{"title":"Comprehensive performance improvement and functional upgrade of Magnolia-based epoxy resins","authors":"Xinru Bai, Zhiyong Li, Yuting Dong, Xinyi Gao, Jingjing Meng","doi":"10.1016/j.reactfunctpolym.2024.106129","DOIUrl":null,"url":null,"abstract":"<div><div>The magnolol- (MEP) and honokiol-epoxy resin (HEP) were prepared from the extract of the natural plant Magnolia officinalis. Those monomers were cured with hardeners, such as 4,4-diamino diphenyl sulfone (DDS) and 4,4′-bis (3-aminophenoxy) diphenyl sulfone (BDS), respectively via solvent-free process to fabricate networks with excellent mechanical properties. The curing procedures occurred in a wide temperature interval (65 °C), which made the concerning vacuum-assisted resin infusion feasible. Notedly, all combinations exhibited increased thermal stability (<em>T</em><sub><em>d5</em></sub>, 359.7–381.9 °C) with <em>T</em><sub><em>max</em></sub> fluctuating around 450 °C. The phase transition temperature (<em>T</em><sub><strong><em>α</em></strong></sub>) screen suggested that except MEP/BDS (<em>T</em><sub><strong><em>α</em></strong></sub>, 147.2 °C), other combinations varied from 264.2 °C to 281.2 °C. In addition, DDS allowed the networks with slightly lower thermal expansion coefficients (<em>CTE,</em> 68.1 ppm/ <sup>o</sup>C, <180 °C for HEP/DDS), while the BDS yielded relatively high <em>CTE</em> values (87.1 ppm/ <sup>o</sup>C, <106 °C, for MEP/BDS). The <em>LOI</em> value (33 %) and vertical burning test (UL-94) indicated their outstanding flame retardancy (UL 94 <em>V</em>-0). Furthermore, for MEP/BDS, the unique solvolysis (in DMF or THF) and thermally induced shape memory properties along with the superior flame retardancy demonstrated its overall high performances. As a whole, these performance improvements further facilitate the high-end applications of sustainable resins in cutting-edge areas.</div></div>","PeriodicalId":20916,"journal":{"name":"Reactive & Functional Polymers","volume":"207 ","pages":"Article 106129"},"PeriodicalIF":4.5000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reactive & Functional Polymers","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1381514824003043","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
The magnolol- (MEP) and honokiol-epoxy resin (HEP) were prepared from the extract of the natural plant Magnolia officinalis. Those monomers were cured with hardeners, such as 4,4-diamino diphenyl sulfone (DDS) and 4,4′-bis (3-aminophenoxy) diphenyl sulfone (BDS), respectively via solvent-free process to fabricate networks with excellent mechanical properties. The curing procedures occurred in a wide temperature interval (65 °C), which made the concerning vacuum-assisted resin infusion feasible. Notedly, all combinations exhibited increased thermal stability (Td5, 359.7–381.9 °C) with Tmax fluctuating around 450 °C. The phase transition temperature (Tα) screen suggested that except MEP/BDS (Tα, 147.2 °C), other combinations varied from 264.2 °C to 281.2 °C. In addition, DDS allowed the networks with slightly lower thermal expansion coefficients (CTE, 68.1 ppm/ oC, <180 °C for HEP/DDS), while the BDS yielded relatively high CTE values (87.1 ppm/ oC, <106 °C, for MEP/BDS). The LOI value (33 %) and vertical burning test (UL-94) indicated their outstanding flame retardancy (UL 94 V-0). Furthermore, for MEP/BDS, the unique solvolysis (in DMF or THF) and thermally induced shape memory properties along with the superior flame retardancy demonstrated its overall high performances. As a whole, these performance improvements further facilitate the high-end applications of sustainable resins in cutting-edge areas.
期刊介绍:
Reactive & Functional Polymers provides a forum to disseminate original ideas, concepts and developments in the science and technology of polymers with functional groups, which impart specific chemical reactivity or physical, chemical, structural, biological, and pharmacological functionality. The scope covers organic polymers, acting for instance as reagents, catalysts, templates, ion-exchangers, selective sorbents, chelating or antimicrobial agents, drug carriers, sensors, membranes, and hydrogels. This also includes reactive cross-linkable prepolymers and high-performance thermosetting polymers, natural or degradable polymers, conducting polymers, and porous polymers.
Original research articles must contain thorough molecular and material characterization data on synthesis of the above polymers in combination with their applications. Applications include but are not limited to catalysis, water or effluent treatment, separations and recovery, electronics and information storage, energy conversion, encapsulation, or adhesion.