| Title: | Utilization of metal-organic frameworks for the adsorptive removal of an aliphatic aldehyde mixture in the gas phase |
| Author(s): | Vikrant K; Qu Y; Szulejko JE; Kumar V; Vellingiri K; Boukhvalov DW; Kim T; Kim KH; |
| Address: | "Department of Civil and Environmental Engineering, Hanyang University, 222 Wangsimni-Ro, Seoul 04763, Republic of Korea. kkim61@hanyang.ac.kr" |
| ISSN/ISBN: | 2040-3372 (Electronic) 2040-3364 (Linking) |
| Abstract: | "Considerable efforts have been undertaken in the domain of air quality management for the removal of hazardous volatile organic compounds, particularly carbonyl compounds (CCs). In this study, the competitive sorptive removal of six CCs (namely, formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, isovaleraldehyde, and valeraldehyde) was assessed using selected metal-organic frameworks (MOFs: MOF-5, MOF-199, UiO-66, and UiO-66-NH(2)) and inexpensive commercial activated carbon as a reference sorbent. The sorption experiments were conducted using a mixture of the six CCs (formaldehyde and acetaldehyde at approximately 1 Pa and propionaldehyde, butyraldehyde, isovaleraldehyde, and valeraldehyde at approximately 0.2 Pa) together with 15 Pa water and 2.6 Pa methanol in 1 bar nitrogen. For all of the carbonyl compounds other than formaldehyde, MOF-199 showed the best 10% breakthrough performance ranging from 34 L g(-1) and 0.14 mol kg(-1) Pa(-1) for acetaldehyde to 1870 L g(-1) and 7.6 mol kg(-1) Pa(-1) for isovaleraldehyde. Among all the sorbents tested, UiO-66-NH(2) exhibited the best 10% breakthrough performance metrics towards the lightest formaldehyde which remains to be one of the most difficult targets for sorptive removal (breakthrough volume: 285 L g(-1) and partition coefficient: 1.1 mol kg(-1) Pa(-1)). Theoretical density functional theory (DFT)-based computations were also conducted to provide better insights into the adsorbate-adsorbent interactions. Accordingly, the magnitude of adsorption energy increased with an increase in the CC molar mass due to an enhancement in the synergetic interaction between C[double bond, length as m-dash]O groups (in adsorbate molecules) and the MOF active centers (open metallic centers and/or NH(2) functionality) as the adsorbent. Such interactions were observed to result in strong distortion of MOF structures. In contrast, weak van der Waals attraction between the hydrocarbon 'tail' of CC molecules and MOF linkers were seen to play a stabilizing role for the sorbent structure. The presence of the NH(2) group in the MOF structure was suspected to play a key role in capturing lighter CCs, while such an effect was less prominent for heavier CCs. Overall, the results of this study provided a basis for the establishment of an effective strategy to enhance the sorption capacity of MOFs against diverse carbonyl species" |
| Notes: | "PubMed-not-MEDLINEVikrant, Kumar Qu, Yao Szulejko, Jan E Kumar, Vanish Vellingiri, Kowsalya Boukhvalov, Danil W Kim, Taejin Kim, Ki-Hyun eng England 2020/04/03 Nanoscale. 2020 Apr 21; 12(15):8330-8343. doi: 10.1039/d0nr00234h. Epub 2020 Apr 1" |
