Journal
ENERGY
Volume 234, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.energy.2021.121261
Keywords
Pd-based catalyst; Dry reforming; Oxidative dehydrogenation; Reaction path; Energy barrier
Categories
Funding
- National Natural Science Foundation of China [51876014]
- Graduate Scientific Research and Innovation Foundation of Chongqing, China [CYB20018]
- Chongqing Science and Technology Bureau [cstc2018jcyjAX0282]
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The catalytic reaction of C2H6 with CO2 can produce ethylene or syngas using shale gas and greenhouse gases as raw materials. The study found that Pd-doped bimetallic catalysts have high selectivity and conversion rates for ethylene and syngas production, playing different roles in the conversion and selectivity of reactants.
The catalytic reaction of C2H6 with CO2 provides an opportunity to use shale gas and the greenhouse gas as source materials to produce ethylene through oxidative dehydrogenation or produce syngas through dry reforming. In this work, the reaction characteristics of ethane with CO2 on Fe/Co/Ni/Cu monometallic catalysts and Pd-doped bimetallic catalysts were studied through activity test, kinetic analysis, catalyst characterization and DFT calculation. It is found that Pd-Fe-6/CeO2 has a high and stable C2H4 selectivity of 80.4%, which is suitable for oxidative dehydrogenation reaction, while Ni-6/CeO2 has a large ethane/CO2 conversion and a high CO selectivity of 96.5%, which is suitable for dry reforming reaction. For Fe-based catalyst, the doping of Pd form double active component structure. It only reduces the energy barrier of ethylene formation and CO2 direct activation to provide O*, but also increases the energy barrier of ethylene deep dehydrogenation, thus increasing the conversion of reactants and selectivity of C2H4. For Ni-based catalysts, the doping of Pd forms the alloy structure, which reduces the energy barrier of O*-assisted dehydrogenation reaction and increases the conversion of reactants, but increases the energy barrier of C-C bond cleavage and CO2 activation reaction, which reduces the selectivity of reforming to syngas. (C) 2021 Elsevier Ltd. All rights reserved.
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