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Effects of Direct Melt Compounding and Masterbatch Dilution on the Structure and Properties of Nanoclay-filled Polyolefins

机译:直接熔融混合和母料稀释对纳米粘土填充聚烯烃结构和性能的影响

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摘要

The differences that direct melt compounding and masterbatch dilution cause in the properties of melt compounded polypropylene (PP) and high density polyethylene-based (PE-HD) nanocomposites are presented. The results include comparison of properties and morphology of directly melt processed organoclay nanocomposites with similar compounds diluted from commercial and in-house-made masterbatches to clay concentrations of 1, 3, 6, and 8 wt%. The compounds were prepared with a co-rotating Brabender twin-screw extruder. The degree of exfoliation and the dispersion of the nanoclay were verified with transmission electron microscopy and X-ray diffraction. Thermal stability of the materials was examined with thermogravimetric analysis and the mechanical properties of the compounded materials were also determined. The most promising results regarding mechanical behavior were achieved with the in-house-made masterbatch in the form of a notable increase in Young's modulus in both matrices. There was also a distinct increase in impact strength when masterbatch was used. Changes were more pronounced in case of PP. [PUBLICATION ABSTRACT]
机译:提出了直接熔融混合和母料稀释导致熔融混合聚丙烯(PP)和高密度聚乙烯基(PE-HD)纳米复合材料性能方面的差异。结果包括将直接熔融加工的有机粘土纳米复合材料的性质和形态进行比较,该复合材料与从商业和内部自制的母料中稀释的相似化合物的粘土浓度分别为1、3、6、8 wt%。用同向旋转的Brabender双螺杆挤出机制备化合物。用透射电子显微镜和X射线衍射证实了纳米粘土的剥离程度和分散性。通过热重分析检查了材料的热稳定性,并确定了复合材料的机械性能。用自制母料以两种基质的杨氏模量均显着增加的形式获得了有关机械性能的最有希望的结果。当使用母料时,冲击强度也明显增加。 PP的变化更为明显。 [出版物摘要]

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    《Polymer Engineering and Science》 |2009年第7期|p.1438-1446|共9页
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    Pirkko Eteläaho, Katja Nevalainen, Reija Suihkonen, Jyrki Vuorinen, KaIIe Hanhi, Pentti JärveläDepartment of Materials Science, Laboratory of Plastics and Elastomer Technology, Tampere University of Technology, Korkeakoulunkatu 6, 33720 Tampere, FinlandCorrespondence to: P. Eteläaho, e-mail: pirkko.etelaaho@tut.fiDOI 10.1002/pen.21270Published online in Wiley InterScience (www.interscience.wiley.com).© 2009 Society of Plastics Engineers,;

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