Oxidation of tungstate-containing green rust (Cl-) in aqueous solution

被引:3
作者
Shinoda, K. [1 ]
Fujieda, S. [1 ]
Tsuri, S. [2 ]
Suzuki, S. [1 ]
机构
[1] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, Sendai, Miyagi 9808577, Japan
[2] JFE Steel Corp, Steel Res Labs, Tokyo, Japan
来源
MATERIALS AND CORROSION-WERKSTOFFE UND KORROSION | 2012年 / 63卷 / 04期
关键词
green rust; iron oxyhydroxide; tungstate; oxidation; X-ray diffraction; X-ray absorption spectroscopy; IRON OXYHYDROXIDES; CORROSION; TRANSFORMATION; CHLORIDE; COPPER; STEEL; SITU; IONS;
D O I
10.1002/maco.201005922
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The influence of tungstate on the oxidation of green rust [GR(Cl)], which contains both Fe(II) and Fe(III), was investigated by synthesizing suspensions of GR(Cl) containing tungstate and oxidizing them via injection of N2 gas containing O2. XRD and TEM analyses were used for characterizing the solid particles formed during synthesis and oxidation. The results showed that the formation of fine a-FeOOH was enhanced by the addition of tungstate to the GR(Cl) suspensions, while GR(Cl) without tungstate was transformed primarily into ?-FeOOH. The pH, oxidation-reduction potential (ORP), and dissolved oxygen (DO) values of the aqueous solution were measured during oxidation of GR(Cl) with and without tungstate. The results showed that whereas the pH value of the solution was decreased and the ORP value was increased monotonically by oxidation of GR(Cl), the pH and ORP values during oxidation the GR(Cl) suspension containing tungstate revealed characteristic changes with time. XAS was also used for characterizing the chemical state and local structure of tungstate in the oxidized particles. The results indicated that the local structure of WO?42 was essentially retained in the particles precipitated from GR(Cl) suspensions.
引用
收藏
页码:343 / 349
页数:7
相关论文
共 26 条
  • [1] Anodic reaction characteristics of tungsten in basic phosphate solutions
    Anik, Mustafa
    [J]. CORROSION SCIENCE, 2010, 52 (09) : 3109 - 3117
  • [2] Electrochemistry of isopolytungstate mixtures
    Borzenko, M. I.
    Botukhova, G. N.
    Tsirlina, G. A.
    Petrii, O. A.
    [J]. ELECTROCHIMICA ACTA, 2008, 53 (11) : 3854 - 3861
  • [3] Cornell R. M, 2003, IRON OXIDES
  • [4] Inhibitory effect of tungstate, molybdate and nitrite ions on the carbon steel pitting corrosion in alkaline formation water containing Cl- ion
    Deyab, M. A.
    El-Rehim, S. S. Abd
    [J]. ELECTROCHIMICA ACTA, 2007, 53 (04) : 1754 - 1760
  • [5] Synthesis of Fe(II-III) hydroxysulphate green rust by coprecipitation
    Géhin, A
    Ruby, C
    Abdelmoula, M
    Benali, O
    Ghanbaja, J
    Refait, P
    Génin, JMR
    [J]. SOLID STATE SCIENCES, 2002, 4 (01) : 61 - 66
  • [6] Structure and thermodynamics of ferrous, stoichiometric and ferric oxyhydroxycarbonate green rusts; redox flexibility and fougerite mineral
    Genin, Jean-Marie R.
    Ruby, Christian
    Upadhyay, Chandan
    [J]. SOLID STATE SCIENCES, 2006, 8 (11) : 1330 - 1343
  • [7] Anion and cation distributions in Fe(II-III) hydroxysalt green rusts from XRD and Mossbauer analysis (carbonate, chloride, sulphate,...);: the "fougerite" mineral
    Génin, JMR
    Ruby, C
    [J]. SOLID STATE SCIENCES, 2004, 6 (07) : 705 - 718
  • [8] Characteristic behavior of nickel ions during transformation of green rust to ferric oxyhydroxides in aqueous solution
    Inoue, Katsuya
    Shinoda, Kozo
    Suzuki, Shigeru
    Waseda, Yoshio
    [J]. MATERIALS TRANSACTIONS, 2008, 49 (03) : 466 - 470
  • [9] Influence of manganese on iron oxyhydroxides and oxides formed in aqueous solution
    Inoue, Katsuya
    Okui, Masato
    Tanaka, Masahiko
    Shinoda, Kozo
    Suzuki, Shigeru
    Waseda, Yoshio
    [J]. CORROSION SCIENCE, 2008, 50 (03) : 811 - 817
  • [10] Analysis of iron oxyhydroxides and oxides converted from green rust in aqueous solution
    Inoue, Katsuya
    Kwon, Sang-Koo
    Kimijima, Ken'ichi
    Kanie, Kiyoshi
    Muramatsu, Atsushi
    Shinoda, Kozo
    Suzuki, Shigeru
    Waseda, Yoshio
    [J]. ISIJ INTERNATIONAL, 2007, 47 (03) : 453 - 457