Abstract
The conversion of methanol to valuable hydrocarbon molecules is of great commercial interest, as the process serves as a sustainable alternative for the production of, for instance, the base chemicals for plastics. The reaction is catalyzed by zeolite materials. By the introduction of magnesium as a cationic metal, the properties of the zeolite, and thereby the catalytic performance, are changed. With atom probe tomography (APT), nanoscale relations within zeolite materials can be revealed: i.e., crucial information for a fundamental mechanistic understanding. We show that magnesium forms clusters within the cages of zeolite SSZ-13, while the framework elements are homogeneously distributed. These clusters of just a few nanometers were analyzed and visualized in 3-D. Magnesium atoms seem to initially be directed to the aluminum sites, after which they aggregate and fill one or two cages in the zeolite SSZ-13 structure. The presence of magnesium in zeolite SSZ-13 increases the lifetime as well as the propylene selectivity. By using operando UV-vis spectroscopy and X-ray diffraction techniques, we are able to show that these findings are related to the suppression of aromatic intermediate products, while maintaining the formation of polyaromatic compounds. Further nanoscale analysis of the spent catalysts showed indications of magnesium redistribution after catalysis. Unlike zeolite H-SSZ-13, for which only a homogeneous distribution of carbon was found, carbon can be either homogeneously or heterogeneously distributed within zeolite Mg-SSZ-13 crystals as the magnesium decreases the coking rate. Carbon clusters were isolated, visualized, and analyzed and were assumed to be polyaromatic compounds. Small one-cage-filling polyaromatic compounds were identified; furthermore, large-cage-crossing aromatic molecules were found by isolating large coke clusters, demonstrating the unique coking mechanism in zeolite SSZ-13. Short-length-scale evidence for the formation of polyaromatic compounds at acid sites is discovered, as clear nanoscale relations between aluminum and carbon atoms exist.
Original language | English |
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Pages (from-to) | 2501-2513 |
Number of pages | 13 |
Journal | JACS Au |
Volume | 2 |
Issue number | 11 |
DOIs | |
State | Published - Nov 28 2022 |
Funding
This work was financially supported by the ARC–CBBC (Advanced Research Center–Chemical Building Blocks Consortium) and is a collaborative study between UU and BASF. APT research was supported by the Center for Nanophase Materials Sciences (CNMS), which is a US Department of Energy, Office of Science User Facility, at Oak Ridge National Laboratory. The authors thank Katarina Stanciakova (UU) for creating the MgO structure files. The authors thank James Burns (ORNL) for assistance in performing the APT sample preparations and running the APT experiments.
Funders | Funder number |
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CBBC | |
Center for Nanophase Materials Sciences | |
U.S. Department of Energy | |
BASF | |
Office of Science | |
Oak Ridge National Laboratory | |
Australian Research Council | |
Universiteit Utrecht |
Keywords
- Atom Probe Tomography
- Methanol-to-Hydrocarbons
- Operando UV-Vis Spectroscopy
- Operando X-ray Diffraction
- Zeolites