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The dependence of Ni-Fe bioxide composites nanoparticles on the FeCl(2) solution used
BACKGROUND: Ni(2)O(3)- γ-Fe(2)O(3) composite nanoparticles coated with a layer of 2FeCl(3)·5H(2)O can be prepared by co-precipitation and processing in FeCl(2) solution. Using vibrating sample magnetometer (VSM), X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532291/ https://www.ncbi.nlm.nih.gov/pubmed/23110795 http://dx.doi.org/10.1186/1752-153X-6-127 |
Sumario: | BACKGROUND: Ni(2)O(3)- γ-Fe(2)O(3) composite nanoparticles coated with a layer of 2FeCl(3)·5H(2)O can be prepared by co-precipitation and processing in FeCl(2) solution. Using vibrating sample magnetometer (VSM), X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) diffraction techniques, the dependence of the preparation on the concentration of the FeCl(2) treatment solution is revealed. RESULTS: The magnetization of the as-prepared products varied non-monotonically as the FeCl(2) concentration increased from 0.020 M to 1.000 M. The Experimental results show that for the composite nanoparticles, the size of the γ-Fe(2)O(3) phase is constant at about 8 nm, the Ni(2)O(3) phase decreased and the 2FeCl(3)·5H(2)O phase increased with increasing concentration of FeCl(2) solution. The magnetization of the as-prepared products mainly results from the γ-Fe(2)O(3) core, and the competition between the reduction of the Ni(2)O(3) phase with the increase of the 2FeCl(3)·5H(2)O phase resulted in the apparent magnetization varying non-monotonically. CONCLUSIONS: When the concentration of FeCl(2) treatment solution did not exceed 0.100 M, the products are spherical nanoparticles of size about 11 nm; their magnetization increased monotonically with increasing the concentration of FeCl(2) solution due to the decreasing proportion of Ni(2)O(3) phase. |
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