Novel Pulse Electrodeposited Co-Cu-Zn Nanowire/tubeCatalysts for C1-C4 Alcohols and C2 - C6 (except C5) Hydrocarbons from CO and H2
Co-Cu-ZnO nanowire/tube catalysts were synthesized using pulse electrodeposition technique from a single aqueous electrolyte solution using a template synthesis technique. They were then tested as catalysts for the hydrogenation of CO to alcohols and higher hydrocarbons. Nanowires/tubes were grown i...
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Veröffentlicht in: | Journal of physical chemistry (1952) 2012-01, Vol.116 (20) |
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creator | Gupta, Mayank Schwartz, Viviane Overbury, Steven {Steve} H More, Karren Leslie Spivey, James J |
description | Co-Cu-ZnO nanowire/tube catalysts were synthesized using pulse electrodeposition technique from a single aqueous electrolyte solution using a template synthesis technique. They were then tested as catalysts for the hydrogenation of CO to alcohols and higher hydrocarbons. Nanowires/tubes were grown inside the pores of membranes using a three-step sequential deposition process. First, a low current of -6.9 mA/cm{sup 2} was applied for 300 ms for Cu deposition, then a high current density of -11.5 mA/cm{sup 2} for t ms (t = 500, 600, 750 ms) was applied for Co deposition, and finally no current was applied for 1200 ms so that the ions near the cathode replenish. The surface had a significantly different composition than the bulk. On the surface, there was more Co, less Cu, and more Zn. The catalyst showed the alcohol (C{sub 1}-C{sub 4}) selectivity of 20.9 %C at H{sub 2}/CO = 3/1, GHSV = 16,000 scc/h gcat, temperature = 270 C, pressure = 15 bar, and time-on-stream = 65 h. |
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(ORNL), Oak Ridge, TN (United States)</creatorcontrib><description>Co-Cu-ZnO nanowire/tube catalysts were synthesized using pulse electrodeposition technique from a single aqueous electrolyte solution using a template synthesis technique. They were then tested as catalysts for the hydrogenation of CO to alcohols and higher hydrocarbons. Nanowires/tubes were grown inside the pores of membranes using a three-step sequential deposition process. First, a low current of -6.9 mA/cm{sup 2} was applied for 300 ms for Cu deposition, then a high current density of -11.5 mA/cm{sup 2} for t ms (t = 500, 600, 750 ms) was applied for Co deposition, and finally no current was applied for 1200 ms so that the ions near the cathode replenish. The surface had a significantly different composition than the bulk. On the surface, there was more Co, less Cu, and more Zn. The catalyst showed the alcohol (C{sub 1}-C{sub 4}) selectivity of 20.9 %C at H{sub 2}/CO = 3/1, GHSV = 16,000 scc/h gcat, temperature = 270 C, pressure = 15 bar, and time-on-stream = 65 h.</description><identifier>ISSN: 0022-3654</identifier><identifier>EISSN: 1541-5740</identifier><language>eng</language><publisher>United States</publisher><subject>ALCOHOLS ; CATALYSTS ; CATHODES ; CURRENT DENSITY ; DEPOSITION ; ELECTRODEPOSITION ; ELECTROLYTES ; HYDROCARBONS ; HYDROGENATION ; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY ; MEMBRANES ; SYNTHESIS</subject><ispartof>Journal of physical chemistry (1952), 2012-01, Vol.116 (20)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/1042882$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Gupta, Mayank</creatorcontrib><creatorcontrib>Schwartz, Viviane</creatorcontrib><creatorcontrib>Overbury, Steven {Steve} H</creatorcontrib><creatorcontrib>More, Karren Leslie</creatorcontrib><creatorcontrib>Spivey, James J</creatorcontrib><creatorcontrib>Shared Research Equipment Collaborative Research Center</creatorcontrib><creatorcontrib>Center for Nanophase Materials Sciences</creatorcontrib><creatorcontrib>Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)</creatorcontrib><title>Novel Pulse Electrodeposited Co-Cu-Zn Nanowire/tubeCatalysts for C1-C4 Alcohols and C2 - C6 (except C5) Hydrocarbons from CO and H2</title><title>Journal of physical chemistry (1952)</title><description>Co-Cu-ZnO nanowire/tube catalysts were synthesized using pulse electrodeposition technique from a single aqueous electrolyte solution using a template synthesis technique. They were then tested as catalysts for the hydrogenation of CO to alcohols and higher hydrocarbons. Nanowires/tubes were grown inside the pores of membranes using a three-step sequential deposition process. First, a low current of -6.9 mA/cm{sup 2} was applied for 300 ms for Cu deposition, then a high current density of -11.5 mA/cm{sup 2} for t ms (t = 500, 600, 750 ms) was applied for Co deposition, and finally no current was applied for 1200 ms so that the ions near the cathode replenish. The surface had a significantly different composition than the bulk. On the surface, there was more Co, less Cu, and more Zn. The catalyst showed the alcohol (C{sub 1}-C{sub 4}) selectivity of 20.9 %C at H{sub 2}/CO = 3/1, GHSV = 16,000 scc/h gcat, temperature = 270 C, pressure = 15 bar, and time-on-stream = 65 h.</description><subject>ALCOHOLS</subject><subject>CATALYSTS</subject><subject>CATHODES</subject><subject>CURRENT DENSITY</subject><subject>DEPOSITION</subject><subject>ELECTRODEPOSITION</subject><subject>ELECTROLYTES</subject><subject>HYDROCARBONS</subject><subject>HYDROGENATION</subject><subject>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</subject><subject>MEMBRANES</subject><subject>SYNTHESIS</subject><issn>0022-3654</issn><issn>1541-5740</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNjjFOAzEQRS0EEkvCHUZUUFjYXm9Ii6ygrRIKKprI8U6URcYTebxAai6OhTgA1W_e039notGd1bJ7sOpcNEoZI9tFZy_FFfObUkq3rW7E95o-MMLzFBlhFTGUTAMeiceCAziSbpKvCdY-0eeY8b5MO3S--HjiwrCnDE5LZ-ExBjpQZPCpagYkuAXc4lfAYwHX3UF_GjIFn3eUqpfpHdzmF-7NXFzsff2__tuZuHlavbheEpdxy6GmhEOglGrdVitrlkvT_gv6AafKTs4</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Gupta, Mayank</creator><creator>Schwartz, Viviane</creator><creator>Overbury, Steven {Steve} H</creator><creator>More, Karren Leslie</creator><creator>Spivey, James J</creator><scope>OTOTI</scope></search><sort><creationdate>20120101</creationdate><title>Novel Pulse Electrodeposited Co-Cu-Zn Nanowire/tubeCatalysts for C1-C4 Alcohols and C2 - C6 (except C5) Hydrocarbons from CO and H2</title><author>Gupta, Mayank ; Schwartz, Viviane ; Overbury, Steven {Steve} H ; More, Karren Leslie ; Spivey, James J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-osti_scitechconnect_10428823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>ALCOHOLS</topic><topic>CATALYSTS</topic><topic>CATHODES</topic><topic>CURRENT DENSITY</topic><topic>DEPOSITION</topic><topic>ELECTRODEPOSITION</topic><topic>ELECTROLYTES</topic><topic>HYDROCARBONS</topic><topic>HYDROGENATION</topic><topic>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</topic><topic>MEMBRANES</topic><topic>SYNTHESIS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gupta, Mayank</creatorcontrib><creatorcontrib>Schwartz, Viviane</creatorcontrib><creatorcontrib>Overbury, Steven {Steve} H</creatorcontrib><creatorcontrib>More, Karren Leslie</creatorcontrib><creatorcontrib>Spivey, James J</creatorcontrib><creatorcontrib>Shared Research Equipment Collaborative Research Center</creatorcontrib><creatorcontrib>Center for Nanophase Materials Sciences</creatorcontrib><creatorcontrib>Oak Ridge National Lab. 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(ORNL), Oak Ridge, TN (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel Pulse Electrodeposited Co-Cu-Zn Nanowire/tubeCatalysts for C1-C4 Alcohols and C2 - C6 (except C5) Hydrocarbons from CO and H2</atitle><jtitle>Journal of physical chemistry (1952)</jtitle><date>2012-01-01</date><risdate>2012</risdate><volume>116</volume><issue>20</issue><issn>0022-3654</issn><eissn>1541-5740</eissn><abstract>Co-Cu-ZnO nanowire/tube catalysts were synthesized using pulse electrodeposition technique from a single aqueous electrolyte solution using a template synthesis technique. They were then tested as catalysts for the hydrogenation of CO to alcohols and higher hydrocarbons. Nanowires/tubes were grown inside the pores of membranes using a three-step sequential deposition process. First, a low current of -6.9 mA/cm{sup 2} was applied for 300 ms for Cu deposition, then a high current density of -11.5 mA/cm{sup 2} for t ms (t = 500, 600, 750 ms) was applied for Co deposition, and finally no current was applied for 1200 ms so that the ions near the cathode replenish. The surface had a significantly different composition than the bulk. On the surface, there was more Co, less Cu, and more Zn. The catalyst showed the alcohol (C{sub 1}-C{sub 4}) selectivity of 20.9 %C at H{sub 2}/CO = 3/1, GHSV = 16,000 scc/h gcat, temperature = 270 C, pressure = 15 bar, and time-on-stream = 65 h.</abstract><cop>United States</cop></addata></record> |
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subjects | ALCOHOLS CATALYSTS CATHODES CURRENT DENSITY DEPOSITION ELECTRODEPOSITION ELECTROLYTES HYDROCARBONS HYDROGENATION INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY MEMBRANES SYNTHESIS |
title | Novel Pulse Electrodeposited Co-Cu-Zn Nanowire/tubeCatalysts for C1-C4 Alcohols and C2 - C6 (except C5) Hydrocarbons from CO and H2 |
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