Catalytic hydrotreatment of kraft lignin into aromatic alcohols over nickel-rhenium supported on niobium oxide catalyst
[Display omitted] •Kraft lignin depolymerization was performed over 5Ni-5Re/Nb2O5 catalyst.•Liquid product was rich in low-molecular-weight aromatic alcohol compounds.•The oxophilicity of Nb2O5 was beneficial for promoting cleavage of C-O bonds.•Ethanol was more favorable for the hydrogenolysis of K...
Gespeichert in:
Veröffentlicht in: | Bioresource technology 2020-03, Vol.299, p.122582-122582, Article 122582 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 122582 |
---|---|
container_issue | |
container_start_page | 122582 |
container_title | Bioresource technology |
container_volume | 299 |
creator | Kong, Liping Zhang, Lilin Gu, Junlin Gou, Le Xie, Longfei Wang, Yuanyuan Dai, Liyi |
description | [Display omitted]
•Kraft lignin depolymerization was performed over 5Ni-5Re/Nb2O5 catalyst.•Liquid product was rich in low-molecular-weight aromatic alcohol compounds.•The oxophilicity of Nb2O5 was beneficial for promoting cleavage of C-O bonds.•Ethanol was more favorable for the hydrogenolysis of Kraft lignin.
Direct hydrogenolysis of Kraft lignin was catalyzed over a series of supported Ni or Re catalysts in ethanol solvent. The best results showed that the oil yield of 96.70 wt% was obtained with less char formation at 330 °C for 3 h over 5Ni-5Re/Nb2O5 catalyst. Product analysis demonstrated that the monomer yield of 35.41 wt% was given under mild condition, and low-molecular-weight aromatic alcohols were the main component in the liquid products. Ethanol was found to be more effective in H2 production and facilitated the transformation of phenolic monomers to aromatic chemicals. The results confirmed that the optimal 5Ni-5Re/Nb2O5 catalyst had superior oxophilicity and appropriate acid sites, which improved the ability to directly remove the methoxyl and hydroxyl groups of lignin-derived phenolic compounds without aromatic ring hydrogenation. In addition, the temperature, time and solvent effects on the lignin depolymerization were also investigated. |
doi_str_mv | 10.1016/j.biortech.2019.122582 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_pubmed_primary_31877480</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0960852419318127</els_id><sourcerecordid>2331250692</sourcerecordid><originalsourceid>FETCH-LOGICAL-c368t-4625cff412eb18fa574eed0cd0f28927f409c50e3a50b31d785afa681e1858243</originalsourceid><addsrcrecordid>eNqFkM1uGyEUhVHUqHGTvkLEsptx-ZkfZtfKappIlrJJ1oiBS4w9Aw4wbv32nYmdbrO6Evc7HPgQuqVkSQmtv2-XnQsxg94sGaHtkjJWCXaBFlQ0vGBtU39CC9LWpBAVK6_Ql5S2hBBOG_YZXfGJakpBFujPSmXVH7PTeHM0MeQIKg_gMw4W76KyGffuxTuPnc8BqxgGNcOq12ET-oTDASL2Tu-gL-IGvBsHnMb9fn6cwcFPu9DNh-GvM4D1W13KN-jSqj7B1_O8Rs93v55W98X68ffD6ue60LwWuShrVmlrS8qgo8KqqikBDNGGWCZa1tiStLoiwFVFOk5NIyplVS0oUDH5KPk1-na6dx_D6wgpy8ElDX2vPIQxScY5ZRWpWzah9QnVMaQUwcp9dIOKR0mJnKXLrXyXLmfp8iR9Ct6eO8ZuAPM_9m55An6cAJh-enAQZdIOvAbjIugsTXAfdfwDVMmZLQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2331250692</pqid></control><display><type>article</type><title>Catalytic hydrotreatment of kraft lignin into aromatic alcohols over nickel-rhenium supported on niobium oxide catalyst</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Kong, Liping ; Zhang, Lilin ; Gu, Junlin ; Gou, Le ; Xie, Longfei ; Wang, Yuanyuan ; Dai, Liyi</creator><creatorcontrib>Kong, Liping ; Zhang, Lilin ; Gu, Junlin ; Gou, Le ; Xie, Longfei ; Wang, Yuanyuan ; Dai, Liyi</creatorcontrib><description>[Display omitted]
•Kraft lignin depolymerization was performed over 5Ni-5Re/Nb2O5 catalyst.•Liquid product was rich in low-molecular-weight aromatic alcohol compounds.•The oxophilicity of Nb2O5 was beneficial for promoting cleavage of C-O bonds.•Ethanol was more favorable for the hydrogenolysis of Kraft lignin.
Direct hydrogenolysis of Kraft lignin was catalyzed over a series of supported Ni or Re catalysts in ethanol solvent. The best results showed that the oil yield of 96.70 wt% was obtained with less char formation at 330 °C for 3 h over 5Ni-5Re/Nb2O5 catalyst. Product analysis demonstrated that the monomer yield of 35.41 wt% was given under mild condition, and low-molecular-weight aromatic alcohols were the main component in the liquid products. Ethanol was found to be more effective in H2 production and facilitated the transformation of phenolic monomers to aromatic chemicals. The results confirmed that the optimal 5Ni-5Re/Nb2O5 catalyst had superior oxophilicity and appropriate acid sites, which improved the ability to directly remove the methoxyl and hydroxyl groups of lignin-derived phenolic compounds without aromatic ring hydrogenation. In addition, the temperature, time and solvent effects on the lignin depolymerization were also investigated.</description><identifier>ISSN: 0960-8524</identifier><identifier>EISSN: 1873-2976</identifier><identifier>DOI: 10.1016/j.biortech.2019.122582</identifier><identifier>PMID: 31877480</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Aromatic alcohols ; Catalysis ; Catalysts ; Hydrogenolysis ; Kraft lignin ; Lignin ; Nickel ; Niobium ; Oxides ; Oxophilicity ; Rhenium</subject><ispartof>Bioresource technology, 2020-03, Vol.299, p.122582-122582, Article 122582</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-4625cff412eb18fa574eed0cd0f28927f409c50e3a50b31d785afa681e1858243</citedby><cites>FETCH-LOGICAL-c368t-4625cff412eb18fa574eed0cd0f28927f409c50e3a50b31d785afa681e1858243</cites><orcidid>0000-0002-9705-4050</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.biortech.2019.122582$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31877480$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kong, Liping</creatorcontrib><creatorcontrib>Zhang, Lilin</creatorcontrib><creatorcontrib>Gu, Junlin</creatorcontrib><creatorcontrib>Gou, Le</creatorcontrib><creatorcontrib>Xie, Longfei</creatorcontrib><creatorcontrib>Wang, Yuanyuan</creatorcontrib><creatorcontrib>Dai, Liyi</creatorcontrib><title>Catalytic hydrotreatment of kraft lignin into aromatic alcohols over nickel-rhenium supported on niobium oxide catalyst</title><title>Bioresource technology</title><addtitle>Bioresour Technol</addtitle><description>[Display omitted]
•Kraft lignin depolymerization was performed over 5Ni-5Re/Nb2O5 catalyst.•Liquid product was rich in low-molecular-weight aromatic alcohol compounds.•The oxophilicity of Nb2O5 was beneficial for promoting cleavage of C-O bonds.•Ethanol was more favorable for the hydrogenolysis of Kraft lignin.
Direct hydrogenolysis of Kraft lignin was catalyzed over a series of supported Ni or Re catalysts in ethanol solvent. The best results showed that the oil yield of 96.70 wt% was obtained with less char formation at 330 °C for 3 h over 5Ni-5Re/Nb2O5 catalyst. Product analysis demonstrated that the monomer yield of 35.41 wt% was given under mild condition, and low-molecular-weight aromatic alcohols were the main component in the liquid products. Ethanol was found to be more effective in H2 production and facilitated the transformation of phenolic monomers to aromatic chemicals. The results confirmed that the optimal 5Ni-5Re/Nb2O5 catalyst had superior oxophilicity and appropriate acid sites, which improved the ability to directly remove the methoxyl and hydroxyl groups of lignin-derived phenolic compounds without aromatic ring hydrogenation. In addition, the temperature, time and solvent effects on the lignin depolymerization were also investigated.</description><subject>Aromatic alcohols</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Hydrogenolysis</subject><subject>Kraft lignin</subject><subject>Lignin</subject><subject>Nickel</subject><subject>Niobium</subject><subject>Oxides</subject><subject>Oxophilicity</subject><subject>Rhenium</subject><issn>0960-8524</issn><issn>1873-2976</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1uGyEUhVHUqHGTvkLEsptx-ZkfZtfKappIlrJJ1oiBS4w9Aw4wbv32nYmdbrO6Evc7HPgQuqVkSQmtv2-XnQsxg94sGaHtkjJWCXaBFlQ0vGBtU39CC9LWpBAVK6_Ql5S2hBBOG_YZXfGJakpBFujPSmXVH7PTeHM0MeQIKg_gMw4W76KyGffuxTuPnc8BqxgGNcOq12ET-oTDASL2Tu-gL-IGvBsHnMb9fn6cwcFPu9DNh-GvM4D1W13KN-jSqj7B1_O8Rs93v55W98X68ffD6ue60LwWuShrVmlrS8qgo8KqqikBDNGGWCZa1tiStLoiwFVFOk5NIyplVS0oUDH5KPk1-na6dx_D6wgpy8ElDX2vPIQxScY5ZRWpWzah9QnVMaQUwcp9dIOKR0mJnKXLrXyXLmfp8iR9Ct6eO8ZuAPM_9m55An6cAJh-enAQZdIOvAbjIugsTXAfdfwDVMmZLQ</recordid><startdate>202003</startdate><enddate>202003</enddate><creator>Kong, Liping</creator><creator>Zhang, Lilin</creator><creator>Gu, Junlin</creator><creator>Gou, Le</creator><creator>Xie, Longfei</creator><creator>Wang, Yuanyuan</creator><creator>Dai, Liyi</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9705-4050</orcidid></search><sort><creationdate>202003</creationdate><title>Catalytic hydrotreatment of kraft lignin into aromatic alcohols over nickel-rhenium supported on niobium oxide catalyst</title><author>Kong, Liping ; Zhang, Lilin ; Gu, Junlin ; Gou, Le ; Xie, Longfei ; Wang, Yuanyuan ; Dai, Liyi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-4625cff412eb18fa574eed0cd0f28927f409c50e3a50b31d785afa681e1858243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aromatic alcohols</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Hydrogenolysis</topic><topic>Kraft lignin</topic><topic>Lignin</topic><topic>Nickel</topic><topic>Niobium</topic><topic>Oxides</topic><topic>Oxophilicity</topic><topic>Rhenium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kong, Liping</creatorcontrib><creatorcontrib>Zhang, Lilin</creatorcontrib><creatorcontrib>Gu, Junlin</creatorcontrib><creatorcontrib>Gou, Le</creatorcontrib><creatorcontrib>Xie, Longfei</creatorcontrib><creatorcontrib>Wang, Yuanyuan</creatorcontrib><creatorcontrib>Dai, Liyi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioresource technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kong, Liping</au><au>Zhang, Lilin</au><au>Gu, Junlin</au><au>Gou, Le</au><au>Xie, Longfei</au><au>Wang, Yuanyuan</au><au>Dai, Liyi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catalytic hydrotreatment of kraft lignin into aromatic alcohols over nickel-rhenium supported on niobium oxide catalyst</atitle><jtitle>Bioresource technology</jtitle><addtitle>Bioresour Technol</addtitle><date>2020-03</date><risdate>2020</risdate><volume>299</volume><spage>122582</spage><epage>122582</epage><pages>122582-122582</pages><artnum>122582</artnum><issn>0960-8524</issn><eissn>1873-2976</eissn><abstract>[Display omitted]
•Kraft lignin depolymerization was performed over 5Ni-5Re/Nb2O5 catalyst.•Liquid product was rich in low-molecular-weight aromatic alcohol compounds.•The oxophilicity of Nb2O5 was beneficial for promoting cleavage of C-O bonds.•Ethanol was more favorable for the hydrogenolysis of Kraft lignin.
Direct hydrogenolysis of Kraft lignin was catalyzed over a series of supported Ni or Re catalysts in ethanol solvent. The best results showed that the oil yield of 96.70 wt% was obtained with less char formation at 330 °C for 3 h over 5Ni-5Re/Nb2O5 catalyst. Product analysis demonstrated that the monomer yield of 35.41 wt% was given under mild condition, and low-molecular-weight aromatic alcohols were the main component in the liquid products. Ethanol was found to be more effective in H2 production and facilitated the transformation of phenolic monomers to aromatic chemicals. The results confirmed that the optimal 5Ni-5Re/Nb2O5 catalyst had superior oxophilicity and appropriate acid sites, which improved the ability to directly remove the methoxyl and hydroxyl groups of lignin-derived phenolic compounds without aromatic ring hydrogenation. In addition, the temperature, time and solvent effects on the lignin depolymerization were also investigated.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31877480</pmid><doi>10.1016/j.biortech.2019.122582</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-9705-4050</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0960-8524 |
ispartof | Bioresource technology, 2020-03, Vol.299, p.122582-122582, Article 122582 |
issn | 0960-8524 1873-2976 |
language | eng |
recordid | cdi_pubmed_primary_31877480 |
source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Aromatic alcohols Catalysis Catalysts Hydrogenolysis Kraft lignin Lignin Nickel Niobium Oxides Oxophilicity Rhenium |
title | Catalytic hydrotreatment of kraft lignin into aromatic alcohols over nickel-rhenium supported on niobium oxide catalyst |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T13%3A50%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Catalytic%20hydrotreatment%20of%20kraft%20lignin%20into%20aromatic%20alcohols%20over%20nickel-rhenium%20supported%20on%20niobium%20oxide%20catalyst&rft.jtitle=Bioresource%20technology&rft.au=Kong,%20Liping&rft.date=2020-03&rft.volume=299&rft.spage=122582&rft.epage=122582&rft.pages=122582-122582&rft.artnum=122582&rft.issn=0960-8524&rft.eissn=1873-2976&rft_id=info:doi/10.1016/j.biortech.2019.122582&rft_dat=%3Cproquest_cross%3E2331250692%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2331250692&rft_id=info:pmid/31877480&rft_els_id=S0960852419318127&rfr_iscdi=true |