This experimental study describes efficient CO₂ capture by 2-amino-2-methyl-1-propanol (AMP)/piperazine (PZ) in ethylene glycol monoethyl ether (EGMEE, 2-ethoxyethanol) containing approximately 15 wt % of water. In these experiments, the solvent is continuously circulated between the absorber (packed-bed reactor at 30, 40, or 45 °C) and the desorber (at 80, 85, or 90 °C). The CO₂ -solvent reaction equilibria have been investigated by using ¹³C NMR spectroscopy, which provides confirmatory evidence that the formation of mono- and biscarbamate derivatives of PZ accounts for most of the CO₂ absorbed by the AMP/PZ/EGMEE/H₂O blend. The solid-state structures of AMP carbamate and of the carbonate salt of protonated AMP have been determined by using XRD. Both AMPCO₂(-) and CO(3)(2-) species completely convert to the monoalkyl carbonates on dissolving the respective salts in methanol, ethanol, or ethylene glycol.
No takes yet. Share an insight, caveat, or question.
Barzagli et al. (2012) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: