Fabrication and characterization of microarc oxidation films on Ti-39Nb-6Zr alloy at different voltages in KOH electrolyte

被引:23
|
作者
Chen, Lin [1 ,2 ]
Qu, Yao [1 ,2 ]
Wei, Kejian [1 ,2 ]
Jin, Xiaoyue [1 ,2 ]
Liao, Bin [1 ,2 ]
Xue, Wenbin [1 ,2 ]
机构
[1] Beijing Normal Univ, Coll Nucl Sci & Technol, Key Lab Beam Technol & Mat Modificat, Minist Educ, Beijing 100875, Peoples R China
[2] Beijing Radiat Ctr, Beijing 100875, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Ti-39Nb-6Zr alloy; Microarc oxidation; TiO2/Nb2O5/ZrO2 ceramic films; Corrosion resistance; IMPEDANCE SPECTROSCOPY; TI-6AL-4V ALLOY; TITANIUM-ALLOYS; ARC OXIDATION; COATINGS; RESISTANCE; ALUMINUM; ANATASE; TIO2;
D O I
10.1016/j.jallcom.2017.07.008
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The TiO2/Nb2O5/ZrO2 ceramic films were successfully prepared on Ti-39Nb-6Zr alloy by microarc oxidation (MAO) at different voltages in KOH electrolyte. Their morphology, phase structure and composition were characterized by scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). Their conducting properties were analyzed by impedance spectroscopy and Mott-Schottky test. Meanwhile, their corrosion behaviors were evaluated by electrochemical impedance spectroscopy (EIS). The MAO films as n-type materials were 8 mu m-15.8 mu m thick with fine micropores on the surface. These films consisted of anatase TiO2, rutile TiO2, Nb2O5, monoclinic ZrO2 (m-ZrO2) and ZrTiO4 phases. Their conductivity gradually increased with the frequency from 4.07 x 10(-15) S cm(-1) at 0.01 Hz to 1.61 x 10(-6) S cm(-1) at 10(7) Hz. Their flat band potential was in the range of 0.34 V-0.77 V, and doping density varied between 3.50 x 10(17) cm(-3) and 5.25 x 10(18) cm(-3) which decreased with increasing positive voltage of MAO process. The Ti-39Nb-6Zr alloy coated at +400 V/-60 V had good corrosion resistance with lower corrosion current density and higher impedance. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:1158 / 1165
页数:8
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