Microporous mixed-metal mixed-ligand metal organic framework for selective CO2 capture

被引:8
|
作者
Maity, Rahul [1 ]
Chakraborty, Debanjan [1 ]
Nandi, Shyamapada [1 ]
Rinku, Kushwaha [1 ]
Vaidhyanathan, Ramanathan [1 ,2 ]
机构
[1] IISER, Dept Chem, Dr HomiBhabha Rd, Pune 411008, Maharashtra, India
[2] Indian Inst Sci Educ & Res, Ctr Energy Sci, Dr HomiBhabha Rd, Pune 411008, Maharashtra, India
来源
CRYSTENGCOMM | 2018年 / 20卷 / 39期
关键词
CARBON-DIOXIDE CAPTURE; GAS SORPTION; FLUE-GAS; ADSORPTION; SEPARATION; MOF; STABILITY; BINDING; SITES; POLYMERS;
D O I
10.1039/c8ce00752g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A microporous mixed-ligand-based metal-organic framework has been synthesized using two different dicarboxylic acid-based ligands (4,4-biphenyldicarboxylate (BPDC) and imino diacetate (IMDA)) and two different metal ions (Ce3+ and Na+), namely Ce3Na3(BPDC)(3)(IMDA)(3)(DMF)(2)(H2O)(9). The framework built from Ce-Na-carboxylate layers and BPDC pillars consists of 2D slit-shaped pores occupied by extra-framework Na+ ions. The desolvated framework is permanently porous with a BET surface area of approximate to 771 m(2) g(-1) and displays moderate CO2 uptake of 2.0 mmol g(-1) with a CO2/N-2 selectivity (S) of 68 at room temperature and 1 bar. A modest heat of adsorption (23 kJ mol(-1)) and smooth diffusion kinetics are observed, as reflected in the facile CO2 cycling. Using GCMC methods, the CO2 adsorption isotherm at 298 K was simulated, which matches the experimental isotherm well. The CO2 positions observed from the simulations showed that Na+ ions in the channels serve as favorable adsorption sites for the oxygen atoms in CO2 pointing toward the Na+ ions (O?C?ONa+ = 3.34-5.87 angstrom), while some CO2 molecules sit flat on the phenyl rings of the BPDC at a CO(2)centroid distance of 3.6-3.7 angstrom.
引用
收藏
页码:6088 / 6093
页数:6
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