Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

Enhanced Carbon Dioxide Adsorption on Post-Synthetically Modified Metal-Organic Frameworks

  • Ko, Na-Keun (Department of Chemistry, Soongsil University) ;
  • Kim, Ja-Heon (Department of Chemistry, Soongsil University)
  • Received : 2011.06.07
  • Accepted : 2011.06.30
  • Published : 2011.08.20
Download PDF
⟨ Previous Next ⟩

Abstract

Four MOFs functionalized with 1-Me, 1-Pr, 1-Ph, and 1-$PhCF_3$ were prepared through post-synthetic modifications of a metal-organic framework (MOF), UMCM-1-$NH_2$ (1) with acetic, butyric, benzoic, and 4-(trifluoromethyl)benzoic anhydrides, respectively. Methane adsorption measurements between 253 and 298 K at pressures up to 1 bar indicated that both 1-Ph and 1-$PhCF_3$ adsorbed more $CH_4$ than the parent MOF, 1. All the functionalized MOFs adsorbed more $CO_2$ than 1 under conditions similar to the $CH_4$ test. The introduction of functional groups promoted adsorption of both $CH_4$ and $CO_2$ despite significantly reducing Brunauer-Emmet-Teller (BET) surface area: 4170 (1), 3550 (1-Me), 2900 (1-Pr), 3680 (1-Ph), and 3520 $m^2/g$ (1-$PhCF_3$). Electron-withdrawing aromatic groups (1-Ph, 1-$PhCF_3$) more effectively enhanced $CO_2$ adsorption than electron-donating alkyl groups (1-Me, 1-Pr). In particular, 1-Ph adsorbed 23% more $CO_2$ at 298 K and 50% more at 253 K than 1.

Keywords

References

  1. Wong-Foy, A. G.; Matzger, A. J.; Yaghi, O. M. J. Am. Chem. Soc. 2006, 128, 3494-3495. https://doi.org/10.1021/ja058213h
  2. Llewellyn, P. L.; Bourrelly, S.; Serre, C.; Vimont, A.; Daturi, M.; Hamon, L.; Weireld, G. D.; Chang, J.-S.; Hong, D.-Y.; Hwang, Y. K.; Jhung, S. H.; Ferey, G. Langmuir 2008, 24, 7245-7250. https://doi.org/10.1021/la800227x
  3. Koh, K.; Wong-Foy, A. G.; Matzger, A. J. Angew. Chem. Int. Ed. 2008, 47, 677-680. https://doi.org/10.1002/anie.200705020
  4. Koh, K.; Wong-Foy, A. G.; Matzger, A. J. J. Am. Chem. Soc. 2009, 131, 4184-4185. https://doi.org/10.1021/ja809985t
  5. Furukawa, H.; Ko, N.; Go, Y. B.; Aratani, N.; Choi, S. B.; Choi, E.; Yazaydin, A. O.; Snurr, R. Q.; O'Keeffe, M.; Kim, J.; Yaghi, O. M. Science 2010, 239, 424-428.
  6. Farha, O. K.; Yazayd n, O.; Eryazici, I.; Malliakas, C.; Hauser, B.; Kanatzidis, M. G.; Nguyen, S. T.; Snurr, R. Q.; Hupp, J. T. Nature Chem. 2010, 2, 944-948. https://doi.org/10.1038/nchem.834
  7. Holst, J. R.; Cooper, A. I. Adv. Mater. 2010, 22, 5212-5216. https://doi.org/10.1002/adma.201002440
  8. Wang, Z.; Cohen, S. M. Chem. Soc. Rev. 2009, 38, 1315-1329. https://doi.org/10.1039/b802258p
  9. Kasinathan, P.; Seo, Y.-K.; Shim, K.-E.; Hwang, Y. K.; Lee, U-H.; Hwang, D.-W.; Hong, D.-Y.; Halligudi, S. B.; Chang, J.-S. Bull. Korean Chem. Soc. 2011, 32, 2073-2075. https://doi.org/10.5012/bkcs.2011.32.6.2073
  10. Tanabe, K. K.; Cohen, S. M. Chem. Soc. Rev. 2011, 40, 498-519. https://doi.org/10.1039/c0cs00031k
  11. Wang, Z.; Cohen, S. M. J. Am. Chem. Soc. 2007, 129, 12368- 12369. https://doi.org/10.1021/ja074366o
  12. Wang, Z.; Cohen, S. M. J. Am. Chem. Soc. 2009, 131, 16675- 16677. https://doi.org/10.1021/ja907742z
  13. Tanabe, K. K.; Wang, Z.; Cohen, S. M. J. Am. Chem. Soc. 2008, 130, 8508-8517. https://doi.org/10.1021/ja801848j
  14. Wang, Z.; Tanabe, K. K.; Cohen, S. M. Inorg. Chem. 2009, 48, 296-306. https://doi.org/10.1021/ic801837t
  15. Wang, Z.; Tanabe, K. K.; Cohen, S. M. Chem. Eur. J. 2010, 16, 212-217. https://doi.org/10.1002/chem.200902158
  16. D'Alessandro, D. M.; Smit, B.; Long, J. R. Angew. Chem. Int. Ed. 2010, 49, 6058-6082. https://doi.org/10.1002/anie.201000431
  17. Choi, S. B.; Seo, M. J.; Cho, M.; Kim, Y.; Jin, M. K.; Jung, D.-Y.; Choi, J.-S.; Ahn, W.-S.; Rowsell, J. L. C.; Kim, J. Cryst. Growth Des. 2007, 7, 2290-2293. https://doi.org/10.1021/cg070640e
  18. Mu, B.; Schoenecker, P. M.; Walton, K. S. J. Phys. Chem. C 2010, 114, 6464-6471. https://doi.org/10.1021/jp906417z
  19. Dietzel, P. D. C.; Johnsen, R. E.; Fjellvag, H.; Bordiga, S.; Groppo, E.; Chavanc, S.; Blom, R. Chem. Commun. 2008, 5125- 5127.
  20. Britt, D.; Furukawa, H.; Wang, B.; Glover, T. G.; Yaghi, O. M. Proc. Natl. Acad. Sci. USA 2009, 106, 20637-20640. https://doi.org/10.1073/pnas.0909718106
  21. Couck, S.; Denayer, J. F. M.; Baron, G. V.; Remy, T.; Gascon, J.; Kapteijn, F. J. Am. Chem. Soc. 2009, 131, 6326-6327. https://doi.org/10.1021/ja900555r

Cited by

  1. Rational Design of Coordination Polymers with Flexible Oxyethylene Side Chains vol.33, pp.4, 2012, https://doi.org/10.5012/bkcs.2012.33.4.1264
  2. Synthesis and Crystal Structure of a 3D Samarium-Organic Framework Containing Vacant Chelating Sites vol.33, pp.4, 2012, https://doi.org/10.5012/bkcs.2012.33.4.1349
  3. CO2 capture by amine-functionalized nanoporous materials: A review vol.31, pp.11, 2014, https://doi.org/10.1007/s11814-014-0257-2
  4. fixation via cyclic carbonate synthesis vol.18, pp.1, 2016, https://doi.org/10.1039/C5GC01763G
  5. Technology for the Remediation of Water Pollution: A Review on the Fabrication of Metal Organic Frameworks vol.6, pp.8, 2018, https://doi.org/10.3390/pr6080122
  6. A post-synthetically modified metal-organic framework for copper catalyzed denitrative C-N coupling of nitroarenes under heterogeneous conditions vol.45, pp.12, 2011, https://doi.org/10.1039/d0nj05711h