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Fabrication of thick nanoporous oxide films on stainless steel via DC anodization and subsequent biofunctionalization

机译:通过直流阳极氧化和随后的生物功能化在不锈钢上制备厚的纳米多孔氧化物膜

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Remarkably thick nanoporous anodic films have been formed through simple DC anodization by adding hydrogen peroxide as an oxidant to a sulfuric acid electrolyte. This result was not possible when using the previously reported pulsed polarization technique. While this anodic film's growth was significantly promoted by DC anodization, having only sulfuric acid resulted in the preferential anodic dissolution of the substrate material. Transmission electron microscopy of the anodic film's cross-section confirmed that the film has numerous fine pores with a size distribution ranging from 5 nm to 20 nm. Energy-dispersive x-ray spectroscopic analysis of the anodized specimens revealed that the films were composed of a complex chromium-rich oxide. In addition, coating stainless steel with thick nanoporous oxide films through anodization in the optimized conditions confirmed that it could act as a highly suitable host for synthetic hydroxyapatite coating, resulting in the enhanced growth of natural apatite in a simulated body environment. The enhancement of the apatite deposition is attributed to the availability of the empty pore volume in the thick anodic porous films, formed on stainless steel surfaces. These findings suggest a novel functionality to stainless-steel surface modification. (C) 2016 Elsevier B.V. All rights reserved.
机译:通过将过氧化氢作为氧化剂添加到硫酸电解质中,通过简单的DC阳极氧化就形成了非常厚的纳米多孔阳极膜。当使用先前报道的脉冲极化技术时,此结果是不可能的。尽管该阳极膜的生长通过DC阳极氧化显着促进,但仅使用硫酸会导致基材优先阳极溶解。阳极膜横截面的透射电子显微镜证实,该膜具有许多细孔,其尺寸分布范围为5 nm至20 nm。对阳极氧化后的样品进行能量色散X射线光谱分析,结果表明该膜由复杂的富铬氧化物组成。此外,在最佳条件下通过阳极氧化在不锈钢上涂上厚厚的纳米多孔氧化膜,证实了它可以用作合成羟基磷灰石涂层的非常合适的基质,从而在模拟的人体环境中增强天然磷灰石的生长。磷灰石沉积的增加归因于在不锈钢表面上形成的厚阳极多孔膜中空孔体积的可用性。这些发现表明不锈钢表面改性具有新颖的功能。 (C)2016 Elsevier B.V.保留所有权利。

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