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CHARACTERIZATION OF IN-CORE WATER CHEMISTRY FOR CORROSION CONTROL OF LWRS

机译:LWRS腐蚀控制中核心水化学特性的表征

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This paper updates scientific bases of water chemistry in applying the author's recent theory, which integrates the elemental radiation- and electro-chemistry reactions in the "Butlar-Volmer equation," presented in ICONE21-16525. For the past several years the author has been trying to establish that the "long-cell" (a kin to macro-cell) corrosion mechanism is inducing practically all sorts of accelerated corrosion phenomena widely observed in water-cooled reactors, especially in aged plants. The theoretical electrochemical potential differences have been benchmarked with the published in-pile test results for both PWR- and BWR water chemistry environments. However the author's previous verification efforts were limited to the extent that the curves were fitted with experimental results at a single point. The author re-formulated the basic theory and found that the redox potential difference consists of an electrochemical part (e.g., Nernst equation of dissolved hydrogen or oxygen) and radiation-induced perturbation term, the latter diminishes to zero without radiation. The author continued his studies to clarify whether our current scientific knowledge is sufficient to explain the in-core "chemistry" to reproduce the experimental results without the fitting parameter. Through his study he realized that the basic mechanism of the potential difference is still not sufficiently known. No fitting parameter was used for the PWR water chemistry in the DH region for practical engineering applications, although it is indispensable to confirm the results with an in-pile test loop. In the BWR-NWC the theoretical redox potential out of core was still necessary to be fitted with the experimental results, due to an effect of residual hydrogen peroxide detected by the reference electrode. In addition the calculated potential shift is several times larger than the experimental observation. With the reformulation the scientific validity of the author's theory is further confirmed. He believes that there is no doubt that the "long-cell" takes place in LWRs, although details are still debatable.
机译:本文运用作者的最新理论来更新水化学的科学基础,该理论将元素辐射和电化学反应整合到了ICONE21-16525中提出的“ Butlar-Volmer方程”中。在过去的几年中,作者一直试图确定“长电池”(类似于大电池)腐蚀机理实际上导致了在水冷反应堆中,尤其是在老化的工厂中广泛观察到的各种加速腐蚀现象。 。理论上的电化学电势差已用已发布的针对PWR-和BWR水化学环境的堆内测试结果进行了基准测试。但是,作者先前的验证工作仅限于曲线在单个点上与实验结果相吻合的程度。作者重新制定了基本理论,发现氧化还原电势差由电化学部分(例如,溶解的氢或氧的能斯特方程)和辐射引起的扰动项组成,后者在没有辐射的情况下减小为零。作者继续进行研究,以澄清我们目前的科学知识是否足以解释核心“化学”,以在没有拟合参数的情况下重现实验结果。通过他的研究,他意识到电势差的基本机制仍不为人所知。对于实际工程应用,在DH地区的PWR水化学中没有使用拟合参数,尽管通过桩内测试回路确认结果是必不可少的。在BWR-NWC中,由于参比电极检测到的残留过氧化氢的影响,仍然需要将核外的理论氧化还原电势与实验结果进行拟合。此外,计算出的电位偏移比实验观察结果大几倍。通过重新制定,进一步证实了作者理论的科学有效性。他认为,毫无疑问,“长电池”是在轻水堆中发生的,尽管细节仍有待商bat。

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