Activated carbon supported silicotungstic acid catalysts for ethyl-tert-butyl ether synthesis
Vapor phase ethyl‐tert‐butyl ether (ETBE) production was conducted in the presence of Cesium salts of silicotungstic acid (Cs‐STA), activated carbon supported silicotungstic acid (AC‐STA), and activated carbon supported Cesium salts of silicotungstic acid (AC‐Cs‐STA) catalysts. Isobutene (IB) conver...
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description | Vapor phase ethyl‐tert‐butyl ether (ETBE) production was conducted in the presence of Cesium salts of silicotungstic acid (Cs‐STA), activated carbon supported silicotungstic acid (AC‐STA), and activated carbon supported Cesium salts of silicotungstic acid (AC‐Cs‐STA) catalysts. Isobutene (IB) conversion to ETBE at 373 K were determined as 0.16 and 0.2 for STA and AC‐STA catalysts on constant space time basis. This increase of activity is one of the highlights of this study considering that STA loading in AC‐STA catalysts had been adjusted to 40%. IB conversion to ETBE obtained at 373 K in the presence of AC‐STA catalyst was found to be close to equilibrium. Stability of the synthesized catalysts were tested by applying a washing procedure with ethanol. Repeated ETBE synthesis with thoroughly washed samples indicated quite stable and active catalyts. © 2011 American Institute of Chemical Engineers AIChE J, 2011 |
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Isobutene (IB) conversion to ETBE at 373 K were determined as 0.16 and 0.2 for STA and AC‐STA catalysts on constant space time basis. This increase of activity is one of the highlights of this study considering that STA loading in AC‐STA catalysts had been adjusted to 40%. IB conversion to ETBE obtained at 373 K in the presence of AC‐STA catalyst was found to be close to equilibrium. Stability of the synthesized catalysts were tested by applying a washing procedure with ethanol. Repeated ETBE synthesis with thoroughly washed samples indicated quite stable and active catalyts. © 2011 American Institute of Chemical Engineers AIChE J, 2011</description><identifier>ISSN: 0001-1541</identifier><identifier>EISSN: 1547-5905</identifier><identifier>DOI: 10.1002/aic.12524</identifier><identifier>CODEN: AICEAC</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Activated carbon ; Applied sciences ; Carbon ; Catalysis ; catalyst ; Catalysts ; Catalytic reactions ; Cesium ; Chemical engineering ; Chemistry ; Conversion ; Cs-STA ; ETBE ; Ethanol ; Ethers ; Ethyl alcohol ; Exact sciences and technology ; General and physical chemistry ; Phase transitions ; Reactors ; Salt ; STA ; Synthesis ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>AIChE journal, 2011-11, Vol.57 (11), p.3171-3181</ispartof><rights>Copyright © 2011 American Institute of Chemical Engineers (AIChE)</rights><rights>2015 INIST-CNRS</rights><rights>Copyright American Institute of Chemical Engineers Nov 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4664-243b632b930270077374ec6c2c98fce5f05777d1fef1bbcaeafd84b40e5889b53</citedby><cites>FETCH-LOGICAL-c4664-243b632b930270077374ec6c2c98fce5f05777d1fef1bbcaeafd84b40e5889b53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Faic.12524$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Faic.12524$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27928,27929,45578,45579</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24686974$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Degirmenci, Levent</creatorcontrib><creatorcontrib>Oktar, Nuray</creatorcontrib><creatorcontrib>Dogu, Gulsen</creatorcontrib><title>Activated carbon supported silicotungstic acid catalysts for ethyl-tert-butyl ether synthesis</title><title>AIChE journal</title><addtitle>AIChE J</addtitle><description>Vapor phase ethyl‐tert‐butyl ether (ETBE) production was conducted in the presence of Cesium salts of silicotungstic acid (Cs‐STA), activated carbon supported silicotungstic acid (AC‐STA), and activated carbon supported Cesium salts of silicotungstic acid (AC‐Cs‐STA) catalysts. Isobutene (IB) conversion to ETBE at 373 K were determined as 0.16 and 0.2 for STA and AC‐STA catalysts on constant space time basis. This increase of activity is one of the highlights of this study considering that STA loading in AC‐STA catalysts had been adjusted to 40%. IB conversion to ETBE obtained at 373 K in the presence of AC‐STA catalyst was found to be close to equilibrium. Stability of the synthesized catalysts were tested by applying a washing procedure with ethanol. Repeated ETBE synthesis with thoroughly washed samples indicated quite stable and active catalyts. © 2011 American Institute of Chemical Engineers AIChE J, 2011</description><subject>Activated carbon</subject><subject>Applied sciences</subject><subject>Carbon</subject><subject>Catalysis</subject><subject>catalyst</subject><subject>Catalysts</subject><subject>Catalytic reactions</subject><subject>Cesium</subject><subject>Chemical engineering</subject><subject>Chemistry</subject><subject>Conversion</subject><subject>Cs-STA</subject><subject>ETBE</subject><subject>Ethanol</subject><subject>Ethers</subject><subject>Ethyl alcohol</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Phase transitions</subject><subject>Reactors</subject><subject>Salt</subject><subject>STA</subject><subject>Synthesis</subject><subject>Theory of reactions, general kinetics. Catalysis. 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Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Degirmenci, Levent</creatorcontrib><creatorcontrib>Oktar, Nuray</creatorcontrib><creatorcontrib>Dogu, Gulsen</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><collection>Aqualine</collection><collection>Water Resources Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy & Non-Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>AIChE journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Degirmenci, Levent</au><au>Oktar, Nuray</au><au>Dogu, Gulsen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activated carbon supported silicotungstic acid catalysts for ethyl-tert-butyl ether synthesis</atitle><jtitle>AIChE journal</jtitle><addtitle>AIChE J</addtitle><date>2011-11</date><risdate>2011</risdate><volume>57</volume><issue>11</issue><spage>3171</spage><epage>3181</epage><pages>3171-3181</pages><issn>0001-1541</issn><eissn>1547-5905</eissn><coden>AICEAC</coden><abstract>Vapor phase ethyl‐tert‐butyl ether (ETBE) production was conducted in the presence of Cesium salts of silicotungstic acid (Cs‐STA), activated carbon supported silicotungstic acid (AC‐STA), and activated carbon supported Cesium salts of silicotungstic acid (AC‐Cs‐STA) catalysts. Isobutene (IB) conversion to ETBE at 373 K were determined as 0.16 and 0.2 for STA and AC‐STA catalysts on constant space time basis. This increase of activity is one of the highlights of this study considering that STA loading in AC‐STA catalysts had been adjusted to 40%. IB conversion to ETBE obtained at 373 K in the presence of AC‐STA catalyst was found to be close to equilibrium. Stability of the synthesized catalysts were tested by applying a washing procedure with ethanol. Repeated ETBE synthesis with thoroughly washed samples indicated quite stable and active catalyts. © 2011 American Institute of Chemical Engineers AIChE J, 2011</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/aic.12524</doi><tpages>11</tpages></addata></record> |
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subjects | Activated carbon Applied sciences Carbon Catalysis catalyst Catalysts Catalytic reactions Cesium Chemical engineering Chemistry Conversion Cs-STA ETBE Ethanol Ethers Ethyl alcohol Exact sciences and technology General and physical chemistry Phase transitions Reactors Salt STA Synthesis Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Activated carbon supported silicotungstic acid catalysts for ethyl-tert-butyl ether synthesis |
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