Intrinsic Millisecond Kinetics of Polyethylene Pyrolysis via Pulse-Heated Analysis of Solid Reactions
Intrinsic Millisecond Kinetics of Polyethylene Pyrolysis via Pulse-Heated Analysis of Solid Reactions
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DOI:
10.1021/acs.chemmater.3c00256
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发表时间:
2023-05
影响因子:
8.6
通讯作者:
Isaac Mastalski;Nathan Sidhu;A. Zolghadr;S. Maduskar;Bryan A. Patel;S. Uppili;Tony Go;Ziwei Wang;M. Neurock;Paul J. Dauenhauer
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文献类型:
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作者:
Isaac Mastalski;Nathan Sidhu;A. Zolghadr;S. Maduskar;Bryan A. Patel;S. Uppili;Tony Go;Ziwei Wang;M. Neurock;Paul J. Dauenhauer
. Continued demand for polyolefins can be met by recycling plastic materials back to their constituent monomers, ethylene and propylene, via thermal cracking in a pyrolysis reactor. During pyrolysis, saturated polyolefin chains break carbon-carbon and carbon-hydrogen bonds, yielding a distribution of alkanes, alkenes, aromatic chemicals, light gases, and solid char residue at temperatures varying from 400-800 °C. To design a pyrolysis reactor that optimizes the chemistry for maximum yield of light olefins, a detailed description of the chemical mechanisms and associated kinetics is required. To that end, the reaction kinetics of isothermal films of low-density polyethylene (LDPE) have been measured by the method of ‘Pulse-Heated Analysis of Solid Reactions,’ or PHASR, which allows for quantification of intrinsic kinetics via isothermal reaction-controlled experimental conditions. The evolution of LDPE films from 20 milliseconds to 2.0 seconds for five temperatures (550, 575, 600, 625