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Morphology, physical and tensile properties of quench-cooled isotactic polypropylene films and spunbonded fabrics.

机译:淬冷等规聚丙烯薄膜和纺粘织物的形态,物理和拉伸性能。

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摘要

The room temperature morphology of quench-cooled isotactic polypropylene (iPP) films and its development were investigated by scanning transmittance electron microscopy (STEM) and differential scanning calorimetry (DSC). STEM dark field images revealed that within an amorphous matrix there exist microcrystalline regions, 160 A in size on the average, having the ;Cross polarization/magic angle spinning (CP/MAS) nuclear magnetic resonance (NMR) spectroscopy was used to monitor morphological changes in the purely crystalline phase of quench-cooled iPP films and spunbonded fabrics during annealing. The spectra were obtained using a pulse sequence that incorporates a delay period with a reduced spin locking field prior to cross polarization. Morphological changes occurring within the purely crystalline phase of iPP were related to observations made by DSC. Upon annealing, the CP/MAS NMR spectrum of the purely crystalline phase of both iPP samples changed by a redistribution in the intensity of the various peaks within a given carbon resonance. This redistribution of intensity was found to reflect the conversion from the ;The tensile properties of the spunbonded iPP fabrics and fibers were enhanced by the dispersion of a silica/silicone additive and by changing the resin characteristics. This additive acts as a nucleating agent for iPP under isothermal crystallization conditions. This nucleating ability manifests itself in smaller crystal sizes and higher nucleation densities in the iPP fibers and bond points. The improved tensile properties are attributed to the smaller crystal sizes which form a more homogeneously dispersed crystalline phase in the amorphous phase as well as to increase the number of load-bearing tie molecules.
机译:通过扫描透射电镜(STEM)和差示扫描量热法(DSC)研究了淬冷等规聚丙烯(iPP)薄膜的室温形态及其发展。 STEM暗场图像显示,在非晶基质中存在平均大小为160 A的微晶区域,并具有;使用交叉极化/魔角旋转(CP / MAS)核磁共振波谱法来监测形态变化退火过程中,iPP膜和纺粘织物的纯结晶相中的相变。光谱是使用脉冲序列获得的,该脉冲序列在交叉极化之前结合了延迟时间和自旋锁定场减小的现象。 iPP的纯结晶相中发生的形态变化与DSC的观察结果有关。退火后,两个iPP样品的纯结晶相的CP / MAS NMR光谱通过在给定碳共振内各个峰强度的重新分布而改变。发现强度的这种重新分布反映了来自的转化。纺粘的iPP织物和纤维的拉伸性能通过二氧化硅/硅氧烷添加剂的分散和改变树脂特性而得到增强。该添加剂在等温结晶条件下充当iPP的成核剂。这种成核能力表现在iPP纤维和结合点中较小的晶体尺寸和较高的成核密度上。拉伸性能的提高归因于较小的晶体尺寸,该晶体尺寸在非晶态相中形成了更均匀分散的晶相,并增加了承载键分子的数量。

著录项

  • 作者

    Caldas, Victor.;

  • 作者单位

    McGill University (Canada).;

  • 授予单位 McGill University (Canada).;
  • 学科 Physical chemistry.;Textile research.
  • 学位 Ph.D.
  • 年度 1995
  • 页码 296 p.
  • 总页数 296
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:49:39

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