{"title":"Unveiling the gradient crystalline structure in the poly(ether-b-amide) foams","authors":"Ping Zhu , Lihui Yuan , Feng Tian , Xia Dong","doi":"10.1016/j.polymer.2026.129802","DOIUrl":null,"url":null,"abstract":"<div><div>The microscopic crystalline structures of unfoamed bead (UFB), foamed bead (FB), foamed bead-welded part (FBWP), extrudate (EXT) and foamed extrudate (FEXT) of poly(ether-<em>b</em>-amide) were investigated by micro-wide-angle X-ray diffraction/small angle X-ray scattering (<em>μ</em>WAXD/SAXS). The crystallinity of the polyamide hard segment was improved after super-critical foaming (SCF), and double-melting peaks were incurred. A gradient crystalline structure with a core-skin difference was found in the FB, EXT, and FEXT, where higher crystallinity and orientation were found in the skin parts, i.e., the crystallinity in the skin could be 1 % higher than that in the core. It is not beneficial for a good steam-welding. The failure mode during tear process of FBWP is majorly adhesive failure, secondly cohesive failure of the skin detachment from the core, confirmed by digital image correlation (DIC) of the tear propagation and scanning electron microscope (SEM) of the fractured surface The tensile strength of FEXT and FBWP was 1/4 and 1/16 of that of hot-pressed film (HPF) respectively. The evolution of the microscopic structures of HPF, FEXT and FBP during tensile elongation were probed by <em>in situ</em> WAXD/SAXS. The long periods were increased remarkably after SCF, due to the increased crystallinity and improved phase separation. The lattice orientation of FEXT increased rapidly upon stretching, during which the strain-induced crystallization occurred. However, that of FBWP was not so high, since the inadequate inter-bead adhesion led the FBWP to break prematurely.</div></div>","PeriodicalId":405,"journal":{"name":"Polymer","volume":"351 ","pages":"Article 129802"},"PeriodicalIF":4.5000,"publicationDate":"2026-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032386126002491","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/28 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
The microscopic crystalline structures of unfoamed bead (UFB), foamed bead (FB), foamed bead-welded part (FBWP), extrudate (EXT) and foamed extrudate (FEXT) of poly(ether-b-amide) were investigated by micro-wide-angle X-ray diffraction/small angle X-ray scattering (μWAXD/SAXS). The crystallinity of the polyamide hard segment was improved after super-critical foaming (SCF), and double-melting peaks were incurred. A gradient crystalline structure with a core-skin difference was found in the FB, EXT, and FEXT, where higher crystallinity and orientation were found in the skin parts, i.e., the crystallinity in the skin could be 1 % higher than that in the core. It is not beneficial for a good steam-welding. The failure mode during tear process of FBWP is majorly adhesive failure, secondly cohesive failure of the skin detachment from the core, confirmed by digital image correlation (DIC) of the tear propagation and scanning electron microscope (SEM) of the fractured surface The tensile strength of FEXT and FBWP was 1/4 and 1/16 of that of hot-pressed film (HPF) respectively. The evolution of the microscopic structures of HPF, FEXT and FBP during tensile elongation were probed by in situ WAXD/SAXS. The long periods were increased remarkably after SCF, due to the increased crystallinity and improved phase separation. The lattice orientation of FEXT increased rapidly upon stretching, during which the strain-induced crystallization occurred. However, that of FBWP was not so high, since the inadequate inter-bead adhesion led the FBWP to break prematurely.
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.