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https://hdl.handle.net/2440/118145
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Type: | Journal article |
Title: | Bifunctionalized metal organic frameworks, UiO-66-NO₂-N (N = -NH₂, -(OH)₂, -(COOH)₂), for enhanced adsorption and selectivity of CO₂ and N₂ |
Other Titles: | Bifunctionalized metal organic frameworks, UiO-66-NO(2)-N (N = -NH(2), -(OH)(2), -(COOH)(2)), for enhanced adsorption and selectivity of CO(2) and N(2) |
Author: | Rada, Z. Abid, H. Sun, H. Wang, S. |
Citation: | Journal of Chemical and Engineering Data, 2015; 60(7):2152-2161 |
Publisher: | American Chemical Society |
Issue Date: | 2015 |
ISSN: | 0021-9568 1520-5134 |
Statement of Responsibility: | Zana Hassan Rada, Hussein Rasool Abid, Hongqi Sun, and Shaobin Wang |
Abstract: | Metal organic frameworks (MOFs), UiO-66-NO2 and UiO-66-NO2–N (N = -NH2, -(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 N2 adsorption/desorption. Gas adsorption of CO2 and N2 on all samples has been evaluated at 760 mmHg and different temperatures. It was found that UiO-66-NO2-NH2 by methanol or chloroform activation presented much higher CO2 adsorption than other samples and the adsorption capacities are around (87 and 74) cm3·g–1 on chloroform-activated and methanol-activated samples, respectively, at 273 K and 760 mmHg. In addition, high selectivity of CO2/N2 has been found on chloroform-activated UiO-66-NO2-NH2 giving a factor of 65 while the selectivity of CO2/N2 is only 40 for chloroform-activated UiO-66-NO2. |
Rights: | © 2015, American Chemical Society |
DOI: | 10.1021/acs.jced.5b00229 |
Published version: | http://dx.doi.org/10.1021/acs.jced.5b00229 |
Appears in Collections: | Aurora harvest 8 Chemical Engineering publications |
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