Issue 11, 2023

Bio-based non-isocyanate poly(hydroxy urethane)s (PHU) derived from vanillin and CO2

Abstract

As an alternative to the use of hazardous phosgene-based isocyanates for polyurethane preparation, non-isocyanate poly(hydroxy urethanes) (PHU) based on 5-membered cyclic carbonates have been developed. However, to date, most aromatic PHUs are oil-based or based on toxic precursors such as bisphenol-A. In this work, bio-based non-isocyanate poly(hydroxy urethanes) (PHUs) prepared from vanillin are reported for the first time. First, three different vanillin-derived bis-cyclic carbonates were synthesized. Subsequently, each monomer was reacted with two different bis-amines to yield six different PHUs, which were characterized in depth by 1H and 13C NMR spectroscopy, FTIR, SEC and DSC. PHUs based on vanillic acid were found to exhibit thermal properties superior to bisphenol A-based PHUs, with a Tg of around 66 °C. It is envisioned that vanillin-based PHUs could potentially be a safer alternative to harmful bisphenol A-based PHUs and provide a useful strategy for CO2 revalorization, especially considering that vanillin is an abundant byproduct of Kraft lignin production.

Graphical abstract: Bio-based non-isocyanate poly(hydroxy urethane)s (PHU) derived from vanillin and CO2

Supplementary files

Article information

Article type
Paper
Submitted
08 Mar 2023
Accepted
15 May 2023
First published
16 May 2023
This article is Open Access
Creative Commons BY-NC license

Mater. Adv., 2023,4, 2437-2448

Bio-based non-isocyanate poly(hydroxy urethane)s (PHU) derived from vanillin and CO2

N. Fanjul-Mosteirín, L. P. Fonseca, A. P. Dove and H. Sardon, Mater. Adv., 2023, 4, 2437 DOI: 10.1039/D3MA00111C

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements