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Polyurethane-based polymer surface modifiers with alkyl ammonium copolyoxetane soft segments: Reaction engineering, surface morphology and antimicrobial behavior.

机译:具有烷基铵共聚氧杂环丁烷软链段的聚氨酯基聚合物表面改性剂:反应工程,表面形态和抗菌性能。

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摘要

Concentrating quaternary (positive) charge at polymer surfaces is important for applications including layer-by-layer polyelectrolyte deposition and antimicrobial coatings. Prior techniques to introduce quaternary charge to the surface involve grafting of quaternary ammonium moieties to a substrate or using polyurethanes with modified hard segments however there are impracticalities involved with these techniques.;In the case of the materials discussed, the quaternary charge is introduced via polyurethane based polymer surface modifiers (PSMs) with quaternized soft segments. The particular advantage to this method is that it utilizes the intrinsic phase separation between the hard and soft segments of polyurethanes. This phase separation results in the surface concentration of the soft segments. Another advantage is that unlike grafting, where modification has to take place after device fabrication, these PSMs can be incorporated with the matrix material during device fabrication.;The soft segments of these quaternized polyurethanes are produced via ring opening co-polymerization of oxetane monomers which possess either a trifluoroethoxy (3FOx) side chains or a quaternary ammonium side chain (C12). These soft segments are subsequently reacted with 4,4'-(methylene bis (p-cyclohexyl isocyanate)), HMDI and butanediol (BD) to form the PSM.;It was initially intended to increase the concentration of quaternary ammonium charge by increasing PSM soft segment molecular weight. Unexpectedly, produced blends with surface microscale phase separation. This observation prompted further investigation of the effect of PSM soft segment molecular weight on phase separation in PSM-base polyurethane blends and the subsequent effects of this phase separation on the biocidal activity.;Analysis of the surface morphology via tapping mode atomic force microscopy (TM-AFM) and scanning electron microscopy (SEM) revealed varying complexities in surface morphology as a function of the PSM soft segment molecular weight and initial annealing temperature. Many of these features include what are described as nanodots (100-300 nm), micropits (0.5-2 mum) and micropeaks (1-10 mum). It was also observed that surface morphology continued to coarsen with time and that the larger features were typically observed in blends containing PSMs with low molecular weight soft segments. This appearance of surface morphological feature correlates with decreased biocidal activity of the PSM blends, that is, the PSM blends exhibit little to no activity upon development of phase separated features. A model has been developed for phase separation and concomitant reduction of surface quaternary charge. This model points the way to future work that will stabilize surface charge and provide durability of surface modification.
机译:对于包括逐层聚电解质沉积和抗菌涂层在内的应用,在聚合物表面集中季电荷(正电荷)非常重要。现有的将季电荷引入表面的技术包括将季铵部分接枝到基材上或使用具有改性硬链段的聚氨酯,但是这些技术不切实际。在讨论的材料中,季电荷通过聚氨酯引入季铵化软链段的高聚物表面改性剂(PSM)。该方法的特别优点是它利用了聚氨酯硬链段和软链段之间的固有相分离。这种相分离导致软链段的表面集中。另一个优点是,与接枝不同,在装置制造后必须进行改性,这些PSM可以在装置制造期间与基质材料结合。这些季铵化聚氨酯的软链段是通过氧杂环丁烷单体的开环共聚反应制得的,具有三氟乙氧基(3FOx)侧链或季铵侧链(C12)。这些软链段随后与4,4'-(亚甲基双(对-环己基异氰酸酯)),HMDI和丁二醇(BD)反应形成PSM .;最初旨在通过增加PSM来增加季铵电荷的浓度软链段分子量。出乎意料的是,产生的混合物具有表面微观相分离。该观察结果促使人们进一步研究PSM软链段分子量对PSM基聚氨酯共混物中相分离的影响以及该相分离对杀生物活性的后续影响。;通过敲击模式原子力显微镜(TM)分析表面形态-AFM)和扫描电子显微镜(SEM)揭示了表面形态的复杂性随PSM软链段分子量和初始退火温度的变化而变化。其中许多功能包括被称为纳米点(100-300 nm),微坑(0.5-2 mum)和微峰(1-10 mum)的特征。还观察到,表面形态随时间持续变粗,并且通常在含有具有低分子量软链段的PSM的共混物中观察到较大的特征。表面形态特征的出现与PSM混合物的杀生物活性降低有关,即,PSM混合物在形成相分离特征时几乎没有或没有活性。已经开发了用于相分离和表面四元电荷减少的模型。该模型为将来的工作指明了方向,该工作将稳定表面电荷并提供表面改性的耐久性。

著录项

  • 作者单位

    Virginia Commonwealth University.;

  • 授予单位 Virginia Commonwealth University.;
  • 学科 Engineering Chemical.;Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 193 p.
  • 总页数 193
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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