Isotopic transient kinetic analysis of CO2 hydrogenation to methanol on Cu/SiO2 promoted by Ga and Zn

Author(s):  
Daviel Gómez ◽  
Claudio Candia ◽  
Romel Jiménez ◽  
Alejandro Karelovic
ACS Catalysis ◽  
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Sabra Hanspal ◽  
Zachary D. Young ◽  
Heng Shou ◽  
Robert J. Davis

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Soo Y. Kim ◽  
Nattaporn Lohitharn ◽  
James G. Goodwin ◽  
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Francesco Pinna ◽  
...  

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Susannah Scott

AbstractThe rate law for CO oxidation over Pd-substituted BaCeO3 was studied. Under CO-rich conditions over a range of pressures and temperatures, changing reaction orders for both CO and O2 suggest the coexistence of both Langmuir-Hinshelwood and BaCeO3-mediated mechanisms. The latter dominates at high P(CO)/P(O2), while both mechanisms contribute significantly at low P(CO)/P(O2). Under CO-lean conditions, the Langmuir-Hinshelwood mechanism dominates the kinetics. The importance of the BaCeO3-mediated mechanism increases with temperature. Steady-state isotopic transient kinetic analysis (SSITKA) using 18O2 confirmed the participation of labile lattice oxygen, thus BaCeO3 behaves as a BaO-stabilized form of CeO2.


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