Pressurization induced crystallization of iPP containing self-assembly β-nucleating agents: role of pressurization rate and temperature

IF 4.1 2区 化学 Q2 POLYMER SCIENCE
Yaxin Liu, Cong Wei, Zipei Ding, Huashen Zhang, Jian Xu, Baobao Chang, Zhen Wang, Chuntai Liu, Changyu Shen, Chunguang Shao
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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.

Abstract Image

含自组装β-成核剂的iPP的加压诱导结晶:加压速率和温度的作用
采用广角x射线衍射、偏光显微镜和差示扫描量热法研究了β-成核剂(β-NA)对等规聚丙烯(iPP)的加压诱导结晶(PIC)作用。在PIC过程中发现了中间相与γ-iPP之间的竞争性形成过程。其中,增大加压速率可以显著抑制γ相的形成,并在临界加压速率R1 ~ R2范围内诱导中间相的形成,但当温度超过280℃左右的临界值时,无论加压速率如何,都只能形成中间相。此外,在PIC处理下,β-NA代替β-iPP作为有效的成核剂,促进γ-iPP的形成,并且其自组装形态也可以通过验证加压速率和/或温度来控制。结果,提出了利用“加压”方法调控iPP材料结晶多态性和形貌的合理机理,并建立了压力-温度结晶结构图,分析了加压速率和温度对iPP结晶多态性的协同效应。这表明,在适当的温度范围内,加压可能是一种通用的方法来定制聚合物结晶。
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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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