Nanoporous amide networks based on tetraphenyladamantane for selective CO2 capture

被引:53
作者
Zulfiqar, Sonia [1 ,2 ]
Mantione, Daniele [2 ]
El Tall, Omar [3 ]
Sarwar, Muhammad Ilyas [1 ,4 ]
Ruiperez, Fernando [2 ]
Rothenberger, Alexander [5 ]
Mecerreyes, David [2 ,6 ]
机构
[1] NUST, SNS, Dept Chem, Islamabad 44000, Pakistan
[2] Univ Basque Country UPV EHU, Joxe Mari Korta Ctr, POLYMAT, Avda Tolosa 72, Donostia San Sebastian 20018, Spain
[3] KAUST, Analyt Core Labs, Thuwal 239556900, Saudi Arabia
[4] Quaid I Azam Univ, Dept Chem, Islamabad 45320, Pakistan
[5] KAUST, Phys Sci & Engn Div, Thuwal 239556900, Saudi Arabia
[6] Basque Fdn Sci, Ikerbasque, E-48011 Bilbao, Spain
关键词
CARBON-DIOXIDE; GAS-STORAGE; MICROPOROUS POLYIMIDES; ORGANIC FRAMEWORKS; FACILE SYNTHESIS; SOLID-STATE; POLYMERS; TRIAZINE; ADSORPTION; HYDROGEN;
D O I
10.1039/c6ta01457g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Reduction of anthropogenic CO2 emissions and CO2 separation from post-combustion flue gases are among the imperative issues in the spotlight at present. Hence, it is highly desirable to develop efficient adsorbents for mitigating climate change with possible energy savings. Here, we report the design of a facile one pot catalyst-free synthetic protocol for the generation of three different nitrogen rich nanoporous amide networks (NANs) based on tetraphenyladamantane. Besides the porous architecture, CO2 capturing potential and high thermal stability, these NANs possess notable CO2/N-2 selectivity with reasonable retention white increasing the temperature from 273 K to 298 K. The quantum chemical calculations also suggest that CO2 interacts mainly in the region of polar amide groups (-CONH-) present in NANs and this interaction is much stronger than that with N-2 thus leading to better selectivity and affirming them as promising contenders for efficient gas separation.
引用
收藏
页码:8190 / 8197
页数:8
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