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Volume 36 Issue 3
Jul.  2021
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Article Contents
CUI Zhong-yu, XIAO Kui, DONG Chao-fang, CUI Tian-yu, LI Xiao-gang. Long-term corrosion behavior of AZ31 magnesium alloy in Xisha marine atmosphere[J]. Chinese Journal of Engineering, 2014, 36(3): 339-344. doi: 10.13374/j.issn1001-053x.2014.03.010
Citation: CUI Zhong-yu, XIAO Kui, DONG Chao-fang, CUI Tian-yu, LI Xiao-gang. Long-term corrosion behavior of AZ31 magnesium alloy in Xisha marine atmosphere[J]. Chinese Journal of Engineering, 2014, 36(3): 339-344. doi: 10.13374/j.issn1001-053x.2014.03.010

Long-term corrosion behavior of AZ31 magnesium alloy in Xisha marine atmosphere

doi: 10.13374/j.issn1001-053x.2014.03.010
  • Received Date: 2012-12-30
    Available Online: 2021-07-10
  • By field exposure test, atmospheric corrosion tests of AZ31 magnesium alloy were conducted in Xisha Islands for 4 a. The surface and cross-section morphologies of corrosion products as well as the corrosion morphologies of the alloy after removing corro-sion products were observed by scanning electron microscopy. Energy dispersive X-ray spectroscopy and X-ray diffraction analysis were used to obtain the element content and phase composition of corrosion products. The results indicate that the alloy undergoes severe corrosion. The average corrosion rate is 11.95μm·a-1. Cl- and CO2 play important roles in the corrosion process. The Cl-—containing absorbed electrolyte layers will destroy the oxidation film and induce anodic dissolution of the alloy. While CO2 dissolved in the absorbed electrolyte layers tends to neutralize the alkali formed in the cathodic area and reacts with Mg (OH) 2 to form Mg5(CO3)4(OH)2·xH2O. The surface corrosion products restrict the transport of CO2 and Cl- to the surface of the alloy, so the inner layer of corrosion products is mainly composed of Mg(OH) 2.

     

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