Massachusetts Institute of Technology
Materials Characterization and Spectroscopy for a Methane Abatement Catalyst
Abstract
dc:description.abstractMethane is the second-most emitted greenhouse gas after carbon dioxide, and it is significantly more powerful as a short-term warmer, making it a valuable target for climate change mitigation efforts. Zeolites are earth-abundant minerals common in catalysis for their low price combined with high conversion and throughput potential. This study evaluates a specific copper-zeolite (mordenite) methane oxidation catalyst for long-term durability and potential performance at 400 and 950 C. Using materials characterization and spectroscopy techniques including scanning-electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), Brunauer-Emmett-Teller analysis (BET), differential scanning calorimetry (DSC), and X-ray diffraction (XRD), chemical and structural changes are tracked, identified, and assessed over the course of three months. Samples treated at 400 °C show no major structural or chemical changes in the catalyst, while samples treated at 950 °C show gradual transformation into a nonporous quartz-mullite-cristobalite mixture. This suggests indefinite catalyst stability at the former temperature and progressive catalyst degradation at the latter temperature, providing plausible long-term operation conditions and peak temporary conditions for this method of methane abatement.
Degree
thesis:*- Name thesis:degree_name
- Master
- Department dc:contributor.department
- Massachusetts Institute of Technology. Department of Civil and Environmental Engineering
- Grantor dc:publisher
- Massachusetts Institute of Technology
- Year dc:date.issued
- 2023
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Wilkinson, Mollie
- Advisor dc:contributor.advisor
-
- Plata, Desiree
Rights
dc:rights- Statement dc:rights
-
- In Copyright - Educational Use Permitted
- Copyright retained by author(s)
- Licence dc:rights.uri
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- https://hdl.handle.net/1721.1/151987
- OAI identifier oai:identifier
- oai:dspace.mit.edu:1721.1/151987