期刊文献+

金属铀在水气气氛中加速腐蚀的实验研究 被引量:2

Experimental Study on Accelerated Corrosion Uranium-water Vapor by Thermogravimetry
下载PDF
导出
摘要 用热重法研究了铀在50~90℃和32%~86%湿度范围的水气气氛中的加速腐蚀,得到了该实验条件下铀的水气腐蚀特性,并对反应的动力学进行了讨论。结果表明:在不同温度、湿度条件下,铀在水气气氛中的腐蚀动力学过程表现为较为明显的3阶段,动力学过程最后为线性反应阶段,该阶段有一稳定的氧化反应速率常数。RH=74.7%时线性反应的活化能约为42.899kJ·mol-1。温度对反应速率的影响明显,温度升高,反应速率加快。 The experimental study on uranium corrosion was carried out over a range of 50-90°C and 32%-86% relative humidity by thermogravimetry (TG). The corrosion degree of uranium-water vapor reaction was evaluated by weighing sample weight gain at appropriate intervals. Under above experimental conditions, the characteristic of uranium corrosion was observed and its kinetics was also discussed. The results indicate that there are three stages in the uranium-water vapor oxidation reaction at various temperatures. First, there is an initial reaction stage followed by the corrosion rate tends to be slow down after the first corrosion stage. At the third stage, the corrosion reaction presents to be a linear reaction with a stable oxidation reaction rate constant. The dynamics curves on the rear part of linear reaction stage are fitted, and the activation energy deduced is about 42.899 kJ&middotmol-1 at RH = 74.7%. Uranium-water vapor reaction is faster at higher temperatures. The effect of relative humidity on the uranium-water reaction is about the same as that of temperature in the range of 70-90°C, but the further study on the effect of relative humidity below 60°C is necessary.
出处 《原子能科学技术》 EI CAS CSCD 北大核心 2005年第3期226-231,共6页 Atomic Energy Science and Technology
关键词 加速腐蚀 水气 实验研究 气氛 金属铀 动力学过程 反应速率常数 腐蚀特性 实验条件 湿度条件 温度升高 热重法 活化能 线性 Activation energy Atmospheric humidity Corrosion Kinetic theory Steam Thermogravimetric analysis Water
  • 相关文献

参考文献12

  • 1王士杰.铀及铀合金在潮湿气氛中长期贮存的腐蚀和氧的抑制作用[J].特种材料,1985,3:5-21.
  • 2Colmenares AC. Oxidation Mechanism and Catalytic Properties of Actinides[J]. Prog Solid State Chem, 1984,15:257-364.
  • 3Ritchie AG. The Kinetics of the Uranium-oxygen-water Vapor Reaction Between 40 and 100℃[J]. J Nucl Mater, 1986, 139:121-136.
  • 4Ritchie AG. A Review of the Rates of Reaction of Uranium With Oxygen and Water Vapor at Temperature up to 300℃[J]. J Nucl Mater,1981,102: 170-182.
  • 5Ritchie AG, Greenwood RC, Randles SJ, et al.Measurements of the Rate of the Uranium-water Vapor Reaction[J]. J Nucl Mater, 1985, 140:197-201.
  • 6Baker MM, Less LN, Orman S. Uranium and Water Reaction Part I- Kinetics, Products and Mechanism[J]. Trans Faraday Soc, 1966,62:2 513-2 524.
  • 7Baker MM, Less LN, Orman S. Uranium and Water Reaction Part Ⅱ-Effect of Oxygenand Other Gases[J]. Trans Faraday Soc, 1966,62:2 525-2 530.
  • 8Orman JB. The Effect of Certain Gases on the Rate of Oxidation of Uranium by Water Vapor[J]. Chem Ind, 1963,19:1 692-1 693.
  • 9Condon JB, Cristy SS, Kirkpatrick JR. Uranium Reaction With Water Vapor: Y/DU-274 DE83010558 [R]. USA:Lawrence Livermore National Laboratory, 1983.
  • 10汪小琳 傅依备 谢仁寿.金属铀在各种气体环境中的表面氧化反应:CNIC-01037/RIPCE-0003[R].北京:原子能出版社,1996..

同被引文献14

引证文献2

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部