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Microemulsion Synthesis of Iron Core/Iron Oxide Shell Magnetic Nanoparticles and Their Physicochemical Properties

Published online by Cambridge University Press:  10 May 2012

Katsiaryna Kekalo
Affiliation:
Thayer School of Engineering at Dartmouth College, Hanover, New Hampshire, USA
Katherine Koo
Affiliation:
Thayer School of Engineering at Dartmouth College, Hanover, New Hampshire, USA
Evan Zeitchick
Affiliation:
Thayer School of Engineering at Dartmouth College, Hanover, New Hampshire, USA
Ian Baker
Affiliation:
Thayer School of Engineering at Dartmouth College, Hanover, New Hampshire, USA
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Abstract

Iron magnetic nanoparticles were synthesized under an inert atmosphere via the reaction between FeCl3 and NaBH4 in droplets of water in a microemulsion consisting of octane with cetyl trimethylammonium bromide and butanol as surfactants. A thin Fe3O4 layer was produced on the iron nanoparticles using slow, controlled oxidation at room temperature. A silica shell was deposited on the Fe3O4 using 3-aminopropyltrimethoxysilane following the method of Zhang et al. [Mater. Sci. Eng. C 30 (2010) 92–97]. The structure and chemistry of the resulting nanoparticles were studied using variety of methods and their magnetic properties were determined. The diameter of the iron core was typically 8-16 nm, while the thickness of the Fe3O4 shell was 2-3 nm. The presence of the silica layer was confirmed using Fourier transform infra-red spectroscopy and the number of NH2-groups on each nanoparticle was determined based on colorimetric tests using ortho-phthalaldehyde.

Type
Research Article
Copyright
Copyright © Materials Research Society 2012

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References

REFERENCES

[1] Zhang, G., Liao, Y. and Baker, I., Materials Science and Engineering C 30(1) (2010) 9297.Google Scholar
[2] Zeng, Q., Baker, I., Loudis, J.A., Liao, Y., Hoopes, P.J. and Weaver, J.B., Appl. Phys. Lett. 90(23) (2007) 233112-1 –; 233112–3.Google Scholar
[3] Hergt, R. et al. . / J Phys Condens Matter 18(38) (2006), pp. S2919S2934 Google Scholar
[4] Klabunde, K. J. and Hadjipanayis, G. C., J. Appl. Phys., 75 (1994) 58765878.Google Scholar
[5] Pileni, M. P., Ninham, B. W., Gulik-Krzywicki, T., Tanori, J., Lisiecki, I. and Filankembo, A., Adv. Mater., 11 (1999) 13581362.Google Scholar
[6] Maillard, M., Giorgio, S. and Pileni, M. P., Adv. Mater., 14 (2002) 10841086.Google Scholar
[7] Sharma, R. K., Sharma, P. and Maitra, A., J. Colloid Interface Sci., 265 (2003) 134140.Google Scholar
[8] Brust, M., Walker, M., Bethell, D., Schiffrin, D.J. and Whyman, R.. J. Chem. Soc., Chem. Commun., 7 (1994) 801802.Google Scholar
[9] O’Connor, C.J., Kolesnichenko, V., Carpenter, E., Sangregorio, C., Zhou, W.L., Kumbhar, A., Sims, J. and Agnoli, F., Synthetic Metals, 122 (2001) 547557.Google Scholar
[10] Pham, T.A., Kumar, N.A. and Jeong, Y.T., Colloids and Surfaces A: Physicochem. Eng. Aspects 370 (2010) 95101.Google Scholar
[11] Seip, C. T. and O’Connor, C. J., NanoStructured Materials, 12 (1999) 183-1 86.Google Scholar
[12] Hoinard, C. et al. ., Spectrofluorometric method for the quantitation of amino groups on solid supports. Journal of Chromatography A, 1986. 355: p. 350353.Google Scholar
[13] Janolino, V. and Swaisgood, H., A spectrophotometric assay for solid phase primary amino groups. Applied Biochemistry and Biotechnology, 1992. 36(2): p. 8185.Google Scholar