Abstract
Abstract
In the present study, Fe
3
O
4
@SiO
2
core–shell microspheres were prepared via two steps. First, Fe
3
O
4
nanoparticles were synthesized by co-precipitation of Fe
+3
and Fe
+2
as reaction substrates and NaOH as precipitant. Second, the surface of Fe
3
O
4
was coated with silica by hydrolysis of tetraethylorthosilicate as the silica source. Subsequently, in order to reduce the amount of interaction and the agglomeration of Fe
3
O
4
@SiO
2
microspheres, the silica shell of these particles was modified by vinyltriethoxysilane as the silane coupling agent. The structural properties of the samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and Fourier transform infrared spectroscopy analyses. The results indicated that the average sizes of Fe
3
O
4
and Fe
3
O
4
@SiO
2
particles were about 50 and 500 nm, respectively. Also, the surface characterization of Fe
3
O
4
@SiO
2
microspheres showed that the silane coupling agent was covalently coupled with the silica surface.
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10.1186/2228-5326-3-23