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The “quiet Goldschmidt”—a mechanochemical, thermoanalytical, and spectroscopic study of selected steps of the aluminothermic reaction
The Goldschmidt reaction (2Al+α-Fe2O3) was investigated both under mechanical and thermal activation by employing a combination of analytical methods such as ESR and Mössbauer spectroscopy, magnetic susceptibility, X-ray powder diffraction, and thermal analysis (TA). Both the mechanical treatment an...
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Published in: | Journal of solid state chemistry 2013-06, Vol.202, p.173-190 |
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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: | The Goldschmidt reaction (2Al+α-Fe2O3) was investigated both under mechanical and thermal activation by employing a combination of analytical methods such as ESR and Mössbauer spectroscopy, magnetic susceptibility, X-ray powder diffraction, and thermal analysis (TA). Both the mechanical treatment and the TA runs under air caused the reaction conditions of “quiet redox reactions” due to a retarding effect and enabled a reaction study in a “slow motion mode”. This allowed to establish distinct partial steps of the integral reaction process depending on the intensity of the mechanical impact, the educt composition, the gas phase composition, and, finally, the thermal excitation in the TA runs. Particular attention was payed to the role of the gas phase and to the reaction of aluminum with differently activated oxygen species. The phlegmatizing effect was traced back to the formation of Al2O3 coverages of the Al particles.
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•The usually extremely violent Goldschmidt reaction was studied in a “slow motion mode”.•Both the mechanochemical and the thermal treatment caused a phlegmatizing effect on the reaction.•Early reaction stages were sensitively indicated by ESR and magnetic measurements.•Intermediates and final products were characterized by XRD and Mössbauer data.•Differently activated oxygen species react with aluminum to form an oxide coverage retarding the vigorous reaction. |
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ISSN: | 0022-4596 1095-726X |
DOI: | 10.1016/j.jssc.2013.02.032 |