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Rheological and mechanical properties of recycled painted automotive bumper materials

机译:再生涂漆汽车保险杠材料的流变和机械性能

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摘要

The use of plastics in the automotive industries has increased significantly in the past few years. Concerns for the environment and the management of waste is encouraging the recycling and proper use of scrap material. Among others, polypropylene (PP) based bumpers are targeted for recycling because of their large volume and relatively simple material composition. Most of these bumpers are coated with polyurethane based paint which becomes dispersed into the matrix during reprocessing influencing the material properties. This seemed to be an important issue to investigate as it was shown by some other workers that the lowering of properties by the presence of paint particles was more significant than the material deterioration itself. So, with the complete recycling process, it is important to understand how the dispersed phase influences the processing and later the behaviour of the matrix so that in future investigations this knowledge can be utilised in further development of the recycled material. This has been the main theme of the project with the following major objectives: (i) to remove paint particles from the painted PP bumpers by melt filtration technique (ii) to determine the rheological and mechanical properties of the rubber toughened PP based composites dispersed with paint particles and glass microspheres and (iii) to understand the effect of dispersed phase on these properties by studying the morphology of the composites. Both commercially recycled material and real system blends prepared in the laboratory were studied to observe the effect of dispersed paint on the polymer matrix. Firstly the following materials were characterised using tensile, impact and rheological tests: virgin bumper bar grade material (PPIEPDMlta1c) ; two batches of material injection moulded from the virgin grade and painted with different levels of paint layers as found on car bumpers (unfiltered and melt filtered) and recycled painted bumpers (unfiltered and melt filtered). Extrusion melt filtration was chosen to remove the paint particles from the pp phase and the quantitative measurement of the dispersed phase was done by digital image analysis. Result of this analysis showed that only about 50% paint was removed following filtration. Little variation was observed in viscosity values for all the samples with unfiltered batches showing slightly higher and filtered samples showing slightly lower viscosity compared to the virgin material. The increased value for the first case was attributed for the paint particles acting as the particulate phase in the matrix. On the other hand, lower viscosity was caused by deterioration of material with chain scission of PP. The elongation and impact strength of the paint dispersed batches decreased drastically compared to the virgin material as the paint particles acted as crack initiators and propagators. For the blends prepared, well characterised paint particles were dispersed into the PP/rubber/talc and PP/rubber matrix to be used as the "real" system. Talc itself is used as a filler in the commercial grades to impart greater stiffness, so composites without talc were worth examining to compare the effect of paint over talc. Also "model" filled systems with glass micro spheres were studied to observe the relative importance of particle shape and filler concentration. The choice to use glass as a model filler was primarily based on its spherical shape, non-deformable nature and relatively small surface area. The glass filled systems served as a comparison and helped in the interpretation of the rheological and mechanical properties of the paint dispersed in the rubber toughened talc filled and unfilled PP. The rheological study over the processing temperature range showed that the presence of small fraction of the dispersed phase (upto 1.9 vol% for glass beads and 2.7 vol% for paint particles) had insignificant effect on viscosity and at these levels the effect of particle size, particle size distribution and particle shape can be neglected. Only with increased filler fraction (5 vol %) a trend in increased viscosity was observed. From mechanical testing it was observed that the retention of tensile yield strength was nearly 100% but elongation at break dropped significantly compared to the base matrices. This reduction was explained by poor interphase between filler and matrix. The modulus values for glass bead filled PP/rubber matrix showed an increasing tendency for high rigidity of the filler itself whereas for paint filled matrix it dropped below the base matrix value. For PP/rubber/talc matrix the scenario was different where a decrease in modulus was observed for all the composites. This was explained by the much high rigidity of talc particles over glass beads and paint particles. Though small sized talc particles acted as reinforcing fillers when added to PP/rubber system, the inclusion of second dispersed phase could not overshadow its effect on matrix thus failing as a weak structure. The drop in modulus for paint dispersed matrices was more significant indicating that irregular shaped paint particles had a smaller degree of interaction with the base matrix compared to spherical glass particles. A sharp decrease in impact strength observed for all the composites again explained the poor adhesion between matrix and dispersed phase which was also attributed from the photomicrographs of the fractured specimens. A separated microstructure was revealed for the composites which emphasised the explanation that the inclusions reduced the ability of the elastomer phase to absorb applied energy by reducing the distance between particles. A decrease in fracture energy and toughness for all the composites was also explained by the same. Models were proposed to predict crack propagation through glass bead and paint particle dispersed in the PP/rubber/talc matrices. For glass beads, crack propagation through the composite was attracted to the equator of particles so fractured surfaces showed clear hemispherical holes and top surfaces of debonded particles. For irregular paint dispersed composites, crack propagated through the interphase of filler and matrix thus debonding the paint particles. The composites under study were also related in terms of their rheology, morphology and mechanical properties. A separated microstructure of the composites as observed from the micrographs leads to the explanation of the slight increase in viscosity of filled composites over unfilled ones. Also poor interphase between filler and matrix leads to decreased property values in mechanical tests compared to base matrices.
机译:在过去几年中,塑料在汽车工业中的使用显着增加。对环境和废物管理的关注鼓励废料的回收和正确使用。其中,基于聚丙烯(PP)的保险杠由于其体积大且材料组成相对简单而被回收利用。这些保险杠大多数都涂有聚氨酯基涂料,在后处理过程中会分散到基体中,从而影响材料性能。这似乎是一个重要的研究课题,因为其他一些工人表明,由于涂料颗粒的存在而导致的性能下降比材料变质本身更重要。因此,在完整的回收过程中,重要的是要了解分散相如何影响加工过程以及随后的基质行为,以便在将来的研究中可以将这一知识用于回收材料的进一步开发中。这一直是该项目的主要主题,其主要目标如下:(i)通过熔体过滤技术从涂漆的PP保险杠上去除涂料颗粒(ii)确定分散在其中的橡胶增韧PP基复合材料的流变和机械性能。涂料颗粒和玻璃微球;以及(iii)通过研究复合材料的形态来了解分散相对这些性能的影响。研究了商业回收材料和实验室制备的实际系统共混物,以观察分散涂料对聚合物基体的影响。首先,使用拉伸,冲击和流变测试对以下材料进行了表征:原始保险杠等级材料(PPIEPDMlta1c);两批由原始级注塑而成的材料,并用汽车保险杠(未过滤和熔体过滤)和回收的涂漆保险杠(未过滤和熔体过滤)上的油漆层进行了不同程度的喷涂。选择挤出熔体过滤以从pp相中除去涂料颗粒,并通过数字图像分析对分散相进行定量测量。分析结果表明,过滤后仅除去了约50%的涂料。与原始材料相比,未过滤批次的样品粘度值几乎没有变化,显示出略高的粘度,过滤后的样品粘度略低。第一种情况的增加值归因于在基体中充当颗粒相的涂料颗粒。另一方面,较低的粘度是由于PP的断链而使材料变质引起的。与原始材料相比,分散的涂料批料的伸长率和冲击强度大大降低,因为涂料颗粒充当了裂纹的引发剂和传播剂。对于制备的共混物,将特征明确的涂料颗粒分散到PP /橡胶/滑石粉和PP /橡胶基质中,以用作“真实”涂料。系统。滑石本身被用作商业级的填料,以赋予其更大的刚度,因此,没有滑石的复合材料值得进行比较,以比较油漆对滑石的影响。同样是“模型”。研究了具有玻璃微球的填充系统,以观察颗粒形状和填料浓度的相对重要性。选择使用玻璃作为模型填充物的选择主要是基于其球形,不可变形的特性和相对较小的表面积。玻璃填充系统用作比较,有助于解释分散在橡胶增韧滑石填充和未填充PP中的涂料的流变学和机械性能。在加工温度范围内的流变学研究表明,存在分散相的一小部分(玻璃珠为1.9%(体积),油漆颗粒为2.7vol%)对粘度的影响不明显,而在这些水平上,粒径的影响,可以忽略粒度分布和颗粒形状。仅当增加填料含量(5体积%)时,才观察到粘度增加的趋势。通过机械测试,观察到拉伸屈服强度的保持率接近100%,但断裂伸长率与基础基质相比显着下降。这种减少的原因是填料和基体之间的不良相间相交。玻璃珠填充的PP /橡胶基体的模量值显示出填料本身具有较高刚性的趋势,而涂料填充的基体的模量值则下降至基础基体值以下。对于PP /橡胶/滑石基料,情况有所不同,其中所有复合材料的模量均下降。滑石粉在玻璃珠和涂料颗粒上的刚性很高,可以解释这一点。尽管小粒径的滑石粉在添加到PP /橡胶体系中时可作为增强填料,第二分散相的加入不能掩盖其对基质的作用,因此作为弱结构失败。涂料分散基质的模量下降更为显着,这表明与球形玻璃颗粒相比,不规则形状的涂料颗粒与基础基质的相互作用程度较小。对所有复合材料观察到的冲击强度的急剧下降再次解释了基体和分散相之间的粘附性差,这也归因于断裂样品的显微照片。揭示了复合材料的分离的微观结构,这强调了以下解释:夹杂物通过减小颗粒之间的距离降低了弹性体相吸收施加的能量的能力。同样,所有复合材料的断裂能和韧性均下降。提出了预测通过玻璃珠和PP /橡胶/滑石基体中分散的涂料颗粒的裂纹扩展的模型。对于玻璃珠,裂纹通过复合材料的传播被吸引到颗粒的赤道上,因此断裂的表面显示出清晰的半球形孔和脱胶颗粒的顶表面。对于不规则的涂料分散的复合材料,裂纹会通过填料和基体的界面扩散,从而使涂料颗粒脱粘。所研究的复合材料在流变性,形态和力学性能方面也具有相关性。从显微照片观察到,复合材料的微观结构是分开的,这导致了填充复合材料的粘度略高于未填充复合材料的粘度的解释。与基础基质相比,填料和基质之间的不良相界面也会导致机械测试中的性能值降低。

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    Quazi R;

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