The CO2−amine chemistry in gas−solid processes was investigated under both humid and dry conditions using aminopropyl-grafted pore-expanded MCM-41 silica (MONO-PE-MCM-41). To draw accurate conclusions, a set of conditions had to be met including (i) the use of an adsorbent with open pore structure and readily accessible adsorption sites, e.g. MONO-PE-MCM-41 with a mean pore size of 7.2 nm; (ii) the CO2 concentration in the feed should be high enough to achieve saturation via chemisorption, but low enough to avoid any additional physisorption, e.g., 5% CO2 in N2; (iii) the use of a reliable method for the accurate measurement of CO2/N ratio. Under such conditions, the obtained CO2/N ratios were reminiscent of those obtained in the CO2 scrubbing process using ethanolamine solutions. Under dry conditions, the CO2/N ratio was close to 0.5, consistent with the formation of carbamate. Streams with relative humidity (RH) of 27, 61, and 74% were studied as well. As RH in the feed increased, CO2/N ratio increased from 0.57 to 0.88, in line with the gradual formation of bicarbonate. As for the determination of CO2/N ratio under dry conditions, both thermogravimetry (TG) and mass spectrometry (MS) were suitable, whereas in the presence of moisture, TG was found to drastically underestimate the CO2 uptake. The seemingly disparate CO2/N ratios reported in the literature for various propylamine-bearing adsorbents were rationalized on the basis of the adsorbent pore structure and/or the experimental conditions used.

Adsorption of CO(2) was investigated on a series of primary, secondary, and tertiary monoamine-grafted pore-expanded mesoporous MCM-41 silicas, referred to as pMONO, sMONO, and tMONO, respectively. The pMONO adsorbent showed the highest CO(2) adsorption capacity, followed by sMONO, whereas tMONO exhibited hardly any CO(2) uptake. As for the stability in the presence of dry CO(2), we showed in a previous contribution [J. Am. Chem. Soc.2010, 132, 6312-6314] that amine-supported materials deactivate in the presence of dry CO(2) via the formation of urea linkages. Here, we showed that only primary amines suffered extensive loss in CO(2) uptake, whereas secondary and tertiary amines were stable even at temperature as high as 200 °C. The difference in the stability of primary vs secondary and tertiary amines was associated with the occurrence of isocyanate as intermediate species toward the formation of urea groups, since only primary amines can be precursors to isocyanate in the presence of CO(2). However, using a grafted propyldiethylenetriamine containing both primary and secondary amines, we demonstrated that while primary amines gave rise to isocyanate, the latter can react with either primary or secondary amines to generate di- and trisubstituted ureas, leading to deactivation of secondary amines as well.

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