欢迎登录材料期刊网

材料期刊网

高级检索

以磷酸二氢锰和无氟添加剂为主要成分,通过化学沉积的方法在AZ31镁合金表面获得了均匀且无氟、无镍和无铬的磷化膜。采用硫酸铜点蚀测试、扫描电镜及电化学极化曲线表征手段,详细地研究了成膜温度、游离酸及酸比工艺对AZ31镁合金磷化膜耐蚀性能及表面形貌的影响。结果表明:在成膜温度95℃,游离酸FA4-5,酸比TA/FA15-20的条件下,可获得晶粒〈20μm的致密磷化膜,耐CuS04点蚀时间〉5min。磷化AZ31镁合金的自腐蚀电位比未处理基体正移110mV,自腐蚀电流密度降低3个数量级。成膜温度〈75℃时,不能得到完整的磷化膜;成膜温度≥75℃时,随着成膜温度的升高,磷化膜颗粒得到细化,膜层更加致密,进而有效地抑制AZ31镁合金的阳极溶解和阴极析氢,提高了耐蚀性能。但升高成膜温度,加速磷酸盐的水解,容易产生大量的磷化渣,而游离酸的控制,能够有效减少磷化渣的产生,降低生产成本,提高膜层质量。

A phosphate solution, free of chromate, fluorides and nitrite, was prepared to form the corrosion resistance conversion film on the AZ31 magnesium alloy surface via chemical deposition, and the effects of film- forming temperature and free acid on surface morphology and corrosion resistance of the film were investigated via CuSO4 pitting corrosion test, scanning electron microscopy and potentiodynamic polarization curves. The denser film with grain of 20 μm, whose time of CuSO4 pitting corrosion resistance is longer than 5 rain, is obtained on the following process: film-forming temperature 95 ℃, FA 4--5, ratio of TA/FA 15-20. The Ecorr with the film is shifted positively 110 mV(vs. SCE), the Icorr is decreased approximately by three orders compared with that of the bare substrate AZ31 respectively. The results show also that the existence of the film has a great inhibitive action on anodic dissolution and restraint action on the cathodic hydrogen evolution. The dense film is not obtained when the film-forming temperature is lower than 75 ~C, but increasing with the film-forming temperature, the grain is refiner and the film is denser, which can improve corrosion resistance performance of AZ31 magnesium alloy. Unfortunately, higher film-forming temperature is easy to accelerate hydrolysis of the phosphate and cause plenty of residues phosphide. But the decreasing of residues phosphide can be effectively controlled by controlling the adding amount of the free acid, which further improve quality of the film and decrease the cost.

参考文献

[1] 崔学军,周吉学,王修春.镁合金AZ31表面无铬磷酸盐转化膜的制备、结构及性能[J].中国腐蚀与防护学报,2012(01):13-17.
[2] Cerium conversion coatings for AZ91D magnesium alloy in ethanol solution and its corrosion resistance[J].Corrosion Science: The Journal on Environmental Degradation of Materials and its Control,2009(12):2916.
[3] 刘妍,卫中领,杨富巍,张昭,曹发和,盛慧博.电解液组成对镁合金阳极氧化膜性能的影响[J].中国腐蚀与防护学报,2011(04):255-259.
[4] 曾荣昌,兰自栋,陈君,莫鲜花,韩恩厚.镁合金表面化学转化膜的研究进展[J].中国有色金属学报,2009(03):397-404.
[5] Wanqiu Zhou;Dayong Shan;En-Hou Han;Wei Ke .Structure and formation mechanism of phosphate conversion coating on die-cast AZ91D magnesium alloy[J].Corrosion Science: The Journal on Environmental Degradation of Materials and its Control,2008(2):329-337.
[6] 刘锋,单大勇,韩恩厚,刘常升.钙对镁合金表面锰系转化膜的影响[J].中国有色金属学报,2008(10):1825-1830.
[7] 刘锋,单大勇,曾荣昌,张津,韩恩厚.AZ31变形镁合金锰系转化膜溶液中锰消耗对膜性能的影响[J].腐蚀科学与防护技术,2010(05):377-379.
[8] Ishizaki, T;Shigematsu, I;Saito, N .Anticorrosive magnesium phosphate coating on AZ31 magnesium alloy[J].Surface & Coatings Technology,2009(16):2288-2291.
[9] Mosia?ek, M.;Mordarski, G.;Nowak, P.;Simka, W.;Nawrat, G.;Hanke, M.;Socha, R.P.;Michalska, J. .Phosphate-permanganate conversion coatings on the AZ81 magnesium alloy: SEM, EIS and XPS studies[J].Surface & Coatings Technology,2011(1):51-62.
[10] 曾荣昌,兰自栋.镀液温度对AZ31镁合金表面锌钙系磷酸盐转化膜耐蚀性的影响[J].中国有色金属学报,2010(08):1461-1466.
[11] 张微,文涛.KH-550型硅烷增强处理AZ31镁合金[J].涂料工业,2009(05):63-65.
[12] Guang-Ling Song;ZhenQing Xu .The surface, microstructure and corrosion of magnesium alloy AZ31 sheet[J].Electrochimica Acta,2010(13):4148-4161.
上一张 下一张
上一张 下一张
计量
  • 下载量()
  • 访问量()
文章评分
  • 您的评分:
  • 1
    0%
  • 2
    0%
  • 3
    0%
  • 4
    0%
  • 5
    0%