Abstract

Despite achieving broadscale commercial applications, Polypropylene (PP) is prone to bacterial contamination, which poses huge threats to public health. Applying antibacterial agents in polymer matrix is recognized as a widespread method to endow PP biocidal properties. Herein, we report a preparation of triclosan (TCS) based antibacterial PP through free radical grafting. As the methyl acrylate group is introduced to the TCS in advance to synthesize a radical-active monomer (f), PP-f products are successfully prepared via two typical free radical grafting reactions, solution grafting (PP-f-sg) and melt grafting (PP-f-mg). Although showing high f content (up to 12.7 mol%), PP-f-sg samples are of low monomer utilization (less than 50%) and the grafting reaction must be assisted by comonomers. On the contrary, PP-f-mg samples with modest f content (from 0.08 to 0.34 mol%) reveal satisfying monomer efficiency (over 80%) without the help of any comonomers, which demonstrates significant advantages. When addition amount of f reaches 0.12 mol% (1.0 wt%), antibacterial rates (R) of PP-f exceed 99% against both E. coli and S. aureus. Since covalent bonds are formed between TCS and PP chains, the biocidal properties of PP-f are durable and non-leaching. The R of PP-f maintains over 90% after ethanol extraction, while those extracted samples made by physical blending of TCS and PP completely lose their antimicrobial properties.

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