A Microporous Metal-Organic Framework with Immobilized -OH Functional Groups within the Pore Surfaces for Selective Gas Sorption

被引:96
作者
Chen, Zhenxia [1 ,2 ]
Xiang, Shengchang [2 ]
Arman, Hadi D. [2 ]
Li, Peng [2 ]
Tidrow, Steven [3 ]
Zhao, Dongyuan [1 ]
Chen, Banglin [2 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[2] Univ Texas San Antonio, Dept Chem, San Antonio, TX 78249 USA
[3] Univ Texas Pan Amer, Dept Phys & Geol, Edinburg, TX 78539 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Copper; Microporous materials; Structure elucidation; Immobilization; Adsorption; ZEOLITIC IMIDAZOLATE FRAMEWORKS; CARBON-DIOXIDE; THERMAL-STABILITY; ADSORPTION; SEPARATION; DESIGN; H-2; ACETYLENE; STORAGE; CO2;
D O I
10.1002/ejic.201000349
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A new two-dimensional microporous metal-organic framework Cu(BDC-OH)(H2O)center dot 0.5DEF [abbreviation: Cu(BDC-OH); H2BDC-OH = 2-hydroxybenzene-1,4-dicarboxylic acid; DEF = diethylformamide] with functional OH groups on the pore surfaces was solvothermally synthesized and structurally characterized. The activated Cu(BDC-OH) exhibits a moderate Langmuir surface of 584 m(2)g(-1), a pore volume of 0.214 cm(3) g(-1), and C2H2/CH4 and CO2/CH4 selectivity of 6.7 and 9.3, respectively, at 296 K, thereby highlighting the promise for its application in gas separation.
引用
收藏
页码:3745 / 3749
页数:5
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