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AFM studies of semicrystalline polymer/inorganic nanocomposites.

机译:半结晶聚合物/无机纳米复合材料的AFM研究。

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摘要

The aims of this work are to elucidate the effects of interaction strength on the crystallization of a polymer near an inorganic surface; connect filler induced polymer crystallinity with resulting property changes, especially for strongly interacting (i.e. hydrogen bonding) systems; and to devise atomic force microscopy (AFM) methods for probing the crystallinity and properties of polymer/layered silicate systems at the nanometer level.; Three inorganically filled systems were studied: (1) poly(vinyl alcohol) (PVA), (2) poly(ethylene oxide) (PEO), and (3) polypropylene (PP). Since it has the strongest, interactions, the PVA system is investigated first. AFM is used in conjunction with x-ray diffraction and differential scanning calorimetry (DSC) to show that strong polymer/filler interactions can promote a different crystalline structure and a different morphology than those seen in the bulk.; The study then proceeds to the weakly interacting PEO/inorganic system where it is found that the inorganic layers disrupt crystalline morphology, but do not change the crystal structure. Furthermore, crystallization always occurs in volumes away from the inorganic filler. The third system (neutral interactions), PP/inorganic is then discussed. The three systems are compared with each other, and is found that the crystalline morphology and structure is highly dependent upon the strength of interaction between the polymer and filler.; Due to its far-reaching morphology changes, the strongly interacting system was chosen for property studies. The composite structure study revealed a coexistence of exfoliated and intercalated MMT layers, especially for low and moderate silicate loadings. The inorganic layers promote a new crystalline phase different than the one of the respective neat PVA, characterized by higher melting temperature and a different crystal structure. This new crystal phase reflects on the composite materials properties, which have mechanical, thermal, and water vapor transmission properties superior to that of the neat polymer and its conventionally filled composites. For example, for a 5wt.% MMT exfoliated composite, the softening temperature increases by 25°C, the Young's modulus triples with a decrease of only 20% in toughness, whereas there is also a 60% reduction in the water permeability. Furthermore, due to the nanoscale dispersion of filler, the nanocomposites retain their optical clarity.; Finally, to better connect changes in morphology with property enhancements, AFM methods were devised which allow direct imaging of morphology as well as local properties.
机译:这项工作的目的是阐明相互作用强度对无机表面附近聚合物结晶的影响。将填料引起的聚合物结晶度与所导致的性能变化联系起来,尤其是对于相互作用强烈的体系(即氢键);并设计原子力显微镜(AFM)方法来探测聚合物/层状硅酸盐体系的结晶度和性质。研究了三种无机填充体系:(1)聚乙烯醇(PVA),(2)聚环氧乙烷(PEO)和(3)聚丙烯(PP)。由于它具有最强的交互作用,因此首先对PVA系统进行了研究。 AFM与X射线衍射和差示扫描量热法(DSC)结合使用,表明与大块聚合物相比,强烈的聚合物/填料相互作用可促进不同的晶体结构和不同的形态。然后,研究继续进行至弱相互作用的PEO /无机系统,在该系统中发现无机层破坏了晶体形态,但没有改变晶体结构。此外,结晶总是在远离无机填料的体积中发生。然后讨论了第三个系统(中性相互作用),PP /无机。将这三种体系相互比较,发现晶体的形态和结构高度依赖于聚合物和填料之间相互作用的强度。由于其深远的形态变化,因此选择了相互作用强烈的系统进行特性研究。复合材料结构研究表明,剥落和插入的MMT层并存,特别是对于中低硅酸盐含量的情况。无机层促进了不同于各自的纯PVA之一的新的结晶相,其特征在于更高的熔融温度和不同的晶体结构。这种新的晶相反映了复合材料的性能,该材料具有比纯聚合物及其常规填充的复合材料更好的机械,热和水蒸气传输性能。例如,对于5wt。%的MMT剥离复合材料,软化温度提高25℃,杨氏模量增加三倍,而韧性仅降低20%,而水渗透率也降低60%。此外,由于填料的纳米级分散,纳米复合材料保持其光学透明度。最后,为了更好地将形态变化与属性增强联系起来,设计了AFM方法,该方法可以对形态以及局部属性进行直接成像。

著录项

  • 作者

    Strawhecker, Kenneth E.;

  • 作者单位

    The Pennsylvania State University.;

  • 授予单位 The Pennsylvania State University.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 151 p.
  • 总页数 151
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;
  • 关键词

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