Pyrolysis characteristics of cathode from spent lithium-ion batteries using advanced TG-FTIR-GC/MS analysis
Autor: | Daidai Wu, Shaoqi Yu, Zhitong Yao, Xiaoshu Lü, Jingjing Xiong, Junhong Tang, Shaodan Xu |
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Přispěvatelé: | Hangzhou Dianzi University, CAS - Guangzhou Institute of Energy Conversion, Department of Civil Engineering, Aalto-yliopisto, Aalto University |
Rok vydání: | 2020 |
Předmět: |
Lithium-ion batteries
Thermogravimetric analysis Materials science Health Toxicology and Mutagenesis Analytical chemistry chemistry.chemical_element Infrared spectroscopy Thermal treatment 010501 environmental sciences 01 natural sciences law.invention law Environmental Chemistry Fourier transform infrared spectroscopy 0105 earth and related environmental sciences General Medicine Electronic waste Pollution Decomposition Cathode Polyvinylidene fluoride binder chemistry Lithium Pyrolysis |
Zdroj: | Environmental Science and Pollution Research. 27:40205-40209 |
ISSN: | 1614-7499 0944-1344 |
DOI: | 10.1007/s11356-020-10108-4 |
Popis: | Thermal treatment offers an alternative method for the separation of Al foil and cathode materials during spent lithium-ion batteries (LIBs) recycling. In this work, the pyrolysis behavior of cathode from spent LIBs was investigated using advanced thermogravimetric Fourier transformed infrared spectroscopy coupled with gas chromatography-mass spectrometer (TG-FTIR-GC/MS) method. The fate of fluorine present in spent batteries was probed as well. TG analysis showed that the cathode decomposition displayed a three-stage process. The temperatures of maximum mass loss rate were located at 470 °C and 599 °C, respectively. FTIR analysis revealed that the release of CO2 increased as the temperature rose from 195 to 928 °C. However, the evolution of H2O showed a decreasing trend when the temperature increased to above 599 °C. The release of fluoride derivatives also exhibited a decreasing trend, and they were not detected after temperatures increasing to above 470 °C. GC-MS analysis indicated that the release of H2O and CO displayed a similar trend, with larger releasing intensity at the first two stages. The evolution of 1,4-difluorobenzene and 1,3,5-trifluorobenzene also displayed a similar trend—larger releasing intensity at the first two stages. However, the release of CO2 showed a different trend, with the largest release intensity at the third stage, as did the release of 1,2,4-trifluorobenzene, with the release mainly focused at the temperature of 300–400 °C. The release intensities of 1,2,4-trifluorobenzene and 1,3,5-trifluorobenzene were comparable, although smaller than that of 1,4-difluorobenzene. This study will offer practical support for the large-scale recycling of spent LIBs. |
Databáze: | OpenAIRE |
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