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Influence of cobalt ions on the precipitation of goethite in highly alkaline media

Published online by Cambridge University Press:  09 July 2018

S. Krehula*
Affiliation:
Division of Materials Chemistry, Ruđer Bošković Institute, P.O. Box 180, HR-10002 Zagreb, Croatia
S. Musić
Affiliation:
Division of Materials Chemistry, Ruđer Bošković Institute, P.O. Box 180, HR-10002 Zagreb, Croatia
*
*E-mail: krehul@irb.hr

Abstract

The effects of cobalt ions on the precipitation of goethite in highly alkaline media were monitored using X-ray diffraction (XRD), Mössbauer, Fourier transform infrared (FTIR) and energy dispersive X-ray (EDS) spectroscopies and field emission scanning electron microscopy (FESEM) techniques. Tetramethylammonium hydroxide was used as a precipitating agent. The precipitates were collected after heating of the precipitation systems at 160ºC for 2 h. The XRD results showed the formation of goethite structure as a single phase up to r = 6.98 (where r = 100·[Co]/([Co]+[Fe])). Cobalt ferrite was found as an additional phase in the precipitates obtained at r = 9.09 and 13.04. Mössbauer spectroscopy showed the formation of solid solutions of α-(Fe,Co)OOH. The incorporation of cobalt ions into the goethite crystal structure was monitored by a decrease in the average hyperfine magnetic field (⟨Bhf⟩). The value ⟨Bhf⟩ decreased linearly up to r = 5.66, whereas a nonlinear dependence was obtained at r = 6.98 to 13.04. Infrared (IR) bands corresponding to the bending vibrations δOH and γOH were shifted from 892 to 903 cm–1 and from 797 to 800 cm–1, respectively, up to r = 6.98. Fourier transform infrared spectroscopy lacked the sensitivity to monitor the effects of cobalt ions, demonstrated by the Mössbauer analysis. Cobalt incorporation into the crystal structure of goethite induced a gradual elongation of α-(Fe,Co)OOH particles along the crystallographic c axis. The formation of α-(Fe,Co)OOH nanowires was shown at r ⩾6.98. These nanowires were ~700 nm long, whereas their diameter was ~15–20 nm. The majority of the cobalt ferrite particles were in the nanosize range, as observed by FE-SEM. On the basis of the Co/Fe ratio measured by EDS, it appears that the cobalt ferrite particles were not fully stoichiometric.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2008

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