Multiscale Structure of Starches Grafted with Hydrophobic Groups: A New Analytical Strategy
Starch, an abundant and low-cost plant-based glucopolymer, has great potential to replace carbon-based polymers in various materials. In order to optimize its functional properties for bioplastics applications chemical groups need to be introduced on the free hydroxyl groups in a controlled manner,...
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doaj-4f113ee01f4b47018e8723aff4b7870b2020-11-25T03:40:35ZengMDPI AGMolecules1420-30492020-06-01252827282710.3390/molecules25122827Multiscale Structure of Starches Grafted with Hydrophobic Groups: A New Analytical StrategyChloé Volant0Alexandre Gilet1Fatima Beddiaf2Marion Collinet-Fressancourt3Xavier Falourd4Nicolas Descamps5Vincent Wiatz6Hervé Bricout7Sébastien Tilloy8Eric Monflier9Claude Quettier10Ahmed Mazzah11Agnès Rolland-Sabaté12Univ. Lille, CNRS, USR3290—MSAP—Miniaturisation pour la Synthèse, l’Analyse et la Protéomique, F-59000 Lille, FranceUniv. Artois, CNRS, Centrale Lille, Univ. Lille, UMR 8181—UCCS—Unité de Catalyse et Chimie du Solide, F-62300 Lens, FranceINRAE, UR BIA, F-44316 Nantes, FranceCIRAD, UPR Recyclage et Risque, F-97743 Saint-Denis, Réunion, FranceINRAE, UR BIA, F-44316 Nantes, FranceROQUETTE Frères, Rue de la Haute Loge, 62136 Lestrem, FranceROQUETTE Frères, Rue de la Haute Loge, 62136 Lestrem, FranceUniv. Artois, CNRS, Centrale Lille, Univ. Lille, UMR 8181—UCCS—Unité de Catalyse et Chimie du Solide, F-62300 Lens, FranceUniv. Artois, CNRS, Centrale Lille, Univ. Lille, UMR 8181—UCCS—Unité de Catalyse et Chimie du Solide, F-62300 Lens, FranceUniv. Artois, CNRS, Centrale Lille, Univ. Lille, UMR 8181—UCCS—Unité de Catalyse et Chimie du Solide, F-62300 Lens, FranceROQUETTE Frères, Rue de la Haute Loge, 62136 Lestrem, FranceUniv. Lille, CNRS, USR3290—MSAP—Miniaturisation pour la Synthèse, l’Analyse et la Protéomique, F-59000 Lille, FranceINRAE, UR BIA, F-44316 Nantes, FranceStarch, an abundant and low-cost plant-based glucopolymer, has great potential to replace carbon-based polymers in various materials. In order to optimize its functional properties for bioplastics applications chemical groups need to be introduced on the free hydroxyl groups in a controlled manner, so an understanding of the resulting structure-properties relationships is therefore essential. The purpose of this work was to study the multiscale structure of highly-acetylated (degree of substitution, 0.4 < DS ≤ 3) and etherified starches by using an original combination of experimental strategies and methodologies. The molecular structure and substituents repartition were investigated by developing new sample preparation strategies for specific analysis including Asymmetrical Flow Field Flow Fractionation associated with Multiangle Laser Light Scattering, Nuclear Magnetic Resonance (NMR), Raman and Time of Flight Secondary Ion Mass spectroscopies. Molar mass decrease and specific ways of chain breakage due to modification were pointed out and are correlated to the amylose content. The amorphous structuration was revealed by solid-state NMR. This original broad analytical approach allowed for the first time a large characterization of highly-acetylated starches insoluble in aqueous solvents. This strategy, then applied to characterize etherified starches, opens the way to correlate the structure to the properties of such insoluble starch-based materials.https://www.mdpi.com/1420-3049/25/12/2827acetylated starchetherified starchchemical compositionmacromolecular characteristicssurface characterization |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chloé Volant Alexandre Gilet Fatima Beddiaf Marion Collinet-Fressancourt Xavier Falourd Nicolas Descamps Vincent Wiatz Hervé Bricout Sébastien Tilloy Eric Monflier Claude Quettier Ahmed Mazzah Agnès Rolland-Sabaté |
spellingShingle |
Chloé Volant Alexandre Gilet Fatima Beddiaf Marion Collinet-Fressancourt Xavier Falourd Nicolas Descamps Vincent Wiatz Hervé Bricout Sébastien Tilloy Eric Monflier Claude Quettier Ahmed Mazzah Agnès Rolland-Sabaté Multiscale Structure of Starches Grafted with Hydrophobic Groups: A New Analytical Strategy Molecules acetylated starch etherified starch chemical composition macromolecular characteristics surface characterization |
author_facet |
Chloé Volant Alexandre Gilet Fatima Beddiaf Marion Collinet-Fressancourt Xavier Falourd Nicolas Descamps Vincent Wiatz Hervé Bricout Sébastien Tilloy Eric Monflier Claude Quettier Ahmed Mazzah Agnès Rolland-Sabaté |
author_sort |
Chloé Volant |
title |
Multiscale Structure of Starches Grafted with Hydrophobic Groups: A New Analytical Strategy |
title_short |
Multiscale Structure of Starches Grafted with Hydrophobic Groups: A New Analytical Strategy |
title_full |
Multiscale Structure of Starches Grafted with Hydrophobic Groups: A New Analytical Strategy |
title_fullStr |
Multiscale Structure of Starches Grafted with Hydrophobic Groups: A New Analytical Strategy |
title_full_unstemmed |
Multiscale Structure of Starches Grafted with Hydrophobic Groups: A New Analytical Strategy |
title_sort |
multiscale structure of starches grafted with hydrophobic groups: a new analytical strategy |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2020-06-01 |
description |
Starch, an abundant and low-cost plant-based glucopolymer, has great potential to replace carbon-based polymers in various materials. In order to optimize its functional properties for bioplastics applications chemical groups need to be introduced on the free hydroxyl groups in a controlled manner, so an understanding of the resulting structure-properties relationships is therefore essential. The purpose of this work was to study the multiscale structure of highly-acetylated (degree of substitution, 0.4 < DS ≤ 3) and etherified starches by using an original combination of experimental strategies and methodologies. The molecular structure and substituents repartition were investigated by developing new sample preparation strategies for specific analysis including Asymmetrical Flow Field Flow Fractionation associated with Multiangle Laser Light Scattering, Nuclear Magnetic Resonance (NMR), Raman and Time of Flight Secondary Ion Mass spectroscopies. Molar mass decrease and specific ways of chain breakage due to modification were pointed out and are correlated to the amylose content. The amorphous structuration was revealed by solid-state NMR. This original broad analytical approach allowed for the first time a large characterization of highly-acetylated starches insoluble in aqueous solvents. This strategy, then applied to characterize etherified starches, opens the way to correlate the structure to the properties of such insoluble starch-based materials. |
topic |
acetylated starch etherified starch chemical composition macromolecular characteristics surface characterization |
url |
https://www.mdpi.com/1420-3049/25/12/2827 |
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