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2021 - Ye - Bio-Based Epoxies From Ferulic Acid and Furfuryl Alcohol - Sup

This document provides supporting information for a research article on the synthesis and properties of high-performance bio-based epoxies made from ferulic acid and furfuryl alcohol. It includes 6 figures showing NMR, GC-MS, and FTIR spectra as well as dynamic mechanical analysis results supporting the findings of the main article. The figures provide chemical analysis of the synthesized compounds and compare the cured and uncured epoxy materials.

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Lina K.
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13 views6 pages

2021 - Ye - Bio-Based Epoxies From Ferulic Acid and Furfuryl Alcohol - Sup

This document provides supporting information for a research article on the synthesis and properties of high-performance bio-based epoxies made from ferulic acid and furfuryl alcohol. It includes 6 figures showing NMR, GC-MS, and FTIR spectra as well as dynamic mechanical analysis results supporting the findings of the main article. The figures provide chemical analysis of the synthesized compounds and compare the cured and uncured epoxy materials.

Uploaded by

Lina K.
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Electronic Supplementary Material (ESI) for Green Chemistry.

This journal is © The Royal Society of Chemistry 2021

Supporting Information

High-performance bio-based epoxies from ferulic acid and furfuryl alcohol:

Synthesis and properties

Jiale Ye1,2, Songqi Ma*,2, Binbo Wang2, Qingming Chen1, Kaifeng Huang2, Xiwei Xu2, Qiong

Li2, Sheng Wang2, Na Lu2, and Jin Zhu2

1College of Materials Science and Engineering, Kunming University of Science and

Technology, Kunming 650093, China;

2 Key Laboratory of Bio-based Polymeric Materials Technology and Application of Zhejiang

Province, Laboratory of Polymers and Composites, Ningbo Institute of Materials Technology

and Engineering, Chinese Academy of Sciences, Ningbo 315201, P. R. China;

*Corresponding author: (Songqi Ma) E-mail [email protected], Tel 86-574-87619806.


Contents
Fig. S1 a) 1H NMR, b) 13C NMR and c) GC-MS spectra of GEFA. ......................................3
Fig. S2 Curing of FAE and DDS. ...........................................................................................3
Fig. S3 1H NMR spectra of a) P-FAE and b) after the reaction between P-FAE and GEFA.4
Fig. S4 1H NMR spectra of the Diels-Alder adducts at 140 °C for 6 h and at 200 °C for 2 h.
................................................................................................................................................5
Fig. S5 FTIR spectra of the FAE1GEFA0 system before and after curing. ............................6
Fig. S6 Storage modulus as a function of temperature for the cured epoxy resins by DMA. 6
Fig. S1 a) 1H NMR, b) 13C NMR and c) GC-MS spectra of GEFA.

Fig. S2 Curing of FAE and DDS.


Fig. S3 1H NMR spectra of a) P-FAE and b) after the reaction between P-FAE and GEFA.
Fig. S4 1H NMR spectra of Diels-Alder adducts at 140 °C for 6 h and at 200 °C for 2 h.
Fig. S5 FTIR spectra of the FAE1GEFA0 system before and after curing.

Fig. S6 Storage modulus as a function of temperature for the cured epoxy resins by DMA.

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