https://doi.org/10.1039/D1DT00602A
“To evaluate the effects of the synthesis method and starting precursors on the CO2 capture performance of the materials, we also tested the CO2 capture capacity of MMOs derived from anion exchanged Mg–Al-acetate LDH. They showed a CO2 capture of 0.57 mmol g−1 at 200 °C under 86% CO2. This observed CO2 capture capacity is similar to the reported value (0.56 mmol g−1) for acetate LDH derived MMOs under similar testing conditions.54 This clearly highlights the need for alternative strategies in developing improved LDH based MMOs for medium-to-high temperature CO2 capture applications. The MMOs derived from Mg–Al-acetate LDHs synthesized by acetamide hydrolysis were tested for cyclic CO2 stability and the results were compared with the CO2 cyclic stability of MMOs derived from the commercial LDH Pural MG70. The results are presented in Fig. 8. The MMOs derived from Mg–Al-acetate LDH (Mg/Al = 4) retained 65% (0.77 mmol g−1 CO2) of their initial capture capacity after 10 adsorption/regeneration cycles. On the other hand, MMOs generated from Mg–Al-acetate LDH (Mg/Al = 3) showed a better stability as the capture capacity loss was around 28% after 10 cycles. This improved CO2 cycling stability might be attributed to the additional aluminium present in the sample compared to the MMOs having Mg/Al = 4 (lower aluminium content).20,70 The commercial LDH based MMO sorbents (Pural MG70) showed a 35% loss in the capture capacity after 10 cycles. The CO2 capture capacity retained by the commercial LDH based MMOs after 10 cycles (0.43 mmol g−1) was much less than the MMOs derived from the Mg–Al-acetate LDHs (0.77 mmol g−1). Overall, MMOs derived from Mg–Al-acetate LDHs synthesized by modified acetamide hydrolysis showed better CO2 capture and cycling stability than the MMOs derived from the anion exchanged and commercial LDHs.”