Interactions of NO2 with Zr-based MOF : effects of the size of organic linkers on NO2 adsorption at ambient conditions
Zirconium-based metal organic framework (Zr-MOF), UiO-66 and UiO-67, were synthesized and used as adsorbents of NO(2) at ambient temperatures in either dry or moist conditions. The samples were characterized before and after exposure to NO(2) by X-ray diffraction, scanning electron microscopy, N(2)-...
| Veröffentlicht in: | Langmuir : the ACS journal of surfaces and colloids. - 1992. - 29(2013), 1 vom: 08. Jan., Seite 168-74 |
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| Format: | Online-Aufsatz |
| Sprache: | English |
| Veröffentlicht: |
2013
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| Zugriff auf das übergeordnete Werk: | Langmuir : the ACS journal of surfaces and colloids |
| Schlagworte: | Journal Article |
| Zusammenfassung: | Zirconium-based metal organic framework (Zr-MOF), UiO-66 and UiO-67, were synthesized and used as adsorbents of NO(2) at ambient temperatures in either dry or moist conditions. The samples were characterized before and after exposure to NO(2) by X-ray diffraction, scanning electron microscopy, N(2)-adsorption at 77 K, thermal analysis, and infrared spectroscopy. The results indicate the important effect of a ligand size on the adsorption of NO(2) on Zr-MOF materials. While the large size of the 4,4-benzenebiphenyldicarboxylic acid (BDPC) ligand has a positive impact on the adsorption of NO(2) on UiO-67 in moist conditions, the opposite effect is found in dry conditions. The large pore volume of UiO-67 enhances the adsorption of moisture and formation of nitric and nitrous acids. The small pore sizes of UiO-66 favor the NO(2) removal in dry conditions via dispersive forces. Upon interaction of NO(2) molecules with the Zr-MOF in dry conditions, the bond between the organic linker and metallic oxide center is broken, leading to the formation of nitrate and nitrite species. Moreover, organic ligands also contribute to the NO(2) reactive adsorption via nitration reaction |
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| Beschreibung: | Date Completed 14.06.2013 Date Revised 08.01.2013 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
| ISSN: | 1520-5827 |
| DOI: | 10.1021/la302869m |