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首页> 外文期刊>Scientific reports. >Micromechanics of ultra-toughened electrospun PMMA/PEO fibres as revealed by in-situ tensile testing in an electron microscope
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Micromechanics of ultra-toughened electrospun PMMA/PEO fibres as revealed by in-situ tensile testing in an electron microscope

机译:超韧电纺PMMA / PEO纤维的微力学,通过电子显微镜的原位拉伸测试显示

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A missing cornerstone in the development of tough microano fibre systems is an understanding of the fibre failure mechanisms, which stems from the limitation in observing the fracture of objects with dimensions one hundredth of the width of a hair strand. Tensile testing in the electron microscope is herein adopted to reveal the fracture behaviour of a novel type of toughened electrospun poly(methyl methacrylate)/poly(ethylene oxide) fibre mats for biomedical applications. These fibres showed a toughness more than two orders of magnitude greater than that of pristine PMMA fibres. The in-situ microscopy revealed that the toughness were not only dependent on the initial molecular alignment after spinning, but also on the polymer formulation that could promote further molecular orientation during the formation of microano-necking. The true fibre strength was greater than 150?MPa, which was considerably higher than that of the unmodified PMMA (17?MPa). This necking phenomenon was prohibited by high aspect ratio cellulose nanocrystal fillers in the ultra–tough fibres, leading to a decrease in toughness by more than one order of magnitude. The reported necking mechanism may have broad implications also within more traditional melt–spinning research.
机译:在开发坚韧的微/纳米纤维系统时,缺少的基石是对纤维破坏机理的理解,这是由于观察到发束宽度的百分之一的物体断裂的局限性所致。本文采用电子显微镜中的拉伸测试来揭示用于生物医学应用的新型增韧电纺聚甲基丙烯酸甲酯/聚环氧乙烷纤维垫的断裂行为。这些纤维的韧性比原始的PMMA纤维高出两个数量级。原位显微镜显示,韧性不仅取决于纺丝后的初始分子排列,而且取决于在微/纳米颈缩形成过程中可促进进一步分子取向的聚合物配方。真正的纤维强度大于150?MPa,大大高于未改性的PMMA(17?MPa)。颈缩现象被超韧纤维中高纵横比的纤维素纳米晶体填料所禁止,从而导致韧性降低了一个数量级以上。在更传统的熔纺研究中,所报道的缩颈机理也可能具有广泛的意义。

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