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      Simulation of Dispersion and Explosion Characteristics of LiFePO 4 Lithium-Ion Battery Thermal Runaway Gases

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          Abstract

          In recent years, as the installed scale of battery energy storage systems (BESS) continues to expand, energy storage system safety incidents have been a fast-growing trend, sparking widespread concern from all walks of life. During the thermal runaway (TR) process of lithium-ion batteries, a large amount of combustible gas is released. In this paper, the 105 Ah lithium iron phosphate battery TR test was conducted, and the flammable gas components released from the battery TR were detected. The simulation tests of the diffusion and explosion characteristics of lithium iron phosphate battery’s (LFP) TR gases with different numbers and positions in the BESS were carried out using FLACS simulation software. It was found that the more batteries TR simultaneously, the shorter the time for the combustible gas concentration in the energy storage cabin to reach the explosion limit. When 48 batteries were in TR simultaneously in the energy storage cabin, the shortest time was 9.8 s, and the further the location of the fire is from the hatch, the largest explosion overpressure is generated to the hatch, up to 583 kPa. When the gas generated by the TR of 48 batteries explodes, the maximum explosion overpressure at 5 m outside the energy storage cabin hatch is more significant than 40 kPa, which will cause serious injury to humans. The causes of TR of batteries in prefabricated chambers are complex, and the location and amount of thermal runaway of batteries as well as the diffusion of combustible fumes can have different effects on the external environment. The research results can provide support for the safety design of BESS.

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          Most cited references34

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          Thermal runaway of commercial 18650 Li-ion batteries with LFP and NCA cathodes – impact of state of charge and overcharge

          Destructive thermal ramp experiments with commercial Li-ion batteries at different state of charge were made. Produced gases were quantified and a causing chemical reaction system is proposed. Thermal runaway characteristics of two types of commercially available 18650 cells, based on Li x FePO 4 and Li x (Ni 0.80 Co 0.15 Al 0.05 )O 2 were investigated in detail. The cells were preconditioned to state of charge (SOC) values in the range of 0% to 143%; this ensured that the working SOC window as well as overcharge conditions were covered in the experiments. Subsequently a series of temperature-ramp tests was performed with the preconditioned cells. Charged cells went into a thermal runaway, when heated above a critical temperature. The following thermal runaway parameters are provided for each experiment with the two cell types: temperature of a first detected exothermic reaction, maximum cell temperature, amount of produced ventgas and the composition of the ventgas. The dependence of those parameters with respect to the SOC is presented and a model of the major reactions during the thermal runaway is made.
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            Explosion hazards from lithium-ion battery vent gas

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              • Article: not found

              Identification and quantification of gases emitted during abuse tests by overcharge of a commercial Li-ion battery

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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                04 April 2024
                16 April 2024
                : 9
                : 15
                : 17036-17044
                Affiliations
                []China Electric Power Research Institute , Beijing 100192, China
                []Jescom Software (Shanghai) Co. , Shanghai 200090, China
                Author notes
                Author information
                https://orcid.org/0009-0007-2018-4504
                Article
                10.1021/acsomega.3c08709
                11025091
                3defdbfe-19e2-4029-ab6c-91f5bc0c1cee
                © 2024 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 02 November 2023
                : 02 February 2024
                : 28 January 2024
                Funding
                Funded by: National Key Research and Development Program of China, doi 10.13039/501100012166;
                Award ID: 2023YFC3009900
                Categories
                Article
                Custom metadata
                ao3c08709
                ao3c08709

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