Modification of silica nanoparticles with hydrophilic sulfonated polymers by using surface-initiated redox polymerization

Sulfonated polymer/silica hybrid nanoparticles were prepared by free radical polymerization of 2-acrylamido-2-methyl-1-propane sulfonic acid (PAMPS-g-SN) and styrene sulfonic acid sodium salt (PSSA-g-SN), initiated on the surfaces of aminopropyl-functionalized silica nanoparticles (ASN). Ce(IV) ammonium nitrate/nitric acid and sodium dodecyl sulfate were used as redox initiator and stabilizer, respectively. ASN Nanoparticles were synthesized by a covalently attached 3-aminopropyltriethoxysilane onto the surface of silica nanoparticles. Sulfonated monomers (AMPS or SSA) were then grafted onto the ASN nanoparticles, ultrasonically dispersed in water, using redox initiator system at 40 A degrees C. ASN, PAMPS-g-SN and PSSA-g-SN nanoparticles were characterized by Fourier transform infrared (FTIR), thermogravimetry, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analyses. FTIR and TGA results indicated that both AMPS and SSA monomers were successfully grafted onto the silica nanoparticles. The grafted amounts of sulfonated polymers onto the silica nanoparticles were estimated from TGA thermograms to be 46 and 22 % for PAMPS and PSSA, respectively. From SEM and TEM micrographs, the average-diameters of the polymer-grafted silica nanoparticles were measured to be < 50 nm with a (semi)spherical morphology, in which several silica nanoparticles were able to form a core with PAMPS or PSSA existing around the silica nanoparticles.