Effect of Cr6+ Concentrations on the Corrosion Behavior of 316LN Stainless Steel in Supercritical Water

Zhenhe Li, Xi Huang, Zixiong Zhan, Qi Zhao, Junxiong Liu, Lihua Wei, Xiaoyan Li
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Abstract

It is well known that the type and concentration of impurity ions in pressurized water reactor environments will significantly alter the corrosion behavior of materials. However, the effect of these water chemistry parameters on the corrosion behavior of candidate materials for future supercritical water-cooled reactor (SCWR) systems is still a lack of understanding. The type and concentration of impurity ions on the corrosion behavior of candidate materials for future supercritical water-cooled reactor (SCWR) systems is still a lack of understanding. In this study, the effect of Cr6+ concentrations on the corrosion behavior of 316LN stainless steel in 550 °C/25 MPa supercritical water (SCW) was investigated. The results show that the weight gain first decreased and subsequently increased with the increasing of Cr6+ concentration, which is 0.40±0.01 mg/cm2 for 0 ppm, 0.28±0.03 mg/cm2 for 0.1 ppm, 0.55±0.02 mg/cm2 for 1.0 ppm, and 0.59±0.01 mg/cm2 for 50 ppm, respectively. The Fe-rich magnetite oxides were gradually covered on the surface of samples, and its proportion on the surface followed a similar alteration trend as the weight gain, which is 44.3% for 0 ppm, 37.8% for 0.1 ppm, 67.7% for 1 ppm, and 87.6% for 50 ppm. A duplex structure of the oxide films, including an Fe-rich outer magnetite layer and a Cr-rich inner spinel layer, was developed on the regions covered with Fe-rich magnetite oxides. The alternation in the thickness of oxide film followed a similar trend as the weight gain, which is 7.67 μm for 0 ppm, 5.80 μm for 0.1 ppm, 9.97 μm for 1 ppm, and 11.23 μm for 50 ppm. However, a Cr-rich spinel oxide film was formed on the region without Ferich magnetite oxides. The thickness of this oxide film was unchanged regardless of Cr6+ ion concentration, which is about 2 μm, but the concentration of Cr in this oxide film is significantly higher than reference sample. These results indicate that the increasing of Cr6+ concentration in SCW will result in the corrosion rate to decrease first and then increase, which means that some measurements should be conducted during the operation of SCWR to keep a lower concentration of Cr6+.
Cr6+浓度对316LN不锈钢在超临界水中腐蚀行为的影响
众所周知,压水堆环境中杂质离子的类型和浓度会显著改变材料的腐蚀行为。然而,这些水化学参数对未来超临界水冷堆(SCWR)系统候选材料腐蚀行为的影响仍然缺乏了解。杂质离子的类型和浓度对未来超临界水冷堆(SCWR)系统候选材料腐蚀行为的影响仍然缺乏认识。研究了不同浓度的Cr6+对316LN不锈钢在550℃/25 MPa超临界水中腐蚀行为的影响。结果表明:随着Cr6+浓度的增加,增重先减小后增大,0 ppm时为0.40±0.01 mg/cm2, 0.1 ppm时为0.28±0.03 mg/cm2, 1.0 ppm时为0.55±0.02 mg/cm2, 50 ppm时为0.59±0.01 mg/cm2。富铁磁铁矿氧化物逐渐覆盖在样品表面,其在样品表面的比例随重量的增加呈变化趋势,0 ppm时为44.3%,0.1 ppm时为37.8%,1 ppm时为67.7%,50 ppm时为87.6%。在富铁磁铁矿氧化物覆盖区域形成富铁外磁铁矿层和富cr内尖晶石层的双相氧化膜结构。氧化膜厚度的变化趋势与增重相似,0 ppm时为7.67 μm, 0.1 ppm时为5.80 μm, 1 ppm时为9.97 μm, 50 ppm时为11.23 μm。而在没有富铁磁铁矿氧化物的区域形成富cr尖晶石氧化膜。无论Cr6+离子浓度如何,氧化膜的厚度基本不变,约为2 μm,但氧化膜中Cr的浓度明显高于参比样品。这些结果表明,随着SCWR中Cr6+浓度的增加,腐蚀速率先降低后增加,因此在SCWR运行过程中应采取措施保持较低的Cr6+浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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