4.6 Article

Enhanced Investigation of CO Methanation over Ni/Al2O3 Catalysts for Synthetic Natural Gas Production

Journal

INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
Volume 51, Issue 13, Pages 4875-4886

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ie300049f

Keywords

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Funding

  1. Chinese Academy of Sciences (CAS) [KGCX2-YW-396]
  2. National Key Technology R&D Program of China [2010BAC66B01]
  3. State Key Laboratory of Multiphase Complex Systems of China [MPCS-2009-C-01]
  4. China Postdoctoral Science Foundation [20100480026, 201104151]

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CO methanation reaction over the Ni/Al2O3 catalysts for synthetic natural gas production was systematically investigated by tuning a number of parameters, including using different commercial Al2O3 supports and varying NiO and MgO loading, calcination temperature, space velocity, H-2/CO ratio, reaction pressure, and time, respectively. The catalytic performance was greatly influenced by the above-mentioned parameters. Briefly, a large surface area of the Al2O3 support, a moderate interaction between Ni and the support Al2O3, a proper Ni content (20 wt %), and a relatively low calcination temperature (400 degrees C) promoted the formation of small NiO particles and reducible beta-type NiO species, which led to high catalytic activities and strong resistance to the carbon deposition, while addition of a small amount of MgO (2 wt %) could improve the catalyst stability by reducing the carbon deposition; other optimized conditions that enhanced the catalytic performance included high reaction pressure (3.0 MPa), high H-2/CO ratio (>= 3:1), low space velocity, and addition of quartz sand as the diluting agent in catalyst bed. The best catalyst combination was 20-40 wt % of NiO supported on a commercial Al2O3 (S-4) with addition of 2-4 wt % of MgO, calcined at 400-500 degrees C and run at a reaction pressure of 3.0 MPa. On this catalyst, 100% of CO conversion could be achieved within a wide range of reaction temperature (300-550 degrees C), and the CH4 selectivity increased with increasing temperature and reached 96.5% at a relatively low temperature of 350 degrees C. These results will be very helpful to develop highly efficient Ni-based catalysts for the methanation reaction, to optimize the reaction process, and to better understand the above reaction.

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