Metal-organic frameworks (MOFs) are characterized by a large specific surface area, a wide variety of porous structures, and the ability to chemically tailor their adsorption sites. Due to these properties, MOFs represent promising adsorbents for direct CO2 capture from the air, where efficient and selective adsorption at CO2 concentrations ranging from 400 to 2000 ppm is crucial. As part of my master’s thesis, I systematically investigated the effect of functionalization with amine compounds–such as glycine, tetraethylpentylamine (TEPA), and polyethyleneimine (PEI)– on capture efficiency at low CO2 concentrations using selected MOF systems. The prepared materials were characterized using selected MOF systems. The prepared materials were characterized using X-ray diffraction, thermogravimetric analysis and Fourier transform infrared spectroscopy. Subsequently, CO2 adsorption isotherms were measured, based on which the effect of functionalization on CO2 capture capacity at concentrations up to 2000 ppm was evaluated. For the functionalized samples exhibiting improved CO2 adsorption compared to the basic MOF systems, nitrogen adsorption isotherms were additionally measured, from which the specific surface areas were determined using the BET method. The regeneration capacity of materials after multiple consecutive cycles of CO2 adsorption and desorption was also tested. Since water vapor significantly affects CO2 adsorption under real-world conditions, water adsorption isotherms were also measured, and CO2 capture performance in the presence of moisture was evaluated.
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