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Investigation of Cross-Linked and Additive Containing Polymer Materials for Membranes with Improved Performance in Pervaporation and Gas Separation

Journal

MEMBRANES
Volume 2, Issue 4, Pages 727-763

Publisher

MDPI AG
DOI: 10.3390/membranes2040727

Keywords

pervaporation; separation; photocrosslinking; membranes; permeability; permselectivity; mixed-matrix membranes; mechanism; crosslinking degree; photochemistry; metal-organic frameworks; MOFs; porosity

Funding

  1. German Research Foundation [KL 531/29-1]
  2. Anton-Betz-Stiftung

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Pervaporation and gas separation performances of polymer membranes can be improved by crosslinking or addition of metal-organic frameworks (MOFs). Crosslinked copolyimide membranes show higher plasticization resistance and no significant loss in selectivity compared to non-crosslinked membranes when exposed to mixtures of CO2/CH4 or toluene/cyclohexane. Covalently crosslinked membranes reveal better separation performances than ionically crosslinked systems. Covalent interlacing with 3-hydroxypropyldimethylmaleimide as photocrosslinker can be investigated in situ in solution as well as in films, using transient UV/Vis and FTIR spectroscopy. The photocrosslinking yield can be determined from the FTIR-spectra. It is restricted by the stiffness of the copolyimide backbone, which inhibits the photoreaction due to spatial separation of the crosslinker side chains. Mixed-matrix membranes (MMMs) with MOFs as additives (fillers) have increased permeabilities and often also selectivities compared to the pure polymer. Incorporation of MOFs into polysulfone and Matrimid polymers for MMMs gives defect-free membranes with performances similar to the best polymer membranes for gas mixtures, such as O-2/N-2 H-2/CH4, CO2/CH4, H-2/CO2, CH4/N-2 and CO2/N-2 (preferentially permeating gas is named first). The MOF porosity, its particle size and content in the MMM are factors to influence the permeability and the separation performance of the membranes.

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