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Extractive desulfurization of fuel oils with low-viscosity dicyanamide-based ionic liquids
Four low-viscosity ionic liquids (ILs) based on the dicyanamide anion ([N(CN)2]-), i.e., 1-butyl-3-methylimdazolium ([BMI][N(CN)2]), 1-ethyl-3-methylimdazolium ([EMI][N(CN)2]), ethylated tetrahydrothiophenium ([S2][N(CN)2]) and ethyldimethylsulfonium ([EtMe2S][N(CN)2]), have been investigated to det...
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Published in: | Green chemistry : an international journal and green chemistry resource : GC 2010-01, Vol.12 (11), p.2030-2037 |
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creator | ASUMANA, Charles GUANGREN YU XI LI JINGJING ZHAO GE LIU XIAOCHUN CHEN |
description | Four low-viscosity ionic liquids (ILs) based on the dicyanamide anion ([N(CN)2]-), i.e., 1-butyl-3-methylimdazolium ([BMI][N(CN)2]), 1-ethyl-3-methylimdazolium ([EMI][N(CN)2]), ethylated tetrahydrothiophenium ([S2][N(CN)2]) and ethyldimethylsulfonium ([EtMe2S][N(CN)2]), have been investigated to determine their extraction capability for thiophene (TS) and dibenzothiophene (DBT) from model fuel oils. Aromatic imidazolium is more efficient than cyclic thiophenium and tetrahedral trialkylsulfonium; specifically, the S-extraction ability follows the order [BMI][N(CN)2] [EMI][N(CN)2] [S2][N(CN)2] [EtMe2S][N(CN)2], with DBT being more efficiently extracted than TS. The S-extraction of [BMI][N(CN)2] has been investigated as a representative with respect to the influence of extraction temperature, IL : oil mass ratio, initial S-content, multiple extractions and reusability, along with its mutual solubility in oil. The percentage of S-removal from gasoline and diesel fuel were 48.5 and 68.7%, respectively, in a single extraction at 25 [degree]C, 1 : 1(w/w) IL : oil, 5 min; the S-content in gasoline decreased from 599 ppm to 4 ppm after 5 extraction cycles and in diesel fuel decreased from 606 ppm to an undetectable value after 4 cycles. The mutual solubility is not pronounced and the extraction efficiency is not conspicuously changed after 6 regeneration cycles. It is worth noting that a short extraction time of 5 min is observed for all the ILs at room temperature, which is understood by their low viscosities and effective mass transfer. This work may offer a new option for the deep desulfurization of fuel oils. |
doi_str_mv | 10.1039/c0gc00118j |
format | article |
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Aromatic imidazolium is more efficient than cyclic thiophenium and tetrahedral trialkylsulfonium; specifically, the S-extraction ability follows the order [BMI][N(CN)2] [EMI][N(CN)2] [S2][N(CN)2] [EtMe2S][N(CN)2], with DBT being more efficiently extracted than TS. The S-extraction of [BMI][N(CN)2] has been investigated as a representative with respect to the influence of extraction temperature, IL : oil mass ratio, initial S-content, multiple extractions and reusability, along with its mutual solubility in oil. The percentage of S-removal from gasoline and diesel fuel were 48.5 and 68.7%, respectively, in a single extraction at 25 [degree]C, 1 : 1(w/w) IL : oil, 5 min; the S-content in gasoline decreased from 599 ppm to 4 ppm after 5 extraction cycles and in diesel fuel decreased from 606 ppm to an undetectable value after 4 cycles. The mutual solubility is not pronounced and the extraction efficiency is not conspicuously changed after 6 regeneration cycles. It is worth noting that a short extraction time of 5 min is observed for all the ILs at room temperature, which is understood by their low viscosities and effective mass transfer. This work may offer a new option for the deep desulfurization of fuel oils.</description><identifier>ISSN: 1463-9262</identifier><identifier>EISSN: 1463-9270</identifier><identifier>DOI: 10.1039/c0gc00118j</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Applied sciences ; Chemical engineering ; Chemistry ; Exact sciences and technology ; Heterocyclic compounds ; Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives ; Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings ; Organic chemistry ; Preparations and properties</subject><ispartof>Green chemistry : an international journal and green chemistry resource : GC, 2010-01, Vol.12 (11), p.2030-2037</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c293t-f8c5ab859f09603ec3e6a1d2a2c321234b1d64411551c6749af524bcc9bb2ed33</citedby><cites>FETCH-LOGICAL-c293t-f8c5ab859f09603ec3e6a1d2a2c321234b1d64411551c6749af524bcc9bb2ed33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23454457$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>ASUMANA, Charles</creatorcontrib><creatorcontrib>GUANGREN YU</creatorcontrib><creatorcontrib>XI LI</creatorcontrib><creatorcontrib>JINGJING ZHAO</creatorcontrib><creatorcontrib>GE LIU</creatorcontrib><creatorcontrib>XIAOCHUN CHEN</creatorcontrib><title>Extractive desulfurization of fuel oils with low-viscosity dicyanamide-based ionic liquids</title><title>Green chemistry : an international journal and green chemistry resource : GC</title><description>Four low-viscosity ionic liquids (ILs) based on the dicyanamide anion ([N(CN)2]-), i.e., 1-butyl-3-methylimdazolium ([BMI][N(CN)2]), 1-ethyl-3-methylimdazolium ([EMI][N(CN)2]), ethylated tetrahydrothiophenium ([S2][N(CN)2]) and ethyldimethylsulfonium ([EtMe2S][N(CN)2]), have been investigated to determine their extraction capability for thiophene (TS) and dibenzothiophene (DBT) from model fuel oils. Aromatic imidazolium is more efficient than cyclic thiophenium and tetrahedral trialkylsulfonium; specifically, the S-extraction ability follows the order [BMI][N(CN)2] [EMI][N(CN)2] [S2][N(CN)2] [EtMe2S][N(CN)2], with DBT being more efficiently extracted than TS. The S-extraction of [BMI][N(CN)2] has been investigated as a representative with respect to the influence of extraction temperature, IL : oil mass ratio, initial S-content, multiple extractions and reusability, along with its mutual solubility in oil. The percentage of S-removal from gasoline and diesel fuel were 48.5 and 68.7%, respectively, in a single extraction at 25 [degree]C, 1 : 1(w/w) IL : oil, 5 min; the S-content in gasoline decreased from 599 ppm to 4 ppm after 5 extraction cycles and in diesel fuel decreased from 606 ppm to an undetectable value after 4 cycles. The mutual solubility is not pronounced and the extraction efficiency is not conspicuously changed after 6 regeneration cycles. It is worth noting that a short extraction time of 5 min is observed for all the ILs at room temperature, which is understood by their low viscosities and effective mass transfer. This work may offer a new option for the deep desulfurization of fuel oils.</description><subject>Applied sciences</subject><subject>Chemical engineering</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives</subject><subject>Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><issn>1463-9262</issn><issn>1463-9270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LAzEYhIMoWKsXf0EuIgir-dxtjlLqBxS86MXLkn2TaEratMlua_31bmmpp5nDM8MwCF1Tck8JVw9AvoAQSkezEzSgouSFYhU5PfqSnaOLnGc7pirFAH1OftqkofVri43NXXBd8r-69XGBo8OuswFHHzLe-PYbh7gp1j5DzL7dYuNhqxd67o0tGp2twX3KAw5-1XmTL9GZ0yHbq4MO0cfT5H38Ukzfnl_Hj9MCmOJt4UYgdTOSyhFVEm6B21JTwzQDzijjoqGmFIJSKSmUlVDaSSYaANU0zBrOh-h237tMcdXZ3NbzfqINQS9s7HKtSEUV4VT25N2ehBRzTtbVy-TnOm1rSurdf_X_fz18c6jVGXRwSS_A52OiHyaFkBX_A0OPcZ4</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>ASUMANA, Charles</creator><creator>GUANGREN YU</creator><creator>XI LI</creator><creator>JINGJING ZHAO</creator><creator>GE LIU</creator><creator>XIAOCHUN CHEN</creator><general>Royal Society of Chemistry</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7U6</scope><scope>C1K</scope></search><sort><creationdate>20100101</creationdate><title>Extractive desulfurization of fuel oils with low-viscosity dicyanamide-based ionic liquids</title><author>ASUMANA, Charles ; GUANGREN YU ; XI LI ; JINGJING ZHAO ; GE LIU ; XIAOCHUN CHEN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c293t-f8c5ab859f09603ec3e6a1d2a2c321234b1d64411551c6749af524bcc9bb2ed33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Applied sciences</topic><topic>Chemical engineering</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Heterocyclic compounds</topic><topic>Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives</topic><topic>Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ASUMANA, Charles</creatorcontrib><creatorcontrib>GUANGREN YU</creatorcontrib><creatorcontrib>XI LI</creatorcontrib><creatorcontrib>JINGJING ZHAO</creatorcontrib><creatorcontrib>GE LIU</creatorcontrib><creatorcontrib>XIAOCHUN CHEN</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ASUMANA, Charles</au><au>GUANGREN YU</au><au>XI LI</au><au>JINGJING ZHAO</au><au>GE LIU</au><au>XIAOCHUN CHEN</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extractive desulfurization of fuel oils with low-viscosity dicyanamide-based ionic liquids</atitle><jtitle>Green chemistry : an international journal and green chemistry resource : GC</jtitle><date>2010-01-01</date><risdate>2010</risdate><volume>12</volume><issue>11</issue><spage>2030</spage><epage>2037</epage><pages>2030-2037</pages><issn>1463-9262</issn><eissn>1463-9270</eissn><abstract>Four low-viscosity ionic liquids (ILs) based on the dicyanamide anion ([N(CN)2]-), i.e., 1-butyl-3-methylimdazolium ([BMI][N(CN)2]), 1-ethyl-3-methylimdazolium ([EMI][N(CN)2]), ethylated tetrahydrothiophenium ([S2][N(CN)2]) and ethyldimethylsulfonium ([EtMe2S][N(CN)2]), have been investigated to determine their extraction capability for thiophene (TS) and dibenzothiophene (DBT) from model fuel oils. Aromatic imidazolium is more efficient than cyclic thiophenium and tetrahedral trialkylsulfonium; specifically, the S-extraction ability follows the order [BMI][N(CN)2] [EMI][N(CN)2] [S2][N(CN)2] [EtMe2S][N(CN)2], with DBT being more efficiently extracted than TS. The S-extraction of [BMI][N(CN)2] has been investigated as a representative with respect to the influence of extraction temperature, IL : oil mass ratio, initial S-content, multiple extractions and reusability, along with its mutual solubility in oil. The percentage of S-removal from gasoline and diesel fuel were 48.5 and 68.7%, respectively, in a single extraction at 25 [degree]C, 1 : 1(w/w) IL : oil, 5 min; the S-content in gasoline decreased from 599 ppm to 4 ppm after 5 extraction cycles and in diesel fuel decreased from 606 ppm to an undetectable value after 4 cycles. The mutual solubility is not pronounced and the extraction efficiency is not conspicuously changed after 6 regeneration cycles. It is worth noting that a short extraction time of 5 min is observed for all the ILs at room temperature, which is understood by their low viscosities and effective mass transfer. This work may offer a new option for the deep desulfurization of fuel oils.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c0gc00118j</doi><tpages>8</tpages></addata></record> |
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subjects | Applied sciences Chemical engineering Chemistry Exact sciences and technology Heterocyclic compounds Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings Organic chemistry Preparations and properties |
title | Extractive desulfurization of fuel oils with low-viscosity dicyanamide-based ionic liquids |
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