Assessment of hydrothermal pretreatment of various lignocellulosic biomass with CO2 catalyst for enhanced methane and hydrogen production.
Identifieur interne : 000653 ( PubMed/Corpus ); précédent : 000652; suivant : 000654Assessment of hydrothermal pretreatment of various lignocellulosic biomass with CO2 catalyst for enhanced methane and hydrogen production.
Auteurs : Cigdem Eskicioglu ; Florian Monlau ; Abdellatif Barakat ; Ivet Ferrer ; Prasad Kaparaju ; Eric Trably ; Hélène CarrèreSource :
- Water research [ 1879-2448 ] ; 2017.
English descriptors
- KwdEn :
- MESH :
- chemical : Hydrogen, Lignin, Methane.
- Anaerobiosis, Biomass.
Abstract
Hydrothermal pretreatment of five lignocellulosic substrates (i.e. wheat straw, rice straw, biomass sorghum, corn stover and Douglas fir bark) were conducted in the presence of CO2 as a catalyst. To maximize disintegration and conversion into bioenergy (methane and hydrogen), pretreatment temperatures and subsequent pressures varied with a range of 26-175 °C, and 25-102 bars, respectively. Among lignin, cellulose and hemicelluloses, hydrothermal pretreatment caused the highest reduction (23-42%) in hemicelluloses while delignification was limited to only 0-12%. These reductions in structural integrity resulted in 20-30% faster hydrolysis rates during anaerobic digestion for the pretreated substrates of straws, sorghum, and corn stover while Douglas fir bark yielded 172% faster hydrolysis/digestion due to its highly refractory nature in the control. Furans and phenolic compounds formed in the pretreated hydrolyzates were below the inhibitory levels for methane and hydrogen production which had a range of 98-340 ml CH4/g volatile solids (VS) and 5-26 ml H2/g VS, respectively. Results indicated that hydrothermal pretreatment is able to accelerate the rate of biodegradation without generating high levels of inhibitory compounds while showing no discernible effect on ultimate biodegradation.
DOI: 10.1016/j.watres.2017.04.068
PubMed: 28478293
Links to Exploration step
pubmed:28478293Le document en format XML
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<author><name sortKey="Eskicioglu, Cigdem" sort="Eskicioglu, Cigdem" uniqKey="Eskicioglu C" first="Cigdem" last="Eskicioglu">Cigdem Eskicioglu</name>
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<author><name sortKey="Monlau, Florian" sort="Monlau, Florian" uniqKey="Monlau F" first="Florian" last="Monlau">Florian Monlau</name>
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<author><name sortKey="Kaparaju, Prasad" sort="Kaparaju, Prasad" uniqKey="Kaparaju P" first="Prasad" last="Kaparaju">Prasad Kaparaju</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Assessment of hydrothermal pretreatment of various lignocellulosic biomass with CO2 catalyst for enhanced methane and hydrogen production.</title>
<author><name sortKey="Eskicioglu, Cigdem" sort="Eskicioglu, Cigdem" uniqKey="Eskicioglu C" first="Cigdem" last="Eskicioglu">Cigdem Eskicioglu</name>
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<author><name sortKey="Monlau, Florian" sort="Monlau, Florian" uniqKey="Monlau F" first="Florian" last="Monlau">Florian Monlau</name>
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<author><name sortKey="Kaparaju, Prasad" sort="Kaparaju, Prasad" uniqKey="Kaparaju P" first="Prasad" last="Kaparaju">Prasad Kaparaju</name>
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<author><name sortKey="Carrere, Helene" sort="Carrere, Helene" uniqKey="Carrere H" first="Hélène" last="Carrère">Hélène Carrère</name>
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<series><title level="j">Water research</title>
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<term>Lignin</term>
<term>Methane</term>
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<term>Lignin</term>
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<front><div type="abstract" xml:lang="en">Hydrothermal pretreatment of five lignocellulosic substrates (i.e. wheat straw, rice straw, biomass sorghum, corn stover and Douglas fir bark) were conducted in the presence of CO2 as a catalyst. To maximize disintegration and conversion into bioenergy (methane and hydrogen), pretreatment temperatures and subsequent pressures varied with a range of 26-175 °C, and 25-102 bars, respectively. Among lignin, cellulose and hemicelluloses, hydrothermal pretreatment caused the highest reduction (23-42%) in hemicelluloses while delignification was limited to only 0-12%. These reductions in structural integrity resulted in 20-30% faster hydrolysis rates during anaerobic digestion for the pretreated substrates of straws, sorghum, and corn stover while Douglas fir bark yielded 172% faster hydrolysis/digestion due to its highly refractory nature in the control. Furans and phenolic compounds formed in the pretreated hydrolyzates were below the inhibitory levels for methane and hydrogen production which had a range of 98-340 ml CH4/g volatile solids (VS) and 5-26 ml H2/g VS, respectively. Results indicated that hydrothermal pretreatment is able to accelerate the rate of biodegradation without generating high levels of inhibitory compounds while showing no discernible effect on ultimate biodegradation.</div>
</front>
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<Abstract><AbstractText>Hydrothermal pretreatment of five lignocellulosic substrates (i.e. wheat straw, rice straw, biomass sorghum, corn stover and Douglas fir bark) were conducted in the presence of CO2 as a catalyst. To maximize disintegration and conversion into bioenergy (methane and hydrogen), pretreatment temperatures and subsequent pressures varied with a range of 26-175 °C, and 25-102 bars, respectively. Among lignin, cellulose and hemicelluloses, hydrothermal pretreatment caused the highest reduction (23-42%) in hemicelluloses while delignification was limited to only 0-12%. These reductions in structural integrity resulted in 20-30% faster hydrolysis rates during anaerobic digestion for the pretreated substrates of straws, sorghum, and corn stover while Douglas fir bark yielded 172% faster hydrolysis/digestion due to its highly refractory nature in the control. Furans and phenolic compounds formed in the pretreated hydrolyzates were below the inhibitory levels for methane and hydrogen production which had a range of 98-340 ml CH4/g volatile solids (VS) and 5-26 ml H2/g VS, respectively. Results indicated that hydrothermal pretreatment is able to accelerate the rate of biodegradation without generating high levels of inhibitory compounds while showing no discernible effect on ultimate biodegradation.</AbstractText>
<CopyrightInformation>Copyright © 2017 Elsevier Ltd. All rights reserved.</CopyrightInformation>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Eskicioglu</LastName>
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<AffiliationInfo><Affiliation>UBC Bioreactor Technology Group, School of Engineering, The University of British Columbia, Okanagan Campus, 3333 University Way, Kelowna, BC V1V 1V7, Canada; LBE, INRA, 11100, Narbonne, France. Electronic address: cigdem.eskicioglu@ubc.ca.</Affiliation>
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