Topics in Catalysis

, Volume 52, Issue 6–7, pp 865–871 | Cite as

Preparation for Size-Controlled MOR Zeolite Nanocrystal Using Water/Surfactant/Organic Solvent

  • Teruoki Tago
  • Daichi Aoki
  • Kazuyuki Iwakai
  • Takao Masuda
Original Paper

Abstract

Recently, the synthesis of nanometer-sized zeolite crystals has attracted considerable attention from many researchers. In this study, the preparation of Mordenite (MOR zeolite) nanocrystals via hydrothermal synthesis in water/surfactant/organic solvent was carried out. Polyoxyethylene-(15)-oleylether (O-15, non-ionic surfactant) and cyclohexane were employed as a surfactant and organic solvent, respectively. Interestingly, it was found that the crystal sizes and morphology of MOR zeolites depended on the surfactant concentration regardless of the same concentrations of Si and Al sources and template in the water solution. The MOR zeolite nanocrystals with average sizes of approximately 80 nm could be obtained. Moreover, the column-like morphology of MOR zeolite was also observed at a high surfactant concentration (0.75 mol/L). Accordingly, the crystal size and morphology of MOR zeolite can be controlled by the surfactant concentration. This result appears to be due to the difference in the nucleation and growth rates of MOR in the solution.

Keywords

MOR zeolite nanocrystal Mordenite Nano-zeolite Surfactant Synthesis 

Notes

Acknowledgement

This work was supported in part by the Industrial Technology Research Grant Program in 2006 from the New Energy and Industrial Technology Development Organization (NEDO) of Japan (06B44702a).

References

  1. 1.
    Taguchi A, Schuth F (2005) Microporous Mesoporous Mater 77:1–45CrossRefGoogle Scholar
  2. 2.
    Corma A, Martinez A (1993) Catal Rev Sci Eng 35:483–570CrossRefGoogle Scholar
  3. 3.
    Kramer GJ, Vansanten RA, Emeis CA, Nowak AK (1993) Nature 363:529–531CrossRefGoogle Scholar
  4. 4.
    Sugi Y, Watanabe S, Imada Y, Waghmode SB, Komura K, Kubota Y, Hanaoka T, Matsuzaki T, Nakajima K, Kunimori K (2008) J Mol Catal A Chem 285:101–110CrossRefGoogle Scholar
  5. 5.
    Selvam T, Mabande GTP, Schwieger W, Sugi Y, Toyama I, Kubota Y, Lee HS, Kim JH (2004) Catal Lett 17–24Google Scholar
  6. 6.
    Tsapatsis M, Lovallo M, Davis ME (1996) Microporous Mater 5:381–388CrossRefGoogle Scholar
  7. 7.
    Mintova S, Olson NH, Valtchev V, Bein T (1999) Science 283:958–960CrossRefGoogle Scholar
  8. 8.
    Hosokawa H, Oki K (2003) Chem Lett 32:586–587CrossRefGoogle Scholar
  9. 9.
    Tago T, Nishi M, Kouno Y, Masuda T (2004) Chem Lett 33:1040–1041CrossRefGoogle Scholar
  10. 10.
    Lee S, Shantz DF (2005) Chem Mater 17:409–417CrossRefGoogle Scholar
  11. 11.
    Tago T, Iwakai K, Nishi M, Masuda T (2006) Stud Surf Sci Catal 159:185–188CrossRefGoogle Scholar
  12. 12.
    Mintova S, Valtchev V, Onfroy T, Marichal C, Knozinger H, Bein T (2006) Microporous Mesoporous Mater 90:237–245CrossRefGoogle Scholar
  13. 13.
    Larlus O, Mintova S, Bein T (2006) Microporous Mesoporous Mater 96:405–412CrossRefGoogle Scholar
  14. 14.
    Tago T, Iwakai K, Nishi M, Masuda T (2009) J Nanosci Nanotechnol 9:612–617Google Scholar
  15. 15.
    Masuda T, Fujikata Y, Mukai SR, Hashimoto K (1997) Appl Catal A Gen 165:57–72CrossRefGoogle Scholar
  16. 16.
    Burkett SL, Davis ME (1994) J Phys Chem 98:4647–4653CrossRefGoogle Scholar
  17. 17.
    Burkett SL, Davis ME (1995) Chem Mater 7:920–928CrossRefGoogle Scholar
  18. 18.
    De-Moor PPEA, Beelen TPM, Komanschek BU, Beck LW, Wagner P, Davis ME, Santen RA (1999) Chem Eur J 5:2083–2088CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2009

Authors and Affiliations

  • Teruoki Tago
    • 1
  • Daichi Aoki
    • 1
  • Kazuyuki Iwakai
    • 1
  • Takao Masuda
    • 1
  1. 1.Chemical Engineering Group, Division of Chemical Process Engineering, Graduate School of EngineeringHokkaido UniversityKita-Ku, SapporoJapan

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