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Study on oxidation and pyrolysis of carbonate esters using a micro flow reactor with a controlled temperature profile. Part I: Reactivities of dimethyl carbonate, ethyl methyl carbonate and diethyl carbonate

碳酸二甲酯 碳酸二乙酯 化学 碳酸盐 热分解 热解 分解 碳酸盐离子 激进的 碳酸乙烯酯 无机化学 分析化学(期刊) 电解质 有机化学 催化作用 物理化学 电极
作者
Keisuke Kanayama,Shintaro Takahashi,Shota Morikura,Hisashi Nakamura,Takuya Tezuka,Kaoru Maruta
出处
期刊:Combustion and Flame [Elsevier]
卷期号:237: 111810-111810 被引量:24
标识
DOI:10.1016/j.combustflame.2021.111810
摘要

Carbonate esters such as dimethyl carbonate (DMC), ethyl methyl carbonate (EMC) and diethyl carbonate (DEC) are widely used as electrolyte solvents in a lithium-ion battery (LIB) and are considered as one of potential fire causes. This study investigates a difference in gas-phase reactivities of DMC, EMC and DEC. Species measurements for oxidation (equivalence ratio of 1.0) and pyrolysis of DMC and DEC at maximum wall temperatures of Tw,max = 700–1300 K and atmospheric pressure were performed using a gas chromatograph connected to a micro flow reactor with a controlled temperature profile (MFR). Measured mole fractions of C2H4 and CO2 in the DEC case started increasing at a low temperature (Tw,max = 750 K), while those of CH4 and CO2 in the DMC case started increasing at an intermediate temperature (Tw,max = 1050 K). Gas-phase reactivities of the three carbonate esters were found to be DMC < EMC ≈ DEC through observation of their weak flames. Computational species and heat release rate profiles of DEC showed a three-stage reaction: thermal decomposition, oxidation of decomposition products to CO and CO oxidation to CO2. This three-stage reaction of DEC is distinct from the one driven by low-temperature oxidation observed with n-heptane and DME in earlier studies. Rate of production analysis indicated that principal fuel consumption reactions of DMC were H-atom abstraction reactions and that of DEC was a thermal decomposition reaction producing C2H4. Based on reaction path analysis of DEC oxidation, initial-stage reactions produced few active radicals at the low temperature region. The reactivity difference between DMC and DEC is, therefore, mainly driven by the difference in the primary fuel consumption reactions that relies on fuel molecular structure. Considering the existence of ethyl ester group in EMC, a dominant EMC consumption reaction would be similar to DEC.

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