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Sol-gel synthesis and washing of amorphous g-FeO(OH) xerogels
Iron(III) oxyhydroxide xerogels were prepared by the sol‐gel technology including a washing step for removal of a salt by‐product. The synthesis involved an iron(III) nitrate nonahydrate as precursor, ethanol as solvent and ammonium hydroxide as gelation agent, following the procedure of an earlier...
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Published in: | Materialwissenschaft und Werkstofftechnik 2012-05, Vol.43 (5), p.427-434 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Iron(III) oxyhydroxide xerogels were prepared by the sol‐gel technology including a washing step for removal of a salt by‐product. The synthesis involved an iron(III) nitrate nonahydrate as precursor, ethanol as solvent and ammonium hydroxide as gelation agent, following the procedure of an earlier work. As this chemical route originates ammonium nitrate as a by‐product dispersed in the iron oxyhydroxide matrix, the removal of this salt by washing the gel before the drying stage is here studied. Two solvents were tested, namely water and ethanol, being the best washing efficiency (95%) achieved with water and two washing batches. Comparing the xerogels obtained without and with the washing step, the later only contained an insignificant amount of ammonium nitrate salt, as confirmed by Elemental Analysis, Fourier Transform Infrared Spectroscopy (FTIR), X‐Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The iron phase in the washed xerogels was found to be g‐FeO(OH), according to FTIR and Mössbauer spectroscopy results, and in consonance with the prevailing iron phase in the unwashed xerogels. The washed xerogels are amorphous and formed by large clusters of well connected nanocrystallites of iron oxyhydroxide. The washing step enhanced the clearing of mesopores, originating materials with a specific surface area of ˜ 250 m2/g, 60 times higher than for unwashed xerogels. |
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ISSN: | 0933-5137 1521-4052 |
DOI: | 10.1002/mawe.201200977 |