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ETS-10, a mixed octahedral/tetrahedral titanosilicate molecular sieve, has a unique architecture where its 0.8 nm pores are lined exclusively with silicon which imparts a high degree of chemical stability, yet the anionic framework can be modified by cation exchange. In this work, the hydrogen-exchanged form of ETS-10 was impregnated with monoethanolamine and the thermal stability and CO2 adsorption characteristics were analyzed. The surface area of the material was characterized by N2 physisorption, the thermal stability of the material assessed through TG-MS experiments, the CO2 capacity was measured via static volumetric adsorption experiments, and the influence of moisture as a carbamate promoter was investigated through a series of gravimetric CO2 adsorption/desorption cycling experiments. Several measurements converge on ~7 wt% monoethanolamine loading which occupies about half of the available pore volume of the sieve. The results suggest that the monoethanolamine is so effectively retained by the molecular sieve that, while the amine is effectively immobilized, under both humid and dry process streams the monoethanolamine is either chemically or sterically hindered and is unable to react measurable quantities of CO2.

A series of nonporous, amine-functionalized sodium titanates was prepared and the thermal and adsorptive behavior of the samples were characterized. Engelhard titanosilicate 2 was chosen as a substrate for its high surface area (300 m 2 /g), native surface hydroxyl concentration, and lack of microporosity; eliminating the risk of fouling the adsorbent under certain process conditions. Aminosilanes containing a single (N1), two (N2), and three (N3) amine groups were chemically grafted to the surface of the substrate and the adsorption capacity for CO 2 measured through thermogravimetry-mass spectroscopy (TG-MS) desorption, volumetric adsorption, and gravimetric adsorption/desorption cycling. The N3 sample displayed complete monolayer coverage and was capable of adsorbing five times as much atmospheric CO 2 as the N1 sample. Testing under anhydrous conditions only engages the primary amine on the tether and the data consistently suggests a correlation between amine utilization and the proportion of monolayer coverage for these adsorbents.