
Summary of CO2 capture capacities using silica based materials
https://doi.org/10.1016/j.apenergy.2016.09.081

https://doi.org/10.1016/j.apenergy.2016.09.081

https://doi.org/10.1093/ce/zkac020 “The adsorption of CO2 was carried out at 25°C and atmospheric pressure using 15/85 vol% CO2/N2 as a feed gas representing the concentration of CO2 in the

https://doi.org/10.1093/ce/zkac020 “Hexagonal mesoporous silica MCM-41 was synthesized by dissolving 2 g of pore-generating agent, CTAB, with 120 mL of deionized water under constant agitation. After

https://doi.org/10.3390/inorganics10070087 “Ordered hierarchical porous silica materials with micro/mesoporous structures were prepared using dextran as a template via the sol-gel technique. First, an aqueous–alcoholic dextran solution

https://doi.org/10.1039/D0RA04497K “As shown in Fig. 8, the CO2 adsorption kinetics of the SASA-3 change with different temperatures. On account of the thermodynamic theory, the CO2 adsorption capacity of

https://doi.org/10.1039/D0RA04497K “As shown in Fig. 7, the CO2 adsorption kinetics of the SASAs change with different grafting times. The CO2 adsorption capacity first increases, then starts to decrease

https://doi.org/10.1039/D0RA04497K “WG, W and HAc were mixed with a volumetrical ratio of 6 : 33 : 1.2 under room temperature (25 °C) to form a water glass solution. The

https://doi.org/10.1590/1980-5373-MR-2019-0285 “In order to better evaluate the results, the performance analysis was repeated for the samples that presented the best CO2 adsorption performances (Ti/M1-P and Zr/M1-P),

https://doi.org/10.1590/1980-5373-MR-2019-0285 “Fig. 12 shows the CO2 adsorption curves at 30 ºC for the PEHA-functionalized samples. According to the cycles presented in the cited figures, it can be

https://doi.org/10.1590/1980-5373-MR-2019-0285 “Monolith M1 was prepared using tetraethoxysilane (TEOS) as a silica source and the cetyltrimethylammonium bromide (CTAB) as surfactant. The methodology for the preparation of
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