TY - JOUR
T1 - Evolution of functional group of lignocellulosic biomass and its delignified form during thermal conversion using synchrotron-based THz and laboratory-based in-situ DRIFT spectroscopy
AU - Kundu, Chandan
AU - Biswas, Saheli
AU - Thomas, Bennet Sam
AU - Appadoo, Dominique
AU - Duan, Alex
AU - Bhattacharya, Sankar
N1 - Funding Information:
The authors thank Sandhya Vijayan and Fatemeh Askari for their assistance during the laboratory work. The authors would like to express their gratitude to Australian Synchrotron and The University of Melbourne for their support and lab facilities. This study was supported by an “Australian Government Research Training Program (RTP) Scholarship”.
Publisher Copyright:
© 2023 The Author(s)
PY - 2023/9/15
Y1 - 2023/9/15
N2 - In the industry, platform chemicals are traditionally synthesized from non-renewable resources. In order to determine the ideal temperature range and associated emissions for the production of platform chemicals from biomass, which is a renewable resource, mechanistic insights into the thermochemical conversion of biomass are needed. Here, the high-resolution synchrotron-based gas-phase THz (Far-IR) spectra and lab-based in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) spectra of both raw and delignified biomass have been studied to identify real-time evolution of the functional groups and any gas-phase secondary reactions during the thermochemical conversion as a function of temperature; these are linked to weight loss measurements through differential thermogravimetry. The high-resolution synchrotron-based technique and DRIFTS were used to acquire the spectra in two different wavenumber ranges of 50–600 cm−1 and 500–4500 cm−1, respectively. The synchrotron-based spectra were used to identify the major gaseous components between 300 and 500 °C of methane, ethane, acetylene and formaldehyde, and their generation followed the order 300 > 400 > 500 °C. The DRIFTS spectra showed that the covalent hydrogen bonds of both raw and delignified biomass was cleaved below 250 °C, between 250 and 300 °C the decarboxylation reaction took place, whereas between 300 and 400 °C platform chemicals (furan, levoglucosan, levoglucosenone) and aromatic compounds were formed from the dehydration of the cellulosic part of the biomass. No changes in the DRIFTS spectra were observed above 400 °C. These results suggest that 300–400 °C is the ideal temperature range for the thermochemical conversion of biomass to platform chemicals. Pyrolysis-gas chromatography/mass spectrometry (Py-GCMS) results demonstrated that the identification of platform chemicals laid the groundwork for large-scale operation.
AB - In the industry, platform chemicals are traditionally synthesized from non-renewable resources. In order to determine the ideal temperature range and associated emissions for the production of platform chemicals from biomass, which is a renewable resource, mechanistic insights into the thermochemical conversion of biomass are needed. Here, the high-resolution synchrotron-based gas-phase THz (Far-IR) spectra and lab-based in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) spectra of both raw and delignified biomass have been studied to identify real-time evolution of the functional groups and any gas-phase secondary reactions during the thermochemical conversion as a function of temperature; these are linked to weight loss measurements through differential thermogravimetry. The high-resolution synchrotron-based technique and DRIFTS were used to acquire the spectra in two different wavenumber ranges of 50–600 cm−1 and 500–4500 cm−1, respectively. The synchrotron-based spectra were used to identify the major gaseous components between 300 and 500 °C of methane, ethane, acetylene and formaldehyde, and their generation followed the order 300 > 400 > 500 °C. The DRIFTS spectra showed that the covalent hydrogen bonds of both raw and delignified biomass was cleaved below 250 °C, between 250 and 300 °C the decarboxylation reaction took place, whereas between 300 and 400 °C platform chemicals (furan, levoglucosan, levoglucosenone) and aromatic compounds were formed from the dehydration of the cellulosic part of the biomass. No changes in the DRIFTS spectra were observed above 400 °C. These results suggest that 300–400 °C is the ideal temperature range for the thermochemical conversion of biomass to platform chemicals. Pyrolysis-gas chromatography/mass spectrometry (Py-GCMS) results demonstrated that the identification of platform chemicals laid the groundwork for large-scale operation.
KW - Biomass
KW - Platform chemicals
KW - Py-GCMS
KW - Synchrotron based THz
KW - Thermochemical conversion
UR - http://www.scopus.com/inward/record.url?scp=85156149218&partnerID=8YFLogxK
U2 - 10.1016/j.fuel.2023.128579
DO - 10.1016/j.fuel.2023.128579
M3 - Article
AN - SCOPUS:85156149218
SN - 0016-2361
VL - 348
JO - Fuel
JF - Fuel
M1 - 128579
ER -