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Kinetic and thermodynamic behavior of co-pyrolysis of olive pomace and thermoplastic waste via thermogravimetric analysis

Author

Listed:
  • Sánchez-Ávila, N.
  • Cardarelli, Alessandro
  • Carmona-Cabello, Miguel
  • Dorado, M.P.
  • Pinzi, Sara
  • Barbanera, Marco

Abstract

This work represents the first attempt to analyze kinetics, thermodynamics and reaction mechanism of olive pomace (OP) and waste plastic materials (PM) co-pyrolysis. Among PM, polypropylene (PP), polystyrene (PS), high density polypropylene (HDPE), polyvinyl chloride (PVC) and poly (ethylene terephthalate) glycol (PETG) were selected. Non-isothermal TG experiments were carried out under inert conditions at four heating rates, namely 5, 10, 20 and 40 °C/min. The kinetic triplet for raw materials and their blends was determined using Starink, Kissinger-Akahira-Sunose and Ozawa-Flynn-Wall iso-conversional models. Pyrolysis mechanism reactions were explained by diverse models, depending on thermal degradation progress. Results shown that co-pyrolysis followed a complex multi-step reaction mechanism. A synergistic effect was detected during co-pyrolysis of OP/PM mixtures. The addition of 50 % (w/w) OP biomass to PM waste decreased the energy of activation (Ea) from 50 to 25 % for all blends, except for PVC/OP. Thermodynamic analysis reveals that adding OP generally reduces the energy barrier (ΔH), except for PS-OP, and improves energy efficiency (ΔG) by facilitating radical formation and molecular chain cleavage.

Suggested Citation

  • Sánchez-Ávila, N. & Cardarelli, Alessandro & Carmona-Cabello, Miguel & Dorado, M.P. & Pinzi, Sara & Barbanera, Marco, 2024. "Kinetic and thermodynamic behavior of co-pyrolysis of olive pomace and thermoplastic waste via thermogravimetric analysis," Renewable Energy, Elsevier, vol. 230(C).
    • Handle: RePEc:eee:renene:v:230:y:2024:i:c:s0960148124009480
    DOI: 10.1016/j.renene.2024.120880
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