Details
| Original language | English |
|---|---|
| Pages (from-to) | 35-47 |
| Number of pages | 13 |
| Journal | Microporous and Mesoporous Materials |
| Volume | 28 |
| Issue number | 1 |
| Early online date | 24 May 1999 |
| Publication status | E-pub ahead of print - 24 May 1999 |
Abstract
Nitrite aluminogermanate sodalite has been obtained from hydrothermal synthesis at a temperature of 473 K. X-ray powder diffraction, and IR, Raman, and NMR spectroscopy of the 27Al and 23Na nuclei, and thermogravimetry were used to characterize these new sodalites. The cystallization field was studied in dependence of both the concentration of the NaNO2 'guest salt' and the concentration of the base NaOH. The investigation of the role of the hydroxide concentration in the starting solution and its effect upon the soldalite formation shows remarkable differences compared to the aluminosilicate system. It was found that increasing the hydroxide concentration led not only to a continuous decrease in the sodalite formation rate but also to an increase in the size and perfection of the crystals. The crystal structure of Na8[AlGeO4]6(NO2)2 [cubic, a0=9.08571(1) Å, space group P4̄3n was refined by the Rietveld method to a final residual of RF=0.021 (Rp=0.064, Rwp=0.087). In contrast to the nitrite aluminosilicate sodalite, where the Si-O and Al-O distances are quite different, the Ge-O and Al-O distances are very similar and the O-Ge-O and O-Al-O angles are almost identical. The NMR investigations show increasing isotropic chemical shift for 23Na and 27Al nucleus of nitrite aluminogermanate sodalite and significantly lower values of quadrupole coupling parameters in comparison to nitrite aluminosilicate sodalite.
Keywords
- Aluminogermanate, Framework structure refinement, Host-guest interaction, Hydrothermal synthesis, Matrix effect, Sodalite
ASJC Scopus subject areas
- Chemistry(all)
- Materials Science(all)
- Physics and Astronomy(all)
- Condensed Matter Physics
- Engineering(all)
- Mechanics of Materials
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In: Microporous and Mesoporous Materials, Vol. 28, No. 1, 24.05.1999, p. 35-47.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Crystallization, characterization and structure of nitrite aluminogermanate sodalite Na8[AlGeO4]6(NO2)2
AU - Bachmann, S.
AU - Buhl, J. Ch
PY - 1999/5/24
Y1 - 1999/5/24
N2 - Nitrite aluminogermanate sodalite has been obtained from hydrothermal synthesis at a temperature of 473 K. X-ray powder diffraction, and IR, Raman, and NMR spectroscopy of the 27Al and 23Na nuclei, and thermogravimetry were used to characterize these new sodalites. The cystallization field was studied in dependence of both the concentration of the NaNO2 'guest salt' and the concentration of the base NaOH. The investigation of the role of the hydroxide concentration in the starting solution and its effect upon the soldalite formation shows remarkable differences compared to the aluminosilicate system. It was found that increasing the hydroxide concentration led not only to a continuous decrease in the sodalite formation rate but also to an increase in the size and perfection of the crystals. The crystal structure of Na8[AlGeO4]6(NO2)2 [cubic, a0=9.08571(1) Å, space group P4̄3n was refined by the Rietveld method to a final residual of RF=0.021 (Rp=0.064, Rwp=0.087). In contrast to the nitrite aluminosilicate sodalite, where the Si-O and Al-O distances are quite different, the Ge-O and Al-O distances are very similar and the O-Ge-O and O-Al-O angles are almost identical. The NMR investigations show increasing isotropic chemical shift for 23Na and 27Al nucleus of nitrite aluminogermanate sodalite and significantly lower values of quadrupole coupling parameters in comparison to nitrite aluminosilicate sodalite.
AB - Nitrite aluminogermanate sodalite has been obtained from hydrothermal synthesis at a temperature of 473 K. X-ray powder diffraction, and IR, Raman, and NMR spectroscopy of the 27Al and 23Na nuclei, and thermogravimetry were used to characterize these new sodalites. The cystallization field was studied in dependence of both the concentration of the NaNO2 'guest salt' and the concentration of the base NaOH. The investigation of the role of the hydroxide concentration in the starting solution and its effect upon the soldalite formation shows remarkable differences compared to the aluminosilicate system. It was found that increasing the hydroxide concentration led not only to a continuous decrease in the sodalite formation rate but also to an increase in the size and perfection of the crystals. The crystal structure of Na8[AlGeO4]6(NO2)2 [cubic, a0=9.08571(1) Å, space group P4̄3n was refined by the Rietveld method to a final residual of RF=0.021 (Rp=0.064, Rwp=0.087). In contrast to the nitrite aluminosilicate sodalite, where the Si-O and Al-O distances are quite different, the Ge-O and Al-O distances are very similar and the O-Ge-O and O-Al-O angles are almost identical. The NMR investigations show increasing isotropic chemical shift for 23Na and 27Al nucleus of nitrite aluminogermanate sodalite and significantly lower values of quadrupole coupling parameters in comparison to nitrite aluminosilicate sodalite.
KW - Aluminogermanate
KW - Framework structure refinement
KW - Host-guest interaction
KW - Hydrothermal synthesis
KW - Matrix effect
KW - Sodalite
UR - http://www.scopus.com/inward/record.url?scp=0032673706&partnerID=8YFLogxK
U2 - 10.1016/S1387-1811(98)00176-0
DO - 10.1016/S1387-1811(98)00176-0
M3 - Article
AN - SCOPUS:0032673706
VL - 28
SP - 35
EP - 47
JO - Microporous and Mesoporous Materials
JF - Microporous and Mesoporous Materials
SN - 1387-1811
IS - 1
ER -