TY - JOUR
T1 - Enhanced Carbon Dioxide Capture from Landfill Gas Using Bifunctionalized Benzimidazole-Linked Polymers
AU - Islamoglu, Timur
AU - Behera, Swayamprabha
AU - Kahveci, Zafer
AU - Tessema, Tsemre Dingel
AU - Jena, Puru
AU - El-Kaderi, Hani M.
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/6/15
Y1 - 2016/6/15
N2 - Tuning the binding affinity of small gases and their selective uptake by porous adsorbents are vital for effective CO2 removal from gas mixtures for environmental protection and fuel upgrading. In this study, an amine-functionalized benzimidazole-linked polymer (BILP-6-NH2) was synthesized by a combination of pre- and postsynthetic modification techniques in two steps. Presynthetic incorporation of nitro groups resulted in stoichiometric functionalization (1 nitro/phenyl) in addition to noninvasive functionalization, where more than 80% of the surface area maintained compared to BILP-6. Experimental studies presented enhanced CO2 uptake and CO2/CH4 selectivity in BILP-6-NH2 compared to BILP-6, which are governed by the synergetic effect of benzimidazole and amine moieties. DFT calculations were used to understand the interaction modes of CO2 with BILP-6-NH2 and confirmed the efficacy of amine groups. Encouraged by the enhanced uptake and selectivity in BILP-6-NH2, we have evaluated its performance in landfill gas separation under vacuum swing adsorption (VSA) settings, which resulted in very promising working capacity and sorbent selection parameters outperforming most of the best solid adsorbent in the literature.
AB - Tuning the binding affinity of small gases and their selective uptake by porous adsorbents are vital for effective CO2 removal from gas mixtures for environmental protection and fuel upgrading. In this study, an amine-functionalized benzimidazole-linked polymer (BILP-6-NH2) was synthesized by a combination of pre- and postsynthetic modification techniques in two steps. Presynthetic incorporation of nitro groups resulted in stoichiometric functionalization (1 nitro/phenyl) in addition to noninvasive functionalization, where more than 80% of the surface area maintained compared to BILP-6. Experimental studies presented enhanced CO2 uptake and CO2/CH4 selectivity in BILP-6-NH2 compared to BILP-6, which are governed by the synergetic effect of benzimidazole and amine moieties. DFT calculations were used to understand the interaction modes of CO2 with BILP-6-NH2 and confirmed the efficacy of amine groups. Encouraged by the enhanced uptake and selectivity in BILP-6-NH2, we have evaluated its performance in landfill gas separation under vacuum swing adsorption (VSA) settings, which resulted in very promising working capacity and sorbent selection parameters outperforming most of the best solid adsorbent in the literature.
KW - CO capture
KW - benzimidazole-linked polymers
KW - functionalization of porous organic polymers
KW - landfill gas purification
KW - sorbent selection parameters
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U2 - 10.1021/acsami.6b05326
DO - 10.1021/acsami.6b05326
M3 - Article
C2 - 27228220
AN - SCOPUS:84975221691
SN - 1944-8244
VL - 8
SP - 14648
EP - 14655
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 23
ER -