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采用扫描电镜、X光电子能谱、失重法和电化学交流阻抗技术研究了铝合金7A04在0.6 mol/L NaCl溶液和0.6 mol/LNaCl+0.02mol/L NaHSO3溶液中干湿周浸后的腐蚀行为和规律,并测试了3种材料力学性能的变化.研究结果表明,随试验时间的延长,铝合金腐蚀产物不断增多,腐蚀失重符合指数规律C=A tn,抗拉强度和延伸率呈下降趋势;表面腐蚀产物形貌呈块状,在0.6 mol/L NaCl溶液中腐蚀产物主要为氢氧化铝和氯化铝,而在0.6 mol/LNaCl+0.02 mol/LNaHSO3溶液中腐蚀产物主要为氢氧化铝、氯化铝和硫酸铝.电化学交流阻抗谱显示铝合金7A04在0.6 mol/L NaCI+0.02 mol/0L NaHSO3溶液中的腐蚀速率远大于在0.6 mol/L NaCl溶液的腐蚀速率,并探讨了其腐蚀机理.

The corrosion behavior of aluminum alloy 7A04 under cyclic wet-dry immersion conditions was investigated in 0.6 mol/L sodium chloride solution and 0.6 mol/L sodium chloride+F0.02 mol/L sodium sulfite solution by Scanning electron microscopy (SEM),energy dispersive X-ray detection (EDS),X-ray photoelectron spectroscopy (XPS),mass loss method,mechanical capability test and electrochemical impedance spectroscopy (EIS).The results showed that the mass loss increases with corrosion time prolonging,and according with the rule as C=Atn,strength and elongation percentage are declining.Surface observation revealed that corrosion product is agglomerated and accidented.The corrosion products are AI(OH)3 and aluminum chloride in 0.6 mol/L sodium chloride solution,and Al(OH)3,aluminum sulfate and chloride in 0.6 mol/L sodium chloride and 0.02 mol/L sodium anlfite solution.The EIS results indicated that corrosion rate in 0.6 mol/L sodium chloride and 0.02 mol/Lsodium sulfite solution is higher than that in 0.6 mol/L sodium chloride solution.The corrosion reaction mechanism was discussed.

参考文献

[1] Andreatta F;Terryn H;Wit J H W .[J].Electrochimica Acta,2004,49:2851.
[2] Panossian Z;Mariaca L;Morcillo M et al.[J].Surface and Coatings Technology,2005,190:225.
[3] Lobnig RE.;Maisono J.;Grundmeier G.;Streckel H. Frankenthal RP.;Stratmann M.;Sinclair JD.;Siconolfi DJ. .ATMOSPHERIC CORROSION OF ALUMINUM IN THE PRESENCE OF AMMONIUM SULFATE PARTICLES[J].Journal of the Electrochemical Society,1996(4):1175-1182.
[4] Gonzalez JA.;Morcillo M.;Escudero E.;Lopez V.;Otero E. .Atmospheric corrosion of bare and anodized aluminium in a wide range of environmental conditions. Part I: Visual observations and gravimetric results[J].Surface & Coatings Technology,2002(2/3):225-234.
[5] López V;González J A;Otero E et al.[J].Surface and Coatings Technology,2002,153:235.
[6] Blucher D B;Lindstrom R;Svensson J E et al.[J].Journal of the Electrochemical Society,2001,148:B127.
[7] EL-Mahdy G A;Nishikata A;Tsuru T .[J].Corrosion Science,2000,42:1509.
[8] Nishikata A;Yamashita Y;Katayama H et al.[J].Corrosion Science,1995,37:2059.
[9] Yadav A P;Nishikata A;Tsuru T .[J].Corrosion Science,2004,46:361.
[10] Dillmann P H;Heerié S;Mazaudier F et al.[J].Corrosion Science,2004,46:1401.
[11] Hoerlé S;Mazaudier F;Dillmann P H et al.[J].Corrosion Science,2004,46:1431.
[12] EL-Mahdy GA;Kim K B .[J].Electrochimica Acta,2004,49:1937.
[13] Wang Z Y;Ma T;Han W .[J].Journal of Chinese Society for Corrosion and Protection,2005,25:321.
[14] Cao F H;Cheng Y L;Zhaag Z.[J].The Chinese Journal of Nonferrous Metals,2002(12):245.
[15] Cao F H;Zhang Z;Li J F et al.[J].The Chinese Journal of Nonferrous Metals,2004,14:619.
[16] Graedel T E .[J].Journal of the Electrochemical Society,1989,136:204.
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