Catalysis on Pd/WO3 and Pd/WO2: Effect of the Modifications of the Surface States Due to Redox Treatments on the Skeletal Rearrangement of Hydrocarbons: Part I. Physical and Chemical Characterizations of Catalysts by BET, TPR, XRD, XAS, and XPS

Bulk and surface properties of Pd/WO3 and Pd/WO2 catalysts were studied using temperature programmed reduction, X-ray diffraction, X-ray absorption, and X-ray photoelectron spectroscopies. Special attention was paid to the oxidation state of tungsten upon reduction under hydrogen at 350 and 600°C. T...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of catalysis 1999-06, Vol.184 (2), p.406-420
Hauptverfasser: Bigey, C., Hilaire, L., Maire, G.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 420
container_issue 2
container_start_page 406
container_title Journal of catalysis
container_volume 184
creator Bigey, C.
Hilaire, L.
Maire, G.
description Bulk and surface properties of Pd/WO3 and Pd/WO2 catalysts were studied using temperature programmed reduction, X-ray diffraction, X-ray absorption, and X-ray photoelectron spectroscopies. Special attention was paid to the oxidation state of tungsten upon reduction under hydrogen at 350 and 600°C. The influence of oxidation treatments was also studied. Our results showed that reduction at 350°C led to the tranformation of bulk WO3 into the stable W20O58 phase. At higher reduction temperature and also at 350°C, if the support WO3 was calcined before impregnation, metallic tungsten was detected and we postulated that this transformation starts with the formation of the metastable W3O phase via W20O58. All these transformations concern the surface as well as the bulk for Pd/WO3 catalysts and the WO3 contamination layer only for Pd/WO2 catalyst. WO2 seems more difficult to reduce than WO3 even if the latter becomes less reducible after oxidation treatment. Autoreduction of the palladium salt was suggested on these catalysts, resulting both from the pretreatment of the supports and the nature of the Pd salt. Addition of a metal to bulk oxides facilitates their reducibility and allows one to obtain a stable surface state.
doi_str_mv 10.1006/jcat.1999.2466
format Article
fullrecord <record><control><sourceid>elsevier_pasca</sourceid><recordid>TN_cdi_pascalfrancis_primary_1837753</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021951799924661</els_id><sourcerecordid>S0021951799924661</sourcerecordid><originalsourceid>FETCH-LOGICAL-e231t-b73f2af32fc1e465bf68bcd192bb10d2fbbdf239616c3ec62d29c65021fb3d893</originalsourceid><addsrcrecordid>eNpFUU1vEzEUtBBIhMKVsw8cs6k_ss66t7INtFJRV0kQvVn-eCYuyW5lu4jwu_kBeJMiLn5-9mhm3huE3lMyo4SI8wer84xKKWdsLsQLNKFEkooJOX-JJoQwWsmaLl6jNyk9EEJpXTcT9KfVWe8OKSQ89Lhz59_uONa9O13ZBV56DzbjweO8BfxlcMGHIhSGPv17XD9Fr22pWWdI-OoJcB7wCtzwC28i6LyHPh_5j-gfsIOiWQA6Rt1_h_F75Lo-uDhYHU3hvsCdjhnfzHC3Le5swY-u2i3sj0271VHbDDH8_m_meZaiZQ7443IzxZtuNcX3q6tyXK6nR4r7bv0WvfJ6l-Ddcz1DXz8tN-11dXv3-aa9vK2AcZors-Ceac-ZtxTmojZeNMY6KpkxlDjmjXGecSmosBysYI5JK-qyaW-4ayQ_Qx9OvI86FdO-TGtDUo8x7HU8KNrwxaLmBdacYFC8_AwQVbIBegsuxLJ75YagKFFjyGoMWY0hqzFk_hfDnpz_</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Catalysis on Pd/WO3 and Pd/WO2: Effect of the Modifications of the Surface States Due to Redox Treatments on the Skeletal Rearrangement of Hydrocarbons: Part I. Physical and Chemical Characterizations of Catalysts by BET, TPR, XRD, XAS, and XPS</title><source>Access via ScienceDirect (Elsevier)</source><creator>Bigey, C. ; Hilaire, L. ; Maire, G.</creator><creatorcontrib>Bigey, C. ; Hilaire, L. ; Maire, G.</creatorcontrib><description>Bulk and surface properties of Pd/WO3 and Pd/WO2 catalysts were studied using temperature programmed reduction, X-ray diffraction, X-ray absorption, and X-ray photoelectron spectroscopies. Special attention was paid to the oxidation state of tungsten upon reduction under hydrogen at 350 and 600°C. The influence of oxidation treatments was also studied. Our results showed that reduction at 350°C led to the tranformation of bulk WO3 into the stable W20O58 phase. At higher reduction temperature and also at 350°C, if the support WO3 was calcined before impregnation, metallic tungsten was detected and we postulated that this transformation starts with the formation of the metastable W3O phase via W20O58. All these transformations concern the surface as well as the bulk for Pd/WO3 catalysts and the WO3 contamination layer only for Pd/WO2 catalyst. WO2 seems more difficult to reduce than WO3 even if the latter becomes less reducible after oxidation treatment. Autoreduction of the palladium salt was suggested on these catalysts, resulting both from the pretreatment of the supports and the nature of the Pd salt. Addition of a metal to bulk oxides facilitates their reducibility and allows one to obtain a stable surface state.</description><identifier>ISSN: 0021-9517</identifier><identifier>EISSN: 1090-2694</identifier><identifier>DOI: 10.1006/jcat.1999.2466</identifier><identifier>CODEN: JCTLA5</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Catalysis ; Catalysts: preparations and properties ; Chemistry ; Exact sciences and technology ; General and physical chemistry ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Journal of catalysis, 1999-06, Vol.184 (2), p.406-420</ispartof><rights>1999 Academic Press</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/jcat.1999.2466$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1837753$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Bigey, C.</creatorcontrib><creatorcontrib>Hilaire, L.</creatorcontrib><creatorcontrib>Maire, G.</creatorcontrib><title>Catalysis on Pd/WO3 and Pd/WO2: Effect of the Modifications of the Surface States Due to Redox Treatments on the Skeletal Rearrangement of Hydrocarbons: Part I. Physical and Chemical Characterizations of Catalysts by BET, TPR, XRD, XAS, and XPS</title><title>Journal of catalysis</title><description>Bulk and surface properties of Pd/WO3 and Pd/WO2 catalysts were studied using temperature programmed reduction, X-ray diffraction, X-ray absorption, and X-ray photoelectron spectroscopies. Special attention was paid to the oxidation state of tungsten upon reduction under hydrogen at 350 and 600°C. The influence of oxidation treatments was also studied. Our results showed that reduction at 350°C led to the tranformation of bulk WO3 into the stable W20O58 phase. At higher reduction temperature and also at 350°C, if the support WO3 was calcined before impregnation, metallic tungsten was detected and we postulated that this transformation starts with the formation of the metastable W3O phase via W20O58. All these transformations concern the surface as well as the bulk for Pd/WO3 catalysts and the WO3 contamination layer only for Pd/WO2 catalyst. WO2 seems more difficult to reduce than WO3 even if the latter becomes less reducible after oxidation treatment. Autoreduction of the palladium salt was suggested on these catalysts, resulting both from the pretreatment of the supports and the nature of the Pd salt. Addition of a metal to bulk oxides facilitates their reducibility and allows one to obtain a stable surface state.</description><subject>Catalysis</subject><subject>Catalysts: preparations and properties</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</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>1999</creationdate><recordtype>article</recordtype><recordid>eNpFUU1vEzEUtBBIhMKVsw8cs6k_ss66t7INtFJRV0kQvVn-eCYuyW5lu4jwu_kBeJMiLn5-9mhm3huE3lMyo4SI8wer84xKKWdsLsQLNKFEkooJOX-JJoQwWsmaLl6jNyk9EEJpXTcT9KfVWe8OKSQ89Lhz59_uONa9O13ZBV56DzbjweO8BfxlcMGHIhSGPv17XD9Fr22pWWdI-OoJcB7wCtzwC28i6LyHPh_5j-gfsIOiWQA6Rt1_h_F75Lo-uDhYHU3hvsCdjhnfzHC3Le5swY-u2i3sj0271VHbDDH8_m_meZaiZQ7443IzxZtuNcX3q6tyXK6nR4r7bv0WvfJ6l-Ddcz1DXz8tN-11dXv3-aa9vK2AcZors-Ceac-ZtxTmojZeNMY6KpkxlDjmjXGecSmosBysYI5JK-qyaW-4ayQ_Qx9OvI86FdO-TGtDUo8x7HU8KNrwxaLmBdacYFC8_AwQVbIBegsuxLJ75YagKFFjyGoMWY0hqzFk_hfDnpz_</recordid><startdate>19990610</startdate><enddate>19990610</enddate><creator>Bigey, C.</creator><creator>Hilaire, L.</creator><creator>Maire, G.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope></search><sort><creationdate>19990610</creationdate><title>Catalysis on Pd/WO3 and Pd/WO2: Effect of the Modifications of the Surface States Due to Redox Treatments on the Skeletal Rearrangement of Hydrocarbons: Part I. Physical and Chemical Characterizations of Catalysts by BET, TPR, XRD, XAS, and XPS</title><author>Bigey, C. ; Hilaire, L. ; Maire, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e231t-b73f2af32fc1e465bf68bcd192bb10d2fbbdf239616c3ec62d29c65021fb3d893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Catalysis</topic><topic>Catalysts: preparations and properties</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bigey, C.</creatorcontrib><creatorcontrib>Hilaire, L.</creatorcontrib><creatorcontrib>Maire, G.</creatorcontrib><collection>Pascal-Francis</collection><jtitle>Journal of catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bigey, C.</au><au>Hilaire, L.</au><au>Maire, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catalysis on Pd/WO3 and Pd/WO2: Effect of the Modifications of the Surface States Due to Redox Treatments on the Skeletal Rearrangement of Hydrocarbons: Part I. Physical and Chemical Characterizations of Catalysts by BET, TPR, XRD, XAS, and XPS</atitle><jtitle>Journal of catalysis</jtitle><date>1999-06-10</date><risdate>1999</risdate><volume>184</volume><issue>2</issue><spage>406</spage><epage>420</epage><pages>406-420</pages><issn>0021-9517</issn><eissn>1090-2694</eissn><coden>JCTLA5</coden><abstract>Bulk and surface properties of Pd/WO3 and Pd/WO2 catalysts were studied using temperature programmed reduction, X-ray diffraction, X-ray absorption, and X-ray photoelectron spectroscopies. Special attention was paid to the oxidation state of tungsten upon reduction under hydrogen at 350 and 600°C. The influence of oxidation treatments was also studied. Our results showed that reduction at 350°C led to the tranformation of bulk WO3 into the stable W20O58 phase. At higher reduction temperature and also at 350°C, if the support WO3 was calcined before impregnation, metallic tungsten was detected and we postulated that this transformation starts with the formation of the metastable W3O phase via W20O58. All these transformations concern the surface as well as the bulk for Pd/WO3 catalysts and the WO3 contamination layer only for Pd/WO2 catalyst. WO2 seems more difficult to reduce than WO3 even if the latter becomes less reducible after oxidation treatment. Autoreduction of the palladium salt was suggested on these catalysts, resulting both from the pretreatment of the supports and the nature of the Pd salt. Addition of a metal to bulk oxides facilitates their reducibility and allows one to obtain a stable surface state.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><doi>10.1006/jcat.1999.2466</doi><tpages>15</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-9517
ispartof Journal of catalysis, 1999-06, Vol.184 (2), p.406-420
issn 0021-9517
1090-2694
language eng
recordid cdi_pascalfrancis_primary_1837753
source Access via ScienceDirect (Elsevier)
subjects Catalysis
Catalysts: preparations and properties
Chemistry
Exact sciences and technology
General and physical chemistry
Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
title Catalysis on Pd/WO3 and Pd/WO2: Effect of the Modifications of the Surface States Due to Redox Treatments on the Skeletal Rearrangement of Hydrocarbons: Part I. Physical and Chemical Characterizations of Catalysts by BET, TPR, XRD, XAS, and XPS
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T12%3A51%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_pasca&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Catalysis%20on%20Pd/WO3%20and%20Pd/WO2:%20Effect%20of%20the%20Modifications%20of%20the%20Surface%20States%20Due%20to%20Redox%20Treatments%20on%20the%20Skeletal%20Rearrangement%20of%20Hydrocarbons:%20Part%20I.%20Physical%20and%20Chemical%20Characterizations%20of%20Catalysts%20by%20BET,%20TPR,%20XRD,%20XAS,%20and%20XPS&rft.jtitle=Journal%20of%20catalysis&rft.au=Bigey,%20C.&rft.date=1999-06-10&rft.volume=184&rft.issue=2&rft.spage=406&rft.epage=420&rft.pages=406-420&rft.issn=0021-9517&rft.eissn=1090-2694&rft.coden=JCTLA5&rft_id=info:doi/10.1006/jcat.1999.2466&rft_dat=%3Celsevier_pasca%3ES0021951799924661%3C/elsevier_pasca%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_els_id=S0021951799924661&rfr_iscdi=true