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Gaseous products from primary reactions of fast plastic pyrolysis
University of Borås, Faculty of Textiles, Engineering and Business. (Swedish Centre for Resource Recovery)ORCID iD: 0000-0003-3239-019x
University of Borås, Faculty of Textiles, Engineering and Business. (Swedish Centre for Resource Recovery)
University of Borås, Faculty of Textiles, Engineering and Business. (Swedish Centre for Resource Recovery)ORCID iD: 0000-0003-0037-3555
2021 (English)In: Journal of Analytical and Applied Pyrolysis, ISSN 0165-2370, E-ISSN 1873-250X, Vol. 158Article in journal (Refereed) Published
Abstract [en]

This study aimed to establish primary reactions and identify gaseous products during fast pyrolysis of low-density polyethylene (LDPE), polypropylene (PP) and polystyrene (PS). Fast pyrolysis was performed by using Py-GC/MS/FID at 574 ± 22 °C for 5 s. Gaseous fractions formed during pyrolysis of LDPE, PP and PS were 14 ± 1 wt%, 31 ± 3 wt% and 103 ± 12 wt%, respectively. The main gaseous compounds from LDPE were butane, 1-pentane and 1-hexene. PP pyrolysis gave propene, pentane and 2,4-dimethyl-1-heptene as the main gaseous compounds. Styrene monomer was the dominant gas from PS. The results showed that polyolefin (PP and PE) produced aliphatic hydrocarbons, while PS formed aromatic hydrocarbons. Furthermore, the proposed mechanism suggests that both inter- and intra-molecular hydrogen transfer occur during PP and PE pyrolysis. PS pyrolysis involves a C-C cleavage at the aliphatic side chain. This work is important to understand the mechanism of gas formation of primary reactions from pyrolysis of common plastics.

Place, publisher, year, edition, pages
2021. Vol. 158
Keywords [en]
Fast pyrolysis, Gas products, Primary reactions, Polyethylene, Polypropylene, Polystyrene
National Category
Energy Engineering
Identifiers
URN: urn:nbn:se:hb:diva-26037DOI: 10.1016/j.jaap.2021.105248ISI: 000687223400008Scopus ID: 2-s2.0-85109107107OAI: oai:DiVA.org:hb-26037DiVA, id: diva2:1579743
Available from: 2021-07-10 Created: 2021-07-10 Last updated: 2025-09-24Bibliographically 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: 2025-09-24Bibliographically approved

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Publisher's full textScopushttps://www.sciencedirect.com/science/article/pii/S0165237021002345

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Supriyanto, SupriyantoYlitervo, PäiviRichards, Tobias

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