TY - JOUR
T1 - Butane Dry Reforming Catalyzed by Cobalt Oxide Supported on Ti2AlC MAX Phase
AU - Ronda-Lloret, Maria
AU - Marakatti, Vijaykumar S.
AU - Sloof, Willem G.
AU - Delgado, Juan José
AU - Sepúlveda-Escribano, Antonio
AU - Ramos-Fernandez, Enrique V.
AU - Rothenberg, Gadi
AU - Shiju, N. Raveendran
PY - 2020
Y1 - 2020
N2 - MAX (Mn+1AXn) phases are layered carbides or nitrides with a high thermal and mechanical bulk stability. Recently, it was shown that their surface structure can be modified to form a thin non-stoichiometric oxide layer, which can catalyze the oxidative dehydrogenation of butane. Here, the use of a Ti2AlC MAX phase as a support for cobalt oxide was explored for the dry reforming of butane with CO2, comparing this new catalyst to more traditional materials. The catalyst was active and selective to synthesis gas. Although the surface structure changed during the reaction, the activity remained stable. Under the same conditions, a titania-supported cobalt oxide catalyst gave low activity and stability due to the agglomeration of cobalt oxide particles. The Co3O4/Al2O3 catalyst was active, but the acidic surface led to a faster deactivation. The less acidic surface of the Ti2AlC was better at inhibiting coke formation. Thanks to their thermal stability and acid-base properties, MAX phases are promising supports for CO2 conversion reactions.
AB - MAX (Mn+1AXn) phases are layered carbides or nitrides with a high thermal and mechanical bulk stability. Recently, it was shown that their surface structure can be modified to form a thin non-stoichiometric oxide layer, which can catalyze the oxidative dehydrogenation of butane. Here, the use of a Ti2AlC MAX phase as a support for cobalt oxide was explored for the dry reforming of butane with CO2, comparing this new catalyst to more traditional materials. The catalyst was active and selective to synthesis gas. Although the surface structure changed during the reaction, the activity remained stable. Under the same conditions, a titania-supported cobalt oxide catalyst gave low activity and stability due to the agglomeration of cobalt oxide particles. The Co3O4/Al2O3 catalyst was active, but the acidic surface led to a faster deactivation. The less acidic surface of the Ti2AlC was better at inhibiting coke formation. Thanks to their thermal stability and acid-base properties, MAX phases are promising supports for CO2 conversion reactions.
KW - butane dry reforming
KW - CO conversion
KW - cobalt oxide
KW - MAX phases
KW - TiAlC support
UR - http://www.scopus.com/inward/record.url?scp=85091145704&partnerID=8YFLogxK
U2 - 10.1002/cssc.202001633
DO - 10.1002/cssc.202001633
M3 - Article
AN - SCOPUS:85091145704
SN - 1864-5631
VL - 13
SP - 6401
EP - 6408
JO - ChemSusChem
JF - ChemSusChem
IS - 23
ER -