ABSTRACT:Maleic anhydride (MAH) was readily grafted onto polypropylene (PP) film by means of introducing the electron donor monomer n-butyl vinyl ether (n-BVE), via two-step method. In the first step, the semibenzopinacol (SBP) groups were introduced onto the film surface under UV irradiation, and they were subsequently detected by both gravimetric method and UV spectra. In the second step, the "dormant" SBP groups were activated and cleaved from the substrate under heat, resulting in the formation of surface free radicals (grafting points) and the immediate initiation of graft polymerization; the temperature required for this process was found to be around 80• C. The grafting resultsshow that the grafting yield (Y g ) of two-step method can be much higher than that of one-step method, and that the novel electron donor-acceptor grafting system is much more effective than that of pure MAH. Properly speaking, the Y g value could reach as high as 180% within 1 h, and the density of polar groups (D p ) on the substrate was 49.5 µmol cm −2 correspondingly. Besides, the maximum Y g can be always attained at 1:1 molar feed ratio of MAH to BVE, indicating that the facile grafting process is attributed to the formation of charge transfer complex (CTC) between the binary monomers. Another significant result is that the good affinity of solvent towards substrate, and especially the desirable solubility for the graft chains are both preferable to heterogeneous graft polymerization. In addition, some phenomena characterizing "living" graft polymerization were revealed in this particular grafting system, which is expected to favor the control of the length and chemical structure of the graft chains.