In situ infrared study of the effect of amine density on the nature of adsorbed CO2 on amine-functionalized solid sorbents.

Abstract

In situ Fourier transform infrared spectroscopy was used to determine the nature of adsorbed CO2 on class I (amine-impregnated) and class II (amine-grafted) sorbents with different amine densities. Adsorbed CO2 on amine sorbents exists in the form of carbamate-ammonium ion pairs, carbamate-ammonium zwitterions, and carbamic acid. The adsorbed CO2 on high-amine density sorbents showed that the formation of ammonium ions correlates with the suppression of CH stretching intensities. An HCl probing technique was used to resolve the characteristic infrared bands of ammonium ions, clarifying that the band observed around 1498 cm(-1) is a combination of the deformation vibration of ammonium ion (NH3(+)) at 1508 and 1469 cm(-1) and the deformation vibration of NH in carbamate (NHCOO(-)) at 1480 cm(-1). Carbamate and carbamic acid on sorbents with low amine density desorbed at a rate faster than those on sorbents with high amine density after switching the flow from CO2 to Ar at 55 °C. Evaluation of the desorption temperature profiles showed that the temperature required to achieve the maximal desorption of CO2 (Tmax.des) increases with amine density. The adsorbed CO2 on sorbents with high amine density is stabilized via hydrogen bonding interactions with adjacent amine sites. These sorbents require higher temperature to desorb CO2 than those with low amine density.