Real-Time Raman Spectroscopy of PhotopolymerizationDynamics in Ethylene Glycol Methyl Ether Acrylate‑<i>g</i>‑Epoxidized Natural Rubber

Natural rubber (NR) is a promising material for polymer electrolytes (PEs) due to its natural abundance and desirable properties, including soft and elastic texture at room temperature, adhesive qualities, and low glass transition temperature (<i>T</i><sub>g</sub>). Additionally, it is more sustainable compared to synthetic polymers. However, its low ion transport capability poses a challenge for electrochemical applications such as lithium-ion batteries. To address this limitation, ethylene glycol methyl ether acrylate (EGMEA) was grafted onto an epoxidized natural rubber (ENR-25) matrix at varying grafting ratios, optimizing the curing time. Photopolymerization was employed due to its rapid reaction kinetics, customizable monomer selection for tailored physical properties, and energy-efficient initiation via illumination. <i>In situ</i> Raman spectroscopy provided insights into the kinetics, mechanisms, and curing times of the reactions. The synthesis of EGMEA-<i>g</i>-ENR was confirmed through infrared (IR) and <sup>1</sup>H NMR analyses, which validated the successful grafting of EGMEA onto ENR-25. A notable decrease in the molecular weight and polydispersity index (PDI) was observed, approaching unity, indicating improved polymer homogeneity. This decrease in molecular weight is likely due to the degradation of ENR-25 during the ultraviolet (UV)-curing process, resulting in a lower <i>T</i><sub>g</sub> (<−43 °C) compared to that of ENR-25 (−35 °C). EGMEA itself has no <i>T</i><sub>g</sub> but exhibits a <i>T</i><sub>m</sub> of −42 °C and a <i>T</i><sub>c</sub> of −65 °C. This is favorable for enhancing the ion transport in polymer electrolytes. Additionally, a significant correlation was found between the grafting efficiency and different EGMEA grafting ratios. The grafting efficiency reached up to 61.95%, with a strong correlation between the grafting efficiency and grafting ratio (<i>R</i><sup>2</sup> = 0.89). This research highlights the potential of rubber-based modification through photopolymerization for developing framework-based solid polymer electrolytes, particularly for applications in lithium-ion batteries.

Publication Details

Journal
Figshare
Published
2025-02-04
DOI
https://doi.org/10.1021/acsapm.4c03593.s001
Primary Topic
Polymer composites and self-healing
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article
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article

Real-Time Raman Spectroscopy of PhotopolymerizationDynamics in Ethylene Glycol Methyl Ether Acrylate‑g‑Epoxidized Natural Rubber

Figshare
Polymer composites and self-healing
article

Real-Time Raman Spectroscopy of PhotopolymerizationDynamics in Ethylene Glycol Methyl Ether Acrylate‑g‑Epoxidized Natural Rubber

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Abstract

Natural rubber (NR) is a promising material for polymer electrolytes (PEs) due to its natural abundance and desirable properties, including soft and elastic texture at room temperature, adhesive qualities, and low glass transition temperature (<i>T</i><sub>g</sub>). Additionally, it is more sustainable compared to synthetic polymers. However, its low ion transport capability poses a challenge for electrochemical applications such as lithium-ion batteries. To address this limitation, ethylene glycol methyl ether acrylate (EGMEA) was grafted onto an epoxidized natural rubber (ENR-25) matrix at varying grafting ratios, optimizing the curing time. Photopolymerization was employed due to its rapid reaction kinetics, customizable monomer selection for tailored physical properties, and energy-efficient initiation via illumination. <i>In situ</i> Raman spectroscopy provided insights into the kinetics, mechanisms, and curing times of the reactions. The synthesis of EGMEA-<i>g</i>-ENR was confirmed through infrared (IR) and <sup>1</sup>H NMR analyses, which validated the successful grafting of EGMEA onto ENR-25. A notable decrease in the molecular weight and polydispersity index (PDI) was observed, approaching unity, indicating improved polymer homogeneity. This decrease in molecular weight is likely due to the degradation of ENR-25 during the ultraviolet (UV)-curing process, resulting in a lower <i>T</i><sub>g</sub> (<−43 °C) compared to that of ENR-25 (−35 °C). EGMEA itself has no <i>T</i><sub>g</sub> but exhibits a <i>T</i><sub>m</sub> of −42 °C and a <i>T</i><sub>c</sub> of −65 °C. This is favorable for enhancing the ion transport in polymer electrolytes. Additionally, a significant correlation was found between the grafting efficiency and different EGMEA grafting ratios. The grafting efficiency reached up to 61.95%, with a strong correlation between the grafting efficiency and grafting ratio (<i>R</i><sup>2</sup> = 0.89). This research highlights the potential of rubber-based modification through photopolymerization for developing framework-based solid polymer electrolytes, particularly for applications in lithium-ion batteries.

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Real-Time Raman Spectroscopy of PhotopolymerizationDynamics in Ethylene Glycol Methyl Ether Acrylate‑<i>g</i>‑Epoxidized Natural Rubber · Figshare (2025) | TGRS Research Map | TGRS