4.6 Article

Sustainable Synthesis of a Highly Stable and Coke-Free Ni@CeO2 Catalyst for the Efficient Carbon Dioxide Reforming of Methane

Journal

CATALYSTS
Volume 12, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/catal12040423

Keywords

dry reforming of methane; coke resistance; durability; deactivation; syngas

Funding

  1. Korea Electric Power Corporation [R20XO02-16]
  2. Korea Institute of Energy Technology Evaluation and Planning (KETEP) - Korean government (MOTIE) (Fostering Human Resources Training in Advanced Hydrogen Energy Industry) [20214000000090]
  3. Korea Institute of Energy Technology Evaluation & Planning (KETEP) [20214000000090] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A facile and green synthetic strategy was developed to construct an efficient Ni@CeO2 catalyst for the dry reforming of methane. The catalyst showed superb syngas production efficiency and stability, with resistance to carbon deposits and sintering. It exhibited high catalytic activity and durability during the DRM reaction.
A facile and green synthetic strategy is developed in this paper for the construction of an efficient catalyst for the industrially important carbon dioxide reforming of methane, which is also named the dry reforming of methane (DRM). Through controlling the synthetic strategy and Ni content, a high-performance Ni@CeO2 catalyst was successfully fabricated. The catalyst showed superb efficiency for producing the syngas with high and stable conversions at prolonged operating conditions. Incorporating Ni during the ceria (CeO2) crystallization resulted in a more stable structure and smaller nanoparticle (NP) size with a more robust interaction with the support than loading Ni on CeO2 supports by the conventional impregnation method. The H-2/CO ratio was almost 1.0, indicating the promising applicability of utilizing the obtained syngas for the Fischer-Tropsch process to produce worthy chemicals. No carbon deposits were observed over the as-synthesized catalyst after operating the DRM reaction for 50.0 h, even at a more coke-favoring temperature (700 degrees C). Owing to the superb resistance to coke and sintering, control of the size of the Ni-NPs, uniform dispersion of the active phase, and potent metal interaction with the support, the synthesized catalyst achieved a magnificent catalytic activity and durability during serving for the DRM reaction for extended operating periods.

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