Abstract

Zinc porphyrins, boasting a coordination environment akin to that of natural carbonic anhydrase (CA), coupled with excellent structural stability, built-in hydrophobic pocket, and suitable charge of center Zn2+, were considered as potential CA-mimics for CO2 capture. To validate this assumption, three zinc porphyrin representatives, zinc porphin (ZnP), zinc protoporphyrin IX (ZnPP), and zinc meso-tetrakis(N-methylpyridinium-4-yl) porphyrin (ZnTMPyP), were prepared, and tested performance in enhancing CO2 absorption in water and K2CO3 solutions. The results from CO2 absorption experiments indicated that ZnTMPyP with the optimal dosage increased CO2 absorption rate by 44.25 % in water, and ZnPP with the optimal dosage increased the CO2 absorption rate by 63.67 % in 20 wt% of K2CO3 solution, which are respectively 1.53 and 2.07 times of CO2 absorption performance of zinc cyclen (ZnC), the most effective CA-mimic reported. Besides, the zinc porphyrins demonstrated excellent stability and reusability throughout five cycles of CO2 absorption and desorption, which are vital aspects for practical applications. Through the calorimetric method and density functional theory (DFT) calculations, it was confirmed that the prepared zinc porphyrins had similar enzymatic behavior and catalytic CO2 hydration pathway to natural CA. According to the results of characterization and DFT calculations, high dispersion, the lowest charge of the Zn2+ center, and the existence of additional CO2 adsorption sites (propionate ions), endow ZnPP with the highest catalytic activity in the K2CO3 solution.

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