Structure of aqueous sodium aluminate solutions: A solution X-ray diffraction study

T. Radnái, Peter M. May, Glenn T. Hefter, P. Sipos

Research output: Contribution to journalArticle

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Abstract

A structural analysis of six alkaline sodium aluminate aqueous solutions by the X-ray diffraction method is reported. On average, each Al atom is surrounded by four oxygens, indicative of the predominance of Al(OH)4 -(aq) in these solutions. Detailed least-squares fitting indicates that a significant contraction of the Al-O distances occurs with increasing aluminate concentration, from 1.80 Å at 2 M to 1.74 Å at 6 M Al-(OH)3 in 8 M NaOH. The local structure has been described by models that have separate hydrated ions in the most dilute aluminate solution but contact sodium aluminate ion pairs in the most concentrated solution. The hydration number of the sodium ion decreases with increasing concentration, but the overall coordination number appears to be unchanged by the ion pair formation. An extensive rearrangement in the hydrogenbonded network of bulk water also occurs as the aluminum concentration rises, with the appearance of new diffraction distances at 3.3 and 3.9 Å. A gradual appearance and disappearance of shorter hydrogen bonds between first neighboring O atoms is observed. The data are consistent with the occurrence of oligomeric aluminate species but are not conclusive within the limits of the experimental error.

Original languageEnglish
Pages (from-to)7841-7850
Number of pages10
JournalJournal of Physical Chemistry A
Volume102
Issue number40
Publication statusPublished - Oct 1 1998

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sodium
Ions
X ray diffraction
diffraction
ions
x rays
Atoms
Aluminum
coordination number
structural analysis
Structural analysis
Hydration
Contacts (fluid mechanics)
contraction
atoms
hydration
Hydrogen bonds
Diffraction
Sodium
occurrences

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

Cite this

Structure of aqueous sodium aluminate solutions : A solution X-ray diffraction study. / Radnái, T.; May, Peter M.; Hefter, Glenn T.; Sipos, P.

In: Journal of Physical Chemistry A, Vol. 102, No. 40, 01.10.1998, p. 7841-7850.

Research output: Contribution to journalArticle

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abstract = "A structural analysis of six alkaline sodium aluminate aqueous solutions by the X-ray diffraction method is reported. On average, each Al atom is surrounded by four oxygens, indicative of the predominance of Al(OH)4 -(aq) in these solutions. Detailed least-squares fitting indicates that a significant contraction of the Al-O distances occurs with increasing aluminate concentration, from 1.80 {\AA} at 2 M to 1.74 {\AA} at 6 M Al-(OH)3 in 8 M NaOH. The local structure has been described by models that have separate hydrated ions in the most dilute aluminate solution but contact sodium aluminate ion pairs in the most concentrated solution. The hydration number of the sodium ion decreases with increasing concentration, but the overall coordination number appears to be unchanged by the ion pair formation. An extensive rearrangement in the hydrogenbonded network of bulk water also occurs as the aluminum concentration rises, with the appearance of new diffraction distances at 3.3 and 3.9 {\AA}. A gradual appearance and disappearance of shorter hydrogen bonds between first neighboring O atoms is observed. The data are consistent with the occurrence of oligomeric aluminate species but are not conclusive within the limits of the experimental error.",
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N2 - A structural analysis of six alkaline sodium aluminate aqueous solutions by the X-ray diffraction method is reported. On average, each Al atom is surrounded by four oxygens, indicative of the predominance of Al(OH)4 -(aq) in these solutions. Detailed least-squares fitting indicates that a significant contraction of the Al-O distances occurs with increasing aluminate concentration, from 1.80 Å at 2 M to 1.74 Å at 6 M Al-(OH)3 in 8 M NaOH. The local structure has been described by models that have separate hydrated ions in the most dilute aluminate solution but contact sodium aluminate ion pairs in the most concentrated solution. The hydration number of the sodium ion decreases with increasing concentration, but the overall coordination number appears to be unchanged by the ion pair formation. An extensive rearrangement in the hydrogenbonded network of bulk water also occurs as the aluminum concentration rises, with the appearance of new diffraction distances at 3.3 and 3.9 Å. A gradual appearance and disappearance of shorter hydrogen bonds between first neighboring O atoms is observed. The data are consistent with the occurrence of oligomeric aluminate species but are not conclusive within the limits of the experimental error.

AB - A structural analysis of six alkaline sodium aluminate aqueous solutions by the X-ray diffraction method is reported. On average, each Al atom is surrounded by four oxygens, indicative of the predominance of Al(OH)4 -(aq) in these solutions. Detailed least-squares fitting indicates that a significant contraction of the Al-O distances occurs with increasing aluminate concentration, from 1.80 Å at 2 M to 1.74 Å at 6 M Al-(OH)3 in 8 M NaOH. The local structure has been described by models that have separate hydrated ions in the most dilute aluminate solution but contact sodium aluminate ion pairs in the most concentrated solution. The hydration number of the sodium ion decreases with increasing concentration, but the overall coordination number appears to be unchanged by the ion pair formation. An extensive rearrangement in the hydrogenbonded network of bulk water also occurs as the aluminum concentration rises, with the appearance of new diffraction distances at 3.3 and 3.9 Å. A gradual appearance and disappearance of shorter hydrogen bonds between first neighboring O atoms is observed. The data are consistent with the occurrence of oligomeric aluminate species but are not conclusive within the limits of the experimental error.

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