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Applications of carbonic acid solution for developing conversion coatings on Mg alloy 被引量:6

Applications of carbonic acid solution for developing conversion coatings on Mg alloy
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摘要 Works on exploring an environmentally clean method for producing an Mg,Al-hydrotalcite(Mg6Al2(OH) 16CO3·4H2O) layer and/or calcium carbonate(CaCO3) layer on Mg alloy in a carbonic acid solution system(aqueous HCO3-/CO3 2-or Ca 2+ /HCO3-) at 50℃ were reviewed.Conversion treatment for the Mg,Al-hydrotalcite conversion coating was as follows.Mg alloy was treated first in acidic HCO3-/CO3 2-aqueous for precursor layer formation on Mg alloy surface and then in alkaline HCO3-/CO3 2-aqueous to form a crystallized Mg,Al-hydrotalcite coating.Duration of an Mg,Al-hydrotalcite coating on Mg alloy surface was reduced from 12 h to 4 h by the conversion treatment.On the other hand,for reducing the formation time of CaCO3 coating on Mg alloy,the aqueous Ca 2+ /HCO3-with a saturated Ca 2+ content was employed for developing a CaCO3 coating on Mg alloy.A dense CaCO3 coating could yield on Mg alloy surface in 2 h.Corrosion rate(corrosion current density,Jcorr) of the Mg,Al-hydrotalcite-coated sample and CaCO3-coated AZ91D sample was 7-10μA/cm 2,roughly two orders less than the Jcorr of the as-diecast sample(about 200μA/cm 2) . No corrosion spot on the Mg,Al-hydrotalcite-coated sample and CaCO3-coated sample was observed after 72 h and 192 h salt spray test,respectively. Works on exploring an environmentally clean method for producing an Mg,Al-hydrotalcite (Mg6Al2(OH)16CO3·4H2O) layer and/or calcium carbonate (CaCO3) layer on Mg alloy in a carbonic acid solution system (aqueous HCO3^- /CO3^2- or Ca^2+/HCO3^-) at 50 ℃ were reviewed. Conversion treatment for the Mg,Al-hydrotalcite conversion coating was as follows. Mg alloy was treated first in acidic HCO3^- /CO3^2- aqueous for precursor layer formation on Mg alloy surface and then in alkaline HCO3^-/CO3^2- aqueous to form a crystallized Mg,Al-hydrotalcite coating. Duration of an Mg,Al-hydrotalcite coating on Mg alloy surface was reduced from 12 h to 4 h by the conversion treatment. On the other hand, for reducing the formation time of CaCO3 coating on Mg alloy, the aqueous Ca^2+/HCO3^- with a saturated Ca^2+ content was employed for developing a CaCO3 coating on Mg alloy. A dense CaCO3 coating could yield on Mg alloy surface in 2 h. Corrosion rate (corrosion current density, Jcorr) of the Mg,Al-hydrotalcite-coated sample and CaCO3-coated AZ91D sample was 7-10 μA/cm^2, roughly two orders less than the Jcorr of the as-diecast sample (about 200 μA/cm^2). No corrosion spot on the Mg,Al-hydrotalcite-coated sample and CaCO3-coated sample was observed after 72 h and 192 h salt spray test, respectively.
出处 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2010年第7期1331-1339,共9页 中国有色金属学报(英文版)
基金 Project supported by the Ministry of Education Under the ATU Plan
关键词 碳酸钙 镁合金 应用程序开发 转化膜 镁铝水滑石 腐蚀电流密度 CACO3 碳酸氢根 Mg alloy AZ91D alloy corrosion conversion coating carbonic acid
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