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Design, Optimization Process and Efficient Analysis for Preparation of Copolymer-Coated Superparamagnetic Nanoparticles
Author(s) -
Mahnaz Mahdavi Shahri
Publication year - 2017
Publication title -
journal of nanostructures
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.251
H-Index - 9
eISSN - 2251-788X
pISSN - 2251-7871
DOI - 10.18502/jns.v7i3.7
Subject(s) - superparamagnetism , materials science , nanoparticle , nanocomposite , ferrofluid , magnetic nanoparticles , chemical engineering , scanning electron microscope , magnetite , iron oxide nanoparticles , transmission electron microscopy , copolymer , polymerization , magnetization , polymer , nanotechnology , composite material , metallurgy , physics , quantum mechanics , magnetic field , engineering
Magnetic nanoparticles (MNPs) are very important systems with potential use in drug delivery systems, ferrofluids, and effluent treatment. In many situations, such as in biomedical applications, it is necessary to cover inorganic magnetic particles with an organic material, such as polymers. A superparamagnetic nanocomposite Fe3O4/poly(maleic anhydride-co-acrylic acid) P(MAH-co-AA) with a core/shell structure was successfully synthesized by a dispersion polymerization route. Iron oxide nanoparticles were used as a core, and P(MAH-co-AA) as a shell was covered on the surface of the Fe3O4 magnetic nanoparticles. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) showed that the Fe3O4/P(MAH-co-AA) magnetic nanocomposite were highly uniform in size and cubic shape with the average size about 17.06 nm. X-ray diffraction confirmed magnetite cores and also indicated that the binding process did not change the phase of Fe3O4. Vibrational sample magnetometer (VSM) revealed the nanoparticles were superparamagnetic and the saturation magnetization was 83.6 and 46.6 emu g-1 for pure Fe3O4 and composite nanoparticles, respectively. Measurements by VSM also showed that the degree of saturation magnetization increased with increasing iron oxide concentration from 1% to 7 wt % of Fe3O4.

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