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dc.contributor.authorRada, Z.
dc.contributor.authorAbid, H.
dc.contributor.authorSun, Hongqi
dc.contributor.authorWang, S.
dc.date.accessioned2017-01-30T10:33:31Z
dc.date.available2017-01-30T10:33:31Z
dc.date.created2015-10-29T04:09:32Z
dc.date.issued2015
dc.identifier.citationRada, Z. and Abid, H. and Sun, H. and Wang, S. 2015. Bifunctionalized Metal Organic Frameworks, UiO-66-NO2-N (N = -NH2, -(OH)2, -(COOH)2), for Enhanced Adsorption and Selectivity of CO2 and N2. Journal of Chemical and Engineering Data. 60 (7): pp. 2152-2161.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/3740
dc.identifier.doi10.1021/acs.jced.5b00229
dc.description.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.

dc.publisherAmerican Chemical Society
dc.titleBifunctionalized Metal Organic Frameworks, UiO-66-NO2-N (N = -NH2, -(OH)2, -(COOH)2), for Enhanced Adsorption and Selectivity of CO2 and N2
dc.typeJournal Article
dcterms.source.volume60
dcterms.source.number7
dcterms.source.startPage2152
dcterms.source.endPage2161
dcterms.source.issn0021-9568
dcterms.source.titleJournal of Chemical and Engineering Data
curtin.departmentSchool of Chemical and Petroleum Engineering
curtin.accessStatusFulltext not available


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