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Vibrational spectroscopic investigation of polymer melt processing

机译:聚合物熔体加工的振动光谱研究

摘要

A polymer is rarely used as a pure material and the baseline physical, chemical and rheological properties such as molecular weight, strength, stiffness and viscosity are often modified by the addition of fillers or by blending with another polymer. However, as many polymers are immiscible, compatibilisation and graft processing polymer blends are very important techniques to increase miscibility of the blends as well as to improve chemical, physical and mechanical properties.ududReactive extrusion, or melt-state processing, is one of the most appropriate techniques for improving polymer properties. Compatibilisation and graft polymer processing are often carried out under reactive extrusion conditions. This technique is an efficient approach because it is easy, inexpensive and has a short processing time. Although reactive extrusion has numerous advantages one of the limitations is degradation of the polymer under the high temperatures and mechanical stresses encountered.ududIn the polymer industry, because of increasing customer demand for improved product quality, optimising the polymerisation process by decreasing product costs and controlling the reaction during polymerisation has become more important. It can be said that any method used for monitoring the polymerisation process has to be fast, accurate and reliable. Both in-line and on-line methods may be involved in in-process monitoring. The primary information from in-process monitoring is used for identifying and understanding molecular structure and changes, optimising and improving process modelling and understanding whether the process is under control. This also involves considering whether the products have the required properties.ududThis thesis describes research in a number of aspects of melt processing of polymers, including examination of extruded products, an in situ spectroscopic study of the reaction of MAH and PP, a study of the melt processing of TPU, and a study of the use of nitroxide radicals as probes for degradation reactions.ududAs mentioned previously, a suitable method for improving polymer properties is polymer blending. Starch is a hydrophilic biodegradable polymer which may be blended with other polymers to produce biodegradable products. In spite of its benefits, it is immiscible with most synthetic polymers, such as polyesters. The main technique for improving the miscibility of starch with the other polymer is a grafting reaction. ududThe reactive extrusion technique was applied to the production of starch and polyester blends, the product of which was a biodegradable aliphatic polyester. In this process dicumyl peroxide (DCP) and maleic anhydride (MAH) were used as an initiator and cross-linker, respectively. Extruded samples were investigated by infrared microscopic mapping using the attenuated total reflectance (ATR) technique. Measurement of various band parameters from the spectra allowed IR maps to be constructed with semi-quantitative information about the distribution of blend components. IR maps were generated by measuring the band area ratio of O-H and C=O stretching bands which are related to starch and polyester, respectively. This was the first time this method has been used for understanding the homogeneity of a polymer blend system. This method successfully indicated that the polyester/starch blend was not a homogenised blend. It was concluded that to improve the homogeneity the reaction conditions should be modified.ududAnother important compatibilisation reaction is the reaction between a polyolefin and MAH. This was investigated by combining a near infrared (NIR) spectrometer with a small laboratory scale extruder, a Haake Minilab. The NIR spectra were collected in situ during melt processing by the use of a fibre optic cable. In addition to this the viscosity of the polymer melt was measured continuously during processing through two pressure transducers within the Minilab extruder. The vinyl C-H stretch overtone of the MAH was clearly seen in the NIR spectra near 6100 cm-1 and diminished over time as the MAH reacted with PP. The spectra obtained were analysed by two techniques: principal component analysis (PCA); and peak area ratios. The peak area ratios were calculated using the =C-H first overtone of MAH with respect to the band observed between 6600 and 7400 cm-1. This band corresponds to a combination band of CH2 and CH3 in PP and was unchanged during the reaction. These data facilitated interpretation of the reaction kinetics and experiments at different temperatures allowed determination of the activation energy of the reaction. These results have thrown new light on the PP-MAH reaction mechanism. It was also shown that although the presence of DCP causes production of a high concentration of macro-radicals it does not have any effect on the rate and kinetics of the reaction. ududAs mentioned previously, one of the limitations of reactive extrusion is degradation of the polymer under high temperatures and shear rates. Hindered amine stabilisers (HAS) are often used as inhibitors to control the thermal-oxidative degradation of polymers. They are used in various polymeric materials but were primarily developed for polyolefins, particularly PP. The stabilisation mechanism of HAS involves interaction firstly with the alkyl peroxyl radicals produced during oxidative degradation so that the hindered amine converts to the corresponding nitroxide. The nitroxide is then able to capture a carbon-centred radical and so retard the subsequent degradation chain reaction.udud1,1,3,3- tetramethyldibenzo[e,g]isoindoline-2-yloxyl (TMDBIO) was used as a probe for investigation of PP during reactive extrusion conditions. The TMDBIO is a profluorescent compound that has been used previously to identify polymer degradation. In the radical form, there is no fluorescence since the unpaired spin on the nitroxide quenches the fluorescence of the phenanthrene moiety. When the radical is removed (by radical trapping or reduction) fluorescence is observed. As a result, the location and intensity of fluorescence can be used as a probe for identification of degradation and to determine the concentration of carbon-centred radicals produced during thermal or mechanical degradation such as occurs during reaction processing. This novel method shows that, the degradation of PP started at the early stage of processing. Also this method can be used as a useful technique to modify the processing conditions to decrease degradation of the polymer during processing. ududThe second system investigated using in situ monitoring via the NIR fibre optic was the melt processing of a TPU nano-composite. This was the first time that the in situ monitoring of TPU nano-composite had been examined. In this investigation the effect of temperature during processing on the TPU molecular structure and rheological behaviour was again investigated. In addition, dispersion of clay nano-particles through the TPU matrix and rheological changes due to this was investigated. This investigation was successful in that it was found that several factors affected the viscosity of the nano-composite. However, to fully understand the degradation mechanism and viscosity changes further studies must be performed.
机译:很少将聚合物用作纯净材料,并且通常通过添加填料或与另一种聚合物共混来改变基线的物理,化学和流变特性,例如分子量,强度,刚度和粘度。但是,由于许多聚合物是不溶混的,因此增容和接枝加工聚合物共混物是提高共混物的混溶性并改善化学,物理和机械性能的非常重要的技术。反应挤出或熔融态加工是其中一种。改善聚合物性能的最合适技术。增容和接枝聚合物加工通常在反应性挤出条件下进行。该技术是一种有效的方法,因为它简单,便宜且处理时间短。尽管反应挤出具有许多优点,但局限性之一是聚合物在高温和遇到的机械应力下会降解。 ud ud在聚合物行业中,由于客户对提高产品质量的需求不断增加,因此通过降低产品成本来优化聚合工艺并且在聚合过程中控制反应变得更加重要。可以说,用于监测聚合过程的任何方法都必须快速,准确和可靠。在线和在线方法都可能参与过程监控。来自过程监控的主要信息用于识别和理解分子结构和变化,优化和改进过程建模以及了解过程是否处于受控状态。这还涉及考虑产品是否具有所需的性能。 ud ud本文介绍了聚合物熔融加工多个方面的研究,包括挤出产品的检查,MAH和PP反应的原位光谱研究,关于TPU熔融加工的研究,以及使用氮氧自由基作为降解反应探针的研究。 ud ud如前所述,一种用于改善聚合物性能的合适方法是聚合物共混。淀粉是一种亲水性可生物降解的聚合物,可以与其他聚合物共混以生产可生物降解的产品。尽管有其优点,但它与大多数合成聚合物(例如聚酯)不能混溶。改善淀粉与其他聚合物混溶性的主要技术是接枝反应。 ud ud反应挤出技术被应用于淀粉和聚酯共混物的生产,其产物是可生物降解的脂肪族聚酯。在该方法中,过氧化二枯基(DCP)和顺丁烯二酸酐(MAH)分别用作引发剂和交联剂。使用衰减全反射率(ATR)技术通过红外显微图对挤压样品进行了研究。从光谱中测量各种波段参数可以使用有关混合成分分布的半定量信息来构建红外图。通过测量分别与淀粉和聚酯有关的O-H和C = O拉伸带的带面积比来产生IR图。这是该方法首次用于理解聚合物共混体系的均匀性。该方法成功地表明聚酯/淀粉共混物不是均质的共混物。得出结论,为改善均质性,应修改反应条件。另一个重要的相容化反应是聚烯烃与MAH之间的反应。通过将近红外(NIR)光谱仪与小型实验室规模的挤出机Haake Minilab结合起来进行了研究。通过使用光缆在熔融加工过程中原位收集NIR光谱。除此之外,在加工过程中通过Minilab挤出机内的两个压力传感器连续测量聚合物熔体的粘度。在6100 cm-1附近的NIR光谱中可以清楚地看到MAH的乙烯基C-H拉伸泛音,并且随着时间的推移,MAH与PP发生反应而逐渐减弱。通过两种技术对获得的光谱进行分析:主成分分析(PCA);主成分分析(PCA)。和峰面积比。使用MAH的= C-H第一泛音相对于6600和7400 cm-1之间观察到的谱带计算峰面积比。该带对应于PP中CH 2和CH 3的组合带,并且在反应过程中没有变化。这些数据有助于解释反应动力学,并且在不同温度下进行的实验可以确定反应的活化能。这些结果为PP-MAH反应机理提供了新的思路。还显示,尽管DCP的存在引起高浓度的大基团的产生,但是它对反应的速率和动力学没有任何影响。 ud ud如前所述,反应挤出的局限性之一是聚合物在高温和剪切速率下的降解。受阻胺稳定剂(HAS)通常用作控制聚合物热氧化降解的抑制剂。它们用于各种聚合材料中,但主要用于聚烯烃,特别是PP。 HAS的稳定机制首先涉及与氧化降解过程中产生的烷基过氧自由基相互作用,从而使受阻胺转化为相应的硝基氧。然后,氮氧化物能够捕获以碳为中心的自由基,因此可延迟后续的降解链反应。 ud ud1,1,1,3,3-四甲基二苯并[e,g]异吲哚啉-2-基氧基(TMDBIO)被用作用于在反应挤出条件下研究PP的探针。 TMDBIO是一种前荧光化合物,以前已用于鉴定聚合物降解。在自由基形式中,没有荧光,因为在氮氧化物上的不成对的自旋猝灭了菲部分的荧光。当自由基被除去(通过自由基捕获或还原)时,观察到荧光。结果,荧光的位置和强度可以用作探针以鉴定降解并确定在热或机械降解例如反应过程中发生的过程中产生的碳中心自由基的浓度。这种新颖的方法表明,PP的降解始于加工的早期阶段。该方法也可以用作改变加工条件以减少加工过程中聚合物降解的有用技术。经由NIR光纤进行现场监测的第二个系统是TPU纳米复合材料的熔融加工。这是首次对TPU纳米复合材料进行现场监测。在这项研究中,再次研究了加工过程中温度对TPU分子结构和流变行为的影响。另外,还研究了粘土纳米颗粒在TPU基质中的分散以及由此引起的流变变化。该研究是成功的,因为发现几种因素影响纳米复合材料的粘度。但是,要完全了解降解机理和粘度变化,必须进行进一步的研究。

著录项

  • 作者

    Moghaddam Lalehvash;

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  • 年度 2008
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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