{"title":"Pressurization induced crystallization of iPP containing self-assembly β-nucleating agents: role of pressurization rate and temperature","authors":"Yaxin Liu, Cong Wei, Zipei Ding, Huashen Zhang, Jian Xu, Baobao Chang, Zhen Wang, Chuntai Liu, Changyu Shen, Chunguang Shao","doi":"10.1016/j.polymer.2025.128026","DOIUrl":null,"url":null,"abstract":"Pressurization-induced crystallization (PIC) of isotactic polypropylene (iPP) with the β-nucleating agent (β-NA) was investigated by wide-angle X-ray diffraction, polarizing microscopy and differential scanning calorimetry measurement. A competitive formation process between the mesophase and γ-iPP was found in the PIC process. Specifically, increasing the pressurization rate can significantly suppress the formation of γ-phase and induce the formation of mesophase with the range between the critical pressurization rate from <strong>R</strong><sub><strong>1</strong></sub> to <strong>R</strong><sub><strong>2</strong></sub>, however, when the temperature exceeds a critical value of about 280 °C, only mesophase forms despite any pressurization rate. Moreover, instead of β-iPP, β-NA serves as an effective nucleating agent and promotes the formation of γ-iPP under PIC treatment, and its self-assembly morphology can also be controlled by verifying pressurization rates and/or temperatures. As a result, a reasonable mechanism was proposed to show how to tune the crystalline polymorphism and morphology of iPP materials by using the “pressurization” method, and a pressure-temperature crystallization structural diagram was established to analyze the synergistic effect of pressurization rate and temperature on the crystallization polymorphism of iPP. It demonstrates that pressurization is likely to be a universal method for tailoring polymer crystallization within an appropriate temperature range.","PeriodicalId":405,"journal":{"name":"Polymer","volume":"5 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-01-03","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.2025.128026","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
Pressurization-induced crystallization (PIC) of isotactic polypropylene (iPP) with the β-nucleating agent (β-NA) was investigated by wide-angle X-ray diffraction, polarizing microscopy and differential scanning calorimetry measurement. A competitive formation process between the mesophase and γ-iPP was found in the PIC process. Specifically, increasing the pressurization rate can significantly suppress the formation of γ-phase and induce the formation of mesophase with the range between the critical pressurization rate from R1 to R2, however, when the temperature exceeds a critical value of about 280 °C, only mesophase forms despite any pressurization rate. Moreover, instead of β-iPP, β-NA serves as an effective nucleating agent and promotes the formation of γ-iPP under PIC treatment, and its self-assembly morphology can also be controlled by verifying pressurization rates and/or temperatures. As a result, a reasonable mechanism was proposed to show how to tune the crystalline polymorphism and morphology of iPP materials by using the “pressurization” method, and a pressure-temperature crystallization structural diagram was established to analyze the synergistic effect of pressurization rate and temperature on the crystallization polymorphism of iPP. It demonstrates that pressurization is likely to be a universal method for tailoring polymer crystallization within an appropriate temperature range.
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.