Abstract

The dependence of magnetic transition on the treatment solution used in the preparation of magnetic nanoparticles was investigated using as-prepared products from paramagnetic FeOOH/Mg(OH)2via a chemically induced transition. Treatment using FeCl3and CuCl solutions led to a product that showed no magnetic transition, whereas the product after treatment with FeSO4or FeCl2solutions showed ferromagnetism. Experiments revealed that the magnetism was caused by the ferrimagneticγ-Fe2O3phase in the nanoparticles, which had a coating of ferric compound. This observation suggests that Fe2+in the treatment solution underwent oxidation to Fe3+, thereby inducing the magnetic transition. The magnetic nanoparticles prepared via treatment with an FeSO4solution contained a larger amount of the nonmagnetic phase. This resulted in weaker magnetization even though these nanoparticles were larger than those prepared by treatment with an FeCl2solution. The magnetic transition of the precursor (FeOOH/Mg(OH)2) was dependent upon treatment solutions and was essentially induced by the oxidation of Fe2+and simultaneous dehydration of FeOOH phase. The transition was independent of the acid radical ions in the treatment solution, but the coating on the magnetic crystallites varied with changes in the acid radical ion.

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