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Catalytic co-pyrolysis of poplar tree and polystyrene with HZSM-5 and Fe/HZSM-5 for production of light aromatic hydrocarbons.

Authors :
Guo, Shuaihua
Wang, Zhiwei
Chen, Gaofeng
Chen, Yan
Wu, Mengge
Zhang, Mengju
Li, Zaifeng
Yang, Shuhua
Lei, Tingzhou
Source :
Energy. Jul2024, Vol. 298, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

The catalytic co-pyrolysis of biomass and plastic waste is a highly effective approach for the production of light aromatic hydrocarbons. In this study, catalytic co-pyrolysis experiments were conducted on poplar tree (PT) and polystyrene (PS) using pyrolyzer coupled with gas chromatography/mass spectrometry (Py-GC/MS). The experiments were carried out at a temperature of 550 °C and a mixing ratio of 1:1. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) techniques were employed for the characterization of HZSM-5 and Fe/HZSM-5 catalysts. The findings indicated that the metallic Fe in the HZSM-5 catalyst led to an enhanced production of monocyclic aromatic hydrocarbons (MAH) during the catalytic co-pyrolysis of PT and PS. The proportion of MAH in the products obtained from HZSM-5 and Fe/HZSM-5 catalyst was determined to be 85.84 % and 90.87 %, respectively. In the catalytic co-pyrolysis of biomass and plastic waste, several crucial reactions took place, including deoxidation, olefins aromatization, and Diels-Alder reaction between furans and olefins. In the presence of Fe metal, the HZSM-5 catalyst exhibited enhanced selectivity towards valuable MAH while effectively suppressing the formation of polycyclic aromatic hydrocarbons, resulting in an increase in MAH production to 90.87 %. • Catalytic co-pyrolysis of biomass and plastic was conducted using Py-GC/MS. • XRD, FTIR and SEM were employed for characterization of HZSM-5 and Fe/HZSM-5. • Fe/HZSM-5 catalyst exhibited enhanced selectivity towards valuable MAH. • Catalytic co-pyrolysis mechanism of biomass and plastic was analyzed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03605442
Volume :
298
Database :
Academic Search Index
Journal :
Energy
Publication Type :
Academic Journal
Accession number :
177063331
Full Text :
https://doi.org/10.1016/j.energy.2024.131433