Alkyl phosphonate/phosphate coating on magnetite nanoparticles: A comparison with fatty acids

Coated magnetite nanoparticles with a 6-8 nm average diameter were prepared . The surfactants used to stabilize the nanoparticles and disperse them in organic solvents were oleic acid (OA), lauric acid, dodecylphosphonate, hex adecylphosphonate, and dihexadecyl phosphate. Transmission electron microsc opy analyses of the aggregation of the coated particles suggest that carbox ylate surfactants provide the particles with better isolation and dispersib ility as compared with phosphonate surfactants. However, Fourier transform infrared spectra of the phosphonate and phosphate coated particles suggest that these surfactants cover the surface of the nanoparticles in islands of high packing density, The thermogravimetric and differential scanning calo rimetry measurements suggest that there is a quasi-bilayer of these surfact ants covering the surface of the nanoparticles, with varying amounts of sur factant in the outer layer and with the second layer weakly bound to the pr imary layer through hydrophobic interactions between the alkyl chains. The desorption temperatures of the alkyl phosphonates and phosphate are higher than those of the carboxylate coated particles. The enthalpy of binding of the ligands suggests strong P-O-Fe bonding on the surface. Nevertheless, re gardless of binding strength, the CA coated particles are better dispersed in organic solvents, Their higher hydrophobicity is likely due to different interactions among the oleyl chains and/or a smaller tendency to form bila yer structures.