Three different commercial Metal-Organic Frameworks (HKUST-1, MIL-53(Al) and ZIF-8) were modified by wetness impregnation of tetraethylenepentamine (TEPA) molecules. These amino-containing MOF materials were studied in CO2 adsorption under post-combustion conditions (45 degrees C and 1 bar) using a simulated exhausted flue gas stream of power plants (75% inert gas; 5% O-2; 14% CO2; 6% H2O; % in vol.). The yield of TEPA incorporation was significantly affected by the physicochemical properties of the MOF precursors. The presence of reactive sites of HKUST-1 (unsaturated copper sites) or MIL 53(Al) (exposed hydroxyl bridges (mu(2)-OH)) as well as their worst textural properties as compared to ZIF-8,led to lower TEPA loadings and porosities of the resultant amino-impregnated HKUST-1 and MIL 53(Al) materials. The ZIF-8 material showed a better distribution of TEPA since reactive surface sites are not present in this support with a higher superficial development. Amino-impregnated ZIF-8 samples exhibited enhanced adsorption capacities by combination of physical and chemical adsorption of CO2 over the TEPA-impregnated microporous framework. The increase of the TEPA content in the ZIF-8 material led to CO2 uptake up to 67 mg(co2)/g(ads) using pure CO2 at 0.15 bar and 45 degrees C. Under post-combustion CO2 capture conditions, TEPA-impregnated ZIF-8 samples underwent a remarkable increase of the carbon dioxide uptake up to 104 mg(co2)/g(ads), due to the presence of moisture, which is responsible of increasing the CO2 capture efficiency of amino groups. After several adsorption/desorption cycles at post-combustion adsorption conditions, TEPA-containing ZIF-8 samples have shown a high structural stability, maintaining the CO2 uptake practically constant. (C) 2015 Elsevier Ltd. All rights reserved.