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Online sample pretreatment for analysis of decomposition products in lithium ion battery by liquid chromatography hyphenated with ion trap-time of flight-mass spectrometry or inductively coupled plasma-sector field-mass spectrometry

化学 色谱法 质谱法 电解质 萃取(化学) 样品制备 检出限 电感耦合等离子体质谱法 固相萃取 离子迁移光谱法 分析化学(期刊) 电极 物理化学
作者
Kristina Kösters,Jonas Henschel,Martin Winter,Sascha Nowak
出处
期刊:Journal of Chromatography A [Elsevier BV]
卷期号:1658: 462594-462594 被引量:4
标识
DOI:10.1016/j.chroma.2021.462594
摘要

Lithium ion batteries are essential power sources for mobile electronic devices like cell phones, tablets and increasingly used in the field of electromobility and energy transition. The commonly applied liquid electrolytes in commercial cells contain a conducting salt at relatively high concentration (LiPF6, ≥1 mol/L). For analytical battery electrolyte investigations, it is necessary to protect the column and mass spectrometer from salt precipitation and clogging. Thus, dilution of the sample is necessary which results in higher limits of detection and limits of quantification. In this study, a comprehensive online sample preparation approach for reversed phase liquid chromatography with an online-solid phase extraction was developed, which allows higher injections volumes and lower dilution factors. For the method development of the online-solid phase extraction, pristine electrolytes were used with trimethyl phosphate and triethyl phosphate as model substances for organo(fluoro)phosphates with weak and strong retention on the extraction column. Organo(fluoro)phosphates are potential hazardous decomposition products, due to their structural similarity to chemical warfare agents like sarin, and therefore their quantification is beneficial for toxicological assessment. The optimization of chromatographic parameters was performed using electrochemically aged electrolytes. For substance independent quantification with a plasma-based technique, an isocratic separation method was implemented. Using optimized conditions, LiPF6 could be removed quantitatively and the injection volume was increased up to a factor of 50, while the dilution factor could be decreased up to a factor of ten. Eleven different organo(fluoro)phosphates with an overall concentration of 133 mg/kg were found. Therefore, limit of detection and limit of quantification were improved significantly (LOQ: ≤100 µg kg-1 phosphorus content, LOD: ≤35 µg kg-1 phosphorus content). In summary, a fast online sample preparation for liquid chromatographic investigations of lithium ion battery electrolytes was implemented, validated on electrochemically aged lithium ion battery electrolyte.
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