4.7 Article

Effective depolymerization of polyethylene plastic wastes under hydrothermal and solvothermal liquefaction conditions

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 446, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.137238

Keywords

Hydrothermal liquefaction; Solvothermal liquefaction; Ionic liquid; Chemical upcycling; E-waste plastics; Polyethylene

Funding

  1. Jiangxi Normal University
  2. SRP-ASU research program [2020-NonEE-01]

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This study evaluates the thermal liquefaction of PE cable plastic waste in a stainless-steel batch reactor, achieving high conversion rate, oil yield, and higher heating values through the solvothermal liquefaction method. The solvent plays a key role in enhancing mass and thermal energy transfer by solvating and dispersing the feedstock, reducing the thermal cracking temperature and facilitating the depolymerization reaction. This work demonstrates the feasibility of an effective technique for chemical upcycling of polyethylene-based plastics.
Depolymerization of polyethylene (PE) is one of the most challenging tasks in the chemical upcycling of PE-based plastic wastes because the disassociation of the stable carbon-carbon bonds in PE is only possible at a very high reaction temperature. The thermal liquefaction of PE cable plastic waste in a stainless-steel batch reactor was thoroughly evaluated in this study. The effect of different liquefaction methods (hydrothermal liquefaction (HTL), ionic liquids catalyzed HTL, and solvothermal liquefaction (STL)) on the yields of product fractions (oil products, solid residue, and gas) and the properties of the oil products were examined. At 350 ? and 90 min reaction duration, the conversion (%) of 75.43%, the oil yield of 39.33%, the energy recovery rate of 39.7%, the higher heating values (HHV) of 43.83 MJ/kg for the oil samples, and the lower boiling range molecular dis-tribution were obtained by the solvothermal liquefaction method with acetone as a solvent. The HHV of the oil samples obtained in the STL method (43.28-43.83 MJ/kg) is comparable to that of gasoline (HHV -43.4 MJ/ kg). The contribution of the solvent to the depolymerization reaction was mainly the dissolution and dispersion of feedstock by solvation, therefore reducing thermal cracking temperature through enhanced mass and thermal energy transfer. In thermal liquefaction, solvent and feedstock had a low level of solvolysis reactions, so the depolymerization reaction mainly follows thermal cracking. The main reaction path is the random scission of PE molecules during heat treatment, with a low level of polymerization, cyclization, and radical recombination reactions, which occurred through the free radical mechanisms. This work has demonstrated the feasibility of a very promising technique for effective chemical upcycling of polyethylene-based plastics.

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