模拟体液
X射线光电子能谱
材料科学
生物活性玻璃
微晶
磷灰石
无定形固体
结晶
扫描电子显微镜
化学工程
微观结构
退火(玻璃)
能量色散X射线光谱学
复合材料
结晶学
化学
冶金
工程类
作者
N. C. Köseoğlu,Aligül Büyükaksoy,Zehra Banu Bahşi Oral,Muhammed Hasan Aslan
标识
DOI:10.1002/adem.200900034
摘要
Abstract Hydroxyapatite (HA) and HA/bioactive glass (49S) films were deposited on Si(100) substrates by a sol–gel dip‐coating method. The microstructure and in vitro bioactivity of the films were investigated by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and X‐ray photoelectron spectroscopy (XPS). Polycrystalline HA and amorphous bioactive glass films were obtained after annealing at 600 and 400 °C, respectively. The crystallization temperature of HA was determined to be around 568 °C. The surfaces of the HA films were covered with an apatite layer consists of spherulites formed by nanosized needle‐like aggregates after the soaking in simulated body fluid (SBF) for 10 days, while amorphous HA/bioactive glass surface was covered with larger spherical crystallites. Both XPS and EDS results obtained from HA/bioactive glass film, after soaking in SBF, showed increasing P amounts on the surface at the expense of Si. The higher density of the newly formed layer on HA/bioactive glass surface than that of the HA surface after 10 days of soaking was evidence of increased reaction rate and apatite forming ability when bioactive glass layer is present on the HA films.
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