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硝酸介质中铀矿冶设备表面放射性污染的规律 被引量:2

Radioactive Contamination Behaviors on Surface of Uranium Mining Industry in Nitric Acid Medium
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摘要 为了掌握铀矿冶生产实践中常用设备材质经放射性污染后表面活度的变化规律,研究了不锈钢、有机玻璃、橡胶3种材质经不同浓度的硝酸铀酰溶液连续浸泡26d后,样品表面活度、表面形貌及铀的存在形式等变化特征。结果表明:在26d内,当铀溶液质量浓度为10.22mg/L时,3种材质表面活度随浸泡时间增加变化不显著,当溶液铀质量浓度分别为563.58mg/L、25.54g/L时,各材质表面活度值均随浸泡时间增加逐渐增大。此外,3种材质表面活度从大到小依次是橡胶>不锈钢>有机玻璃。样品表面活度的增加主要是由于样品被腐蚀,导致铀在样品表面的附着沉积引起,并且表面的铀主要以UO2(NO3)2·6H2O及少量UO3的形式存在。 In order to master the rule of surface activity of radioactively contaminated materials commonly used in uranium mining and metallurgy, the characteristics of surface activity, surface morphology and the form of uranium were studied with stainless steel, plexiglass and rubber soaked in different uranium nitrate milling concentrations solution for 26 days. The results show that the surface activities of three kinds of materials do not change significantly over time as the mass concentration of uranium solution is 10.22 mg/L;the surface activity value of each material increases gradually over time, as the uranium mass concentrations are 563.58 mg/L and 25.54 g/L, within 26 days. In addition, the contamination degree of three kinds of materials from large to small in the order is rubber, stainless steel and plexiglass. The increase of activity on the surface of the sample is mainly due to the corrosion of samples, which leads to the deposition of uranium on the surface of the sample. The forms of uranium on the sample surface are mainly UO2(NO3)2 ·6H2O and a small amount of UO3.
作者 刘宇 王清良 王红强 胡鄂明 苟浩然 LIU Yu;WANG Qing-liang;WANG Hong-qiang;HU E-ming;GOU Hao-ran(School of Resource Environment and Safety Engineering,University of South China,Hengyang 421001,China)
出处 《核化学与放射化学》 CAS CSCD 北大核心 2019年第3期304-310,共7页 Journal of Nuclear and Radiochemistry
基金 湖南省自然科学基金资助项目(2017JJ4010)
关键词 表面活度 污染规律 uranium surface activity contamination rule
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  • 1谭昭怡,孙宇,李烨,曾俊辉,张东.^(241)Am火警源生产线退役中金属去污实践[J].环境工程,2009,27(S1):375-378. 被引量:1
  • 2唐任寰 刘元方 张青莲.锕系一锕系后元素[M].北京:科学出版社,1998.173.
  • 3Ogura K, Sato K. Cathodic dissolution of the passive film on iron- I . Kinetics and mechanism [J]. Electrochimica Acta , 1979,25:857-862.
  • 4Lorbeer P, Lorenz W J. The kinetics of iron dissolution and passivation in solutions containing oxygen [J]. Electrochimica Acta , 1979,25:375 -381.
  • 5Videm K, Koren A M. Corroison, passivity, and pitting of carbon steel in aqueous solutions of HCO^3- ,C02,and Cl^- [J]. Corrosion Science, 1993,49(9) :746 - 754.
  • 6Engelhardt J, Marx G. Contact corrosion measurements on the pair U02 +x and carbon steel 1. 0330 in brines and bentonite porewater with respect to direct waste disposal [J]. J Nuclear Materials, 1999,264:161 - 168.
  • 7Man-Sung Yim.Radiation dose management in nuclear power plants[J].Progress in Nuclear Energy,2001,39(1):31-51.
  • 8欧洲原子能共同体主编.核设施退役手册(1995)[M].吴春喜等译.北京:核科学技术情报研究所,1998.129.
  • 9Manion W J,Laguardia T S.Decommissioning Handbook[M].US:America DOE,1980.67-73.
  • 10马鹏勋,张涛革,武明亮,张玉霞.Ce(Ⅳ)/HNO_3去污技术工程应用安全性的初步研究[J].辐射防护,2007,27(6):329-335. 被引量:4

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