Synthesis of Polymer-coated Magnetic Nanoparticles (original) (raw)

2005, T. Dey, C. J. O’Connor (2005). Synthesis of Polymer-coated Magnetic Nanoparticles. Proc. NSTI Nanotech. 2, 13-16.

ATRP (atom transfer radical polymerization) approach was employed to synthesis polymer-coated magnetite nanoparticles with an average diameter of 7.1 nm and of narrow size distribution, followed by various characterization techniques like Transmission Electron Microscopy (TEM), Ultraviolet-Visible spectroscopy (UV-vis), Fourier Transform Infrared spectroscopy (FTIR) and Atomic Force Microscopy (AFM). The challenge was to obtain a thin shell and particles in an unagglomerated state. Several factors like presence/choice of solvent, monomer-to-initiator concentration and structure of initiator were found to play a key role in this study. Attempts have been made to tailor the polymer shells by end-functionalization. This work has an enormous biomedical application potential.

The polymerisation of oligo (ethylene glycol methyl ether) methacrylate from a multifunctional poly (ethylene imine) derived amide: a stabiliser for the synthesis and dispersion of magnetite nanoparticles

A facile synthetic route to poly(ethylene imine)-graft-poly(oligo(ethylene glycol methyl ether)) (PEI-graft-POEGMA) functionalised superparamagnetic magnetite nanoparticles is described. The polymerisation of OEGMA from a model molecular amide demonstrated the feasibility of POEGMA synthesis under mild ATRP conditions (20 °C in ethanol) albeit with low initiator efficiencies. DFT studies suggest that the amide functionality is intrinsically of lower activity than ester functional monomers and initiators for atom transfer polymerisation (ATRP) as a consequence of higher bond dissociation energies and bond dissociation free energies (BDFE). However these studies further highlighted that use of an appropriate solvent could reduce the free energy of dissociation thereby reducing the relative difference in BDFE between the ester and amide groups. A commercial branched PEI sample was functionalised by reaction with 2-bromo-2-methylpropanoyl bromide giving an amide macroinitiator suitable for the atom transfer radical polymerisation (ATRP) of oligo(ethylene glycol methyl ether) methacrylate. The resulting PEI-graft-POEGMA copolymers were characterised by SEC, FT-IR and 1H and 13C NMR spectroscopy. PEI-graft-POEGMA coated magnetite nanoparticles were synthesised by a basic aqueous co-precipitation method and were characterised by transmission electron microscopy, thermogravimetric analysis and vibrating sample magnetometry and dynamic light scattering. These copolymer coated magnetite nanoparticles were demonstrated to be effectively stabilised in an aqueous medium. Overall the particle sizes and magnetic and physical properties of the coated samples were similar to those of uncoated samples.

High Encapsulation Efficiency of Magnetite Nanoparticles in Hydrophobic Polymer Microcapsules using Microsuspension Conventional Radical Polymerization

Oriental Journal of Chemistry

High encapsulation efficiency of magnetite nanoparticles (MNPs; Fe3O4) in microcapsules using PDVB as a hydrophobic polymer shell was successfully achieved by microsuspension conventional radical polymerization (ms CRP). MNPs were initially synthesized by co-precipitation of Fe2+/Fe3+ in a binary phase. During the nucleation of MNPs in alkaline aqueous solution existing oleic acid (OA), MNPs were coated with OA (MNPs-OA) before moving to the toluene phase with the addition of salt. At OA concentration of 0.3 wt%, most of the nucleated MNPs were hydrophobic and well dispersed in the toluene phase. Using DVB as a monomer for ms CRP, high encapsulation efficiency (92 %EE) of MNPs-OA was obtained, with low free polymer particle formation. By contrast, large amounts of free polymer particles were observed at low %EE (32%) of MNPs. The main driving force for high %EE was obtained by coating the surface of the MNPs by OA which increased hydrophobicity.

Aminopropylimidazole as an Advantageous Coating in the Synthesis of Functionalized Magnetite Nanoparticles

Nanomaterials

Implementing new methods to prepare magnetite nanoparticles with a covered or uncovered surface has been, and still is, a significant challenge. In this work, we describe a very clear and effortless way for the preparation of magnetite nanoparticles using two types of bases, namely: 1-(3-aminopropyl)imidazole and sodium hydroxide. Fourier transform infrared spectroscopy (FTIR) served as a tool for the structural investigation of the as-prepared magnetite nanoparticles. The morphology of the samples was investigated using Transmission Electron Microscopy (TEM). Comprehensive high-resolution X-ray photoelectron spectroscopy investigations (XPS) were applied as an effective tool for analyzing the composition of the various types of magnetic nanoparticles. Further polymer linkage was accomplished with poly(benzofuran-co-arylacetic acid) on the amino-functionalized surface of aminopropylimidazole-containing magnetic nanoparticles. The findings are promising for biomedicine, catalysis, an...

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