Assessment of the UCST-type liquid-liquid phase separation mechanism of imidazolium-based ionic liquid, [Cmim][TFSI], and 1,4-dioxane by SANS, NMR, IR, and MD simulations
Liquid-liquid phase separation of binary systems for imidazolium-based ionic liquids (ILs), 1-alkyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([C n mim][TFSI], where n represents the alkyl chain length of the cation), with 1,4-dioxane (1,4-DIO) was observed as a function of temperature...
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creator | Kawano, Masahiro Sadakane, Koichiro Iwase, Hiroki Matsugami, Masaru Marekha, Bogdan A Idrissi, Abdenacer Takamuku, Toshiyuki |
description | Liquid-liquid phase separation of binary systems for imidazolium-based ionic liquids (ILs), 1-alkyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([C
n
mim][TFSI], where
n
represents the alkyl chain length of the cation), with 1,4-dioxane (1,4-DIO) was observed as a function of temperature and 1,4-DIO mole fraction,
x
1,4-DIO
. The phase diagrams obtained for [C
n
mim][TFSI]-1,4-DIO systems showed that the miscible region becomes wider with an increase in the alkyl chain length,
n
. For
n
= 6 and 8, an upper critical solution temperature (UCST) was found. To clarify the mechanism of the UCST-type phase separation, small-angle neutron scattering (SANS) experiments were conducted on the [C
8
mim][TFSI]-1,4-DIO-
d
8
system at several
x
1,4-DIO
. The critical exponents of
γ
and
ν
determined from the SANS experiments showed that phase separation of the system at the UCST mole fraction occurs
via
the 3D-Ising mechanism, while that on both sides of UCST occurs
via
the mean field mechanism. Thus, the crossover of mechanism was observed for this system. The microscopic interactions among the cation, anion, and 1,4-DIO were elucidated using
1
H and
13
C NMR and IR spectroscopic techniques, together with the theoretical method of molecular dynamics (MD) simulations. The results on the microscopic interactions suggest that 1,4-DIO molecules cannot strongly interact with H atoms on the imidazolium ring, while they interact with the octyl chain of the cation through dispersion force. With a decrease in temperature, 1,4-DIO molecules gradually aggregate to form 1,4-DIO clusters in the binary solutions. The strengthening of the C-H O interaction between 1,4-DIO molecules by cooling is the key to the phase separation. Of course, the electrostatic interaction between the cations and anions results in the formation of IL clusters. When IL clusters are excluded from 1,4-DIO clusters, liquid-liquid phase separation occurs. Accordingly, the balance between the electrostatic force between the cations and anions and the C-H O interaction between the 1,4-DIO determines the 3D-Ising or the mean field mechanism of phase separation.
UCST-type phase separation of binary solutions of [C
n
mim][TFSI]-1,4-DIO. |
doi_str_mv | 10.1039/d1cp01940f |
format | Article |
fullrecord | <record><control><sourceid>proquest_rsc_p</sourceid><recordid>TN_cdi_rsc_primary_d1cp01940f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2592263052</sourcerecordid><originalsourceid>FETCH-LOGICAL-c414t-76a83ddf7ae7f6651f1885d201eee3fb5359b8b03f8ba0fb3574a7fb7bf595d03</originalsourceid><addsrcrecordid>eNpd0s1q3DAQAGBTWmia9tJ7QdBLW-xWsiT_HBen2yxs0pLdnEIwkiWxCpbleOySzSP1KauNwxZ6mkF8mtEwiqL3BH8lmJbfFGl6TEqGzYvohLCMJiUu2MtjnmevozcAdxhjwgk9if4sADSA092IvEHjTqPrarNNxn2vUWvvJ6uSOaB-J0Aj0L0YxGh9h5xudqKz4A43rbNKPPrWTi6RASoUiG2ea8TopnLW3d5sl5vVbYxEpxCJWaKsfxCdRnKPNovLTYwuL65itLqaxcUZAuum9qkdvI1eGdGCfvccT6Pr5fdtdZ6sf_5YVYt10jDCxiTPREGVMrnQuckyTgwpCq5STLTW1EhOeSkLiakppMBGUp4zkRuZS8NLrjA9jT7PdXeirfvBOjHsay9sfb5Y14czzDDjvEh_k2A_zbYf_P2kYaydhUa3bRjKT1CnvMgYJynmgX78j975aejCJEGVaZpRzNOgvsyqGTzAoM3xBQTXhxXXZ6T69bTiZcAfZjxAc3T_vgD9C18yoXs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2592263052</pqid></control><display><type>article</type><title>Assessment of the UCST-type liquid-liquid phase separation mechanism of imidazolium-based ionic liquid, [Cmim][TFSI], and 1,4-dioxane by SANS, NMR, IR, and MD simulations</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Kawano, Masahiro ; Sadakane, Koichiro ; Iwase, Hiroki ; Matsugami, Masaru ; Marekha, Bogdan A ; Idrissi, Abdenacer ; Takamuku, Toshiyuki</creator><creatorcontrib>Kawano, Masahiro ; Sadakane, Koichiro ; Iwase, Hiroki ; Matsugami, Masaru ; Marekha, Bogdan A ; Idrissi, Abdenacer ; Takamuku, Toshiyuki</creatorcontrib><description>Liquid-liquid phase separation of binary systems for imidazolium-based ionic liquids (ILs), 1-alkyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([C
n
mim][TFSI], where
n
represents the alkyl chain length of the cation), with 1,4-dioxane (1,4-DIO) was observed as a function of temperature and 1,4-DIO mole fraction,
x
1,4-DIO
. The phase diagrams obtained for [C
n
mim][TFSI]-1,4-DIO systems showed that the miscible region becomes wider with an increase in the alkyl chain length,
n
. For
n
= 6 and 8, an upper critical solution temperature (UCST) was found. To clarify the mechanism of the UCST-type phase separation, small-angle neutron scattering (SANS) experiments were conducted on the [C
8
mim][TFSI]-1,4-DIO-
d
8
system at several
x
1,4-DIO
. The critical exponents of
γ
and
ν
determined from the SANS experiments showed that phase separation of the system at the UCST mole fraction occurs
via
the 3D-Ising mechanism, while that on both sides of UCST occurs
via
the mean field mechanism. Thus, the crossover of mechanism was observed for this system. The microscopic interactions among the cation, anion, and 1,4-DIO were elucidated using
1
H and
13
C NMR and IR spectroscopic techniques, together with the theoretical method of molecular dynamics (MD) simulations. The results on the microscopic interactions suggest that 1,4-DIO molecules cannot strongly interact with H atoms on the imidazolium ring, while they interact with the octyl chain of the cation through dispersion force. With a decrease in temperature, 1,4-DIO molecules gradually aggregate to form 1,4-DIO clusters in the binary solutions. The strengthening of the C-H O interaction between 1,4-DIO molecules by cooling is the key to the phase separation. Of course, the electrostatic interaction between the cations and anions results in the formation of IL clusters. When IL clusters are excluded from 1,4-DIO clusters, liquid-liquid phase separation occurs. Accordingly, the balance between the electrostatic force between the cations and anions and the C-H O interaction between the 1,4-DIO determines the 3D-Ising or the mean field mechanism of phase separation.
UCST-type phase separation of binary solutions of [C
n
mim][TFSI]-1,4-DIO.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/d1cp01940f</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Anions ; Binary systems ; Cations ; Chains ; Chemical Sciences ; Clusters ; Ionic liquids ; Ions ; Ising model ; Liquid phases ; Molecular dynamics ; Neutron scattering ; NMR ; Nuclear magnetic resonance ; or physical chemistry ; Phase diagrams ; Phase separation ; Theoretical and</subject><ispartof>Physical chemistry chemical physics : PCCP, 2021-11, Vol.23 (42), p.24449-24463</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-76a83ddf7ae7f6651f1885d201eee3fb5359b8b03f8ba0fb3574a7fb7bf595d03</citedby><cites>FETCH-LOGICAL-c414t-76a83ddf7ae7f6651f1885d201eee3fb5359b8b03f8ba0fb3574a7fb7bf595d03</cites><orcidid>0000-0002-6924-6434 ; 0000-0003-4038-7839 ; 0000-0003-3142-8029 ; 0000-0002-1975-5476</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04045582$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Kawano, Masahiro</creatorcontrib><creatorcontrib>Sadakane, Koichiro</creatorcontrib><creatorcontrib>Iwase, Hiroki</creatorcontrib><creatorcontrib>Matsugami, Masaru</creatorcontrib><creatorcontrib>Marekha, Bogdan A</creatorcontrib><creatorcontrib>Idrissi, Abdenacer</creatorcontrib><creatorcontrib>Takamuku, Toshiyuki</creatorcontrib><title>Assessment of the UCST-type liquid-liquid phase separation mechanism of imidazolium-based ionic liquid, [Cmim][TFSI], and 1,4-dioxane by SANS, NMR, IR, and MD simulations</title><title>Physical chemistry chemical physics : PCCP</title><description>Liquid-liquid phase separation of binary systems for imidazolium-based ionic liquids (ILs), 1-alkyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([C
n
mim][TFSI], where
n
represents the alkyl chain length of the cation), with 1,4-dioxane (1,4-DIO) was observed as a function of temperature and 1,4-DIO mole fraction,
x
1,4-DIO
. The phase diagrams obtained for [C
n
mim][TFSI]-1,4-DIO systems showed that the miscible region becomes wider with an increase in the alkyl chain length,
n
. For
n
= 6 and 8, an upper critical solution temperature (UCST) was found. To clarify the mechanism of the UCST-type phase separation, small-angle neutron scattering (SANS) experiments were conducted on the [C
8
mim][TFSI]-1,4-DIO-
d
8
system at several
x
1,4-DIO
. The critical exponents of
γ
and
ν
determined from the SANS experiments showed that phase separation of the system at the UCST mole fraction occurs
via
the 3D-Ising mechanism, while that on both sides of UCST occurs
via
the mean field mechanism. Thus, the crossover of mechanism was observed for this system. The microscopic interactions among the cation, anion, and 1,4-DIO were elucidated using
1
H and
13
C NMR and IR spectroscopic techniques, together with the theoretical method of molecular dynamics (MD) simulations. The results on the microscopic interactions suggest that 1,4-DIO molecules cannot strongly interact with H atoms on the imidazolium ring, while they interact with the octyl chain of the cation through dispersion force. With a decrease in temperature, 1,4-DIO molecules gradually aggregate to form 1,4-DIO clusters in the binary solutions. The strengthening of the C-H O interaction between 1,4-DIO molecules by cooling is the key to the phase separation. Of course, the electrostatic interaction between the cations and anions results in the formation of IL clusters. When IL clusters are excluded from 1,4-DIO clusters, liquid-liquid phase separation occurs. Accordingly, the balance between the electrostatic force between the cations and anions and the C-H O interaction between the 1,4-DIO determines the 3D-Ising or the mean field mechanism of phase separation.
UCST-type phase separation of binary solutions of [C
n
mim][TFSI]-1,4-DIO.</description><subject>Anions</subject><subject>Binary systems</subject><subject>Cations</subject><subject>Chains</subject><subject>Chemical Sciences</subject><subject>Clusters</subject><subject>Ionic liquids</subject><subject>Ions</subject><subject>Ising model</subject><subject>Liquid phases</subject><subject>Molecular dynamics</subject><subject>Neutron scattering</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>or physical chemistry</subject><subject>Phase diagrams</subject><subject>Phase separation</subject><subject>Theoretical and</subject><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpd0s1q3DAQAGBTWmia9tJ7QdBLW-xWsiT_HBen2yxs0pLdnEIwkiWxCpbleOySzSP1KauNwxZ6mkF8mtEwiqL3BH8lmJbfFGl6TEqGzYvohLCMJiUu2MtjnmevozcAdxhjwgk9if4sADSA092IvEHjTqPrarNNxn2vUWvvJ6uSOaB-J0Aj0L0YxGh9h5xudqKz4A43rbNKPPrWTi6RASoUiG2ea8TopnLW3d5sl5vVbYxEpxCJWaKsfxCdRnKPNovLTYwuL65itLqaxcUZAuum9qkdvI1eGdGCfvccT6Pr5fdtdZ6sf_5YVYt10jDCxiTPREGVMrnQuckyTgwpCq5STLTW1EhOeSkLiakppMBGUp4zkRuZS8NLrjA9jT7PdXeirfvBOjHsay9sfb5Y14czzDDjvEh_k2A_zbYf_P2kYaydhUa3bRjKT1CnvMgYJynmgX78j975aejCJEGVaZpRzNOgvsyqGTzAoM3xBQTXhxXXZ6T69bTiZcAfZjxAc3T_vgD9C18yoXs</recordid><startdate>20211103</startdate><enddate>20211103</enddate><creator>Kawano, Masahiro</creator><creator>Sadakane, Koichiro</creator><creator>Iwase, Hiroki</creator><creator>Matsugami, Masaru</creator><creator>Marekha, Bogdan A</creator><creator>Idrissi, Abdenacer</creator><creator>Takamuku, Toshiyuki</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-6924-6434</orcidid><orcidid>https://orcid.org/0000-0003-4038-7839</orcidid><orcidid>https://orcid.org/0000-0003-3142-8029</orcidid><orcidid>https://orcid.org/0000-0002-1975-5476</orcidid></search><sort><creationdate>20211103</creationdate><title>Assessment of the UCST-type liquid-liquid phase separation mechanism of imidazolium-based ionic liquid, [Cmim][TFSI], and 1,4-dioxane by SANS, NMR, IR, and MD simulations</title><author>Kawano, Masahiro ; Sadakane, Koichiro ; Iwase, Hiroki ; Matsugami, Masaru ; Marekha, Bogdan A ; Idrissi, Abdenacer ; Takamuku, Toshiyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-76a83ddf7ae7f6651f1885d201eee3fb5359b8b03f8ba0fb3574a7fb7bf595d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anions</topic><topic>Binary systems</topic><topic>Cations</topic><topic>Chains</topic><topic>Chemical Sciences</topic><topic>Clusters</topic><topic>Ionic liquids</topic><topic>Ions</topic><topic>Ising model</topic><topic>Liquid phases</topic><topic>Molecular dynamics</topic><topic>Neutron scattering</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>or physical chemistry</topic><topic>Phase diagrams</topic><topic>Phase separation</topic><topic>Theoretical and</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawano, Masahiro</creatorcontrib><creatorcontrib>Sadakane, Koichiro</creatorcontrib><creatorcontrib>Iwase, Hiroki</creatorcontrib><creatorcontrib>Matsugami, Masaru</creatorcontrib><creatorcontrib>Marekha, Bogdan A</creatorcontrib><creatorcontrib>Idrissi, Abdenacer</creatorcontrib><creatorcontrib>Takamuku, Toshiyuki</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawano, Masahiro</au><au>Sadakane, Koichiro</au><au>Iwase, Hiroki</au><au>Matsugami, Masaru</au><au>Marekha, Bogdan A</au><au>Idrissi, Abdenacer</au><au>Takamuku, Toshiyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessment of the UCST-type liquid-liquid phase separation mechanism of imidazolium-based ionic liquid, [Cmim][TFSI], and 1,4-dioxane by SANS, NMR, IR, and MD simulations</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><date>2021-11-03</date><risdate>2021</risdate><volume>23</volume><issue>42</issue><spage>24449</spage><epage>24463</epage><pages>24449-24463</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>Liquid-liquid phase separation of binary systems for imidazolium-based ionic liquids (ILs), 1-alkyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([C
n
mim][TFSI], where
n
represents the alkyl chain length of the cation), with 1,4-dioxane (1,4-DIO) was observed as a function of temperature and 1,4-DIO mole fraction,
x
1,4-DIO
. The phase diagrams obtained for [C
n
mim][TFSI]-1,4-DIO systems showed that the miscible region becomes wider with an increase in the alkyl chain length,
n
. For
n
= 6 and 8, an upper critical solution temperature (UCST) was found. To clarify the mechanism of the UCST-type phase separation, small-angle neutron scattering (SANS) experiments were conducted on the [C
8
mim][TFSI]-1,4-DIO-
d
8
system at several
x
1,4-DIO
. The critical exponents of
γ
and
ν
determined from the SANS experiments showed that phase separation of the system at the UCST mole fraction occurs
via
the 3D-Ising mechanism, while that on both sides of UCST occurs
via
the mean field mechanism. Thus, the crossover of mechanism was observed for this system. The microscopic interactions among the cation, anion, and 1,4-DIO were elucidated using
1
H and
13
C NMR and IR spectroscopic techniques, together with the theoretical method of molecular dynamics (MD) simulations. The results on the microscopic interactions suggest that 1,4-DIO molecules cannot strongly interact with H atoms on the imidazolium ring, while they interact with the octyl chain of the cation through dispersion force. With a decrease in temperature, 1,4-DIO molecules gradually aggregate to form 1,4-DIO clusters in the binary solutions. The strengthening of the C-H O interaction between 1,4-DIO molecules by cooling is the key to the phase separation. Of course, the electrostatic interaction between the cations and anions results in the formation of IL clusters. When IL clusters are excluded from 1,4-DIO clusters, liquid-liquid phase separation occurs. Accordingly, the balance between the electrostatic force between the cations and anions and the C-H O interaction between the 1,4-DIO determines the 3D-Ising or the mean field mechanism of phase separation.
UCST-type phase separation of binary solutions of [C
n
mim][TFSI]-1,4-DIO.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d1cp01940f</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-6924-6434</orcidid><orcidid>https://orcid.org/0000-0003-4038-7839</orcidid><orcidid>https://orcid.org/0000-0003-3142-8029</orcidid><orcidid>https://orcid.org/0000-0002-1975-5476</orcidid></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Anions Binary systems Cations Chains Chemical Sciences Clusters Ionic liquids Ions Ising model Liquid phases Molecular dynamics Neutron scattering NMR Nuclear magnetic resonance or physical chemistry Phase diagrams Phase separation Theoretical and |
title | Assessment of the UCST-type liquid-liquid phase separation mechanism of imidazolium-based ionic liquid, [Cmim][TFSI], and 1,4-dioxane by SANS, NMR, IR, and MD simulations |
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