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Effects of perfluoroether concentration and curing protocol on morphology and mechanicla properties of toughened TGDDM/MNA resin systems

机译:全氟醚浓度和固化方案对增韧的TGDDM / MNA树脂体系的形态和力学性能的影响

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Previous published work has shown that hydroxyl terminated perfluoroether oligomers can be suitably modified and functionalised to make them miscible with epoxy resins in the uncured state.The reaction conditions can adjusted to induce phase separation either through spinodal decomposition to produce an IPN type morphology,or by nucleation and growth if a dispersed-particle microstructure is required.In the present work we examine the relative toughening enhancement efficiency of the two possible heterophase morpholgies.Both systems show a sigmoidal increase in fracture toughness,with increasing concentration of the modifier.However,this takes place at much lower modifier concentrations for the systems with a particulate morphology (about 3.5% w/w) than for IPN systems (about 7.5% w/w).The maximum fracture toughness achievable for the two systems,on the other hand,is very similar and coincides with the concentration at which co-continuous phases are formed.These differences in morphology,however,are not reflected in the variation of modulus and compressive yield strength with increasing concentration of perfluoroether modifier,in so far as both systems exhibit a gradual and small reduction in property with increasing concentration.Furthermore,the dynamic mechanical spectra of the two systems are very different,but the changes resulting from increasing the concentration of toughening agent are relatively smallin eitgher case.Nanoindentation tests indicate that it is the local plasticity,brought about by the presenceof the softer perfluoroether phase,which is responsible for the enhancement of fracture toughness.This is corroborated by AFM examinations,which reveal local plastic deformations in the regions surrounding the softer particles.
机译:先前发表的工作表明,可以对羟基封端的全氟醚低聚物进行适当的改性和功能化,使其与未固化状态的环氧树脂互溶。反应条件可以通过旋节线分解产生IPN型形态或通过如果需要分散颗粒的微结构,则成核和生长。在本工作中,我们研究了两种可能的异相形态的相对增韧增强效率。两个系统均显示出随着改善剂浓度的增加,断裂韧度呈S形增长。与IPN系统(约7.5%w / w)相比,具有颗粒形态的系统(约3.5%w / w)发生的改性剂浓度低得多。另一方面,两个系统可实现的最大断裂韧性这些非常相似,并且与共连续相形成时的浓度相吻合。但是,gy并没有反映在全氟醚改性剂浓度增加的情况下模量和抗压屈服强度的变化中,只要这两个系统都显示出随着浓度的增加逐渐降低的性能。纳米压痕试验表明,这是局部塑性,是由于存在较软的全氟醚相造成的,这是造成断裂的原因。 AFM检查证实了这一点,该检查揭示了较软颗粒周围区域的局部塑性变形。

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