Characterization of synthetic Cs-Li cancrinite grown in a butanediol-water system: An NMR spectroscopic and Rietveld refinement study

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autorschaft

  • M. Fechtelkord
  • B. Posnatzki
  • J. C. Buhl
  • C. A. Fyfe
  • L. A. Groat
  • M. Raudsepp

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OriginalspracheEnglisch
Seiten (von - bis)881-888
Seitenumfang8
FachzeitschriftAmerican mineralogist
Jahrgang86
Ausgabenummer7-8
PublikationsstatusVeröffentlicht - 1 Juli 2001

Abstract

A Cs-Li-analogue of cancrinite has been synthesized from tetraethoxysilane and Al sec-butoxide in a mixture of 1,3-butanediol and water. Cs and Li were introduced as hydroxides. Synthesis was done at autogeneous pressure and T = 473 K for 100 h. The synthesis product was characterized by powder X-ray diffraction, IR-spectroscopy, thermogravimetry, 1H, 6Li, 133Cs, 27Al, 29Si MAS, and (1H) 13C CPMAS NMR and Rietveld structure refinement. 29Si MAS NMR and 27Al MAS NMR spectroscopy show a framework with strong alternating order of the SiO4 and AlO4 tetrahedra and an Si/Al ratio of one. 6Li MAS NMR suggests the existence of two different signals that cannot be resolved in the 7Li MAS NMR spectrum. 133Cs MAS NMR shows only a single resonance. The thermogravimetric analysis reveals a continuous weight loss in several steps, indicating the evaporation of water of hydration. IR spectroscopy shows evidence for hydroxyl anions and water included in the cancrinite framework. The Rietveld structure refinement is consistent with a completely ordered alumosilicate framework with an Si/Al ratio of one and the presence of both molecular water and hydroxyl groups in the hexagonal channel, a result different from the previously published structure. Cs is exclusively located in the ε-cages; Li ions are located in the channels and are coordinated by water molecules.

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Characterization of synthetic Cs-Li cancrinite grown in a butanediol-water system: An NMR spectroscopic and Rietveld refinement study. / Fechtelkord, M.; Posnatzki, B.; Buhl, J. C. et al.
in: American mineralogist, Jahrgang 86, Nr. 7-8, 01.07.2001, S. 881-888.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Fechtelkord M, Posnatzki B, Buhl JC, Fyfe CA, Groat LA, Raudsepp M. Characterization of synthetic Cs-Li cancrinite grown in a butanediol-water system: An NMR spectroscopic and Rietveld refinement study. American mineralogist. 2001 Jul 1;86(7-8):881-888. doi: 10.2138/am-2001-0711
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title = "Characterization of synthetic Cs-Li cancrinite grown in a butanediol-water system: An NMR spectroscopic and Rietveld refinement study",
abstract = "A Cs-Li-analogue of cancrinite has been synthesized from tetraethoxysilane and Al sec-butoxide in a mixture of 1,3-butanediol and water. Cs and Li were introduced as hydroxides. Synthesis was done at autogeneous pressure and T = 473 K for 100 h. The synthesis product was characterized by powder X-ray diffraction, IR-spectroscopy, thermogravimetry, 1H, 6Li, 133Cs, 27Al, 29Si MAS, and (1H) 13C CPMAS NMR and Rietveld structure refinement. 29Si MAS NMR and 27Al MAS NMR spectroscopy show a framework with strong alternating order of the SiO4 and AlO4 tetrahedra and an Si/Al ratio of one. 6Li MAS NMR suggests the existence of two different signals that cannot be resolved in the 7Li MAS NMR spectrum. 133Cs MAS NMR shows only a single resonance. The thermogravimetric analysis reveals a continuous weight loss in several steps, indicating the evaporation of water of hydration. IR spectroscopy shows evidence for hydroxyl anions and water included in the cancrinite framework. The Rietveld structure refinement is consistent with a completely ordered alumosilicate framework with an Si/Al ratio of one and the presence of both molecular water and hydroxyl groups in the hexagonal channel, a result different from the previously published structure. Cs is exclusively located in the ε-cages; Li ions are located in the channels and are coordinated by water molecules.",
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T1 - Characterization of synthetic Cs-Li cancrinite grown in a butanediol-water system

T2 - An NMR spectroscopic and Rietveld refinement study

AU - Fechtelkord, M.

AU - Posnatzki, B.

AU - Buhl, J. C.

AU - Fyfe, C. A.

AU - Groat, L. A.

AU - Raudsepp, M.

PY - 2001/7/1

Y1 - 2001/7/1

N2 - A Cs-Li-analogue of cancrinite has been synthesized from tetraethoxysilane and Al sec-butoxide in a mixture of 1,3-butanediol and water. Cs and Li were introduced as hydroxides. Synthesis was done at autogeneous pressure and T = 473 K for 100 h. The synthesis product was characterized by powder X-ray diffraction, IR-spectroscopy, thermogravimetry, 1H, 6Li, 133Cs, 27Al, 29Si MAS, and (1H) 13C CPMAS NMR and Rietveld structure refinement. 29Si MAS NMR and 27Al MAS NMR spectroscopy show a framework with strong alternating order of the SiO4 and AlO4 tetrahedra and an Si/Al ratio of one. 6Li MAS NMR suggests the existence of two different signals that cannot be resolved in the 7Li MAS NMR spectrum. 133Cs MAS NMR shows only a single resonance. The thermogravimetric analysis reveals a continuous weight loss in several steps, indicating the evaporation of water of hydration. IR spectroscopy shows evidence for hydroxyl anions and water included in the cancrinite framework. The Rietveld structure refinement is consistent with a completely ordered alumosilicate framework with an Si/Al ratio of one and the presence of both molecular water and hydroxyl groups in the hexagonal channel, a result different from the previously published structure. Cs is exclusively located in the ε-cages; Li ions are located in the channels and are coordinated by water molecules.

AB - A Cs-Li-analogue of cancrinite has been synthesized from tetraethoxysilane and Al sec-butoxide in a mixture of 1,3-butanediol and water. Cs and Li were introduced as hydroxides. Synthesis was done at autogeneous pressure and T = 473 K for 100 h. The synthesis product was characterized by powder X-ray diffraction, IR-spectroscopy, thermogravimetry, 1H, 6Li, 133Cs, 27Al, 29Si MAS, and (1H) 13C CPMAS NMR and Rietveld structure refinement. 29Si MAS NMR and 27Al MAS NMR spectroscopy show a framework with strong alternating order of the SiO4 and AlO4 tetrahedra and an Si/Al ratio of one. 6Li MAS NMR suggests the existence of two different signals that cannot be resolved in the 7Li MAS NMR spectrum. 133Cs MAS NMR shows only a single resonance. The thermogravimetric analysis reveals a continuous weight loss in several steps, indicating the evaporation of water of hydration. IR spectroscopy shows evidence for hydroxyl anions and water included in the cancrinite framework. The Rietveld structure refinement is consistent with a completely ordered alumosilicate framework with an Si/Al ratio of one and the presence of both molecular water and hydroxyl groups in the hexagonal channel, a result different from the previously published structure. Cs is exclusively located in the ε-cages; Li ions are located in the channels and are coordinated by water molecules.

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