Affiliation:
1. Institute of Technology of Materials (ITM) Universitat Politècnica de València (UPV) Camí de Vera s/n Valencia 46022 Spain
2. Department of Chemical Engineering (DEQ) Universitat Rovira i Virgili (URV) Av. Païssos Catalans, 26 Tarragona 43007 Spain
3. Department of Analytical Chemistry and Organic Chemistry Universitat Rovira i Virgili (URV) C/ Marcel·lí Domingo s/n Tarragona 43007 Spain
Abstract
AbstractPolysulfone membranes, used as contactors for CO2 capture, are blended with two different hyperbranched polyethyleneimines modified with benzoyl chloride (Additive 1) and phenyl isocyanate (Additive 2) in different percentages. Fourier‐transformed infrared spectra evidence the presence of urea and amide groups, whereas the field emission scanning electron microscopy images show differences in the microstructure of the blended membranes. Dielectric spectra determine the motions of the side and backbone chains, which can facilitate the diffusion of CO2. The spectra consist of six dielectric processes; three of them are due to the polysulfone (γPSf, βPSf, and αPSf), whereas the rest are characteristic of the additive (γHPEI, βHPEI, and αHPEI). The benzoyl chloride and phenyl isocyanate functional groups introduce variations in molecular mobility and modify the relaxations associated with the hyperbranched polyethyleneimine (HPEI). The additives also increase the conductivity of the blended membranes, which can compromise the performance of the membranes, specifically in the case of Additive 1. Ion hopping is found to be the prevailing charge transport mechanism while both relaxations, αHPEI and αPSf, are actives. These results, together with the final morphology of the membranes, may explain the greater absorption capacity of the membranes prepared with the hyperbranched polyethyleneimine modified with Additive 2.
Funder
Ministerio de Ciencia e Innovación
Subject
Materials Chemistry,Polymers and Plastics,Organic Chemistry
Cited by
1 articles.
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