Abstract

The controlled release of antifoulant is critical in marine antifouling, which is profoundly influenced by the compatibility between polymer resin and antifoulant. Conjugation of polymers with active molecules provides a promising strategy to solve the problem. In this study, we report the synthesis of hyperbranched polymers containing antifouling main-chains and degradable branching points by using reversible addition-fragmentation chain-transfer (RAFT) polymerization. The copolymerization of butyl methacrylate, vinyl-functional Econea and divinyl-functional poly(ε-caprolactone) (PCL) yields a degradable hyperbranched antifouling polymer (DHAP). As revealed by 1H NMR, the vinyl conversion linearly increases over reaction time during RAFT polymerization with a final conversion rate above 90 % after 24 h. The branching degree of DHAP increases with the content of PCL segment. Quartz crystal microbalance with dissipation (QCM-D) measurements show the degradation of DHAP is controlled. Antibacterial assays indicate that DHAP coating has good antibacterial activity. Thus, DHAP represents a promising system for antifouling coatings.

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