Ionic liquids (ILs) physical immobilization in solid materials is a key strategy for developing efficient and low cost CO2 capture processes. In this work, two porous commercial substrates with different characteristics (silica and alumina) were impregnated with ILs by physical wet method. Imidazolium based IL combined with [Br]- and [Tf2N]- anions were used in impregnation process. CO2 sorption capacity and selectivity (CO2/N2) of these materials were investigated. The best results regarding CO2/N2 selectivity and CO2 sorption were obtained with [Tf2N]- anion. In relation to solid support, commercial alumina exhibited enhanced CO2 uptake and higher selective capacity (CO2/N2) (6.1 (± 0.1)). Combination of commercial alumina as support and 20 wt% of mbmim [Tf2N] resulted in higher CO2/N2 selectivity of 9.5 ± 1.0. In addition, this material also showed fast sorption kinetics when compared to pure IL besides reuse capacity.

The development of both versatile and inexpensive sorbents for CO2/CH4 separation has become one of the greatest challenges to the environment and natural gas processing. This study reports the preparation and characterization of polyurethane (PU)/ cellulose based poly(ionic liquid)(CPIL) composites for CO2/CH4 separation. PU matrix was reinforced with CPIL in the range of 10-30 wt%. Several characterization techniques (TGA, DSC, DMTA and FESEM ) were used to study the physical properties of composites when the PU matrix is reinforced with cellulose based poly (ionic liquids) (CPIL) up to 30%. CO2 sorption, reusability and CO2/CH4 selectivity were assessed by pressure-decay technique. Results showed that CPIL addition in PU matrix promoted the increase in both thermal stability and mechanical properties when compared to PU. The best result for CO2 sorption (35.0 mgCO2/g) was obtained for PU/CPIL-TBP 10% which presented a higher sorption value when compared to PU (24.1 mgCO2/g) and PU/CELLULOSE 10% (26.8 mgCO2/g). PU/CPIL-TBP 20% demonstrated higher CO2/CH4 selectivity. PU/CPIL composites appear as promissory materials for CO2 capture. These compounds combine the benefits of ionic liquids (ILs) (high ionic conductivity, chemical and thermal stability) and cellulose (thermal stability) with PU properties (mechanical stability, processing and tunable macromolecular design).

Capturing carbon dioxide (CO2) from exhaust gases is an important strategy to prevent climate change. There is a great interest in developing novel CO2 sorbents. Thus, a series of polyurethane (PU) / silica xerogels functionalized with RTILs (bmim Cl and bmim TF2N) composites were prepared and characterized. PU matrix was reinforced with functionalized silica xerogels in the range of 0.5-20 wt%. PU / functionalized silica xerogels were characterized by NMR, FTIR, DSC, TGA, DMTA and FESEM. CO2 sorption capacity and reusability were assessed by the pressure-decay technique at 298.15 K and 1 bar. Results showed that the filler aggregation in PU matrix promoted the reduction of mechanical properties. However, addition of silica xerogels functionalized with RTILs in PU matrix led to increased CO2 uptake. CO2 sorption capacity tends to increase with the incorporation of silica xerogels functionalized with RTILs in PU matrix. The best CO2 sorption value was found for PU/SX-[Bmim]-[TF2N] 0.5 composite (48.5 mgCO2/g at 298.15 K and 1 bar). Moreover, the PU/SX-[Bmim]-[TF2N] 0.5 composite showed reuse capacity and higher CO2 sorption value as compared to other reported composites.