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Modification of electrophoretic deposition of chitosan-bioactive glass-hydroxyapatite nanocomposite coatings for orthopedic applications by changing voltage and deposition time

机译:通过改变电压和沉积时间,改变用于骨科应用的壳聚糖-生物活性玻璃-羟基磷灰石纳米复合涂料的电泳沉积

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摘要

This article presents electrophoretic depositions of chitosan (CS), bioactive glass (BG), and hydroxyapatite (HA) applied on titanium (Ti) substrate from ethanol-based suspension. The strategy was utilized to modify the deposition of particles with different values of sizes and Zeta potentials, and consequently obtain desirable nanocomposite coating. SEM studies showed that uniform distribution of particles was obtained on isolated substrate at pH 4.5. Moreover, modified deposition of BG microparticles (<37 mu m) and HA nanoparticles (<150 nm) in chitosan matrix was reached by changing voltage and deposition time. The results of X-ray diffraction (XRD) revealed a composite with high content of HA was fabricated at pH 4.5, V=20 V, and t=15 min. The deposition mechanism at the initial and final times was significantly related to self-assembly of HA nanoparticles that chelated by cationic macromolecular chains and located on BG microparticles, and CS-coated particulates of HA nanoparticles, respectively. The results of potentiodynamic polarization and electrochemical impedance spectroscopy studies demonstrated that the CS-BG-HA composite coating acts as a bather layer in corrected simulated body fluid (C-SBF). (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
机译:本文介绍了基于乙醇的悬浮液在钛(Ti)基材上应用的壳聚糖(CS),生物活性玻璃(BG)和羟基磷灰石(HA)的电泳沉积。该策略用于修改具有不同大小和Zeta电位值的颗粒的沉积,并因此获得理想的纳米复合涂层。 SEM研究表明,在pH 4.5下在分离的基底上获得了均匀的颗粒分布。此外,通过改变电压和沉积时间,可以在壳聚糖基质中实现BG微粒(<37μm)和HA纳米颗粒(<150 nm)的改良沉积。 X射线衍射(XRD)结果表明,在pH 4.5,V = 20 V和t = 15分钟的条件下,制备了高HA含量的复合材料。初始和最终时间的沉积机理与被阳离子大分子链螯合并分别位于BG微粒和CS涂层的HA纳米颗粒的HA纳米颗粒的自组装显着相关。电位动力学极化和电化学阻抗谱研究的结果表明,CS-BG-HA复合涂层在校正后的模拟体液(C-SBF)中充当隔离层。 (C)2015 Elsevier Ltd和Techna Group S.r.l.版权所有。

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