A supermolecular building layer approach for gas separation and storage applications: the eea and rtl MOF platforms for CO2 capture and hydrocarbon separation

被引:101
作者
Chen, Zhijie [1 ]
Adil, Karim [1 ]
Weselinski, Lukasz J. [1 ]
Belmabkhout, Youssef [1 ]
Eddaoudi, Mohamed [1 ]
机构
[1] King Abdullah Univ Sci & Technol KAUST, Funct Mat Design Discovery & Dev Res Grp FMD3, Adv Membranes & Porous Mat Ctr AMPM, Div Phys Sci & Engn, Thuwal 239556900, Saudi Arabia
关键词
METAL-ORGANIC FRAMEWORKS; ADSORPTION; FUNCTIONALIZATION; THERMODYNAMICS; SELECTIVITY; CHEMISTRY; CO2/N-2; DESIGN;
D O I
10.1039/c4ta07115h
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
The supermolecular building layer (SBL) approach was employed to deliberately synthesize five novel metal-organic frameworks (1-5) with an exposed array of amide or amine functionalities within their pore system. The ability to decorate the pores with nitrogen donor moieties offers potential to evaluate/elucidate the structure-adsorption property relationship. Two MOF platforms, eea-MOF and rtl-MOF, based on pillaring of kgm-a or sql-a layers with heterofunctional 3-connected organic building blocks were targeted and constructed to purposely introduce and expose the desired amide or amine functionalities. Interestingly, gas adsorption properties of eea-MOF-4 (1) and eea-MOF-5 (2) showed that by simply altering the nitrogen donor position within the ligand, it is possible to relatively reduce the pore size of the related eea-MOF material and subsequently increase the associated CO2 uptake. The slightly confined pore space in 2, relative to 1, has enabled an enhancement of the pore local charge density and thus the observed relative increase in the CO2 and H-2 isosteric heat of adsorption (Q(st)). In addition, light hydrocarbon adsorption studies revealed that 2 is more selective toward C2H6 and C3H8 over CH4 than 1, as exemplified for C2H6 : CH4 (5 : 95) or C3H8 : CH4 (5 : 95) binary gas mixtures.
引用
收藏
页码:6276 / 6281
页数:6
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