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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Kononenko, Denys |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Šuljagić, Marija |
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| Kalteremidou, Kalliopi-Artemi | Brussels |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Blanpain, Bart |
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| Ali, M. A. |
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| Popa, V. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Farmer, Thomas James
University of York
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (12/12 displayed)
- 2020Effects of Methyl Branching on the Properties and Performance of Furandioate-Adipate Copolyesters of Bio-Based Secondary Diolscitations
- 2019Fabrication of PES/PVP Water Filtration Membranes Using Cyrene®, a Safer Bio-Based Polar Aprotic Solventcitations
- 2019Improving the Post-polymerization Modification of Bio-Based Itaconate Unsaturated Polyesters: Catalyzing Aza-Michael Additions With Reusable Iodine on Acidic Aluminacitations
- 2018A methodical selection process for the development of ketones and esters as bio-based replacements for traditional hydrocarbon solventscitations
- 2018Post-polymerization modification of bio-based polymerscitations
- 2018Elucidating enzymatic polymerisationscitations
- 2017Wholly biomass derivable sustainable polymers by ring-opening metathesis polymerisation of monomers obtained from furfuryl alcohol and itaconic anhydridecitations
- 20172,2,5,5-Tetramethyltetrahydrofuran (TMTHF)citations
- 2017New bio-based monomers::Tuneable polyester properties using branched diols from biomasscitations
- 2017New bio-based monomers:citations
- 2016Ring opening metathesis polymerisation of a new bio-derived monomer from itaconic anhydride and furfuryl alcoholcitations
- 2015Bio-derived materials as a green route for precious & critical metal recovery and re-usecitations
Places of action
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article
New bio-based monomers:
Abstract
A family of monomers including 2,5-hexandiol, 2,7-octandiol, 2,5-furandicarboxylic acid (FDCA) , terephthalic acid (TA), and branched-chain adipic and pimelic acid derivatives all find a common derivation in the biomass-derived platform molecule 5-(chloromethyl)furfural (CMF). The diol monomers, previously little known to polymer chemistry, have been combined with FDCA and TA derivatives to produce a range of novel polyesters. It is shown that the use of secondary diols leads to polymers with higher glass transition temperatures (Tg) than those prepared from their primary diol equivalents. Two methods of polymerisation were investigated, the first employing activation of the aromatic diacids via the corresponding diacid chlorides and the second using a transesterification procedure. Longer chain diols were found to be more reactive than the shorter chain alternatives, generally giving rise to higher molecular weight polymers, an effect shown to be most dramatic when using the transesterification route. Finally, novel diesters with high degrees of branching in their hydrocarbon chains are introduced as potential monomers for low surface energy materials applications.