Apatite formation on surface titanate layer with different Na content on Ti metal

被引:29
|
作者
Kawai, Takahiro [1 ]
Kizuki, Takashi [2 ]
Takadama, Hiroaki [2 ]
Matsushita, Tomiharu [2 ]
Unuma, Hidero [1 ]
Nakamura, Takashi [3 ]
Kokubo, Tadashi [2 ]
机构
[1] Yamagata Univ, Grad Sch Sci & Engn, Dept Chem & Chem Engn, Yamagata 9928510, Japan
[2] Chubu Univ, Coll Life & Hlth Sci, Dept Biomed Sci, Aichi 4878501, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Orthopaed Surg, Sakyo Ku, Kyoto 6068507, Japan
关键词
Titanium; Surface ceramic layer; Sodium content; Apatite-forming ability; Scratch resistance; TREATED TITANIUM; NANOTUBES; STABILITY; MECHANISM;
D O I
10.2109/jcersj2.118.19
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
It was early shown that Ti metal spontaneously bonds to living bone through,in apatite layer formed on its surface in the living body, when it was subjected to NaOH and heat treatment to form a sodium titanate on its surface. This kind of bioactive Ti metal was applied to artificial hip joint and already clinically used in Japan. During the study of fabrication process of the hip joint, it was found that sodium content of the surface layer of the Ti metal is largely varied with washing condition after the NaOH treatment, and that apatite-forming ability of the NaOH- and heat-treated Ti metal is liable to decrease in humid environment for a long period. In the present study, the sodium content of the surface layer of the Ti metal was systematically changed by water or HCl treatment after NaOH treatment. Effect of the sodium content of the surface layer on apatite-forming ability in a simulated body fluid and its stability in humid environment of the NaOH- and heat-treated Ti metal were investigated. As a result, it was found that the NaOH- and heat-treated Ti metal gives high and stable apatite-forming ability, when the Ti metal was treated with water after the NaOH treatment to remove partially sodium ions in the surface layer, and subjected to heat treatment. (C)2010 The Ceramic Society of Japan. All rights reserved.
引用
收藏
页码:19 / 24
页数:6
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