Characteristic and in vitro bioactivity of a microarc-oxidized TiO2-based coating after chemical treatment

被引:142
作者
Wei, Daqing [1 ]
Zhou, Yu [1 ]
Jia, Dechang [1 ]
Wang, Yaming [1 ]
机构
[1] Harbin Inst Technol, Inst Adv Ceram, Harbin 150001, Peoples R China
关键词
coating; titanium alloy; biomimetic apatite; microarc oxidation; alkali treatment;
D O I
10.1016/j.actbio.2007.03.001
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Microarc oxidation (MAO) was used to prepare a TiO2-based coating containing Ca and P on titanium alloy. An alkali treatment was developed to modify the surface of the MAO coating to improve the apatite-forming ability of the coating. The chemically treated MAO coating exhibits a modified layer, with the main constituents being 0, Ti, Ca and Na, showing anatase. The modified MAO coating shows a rough and porous morphology containing numerous nanoflakes of similar to 100 nm thickness. During the alkali treatment process, P on the surface of the MAO coating shows a main dynamic process of dissolution; however, Ca exhibits a re-deposition process as well as dissolution. The formation of the modified layer could be explained by this mechanism: negatively charged HTiO3- ions are formed on the MAO coating due to the attack of OH- ions on the TiO2 phase. The HTiO3 ions could incorporate sodium from the alkali solution and calcium from the alkali solution and MAO coating. The apatite-forming ability of the MAO coating is improved remarkably by the simple chemical treatment, since the surface of the alkali-treated MAO coating could provide abundant Ti-OH groups probably formed by ionic exchanges between (Ca2+, Na+) ions of the alkali-treated MAO coating and H3O+ ions of a simulated body fluid (SBF). Moreover, Ca released from the alkali-treated MAO coating increases the degree of supersaturation of SBF, promoting the formation of apatite. The apatite induced by the alkali-treated MAO coating possesses carbonated structure and pore networks on the nanometer scale. (c) 2007 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:817 / 827
页数:11
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