An investigation on the heat dissipation in Zn-substituted magnetite nanoparticles, coated with citric acid and pluronic F127 for hyperthermia application

Zinc substituted spinel ferrite nanoparticles are appropriate for magnetic fluid hyperthermia. Stable suspensions of Zn2+ substituted magnetite (ZnxFe3-xO4, 0 ≤ x ≤ 0.20) nanoparticles in aqueous solutions (pH 5.5) were synthesized by means of co-precipitation approach, using citric acid (CA) and pluronic F127 as surfactants for hyperthermia application. The specimens were characterized by different methods. XRD patterns of the precipitates confirmed that all specimens have single phase cubic spinel structures and their lattice parameters increased as Zn2+ content increased. Mean crystallite sizes of the uncoated specimens were determined to be around 28 nm, using Scherrer's formula. By increasing the Zn2+ content, Curie temperature of the uncoated specimens reduced from 545 to 410 °C monotonically caused by reduction in super-exchange interactions. Room temperature saturation magnetizations of the uncoated specimens increased to 98.8 emu/g for x = 0.10 initially, and then decreased to 79.6 emu/g for x = 0.20. It is attributed to the replacement of paramagnetic Fe3+ ions by diamagnetic Zn2+ ones and spin canting. FTIR spectra reconfirmed formation of pure magnetite and Zn2+ substituted magnetite nanoparticles and also proved the presence of ligands on the surface of the nanoparticles. TEM investigation showed that mean particle sizes of the coated nanoparticles were in the range of 35–40 nm. The obtained ferrofluids showed a good stability in aqueous medium (pH 5.5) and according to the room temperature magnetic measurements, heating efficiency is scarcely released due to relaxation processes. Maximum obtained specific loss power (SLP) was 539 W/g and that of intrinsic loss power (ILP) was 7.26 nHm2/kg for x = 0.05 (f = 290 kHz, H = 16 kA/m) with a nanoparticle concentration as low as 1.2 mg/ml, which is a promising candidate for magnetic hyperthermia applications potentially.