Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 degrees C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main...
Gespeichert in:
Veröffentlicht in: | Journal of catalysis 2008-02, Vol.254 (1), p.71-78 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 78 |
---|---|
container_issue | 1 |
container_start_page | 71 |
container_title | Journal of catalysis |
container_volume | 254 |
creator | CAMPO, Betiana PETIT, Corinne VOLPE, Maria A |
description | The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 degrees C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main product in the deactivation period, whereas crotyl alcohol, butanal, butanol, and condensation products were produced under steady-state conditions. The activity and selectivity to crotyl alcohol (in the 20-32% range) were lower than those for the high-surface area ceria catalysts studied previously [B. Campo, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 242 (2006) 162]. Samples were characterized by TPR, XPS, TEM, and XRD. The analysis of catalytic and characterization results indicates that gold particles supported on low- and medium-surface area ceria were relatively large, and the promotional effect of Ce3+ species was not achieved for the corresponding catalysts. Moreover, under reductive conditions, sintering still increased gold particle size. [PUBLICATION ABSTRACT] |
doi_str_mv | 10.1016/j.jcat.2007.11.018 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_195453651</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1574228291</sourcerecordid><originalsourceid>FETCH-LOGICAL-c348t-a711d1d65e9e5b91c370442183853bd1961acd716e7a0240badc64164e72b9cc3</originalsourceid><addsrcrecordid>eNo9kE9LxDAQxYMouK5-AU9F8NjuTJo_zUVYFnWFhb3oOaRJqi21XZPuod_eLC6eBob33sz7EXKPUCCgWHVFZ81UUABZIBaA1QVZICjIqVDskiwAKOaKo7wmNzF2AIicVwvytJ1dGD_9YKZ2HLKxyWwYp3EwvfNfs_NZWrq2aXzww5Stj6uN39Ms3TL9HKd4S64a00d_d55L8vHy_L7Z5rv969tmvcttyaopNxLRoRPcK89rhbaUwBjFqqx4WTtUAo11EoWXBiiD2jgrGArmJa2VteWSPPzlHsL4c_Rx0t14DOnLqFFxxkvBMYnonyhViDH4Rh9C-23CrBH0CZPu9AmTPmHSiDphSqbHc7KJ1vRNMINt478zSYWUnJa_h_Fn8w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>195453651</pqid></control><display><type>article</type><title>Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts</title><source>Access via ScienceDirect (Elsevier)</source><creator>CAMPO, Betiana ; PETIT, Corinne ; VOLPE, Maria A</creator><creatorcontrib>CAMPO, Betiana ; PETIT, Corinne ; VOLPE, Maria A</creatorcontrib><description>The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 degrees C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main product in the deactivation period, whereas crotyl alcohol, butanal, butanol, and condensation products were produced under steady-state conditions. The activity and selectivity to crotyl alcohol (in the 20-32% range) were lower than those for the high-surface area ceria catalysts studied previously [B. Campo, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 242 (2006) 162]. Samples were characterized by TPR, XPS, TEM, and XRD. The analysis of catalytic and characterization results indicates that gold particles supported on low- and medium-surface area ceria were relatively large, and the promotional effect of Ce3+ species was not achieved for the corresponding catalysts. Moreover, under reductive conditions, sintering still increased gold particle size. [PUBLICATION ABSTRACT]</description><identifier>ISSN: 0021-9517</identifier><identifier>EISSN: 1090-2694</identifier><identifier>DOI: 10.1016/j.jcat.2007.11.018</identifier><identifier>CODEN: JCTLA5</identifier><language>eng</language><publisher>Amsterdam: Elsevier</publisher><subject>Alcohol ; Catalysis ; Catalysts ; Chemical reactions ; Chemistry ; Exact sciences and technology ; General and physical chemistry ; Gold ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Journal of catalysis, 2008-02, Vol.254 (1), p.71-78</ispartof><rights>2008 INIST-CNRS</rights><rights>Copyright © 2008 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c348t-a711d1d65e9e5b91c370442183853bd1961acd716e7a0240badc64164e72b9cc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20067752$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>CAMPO, Betiana</creatorcontrib><creatorcontrib>PETIT, Corinne</creatorcontrib><creatorcontrib>VOLPE, Maria A</creatorcontrib><title>Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts</title><title>Journal of catalysis</title><description>The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 degrees C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main product in the deactivation period, whereas crotyl alcohol, butanal, butanol, and condensation products were produced under steady-state conditions. The activity and selectivity to crotyl alcohol (in the 20-32% range) were lower than those for the high-surface area ceria catalysts studied previously [B. Campo, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 242 (2006) 162]. Samples were characterized by TPR, XPS, TEM, and XRD. The analysis of catalytic and characterization results indicates that gold particles supported on low- and medium-surface area ceria were relatively large, and the promotional effect of Ce3+ species was not achieved for the corresponding catalysts. Moreover, under reductive conditions, sintering still increased gold particle size. [PUBLICATION ABSTRACT]</description><subject>Alcohol</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chemical reactions</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Gold</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><issn>0021-9517</issn><issn>1090-2694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNo9kE9LxDAQxYMouK5-AU9F8NjuTJo_zUVYFnWFhb3oOaRJqi21XZPuod_eLC6eBob33sz7EXKPUCCgWHVFZ81UUABZIBaA1QVZICjIqVDskiwAKOaKo7wmNzF2AIicVwvytJ1dGD_9YKZ2HLKxyWwYp3EwvfNfs_NZWrq2aXzww5Stj6uN39Ms3TL9HKd4S64a00d_d55L8vHy_L7Z5rv969tmvcttyaopNxLRoRPcK89rhbaUwBjFqqx4WTtUAo11EoWXBiiD2jgrGArmJa2VteWSPPzlHsL4c_Rx0t14DOnLqFFxxkvBMYnonyhViDH4Rh9C-23CrBH0CZPu9AmTPmHSiDphSqbHc7KJ1vRNMINt478zSYWUnJa_h_Fn8w</recordid><startdate>20080215</startdate><enddate>20080215</enddate><creator>CAMPO, Betiana</creator><creator>PETIT, Corinne</creator><creator>VOLPE, Maria A</creator><general>Elsevier</general><general>Elsevier BV</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20080215</creationdate><title>Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts</title><author>CAMPO, Betiana ; PETIT, Corinne ; VOLPE, Maria A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-a711d1d65e9e5b91c370442183853bd1961acd716e7a0240badc64164e72b9cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Alcohol</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Chemical reactions</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Gold</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CAMPO, Betiana</creatorcontrib><creatorcontrib>PETIT, Corinne</creatorcontrib><creatorcontrib>VOLPE, Maria A</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CAMPO, Betiana</au><au>PETIT, Corinne</au><au>VOLPE, Maria A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts</atitle><jtitle>Journal of catalysis</jtitle><date>2008-02-15</date><risdate>2008</risdate><volume>254</volume><issue>1</issue><spage>71</spage><epage>78</epage><pages>71-78</pages><issn>0021-9517</issn><eissn>1090-2694</eissn><coden>JCTLA5</coden><abstract>The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 degrees C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main product in the deactivation period, whereas crotyl alcohol, butanal, butanol, and condensation products were produced under steady-state conditions. The activity and selectivity to crotyl alcohol (in the 20-32% range) were lower than those for the high-surface area ceria catalysts studied previously [B. Campo, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 242 (2006) 162]. Samples were characterized by TPR, XPS, TEM, and XRD. The analysis of catalytic and characterization results indicates that gold particles supported on low- and medium-surface area ceria were relatively large, and the promotional effect of Ce3+ species was not achieved for the corresponding catalysts. Moreover, under reductive conditions, sintering still increased gold particle size. [PUBLICATION ABSTRACT]</abstract><cop>Amsterdam</cop><pub>Elsevier</pub><doi>10.1016/j.jcat.2007.11.018</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9517 |
ispartof | Journal of catalysis, 2008-02, Vol.254 (1), p.71-78 |
issn | 0021-9517 1090-2694 |
language | eng |
recordid | cdi_proquest_journals_195453651 |
source | Access via ScienceDirect (Elsevier) |
subjects | Alcohol Catalysis Catalysts Chemical reactions Chemistry Exact sciences and technology General and physical chemistry Gold Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T23%3A16%3A41IST&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=Hydrogenation%20of%20crotonaldehyde%20on%20different%20Au/CeO2%20catalysts&rft.jtitle=Journal%20of%20catalysis&rft.au=CAMPO,%20Betiana&rft.date=2008-02-15&rft.volume=254&rft.issue=1&rft.spage=71&rft.epage=78&rft.pages=71-78&rft.issn=0021-9517&rft.eissn=1090-2694&rft.coden=JCTLA5&rft_id=info:doi/10.1016/j.jcat.2007.11.018&rft_dat=%3Cproquest_cross%3E1574228291%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=195453651&rft_id=info:pmid/&rfr_iscdi=true |