Cengiz Sezgin, Azakli Yunus, Tarakci Mehmet, Stanciu Lia, Gencer Yucel
Department of Materials Science and Engineering, Gebze Technical University, 41400 Gebze, Kocaeli, Turkey; School of Materials Engineering, Purdue University, 701 West Stadium Avenue, West Lafayette, IN, United States.
Department of Materials Science and Engineering, Gebze Technical University, 41400 Gebze, Kocaeli, Turkey.
Mater Sci Eng C Mater Biol Appl. 2017 Aug 1;77:374-383. doi: 10.1016/j.msec.2017.03.230. Epub 2017 Mar 29.
This study is an attempt for gaining a better understanding on relationship between microarc oxidation (MAO) coating discharge types and bioactivity of an oxide-based coating synthesized on a Zr substrate. The discharge types and the coating growth mechanism were identified by the examination of the real cross-section image of the coating microstructure. The coating was conducted by using MAO in an electrolyte containing NaSiO, Ca(CHCOO) and CHNaOP, for different durations of 2.5, 5, 15, and 30mins. The effect of the process duration on the different discharge model types (Type-A, B, and C) and bioactivity of the coatings were investigated by using X-ray Diffractometry (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy-Energy-Dispersive X-ray spectroscopy measurements (SEM-EDS) and Optical Surface Profilometry (OSP). It was found that the increasing MAO duration resulted in thicker and rougher coatings. The XRD data revealed that all the samples prepared at different process durations contained the t-ZrO (tetragonal zirconia) phase. During the MAO process, non-crystalline hydroxyapatite (HA) formed, which was confirmed from the FTIR data. The surface morphology, the amount and distribution of the features of the coating surface were modified by increasing voltage. The simulated body fluid (SBF) tests showed that the more bioactive surface with more HA crystals formed owing to chemical composition and high surface roughness of the coating. The pore, crack and discharge structures played a key role in apatite nucleation and growth, and provided ingrowth of apatite into discharge channels on the coating surface.
本研究旨在更好地理解微弧氧化(MAO)涂层放电类型与在Zr基底上合成的氧化物基涂层生物活性之间的关系。通过检查涂层微观结构的真实横截面图像来确定放电类型和涂层生长机制。在含有NaSiO、Ca(CHCOO)和CHNaOP的电解液中,使用MAO进行不同时长(2.5、5、15和30分钟)的涂层制备。通过X射线衍射仪(XRD)、傅里叶变换红外光谱仪(FTIR)、扫描电子显微镜-能量色散X射线光谱测量仪(SEM-EDS)和光学表面轮廓仪(OSP)研究了处理时长对不同放电模型类型(A型、B型和C型)及涂层生物活性的影响。结果发现,MAO时长增加会导致涂层更厚且更粗糙。XRD数据显示,在不同处理时长下制备的所有样品均含有t-ZrO(四方氧化锆)相。在MAO过程中,形成了非晶态羟基磷灰石(HA),这从FTIR数据中得到了证实。通过增加电压可改变涂层表面的形态、特征的数量和分布。模拟体液(SBF)测试表明,由于涂层的化学成分和高表面粗糙度,形成了具有更多HA晶体的更具生物活性的表面。孔隙、裂纹和放电结构在磷灰石的成核和生长中起关键作用,并使磷灰石在涂层表面的放电通道中向内生长。