Impact of organic interlayer anions on the CO2 adsorption performance of Mg-Al layered double hydroxides derived mixed oxides

Herein we report a systematical investigation on the promoting effect of the carbon chain length of the intercalated carboxylic anions on the COcapture performance of Mg-Al layer double hydroxides（LDHs）.A series of organo-LDHs were successfully synthesized via co-precipitation and calcination-rehydration methods. All as-prepared samples were characterized by many techniques including XRD, ATR-FTIR, BET,and TGA. The XRD and ATR-FTIR studies indicated that organic anions were successfully intercalated into LDHs. The influence of some important parameters such as calcination temperature, adsorption temperature, and coating with（Li-Na-K）NOmolten salt was investigated. The results exhibited that when the number of carbon is greater than 10, the COcapture capacity steadily increased with the increase in carbon number. After coating with 55 mol%（Li-Na-K）NOmolten salt, the COuptake of LDH-C16 sample with high Mg/Al ratios can be increased up to 3.25 mmol/g. The COadsorption/desorption cycling stability was also studied using temperature swing adsorption, which showed a stable COcapture performance even after 22 cycles. Considering its high COcapture capacity and good cycling stability, this novel COadsorbent is very promising in the sorption-enhanced water gas shift（SEWGS） processes.

Efficient fixation of CO_2 at mild conditions by a Cr-conjugated microporous polymer

We reported a bifunctional material, Cr-salen implanted conjugated microporous polymer(Cr-CMP), which is able to capture excellent CO2amounts and has a remarkable catalytic activity towards the cycloaddition reaction of CO2to epoxides forming cyclic carbonates at mild conditions without additional solvents. This heterogeneous Cr-CMP catalyst has a superior catalytic activity to its related homogeneous catalyst and can be reused more than ten times without a significant decrease in catalytic activity.