摘要
Abstract： Maghemite-silica particulate nanocomposites were prepared by modified 2-step sol-gel process. Superparamagnetic maghemite nanoparticles were successfully produced using Massart＇s procedure. Nanocomposites consisting of synthesized maghemite nanoparticles and silica were produced by dispersing the as-synthesized maghemite nanoparticles into the silica particulate form. The system was then heated at 140 ℃for 3 d. A variety of mass ratios of Fe2O3/SiO2 was investigated. Moreover, no surfactant or other unnecessary precursor was involved. The nanocomposites were characterized using XRD, BET and AGM. The XRD diffraction patterns show the reflection corresponding to maghemite nanoparticles and a visible wide band at 20 from 20° to 35° which are the characteristics of the amorphous phase of the silica gel. The patterns also exhibit the presence of only maghemite and SiO2 amorphous phase, which indicates that there is no chemical reaction between the silica particulate gel and maghemite nanoparticles to form other compounds. The calculated crystallite size for encapsulated maghemite nanoparticles is smaller than the as-synthesized maghemite nanoparticles indicating the dissolution of the nanoparticles. Very high surface area is attained for the produced nanocomposites （360-390 m^2/g）. This enhances the sensitivity and the reactivity of the nanocomposites. The shapes of the magnetization curves for nanocomposites are very similar to the as-synthesized maghemite nanoparticles. Superparamagnetic behaviour is exhibited by all samples, indicating that the size of the maghemite nanoparticles is always within the nanometre range. The increase in iron content gives rise to a small particle growth.
Maghemite-silica particulate nanocomposites were prepared by modified 2-step sol-gel process.Superparamagnetic maghemite nanoparticles were successfully produced using Massart’s procedure.Nanocomposites consisting of synthesized maghemite nanoparticles and silica were produced by dispersing the as-synthesized maghemite nanoparticles into the silica particulate form.The system was then heated at 140°C for 3 d.A variety of mass ratios of Fe2O3/SiO2was investigated.Moreover,no surfactant or other unnecessary precursor was involved.The nanocomposites were characterized using XRD,BET and AGM.The XRD diffraction patterns show the reflection corresponding to maghemite nanoparticles and a visible wide band at 2θfrom 20°to35°which are the characteristics of the amorphous phase of the silica gel.The patterns also exhibit the presence of only maghemite and SiO2amorphous phase,which indicates that there is no chemical reaction between the silica particulate gel and maghemite nanoparticles to form other compounds.The calculated crystallite size for encapsulated maghemite nanoparticles is smaller than the as-synthesized maghemite nanoparticles indicating the dissolution of the nanoparticles.Very high surface area is attained for the produced nanocomposites(360–390 m2/g).This enhances the sensitivity and the reactivity of the nanocomposites.The shapes of the magnetization curves for nanocomposites are very similar to the as-synthesized maghemite nanoparticles.Superparamagnetic behaviour is exhibited by all samples,indicating that the size of the maghemite nanoparticles is always within the nanometre range.The increase in iron content gives rise to a small particle growth.
基金
Project(RP021-2012C)supported by University of Malaya under the UMRG Fund,Malaysia
