化学
热重分析
氯仿
吸附
选择性
傅里叶变换红外光谱
金属有机骨架
甲醇
无机化学
活性炭
核化学
解吸
红外光谱学
扫描电子显微镜
催化作用
有机化学
化学工程
材料科学
工程类
复合材料
作者
Zana Hassan Rada,Hussein Rasool Abid,Hongqi Sun,Shaobin Wang
标识
DOI:10.1021/acs.jced.5b00229
摘要
Metal organic frameworks (MOFs), UiO-66-NO 2 and UiO-66-NO 2 –N (N = -NH 2, -(OH) 2, -COOH) 2 ), were synthesized under solvothemal conditions using different functionalized organic linkers. The synthesized samples were further activated by solvent exchange using methanol and chloroform. All samples were characterized by X-ray diffraction, Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and N 2 adsorption/desorption. Gas adsorption of CO 2 and N 2 on all samples has been evaluated at 760 mmHg and different temperatures. It was found that UiO-66-NO 2 -NH 2 by methanol or chloroform activation presented much higher CO 2 adsorption than other samples and the adsorption capacities are around (87 and 74) cm 3 ·g –1 on chloroform-activated and methanol-activated samples, respectively, at 273 K and 760 mmHg. In addition, high selectivity of CO 2 /N 2 has been found on chloroform-activated UiO-66-NO 2 -NH 2 giving a factor of 65 while the selectivity of CO 2 /N 2 is only 40 for chloroform-activated UiO-66-NO 2 .
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