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Direct Air Capture of CO2 with Aqueous Amino Acids and Solid Bis-iminoguanidines (BIGs)

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We report a bench-scale direct air capture (DAC) process comprising CO2 absorption with aqueous amino acid salts (i.e., potassium glycinate, potassium sarcosinate), followed by room-temperature regeneration of the amino acids… Click to show full abstract

We report a bench-scale direct air capture (DAC) process comprising CO2 absorption with aqueous amino acid salts (i.e., potassium glycinate, potassium sarcosinate), followed by room-temperature regeneration of the amino acids by reaction with solid meta-benzene-bis(iminoguanidine) (m-BBIG), resulting in crystallization of the hydrated m-BBIG carbonate salt, (m-BBIGH2)(CO3)(H2O)n (n = 3-4). The CO2 is subsequently released by mild heating (60-120 C) of the carbonate crystals, which regenerates the m-BBIG solid quantitatively. This low-temperature crystallization-based DAC process circumvents the need to heat the aqueous amino acid sorbents, thereby minimizing their loss through thermal and oxidative degradation. The CO2 cyclic capacity for the sarcosine/m-BBIG system, measured over three consecutive absorption/regeneration cycles, is in the range of 0.12–0.20 mol/mol. The regeneration energy of m-BBIG, comprising the enthalpy of CO2 and water release, and the sensible heat, is 360 kJ/mol (8.2 GJ/ton CO2)....

Keywords: amino; amino acids; air capture; aqueous amino; direct air

Journal Title: Industrial & Engineering Chemistry Research
Year Published: 2019

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