Separations, Vol. 12, Pages 71: Polyethylene Glycol (PEG) Additive in Polymer Membranes for Carbon Dioxide Separation: A Critical Review on Performances and Correlation with Membrane Structure


Separations, Vol. 12, Pages 71: Polyethylene Glycol (PEG) Additive in Polymer Membranes for Carbon Dioxide Separation: A Critical Review on Performances and Correlation with Membrane Structure

Separations doi: 10.3390/separations12030071

Authors:
Riccardo Checchetto

The efficient separation and removal of carbon dioxide (CO2) from its mixtures is an important technological challenge to limit effects resulting from the increase of the carbon dioxide concentration in the atmosphere. Membrane technology is an environmentally friendly approach, highly scalable and less energy-consuming than conventional methods such as adsorption, absorption and cryogenic separation. Hybrid membrane materials incorporating inorganic filler nanostructures in polymer matrices having polyethylene glycol (PEG) as a plasticized additive are promising membrane materials given the presence of CO2-philic polar functional groups of PEGs and the structural refinements on the blend matrix consequent to the filler distribution. In this review, literature information on hybrid polymer/PEG membranes are critically reviewed to discuss how filler dispersion in the blend matrix gives rise to enhanced CO2 separation performances with respect to those obtained with traditional mixed matrix membranes where filler nanostructures are dispersed in the neat polymer. The discussion will be focused on the correlation between the CO2 transport properties, membrane structural properties and defect resulting from the polymer-filler incompatibility. It is shown that hybrid polymer/PEG membranes with dispersed filler nanostructures simultaneously offer improved CO2 separation performances and enhanced mechanical properties compared with nanocomposite ones where filler particles are dispersed in the neat polymer matrix. PEG addition enhances the filler-matrix compatibility, delays filler aggregation and limits the formation of filler-matrix interface defects.



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Riccardo Checchetto www.mdpi.com