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The increasing amount of CO2 in the atmosphere is recognized as a major cause of global warming and its harmful consequences. Industrially, CO2 is captured by chemisorption using amine-based solvents. However, there are major drawbacks to the wet-scrubbing process, including corrosion and high regeneration energy. The physical adsorption of CO2 by using porous solid adsorbents is a viable and efficient alternative. Therefore, designing effective porous polymers with microporosity and polar functional groups using a simple approach is important for efficient carbon dioxide capture. This work describes the design, characterization, and CO2 capture studies of a 3D-triptycene and phenanthroline-based microporous polymer (TPPM). The polymeric framework of TPPM is incorporated with 3D triptycene and phenanthroline as robust motifs to yield inflexible, twisted polymeric frameworks with an abundance of micropores and ultramicropores. This confers desirable features such as higher surface area, abundance microporosity, and physiochemical and thermal stability. TPPM demonstrated excellent thermal stability (Td > 380 °C) with a larger BET-specific surface area of 1120 m2 g–1 and considerable microporosity, which makes it a promising adsorbent for CO2 capture applications. The Morphological characterization of the polymer sample shows the formation of microspheres with diameters around 0.5–1 μm. TPPM has a strong affinity for CO2 with Qst of 23 kJ mol–1 demonstrating promising CO2 capture capacity of 2.76 mmol g–1 at 273 K and 1.85 mmol g–1 at 298 K where the micropore volume (Vmic = 0.445 cm3 g–1) plays a potential role. The CO2 capture capacity of TPPM outperforms several other literature-reported porous polymers. TPPM also demonstrated promising CO2 selectivity over CH4 and N2, suggesting good promise for CO2 adsorption and separation.
Ansari et al. (Wed,) studied this question.