Development of catalysts for ammonia synthesis based on metal phthalocyanine materials
AuthorsMorlanes, Natalia Sanchez
Rai, Rohit Kumar
Ali, Mohammed M.
Al-Sabban, Bedour E.
KAUST DepartmentChemical Science Program
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
SABIC Corporate Research and Development Center at KAUST, Saudi Basic Industries Corporation Thuwal 23955 Kingdom of Saudi Arabia
Permanent link to this recordhttp://hdl.handle.net/10754/661947
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AbstractHighly efficient and very stable iron and/or cobalt-based catalysts for the ammonia synthesis reaction were synthesized by one-step pyrolysis of metal phthalocyanine precursors. The presence of alkaline earth or alkali metals is found to be essential for accelerating the reaction rate for the ammonia synthesis process. When promoted by alkali metals, the catalysts show a 3-fold increase in their catalytic performance (at 400 °C and 0.1-7 MPa) compared to a commercial benchmark iron-based catalyst, widely used for the Haber-Bosch process. TEM images reveal the local structure of the catalysts obtained upon pyrolysis of the metal phthalocyanine precursor, with metal nanoparticles (5-50 nm) confined in a nitrogen-doped carbon mesoporous matrix, where the alkali metal promoters are located on the top of the iron nanoparticles but also on the carbon support. Finally, kinetic analysis shows a lower activation energy for the Fe phthalocyanine-derived catalyst (42 kJ mol-1) versus 70 kJ mol-1 reported for the iron-benchmark catalyst. Furthermore, this kinetic analysis suggests that the rate-determining step shifts from nitrogen activation to NHx formation, which only few catalysts have achieved.
CitationMorlanés, N., Almaksoud, W., Rai, R. K., Ould-Chikh, S., Ali, M. M., Vidjayacoumar, B., … Basset, J.-M. (2020). Development of catalysts for ammonia synthesis based on metal phthalocyanine materials. Catalysis Science & Technology, 10(3), 844–852. doi:10.1039/c9cy02326g
SponsorsThis research was supported by the SABIC Company. The authors acknowledge the resources and facilities provided by the King Abdullah University of Science and Technology. The authors also acknowledge the KAUST Analytical Core Lab (ACL) and especially the scientist Mohammed Khalid.
PublisherRoyal Society of Chemistry (RSC)
JournalCatalysis Science and Technology