{"title":"SEPS Elastomer-induced β-Crystallization and the Role of Isothermal Crystallization on Enhancing the Low-Temperature Toughness of Polypropylene","authors":"Jiayi Wang, Wenwen Yu, Zhiyi Zhang, Jiahao Shen, Ruimiao Liang, Xiaotian Nan, Fuyong Liu, Fengbo Zhu, Yonggang Shangguan, Qiang Zheng","doi":"10.1016/j.polymer.2024.127948","DOIUrl":null,"url":null,"abstract":"In the quest to develop high-performance polypropylene (PP) blends with enhanced toughness, a blend was prepared by integrating poly(styrene-ethylene/propylene-styrene) (SEPS), which functions not only as an elastomer but also as a <em>β</em>-nucleating agent. The dispersion with a smaller interparticle distance of SEPS and its formation of an entangled network within PP significantly enhance the material’s toughness, shifting the brittle-ductile transition temperature to lower values. Under natural cooling conditions, only a low amount of <em>β</em>-crystals forms. However, isothermal crystallization of PP with only elastomer added leads to a substantial increase in the quantity and aggregation of <em>β</em>-spherulites, resulting in enhanced intercrystalline connectivity and the development of “flower”-like aggregates. This unique microstructure, facilitated by SEPS, is highly effective in stress transfer and impact energy absorption. After isothermal crystallization, the relative content of <em>β</em>-crystals increases significantly, from 9.00% to 29.55%, leading to a remarkable 89.95% increase in the impact strength of PP/SEPS blends at -10°C. Importantly, the <em>β</em>-crystals produced through isothermal crystallization with SEPS as a nucleating agent exhibit greater stability compared to those formed using other <em>β</em>-nucleating agents.","PeriodicalId":405,"journal":{"name":"Polymer","volume":"40 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.polymer.2024.127948","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
In the quest to develop high-performance polypropylene (PP) blends with enhanced toughness, a blend was prepared by integrating poly(styrene-ethylene/propylene-styrene) (SEPS), which functions not only as an elastomer but also as a β-nucleating agent. The dispersion with a smaller interparticle distance of SEPS and its formation of an entangled network within PP significantly enhance the material’s toughness, shifting the brittle-ductile transition temperature to lower values. Under natural cooling conditions, only a low amount of β-crystals forms. However, isothermal crystallization of PP with only elastomer added leads to a substantial increase in the quantity and aggregation of β-spherulites, resulting in enhanced intercrystalline connectivity and the development of “flower”-like aggregates. This unique microstructure, facilitated by SEPS, is highly effective in stress transfer and impact energy absorption. After isothermal crystallization, the relative content of β-crystals increases significantly, from 9.00% to 29.55%, leading to a remarkable 89.95% increase in the impact strength of PP/SEPS blends at -10°C. Importantly, the β-crystals produced through isothermal crystallization with SEPS as a nucleating agent exhibit greater stability compared to those formed using other β-nucleating agents.
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.