Surface characterization, shear strength, and bioactivity of anodized titanium prepared in mixed-acid electrolytes

被引:17
|
作者
Jain, Sakshi [1 ]
Williamson, R. Scott [1 ]
Roach, Michael D. [1 ]
机构
[1] Univ Mississippi, Med Ctr, Biomed Mat Sci, Jackson, MS 39216 USA
来源
关键词
Bioactivity; Titanium; Anodization; Apatite; Anatase; Rutile; COMMERCIALLY PURE TITANIUM; BOND STRENGTH; OXIDE FILMS; ANODIZATION; OXIDATION; TI6AL4V; ANATASE; LAYERS; METAL;
D O I
10.1016/j.surfcoat.2017.07.010
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The present study focused on evaluation of anodized oxides prepared in four mixed acid electrolytes with and without phosphoric acid as a function of forming voltage. Specifically the oxide surface characteristics, the mechanical integrity, and the bioactive performance were evaluated for a range of forming voltages in each electrolyte. Surface analyses showed phosphorus incorporation into the oxide layer started at localized areas after a threshold forming voltage, but became more uniform at higher voltages. Oxide crystallinity and thickness were retarded by the phosphoric acid levels present in the anodization electrolytes. Surface roughness was shown to be electrolyte dependent as a function of forming voltage, and in general was shown to increase with increasing voltage. Samples anodized up to a forming voltage of 144 V did not show any oxide failure through shear strength testing with only epoxy delamination for three of the electrolytes. At 180 V, the oxide layers showed failure or partial failure at approximately 30-35 MPa, which is stronger than many values previously reported for anodized coatings in the literature. Additionally, oxide films prepared in phosphoric acid containing electrolytes showed greater bioactivity through enhanced apatite formation. These anodized coatings exhibiting enhanced bioactivity show promise for promoting faster osseointegration while providing better implant stability due to the superior coating adhesion strengths. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:594 / 603
页数:10
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