Synthesis of carbon nanofibers supported cobalt catalysts for Fischer–Tropsch process
•Support crystallinity clearly influenced on the metal particle size.•Co/CNF-1 and Co/CNF-2 showed the highest activity and selectivity to CO2 and CH4.•Co/CNF-3 sample presented the highest selectivity to long-chained hydrocarbons.•Metal sintering was significant in catalysts with small metal partic...
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Veröffentlicht in: | Fuel (Guildford) 2013-09, Vol.111, p.422-429 |
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creator | Díaz, José Antonio Martínez-Fernández, Miriam Romero, Amaya Valverde, José Luis |
description | •Support crystallinity clearly influenced on the metal particle size.•Co/CNF-1 and Co/CNF-2 showed the highest activity and selectivity to CO2 and CH4.•Co/CNF-3 sample presented the highest selectivity to long-chained hydrocarbons.•Metal sintering was significant in catalysts with small metal particles.•Catalyst fouling by long-chained hydrocarbons slow down the reaction.
In this paper, CNFs prepared at three different temperatures (1023, 873 and 723K, called CNF-1, CNF-2 and CNF-3, respectively) were used as supports for cobalt-based catalysts in the Fischer–Tropsch Synthesis (FTS). The supports and cobalt catalysts were characterized by nitrogen adsorption–desorption, temperature-programmed reduction (TPR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA) techniques; the metal content of the cobalt-based catalysts was analyzed by atomic absorption. The activity and selectivity of the CNFs supported catalysts were studied at 523K, 20bar and H2/CO=2. Co/CNF-1 and Co/CNF-2 were very active and showed high selectivity to CH4 and CO2, without further deactivation, whereas the less active catalyst Co/CNF-3 led to the highest selectivity to long-chained hydrocarbons (C5+) and under was a remarkable deactivation. Used catalysts were characterized by nitrogen adsorption–desorption, XRD and TGA. Results confirmed that all the catalysts underwent catalyst fouling as a consequence of C5+ hydrocarbons formation whereas catalyst Co/CNF-3 presented a notably metal sintering by coalescence. |
doi_str_mv | 10.1016/j.fuel.2013.04.003 |
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In this paper, CNFs prepared at three different temperatures (1023, 873 and 723K, called CNF-1, CNF-2 and CNF-3, respectively) were used as supports for cobalt-based catalysts in the Fischer–Tropsch Synthesis (FTS). The supports and cobalt catalysts were characterized by nitrogen adsorption–desorption, temperature-programmed reduction (TPR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA) techniques; the metal content of the cobalt-based catalysts was analyzed by atomic absorption. The activity and selectivity of the CNFs supported catalysts were studied at 523K, 20bar and H2/CO=2. Co/CNF-1 and Co/CNF-2 were very active and showed high selectivity to CH4 and CO2, without further deactivation, whereas the less active catalyst Co/CNF-3 led to the highest selectivity to long-chained hydrocarbons (C5+) and under was a remarkable deactivation. Used catalysts were characterized by nitrogen adsorption–desorption, XRD and TGA. Results confirmed that all the catalysts underwent catalyst fouling as a consequence of C5+ hydrocarbons formation whereas catalyst Co/CNF-3 presented a notably metal sintering by coalescence.</description><identifier>ISSN: 0016-2361</identifier><identifier>EISSN: 1873-7153</identifier><identifier>DOI: 10.1016/j.fuel.2013.04.003</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Applied sciences ; Carbon nanofibers ; Catalysis ; Catalyst deactivation ; Catalysts ; Cobalt ; Deactivation ; Energy ; Energy. Thermal use of fuels ; Exact sciences and technology ; Fischer–Tropsch ; Fouling ; Fuels ; Hydrocarbons ; Selectivity ; Synthesis</subject><ispartof>Fuel (Guildford), 2013-09, Vol.111, p.422-429</ispartof><rights>2013 Elsevier Ltd</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-4e214d19aace917d7d98434fabb3af7cd0f5864c7d03f5ace48ad3280df3de033</citedby><cites>FETCH-LOGICAL-c433t-4e214d19aace917d7d98434fabb3af7cd0f5864c7d03f5ace48ad3280df3de033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.fuel.2013.04.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27502085$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Díaz, José Antonio</creatorcontrib><creatorcontrib>Martínez-Fernández, Miriam</creatorcontrib><creatorcontrib>Romero, Amaya</creatorcontrib><creatorcontrib>Valverde, José Luis</creatorcontrib><title>Synthesis of carbon nanofibers supported cobalt catalysts for Fischer–Tropsch process</title><title>Fuel (Guildford)</title><description>•Support crystallinity clearly influenced on the metal particle size.•Co/CNF-1 and Co/CNF-2 showed the highest activity and selectivity to CO2 and CH4.•Co/CNF-3 sample presented the highest selectivity to long-chained hydrocarbons.•Metal sintering was significant in catalysts with small metal particles.•Catalyst fouling by long-chained hydrocarbons slow down the reaction.
In this paper, CNFs prepared at three different temperatures (1023, 873 and 723K, called CNF-1, CNF-2 and CNF-3, respectively) were used as supports for cobalt-based catalysts in the Fischer–Tropsch Synthesis (FTS). The supports and cobalt catalysts were characterized by nitrogen adsorption–desorption, temperature-programmed reduction (TPR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA) techniques; the metal content of the cobalt-based catalysts was analyzed by atomic absorption. The activity and selectivity of the CNFs supported catalysts were studied at 523K, 20bar and H2/CO=2. Co/CNF-1 and Co/CNF-2 were very active and showed high selectivity to CH4 and CO2, without further deactivation, whereas the less active catalyst Co/CNF-3 led to the highest selectivity to long-chained hydrocarbons (C5+) and under was a remarkable deactivation. Used catalysts were characterized by nitrogen adsorption–desorption, XRD and TGA. Results confirmed that all the catalysts underwent catalyst fouling as a consequence of C5+ hydrocarbons formation whereas catalyst Co/CNF-3 presented a notably metal sintering by coalescence.</description><subject>Applied sciences</subject><subject>Carbon nanofibers</subject><subject>Catalysis</subject><subject>Catalyst deactivation</subject><subject>Catalysts</subject><subject>Cobalt</subject><subject>Deactivation</subject><subject>Energy</subject><subject>Energy. Thermal use of fuels</subject><subject>Exact sciences and technology</subject><subject>Fischer–Tropsch</subject><subject>Fouling</subject><subject>Fuels</subject><subject>Hydrocarbons</subject><subject>Selectivity</subject><subject>Synthesis</subject><issn>0016-2361</issn><issn>1873-7153</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkMFq3DAQhkVJoZu0L9CTL4Vc7IwseeWFXMKSTQMLOTSlRyFLI6LFsVyNN7C3vkPesE8SuRt6TE4zh2_mn_kY-8qh4sCXF7vK77GvauCiAlkBiA9swVslSsUbccIWkKmyFkv-iZ0S7QBAtY1csF8_DsP0gBSoiL6wJnVxKAYzRB86TFTQfhxjmtAVNnamnzIymf5AExU-pmITyD5g-vvn-T7FMffFmKJFos_sozc94ZfXesZ-bq7v19_L7d3N7fpqW1opxFRKrLl0fGWMxRVXTrlVK4X0puuE8co68E27lFY5EL7JkGyNE3ULzguHIMQZOz_uzbm_90iTfswnYd-bAeOedP4-CxINqPdRuZQ5rG5ntD6iNkWihF6PKTyadNAc9Cxc7_QsXM_CNUgN_0759rrfkDW9T2awgf5P1qqBGtomc5dHDrOXp4BJkw04WHQhoZ20i-GtmBdlLpjl</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Díaz, José Antonio</creator><creator>Martínez-Fernández, Miriam</creator><creator>Romero, Amaya</creator><creator>Valverde, José Luis</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7TB</scope><scope>7U5</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>20130901</creationdate><title>Synthesis of carbon nanofibers supported cobalt catalysts for Fischer–Tropsch process</title><author>Díaz, José Antonio ; Martínez-Fernández, Miriam ; Romero, Amaya ; Valverde, José Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-4e214d19aace917d7d98434fabb3af7cd0f5864c7d03f5ace48ad3280df3de033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Applied sciences</topic><topic>Carbon nanofibers</topic><topic>Catalysis</topic><topic>Catalyst deactivation</topic><topic>Catalysts</topic><topic>Cobalt</topic><topic>Deactivation</topic><topic>Energy</topic><topic>Energy. Thermal use of fuels</topic><topic>Exact sciences and technology</topic><topic>Fischer–Tropsch</topic><topic>Fouling</topic><topic>Fuels</topic><topic>Hydrocarbons</topic><topic>Selectivity</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Díaz, José Antonio</creatorcontrib><creatorcontrib>Martínez-Fernández, Miriam</creatorcontrib><creatorcontrib>Romero, Amaya</creatorcontrib><creatorcontrib>Valverde, José Luis</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Fuel (Guildford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Díaz, José Antonio</au><au>Martínez-Fernández, Miriam</au><au>Romero, Amaya</au><au>Valverde, José Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of carbon nanofibers supported cobalt catalysts for Fischer–Tropsch process</atitle><jtitle>Fuel (Guildford)</jtitle><date>2013-09-01</date><risdate>2013</risdate><volume>111</volume><spage>422</spage><epage>429</epage><pages>422-429</pages><issn>0016-2361</issn><eissn>1873-7153</eissn><abstract>•Support crystallinity clearly influenced on the metal particle size.•Co/CNF-1 and Co/CNF-2 showed the highest activity and selectivity to CO2 and CH4.•Co/CNF-3 sample presented the highest selectivity to long-chained hydrocarbons.•Metal sintering was significant in catalysts with small metal particles.•Catalyst fouling by long-chained hydrocarbons slow down the reaction.
In this paper, CNFs prepared at three different temperatures (1023, 873 and 723K, called CNF-1, CNF-2 and CNF-3, respectively) were used as supports for cobalt-based catalysts in the Fischer–Tropsch Synthesis (FTS). The supports and cobalt catalysts were characterized by nitrogen adsorption–desorption, temperature-programmed reduction (TPR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA) techniques; the metal content of the cobalt-based catalysts was analyzed by atomic absorption. The activity and selectivity of the CNFs supported catalysts were studied at 523K, 20bar and H2/CO=2. Co/CNF-1 and Co/CNF-2 were very active and showed high selectivity to CH4 and CO2, without further deactivation, whereas the less active catalyst Co/CNF-3 led to the highest selectivity to long-chained hydrocarbons (C5+) and under was a remarkable deactivation. Used catalysts were characterized by nitrogen adsorption–desorption, XRD and TGA. Results confirmed that all the catalysts underwent catalyst fouling as a consequence of C5+ hydrocarbons formation whereas catalyst Co/CNF-3 presented a notably metal sintering by coalescence.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.fuel.2013.04.003</doi><tpages>8</tpages></addata></record> |
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subjects | Applied sciences Carbon nanofibers Catalysis Catalyst deactivation Catalysts Cobalt Deactivation Energy Energy. Thermal use of fuels Exact sciences and technology Fischer–Tropsch Fouling Fuels Hydrocarbons Selectivity Synthesis |
title | Synthesis of carbon nanofibers supported cobalt catalysts for Fischer–Tropsch process |
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