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Microrheological study on polyethylene/thermotropic liquid crystalline polymer/layered silicates nanocomposites.

机译:聚乙烯/热致液晶聚合物/层状硅酸盐纳米复合材料的微流变研究。

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摘要

The objective of the thesis is investigation microrheology and microstructure behaviors to understanding mechanisms of bulk viscosity reduction in layer silicate (organoclay)/thermotropic liquid crystalline copolyester (TLCP)/high molecular weight polyethylene (PE) nanocomposites.; Before illustrate mechanisms of ternary blends, the interactions between layered silicate and liquid crystalline polymer have been characterized by microrheological and microstructural methods first. Four typical kinds of binary composites have been studied with nominal 3.0 wt% organoclay in TLCP, i.e., TC3. (1) TC3 UP is a typical partial intercalated and partial exfoliated nanocomposite. Phase separation occurred during steady shear experiments and observed by POM at 190°C. Separation of TC3 UP was performed and two hybrids were obtained: TC3 white and TC3 dark. (2) In TC3 white, organoclays formed exfoliated morphologies and well dispersed in TLCP matrix with uniform sizes 15-25 nm. The presence of organoclay did not affect liquid crystallinity of matrix but enhanced the rigidity of TLCP molecules. The molecular level interactions between organoclay and TLCP molecules held molecular orientation in the flow direction during relaxation after steady shear. The bulk viscosity mechanism of this binary filler in PE has been analyzed in detailed. (3) Organoclays in TC3 dark hybrid totally destroyed matrix liquid crystallinity and deteriorated thermal properties. Due to intercalated morphologies, TC3 dark has strong solid-like behaviors with high viscosities, long relaxation time but short linear viscoelastic region. (4) TC3 FS is the nanocomposite having comparable lengths for organoclays and TLCP molecules. Exfoliated structures formed in the nanocomposite with slightly modified matrix liquid crystallinity. It has the similar rheological behavior with TLCP.; PE/TLCP/organoclay blends, i.e., PTC, have been prepared to analyze the concentrations and preparation sequences effects. (1) Increasing TLCP concentration in PE as well as in organoclay/PE matrix can effectively reduce the bulk viscosities, but too much would cause shear-induced agglomeration of TLCP in matrix. (2) The same ratio of TLCP and as-received organoclay (1/1) in PE matrix can cause bulk viscosities reduction but no processing window increasing at the same time. (3) With suitable preparation sequences and optimal TLCP/organoclay ratio, the blend (3 wt% TLCP/PE)/1 wt% clay ((PT3) C1) has even lower viscosities than the corresponding 3wt% TLCP/PE blend (PT3) with the dramatic improved processing window. A binary flow pattern model, originally developed for viscosity reduction in HMMPE/TLCP blend, successfully predicted both the dramatic viscosity reduction effects and the critical yielding stress for the above blends.; Organoclay enhanced TLCP in PE matrix have been characterized mainly by rheological method with adding 1 wt% of above four kinds TC3 in PE. Relative lower yield stresses and shear rates as well as higher viscosity reduction abilities than 1 wt% TLCP/PE (PTI) blend have been observed. P (TC3 dark 1.0 wt%) and P (TC3 UP 1.0 wt%) rheological behaviors can not be predicted by the model, due to the dramatic impact of organoclay to TLCP in PE at high shear rates regions. P (TC3 FS 1.0 wt%) and P (TC3 white 1.0 wt%) showed highest viscosity reduction ability in the four blends with P (TC3 FS 1.0 wt%) having the same processing window and P (TC3 white 1.0 wt%) holding a relatively broad processing window than PT1. The model has been successfully proposed for these two blends. Shear-induced phase transition with the combination of synergic effect of organoclay with TLCP is the mechanism for bulk viscosity reduction as well as low yielding stress and shear rate in P(TC3 white 1 wt%).; Fibrillation with different fibre lengths, widths and shapes controlled the final rheological properties of PE blends, which were controlled by different organoclay morphologies and interaction types
机译:本文的目的是研究微观流变学和微观结构行为,以了解层状硅酸盐(有机粘土)/热致液晶共聚酯(TLCP)/高分子量聚乙烯(PE)纳米复合材料的体积粘度降低的机理。在说明三元共混物的机理之前,首先通过微流变和微结构方法表征了层状硅酸盐与液晶聚合物之间的相互作用。已经研究了四种典型的二元复合材料,它们在TLCP中具有标称的3.0 wt%有机粘土,即TC3。 (1)TC3 UP是一种典型的部分嵌入和部分剥离的纳米复合材料。在稳态剪切实验中发生相分离,并在190°C下通过POM观察到。进行TC3 UP的分离,获得了两个杂种:TC3白色和TC3黑色。 (2)在TC3白色中,有机粘土形成了剥落的形态,并很好地分散在TLCP基质中,均匀大小为15-25 nm。有机粘土的存在不会影响基质的液晶性,但会增强TLCP分子的刚性。在稳定剪切后的松弛过程中,有机粘土和TLCP分子之间的分子水平相互作用在流动方向上保持分子取向。详细分析了这种二元填料在PE中的体积粘度机理。 (3)TC3暗杂化物中的有机粘土完全破坏了基质的液晶性并降低了其热性能。由于层状形态,TC3暗色具有强固形的行为,具有高粘度,长弛豫时间但线性粘弹性区域短。 (4)TC3 FS是具有与有机粘土和TLCP分子相当的长度的纳米复合材料。纳米复合材料中形成的剥落结构,基体液晶度稍有改变。它具有与TLCP相似的流变行为。已经制备了PE / TLCP /有机粘土混合物,即PTC,以分析浓度和制备顺序的影响。 (1)增加PE和有机粘土/ PE基质中的TLCP浓度可以有效降低整体粘度,但过多会引起剪切诱导的TLCP在基质中的团聚。 (2)在PE基质中相同比例的TLCP和按原样接收的有机粘土(1/1)可以导致体积粘度降低,但同时没有增加加工窗口。 (3)通过适当的制备顺序和最佳的TLCP /有机粘土比率,共混物(3 wt%TLCP / PE)/ 1 wt%粘土((PT3)C1)的粘度甚至比相应的3wt%TLCP / PE共混物(PT3)低),并大大改善了处理窗口。最初为降低HMMPE / TLCP共混物的粘度而开发的二元流模式模型成功地预测了上述共混物的显着粘度降低效果和临界屈服应力。 PE基质中有机粘土增强的TLCP主要通过流变学方法表征,在PE中添加1 wt%的上述四种TC3。已经观察到相对于1wt%的TLCP / PE(PTI)共混物而言,相对较低的屈服应力和剪切速率以及较高的粘度降低能力。由于有机粘土对高剪切速率区域中PE中TLCP的巨大影响,因此该模型无法预测P(TC3暗含量为1.0 wt%)和P(TC3 UP含量为1.0 wt%)的流变行为。 P(TC3 FS 1.0 wt%)和P(TC3白色1.0 wt%)在具有相同加工窗口且P(TC3白色1.0 wt%)保持不变的四种共混物中显示出最高的降粘能力比PT1相对更宽的处理窗口。该模型已成功地针对这两种混合物提出。剪切诱导相变与有机粘土与TLCP的协同作用相结合是降低P(TC3白1 wt%)的整体粘度以及降低屈服应力和剪切速率的机制。具有不同纤维长度,宽度和形状的原纤化控制了PE共混物的最终流变性能,而该流变性能则受不同的有机粘土形态和相互作用类型的控制

著录项

  • 作者

    Tang, Youhong.;

  • 作者单位

    Hong Kong University of Science and Technology (People's Republic of China).;

  • 授予单位 Hong Kong University of Science and Technology (People's Republic of China).;
  • 学科 Engineering Chemical.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 288 p.
  • 总页数 288
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化工过程(物理过程及物理化学过程);
  • 关键词

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