2021
DOI: 10.1039/d1cy00362c
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CO2-assisted ethane oxidative dehydrogenation over MoOx catalysts supported on reducible CeO2–TiO2

Abstract: Supported MoOx on mixed CeO2-TiO2 were investigated for the oxidative dehydrogenation of ethane (ODHE) using CO2 as a mild oxidant. Raman spectroscopic characterization of the synthesized catalysts under dehydrated conditions...

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Cited by 14 publications
(8 citation statements)
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“…149 Another important function of CO 2 is re-oxidation of the reduced active phase. Such phenomenon was observed in the systems with reducible oxides, for example, MoO x , 166 Pd/CeZrAlO x , 167 Ga 2 O 3 . 168 This process occurs in the case of the one-stage “looping-like” ODH, when alkane is directly oxidized by lattice oxygen resulting in the olefin and water production, after which the reduced metal species are re-oxidized by CO 2 .…”
Section: Light Olefin Synthesis From Hydrocarbonsmentioning
confidence: 72%
“…149 Another important function of CO 2 is re-oxidation of the reduced active phase. Such phenomenon was observed in the systems with reducible oxides, for example, MoO x , 166 Pd/CeZrAlO x , 167 Ga 2 O 3 . 168 This process occurs in the case of the one-stage “looping-like” ODH, when alkane is directly oxidized by lattice oxygen resulting in the olefin and water production, after which the reduced metal species are re-oxidized by CO 2 .…”
Section: Light Olefin Synthesis From Hydrocarbonsmentioning
confidence: 72%
“…13), indicating that a large part of hydrogen derived from C3H8 was consumed by reverse water-gas shift reaction. This also suggests that the contribution of DDP versus CO2-ODP to the overall C3H6 production, which is reflected roughly by the H2 yield/C3H6 yield ratio, 35 was considerably low (~10%). Considering that H2 can also be formed by dry reforming to a small extent, the actual contribution of DDP should be much lower than 10%.…”
Section: Catalytic Reactionsmentioning
confidence: 99%
“…49,50 However, it is worth mentioning that the effect of CO 2 on the overall propane conversion and propylene formation depends on multiple factors that may include the nature of active sites present which in turn may govern the relative contribution of simultaneous reactions such as DH vs. reforming 51 and/or DH/ ODH. 52 Moreover, CO 2 may participate directly in reoxidizing reduced metal oxide centers; thus, its conversion competes with the reverse water gas shift reaction.…”
Section: Catalysis Science and Technology Papermentioning
confidence: 99%