Minhas Badar, Dino Sahib, Zuo Yu, Qian Hongchang, Zhao Xuhui
School of Material Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China.
Institute for Advanced Materials and Technology, University of Science & Technology Beijing, Beijing 100083, China.
Materials (Basel). 2021 Mar 3;14(5):1188. doi: 10.3390/ma14051188.
By anodization and thermal oxidation at 600 °C, an oxide layer on Ti with excellent corrosion resistance in strong acid solutions was prepared. The structural properties of TiO films before and after thermal oxidation were investigated with methods of Scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The electrochemical characterization was recorded via electrochemical impedance spectroscopy, potentiodynamic polarization and Mott-Schottky methods. XRD results show that a duplex rutile/anatase structure formed after oxidation, and the amount of anatase phase increased as the treatment time was prolonged from 3 to 9 h. XPS analysis indicates that as the thermal oxidation time increased, more Ti vacancies were present in the titanium oxide films, with decreased donor concentration. Longer thermal oxidation promoted the formation of hydroxides of titanium on the surface, which is helpful to improve the passive ability of the film. The anodized and thermally oxidized Ti samples showed relatively high corrosion resistance in 4 M HCl and 4 M HSO solutions at 100 ± 5 °C. The passive current density values of the thermally oxidized samples were five orders of magnitude under the testing condition compared with that of the anodized sample. With the oxidation time prolonged, the passive current density decreased further to some extent.
通过在600℃下进行阳极氧化和热氧化,制备了在强酸溶液中具有优异耐腐蚀性的钛氧化物层。采用扫描电子显微镜(SEM)、X射线光电子能谱(XPS)和X射线衍射(XRD)方法研究了热氧化前后TiO薄膜的结构性能。通过电化学阻抗谱、动电位极化和莫特-肖特基方法记录了电化学表征结果。XRD结果表明,氧化后形成了金红石/锐钛矿双相结构,随着处理时间从3小时延长到9小时,锐钛矿相的含量增加。XPS分析表明,随着热氧化时间的增加,氧化钛薄膜中存在更多的钛空位,施主浓度降低。更长时间的热氧化促进了表面钛氢氧化物的形成,这有助于提高薄膜的钝性。阳极氧化和热氧化后的钛样品在100±5℃的4M HCl和4M HSO溶液中表现出相对较高的耐腐蚀性。在测试条件下,热氧化样品的钝化电流密度值比阳极氧化样品低五个数量级。随着氧化时间的延长,钝化电流密度在一定程度上进一步降低。