Conformation of poly(ethylene oxide) dissolved in the solvate ionic liquid [Li(G4)]TFSI
Author(s) -
Zhengfei Chen,
Paul A. FitzGerald,
Gregory G. Warr,
Rob Atkin
Publication year - 2015
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c5cp02033f
Subject(s) - ethylene oxide , ionic liquid , oxide , ethylene , poly ethylene , chemistry , ionic bonding , polymer chemistry , organic chemistry , ion , polymer , catalysis , copolymer
The conformation of 38 kDa PEO in a solvate ionic liquid (SIL), lithium tetraglyme bis(trifluoromethane-sulfonyl)amide ([Li(G4)]TFSI) from dilute to concentrated solution regimes has been determined by small angle neutron scattering and rheology. SANS analysis reveals that [Li(G4)]TFSI is better than a theta solvent (theta-good) for PEO. The variation of the radius of gyration (Rg) and viscosity as a function of polymer concentration allow the overlap concentrations, c* and c**, to be identified at 13 mg mL(-1) and 50 mg mL(-1), respectively, which are similar to values reported previously for conventional ionic liquids. Unlike water and conventional ionic liquids, [Li(G4)]TFSI cannot form hydrogen bonds with PEO. Thermal gravimetric analysis indicates that the solvation of PEO by [Li(G4)]TFSI is a consequence of PEO forming coordinate bonds with the lithium by displacing the anion, but without displacing the glyme molecule.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom