Separation of ethyl acetate–isooctane mixture by heteroazeotropic batch distillation
Heteroazeotropic batch distillation process to recover isooctane as product from ethyl acetate–isooctane mixture with using acetonitrile. 3.0-2 class ternary diagram and liquid–liquid and liquid–liquid–vapour equilibrium envelopes estimated by the original UNIFAC model. •Distillation of isooctane fr...
Gespeichert in:
Veröffentlicht in: | Chemical engineering research & design 2014-06, Vol.92 (6), p.995-1004 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1004 |
---|---|
container_issue | 6 |
container_start_page | 995 |
container_title | Chemical engineering research & design |
container_volume | 92 |
creator | Ooms, Tom Vreysen, Steven Van Baelen, Guy Gerbaud, Vincent Rodriguez-Donis, Ivonne |
description | Heteroazeotropic batch distillation process to recover isooctane as product from ethyl acetate–isooctane mixture with using acetonitrile. 3.0-2 class ternary diagram and liquid–liquid and liquid–liquid–vapour equilibrium envelopes estimated by the original UNIFAC model.
•Distillation of isooctane from an ethyl acetate–isooctane mixture.•Heterogeneous azeotropic distillation in a batch rectification column.•Methanol and acetonitrile heterogeneous entrainers selected among 60 candidates.•Experiments carried out in a laboratory scale column with decanter at the top.•Isooctane is the distillate product while acetonitrile achieves the best separation.
This paper studies the separation of an ethyl acetate–isooctane mixture by heterogeneous azeotropic distillation in a batch rectifying column. An initial list of 60 candidates was studied but only methanol and acetonitrile were obtained as potential heterogeneous entrainers. These entrainers form a low boiling heterogeneous azeotrope with isooctane. Experimental verification of the miscibility gap with isooctane was performed at 25°C for each entrainer giving a smaller region for methanol than for acetonitrile. Feasibility of the heterogeneous azeotropic batch distillation was carried out experimentally in a laboratory batch distillation column having 44 theoretical equilibrium stages and using a high reflux ratio. Several distillate fractions were taken as a function of the temperature at the top of the column. For both methanol and acetonitrile, the main fraction was defined by the condensed vapor providing a liquid–liquid split of the isooctane/entrainer heteroazeotrope into the decanter. Ethyl acetate impurity was detected in both decanted phases, but in much lower amount when using acetonitrile as entrainer. The process with acetonitrile also resulted in a shorter operating time and higher purity and recovery yield of isooctane as the main distillate product. Pure ethyl acetate remained into the boiler at the end of each process. |
doi_str_mv | 10.1016/j.cherd.2013.10.010 |
format | Article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_03521173v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0263876213004309</els_id><sourcerecordid>1560126048</sourcerecordid><originalsourceid>FETCH-LOGICAL-c485t-e493523ba6e0c64139df3e0b3ab9856e7af050131f61e760c338c118a73938383</originalsourceid><addsrcrecordid>eNqFUUFu2zAQJIoEqOv0Bb3o2Bzk7IoSJR1yMIymDmCghza9EhS1gmjIpkPSRp1T_5Af5iWl7CDHBntYYDgzmOUw9gVhhoDiZj3TPbl2lgHyiMwA4QObYJnnKS8Ev2ATyARPq1JkH9kn79cAEF-rCfv9k3bKqWDsNrFdQqE_DonSFFSgl7_Pxlurg9pSsjF_wt5R0hyTngI5q57IBmd3RieNCrpPWuODGYaT1xW77NTg6fPrnrKHu2-_Fst09eP7_WK-SnVeFSGlvOZFxhslCLTIkddtxwkarpq6KgSVqoMi3oSdQCoFaM4rjVipkte8ijNl12ffXg1y58xGuaO0ysjlfCVHDKI_YskPGLlfz9yds4978kFujNcUE2_J7r1EUZZ1nuUFvE8tBGAmIB8T8DNVO-u9o-4tBoIcy5FreSpHjuWMYCwnqm7PKoqfczDkpNeGtppa40gH2VrzX_0_bNSY6w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1560126048</pqid></control><display><type>article</type><title>Separation of ethyl acetate–isooctane mixture by heteroazeotropic batch distillation</title><source>Elsevier ScienceDirect Journals</source><creator>Ooms, Tom ; Vreysen, Steven ; Van Baelen, Guy ; Gerbaud, Vincent ; Rodriguez-Donis, Ivonne</creator><creatorcontrib>Ooms, Tom ; Vreysen, Steven ; Van Baelen, Guy ; Gerbaud, Vincent ; Rodriguez-Donis, Ivonne</creatorcontrib><description>Heteroazeotropic batch distillation process to recover isooctane as product from ethyl acetate–isooctane mixture with using acetonitrile. 3.0-2 class ternary diagram and liquid–liquid and liquid–liquid–vapour equilibrium envelopes estimated by the original UNIFAC model.
•Distillation of isooctane from an ethyl acetate–isooctane mixture.•Heterogeneous azeotropic distillation in a batch rectification column.•Methanol and acetonitrile heterogeneous entrainers selected among 60 candidates.•Experiments carried out in a laboratory scale column with decanter at the top.•Isooctane is the distillate product while acetonitrile achieves the best separation.
This paper studies the separation of an ethyl acetate–isooctane mixture by heterogeneous azeotropic distillation in a batch rectifying column. An initial list of 60 candidates was studied but only methanol and acetonitrile were obtained as potential heterogeneous entrainers. These entrainers form a low boiling heterogeneous azeotrope with isooctane. Experimental verification of the miscibility gap with isooctane was performed at 25°C for each entrainer giving a smaller region for methanol than for acetonitrile. Feasibility of the heterogeneous azeotropic batch distillation was carried out experimentally in a laboratory batch distillation column having 44 theoretical equilibrium stages and using a high reflux ratio. Several distillate fractions were taken as a function of the temperature at the top of the column. For both methanol and acetonitrile, the main fraction was defined by the condensed vapor providing a liquid–liquid split of the isooctane/entrainer heteroazeotrope into the decanter. Ethyl acetate impurity was detected in both decanted phases, but in much lower amount when using acetonitrile as entrainer. The process with acetonitrile also resulted in a shorter operating time and higher purity and recovery yield of isooctane as the main distillate product. Pure ethyl acetate remained into the boiler at the end of each process.</description><identifier>ISSN: 0263-8762</identifier><identifier>EISSN: 1744-3563</identifier><identifier>DOI: 10.1016/j.cherd.2013.10.010</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Acetonitrile ; Batch distillation ; Chemical and Process Engineering ; Chemical engineering ; Chemical Sciences ; Decantation ; Distillation ; Engineering Sciences ; Entrainer selection ; Entrainment ; Ethyl acetate ; Ethyl acetate–isooctane mixture ; Heteroazeotropic distillation ; Isooctane ; Methanol ; Methyl alcohol ; Separation ; Solvent recovery</subject><ispartof>Chemical engineering research & design, 2014-06, Vol.92 (6), p.995-1004</ispartof><rights>2013 The Institution of Chemical Engineers</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-e493523ba6e0c64139df3e0b3ab9856e7af050131f61e760c338c118a73938383</citedby><cites>FETCH-LOGICAL-c485t-e493523ba6e0c64139df3e0b3ab9856e7af050131f61e760c338c118a73938383</cites><orcidid>0000-0003-2738-7922 ; 0000-0002-7809-0910</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cherd.2013.10.010$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,777,781,882,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://hal.science/hal-03521173$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Ooms, Tom</creatorcontrib><creatorcontrib>Vreysen, Steven</creatorcontrib><creatorcontrib>Van Baelen, Guy</creatorcontrib><creatorcontrib>Gerbaud, Vincent</creatorcontrib><creatorcontrib>Rodriguez-Donis, Ivonne</creatorcontrib><title>Separation of ethyl acetate–isooctane mixture by heteroazeotropic batch distillation</title><title>Chemical engineering research & design</title><description>Heteroazeotropic batch distillation process to recover isooctane as product from ethyl acetate–isooctane mixture with using acetonitrile. 3.0-2 class ternary diagram and liquid–liquid and liquid–liquid–vapour equilibrium envelopes estimated by the original UNIFAC model.
•Distillation of isooctane from an ethyl acetate–isooctane mixture.•Heterogeneous azeotropic distillation in a batch rectification column.•Methanol and acetonitrile heterogeneous entrainers selected among 60 candidates.•Experiments carried out in a laboratory scale column with decanter at the top.•Isooctane is the distillate product while acetonitrile achieves the best separation.
This paper studies the separation of an ethyl acetate–isooctane mixture by heterogeneous azeotropic distillation in a batch rectifying column. An initial list of 60 candidates was studied but only methanol and acetonitrile were obtained as potential heterogeneous entrainers. These entrainers form a low boiling heterogeneous azeotrope with isooctane. Experimental verification of the miscibility gap with isooctane was performed at 25°C for each entrainer giving a smaller region for methanol than for acetonitrile. Feasibility of the heterogeneous azeotropic batch distillation was carried out experimentally in a laboratory batch distillation column having 44 theoretical equilibrium stages and using a high reflux ratio. Several distillate fractions were taken as a function of the temperature at the top of the column. For both methanol and acetonitrile, the main fraction was defined by the condensed vapor providing a liquid–liquid split of the isooctane/entrainer heteroazeotrope into the decanter. Ethyl acetate impurity was detected in both decanted phases, but in much lower amount when using acetonitrile as entrainer. The process with acetonitrile also resulted in a shorter operating time and higher purity and recovery yield of isooctane as the main distillate product. Pure ethyl acetate remained into the boiler at the end of each process.</description><subject>Acetonitrile</subject><subject>Batch distillation</subject><subject>Chemical and Process Engineering</subject><subject>Chemical engineering</subject><subject>Chemical Sciences</subject><subject>Decantation</subject><subject>Distillation</subject><subject>Engineering Sciences</subject><subject>Entrainer selection</subject><subject>Entrainment</subject><subject>Ethyl acetate</subject><subject>Ethyl acetate–isooctane mixture</subject><subject>Heteroazeotropic distillation</subject><subject>Isooctane</subject><subject>Methanol</subject><subject>Methyl alcohol</subject><subject>Separation</subject><subject>Solvent recovery</subject><issn>0263-8762</issn><issn>1744-3563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFUUFu2zAQJIoEqOv0Bb3o2Bzk7IoSJR1yMIymDmCghza9EhS1gmjIpkPSRp1T_5Af5iWl7CDHBntYYDgzmOUw9gVhhoDiZj3TPbl2lgHyiMwA4QObYJnnKS8Ev2ATyARPq1JkH9kn79cAEF-rCfv9k3bKqWDsNrFdQqE_DonSFFSgl7_Pxlurg9pSsjF_wt5R0hyTngI5q57IBmd3RieNCrpPWuODGYaT1xW77NTg6fPrnrKHu2-_Fst09eP7_WK-SnVeFSGlvOZFxhslCLTIkddtxwkarpq6KgSVqoMi3oSdQCoFaM4rjVipkte8ijNl12ffXg1y58xGuaO0ysjlfCVHDKI_YskPGLlfz9yds4978kFujNcUE2_J7r1EUZZ1nuUFvE8tBGAmIB8T8DNVO-u9o-4tBoIcy5FreSpHjuWMYCwnqm7PKoqfczDkpNeGtppa40gH2VrzX_0_bNSY6w</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Ooms, Tom</creator><creator>Vreysen, Steven</creator><creator>Van Baelen, Guy</creator><creator>Gerbaud, Vincent</creator><creator>Rodriguez-Donis, Ivonne</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TB</scope><scope>7U5</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>L7M</scope><scope>7SR</scope><scope>8BQ</scope><scope>JG9</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-2738-7922</orcidid><orcidid>https://orcid.org/0000-0002-7809-0910</orcidid></search><sort><creationdate>20140601</creationdate><title>Separation of ethyl acetate–isooctane mixture by heteroazeotropic batch distillation</title><author>Ooms, Tom ; Vreysen, Steven ; Van Baelen, Guy ; Gerbaud, Vincent ; Rodriguez-Donis, Ivonne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-e493523ba6e0c64139df3e0b3ab9856e7af050131f61e760c338c118a73938383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acetonitrile</topic><topic>Batch distillation</topic><topic>Chemical and Process Engineering</topic><topic>Chemical engineering</topic><topic>Chemical Sciences</topic><topic>Decantation</topic><topic>Distillation</topic><topic>Engineering Sciences</topic><topic>Entrainer selection</topic><topic>Entrainment</topic><topic>Ethyl acetate</topic><topic>Ethyl acetate–isooctane mixture</topic><topic>Heteroazeotropic distillation</topic><topic>Isooctane</topic><topic>Methanol</topic><topic>Methyl alcohol</topic><topic>Separation</topic><topic>Solvent recovery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ooms, Tom</creatorcontrib><creatorcontrib>Vreysen, Steven</creatorcontrib><creatorcontrib>Van Baelen, Guy</creatorcontrib><creatorcontrib>Gerbaud, Vincent</creatorcontrib><creatorcontrib>Rodriguez-Donis, Ivonne</creatorcontrib><collection>CrossRef</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>Advanced Technologies Database with Aerospace</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Materials Research Database</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Chemical engineering research & design</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ooms, Tom</au><au>Vreysen, Steven</au><au>Van Baelen, Guy</au><au>Gerbaud, Vincent</au><au>Rodriguez-Donis, Ivonne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Separation of ethyl acetate–isooctane mixture by heteroazeotropic batch distillation</atitle><jtitle>Chemical engineering research & design</jtitle><date>2014-06-01</date><risdate>2014</risdate><volume>92</volume><issue>6</issue><spage>995</spage><epage>1004</epage><pages>995-1004</pages><issn>0263-8762</issn><eissn>1744-3563</eissn><abstract>Heteroazeotropic batch distillation process to recover isooctane as product from ethyl acetate–isooctane mixture with using acetonitrile. 3.0-2 class ternary diagram and liquid–liquid and liquid–liquid–vapour equilibrium envelopes estimated by the original UNIFAC model.
•Distillation of isooctane from an ethyl acetate–isooctane mixture.•Heterogeneous azeotropic distillation in a batch rectification column.•Methanol and acetonitrile heterogeneous entrainers selected among 60 candidates.•Experiments carried out in a laboratory scale column with decanter at the top.•Isooctane is the distillate product while acetonitrile achieves the best separation.
This paper studies the separation of an ethyl acetate–isooctane mixture by heterogeneous azeotropic distillation in a batch rectifying column. An initial list of 60 candidates was studied but only methanol and acetonitrile were obtained as potential heterogeneous entrainers. These entrainers form a low boiling heterogeneous azeotrope with isooctane. Experimental verification of the miscibility gap with isooctane was performed at 25°C for each entrainer giving a smaller region for methanol than for acetonitrile. Feasibility of the heterogeneous azeotropic batch distillation was carried out experimentally in a laboratory batch distillation column having 44 theoretical equilibrium stages and using a high reflux ratio. Several distillate fractions were taken as a function of the temperature at the top of the column. For both methanol and acetonitrile, the main fraction was defined by the condensed vapor providing a liquid–liquid split of the isooctane/entrainer heteroazeotrope into the decanter. Ethyl acetate impurity was detected in both decanted phases, but in much lower amount when using acetonitrile as entrainer. The process with acetonitrile also resulted in a shorter operating time and higher purity and recovery yield of isooctane as the main distillate product. Pure ethyl acetate remained into the boiler at the end of each process.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.cherd.2013.10.010</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-2738-7922</orcidid><orcidid>https://orcid.org/0000-0002-7809-0910</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0263-8762 |
ispartof | Chemical engineering research & design, 2014-06, Vol.92 (6), p.995-1004 |
issn | 0263-8762 1744-3563 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_03521173v1 |
source | Elsevier ScienceDirect Journals |
subjects | Acetonitrile Batch distillation Chemical and Process Engineering Chemical engineering Chemical Sciences Decantation Distillation Engineering Sciences Entrainer selection Entrainment Ethyl acetate Ethyl acetate–isooctane mixture Heteroazeotropic distillation Isooctane Methanol Methyl alcohol Separation Solvent recovery |
title | Separation of ethyl acetate–isooctane mixture by heteroazeotropic batch distillation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T06%3A30%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Separation%20of%20ethyl%20acetate%E2%80%93isooctane%20mixture%20by%20heteroazeotropic%20batch%20distillation&rft.jtitle=Chemical%20engineering%20research%20&%20design&rft.au=Ooms,%20Tom&rft.date=2014-06-01&rft.volume=92&rft.issue=6&rft.spage=995&rft.epage=1004&rft.pages=995-1004&rft.issn=0263-8762&rft.eissn=1744-3563&rft_id=info:doi/10.1016/j.cherd.2013.10.010&rft_dat=%3Cproquest_hal_p%3E1560126048%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1560126048&rft_id=info:pmid/&rft_els_id=S0263876213004309&rfr_iscdi=true |