{"title":"Sustainable soybean oil acrylate for boronic ester vitrimer: Self-healing, reprocessable and extensive elongation performance","authors":"Chandan Bodhak , Pranabesh Sahu , Ram K. Gupta","doi":"10.1016/j.polymer.2025.128095","DOIUrl":null,"url":null,"abstract":"<div><div>Vitrimers have currently emerged as an ideal alternative to conventional thermosetting resins combining the benefits of both thermoplastic and thermoset. But, maintaining the superior performance of vitrimers with good mechanical and stimuli-responsive properties still presents significant challenges. Epoxidized plant oil-derived thermosets are typically constrained by their non-processability and poor mechanical qualities. Henceforth, the development of smart, recyclable, and eco-friendly benevolent thermosets by integrating dynamic covalent bonds into cross-linked polymer networks can resolve the trade-off to overcome these drawbacks. In this work, we demonstrate a one-pot thermally-controlled “<em>thiol-acrylate”</em> coupling between a novel soybean oil acrylate (ESBO_HEA) and dynamic diboronic ester dithiol (DBDT) cross-linker to prepare a self-healable biobased vitrimer employing the green chemistry protocols. The synthesized ESBO_HEA-DBDT vitrimers with covalently cross-linked networks can alter the topologies through the exchange of reversible bonds of boronic ester, which allows room temperature self-healing phenomenon. Thermomechanical characteristics and vitrimeric features have been studied by dynamic mechanical analysis, showing that stress relaxes very quickly at low temperatures, leveraging the dioxaborolane exchange metathesis. The absolute value of glass transition temperature (T<sub>g</sub>) determined from DMA analysis was 5.22 °C, above which the vitrimer exhibits dynamic nature by associative boronic ester exchange. Moreover, the developed vitrimer demonstrates extensive elongation (700–1200 %) properties and excellent reprocessability. Even after 2 cycles of reprocessing, the mechanical characteristics of the reprocessed vitrimers were retained as compared to the original materials. The self-healing efficiency of the biobased vitrimers reached 100 % at room temperature in less than 15 h, whereas the sample achieved complete healing within 4 h when thermally triggered at 50 °C. Through dynamic-mechanical analyses, ESBO_HEA vitrimer reveals remarkably short relaxation time of 15.6 s at 25 °C and an activation energy of 8.70 kJ/mol. In addition, it can be easily recycled by reversibly hydrolyzing in 95 % ethanol and then evaporating the solvent to regenerate the original vitrimer. Briefly, the present research illustrates the potent malleability, reprocessability, self-healing, and extensive elongation properties of the covalently cross-linked vitrimers derived exclusively from renewable resources.</div></div>","PeriodicalId":405,"journal":{"name":"Polymer","volume":"320 ","pages":"Article 128095"},"PeriodicalIF":4.1000,"publicationDate":"2025-01-29","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/S0032386125000813","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
Vitrimers have currently emerged as an ideal alternative to conventional thermosetting resins combining the benefits of both thermoplastic and thermoset. But, maintaining the superior performance of vitrimers with good mechanical and stimuli-responsive properties still presents significant challenges. Epoxidized plant oil-derived thermosets are typically constrained by their non-processability and poor mechanical qualities. Henceforth, the development of smart, recyclable, and eco-friendly benevolent thermosets by integrating dynamic covalent bonds into cross-linked polymer networks can resolve the trade-off to overcome these drawbacks. In this work, we demonstrate a one-pot thermally-controlled “thiol-acrylate” coupling between a novel soybean oil acrylate (ESBO_HEA) and dynamic diboronic ester dithiol (DBDT) cross-linker to prepare a self-healable biobased vitrimer employing the green chemistry protocols. The synthesized ESBO_HEA-DBDT vitrimers with covalently cross-linked networks can alter the topologies through the exchange of reversible bonds of boronic ester, which allows room temperature self-healing phenomenon. Thermomechanical characteristics and vitrimeric features have been studied by dynamic mechanical analysis, showing that stress relaxes very quickly at low temperatures, leveraging the dioxaborolane exchange metathesis. The absolute value of glass transition temperature (Tg) determined from DMA analysis was 5.22 °C, above which the vitrimer exhibits dynamic nature by associative boronic ester exchange. Moreover, the developed vitrimer demonstrates extensive elongation (700–1200 %) properties and excellent reprocessability. Even after 2 cycles of reprocessing, the mechanical characteristics of the reprocessed vitrimers were retained as compared to the original materials. The self-healing efficiency of the biobased vitrimers reached 100 % at room temperature in less than 15 h, whereas the sample achieved complete healing within 4 h when thermally triggered at 50 °C. Through dynamic-mechanical analyses, ESBO_HEA vitrimer reveals remarkably short relaxation time of 15.6 s at 25 °C and an activation energy of 8.70 kJ/mol. In addition, it can be easily recycled by reversibly hydrolyzing in 95 % ethanol and then evaporating the solvent to regenerate the original vitrimer. Briefly, the present research illustrates the potent malleability, reprocessability, self-healing, and extensive elongation properties of the covalently cross-linked vitrimers derived exclusively from renewable resources.
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.