Please use this identifier to cite or link to this item: https://doi.org/10.1142/S1793604708000381
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dc.titleSynthesis of magnetite nanoparticles by thermal decomposition: Time, temperature, surfactant and solvent effects
dc.contributor.authorMaity, D.
dc.contributor.authorDing, J.
dc.contributor.authorXue, J.-M.
dc.date.accessioned2014-10-07T09:54:29Z
dc.date.available2014-10-07T09:54:29Z
dc.date.issued2008-12
dc.identifier.citationMaity, D., Ding, J., Xue, J.-M. (2008-12). Synthesis of magnetite nanoparticles by thermal decomposition: Time, temperature, surfactant and solvent effects. Functional Materials Letters 1 (3) : 189-193. ScholarBank@NUS Repository. https://doi.org/10.1142/S1793604708000381
dc.identifier.issn17936047
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/86760
dc.description.abstractMonodispersed magnetite (Fe 3O 4) nanoparticles can be synthesized by thermal decomposition of iron(III) acetylacetonate, Fe(acac) 3. High saturation magnetization M S of the magnetite particles is extremely important to realize the full potential of magnetite materials in biomedical application. In this work, we have studied the different effects (time, temperature and surfactant) on structure and magnetic properties of Fe 3O 4 nanoparticles. The M S of the particles are enhanced after the synthesis at a higher reaction temperature and/or a longer reaction time. However, the increase in reaction temperature and/or reaction time resulted in particle size increase and the broadening of the particle size distribution. In this work, high M S value of the magnetite particles has been achieved through adopting surfactant or modification of solvent to overcome the temperature and time effects, while the smaller size particles with an acceptable size distribution has been maintained. Size and morphology of the particles were studied by TEM while magnetic properties of the particles were measured using VSM. The saturation magnetization M S of the particles can be increased at higher reaction temperature and/or longer reaction time, while narrow size distribution of the particles can be maintained either by the selective adsorption of oleic acid to the particle surface or by synthesizing them using solvent free thermal decomposition reaction. © 2008 World Scientific Publishing Company.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1142/S1793604708000381
dc.sourceScopus
dc.subjectIron oxide
dc.subjectmagnetite nanoparticles
dc.subjectoleic acid
dc.subjectoleylamine
dc.subjectsuperparamagnetic
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1142/S1793604708000381
dc.description.sourcetitleFunctional Materials Letters
dc.description.volume1
dc.description.issue3
dc.description.page189-193
dc.identifier.isiut000271076800005
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