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Deposition Kinetics of Bioinspired Phenolic Coatings on Titanium Surfaces

机译:钛表面生物启发型酚醛涂层的沉积动力学

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摘要

Polyphenols can form functional coatings on a variety of different materials through auto-oxidative surface polymerization in a manner similar to polydopamine coatings. However, the mechanisms behind the coating deposition are poorly understood. We report the coating deposition kinetics of the polyphenol tannic acid (TA) and the simple phenolic compound pyrogallol (PG) on titanium surfaces. The coating deposition was followed in real time over a period of 24 h using a quartz crystal microbalance with dissipation monitoring (QCM-D). TA coatings revealed a multiphasic layer formation: the deposition of an initial rigid layer was followed by the buildup of an increasingly dissipative layer, before mass adsorption stopped after approximately 5 h of coating time. The PG deposition was biphasic, starting with the adsorption of a nonrigid viscoelastic layer which was followed by layer stiffening upon further mass adsorption. Coating evaluation by ellipsometry and AFM confirmed the deposition kinetics determined by QCM-D and revealed maximum coating thicknesses of approximately 50 and 75 nm for TA and PG, respectively. Chemical characterization of the coatings and polymerized polyphenol particles indicated the involvement of both physical and chemical interactions in the auto-oxidation reactions.
机译:多酚可以通过自动氧化表面聚合,以类似于聚多巴胺涂料的方式,在多种不同的材料上形成功能性涂料。但是,对涂层沉积背后的机理了解甚少。我们报告了钛表面上多酚鞣酸(TA)和简单酚类化合物邻苯三酚(PG)的涂层沉积动力学。使用带有耗散监测(QCM-D)的石英晶体微天平,在24小时内实时跟踪涂层沉积。 TA涂层显示出多相层的形成:初始刚性层的沉积之后,是逐渐耗散的层的堆积,在约5小时的涂覆时间后质量吸附停止。 PG的沉积是两相的,首先是吸附非刚性粘弹性层,然后是在进一步吸附质量时变硬。通过椭圆光度法和原子力显微镜的涂层评估证实了由QCM-D确定的沉积动力学,并揭示了TA和PG的最大涂层厚度分别约为50和75 nm。涂层和聚合的多酚颗粒的化学表征表明,物理和化学相互作用都参与了自动氧化反应。

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