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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Veröffentlicht in:Physical chemistry chemical physics : PCCP 2021-11, Vol.23 (42), p.24449-24463
Hauptverfasser: Kawano, Masahiro, Sadakane, Koichiro, Iwase, Hiroki, Matsugami, Masaru, Marekha, Bogdan A, Idrissi, Abdenacer, Takamuku, Toshiyuki
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container_issue 42
container_start_page 24449
container_title Physical chemistry chemical physics : PCCP
container_volume 23
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.
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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. 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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 ; 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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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