Synthesis and characterization of magnetic nanoparticles in spontaneously generated vesicles
Document Type
Article
Date of Original Version
1-1-1994
Abstract
Unilamellar vesicles, formed spontaneously by mixing single-tailed anionic and cationic surfactants (dodecylbenzenesulfonic acid (HDBS) and cetyltrimethylammonium bromide (CTAB), respectively), have been used as reactors for the synthesis of magnetic nanoparticles. The micellar cationic surfactant solution containing ferrous chloride was mixed with the micellar anionic surfactant solution, resulting in the formation of defect-free unilamellar vesicles, with ferrous chloride within the cores as well as in the extravesicular spaces. The external ferrous ions were replaced with sodium ions by gel permeation chromatography. Sodium hydroxide was then added to the extravesicular region. Hydroxyl ions penetrated the vesicle cores and reacted with the available ferrous ions to initiate particle formation. The presence of intravesicular particles was confirmed by cryogenic transmission electron microscopy. Absorbance measurement showed that the reaction proceeded over a period of several minutes. To form the magnetic nanoparticles, the suspension was heated to about 70°C for 1 min, and then cooled back to room temperature. The resulting particles had a mean diameter of approximately 2.6 nm and displayed superparamagnetic behavior. Wide-area electron diffraction showed the particles to be either I-ferrite or magnetite. Magnetization measurements yielded a least upper bound for the magnetic diameter of these particles of 0.61 nm. These results are consistent with the presence of a magnetically disordered surface layer on the order of 1 nm thick. © 1994 by Academic Press, Inc.
Publication Title, e.g., Journal
Journal of Colloid And Interface Science
Volume
168
Issue
2
Citation/Publisher Attribution
Yaacob, Iskandar I., Anthony C. Nunes, Arijit Bose, and Dinesh O. Shah. "Synthesis and characterization of magnetic nanoparticles in spontaneously generated vesicles." Journal of Colloid And Interface Science 168, 2 (1994): 289-301. doi: 10.1006/jcis.1994.1423.