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Catalytic hydroconversion of pyrolytic bio-oil: Understanding and limiting macromolecules formation
Fast pyrolysis followed by catalytic hydroconversion is a value chain aimed to transform lignocellulosic biomass into biofuel or chemicals. During hydroconversion, desired catalytic deoxygenation reactions are in competition with thermal side reactions like condensation or oligomerization. These und...
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Published in: | Biomass & bioenergy 2018-01, Vol.108, p.501-510 |
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creator | Ozagac, Mathieu Bertino-Ghera, C. Uzio, D. Quignard, A. Laurenti, D. Geantet, C. |
description | Fast pyrolysis followed by catalytic hydroconversion is a value chain aimed to transform lignocellulosic biomass into biofuel or chemicals. During hydroconversion, desired catalytic deoxygenation reactions are in competition with thermal side reactions like condensation or oligomerization. These undesired pathways lead to high molecular weight compounds (i.e. macromolecules) that are responsible for catalyst deactivation and severe plugging of the reactor. We investigate here the impact of a phenolic compound on the formation of these macromolecules. Catalytic hydroconversion of a fast pyrolysis bio-oil and a bio-oil/guaiacol (50/50 wt%) mixture were carried out in a batch reactor using a NiMo/alumina catalyst. An extended analytical strategy has been developed involving size-exclusion chromatography (SEC) and liquid state 13C NMR dedicated to the in depth characterization of effluents as well as physicochemical analysis of the fresh and used catalyst (XRD, Hg porosimetry, N2 physisorption, STEM). This strategy allowed bringing new insights on aromatic structures larger than 1000 g.mol−1 and their formation mechanism. This formation can be chemically inhibited by the introduction of organic component such as guaiacol. This stabilization was mainly observed and explained at low temperature and short reaction time.
[Display omitted]
•Macromolecules formation was investigated depending on operating conditions.•Crossing SEC, GC and 13C NMR analyses was performed to describe the macromolecules.•SEC analysis highlighted structures beyond 5000 g.mol−1 during BO catalytic hydroconversion.•Guaiacol reacts with macromolecules precursors limiting their extension.•Stabilization was mainly observed at low temperature and short reaction time. |
doi_str_mv | 10.1016/j.biombioe.2017.10.002 |
format | article |
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[Display omitted]
•Macromolecules formation was investigated depending on operating conditions.•Crossing SEC, GC and 13C NMR analyses was performed to describe the macromolecules.•SEC analysis highlighted structures beyond 5000 g.mol−1 during BO catalytic hydroconversion.•Guaiacol reacts with macromolecules precursors limiting their extension.•Stabilization was mainly observed at low temperature and short reaction time.</description><identifier>ISSN: 0961-9534</identifier><identifier>EISSN: 1873-2909</identifier><identifier>DOI: 10.1016/j.biombioe.2017.10.002</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Biofuel ; Catalysis ; Chemical engineering ; Chemical Sciences ; Guaiacol ; Humins ; Hydrodeoxygenation ; Oligomers ; SEC</subject><ispartof>Biomass & bioenergy, 2018-01, Vol.108, p.501-510</ispartof><rights>2017 Elsevier Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-5bd447151591cafdf0269b98e3fe1dae7e82287160f0719bc2f794f752fde4ff3</citedby><cites>FETCH-LOGICAL-c431t-5bd447151591cafdf0269b98e3fe1dae7e82287160f0719bc2f794f752fde4ff3</cites><orcidid>0000-0001-6645-6789 ; 0000-0002-3582-9244</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><backlink>$$Uhttps://hal.science/hal-01688399$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Ozagac, Mathieu</creatorcontrib><creatorcontrib>Bertino-Ghera, C.</creatorcontrib><creatorcontrib>Uzio, D.</creatorcontrib><creatorcontrib>Quignard, A.</creatorcontrib><creatorcontrib>Laurenti, D.</creatorcontrib><creatorcontrib>Geantet, C.</creatorcontrib><title>Catalytic hydroconversion of pyrolytic bio-oil: Understanding and limiting macromolecules formation</title><title>Biomass & bioenergy</title><description>Fast pyrolysis followed by catalytic hydroconversion is a value chain aimed to transform lignocellulosic biomass into biofuel or chemicals. During hydroconversion, desired catalytic deoxygenation reactions are in competition with thermal side reactions like condensation or oligomerization. These undesired pathways lead to high molecular weight compounds (i.e. macromolecules) that are responsible for catalyst deactivation and severe plugging of the reactor. We investigate here the impact of a phenolic compound on the formation of these macromolecules. Catalytic hydroconversion of a fast pyrolysis bio-oil and a bio-oil/guaiacol (50/50 wt%) mixture were carried out in a batch reactor using a NiMo/alumina catalyst. An extended analytical strategy has been developed involving size-exclusion chromatography (SEC) and liquid state 13C NMR dedicated to the in depth characterization of effluents as well as physicochemical analysis of the fresh and used catalyst (XRD, Hg porosimetry, N2 physisorption, STEM). This strategy allowed bringing new insights on aromatic structures larger than 1000 g.mol−1 and their formation mechanism. This formation can be chemically inhibited by the introduction of organic component such as guaiacol. This stabilization was mainly observed and explained at low temperature and short reaction time.
[Display omitted]
•Macromolecules formation was investigated depending on operating conditions.•Crossing SEC, GC and 13C NMR analyses was performed to describe the macromolecules.•SEC analysis highlighted structures beyond 5000 g.mol−1 during BO catalytic hydroconversion.•Guaiacol reacts with macromolecules precursors limiting their extension.•Stabilization was mainly observed at low temperature and short reaction time.</description><subject>Biofuel</subject><subject>Catalysis</subject><subject>Chemical engineering</subject><subject>Chemical Sciences</subject><subject>Guaiacol</subject><subject>Humins</subject><subject>Hydrodeoxygenation</subject><subject>Oligomers</subject><subject>SEC</subject><issn>0961-9534</issn><issn>1873-2909</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LxDAQhoMouK7-BenVQ9dMmjaNJ5fFL1jw4p5Dmg83S9ssSV3ovzel6tXDMMw7874kD0K3gFeAobo_rBrnu1RmRTCwJK4wJmdoATUrcsIxP0cLzCvIeVnQS3QV4wFjoJjCAqmNHGQ7Dk5l-1EHr3x_MiE632feZscx-HmZ4nPv2ods1-u0H2SvXf-ZpZa1rnPDNHRSBd_51qiv1sTM-tDJISVdowsr22hufvoS7Z6fPjav-fb95W2z3uaKFjDkZaMpZVBCyUFJqy0mFW94bQprQEvDTE1IzaDCFjPgjSKWcWpZSaw21Npiie7m3L1sxTG4ToZReOnE63orJi3RquuC8xOk22q-TU-OMRj7ZwAsJqziIH6xignrpCesyfg4G036ycmZIKJypldGu2DUILR3_0V8A0sYhqc</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Ozagac, Mathieu</creator><creator>Bertino-Ghera, C.</creator><creator>Uzio, D.</creator><creator>Quignard, A.</creator><creator>Laurenti, D.</creator><creator>Geantet, C.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-6645-6789</orcidid><orcidid>https://orcid.org/0000-0002-3582-9244</orcidid></search><sort><creationdate>201801</creationdate><title>Catalytic hydroconversion of pyrolytic bio-oil: Understanding and limiting macromolecules formation</title><author>Ozagac, Mathieu ; Bertino-Ghera, C. ; Uzio, D. ; Quignard, A. ; Laurenti, D. ; Geantet, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-5bd447151591cafdf0269b98e3fe1dae7e82287160f0719bc2f794f752fde4ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Biofuel</topic><topic>Catalysis</topic><topic>Chemical engineering</topic><topic>Chemical Sciences</topic><topic>Guaiacol</topic><topic>Humins</topic><topic>Hydrodeoxygenation</topic><topic>Oligomers</topic><topic>SEC</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ozagac, Mathieu</creatorcontrib><creatorcontrib>Bertino-Ghera, C.</creatorcontrib><creatorcontrib>Uzio, D.</creatorcontrib><creatorcontrib>Quignard, A.</creatorcontrib><creatorcontrib>Laurenti, D.</creatorcontrib><creatorcontrib>Geantet, C.</creatorcontrib><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Biomass & bioenergy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ozagac, Mathieu</au><au>Bertino-Ghera, C.</au><au>Uzio, D.</au><au>Quignard, A.</au><au>Laurenti, D.</au><au>Geantet, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catalytic hydroconversion of pyrolytic bio-oil: Understanding and limiting macromolecules formation</atitle><jtitle>Biomass & bioenergy</jtitle><date>2018-01</date><risdate>2018</risdate><volume>108</volume><spage>501</spage><epage>510</epage><pages>501-510</pages><issn>0961-9534</issn><eissn>1873-2909</eissn><abstract>Fast pyrolysis followed by catalytic hydroconversion is a value chain aimed to transform lignocellulosic biomass into biofuel or chemicals. During hydroconversion, desired catalytic deoxygenation reactions are in competition with thermal side reactions like condensation or oligomerization. These undesired pathways lead to high molecular weight compounds (i.e. macromolecules) that are responsible for catalyst deactivation and severe plugging of the reactor. We investigate here the impact of a phenolic compound on the formation of these macromolecules. Catalytic hydroconversion of a fast pyrolysis bio-oil and a bio-oil/guaiacol (50/50 wt%) mixture were carried out in a batch reactor using a NiMo/alumina catalyst. An extended analytical strategy has been developed involving size-exclusion chromatography (SEC) and liquid state 13C NMR dedicated to the in depth characterization of effluents as well as physicochemical analysis of the fresh and used catalyst (XRD, Hg porosimetry, N2 physisorption, STEM). This strategy allowed bringing new insights on aromatic structures larger than 1000 g.mol−1 and their formation mechanism. This formation can be chemically inhibited by the introduction of organic component such as guaiacol. This stabilization was mainly observed and explained at low temperature and short reaction time.
[Display omitted]
•Macromolecules formation was investigated depending on operating conditions.•Crossing SEC, GC and 13C NMR analyses was performed to describe the macromolecules.•SEC analysis highlighted structures beyond 5000 g.mol−1 during BO catalytic hydroconversion.•Guaiacol reacts with macromolecules precursors limiting their extension.•Stabilization was mainly observed at low temperature and short reaction time.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.biombioe.2017.10.002</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-6645-6789</orcidid><orcidid>https://orcid.org/0000-0002-3582-9244</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biofuel Catalysis Chemical engineering Chemical Sciences Guaiacol Humins Hydrodeoxygenation Oligomers SEC |
title | Catalytic hydroconversion of pyrolytic bio-oil: Understanding and limiting macromolecules formation |
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