Bioplastics possess the potential to foster a sustainable circular plastic economy, but their end-of-life is still challenging. To sustainably overcome this problem, this work proposes the hydrothermal carbonization (HTC) of residual bioplastics as an alternative green path. The focus is on cellulose acetate - a bioplastic used for eyewear, cigarette filters and other applications - showing the proof of concept and the chemistry behind the conversion, including a reaction kinetics model. HTC of pure and commercial cellulose acetates was assessed under various operating conditions (180-250 °C and 0-6 h), with analyses on the solid and liquid products. Results show the peculiar behavior of these substrates under HTC. At 190-210 °C, the materials almost completely dissolve into the liquid phase forming 5‑hydroxymethylfurfural and organic acids. Above 220 °C, intermediates repolymerize into carbon-rich microspheres (secondary char), achieving solid yields up to 23 %, while itaconic and citric acid form. A comparison with pure substrates and additives demonstrates that the amounts of acetyl groups and derivatives of the plasticizers are crucial in catalyzing HTC reactions, creating a unique environment capable of leading to a total rearrangement of cellulose acetates. HTC can thus represent a cornerstone in establishing a biorefinery for residual cellulose acetate.

Cellulose Acetates in Hydrothermal Carbonization: a Green Pathway to Valorize Residual Bioplastics / Ischia, Giulia; Marchelli, Filippo; Bazzanella, Nicola; Ceccato, Riccardo; Calvi, Marco; Guella, Graziano; Gioia, Claudio; Fiori, Luca. - In: CHEMSUSCHEM. - ISSN 1864-5631. - STAMPA. - 2024:(2024). [10.1002/cssc.202401163]

Cellulose Acetates in Hydrothermal Carbonization: a Green Pathway to Valorize Residual Bioplastics

Ischia, Giulia
Primo
;
Marchelli, Filippo
Secondo
;
Bazzanella, Nicola;Ceccato, Riccardo;Guella, Graziano;Gioia, Claudio
Penultimo
;
Fiori, Luca
Ultimo
2024-01-01

Abstract

Bioplastics possess the potential to foster a sustainable circular plastic economy, but their end-of-life is still challenging. To sustainably overcome this problem, this work proposes the hydrothermal carbonization (HTC) of residual bioplastics as an alternative green path. The focus is on cellulose acetate - a bioplastic used for eyewear, cigarette filters and other applications - showing the proof of concept and the chemistry behind the conversion, including a reaction kinetics model. HTC of pure and commercial cellulose acetates was assessed under various operating conditions (180-250 °C and 0-6 h), with analyses on the solid and liquid products. Results show the peculiar behavior of these substrates under HTC. At 190-210 °C, the materials almost completely dissolve into the liquid phase forming 5‑hydroxymethylfurfural and organic acids. Above 220 °C, intermediates repolymerize into carbon-rich microspheres (secondary char), achieving solid yields up to 23 %, while itaconic and citric acid form. A comparison with pure substrates and additives demonstrates that the amounts of acetyl groups and derivatives of the plasticizers are crucial in catalyzing HTC reactions, creating a unique environment capable of leading to a total rearrangement of cellulose acetates. HTC can thus represent a cornerstone in establishing a biorefinery for residual cellulose acetate.
2024
Ischia, Giulia; Marchelli, Filippo; Bazzanella, Nicola; Ceccato, Riccardo; Calvi, Marco; Guella, Graziano; Gioia, Claudio; Fiori, Luca
Cellulose Acetates in Hydrothermal Carbonization: a Green Pathway to Valorize Residual Bioplastics / Ischia, Giulia; Marchelli, Filippo; Bazzanella, Nicola; Ceccato, Riccardo; Calvi, Marco; Guella, Graziano; Gioia, Claudio; Fiori, Luca. - In: CHEMSUSCHEM. - ISSN 1864-5631. - STAMPA. - 2024:(2024). [10.1002/cssc.202401163]
File in questo prodotto:
File Dimensione Formato  
ChemSusChem - 2024 - Ischia - Cellulose Acetates in Hydrothermal Carbonization A Green Pathway to Valorize Residual.pdf

accesso aperto

Descrizione: online first
Tipologia: Versione editoriale (Publisher’s layout)
Licenza: Creative commons
Dimensione 4.01 MB
Formato Adobe PDF
4.01 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11572/431051
Citazioni
  • ???jsp.display-item.citation.pmc??? 0
  • Scopus 0
  • ???jsp.display-item.citation.isi??? ND
  • OpenAlex ND
social impact