TY - JOUR
T1 - Multifunctional Catalyst Combination for the Direct Conversion of CO2 to Propane
AU - Ramirez, Adrian
AU - Ticali, Pierfrancesco
AU - Salusso, Davide
AU - Cordero-Lanzac, Tomas
AU - Ould-Chikh, Samy
AU - Ahoba-Sam, Christian
AU - Bugaev, Aram L.
AU - Borfecchia, Elisa
AU - Morandi, Sara
AU - Signorile, Matteo
AU - Bordiga, Silvia
AU - Gascon, Jorge
AU - Olsbye, Unni
N1 - KAUST Repository Item: Exported on 2021-09-07
Acknowledgements: This project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement 837733. The XAS measurements were supported by a public grant overseen by the French National Research Agency (ANR) as part of the “Investissements d’Avenir” program (reference: ANR-10-EQPX-45). The authors are grateful to C. La Fontaine and V. Briois, as well as to K. A. Lomachenko and A. Lazzarini for the help with the XAS experiment at ROCK, Soleil. Dr. Idoia Hita Del Olmo is acknowledged for her help with the TGA measurements. A.R., S.O.C., and J.G. acknowledge financial support from King Abdullah University of Science and Technology (KAUST). C.A.S. acknowledges the Norwegian Research Council for financial support through project no. 288331 (CO2LO). A.L.B. acknowledges the President’s Grant of Russian Federation MK-5853.2021.1.2.
PY - 2021/9/2
Y1 - 2021/9/2
N2 - The production of carbon-rich hydrocarbons via CO2 valorization is essential for the transition to renewable, non-fossil-fuel-based energy sources. However, most of the recent works in the state of the art are devoted to the formation of olefins and aromatics, ignoring the rest of the hydrocarbon commodities that, like propane, are essential to our economy. Hence, in this work, we have developed a highly active and selective PdZn/ZrO2+SAPO-34 multifunctional catalyst for the direct conversion of CO2 to propane. Our multifunctional system displays a total selectivity to propane higher than 50% (with 20% CO, 6% C1, 13% C2, 10% C4, and 1% C5) and a CO2 conversion close to 40% at 350 °C, 50 bar, and 1500 mL g–1 h–1. We attribute these results to the synergy between the intimately mixed PdZn/ZrO2 and SAPO-34 components that shifts the overall reaction equilibrium, boosting CO2 conversion and minimizing CO selectivity. Comparison to a PdZn/ZrO2+ZSM-5 system showed that propane selectivity is further boosted by the topology of SAPO-34. The presence of Pd in the catalyst drives paraffin production via hydrogenation, with more than 99.9% of the products being saturated hydrocarbons, offering very important advantages for the purification of the products.
AB - The production of carbon-rich hydrocarbons via CO2 valorization is essential for the transition to renewable, non-fossil-fuel-based energy sources. However, most of the recent works in the state of the art are devoted to the formation of olefins and aromatics, ignoring the rest of the hydrocarbon commodities that, like propane, are essential to our economy. Hence, in this work, we have developed a highly active and selective PdZn/ZrO2+SAPO-34 multifunctional catalyst for the direct conversion of CO2 to propane. Our multifunctional system displays a total selectivity to propane higher than 50% (with 20% CO, 6% C1, 13% C2, 10% C4, and 1% C5) and a CO2 conversion close to 40% at 350 °C, 50 bar, and 1500 mL g–1 h–1. We attribute these results to the synergy between the intimately mixed PdZn/ZrO2 and SAPO-34 components that shifts the overall reaction equilibrium, boosting CO2 conversion and minimizing CO selectivity. Comparison to a PdZn/ZrO2+ZSM-5 system showed that propane selectivity is further boosted by the topology of SAPO-34. The presence of Pd in the catalyst drives paraffin production via hydrogenation, with more than 99.9% of the products being saturated hydrocarbons, offering very important advantages for the purification of the products.
UR - http://hdl.handle.net/10754/670955
UR - https://pubs.acs.org/doi/10.1021/jacsau.1c00302
U2 - 10.1021/jacsau.1c00302
DO - 10.1021/jacsau.1c00302
M3 - Article
C2 - 34723275
SN - 2691-3704
JO - JACS Au
JF - JACS Au
ER -