4.7 Article

Pyrolysis of long chain hydrocarbon-based plastics via self-exothermic effects: The origin and influential factors of exothermic processes

期刊

JOURNAL OF HAZARDOUS MATERIALS
卷 424, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jhazmat.2021.127476

关键词

Pyrolysis; Phase transition; Polyethylene; Long chain hydrocarbon; Exotherm

资金

  1. National Key Research and Development Program of China [2018YFC1901200]
  2. National Natural Science Foundation of China [51976223]
  3. Key Special Project for Introduced Talents Team of Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) [GML2019ZD0101]
  4. Guang-dong Province Science and Technology Planning Project [2019B110210003]

向作者/读者索取更多资源

Converting plastic wastes into high-value products through energy-efficient pyrolysis is crucial, requiring lower temperatures and shorter processing times than traditional methods. The exothermic phase transition observed during the process can lead to deep cracking of polyethylene with a high yield of liquid products and minimal gas production. This self-exothermic pyrolysis offers a viable approach for plastic recycling at low temperatures and short heating times, without the need for a catalyst.
Converting plastic wastes into value-added products through energy-efficient pyrolysis is essential, and it requires lower pyrolysis temperatures and shorter processing times than that of other processes. An exothermic phenomenon was observed during the process high-pressure polyethylene pyrolysis. It was proven for the first time that the exotherm is caused by a pressure-induced phase transition, in which colossal heat release can be driven by relatively small pressures. A large temperature change (> 100 degrees C) leads to the deep cracking of polyethylene, although the set temperature is far lower than the required temperature for thermal cracking. Importantly, the heat input stops immediately when the set temperature is reached; thus, the external heating time is short. Polyethylene can be completely converted into liquid products in similar to 90 wt% yield and with a small number of gases. The self-exothermic phase transition only occurs within a certain range of material thickness, which is related to the corresponding phase behavior. In the self-exothermic pyrolysis process, with an increase in the thickness of polyethylene, the proportion of low-value olefins in oil products decreases gradually, while alkanes, isoalkanes and aromatics show an increasing trend, making the product composition closer to the fuel standard. This work provides a viable approach for plastic recycling at low pyrolysis temperatures and short external heating times with the help of a self-exothermic phase transition in the absence of a catalyst.

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