Grafting of polypropylene and its potential use as metal ion adsorption resin

Polypropylene (PP) was modified by radical grafting of acrylic acid (AA) in the melt by using dicumyl peroxide (DCP) as initiator. To reach a high grafting degree (GD) without substantially modifying PP‐chain structure, a few runs were carried out by employing butyl 3‐(2‐furanyl)propenoate (BFA), which is a coagent able to preserve the molecular weight (MW) of PP macromolecules in the presence of radical grafting reagents. All the samples were extracted with selective solvents to remove unreacted chemicals and free poly(acrylic acid) (PAA), and the GD was accurately determined by using the FTIR methodology. The GD ranged from 1.51 to 4.67 mol %. High‐temperature size permeation chromatography analysis was used to evaluate MW behavior, confirming the control exerted by the presence of BFA on the degradation reactions. DSC, TGA, and SEM analyses were performed to analyze the chemical modification effects on the polymer products' thermal and morphological properties. Finally, selected samples, with a particle size distribution in the range 100–850 μm, were tested as metal ion adsorption resins. Al(III), Cr(III), Zn(II), Cd(II), Pb(II), and Hg(II) were studied, and the highest adsorption efficiency values (in percentage) were obtained for Al(III) (15–20%) and Hg(II) (25–30%). © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009