欢迎登录材料期刊网

材料期刊网

高级检索

以四硼酸钠为添加剂,Ce(NO3)3-KMnO4为主要成膜剂,室温下在AZ91镁合金表面制备了Ce-Mn转化膜。基于优化的成膜剂浓度比,主要研究了成膜时间对膜层组织和耐蚀性的影响。结果表明转化膜层主要由O、Mg、Al、Mn、Ce等元素组成,随成膜时间延长,膜层不断增厚,且产生裂纹甚至膜层剥落。Ce(NO3)3/KMnO4浓度比较低时成膜速率较慢,膜层中Ce/Mn原子较小,但膜层的电化学性能较优。开路电位随成膜时间延长呈现先急剧增大,后缓慢增加并在2min后趋于平稳的趋势。室温下处理2min即可获得组织致密且耐腐蚀性能较好的转化膜,与基体相比,经配方A和B成膜后的试样,其自腐蚀电流密度由34.099μA/cm2分别下降到0.822和1.367μA/cm2,电阻由0.64kΩ.cm2分别增大到32.01和20.96kΩ.cm2。

Using sodium borate as additive,Ce-Mn chemical conversion coating was prepared on the surface of AZ91 magnesium alloy in Ce(NO3)3 and KMnO4 solution at room temperature.Based on the optimized concentration ratio of Ce(NO3)3/KMnO4,the influence of processing time on the morphology,composition and corrosion resistance was analyzed.The results show that Ce-Mn chemical conversion coating is mainly composed of O,Mg,Al,Mn and Ce elements.With extending processing time,the thickness of Ce-Mn chemical conversion coating was increased,but cracks in the coating appear and the coating even peels off.When the concentration ratio of Ce(NO3)3/KMnO4 was low,the forming rate and the atomic ratio of Ce/Mn of the coating was low while the corrosion resistance was better.The open circuit potential increases sharply during the first minute,and then gradually approaches a constant value.After 2min,it almost maintains steady.The best compact and corrosion resistant coating can be obtained when treating specimens for 2min.Compared with magnesium matrix,the corrosion current density of samples A and B after treating was decrease from 34.099 to 0.822 and 1.367μA/cm2,and the electric resistance was increase from 0.64 to 32.01 and 20.96kΩ·cm2,respectively.

参考文献

[1] 慕伟意,李争显,杜继红,奚正平.镁合金的应用及其表面处理研究进展[J].表面技术,2011(02):86-91.
[2] 苏鸿英.镁合金的应用前景和局限性[J].世界有色金属,2011(02):69.
[3] Amy L. Rudd;Carmel B. Breslin;Florian Mansfeld .The corrosion protection afforded by rare earth conversion coatings applied to magnesium[J].Corrosion Science,2000(2):275-288.
[4] Dabala M.;Brunelli K.;Napolitani E.;Magrini M. .Cerium-based chemical conversion coating on AZ63 magnesium alloy[J].Surface & Coatings Technology,2003(2/3):227-232.
[5] H. Ardelean;C. Fiaud;P. Marcus .Enhanced corrosion resistance of magnesium and its alloys through the formation of cerium (and aluminium) oxide surface films[J].Materials and Corrosion,2001(12):889-895.
[6] M.F. Montemor;A.M. Simoes;M.J. Carmezim .Characterization of rare-earth conversion films formed on the AZ31 magnesium alloy and its relation with corrosion protection[J].Applied Surface Science: A Journal Devoted to the Properties of Interfaces in Relation to the Synthesis and Behaviour of Materials,2007(16):6922-6931.
[7] Lin C S;Fang S K .Formation of cerium conversion coat- ings on AZ31 magnesium alloys[J].Journal of The Elec- trochemical Society,2005,152(02):54-59.
[8] Lu Yanling;Guo Yi;Chen Yankun et al.Influence of He 02 on formation and corrosion protection properties of cerium conversion coatings on AZ91D magnesium alloys[J].Journal of Functional Materials,2011,42(z2):275-279.
[9] Lu Yanling;Guo Yi;Chen Yankun et al.Formation and structure characterization of cerium conversion coatings on AZglD magnesium alloy[J].Journal of Functional Materials,2011,42(z2):218-222.
[10] 李凌杰,雷惊雷,于生海,田钰靖,蒋齐全,潘复生.镁合金铈转化膜的形成及表征[J].中国稀土学报,2007(06):736-740.
[11] 钟丽应,曹发和,施彦彦,文强,张昭,张鉴清.AZ91镁合金表面铈基稀土转化膜的制备及腐蚀电化学行为[J].金属学报,2008(08):979-985.
[12] 张永君,严川伟,王福会.Mg及Mg合金表面稀土转化处理及其耐蚀性研究[J].腐蚀科学与防护技术,2001(z1):467-470.
[13] 许越,陈湘,吕祖舜,李英杰.AZ91镁合金表面稀土转化膜的制备及耐蚀性能研究[J].中国稀土学报,2005(01):40-43.
[14] 杨潇潇;王桂香;董国君 等.AZ31镁合金稀土转化膜及耐蚀性能的研究[J].电镀与环保,2008,28(02):31-34.
[15] R. F. Zheng;C. H. Liang .Conversion coating treatment for AZ91 magnesium alloys by a permanganate-REMS bath[J].Materials and Corrosion,2007(3):193-197.
[16] Umehara H.;Takaya M.;Terauchi S. .Chrome-free surface treatments for magnesium alloy[J].Surface & Coatings Technology,2003(0):666-669.
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%