Corrosion of iron: A study for radioactive waste canisters

被引:11
作者
Ben Lagha, S.
Crusset, D.
Mabille, I.
Tran, M.
Bernard, M. C.
Sutter, E.
机构
[1] UPMC, EA349, Lab Genie Proc Plasmas & Traitements Surface, F-75231 Paris 05, France
[2] ANDRA, F-92298 Malabry, France
[3] CNRS, UPR15, UPMC, Lab Interfaces & Syst Electrochim, F-75252 Paris 05, France
关键词
D O I
10.1016/j.jnucmat.2007.01.257
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The purpose of this study is to examine the risks of atmospheric corrosion of steel waste canisters following their deep geological disposal in the temperature range from 303 to 363 K. The work was performed using iron samples deposited as thin films on a quartz crystal microbalance (QCM) and disposed in a climatic chamber. The experiments showed that, in the temperature under study (298-363 K), the mass increase due to the formation of oxide/hydroxide rose sharply above 70% R-H, as is commonly observed at room temperatures, indicating that the phenomenon remains electrochemical in nature. Ex. situ Raman spectrometric analyses indicate the formation of magnetite, maghemite and oxyhydroxides species in the 298-363 K temperature range, and for oxygen contents above 1 vol.%, whereas only Fe3O4 and gamma-Fe2O3 are detected at 363 K. In this work, the kinetics of the rust growth is discussed, on the bases of the rate of mass increase and of the composition of the rust, as a function of the climatic parameters and the oxygen content of the atmosphere. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:485 / 492
页数:8
相关论文
共 14 条
[1]   Experimental in situ studies of copper exposed to humidified air [J].
Aastrup, T ;
Wadsak, M ;
Schreiner, M ;
Leygraf, C .
CORROSION SCIENCE, 2000, 42 (06) :957-967
[2]  
CHIVOT J, 2004, SCI TECHNIQUES SERIE, P4
[3]   THE EVOLUTION OF THE ADSORBED SOLUTION LAYER DURING ATMOSPHERIC CORROSION AND ITS EFFECTS ON THE CORROSION RATE OF COPPER [J].
DANTE, JF ;
KELLY, RG .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1993, 140 (07) :1890-1897
[4]   Influence of metal ions on the transformation of γ-FeOOH into α-FeOOH [J].
Ishikawa, T ;
Minamigawa, M ;
Kandori, K ;
Nakayama, T ;
Tsubota, T .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (09) :B512-B518
[5]   Oxidation of iron in 288°C, oxygen-containing water [J].
Kumai, CS ;
Devine, TM .
CORROSION, 2005, 61 (03) :201-218
[6]   Adsorption of water on copper, nickel, and iron [J].
Lee, S ;
Staehle, RW .
CORROSION, 1997, 53 (01) :33-42
[7]  
LEYGRAF C, 2000, ATMOSPHERIC CORROSIO, P10
[8]   EFFECT OF TEMPERATURE AND DISSOLVED-OXYGEN ON THE CORROSION BEHAVIOR OF CARBON-STEEL IN HIGH-TEMPERATURE WATER [J].
MABUCHI, K ;
HORII, Y ;
TAKAHASHI, H ;
NAGAYAMA, M .
CORROSION, 1991, 47 (07) :500-508
[9]   In situ Raman spectroscopic investigation of aqueous iron corrosion at elevated temperatures and pressures [J].
Maslar, JE ;
Hurst, WS ;
Bowers, WJ ;
Hendricks, JH ;
Aquino, MI .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (07) :2532-2542
[10]   RAMAN-SPECTROSCOPY OF THIN CORROSION FILMS ON IRON AT 100-C TO 150-C IN AIR [J].
OHTSUKA, T ;
KUBO, K ;
SATO, N .
CORROSION, 1986, 42 (08) :476-481