Composition of the isopropanol-soluble portion and fast pyrolysis product distribution of the insoluble part from Pakistani lignite

Pakistani lignite (PLC) was thermally dissolved at 300 °C using isopropanol (IPA) to obtain a soluble portion (SP) and insoluble portion (ISP). Proximate analysis, ultimate analysis, Fourier transform infrared spectrometry (FTIR), thermogravimetric analysis (TG-DTG) and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) results were compared to explore the influence of the thermal dissolution process on the pyrolysis for PLC and ISP. Results showed that the thermal dissolution process mainly dissolved some light components of low-rank coal, and more phenols, aldehydes, esters and ethers were found in the SP, indicating that low-carbon alcohols can break the ether bridge bond in coal and generate oxygen-containing organic compounds (OCOCs). Compared with PLC, ISP had better thermal stability, low activation energy and pre-exponential factor. Furthermore, thermal dissolution dissolves small molecular compounds in coal channels, enlarges the pore structure and mass transfer rate, and enables the compounds produced in the pyrolysis process to diffuse to the surface of coal faster. On the other hand, IPA could be used as a hydrogen supply solvent to weaken the oxygen bridge bond in the macromolecular structure of coal, so that it is easier to break during pyrolysis. Thus, it was demonstrated that the low molecular weight compounds have a significant effect on the low temperature pyrolysis characteristics of PLC, and these two processes could potentially improve the added value of coal.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d4ra07749k
Citations
3
Primary Topic
Thermochemical Biomass Conversion Processes
Type
article
Field-Weighted Citation Impact
2.02
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article

Composition of the isopropanol-soluble portion and fast pyrolysis product distribution of the insoluble part from Pakistani lignite

Guihan Zhao, Xian‐Yong Wei, Naeem Akram, Yaya Ma et al.
3 citations
RSC Advances
Thermochemical Biomass Conversion Processes
2.02
article

Composition of the isopropanol-soluble portion and fast pyrolysis product distribution of the insoluble part from Pakistani lignite

Guihan Zhao, Xian‐Yong Wei, Naeem Akram, Yaya Ma, Wen‐Long Mo, Xing Fan, Jun Xiao, Jia Guo, Yuan Ren
article en
3 citations

Abstract

Pakistani lignite (PLC) was thermally dissolved at 300 °C using isopropanol (IPA) to obtain a soluble portion (SP) and insoluble portion (ISP). Proximate analysis, ultimate analysis, Fourier transform infrared spectrometry (FTIR), thermogravimetric analysis (TG-DTG) and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) results were compared to explore the influence of the thermal dissolution process on the pyrolysis for PLC and ISP. Results showed that the thermal dissolution process mainly dissolved some light components of low-rank coal, and more phenols, aldehydes, esters and ethers were found in the SP, indicating that low-carbon alcohols can break the ether bridge bond in coal and generate oxygen-containing organic compounds (OCOCs). Compared with PLC, ISP had better thermal stability, low activation energy and pre-exponential factor. Furthermore, thermal dissolution dissolves small molecular compounds in coal channels, enlarges the pore structure and mass transfer rate, and enables the compounds produced in the pyrolysis process to diffuse to the surface of coal faster. On the other hand, IPA could be used as a hydrogen supply solvent to weaken the oxygen bridge bond in the macromolecular structure of coal, so that it is easier to break during pyrolysis. Thus, it was demonstrated that the low molecular weight compounds have a significant effect on the low temperature pyrolysis characteristics of PLC, and these two processes could potentially improve the added value of coal.

RSC AdvancesVol. 15(1)
Minhaj University Lahore (PK), Xinjiang New Energy Research Institute (China) (CN), Xinjiang University (CN)
Openalex Percentile: Top 16%
Thermochemical Biomass Conversion Processes
2.02
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