Abstract

Ni-Mg-Mn-Fe-O catalysts were prepared via co-precipitation through layered double hydroxide (LDH) precursors and tested for hydrogen production from ethanol by auto-thermal reforming (ATR). With Mn and Fe in the precursor of the Ni0.35 Mg2.65Mn0.5Fe0.5O4.5±δ catalyst, an LDH structure formed via co-precipitation, and after calcination, a cubic MgO skeleton formed with spinel phases of NiMn2O4 and NiFe2O4. The H2 yield reached 4.0mol-H2/mol-EtOH and remained stable in a 30-h ATR test, which can be attributed to the improvement of reduction behavior and stability of Ni0 species.

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