Polymer brush coatings for combating marine biofouling |
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Authors: | Wen Jing Yang Koon-Gee Neoh En-Tang Kang Serena Lay-Ming Teo Daniel Rittschof |
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Affiliation: | 1. Key Laboratory for Organic Electronics & Information Displays, Institute of Advanced Materials, Nanjing University of Posts and Telecommunications, Wenyuan Road 9, Nanjing 210046, PR China;2. Department of Chemical & Biomolecular Engineering, National University of Singapore, Kent Ridge, Singapore 119260, Singapore;3. Tropical Marine Science Institute, National University of Singapore, Kent Ridge, Singapore 119223, Singapore;4. Duke University Marine Laboratory, Nicholas School of the Environment, 135 Duke Marine Lab Road, Beaufort, NC 28516-9721, USA |
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Abstract: | A variety of functional polymer brushes and coatings have been developed for combating marine biofouling and biocorrosion with much less environmental impact than traditional biocides. This review summarizes recent developments in marine antifouling polymer brushes and coatings that are tethered to material surfaces and do not actively release biocides. Polymer brush coatings have been designed to inhibit molecular fouling, microfouling and macrofouling through incorporation or inclusion of multiple functionalities. Hydrophilic polymers, such as poly(ethylene glycol), hydrogels, zwitterionic polymers and polysaccharides, resist attachment of marine organisms effectively due to extensive hydration. Fouling release polymer coatings, based on fluoropolymers and poly(dimethylsiloxane) elastomers, minimize adhesion between marine organisms and material surfaces, leading to easy removal of biofoulants. Polycationic coatings are effective in reducing marine biofouling partly because of their good bactericidal properties. Recent advances in controlled radical polymerization and click chemistry have also allowed better molecular design and engineering of multifunctional brush coatings for improved antifouling efficacies. |
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Keywords: | AA, alginic acid AAm, acrylamide AFM, atomic force microscope AMPS, 2-acrylamide-2-methyl-1-propanesulfonate ATRP, atom transfer radical polymerization CBMA, carboxybetaine methacrylate CRP, controlled/living radical polymerization GPS, 3-(glycidoxypropyl)trimethoxysilane HA, hyaluronic acid HBFP, hyperbranched fluoropolymer HEMA, 2-hydroxyethyl methacrylate IDT, isophorone diisocyanate trimer META, 2-(methacryloyloxy)ethyl trimethylammonium chloride MIC, microbiologically influenced corrosion MPC, 2-methacryloyloxyethyl phosphorylcholine MWCNT, multi-wall carbon nanotubes NA, noradrenaline OEG, oligo(ethylene glycol) P4VP, poly(4-vinylpridine) PA, pectic acid PAA, poly(acrylic acid) PANI, polyaniline PDMAEMA, poly(2-dimethylaminoethyl methacrylate) PDMS, poly(dimethylsiloxane) PEG, poly(ethylene glycol) PEGMA, poly(ethylene glycol) methacrylate PEI, polyethyleneimine PFPE, penfluoropolyether PFS, 2,3,4,5,6-pentafluorostyrene PGMA, poly(glycidyl methacrylate) PS-b-P(EO-stat-AGE), polystyrene-block-poly[(ethylene oxide)-stat-(allyl glycidyl ether)] PSPMA, poly(3-sulfopropyl methacrylate) PTMSPMA, poly(3-(trimethoxysilyl) propyl methacrylate) PVA-SbQ, poly(vinyl alcohol) with stilbazolium QAC, quaternary ammonium cations QAS, quaternary ammonium salts SABC, surface-active block copolymers SBMA, sulfobetaine methacrylate SEBS, polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene SI-ATRP, surface-initiated atom transfer radical polymerization SPC, self-polishing copolymer SQTC, semifluorinated-quaternized triblock copolymers TBT, tributyltin TEM, transmission electron microscopy TPCL, polycaprolactone polyol |
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