条件下的不锈钢材料释放。在不同浓度的铁,镍和锌物种的金属掺杂剂被用来研究水化学的影响。活动集结和释放不同的曝光间隔3个月的长期高压实验过程进行了研究。吸收速率的放射性看到从氧化换档水化学还原条件时增加。从降低到氧化化学相应变化导致降低的速率。具有和不具有在铁和镍掺杂剂的存在锌注射观察到不同的活动摄取速率。与注入锌,钴60的瞬间释放被认为在缀合到从氧化任何水化学位移以减少或从降低到氧化条件。这项研究的结果与先前获得的洒在活动积聚和水化学条件的影响背后的可能机制一些光比较。

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