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Modes of Interaction in Binary Blends of Hydrophobic Polyethers and Imidazolium Bis(trifluoromethylsulfonyl)imide Ionic Liquids
被引:9
作者:
Bentley, Caitlin L.
[1
]
Chwatko, Malgorzata
[1
]
Wheatle, Bill K.
[1
]
Burkey, Aaron A.
[1
]
Helenic, Alysha
[1
]
Morales-Collazo, Oscar
[1
]
Ganesan, Venkat
[1
]
Lynd, Nathaniel A.
[1
]
Brennecke, Joan F.
[1
]
机构:
[1] Univ Texas Austin, McKetta Dept Chem Engn, Austin, TX 78712 USA
基金:
美国国家科学基金会;
关键词:
TEMPERATURE PHASE-BEHAVIOR;
POLY(ETHYLENE OXIDE);
SEPARATION BEHAVIOR;
POLYMER BLENDS;
CARBON-DIOXIDE;
CO2;
SOLVENTS;
EXTRACTION;
MIXTURES;
GELS;
D O I:
10.1021/acs.macromol.0c01155
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
Lower critical solution behavior in binary blends of hydrophobic polyethers with 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ahmim][Tf2N]) exhibited a difference in lower critical solution temperature (LCST) greater than 80 degrees C between structurally homologous poly(isopropyl glycidyl ether) (PiPGE) and poly(n-butyl glycidyl ether) (PnBGE). Replacement of the acidic hydrogen on the imidazolium ring with a methyl group (i.e., 2,3-dimethyl-1-hexyl-imidazolium bis(trifluoromethylsulfonyl)imide ([hmmim] [Tf2N])) significantly reduced the LCST of both the PnBGE/ionic liquid (IL) mixture and the PiPGE/IL mixture. Differing degrees of hydrogen bonding between the polymer and the cation cannot alone explain the observed behavior. Similar hydrogen bonding between the [hmim](+ )cation and both polymers from molecular dynamics simulations was consistent with this conclusion. However, stronger [hmim](+) cation tail/polymer alkyl side-chain interactions for PnBGE, with consequently stronger cation/anion interactions, point to solvophobic interactions as the basis for the large LCST difference between the PnBGE/[hmim][Tf2N] and PiPGE/[hmim][Tf2N] blends.
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页码:6519 / 6528
页数:10
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