首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >CeO2-modified Au/TiO2 catalysts with outstanding stability under harsh CO oxidation conditions
【24h】

CeO2-modified Au/TiO2 catalysts with outstanding stability under harsh CO oxidation conditions

机译:CeO2改性的Au / TiO2催化剂在苛刻的CO氧化条件下具有出色的稳定性

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

The 1.5 wt% Au/TiO2 World Gold Council catalyst (WGC) was modified by depositing on its surface a 5:4 wt% CeO2 loading by incipient wetness impregnation. Calcination at 673 K of the resulting, surface modified, catalyst yielded a material in which the system of gold particles was not significantly modified with respect to that of the starting 1.5% Au/TiO2 WGC catalyst, neither in terms of its size distribution or metallic dispersion. The latter parameter remained, as in the catalyst prior to CeO2 deposition, in a value about 36%. Both catalysts, Au(1.5%)/TiO2 WGC and Ce02(5.4%)/Au(1.5%)/TiO2, were tested in consecutive CO oxidation reaction loops at increasing final temperatures. In these cycles, the ceria-modified catalyst showed notonly a higher activity but, more importantly, a largely enhanced stability against deactivation. Scanning Transmission Electron Microscopy (STEM) studies clearly revealed the presence of nanometersized ceria rafts, less than 1 nm thick, on the surface of the fresh CeO2(5.4%)/Au(1.5%)/TiO2 catalysts. After the CO oxidation test at the highest temperature, 1223 K, the WGC catalyst suffered from a very severe Au nanoparticle sintering whereas Au nanoparticle growth was very much limited in the ceria-modified catalyst after the same aging test. STEM results reveal that a major fraction of the Au nanoparticles (75%), comprising all the smaller ones (<5 nm), was contacting the ceria phase. This evidences an important stabilizing effect of the proposed surface modification. Moreover, these results open up possibilities for gold catalysts in applications where high temperatures are reached under working conditions. (C) 2016 Elsevier B.V. All rights reserved.
机译:通过初湿浸渍通过在其表面上沉积5:4 wt%的CeO2负载量来改性1.5 wt%的Au / TiO2世界黄金协会催化剂(WGC)。所得的表面改性催化剂在673 K下煅烧,得到的材料中,金颗粒体系相对于起始的1.5%Au / TiO2 WGC催化剂而言,没有明显的改性,无论是从粒度分布还是金属方面分散。如在CeO 2沉积之前的催化剂中,后一个参数保持为约36%的值。两种催化剂Au(1.5%)/ TiO2 WGC和Ce02(5.4%)/ Au(1.5%)/ TiO2在连续的CO氧化反应回路中以升高的最终温度进行了测试。在这些循环中,二氧化铈改性的催化剂不仅显示出较高的活性,而且更重要地,显示出对失活的稳定性大大提高。扫描透射电子显微镜(STEM)研究清楚地表明,在新鲜的CeO2(5.4%)/ Au(1.5%)/ TiO2催化剂表面上存在小于1 nm厚的纳米级氧化铈筏。在最高温度1223 K的CO氧化测试后,WGC催化剂遭受非常严重的Au纳米粒子烧结,而在相同的老化测试后,二氧化铈改性的催化剂中Au纳米粒子的生长受到很大限制。 STEM结果显示,包括所有较小的Au纳米颗粒(<5 nm)的大部分(75%)与二氧化铈相接触。这证明了所提出的表面改性的重要稳定作用。此外,这些结果为金催化剂在工作条件下达到高温的应用提供了可能性。 (C)2016 Elsevier B.V.保留所有权利。

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