空气气氛中pb44,6bi55,4共晶熔体的表面张力

B. Alchagirov, A. Khibiev
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引用次数: 1

摘要

在20世纪50年代,液态铅和铅铋共晶合金(Pb45Bi55)被认为是苏联和美国核电系统冷却剂的候选材料。与此同时,由A.I.雷普斯基首先提出的合金(Pb45Bi55)被选为“阿尔法”号核潜艇的冷却剂,在战术和技术数据上都领先于当时。然而,1968年,其中一艘遭遇了严重的辐射事故,由于冷却剂的氧化物沉淀和积聚,导致船载核反应堆堆芯燃料元件熔化,堵塞了管道截面,急剧恶化了反应堆的冷却,导致其失效。事实上,事故的主要原因是缺乏对铅铋冷却剂的物理化学和技术特性的了解。因此,Pb45Bi55冷却剂的主要缺点是对核电站结构材料的腐蚀性。但研究发现,通过调节冷却剂中的含氧量,可以减少液铅合金的腐蚀。例如,在770 K时,马氏体钢在Pb45Bi55无氧流动冷却液中的腐蚀速率约为1 mm /年,而在Pb45Bi55冷却液中溶解氧气并保持其质量浓度为0.01 ppm的情况下,腐蚀速率可降至0.01 mm /年,即100次。观察到的效果是由管道钢表面形成的氧化层提供的保护来解释的。因此,为了更深入地了解液态金属“冷却剂-气体”部分边界上发生的现象,研究保护氧化层的形成和破坏过程及其在冷却剂流体中的行为,特别是从核电厂长期运行的角度来看,仍然具有重要意义。在这方面,关于“冷却剂-气体”相界面表面张力的数据具有重要的科学和实际意义。为此,本工作的任务是实验研究大气对Pb45Bi55共晶熔体表面张力的影响。在静态真空和常压条件下,对制备的共晶熔体Pb44, 6bi55,4的表面张力进行了连续测量。在这项工作中获得的大约300个实验点使得描述表面张力变化过程的动力学成为可能,这取决于冷却剂表面在真空和大气中暴露的时间。结果表明,与作者在静态真空中采用大垂滴法得到的结果相比,共晶熔体在大气压力约300 mmHg下暴露后的前10分钟内,共晶Pb44.6Bi55.4的表面张力下降了55 mN/m以上,比我们测量的总误差(2%)高一个数量级。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SURFACE TENSION OF Pb44,6Bi55,4 EUTECTIC MELT IN AIR ATMOSPHERE
In the 1950s liquid lead and the lead-bismuth eutectic alloy (Pb45Bi55) were considered candidates for their use as coolants for nuclear power systems in the USSR and the USA. At the same time, the alloy (Pb45Bi55), first proposed by A.I. Leypunsky, was chosen as a coolant for the nuclear submarine “Alpha”, which was ahead of its time in terms of its tactical and technical data. However, in 1968, one of them suffered a severe radiation accident caused by the melting of fuel elements in the core of an onboard nuclear reactor due to the precipitation of oxides from the coolant and their accumulation, which blocked the pipeline cross-section and sharply worsened the cooling of the reactor, which led to its failure. In fact, the primary cause of the accident was a lack of knowledge about the physicochemical and technological properties of the lead-bismuth coolant. Thus, the main disadvantage of the Pb45Bi55 coolant is its corrosiveness to structural materials used in the nuclear power plant. But it has been found that corrosion by liquid lead alloys can be reduced by adjusting the oxygen level in the coolant. For example, the corrosion rate of martensitic steel at 770 K in a Pb45Bi55 flowing coolant without oxygen is about 1 mm per year, but it can be reduced to 0.01 mm per year, i.e. 100 times, if oxygen is dissolved in Pb45Bi55 coolant and its mass concentration is maintained at the level of 0.01 ppm. The observed effect is explained by the protection provided by the oxide layer formed on the steel surface of the pipeline. Thus, for a deeper understanding of the phenomena occurring at the boundaries of the liquid metal “coolants - gases” section, it remains relevant to study the processes of formation and destruction of the protective oxide layer and its behavior in coolant fluids, especially from the point of view of long-term operation of nuclear power plants. In this regard, data on the surface tension of the “coolant - gas” interphase boundaries are of great scientific and practical importance. In this connection, the present work sets the task of experimentally studying the influence of atmospheric air on the surface tension of Pb45Bi55 eutectic melt. Measurements of the surface tension of the eutectic melt Pb44,6Bi55,4 prepared by the authors were carried out in a non-stop mode sequentially, under static vacuum and atmospheric air, on the same surface. About three hundred experimental points obtained in this work made it possible to describe the dynamics of the surface tension changing process depending on the time of exposure of the coolant surface in vacuum and atmospheric air. It is shown that in comparison with the results obtained by the authors by the large lying drop method in a static vacuum, in the first 10 minutes from the beginning of the exposure of the eutectic melt in atmospheric air at a pressure of about 300 mmHg), the surface tension of the eutectic Pb44.6Bi55.4 decreases by 55 mN/m and more, which is an order of magnitude higher than the total error (2 %) of our measurements.
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