a Department of Chemistry and Chemical Biology , Cornell University , Ithaca , New York 14853 , USA.
Biofouling. 2014;30(5):589-604. doi: 10.1080/08927014.2014.897335. Epub 2014 Apr 14.
The ideal marine antifouling (AF)/fouling-release (FR) coating should be non-toxic, while effectively either resisting the attachment of marine organisms (AF) or significantly reducing their strength of attachment (FR). Many recent studies have shown that amphiphilic polymeric materials provide a promising solution to producing such coatings due to their surface dual functionality. In this work, poly(ethylene glycol) (PEG) of different molecular weights (Mw = 350, 550) was coupled to a saturated difunctional alkyl alcohol to generate amphiphilic surfactants (PEG-hydrocarbon-OH). The resulting macromolecules were then used as side chains to covalently modify a pre-synthesized PS8 K-b-P(E/B)25 K-b-PI10 K (SEBI or K3) triblock copolymer, and the final polymers were applied to glass substrata through an established multilayer surface coating technique to prepare fouling resistant coatings. The coated surfaces were characterized with AFM, XPS and NEXAFS, and evaluated in laboratory assays with two important fouling algae, Ulva linza (a green macroalga) and Navicula incerta, a biofilm-forming diatom. The results suggest that these polymer-coated surfaces undergo surface reconstruction upon changing the contact medium (polymer/air vs polymer/water), due to the preferential interfacial aggregation of the PEG segment on the surface in water. The amphiphilic polymer-coated surfaces showed promising results as both AF and FR coatings. The sample with longer PEG chain lengths (Mw = 550 g mol(-1)) exhibited excellent properties against both algae, highlighting the importance of the chemical structures on ultimate biological performance. Besides reporting synthesis and characterization of this new type of amphiphilic surface material, this work also provides insight into the nature of PEG/hydrocarbon amphiphilic coatings, and this understanding may help in the design of future generations of fluorine-free, environmentally friendly AF/FR polymeric coatings.
理想的海洋防污(AF)/防污释放(FR)涂层应该是无毒的,同时有效地抵抗海洋生物的附着(AF)或显著降低其附着强度(FR)。许多最近的研究表明,两亲聚合物材料由于其表面双重功能,为生产这种涂层提供了一种有前途的解决方案。在这项工作中,不同分子量(Mw=350、550)的聚乙二醇(PEG)与饱和二官能烷基醇偶联,生成两亲性表面活性剂(PEG-烃基-OH)。然后,将得到的大分子用作侧链,通过共价修饰预先合成的 PS8 K-b-P(E/B)25 K-b-PI10 K(SEBI 或 K3)三嵌段共聚物,最终聚合物通过已建立的多层表面涂层技术应用于玻璃衬底,以制备抗污涂层。用 AFM、XPS 和 NEXAFS 对涂层表面进行了表征,并通过两种重要的污损藻类(绿藻 Ulva linza 和生物膜形成硅藻 Navicula incerta)的实验室试验进行了评估。结果表明,这些聚合物涂层表面在改变接触介质(聚合物/空气与聚合物/水)时会发生表面重构,这是由于在水中,PEG 段在表面上优先界面聚集所致。两亲聚合物涂层表面在作为 AF 和 FR 涂层方面表现出良好的效果。具有较长 PEG 链长(Mw=550gmol(-1))的样品对两种藻类都表现出优异的性能,突出了化学结构对最终生物性能的重要性。除了报道这种新型两亲表面材料的合成和表征外,本工作还深入了解了 PEG/烃基两亲性涂层的性质,这一认识可能有助于设计新一代无氟、环保的 AF/FR 聚合物涂层。