首页> 外文期刊>PowerPlant Chemistry: The Journal of All Power Plant Chemistry Areas >Chloride Contamination of the Water/Steam Cycle in Power Plants Part IV: Association with Tubesheet Dealloying as Evident during a Condenser Re-tubing
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Chloride Contamination of the Water/Steam Cycle in Power Plants Part IV: Association with Tubesheet Dealloying as Evident during a Condenser Re-tubing

机译:电厂水/蒸汽循环中的氯化物污染第四部分:与冷凝器换管过程中明显出现的管板脱合金有关

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This paper is a continuation of a series of publications on investigations performed at the Shand Power Station (SaskPower) to determine a hitherto unfamiliar source(s) of chloride contamination to the water/steam circuit. The first showed that current popularly known causative factors were not individually or cumulatively responsible root causes of the chloride ingress. The second provided evidence from overhaul inspections and sample test results that the chloride ingress emanates from a cooling water source, but through two different (gaseous and water-borne) pathways, each of which is distinctly different from the common condenser tube water leaks. The gaseous ingress pathway was identified as the likely main source of the contamination. In the third paper, computational analysis and plant operational data were used in support of this idea. The working hypothesis was that chlorinated compounds with significant vapor pressures (e.g. free chlorine species HOCI and Cl2, chloramines NH2CI, NHCI2 and NCI3, trihalomethanes (THMs), haloacetic acids, HCI, etc.) ingress in gaseous forms into the condenser hotwell through weak seals of tube-to-tubesheet joints. Apart from some THMs (i.e. CHCI3 and CBrCI2), which are likely to be lost significantly through air ejection and deaeration processes, NH2CI, HOCI and NHCI2 were noted to be potential significant contributors of chlorides to the water/steam cycle from the re-circulating cooling water. Dezincification was implicated as the corrosion mechanism occurring from the attack of these oxidizing chlorinated compounds on weak naval brass tube-to-tubesheet joints, thus creating a pathway for the vapor of these relatively volatile inorganic solutions to enter the shell side of the condenser. This fourth paper first provides a brief literature background and follows up with pictorial evidence of the dezincification process and results of more detailed laboratory analyses of samples collected during the condenser tube removal and re-tubing periods in support of the above hypotheses.
机译:本文是在Shand电站(SaskPower)进行的一系列调查研究的后续出版物,以确定迄今不熟悉的水/蒸汽回路中氯化物污染的来源。第一个结果表明,当前广为人知的致病因素并不是氯化物进入的单独或累积的根本原因。第二个从大修检查和样本测试结果中提供了证据,表明氯化物的进入是从冷却水源发出的,但是是通过两种不同的(气态和水传播)途径而来的,每种途径与常见的冷凝器管漏水明显不同。气体进入途径被确定为可能的主要污染源。在第三篇论文中,使用了计算分析和工厂运营数据来支持这一想法。可行的假设是,蒸气压较高的氯化物(例如游离氯物质HOCI和Cl2,氯胺NH2Cl,NHCI2和NCI3,三卤甲烷(THMs),卤乙酸,HCl等)以气体形式通过弱气进入冷凝器热井。管对管板接头的密封件。除了一些THM(即CHCl3和CBrCl2),它们很可能会通过空气喷射和脱气过程而大量损失,此外,NH2Cl,HOCI和NHCI2可能是氯从再循环到水/蒸汽循环的重要贡献者。冷却水。脱锌被认为是由于这些氧化的氯化物对海军薄弱的黄铜管-管板接头的侵蚀而发生的腐蚀机理,从而为这些相对易挥发的无机溶液的蒸气进入冷凝器的壳侧提供了一条途径。这第四篇文章首先提供了简要的文献背景,并为脱锌过程提供了图形证据,并为冷凝器管拆除和重新装管期间收集的样品提供了更详细的实验室分析结果,以支持上述假设。

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