{"title":"Solvent induced crystallization and phase transition of syndiotactic polymethoxystyrene investigated using In situ wide angle X-ray diffraction","authors":"Hai Wang , Xue Jin , Dongmei Cui","doi":"10.1016/j.polymer.2024.127803","DOIUrl":null,"url":null,"abstract":"<div><div>Solvent induced crystallization and phase transition is an interesting phenomenon that has been observed in many kinds of semicrystalline polymer. In the case of syndiotactic polystyrene (SPS) which exhibits complicated phase transition behavior, this process may be different when the phenyl rings are substituted by polarity groups. In our previous work, the crystal structures of a series of –OCH<sub>3</sub> (OMe) substituted SPS and OMe-SPS/solvent complexes were analyzed (<em>Macromolecules</em> <strong>2021</strong>, <em>54</em>, 1881 and <em>Macromolecules</em> <strong>2022</strong>, 55, <em>8222</em>). In this particular work, the phase transition behavior of OMe-SPS, especially meta-OMe-SPS with different initial crystalline structures was discussed based on in situ 2-dimensional wide-angle X-ray diffractions (2D-WAXD) in the presence of organic solvent. It is found that meta-OMe-SPS in amorphous state and mesophase shows similar solvent induced phase transition like the cases of SPS. <del>However</del> Meanwhile, highly crystalline and oriented meta-OMe-SPS also exhibits organic solvent induced phase transition from β form with planar zigzag conformation into δ form with helical conformation, which<del>is</del> has not been observed in SPS. The subsequent heating of meta-OMe-SPS δ and γ forms does not form β form, which is <del>also</del> unlike the situation of SPS δ/δ<sub>e</sub>-γ-α/β transition. The OMe substituted group that changes the polarity of the phenyl rings may be the chemical structure region of affecting the chain conformation energy and phase transition behavior.</div></div>","PeriodicalId":405,"journal":{"name":"Polymer","volume":"315 ","pages":"Article 127803"},"PeriodicalIF":4.1000,"publicationDate":"2024-11-07","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/S003238612401139X","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
Solvent induced crystallization and phase transition is an interesting phenomenon that has been observed in many kinds of semicrystalline polymer. In the case of syndiotactic polystyrene (SPS) which exhibits complicated phase transition behavior, this process may be different when the phenyl rings are substituted by polarity groups. In our previous work, the crystal structures of a series of –OCH3 (OMe) substituted SPS and OMe-SPS/solvent complexes were analyzed (Macromolecules2021, 54, 1881 and Macromolecules2022, 55, 8222). In this particular work, the phase transition behavior of OMe-SPS, especially meta-OMe-SPS with different initial crystalline structures was discussed based on in situ 2-dimensional wide-angle X-ray diffractions (2D-WAXD) in the presence of organic solvent. It is found that meta-OMe-SPS in amorphous state and mesophase shows similar solvent induced phase transition like the cases of SPS. However Meanwhile, highly crystalline and oriented meta-OMe-SPS also exhibits organic solvent induced phase transition from β form with planar zigzag conformation into δ form with helical conformation, whichis has not been observed in SPS. The subsequent heating of meta-OMe-SPS δ and γ forms does not form β form, which is also unlike the situation of SPS δ/δe-γ-α/β transition. The OMe substituted group that changes the polarity of the phenyl rings may be the chemical structure region of affecting the chain conformation energy and phase transition behavior.
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.