Experimental and Numerical Study of the Impact of Pressure During the Pyrolysis of Diethyl Carbonate and Ethyl Methyl Carbonate
During a thermal runaway, Lithium-ion battery cells are subjected to a large increase in temperature, which will vaporize and potentially thermally degrade their liquid electrolyte. The formation of gas in the battery cell will increase the pressure until the flammable gases vent and potentially lead to a fire incident. While the pyrolysis chemistry of the electrolyte components has been studied near atmospheric pressure, the effect of pressure has not been investigated. This study was undertaken to better understand the effect of pressure on the thermal dissociation of two common linear electrolyte components, diethyl carbonate (DEC) and ethyl methyl carbonate (EMC). The pyrolysis of DEC and EMC was studied in the gas phase, in 99.75% He/Ar, and was carried out at high temperatures and for pressures near 5.5 atm. The time-resolved CO formation was measured using a quantum cascade laser, providing a unique experimental dataset. A detailed chemical kinetics analysis was performed to understand the effect of pressure on DEC and EMC, with CO time-history results obtained in similar conditions at near-atmospheric pressure for DEC and EMC serving as baselines for comparison. Numerical predictions using detailed chemical kinetics mechanisms from the literature were carried out, and reaction pathways at different pressures were highlighted to emphasize the effect of pressure on the pyrolysis chemistry.
Authors
- Olivier E. Mathieu (ORCID: https://orcid.org/0000-0002-8658-6326)
- Eric L. Petersen (ORCID: https://orcid.org/0000-0002-4572-5916)
- Claire M. Grégoire (ORCID: https://orcid.org/0000-0002-0085-0553)
Institutions
- Walker (United States) (US)
- Texas A&M University (US)
Publication Details
- Journal
- Batteries
- Published
- 2025-08-08
- DOI
- https://doi.org/10.3390/batteries11080303
- Primary Topic
- Advanced Battery Technologies Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation