Marine biofouling is a worldwide problem in marine systems. Nowadays, innovative non-toxic antifouling and fouling-release materials are highly desirable. In this study, a strategy for preparing antifouling and fouling-release materials via one-step dip coating is reported. Copolymers were synthesized via the polymerization of a monomer with catechol sticky functional groups and four monomers with antifouling- or fouling-release functional groups, respectively. The copolymers could assemble onto different material surfaces, such as metals and plastics, using biomimetic catechol groups via multivalent complex bonding. The catechol groups were helpful for adhesion onto the surfaces, while the other functional groups endowed the coatings with antifouling or fouling-release properties. The effects of modifying the substrates using these copolymer coatings were verified via X-ray photoelectron spectroscopy; images of Chlorella cell and Ulva zoospore settlement were taken using a microscope and scanning electron microscope. The copolymer-coated surfaces, especially the surface modified by DOPA–PSPMA, displayed the best antifouling activity, and surface modification via DOPA–PTMETH was shown to be the most effective for producing the fouling-release property in the settlement assay.

Epoxy resins often require toughening to broaden their engineering applications, such as in durable concrete repair. This study addresses this need by developing high-performance polyurethane/epoxy (PU/EP) interpenetrating polymer networks (IPNs). The composites were synthesized via prepolymer and stepwise methods using polyether polyol (PPG-1000), isocyanate (MDI-50), and E51 epoxy. At an optimal PU prepolymer content of 15 wt%, the polyether-based IPNs achieved a balanced mechanical profile (tensile strength: 59.90 MPa; elongation at break: 6.46%; compressive strength: 69.99 MPa). Further tuning of the soft segment by introducing polyester polyol (PS-2412) yielded superior performance at a PS-2412/PPG-1000 ratio of 30/70. This formulation increased tensile and compressive strengths by 11.4% and 6.07% (to 66.74 MPa and 74.24 MPa), and dry and wet bond strengths by 12.1% and 36.3% (to 5.68 MPa and 4.62 MPa), respectively. The enhancement is attributed to the increased crosslinking density and more uniform network structure imparted by PS-2412, which improves stress distribution and interfacial adhesion. This work provides an effective soft-segment design strategy for fabricating toughened epoxy composites with robust mechanical and adhesive properties.

A combination of surface wettability and antibacterial performance is highly imperative for construction of antibacterial coatings. In this study, motivated by the antibacterial properties of zwitterionic polymer, mussel-inspired adhesion, and the “grafting to”, a novel DOMA-SBMA copolymer with adhesion and wettability is developed for constructing a bacteriostatic surface. Specifically, the antibacterial coating is prepared via free radical polymerization and grafting to methods on the surface of stainless steel, and characterized by SCA, FTIR, XPS, SEM, and AFM to confirm the modification process. Antibacterial activity evaluation using Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) shows that the coating presents satisfactory antibacterial performance. The results showed that DOMA-SBMA coating is enough for antibacterial application, with high antibacterial efficiency against E. coli (92.2%) and S. aureus (95.0%). In summary, the bioinspired coating developed here may improve the stability of zwitterionic coatings and provides a simple preparation strategy for constructing antibacterial coatings.