Issue 41, 2016

Formation mechanism and cytocompatibility of nano-shaped calcium silicate hydrate/calcium titanium silicate/TiO2 composite coatings on titanium

Abstract

Bilayered (HT0.5h and HT1h) and triple-layered (HT2h, HT6h and HT24h) coatings were fabricated on Ti using a hybrid process of microarc oxidation (MAO) and hydrothermal treatment (HT). The bilayered coatings comprise an outer layer of nanofloc Ca(Si1.9Ti0.1)O5 and an inner layer of microporous TiO2. The triple-layered coatings comprise an outer layer of nanoleaf or nanoribbon Ca3Si6O15(H2O)7, a middle layer of nanograined Ca(Si1.9Ti0.1)O5 and an inner layer of microporous TiO2. The hydrothermal formation mechanism of the coatings was explored. The adhesion strength, hydrophilicity and cytocompatibility of selected coatings were investigated. During HT, Ca2+ incorporated into the TiO2 layer migrates out and reacts with SiO32− as well as HTiO3, resulting in the formation of Ca(Si1.9Ti0.1)O5. Ca3Si6O15(H2O)7 nanoleaves nucleate from Ca(Si1.9Ti0.1)O5 preformed on the TiO2 and grow in length and width to nanoribbons at the expense of Ca2+ and SiO32− ions. The nanofloc (HT0.5h and HT1h), nanoleaf (HT2h) and nanoribbon (HT6h) coated surfaces display firm adhesion to substrates and super hydrophilicity. Compared with as-MAOed TiO2, HTed coatings including HT0.5h, HT1h and HT2h enhance the mitochondrial activity, adhesion and proliferation of osteoblasts, and HT2h appears far more effective in accelerating the differentiation of osteoblasts.

Graphical abstract: Formation mechanism and cytocompatibility of nano-shaped calcium silicate hydrate/calcium titanium silicate/TiO2 composite coatings on titanium

Supplementary files

Article information

Article type
Paper
Submitted
08 Jul 2016
Accepted
22 Sep 2016
First published
23 Sep 2016

J. Mater. Chem. B, 2016,4, 6734-6745

Formation mechanism and cytocompatibility of nano-shaped calcium silicate hydrate/calcium titanium silicate/TiO2 composite coatings on titanium

L. Zhang, X. Huang and Y. Han, J. Mater. Chem. B, 2016, 4, 6734 DOI: 10.1039/C6TB01699E

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