4.2 Article

Effect of Sr content on hydrogen production by steam reforming,of ethanol over Ni-Sr/Al2O3-ZrO2 xerogel catalysts

Journal

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
Volume 418, Issue -, Pages 68-77

Publisher

ELSEVIER
DOI: 10.1016/j.molcata.2016.03.035

Keywords

Hydrogen production; Steam reforming of ethanol; Ni-Sr/Al2O3-ZrO2 catalyst; Strontium promoter; Nickel surface area

Funding

  1. Global Frontier RAMP
  2. D Program on Center for Multiscale Energy System - National Research Foundation under the Ministry of Science, ICT AMP
  3. Future Planning, Korea [20110031575]

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A series of Ni-Sr/Al2O3-ZrO2 (15Ni-XSr/AZ) xerogel catalysts with different strontium content (X, wt%) were prepared by an epoxide-driven sol-gel method followed by a co-impregnation method. Unpromoted Ni/Al2O3-ZrO2 (15Ni/AZ) xerogel catalyst was also prepared according to the similar methods for comparison. Surface area of the catalysts decreased with increasing strontium content. Excess amount of impregnated strontium on the catalyst led to weakened metal-support interaction, inducing formation of large nickel particles in the reduced catalysts with high Sr loading. Introduction of strontium promoter reduced acidity of the catalysts, leading to a more favorable reaction pathway during the ethanol steam reforming reaction. Promotion with strontium generally had a positive effect on the catalytic activity due to enhanced nickel dispersion and suppressed acidity. Nickel surface area and ethanol adsorption capacity exhibited volcano-shaped trends with respect to strontium content. Hydrogen yield increased with increasing nickel surface area and with increasing ethanol adsorption capacity of the catalyst. Among the catalysts tested, 15Ni-6Sr/AZ, which retained the highest nickel surface area and the largest ethanol adsorption capacity, showed the highest hydrogen yield in the steam reforming of ethanol. It was concluded that an optimal amount of strontium promoter was required to achieve the best catalytic performance. (C) 2016 Elsevier B.V. All rights reserved.

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