...
首页> 外文期刊>Surface and Interface Analysis: SIA: An International Journal Devoted to the Development and Application of Techniques for the Analysis of Surfaces, Interfaces and Thin Films >Chemical composition and structural changes of porous templates obtained by anodising aluminium in phosphoric acid electrolyte
【24h】

Chemical composition and structural changes of porous templates obtained by anodising aluminium in phosphoric acid electrolyte

机译:铝在磷酸电解质中阳极氧化制得的多孔模板的化学组成和结构变化

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Ordered anodic aluminium oxide (AAO) films were first prepared by anodising in a phosphoric acid electrolyte and then studied extensively and characterised by field emission gun-scanning electron microscopy (FEG-SEM), X-ray diffraction, Raman and infrared spectroscopy at a macroscopic scale. These analyses showed that the as-prepared AAO film is in fact amorphous, partially hydrated and that its initial global chemical composition can be described, in agreement with previous works, as: Al2O3, 0.186AlPO(4)center dot 0.005H(2)O. Additional analyses (thermogravimetric analysis, differential thermal analysis and FEG-SEM) showed geometrical changes of the film structure at different scales, explained by various steps of dehydration and allotropic transformations of the resulting crystallised alumina. However, because their structure remains unchanged up to 900 degrees C, the phosphoric templates appear to be particularly suitable for applications or processes at medium or high temperatures, such as the preparation of carbon nanotubes or oxide rods. Copyright
机译:首先通过在磷酸电解质中进行阳极氧化来制备有序的阳极氧化铝(AAO)膜,然后进行了广泛的研究,并通过宏观的场发射枪扫描电子显微镜(FEG-SEM),X射线衍射,拉曼光谱和红外光谱进行了表征规模。这些分析表明,所制备的AAO膜实际上是无定形的,部分水合的,并且其初始整体化学组成可以与以前的作品相描述为:Al2O3、0.186AlPO(4)中心点0.005H(2)哦额外的分析(热重分析,差热分析和FEG-SEM)显示了膜结构在不同尺度上的几何变化,这可以通过脱水和结晶结晶氧化铝的同素异形转变的各个步骤来解释。但是,由于其结构在900摄氏度以下仍保持不变,因此磷模板似乎特别适用于中温或高温下的应用或过程,例如碳纳米管或氧化棒的制备。版权

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号