Synthesis of Phosphorus-Modified AFX Zeolite by the Hydrothermal Conversion of Tetraalkylphosphonium Hydroxide-Impregnated FAU Zeolite

  • Misae Onishi
    Applied Chemistry Program, Graduate School of Advanced Science and Engineering, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8527 , Japan
  • Nao Tsunoji
    Applied Chemistry Program, Graduate School of Advanced Science and Engineering, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8527 , Japan
  • Masahiro Sadakane
    Applied Chemistry Program, Graduate School of Advanced Science and Engineering, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8527 , Japan
  • Tsuneji Sano
    Applied Chemistry Program, Graduate School of Advanced Science and Engineering, Hiroshima University, Higashi-Hiroshima, Hiroshima 739-8527 , Japan

書誌事項

公開日
2020-08-25
資源種別
journal article
権利情報
  • https://academic.oup.com/pages/standard-publication-reuse-rights
DOI
  • 10.1246/bcsj.20200224
公開者
Oxford University Press (OUP)

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説明

<jats:title>Abstract</jats:title> <jats:p>Phosphorus-modified AFX zeolite was synthesized by the hydrothermal conversion of FAU zeolite, which was impregnated with tetraethylphosphonium hydroxide (TEPOH). For the optimization of the introduced phosphorus, we investigated the influence of the loaded amount of TEPOH on FAU zeolite and tested the combination of the starting materials, composed of phosphorus-free and TEPOH-impregnated FAU zeolites. The synthesis system, employing the combined starting materials, effectively incorporated phosphorus into AFX zeolite while the TEPOH-impregnated FAU zeolite was not effective as a solo starting material. X-ray diffractometry, N2 adsorption, and elemental analysis were employed to confirm the high purity of the AFX zeolite, obtained from the utilization of combined starting materials. Moreover, 13C and 31P magic angle spinning (MAS) NMR spectroscopy further revealed the modification of phosphorus in which the phosphorus species interacting with the zeolite framework was formed via the decomposition of tetraethylphosphonium (TEP) by calcination.</jats:p>

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