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Fast co-pyrolysis of wood and plastic: Evaluation of the primary gaseous products
University of Borås, Faculty of Textiles, Engineering and Business.ORCID iD: 0000-0003-3239-019x
University of Borås, Faculty of Textiles, Engineering and Business.
University of Borås, Faculty of Textiles, Engineering and Business.ORCID iD: 0000-0003-0037-3555
2024 (English)In: Energy Conversion and Management: X, E-ISSN 2590-1745, Vol. 22, article id 100613Article in journal (Refereed) Published
Abstract [en]

Bio-oil derived from fast pyrolysis of wood contains oxygenates and has a relatively low heating value. These are challenges that need to be tackled if wood-derived bio-oil is to be used as drop-in fuels. The bio-oil can be obtained by condensation of gaseous products. Using a material with no oxygen in addition to wood during fast pyrolysis could be a technique to reduce the formation of oxygenates and promote a hydrocarbon-rich product. This work aims to evaluate the primary gaseous products formed during fast co-pyrolysis of birch wood and plastic. The pyrolysis was performed in a micropyrolyser at 600 °C with a residence time of 5 s. Birch wood and plastic were melt-mixed at different weight ratios to study possible interaction effects upon pyrolysis. The different plastics used were low-density polyethylene (LDPE), polypropylene (PP) and polystyrene (PS). The total gaseous product was between 10–20 wt% from Wood-LDPE or Wood-PP, while it was in the range 15–90 wt% from Wood-PS. The analysis of gas product found that the formation of oxygenates (up to 9 wt%) was lower than expected (up to 14 wt%) for the mixtures of wood and plastic compared to the pure materials (about 18 wt%). The reduction of oxygenates (up to 90 %) was mainly due to a lower production of ketones, carboxylic acids and aldehydes. Maximum hydrocarbons in the gas phase from binary mixtures were around 8, 15 and 55 wt% from Wood-LDPE, Wood-PP and Wood-PS, respectively. The most significant difference between experimental and estimated values assuming no interaction among hydrocarbons was observed in the case of alkenes and alkanes for Wood-LDPE, as well as alkanes for Wood-PS, while the Wood and PP mixture showed almost no signs of interaction. This work is beneficial for understanding interactions between wood and plastics, and could be used to reduce the amount of oxygenates from wood pyrolysis and reduce the need for upgrading.

Place, publisher, year, edition, pages
2024. Vol. 22, article id 100613
Keywords [en]
Fast co-pyrolysis, Hydrocarbons, Oxygenates, Plastic, Wood
National Category
Chemical Engineering
Identifiers
URN: urn:nbn:se:hb:diva-31797DOI: 10.1016/j.ecmx.2024.100613ISI: 001237445800001Scopus ID: 2-s2.0-85192449008OAI: oai:DiVA.org:hb-31797DiVA, id: diva2:1856055
Available from: 2024-05-05 Created: 2024-05-05 Last updated: 2025-02-27Bibliographically approved
In thesis
1. Fast Co-pyrolysis of Wood and Plastic: Evaluation of Gases from Primary Reactions
Open this publication in new window or tab >>Fast Co-pyrolysis of Wood and Plastic: Evaluation of Gases from Primary Reactions
2025 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Fast co-pyrolysis (FCP) of wood and plastic offers a promising strategy not only to reduce dependence on fossil fuels for feedstock and chemical production but also to mitigate plastic waste accumulation. This thermochemical process decomposes wood and plastic in the absence of oxygen. It involves complex chemical reactions that yield valuable solid, liquid and gaseous products. These reactions include both primary and secondary reactions. However, limited research has been conducted on gases produced during primary reactions. In this work, micropyrolyser connected with a gas chromatography, a mass spectrometry, a flame ionization detector, and a thermal conductivity detector (Py-GC/MS/FID/TCD) have been employed to analyse gaseous products from primary reactions during both non-catalytic and catalytic FCP of wood and plastic.

Primary gaseous products from the fast pyrolysis of cellulose, xylan, and lignin were successfully promoted, showing increased gas yields at higher temperatures and longer residence times. Additionally, fast pyrolysis of low-density polyethylene (LDPE), polypropylene (PP), and polystyrene (PS) has been performed. Fast pyrolysis of lignocellulosic biomass primarily produces oxygenated compounds such as sugars, phenols, carboxylic acids, aldehydes and ketones. Meanwhile, fast pyrolysis of plastics yields aliphatic and aromatic hydrocarbons, including alkanes, alkenes and alkynes. The underlying reaction mechanisms for primary reactions were proposed.

The evaluation of gaseous products from the pyrolysis of individual materials was further used to assess interaction effects during FCP of birch wood with plastics (Wood-LDPE, Wood-PP, and Wood-PS). Significant interactions were observed, with a 90% reduction in oxygenate content in the gases at 75 wt% wood content, regardless of plastic type. Furthermore, catalytic FCP using calcium carbonate (CaCO₃) was conducted to explore the role of in-situ catalysts in enhancing gas yield. Adding 10 wt% CaCO₃ doubled the total gas yield, with a significant increase in volatile compounds containing fewer than 10 carbon atoms.

The findings contribute to optimising fuel and chemical production by fine-tuning the wood-to-plastic ratio and selecting appropriate plastic types.

Place, publisher, year, edition, pages
Borås: Högskolan i Borås, 2025
Series
Skrifter från Högskolan i Borås, ISSN 0280-381X ; 155
Keywords
calcium carbonate, catalyst, fast co-pyrolysis, gases, plastic, primary reactions, wood
National Category
Chemical Engineering
Research subject
Resource Recovery
Identifiers
urn:nbn:se:hb:diva-33286 (URN)978-91-89833-66-1 (ISBN)978-91-89833-67-8 (ISBN)
Public defence
C203, Allégatan 1, Borås (English)
Opponent
Supervisors
Available from: 2025-02-28 Created: 2025-02-12 Last updated: 2025-03-24Bibliographically approved

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Supriyanto, SupriyantoYlitervo, PäiviRichards, Tobias

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