Fe2O3–SiO2 nanocomposites were prepared by a sol–gel method using various evaporation surface to volume (S/V) ratios ranging from 0.03 to 0.2. The Fe2O3–SiO2 sols were gelated at various temperatures
ranging from 50 °C to 70 °C, and subsequently they were calcined in air at 400 °C for 4 hours. The structure and the magnetic properties of the prepared Fe2O3–SiO2 nanocomposites were characterized using X-ray diffraction (XRD), transmission
electron microscopy (TEM), differential thermal analysis (DTA), and vibrating sample magnetometer (VSM) measurements. The gelation temperature of the Fe2O3–SiO2 sols influenced strongly the particle size and crystallinity of the maghemite nanoparticles.
It was observed that the particle size of maghemite nanoparticles increased with the increasing of the gelation temperature of the sols, which may be due to the agglomeration of the maghemite particles at elevated temperatures inside the microporosity of the silica matrix during the gelation
process, and the subsequent calcination of these gels at 400 °C resulted in the formation of large size iron oxide particles. Magnetization studies at temperatures of 10, 195, and 300 K showed superparamagnetic behavior for all the nanocomposites prepared using the evaporation surface
to volume ratio (S/V) of 0.1, 0.2, 0.09, and 0.08. The saturation magnetization, Ms, values measured at 10K were 5.5, 8.5, and 9.5 emu/g, for the samples gelated at 50, 60, and 70 °C, respectively. At the gelation temperature of 70 °C, γ-Fe2O3
crystalline superparamagnetic nanoparticles with the particle size of 9±2 nm were formed in 12 hours for the samples prepared at the S/V ratio of 0.2.
Synthesis, Structural, Morphological and Thermal Characterization of Five Different Silica-Polyethylene Glycol-Chlorogenic Acid Hybrid Materials