4.7 Article

The active phase of NaCo/ZnO catalyst for ethanol steam reforming: EXAFS and in situ XANES studies

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 35, 期 11, 页码 5378-5382

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2010.02.128

关键词

NaCo/ZnO catalyst; Ethanol steam reforming; XANES; EXAFS

资金

  1. Dankook University
  2. National Research Foundation of Korea [2008-56529] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The NaCo/ZnO catalyst was prepared by a co-precipitation method and the active phase for the catalyst was studied. Extended X-ray absorption fine structure (EXAFS) studies were used to obtain structural parameters of the active phase of the catalyst. In situ X-ray absorption near edge structure (XANES) studies were also employed to better understand the phase transition of the catalyst in the course of H-2-temperature-programmed reduction followed by ethanol steam reforming. The XANES analysis confirmed that the oxidic precursor of Co3O4 phase was transformed to CoO followed by Co metal in the course of H-2-TPR, and the Co metal phase remained stable during the reaction. The EXAFS analysis for the fresh and spent catalyst samples revealed that the characteristic features corresponding to Co Co distance of Co metallic phase were being developed during reaction, which demonstrated that Co phase is most likely the active phase of NaCo/ZnO catalyst for the ethanol steam reforming. The catalytic activity in ethanol steam reforming for hydrogen production over the oxidized and reduced catalyst samples was measured at 773 K and 1 atm in a fixed bed reactor using a model liquid feed containing 21 vol% ethanol in water. The prereduced NaCo/ZnO catalyst gave high ethanol conversion of 99% with product distributions of 73.0% H-2, 2.2% CO, 22.1% CO2, and 2.7% CH4, while the calcined oxidic one exhibited poor ethanol conversion below 44% at 773 K. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.

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