There is a strong demand for antifouling surface. To create such antifouling surface, there are some approaches such as chemical reaction at the surface, coatings, internal additives, etc. We are developing polymers that can modify the surface property by easy treatments based on precise design and synthesis of the polymers. Biomedical synthetic materials, such as poly(ethylene terephthalate) (PET) and polypropylene (PP), are prone to adhesion of proteins, cells, and bacteria, causing functional failures in implants, artificial organs, catheters, and diagnostic devices, and increasing the risk of secondary infections. One of the promising answers is a hydrophilic polymer brush surface on which many polymer chains are connected in high density to inhibit adsorption of proteins and following adhesion of related biomolecules and cells. Such high density polymer brush is usually built by surface-initiated living radical polymerization through several chemical steps and polymers applied for medical devices are rather inert to chemical modification than inorganic materials. We thus created a new star shaped heteroarm polymer consisting of hydrophilic chains, as an antifouling block, and hydrophobic chains, as a substrate attaching block, for a biocompatible coating material, which is supposed to form polymer brush-like structure by simple coating procedure. The coating surface exhibited very good resistance to adhesion of platelets, bacteria, fibroblasts, and proteins although the corresponding linear polymer exhibited moderate resistance. This result indicates utilization of unique architecture of the star polymer is effective for building condensed polymer brush structure at the surface. Perfluoroalkyl group-containing polymer shows water/oil repellency. Although long perfluoroalkyl groups (longer than C8) exhibit high repellency, they can not be employed because of the environmental reason, nowadays. Shorter perfluoroalkyl groups (less than C8) give less effect to environment but they have less repellency. We thud designed block copolymers consisting of fluorine and non-fluorine containing monomers and evaluated the sequence effects as an internal additive to PP resin to improve oil repellency. By controlling fluorinated/non-fluorinated monomer sequence, the oil repellency of the fluorinated polymer-added polypropylene (PP) was dramatically improved compared to that modified with the randomly sequenced fluoropolymer. For instance, random copolymer consisting of 2-(perfluorohexyl)ethyl methacrylate (C6FMA) and stearyl methacrylate (StMA) gave slightly higher contact angle (13º) than that of non-additive PP (6º). Compared to the random copolymer, the diblock and triblock copolymer lead much higher contact angles (23º and 38º, respectively) when only 1wt% of the fluoropolymer was mixed into PP. This result indicates sequence regulation of fluorinated/non-fluorinated monomer in the fluoropolymer is effective to concentrate fluorine groups at the resin surface resulting in improvement of water/oil repellency.
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