Comparison of plasma electrolytic oxidation of zirconium alloy in silicate- and aluminate-based electrolytes and wear properties of the resulting coatings
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作者:
Cheng, Yingliang
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Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R ChinaHunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
Cheng, Yingliang
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Wu, Fan
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Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R ChinaHunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
Wu, Fan
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Dong, Jiali
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Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R ChinaHunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
Dong, Jiali
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Wu, Xiangquan
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Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R ChinaHunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
Wu, Xiangquan
[1
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Xue, Zhigang
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Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R ChinaHunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
Xue, Zhigang
[1
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Matykina, E.
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Univ Complutense Madrid, Fac Ciencias Quim, Dept Ciencia Mat & Ingn Met, E-28040 Madrid, SpainHunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
Matykina, E.
[2
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Skeldon, P.
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Univ Manchester, Sch Mat, Ctr Corros & Protect, Manchester M13 9PL, Lancs, EnglandHunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
Skeldon, P.
[3
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Thompson, G. E.
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Univ Manchester, Sch Mat, Ctr Corros & Protect, Manchester M13 9PL, Lancs, EnglandHunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
Thompson, G. E.
[3
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机构:
[1] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
[2] Univ Complutense Madrid, Fac Ciencias Quim, Dept Ciencia Mat & Ingn Met, E-28040 Madrid, Spain
[3] Univ Manchester, Sch Mat, Ctr Corros & Protect, Manchester M13 9PL, Lancs, England
Plasma electrolytic oxidation of Zircaloy-2 at constant rms current is examined in silicate and aluminate electrolytes, revealing significantly different behaviors in the growth kinetics and properties of the coatings. Coatings thicken continuously in the silicate electrolyte, while in the aluminate electrolyte, the thickness reaches a relatively constant value. The latter coincides with changing appearances of discharges and detachment of an outer coating layer. Dissolution of zirconium is faster in the silicate electrolyte in the early stage of PEO, but is faster in the aluminate electrolyte following coating breakdown. The pre-spallation coating formed in the aluminate electrolyte shows superior wear resistance, which can be ascribed to its relative compactness, associated with the presence of tetragonal zirconia stabilized by aluminium species. (C) 2012 Elsevier Ltd. All rights reserved.