Synthesis and gas separation properties of poly(ionic liquid)-ionic liquid composite membranes containing a copper salt
Composite poly(ionic liquid)-ionic liquid membranes containing copper (I) chloride (CuCl) have been successfully fabricated via photopolymerization of an IL monomer, 1-vinyl-3-butylimidazolium bistriflimide ([C4vim][Tf2N]), in the presence of CuCl and a non-polymerizable IL, 1-butyl-3-methylimidazol...
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Published in: | Journal of membrane science Vol. 515; pp. 109 - 114 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier B.V
01-10-2016
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Subjects: | |
Online Access: | Get full text |
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Summary: | Composite poly(ionic liquid)-ionic liquid membranes containing copper (I) chloride (CuCl) have been successfully fabricated via photopolymerization of an IL monomer, 1-vinyl-3-butylimidazolium bistriflimide ([C4vim][Tf2N]), in the presence of CuCl and a non-polymerizable IL, 1-butyl-3-methylimidazolium chloride ([C4mim][Cl]), forming the chlorocuprate anion ([CuCl2]−) in situ. The influence of the metal salt content on the gas separation performance of the composite membranes was assessed. Results showed that increasing the content of non-polymerizable IL enhanced the permeabilities of CO2, H2, N2 and CO relative to those obtained in the pristine poly([C4vim][Tf2N]); whereas the addition of CuCl induced a general reduction of gas diffusivity. On the whole, an enhancement of both gas permeability and ideal gas pair selectivity were observed for CO2/N2 and H2/N2 separations in the Cu-containing composite membranes with respect to the neat poly([C4vim][Tf2N]).
•Poly(IL)-IL composites containing Cu+ (as CuCl2−) fabricated via photopolymerization.•Presence of Cu+ did not promote facilitated transport of carbon monoxide.•Design approach could enable new poly(IL) materials with other transition metals. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0376-7388 1873-3123 |
DOI: | 10.1016/j.memsci.2016.05.045 |