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CeO_2-promoted Ni/activated carbon catalysts for the water-gas shift (WGS) reaction

机译:CeO_2促进的Ni /活性炭催化剂用于水煤气变换(WGS)反应

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摘要

The low temperature water-gas shift (WGS) reaction has been studied over carbon-supported nickel catalysts promoted by ceria. To this end, cerium oxide has been dispersed (at different loadings: 10, 20, 30 and 40 wt.%) on the activated carbon surface with the aim of obtaining small ceria particles and a highly available surface area. Furthermore, carbon- and ceria-supported nickel catalysts have also been studied as . A combination of N_2 adsorption analysis, powder X-ray diffraction, temperature-programmed reduction with H_2, X-ray photoelectron spectroscopy and TEM analysis were used to characterize the Ni-CeO_2 interactions and the CeO_2 dispersion over the activated carbon support. Catalysts were tested in the low temperature WGS reaction with two different feed gas mixtures: the idealized one (with only CO and H_2O) and a slightly harder one (with CO, CO_2, H_2, and H_2O). The obtained results show that there is a clear effect of the ceria loading on the catalytic activity. In both cases, catalysts with 20 and 10 wt.% CeO_2 were the most active materials at low temperature. On the other hand, Ni/C shows a lower activity, this assessing the determinant role of ceria in this reaction. Methane, a product of side reactions, was observed in very low amounts, when CO_2 and H_2 were included in the WGS feed. Nevertheless, our data indicate that the methanation process is mainly due to CO_2, and no CO consumption via methanation takes place at the relevant WGS temperatures. Finally, a stability test was carried out, obtaining CO conversions greater than 40% after 150 h of reaction.
机译:已经对二氧化铈促进的碳载镍催化剂进行了低温水煤气变换(WGS)反应的研究。为此,氧化铈已经以不同的负载量:10、20、30和40wt。%分散在活性炭表面上,目的是获得小的二氧化铈颗粒和高可用表面积。此外,还已经研究了碳和二氧化铈负载的镍催化剂。 N_2吸附分析,粉末X射线衍射,H_2程序升温还原,X射线光电子能谱和TEM分析相结合,用于表征Ni-CeO_2相互作用和CeO_2在活性炭载体上的分散。在低温WGS反应中使用两种不同的进料气体混合物测试了催化剂:理想化的一种(仅含CO和H_2O)和稍硬的一种(含CO,CO_2,H_2和H_2O)。所得结果表明二氧化铈负载量对催化活性具有明显的影响。在两种情况下,具有20和10重量%的CeO 2的催化剂在低温下都是最活跃的材料。另一方面,Ni / C显示较低的活性,这评估了二氧化铈在该反应中的决定性作用。当WGS进料中包含CO_2和H_2时,发现副产物甲烷的含量非常低。但是,我们的数据表明,甲烷化过程主要是由于CO_2,在相关的WGS温度下,甲烷化不会消耗CO。最后,进行了稳定性测试,反应150小时后,CO转化率大于40%。

著录项

  • 来源
    《International journal of hydrogen energy》 |2014年第31期|17589-17599|共11页
  • 作者单位

    Laboratorio de Materiales Avanzados, Departamento de Quimica Inorganica - Instituto, Universitario de Materiales de Alicante, Universidad de Alicante, Apartado 99, E-03080 Alicante, Spain;

    Grupo de Materiales Avanzados y Energia, Facultad de Ingenieria, Instituto Tecnologico Metropolitano ITM, Apartado 54959, Medellin, Colombia;

    Laboratorio de Materiales Avanzados, Departamento de Quimica Inorganica - Instituto, Universitario de Materiales de Alicante, Universidad de Alicante, Apartado 99, E-03080 Alicante, Spain;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Ni; CeO_2; Activated carbon; WGS; Low temperature;

    机译:你;CeO_2;活性炭;WGS;低温;

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