Towards sugar- and lignin-based polyesters and polyurethanes with enhanced properties
Författare
Summary, in English
The enormous production and consumption of fossil-based plastics has caused severe environmental challenges such as pollution of the ocean, increased CO2-emissions, and various health problems. Many of
these concerns are intimately connected to the use of fossil fuels in the production of polymers. For this reason, there is a considerable interest to develop bio-based monomers to mitigate some of the issues connected to
fossil-based plastics. However, new bio-based monomers are often expensive and need some material advantages to facilitate their market entry. In this context, we have designed several new monomers by
converting bio-based molecules such as 5-chloromethylfurfural (CMF), 5-hydroxymethylfurfural (HMF) and vanillin into rigid diols for polyester and polyurethane synthesis. This thesis has been divided into 5 chapters
describing the most important findings from each underlying project.
In Chapter 1 and 2, HMF was reacted with pentaerythritol and di(trimethylolpropane) to make two rigid diols with cyclic acetal structures. The monomer made from HMF and pentaerythritol was predicted to have an
exceptionally low carbon footprint according to our LCA calculations. These diols were further used to synthesize a series of polyesters and polyurethanes with increased glass transition temperatures. Polyurethane
synthesis was deemed more suitable for this type of monomers, since degradation occurred at the high temperatures required for polyester synthesis. The obtained polyurethanes were used to prepare coatings and
textile fibers. Furthermore, the cyclic acetal structure of the monomers enabled chemical recycling under acidic conditions. In Chapter 3, HMF was produced in a continuous process from fructose, using water and
dimethylcarbonate (DMC) in a biphasic system. Both yield and conversion were excellent, demonstrating the utility of DMC for HMF synthesis. The HMF synthesized by this method was sufficiently pure for preparation of
the monomers in Chapters 1 and 2 in comparable yields to commercial HMF. In Chapter 4, three rigid diols were prepared from CMF and various lignin-based monomeric aldehydes including 4-hydroxybenzaldehyde, vanillin and syringaldehyde. The diol made from vanillin and CMF was used to prepare a series of thermoplastic polyurethanes with increased glass transition temperatures. The polymers were then cross-linked with DielsAlder chemistry, which could be reversed at higher temperature. This may facilitate its reprocessing and recycling. In Chapter 5, two rigid monomers were produced from potentially lignin-derived phenols, and used to prepare a series of polyesters with tunable thermal properties. The polymers could potentially be chemically recycled by acid hydrolysis.
these concerns are intimately connected to the use of fossil fuels in the production of polymers. For this reason, there is a considerable interest to develop bio-based monomers to mitigate some of the issues connected to
fossil-based plastics. However, new bio-based monomers are often expensive and need some material advantages to facilitate their market entry. In this context, we have designed several new monomers by
converting bio-based molecules such as 5-chloromethylfurfural (CMF), 5-hydroxymethylfurfural (HMF) and vanillin into rigid diols for polyester and polyurethane synthesis. This thesis has been divided into 5 chapters
describing the most important findings from each underlying project.
In Chapter 1 and 2, HMF was reacted with pentaerythritol and di(trimethylolpropane) to make two rigid diols with cyclic acetal structures. The monomer made from HMF and pentaerythritol was predicted to have an
exceptionally low carbon footprint according to our LCA calculations. These diols were further used to synthesize a series of polyesters and polyurethanes with increased glass transition temperatures. Polyurethane
synthesis was deemed more suitable for this type of monomers, since degradation occurred at the high temperatures required for polyester synthesis. The obtained polyurethanes were used to prepare coatings and
textile fibers. Furthermore, the cyclic acetal structure of the monomers enabled chemical recycling under acidic conditions. In Chapter 3, HMF was produced in a continuous process from fructose, using water and
dimethylcarbonate (DMC) in a biphasic system. Both yield and conversion were excellent, demonstrating the utility of DMC for HMF synthesis. The HMF synthesized by this method was sufficiently pure for preparation of
the monomers in Chapters 1 and 2 in comparable yields to commercial HMF. In Chapter 4, three rigid diols were prepared from CMF and various lignin-based monomeric aldehydes including 4-hydroxybenzaldehyde, vanillin and syringaldehyde. The diol made from vanillin and CMF was used to prepare a series of thermoplastic polyurethanes with increased glass transition temperatures. The polymers were then cross-linked with DielsAlder chemistry, which could be reversed at higher temperature. This may facilitate its reprocessing and recycling. In Chapter 5, two rigid monomers were produced from potentially lignin-derived phenols, and used to prepare a series of polyesters with tunable thermal properties. The polymers could potentially be chemically recycled by acid hydrolysis.
Avdelning/ar
Publiceringsår
2022-05-25
Språk
Engelska
Fulltext
Dokumenttyp
Doktorsavhandling
Förlag
Centre for Analysis and Synthesis, Department of Chemistry, Lund University
Ämne
- Polymer Chemistry
Nyckelord
- Polyesters
- Polyurethane
- Bio-based Materials
- HMF
- Recycling
- Vanillin
Status
Published
Handledare
ISBN/ISSN/Övrigt
- ISBN: 978-91-7422-890-8
- ISBN: 978-91-7422-889-2
Försvarsdatum
25 maj 2022
Försvarstid
09:00
Försvarsplats
Lecture Hall KC:B, Kemicentrum, Naturvetarvägen 14, Faculty of Engineering LTH, Lund University, Lund.
Opponent
- Filip Du Prez (Prof.)