The effects of stretching on the mechanical properties of neat and nucleated isotactic polypropylene and its enhancement mechanism

IF 4.1 2区 化学 Q2 POLYMER SCIENCE
Enci Zhu , Lijuan Wei , Zhilan Jin , Zhipeng Liu , Shicheng Zhao
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Abstract

Both stretching and adding nucleating agent can improve the mechanical properties of isotactic polypropylene (iPP), but their combined effects and mechanisms remain unclear. In this paper, α-PP and β-PP were induced by different nucleating agents and the effects of stretching on their mechanical properties and their mechanisms were studied. According to the results, stiffness and toughness of iPP can be enhanced simultaneously through stretching. After stretching, the flexural modulus, tensile strength, and impact strength of α-PP were increased by 145 %, 379 % and 816 % while those of β-PP were increased by 208 %, 486 % and 1316 % individually at 23 °C. Typically, the mechanical properties of iPP will significantly decrease at low temperature. The impact strengths of α-PP and β-PP were reduced by 51.0 % and 75.2 % at −20 °C respectively. However, after stretching, their toughness hardly decreased. Then the enhancement mechanism was investigated by differential scanning calorimeter (DSC), dynamic mechanical analysis (DMA), Raman laser spectrometer (RLS), scanning electron microscope (SEM) and micro computed tomography (micro-CT). The results indicated that the cavities were generated during stretching, which can absorb energy when fractured and improve the toughness of iPP. The increases in crystallinity, the interphase iPP content and orientation result in the improved stiffness. The amorphous phase almost disappeared, which contributes to the improvement of mechanical properties of iPP at low temperature. Additionally, stretched β-PP exhibited a higher orientation and more obvious cavitation phenomenon than stretched α-PP, leading to its superior mechanical performance. This paper not only provides a new method to improve the stiffness and toughness of iPP, especially the toughness at low temperature, but also elucidates the enhancement mechanisms.

Abstract Image

Abstract Image

拉伸对整齐成核等规聚丙烯力学性能的影响及其增强机理
拉伸和加入成核剂都能改善等规聚丙烯(iPP)的力学性能,但两者的共同作用及其机理尚不清楚。本文采用不同成核剂诱导α-PP和β-PP,研究拉伸对其力学性能的影响及其机理。结果表明,拉伸可以同时提高iPP的刚度和韧性。在23℃拉伸后,α-PP的抗弯模量、抗拉强度和冲击强度分别提高了145%、379%和816%,β-PP的抗弯模量、抗拉强度和冲击强度分别提高了208%、486%和1316%。通常情况下,低温下iPP的力学性能会显著下降。α-PP和β-PP在-20℃时的冲击强度分别降低51.0%和75.2%。拉伸后,其韧性几乎没有下降。然后通过差示扫描量热仪(DSC)、动态力学分析(DMA)、拉曼激光光谱仪(RLS)、扫描电镜(SEM)和微计算机断层扫描(micro- ct)研究了增强机理。结果表明:在拉伸过程中产生空腔,可吸收断裂时的能量,提高iPP的韧性;结晶度、相间iPP含量和取向的增加导致硬度的提高。非晶相几乎消失,有利于iPP低温力学性能的提高。与拉伸后的α-PP相比,拉伸后的β-PP具有更高的取向和更明显的空化现象,从而具有更优越的力学性能。本文不仅为提高iPP的刚度和韧性,特别是低温韧性提供了一种新的方法,而且阐明了增强机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Polymer
Polymer 化学-高分子科学
CiteScore
7.90
自引率
8.70%
发文量
959
审稿时长
32 days
期刊介绍: Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics. The main scope is covered but not limited to the following core areas: Polymer Materials Nanocomposites and hybrid nanomaterials Polymer blends, films, fibres, networks and porous materials Physical Characterization Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films Polymer Engineering Advanced multiscale processing methods Polymer Synthesis, Modification and Self-assembly Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization Technological Applications Polymers for energy generation and storage Polymer membranes for separation technology Polymers for opto- and microelectronics.
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