Crossing the Great Divide Between Model Studies and Applied Reactors in Catalysis
Controlled pulses of chemicals over a wide pressure range can link fundamental studies to practical performance, informing catalyst design.
The Science
Just because a model catalyst effectively drives a reaction in a well-controlled environment doesn’t mean it will work as well under more practical conditions. For years, scientists have strived to predict catalysts’ performance. In an ultrahigh vacuum model reactor, catalysts typically work at lower pressures and temperatures than in applied catalytic reactor studies. Now, a team devised a way to bridge the gap between these two extremes. Using their approach, they can predict catalyst performance across a wider range of temperatures and pressures.
The Impact
The findings show that scientists can use fundamental surface science to predict behavior in applied catalytic reactor studies. The study is a stepping stone in designing efficient catalytic processes. Further, this work offers in-depth insight into a series of reactions that turn alcohols to higher-value chemicals.
Summary
Researchers often use model catalysts to study selectivity, a measure of a catalyst’s performance. However, for years, researchers did not have a way to scale-up the selectivity calculations from model catalysts to applied reactor studies. These reactors typically operated at higher temperatures and pressures than model studies, which operated in ultrahigh vacuum reactors. Researchers changed that situation. Their work focused on the oxidative self-coupling of methanol over gold. The team found that kinetic and mechanistic information derived from model system single crystal studies was predictive of those measured on nanoporous gold catalysts under practical catalytic conditions. They identified adsorbed atomic oxygen as the initiator of the catalytic cycle, in accord with the ultrahigh vacuum studies. Indeed, the principles of surface reactivity governing the elementary steps known from the fundamental studies applied equally to the two vastly different circumstances.
The researchers provided the link between the fundamental and applied settings by determining the time constants for product formation in response to reactant pulses over the actual catalyst at reactor temperature over a wide range of active oxygen coverages. They re-created these time constants numerically to high precision from the kinetics and mechanism determined on the gold single crystal with only minor adjustments. The numerical simulation, when expanded to higher pressures, predicted the selectivity patterns seen under catalytic conditions in the fixed bed reactors, demonstrating continuity between model systems and applied catalysis. The numerical analysis showed a strong positive correlation between the surface lifetime of surface-bound methoxy and the selectivity to the desired product (methyl formate), indicating that achieving high selectivity of the coupling product hinges on optimizing the surface coverage of methoxy. The work builds a pathway for extending these results to other analogous reactions.
Contact
Robert J. Madix
Harvard University
[email protected]
Funding
This work was supported as part of the Integrated Mesoscale Architectures for Sustainable Catalysis (IMASC), an Energy Frontier Research Center funded by the Department of Energy, Office of Science, Basic Energy Sciences. R.J.M. and E.A.R. guided the research. C.R. and S.K. performed the experiments. C.R. performed the microkinetic modeling. R.J.M., C.R., E.A.R., S.K., and C.M.F. all participated in frequent discussions and contributed significantly to writing the manuscript. E.A.R. acknowledges the Norwegian Research Council for financial support.
Publications
C. Reece, E.A. Redekop, S. Karakalos, C.M. Friend, and R.J. Madix, “Crossing the great divide between single-crystal reactivity and actual catalyst selectivity with pressure transients.” Nature Catalysis 1, 52 (2018). [DOI: 10.1038/s41929-018-0167-5]
Highlight Categories
Performer: University
Additional: Collaborations , International Collaboration
