LAPSE:2024.1731v1
Published Article

LAPSE:2024.1731v1
Hydrothermal Co-Liquefaction of Sugarcane Bagasse and Residual Cooking Soybean Oil for Bio-Crude Production
August 23, 2024
Abstract
Hydrothermal co-liquefaction (co-HTL) is a process involving two sources of biomasses aiming at bio-crude production. Since there is a lack of studies performed with sugarcane bagasse and residual soybean oil, this study investigated different conditions for the co-HTL of these biomasses, with and without the presence of ethanol as a co-solvent to maximize the bio-crude yield. All co-HTL reactions were carried out in a 300 mL Parr® reactor at temperatures ranging from 200 to 300 °C. After the reaction, a vacuum filtration was performed to separate the bio-char, later washed with ethanol to extract heavy bio-crude, while the liquid-phase was mixed with dichloromethane to recover light bio-crude. Bio-crude yields of around 95 wt.% were obtained at 300 °C using ethanol and water as solvents. The highest bio-char yield (16.6 wt.%) was achieved when using only sugarcane bagasse as the substrate, without the presence of soybean oil. Bio-crude samples obtained at higher temperatures (280 °C and 300 °C) using ethanol as a hydrogen donor presented higher contents of both free fatty acids and fatty acid ethyl esters. This work presents a promising process to produce high-quality bio-crude using an abundant feedstock (sugarcane bagasse) in the presence of a lipid source which could cause environmental problems if poorly handled.
Hydrothermal co-liquefaction (co-HTL) is a process involving two sources of biomasses aiming at bio-crude production. Since there is a lack of studies performed with sugarcane bagasse and residual soybean oil, this study investigated different conditions for the co-HTL of these biomasses, with and without the presence of ethanol as a co-solvent to maximize the bio-crude yield. All co-HTL reactions were carried out in a 300 mL Parr® reactor at temperatures ranging from 200 to 300 °C. After the reaction, a vacuum filtration was performed to separate the bio-char, later washed with ethanol to extract heavy bio-crude, while the liquid-phase was mixed with dichloromethane to recover light bio-crude. Bio-crude yields of around 95 wt.% were obtained at 300 °C using ethanol and water as solvents. The highest bio-char yield (16.6 wt.%) was achieved when using only sugarcane bagasse as the substrate, without the presence of soybean oil. Bio-crude samples obtained at higher temperatures (280 °C and 300 °C) using ethanol as a hydrogen donor presented higher contents of both free fatty acids and fatty acid ethyl esters. This work presents a promising process to produce high-quality bio-crude using an abundant feedstock (sugarcane bagasse) in the presence of a lipid source which could cause environmental problems if poorly handled.
Record ID
Keywords
bio-crude, Ethanol, hydrothermal co-liquefaction, residual soybean oil, sugarcane bagasse
Subject
Suggested Citation
Oliveira MVD, Pelisson M, Hamerski F, Kanda LRS, Voll FAP, Ramos LP, Corazza ML. Hydrothermal Co-Liquefaction of Sugarcane Bagasse and Residual Cooking Soybean Oil for Bio-Crude Production. (2024). LAPSE:2024.1731v1
Author Affiliations
Oliveira MVD: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil
Pelisson M: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil
Hamerski F: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil
Kanda LRS: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil [ORCID]
Voll FAP: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil
Ramos LP: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil [ORCID]
Corazza ML: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil
Pelisson M: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil
Hamerski F: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil
Kanda LRS: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil [ORCID]
Voll FAP: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil
Ramos LP: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil [ORCID]
Corazza ML: Department of Chemical Engineering, Federal University of Paraná, Rua Coronel Francisco Heráclito dos Santos 100, Curitiba 81531-980, PR, Brazil
Journal Name
Processes
Volume
12
Issue
7
First Page
1371
Year
2024
Publication Date
2024-07-01
ISSN
2227-9717
Version Comments
Original Submission
Other Meta
PII: pr12071371, Publication Type: Journal Article
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LAPSE:2024.1731v1
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https://doi.org/10.3390/pr12071371
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[v1] (Original Submission)
Aug 23, 2024
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Aug 23, 2024
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