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From petrochemical polyurethanes to biobased polyhydroxyurethanes

Authors :
Zéphirin Mouloungui
Bassam Nohra
Celine Guerin
Laure Candy
Jean-François Blanco
Yann Raoul
Centre National de la Recherche Scientifique - CNRS (FRANCE)
CONDAT (FRANCE)
Institut National Polytechnique de Toulouse - Toulouse INP (FRANCE)
Institut National de la Recherche Agronomique - INRA (FRANCE)
Université Toulouse III - Paul Sabatier - UT3 (FRANCE)
ONIDOL (FRANCE)
Chimie Agro-Industrielle (CAI)
Institut National Polytechnique (Toulouse) (Toulouse INP)
Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Ecole nationale supérieure des ingénieurs en arts chimiques et technologiques-Institut National de la Recherche Agronomique (INRA)
Université Fédérale Toulouse Midi-Pyrénées
LGC - Laboratoire de Génie Chimique
CONDAT
Organisation Nationale Interprofessionnelle des Oléagineux (ONIDOL)
Institut National Polytechnique de Toulouse - INPT (FRANCE)
Source :
Macromolecules, Macromolecules, American Chemical Society, 2013, 46 (10), pp.3771-3792. ⟨10.1021/ma400197c⟩
Publication Year :
2013
Publisher :
American Chemical Society, 2013.

Abstract

International audience; From a green and sustainable chemistry standpoint, the current challenge in the polyurethane's industry is to switch from petrobased polyurethanes (PUs) to biobased polyhydroxyurethanes (PHUs). This review describes the main alternative strategies being developed with a focus on PHUs from vegetable oils and derivatives. The substitution of petrobased polyols by natural oil based polyols was the first route to biobased PUs to be developed. The second strategy involves synthesis without the need of harmful isocyanate by the nucleophilic polyaddition of polyamines to polycyclic carbonates. The technological barrier to the synthesis of biobased cyclic carbonates could be overcome by the chemical transformation of epoxidized vegetable oils or by the use of glycerine carbonate-based intermediates. New families of biobased PHUs with a lower environmental footprint could be generated.

Details

Language :
English
ISSN :
00249297 and 15205835
Database :
OpenAIRE
Journal :
Macromolecules, Macromolecules, American Chemical Society, 2013, 46 (10), pp.3771-3792. ⟨10.1021/ma400197c⟩
Accession number :
edsair.doi.dedup.....f996463254ac104d36c29bfc5b769a2d