Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review
International audience The use of 1,4:3,6-dianhydrohexitols, isosorbide, isomannide and isoidide in polymers is reviewed. 1,4:3,6-Dianhydrohexitols are derived from renewable resources from cereal-based polysaccharides. In the field of polymeric materials, these diols are essentially employed to syn...
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Online Access: | https://hal.archives-ouvertes.fr/hal-00587040 https://doi.org/10.1016/j.progpolymsci.2009.10.001 |
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ftunivnantes:oai:HAL:hal-00587040v1 2023-05-15T15:52:44+02:00 Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review Fenouillot, Françoise Alain, Rousseau Colomines, Gael Saint Loup, René Pascault, Jean-Pierre Ingénierie des Matériaux Polymères - Laboratoire des Matériaux Macromoléculaires (IMP-LMM) Université Claude Bernard Lyon 1 (UCBL) Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon) Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Université Jean Monnet Saint-Étienne (UJM)-Centre National de la Recherche Scientifique (CNRS) Institut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier (ICGM ICMMM) Université Montpellier 1 (UM1)-Université Montpellier 2 - Sciences et Techniques (UM2)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS) Centre d'enseignement Cnam Paris (CNAM Paris) Conservatoire National des Arts et Métiers CNAM (CNAM) HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM) Laboratoire de chimie Macromoléculaire (CNRS UMR 5076) Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM) 2010-05 https://hal.archives-ouvertes.fr/hal-00587040 https://doi.org/10.1016/j.progpolymsci.2009.10.001 en eng HAL CCSD Elsevier info:eu-repo/semantics/altIdentifier/doi/10.1016/j.progpolymsci.2009.10.001 hal-00587040 https://hal.archives-ouvertes.fr/hal-00587040 doi:10.1016/j.progpolymsci.2009.10.001 ISSN: 0079-6700 Progress in Polymer Science https://hal.archives-ouvertes.fr/hal-00587040 Progress in Polymer Science, Elsevier, 2010, pp.578-622. ⟨10.1016/j.progpolymsci.2009.10.001⟩ PHASE-TRANSFER CATALYSIS DICARBOXYLIC-ACID UNITS MICROWAVE-ASSISTED POLYCONDENSATION LIQUID-CRYSTALLINE POLYIMIDES SILYLATED ALIPHATIC DIOLS CARBONIC-ACID LC-POLYIMIDES MAIN-CHAIN AMINO-ACID BIOANALOGOUS POLYMERS [CHIM.POLY]Chemical Sciences/Polymers [CHIM.MATE]Chemical Sciences/Material chemistry info:eu-repo/semantics/article Journal articles 2010 ftunivnantes https://doi.org/10.1016/j.progpolymsci.2009.10.001 2022-10-04T22:58:08Z International audience The use of 1,4:3,6-dianhydrohexitols, isosorbide, isomannide and isoidide in polymers is reviewed. 1,4:3,6-Dianhydrohexitols are derived from renewable resources from cereal-based polysaccharides. In the field of polymeric materials, these diols are essentially employed to synthesize or modify polycondensates. Their attractive features as monomers are linked to their rigidity, chirality, non-toxicity, and the fact that they are not derived from petroleum. First, the synthesis of high glass transition temperature polymers with good thermomechanical resistance is possible. Second, the chiral nature of 1,4:3,6-dianhydrohexitols may lead to specific optical properties. Finally, biodegradable polymers can be obtained. The production of isosorbide at the industrial scale with a purity satisfying the requirements for polymer synthesis suggests that isosorbide will soon emerge in industrial polymer applications. However, a deciding factor will be the reduction of polymerization time of these low-reactivity monomers to values compatible with economically viable production processes. (C) 2009 Elsevier Ltd. All rights reserved. Article in Journal/Newspaper Carbonic acid Université de Nantes: HAL-UNIV-NANTES Progress in Polymer Science 35 5 578 622 |
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Université de Nantes: HAL-UNIV-NANTES |
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ftunivnantes |
language |
English |
topic |
PHASE-TRANSFER CATALYSIS DICARBOXYLIC-ACID UNITS MICROWAVE-ASSISTED POLYCONDENSATION LIQUID-CRYSTALLINE POLYIMIDES SILYLATED ALIPHATIC DIOLS CARBONIC-ACID LC-POLYIMIDES MAIN-CHAIN AMINO-ACID BIOANALOGOUS POLYMERS [CHIM.POLY]Chemical Sciences/Polymers [CHIM.MATE]Chemical Sciences/Material chemistry |
spellingShingle |
PHASE-TRANSFER CATALYSIS DICARBOXYLIC-ACID UNITS MICROWAVE-ASSISTED POLYCONDENSATION LIQUID-CRYSTALLINE POLYIMIDES SILYLATED ALIPHATIC DIOLS CARBONIC-ACID LC-POLYIMIDES MAIN-CHAIN AMINO-ACID BIOANALOGOUS POLYMERS [CHIM.POLY]Chemical Sciences/Polymers [CHIM.MATE]Chemical Sciences/Material chemistry Fenouillot, Françoise Alain, Rousseau Colomines, Gael Saint Loup, René Pascault, Jean-Pierre Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review |
topic_facet |
PHASE-TRANSFER CATALYSIS DICARBOXYLIC-ACID UNITS MICROWAVE-ASSISTED POLYCONDENSATION LIQUID-CRYSTALLINE POLYIMIDES SILYLATED ALIPHATIC DIOLS CARBONIC-ACID LC-POLYIMIDES MAIN-CHAIN AMINO-ACID BIOANALOGOUS POLYMERS [CHIM.POLY]Chemical Sciences/Polymers [CHIM.MATE]Chemical Sciences/Material chemistry |
description |
International audience The use of 1,4:3,6-dianhydrohexitols, isosorbide, isomannide and isoidide in polymers is reviewed. 1,4:3,6-Dianhydrohexitols are derived from renewable resources from cereal-based polysaccharides. In the field of polymeric materials, these diols are essentially employed to synthesize or modify polycondensates. Their attractive features as monomers are linked to their rigidity, chirality, non-toxicity, and the fact that they are not derived from petroleum. First, the synthesis of high glass transition temperature polymers with good thermomechanical resistance is possible. Second, the chiral nature of 1,4:3,6-dianhydrohexitols may lead to specific optical properties. Finally, biodegradable polymers can be obtained. The production of isosorbide at the industrial scale with a purity satisfying the requirements for polymer synthesis suggests that isosorbide will soon emerge in industrial polymer applications. However, a deciding factor will be the reduction of polymerization time of these low-reactivity monomers to values compatible with economically viable production processes. (C) 2009 Elsevier Ltd. All rights reserved. |
author2 |
Ingénierie des Matériaux Polymères - Laboratoire des Matériaux Macromoléculaires (IMP-LMM) Université Claude Bernard Lyon 1 (UCBL) Université de Lyon-Université de Lyon-Institut National des Sciences Appliquées de Lyon (INSA Lyon) Université de Lyon-Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Université Jean Monnet Saint-Étienne (UJM)-Centre National de la Recherche Scientifique (CNRS) Institut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier (ICGM ICMMM) Université Montpellier 1 (UM1)-Université Montpellier 2 - Sciences et Techniques (UM2)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS) Centre d'enseignement Cnam Paris (CNAM Paris) Conservatoire National des Arts et Métiers CNAM (CNAM) HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM) Laboratoire de chimie Macromoléculaire (CNRS UMR 5076) Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM) |
format |
Article in Journal/Newspaper |
author |
Fenouillot, Françoise Alain, Rousseau Colomines, Gael Saint Loup, René Pascault, Jean-Pierre |
author_facet |
Fenouillot, Françoise Alain, Rousseau Colomines, Gael Saint Loup, René Pascault, Jean-Pierre |
author_sort |
Fenouillot, Françoise |
title |
Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review |
title_short |
Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review |
title_full |
Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review |
title_fullStr |
Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review |
title_full_unstemmed |
Polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): A review |
title_sort |
polymers from renewable 1,4:3,6-dianhydrohexitols (isosorbide, isomannide and isoidide): a review |
publisher |
HAL CCSD |
publishDate |
2010 |
url |
https://hal.archives-ouvertes.fr/hal-00587040 https://doi.org/10.1016/j.progpolymsci.2009.10.001 |
genre |
Carbonic acid |
genre_facet |
Carbonic acid |
op_source |
ISSN: 0079-6700 Progress in Polymer Science https://hal.archives-ouvertes.fr/hal-00587040 Progress in Polymer Science, Elsevier, 2010, pp.578-622. ⟨10.1016/j.progpolymsci.2009.10.001⟩ |
op_relation |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.progpolymsci.2009.10.001 hal-00587040 https://hal.archives-ouvertes.fr/hal-00587040 doi:10.1016/j.progpolymsci.2009.10.001 |
op_doi |
https://doi.org/10.1016/j.progpolymsci.2009.10.001 |
container_title |
Progress in Polymer Science |
container_volume |
35 |
container_issue |
5 |
container_start_page |
578 |
op_container_end_page |
622 |
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