Abstract
The transformation of vivianite and the direct synthesis starting from pure chemicals lead to the formation of lipscombite {Fe 2+x Fe 3+3−x [(OH)3−x/(PO4)2]} with varying Fe2+/Fe3+ molar ratios. The influence of this ratio on the Mössbauer spectra, solubility, electrokinetic potential and infrared spectra has been studied. By means of Mössbauer spectroscopy, the distribution of the Fe2+ and Fe3+ ions between the octahedral sites I and II has been investigated.
The unit cell dimensions have been determined from Guinier-Hägg X-ray diffraction patterns. The crystal system is tetragonal for synthetic lipscombite with a=5.3020±0.0005 Å and c=12.8800±0.0005 Å.
Lipscombite has been found to show a negative and time-dependent zeta-potential which, moreover, is influenced by the pH of the suspension and the Fe2+/Fe3+ molar ratio. An explanation of the time-dependence of the zeta-potential on variations of solubility is proposed.
Infrared absorption spectrum only is characterized by two absorption bands: v OH(3,500 cm−1) and v P−O(1,100-960 cm−1). The density at 25° C is determined in toluene as 3.36±0.01 g·cm−3.
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Vochten, R., De Grave, E. Crystallographic, Mössbauer and electrokinetic study of synthetic lipscombite. Phys Chem Minerals 7, 197–203 (1981). https://doi.org/10.1007/BF00311889
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DOI: https://doi.org/10.1007/BF00311889