Electrodeposition of Zn-Mn alloys on steel using an alkaline pyrophosphate-based electrolytic bath

被引:58
作者
Sylla, D [1 ]
Savall, C [1 ]
Gadouleau, M [1 ]
Rebere, C [1 ]
Creus, J [1 ]
Refait, P [1 ]
机构
[1] Univ Rochelle, Lab Etud Mat Milieux Agress, Pole Sci & Technol, F-17042 La Rochelle 01, France
关键词
plating; zinc alloy; manganese; scanning electron microscopy; X-ray diffraction;
D O I
10.1016/j.surfcoat.2004.11.020
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Electrodeposited coatings of zinc are commonly used to protect carbon steels from corrosion. However, this protection is not acceptable under severe atmospheric conditions and various alternative materials are investigated. Among those materials are the Zn-Mn alloys, which seem to display both improved corrosion resistance and environmental compatibility. The electrodeposition of Zn-Mn alloys from an alkaline bath was achieved for the first time. The bath consisted of dissolved (MnSO4)-S-II and (ZnSO4)-S-II in a pyrophosphate+hydroxylamine matrix. Pyrophosphate was used as a necessary complexing agent to avoid the precipitation of Mn(II) and Zn(II) hydroxides whereas hydroxylamine was added to prevent oxidation of dissolved Mn(II) species by O-2. The effects of the Zn(II)/Mn(II) ratio were studied, allowing to determine the optimal conditions for the electrodeposition. The redox processes involving Zn(II), Mn(II), and the components of the bath were studied by cyclic voltammetry. The potentiostatically electrodeposited Zn-Mn films were finally investigated by means of scanning electron microscopy, energy dispersive X-ray spectrometry, and X-ray diffraction. They presented a cauliflower morphology and a Mn content up to similar to 25 at.%. They were monophasic, constituted of the metastable epsilon-ZnMn phase, or biphasic epsilon-ZrMn+Zn (eta) depending on the Mn content. The use of a commercial additive improved appreciably the appearance of the deposits and induced the formation of the stable gamma-ZnMn phase. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:2137 / 2145
页数:9
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