4.7 Article

Ni/La2O3 catalysts for dry reforming of methane: Effect of La2O3 synthesis conditions on the structural properties and catalytic performances

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 11, Pages 7939-7953

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2020.12.026

Keywords

La2O3 synthesis; Sol-gel citric method; NH3 effect; LaNiO3; NiO; La3Ni2O6 phases

Funding

  1. Russian Science Foundation [19-73-30026]
  2. Project PON (2015-2020) Energie per l'Ambiente - TARANTO [ARS01_00637]

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10 wt% Ni/La2O3 catalysts for dry reforming of methane were synthesized by wetness impregnation of lanthana supports prepared using sol-gel citric method with and without NH3 addition. The Ni-La CA catalyst showed higher catalytic activity at 650 degrees Celsius, while Ni-La CA-NH3 exhibited higher stability under the same temperature and time conditions. After long run tests, both catalysts formed La2O2CO3 phase, but Ni-La CA showed more severe deactivation.
10 wt%Ni/La2O3 catalysts for dry reforming of methane (DRM) were synthesized by wetness impregnation of lanthana supports prepared using sol-gel citric method with and without NH3 addition (Ni-La CA-NH3 and Ni-La CA, respectively). The support preparation conditions affect the nature, phase composition, and distribution of Ni phases (LaNiO3, NiO and La3Ni2O6). The gradient temperature DRM tests (400-800 degrees C) reveal higher catalytic activity of Ni-La CA (at 650 degrees C, X(CO2) = 65.7%, X(CH4) = 54.6%, H-2/CO = 0.71). The Ni-La CA-NH3 shows higher stability (at 650 degrees C and 24 h, X(CO2): 73.7% => 76.4%, X(CH4): 64.7% => 64.6%, H-2/CO: 0.77 => 0.72). For both catalysts, La2O2CO3 phase is formed after long run tests at 650 degrees C 24 h, with the greater TGA weight loss and stronger deactivation being observed for Ni-La CA. The H-2-reduced Ni La CA-NH3 features ultrasmall (1-2 nm) Ni NPs strongly interacting with the support. Catalyst nature affects the amount of carbon coke formed. (c) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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