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Gildas Coativy

Bio: Gildas Coativy is an academic researcher from Institut national de la recherche agronomique. The author has contributed to research in topics: Materials science & Extrusion. The author has an hindex of 5, co-authored 5 publications receiving 197 citations. Previous affiliations of Gildas Coativy include Centre national de la recherche scientifique.

Papers
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Journal ArticleDOI
TL;DR: The characterization of the materials indicates that, compared to glycerol, the use of [BMIM]Cl leads to less hygroscopicity, a more efficient plasticization of both starch and zein phases and a compatibilization of starch/zein blends.

94 citations

Journal ArticleDOI
TL;DR: Deep eutectic solvents (DES) based on choline chloride and hydrogen bond donors are shown to be efficient functional additives for thermoplastic starch, able to act as efficient plasticizers, water uptake inhibitors, and as compatibilizers in the case of blends with a hydrophobic phase.

82 citations

Journal ArticleDOI
TL;DR: In mechanically constrained conditions, the maximum recovered stress was significantly improved for the bionanocomposites compared to unreinforced starch, opening promising perspectives for the design of sensors and actuators.

36 citations

Journal ArticleDOI
TL;DR: Starch-clay bionanocomposites containing 1-10% of natural montmorillonite were elaborated by melt processing in the presence of water and it seems that for high clay content, the slowdown of segmental relaxation due to confinement of the starch macromolecules between the clay tactoïds is the predominant phenomenon.

13 citations

Journal ArticleDOI
23 Oct 2015-Polymer
TL;DR: In this article, an X-ray diffraction of amorphous starch obtained by extrusion exhibits shape memory properties when submitted to a specific type of thermomechanical treatment, called Shape Memory Creation Procedure (SMCP).

7 citations


Cited by
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Journal ArticleDOI
TL;DR: This article aims to review the literature concerning the choice of selectivity for hydrogels based on classification, application and processing to assess their potential in hi-tech applications in the biomedical, pharmaceutical, biotechnology, bioseparation, biosensor, agriculture, oil recovery and cosmetics fields.

905 citations

Journal ArticleDOI
TL;DR: A review of the most common bio-based polymeric materials can be found in this paper, which provides an overview of recent advances in the selection and use of plasticizers, and their effect on the performance of these materials.
Abstract: Over the coming few decades bioplastic materials are expected to complement and gradually replace some of the fossil oil based materials. Multidisciplinary research efforts have generated a significant level of technical and commercial success towards these bio-based materials. However, extensive application of these bio-based plastics is still challenged by one or more of their possible inherent limitations, such as poor processability, brittleness, hydrophilicity, poor moisture and gas barrier, inferior compatibility, poor electrical, thermal and physical properties. The incorporation of additives such as plasticizers into the biopolymers is a common practice to improve these inherent limitations. Generally, plasticizers are added to both synthetic and bio-based polymeric materials to impart flexibility, improve toughness, and lower the glass transition temperature. This review introduces the most common bio-based plastics and provides an overview of recent advances in the selection and use of plasticizers, and their effect on the performance of these materials. In addition to plasticizers, we also present a perspective of other emerging techniques of improving the overall performance of bio-based plastics. Although a wide variety of bio-based plastics are under development, this review focuses on plasticizers utilized for the most extensively studied bioplastics including poly(lactic acid), polyhydroxyalkanoates, thermoplastic starch, proteinaceous plastics and cellulose acetates. The ongoing challenge and future potentials of plasticizers for bio-based plastics are also discussed.

567 citations

Journal ArticleDOI
TL;DR: Deep eutectic solvents (DESs) as mentioned in this paper have been considered green solvent alternatives to conventional Solvents and have attracted considerable attention in recent years, with an in-depth understanding of the common and novel properties of DESs, many of them have been prepared and applied to various areas of chemistry.
Abstract: In recent years, deep eutectic solvents (DESs) have been considered green solvent alternatives to conventional solvents and have attracted considerable attention. With an in-depth understanding of the common and novel properties of DESs, many of them have been prepared and applied to various areas of chemistry. To summarize the full-scale development of DESs, we reviewed this field from its inception. This review summarizes the general trends in the development of DESs and evaluates the major aspects of DESs, such as their properties, preparations, and applications. This work is expected to be helpful for the further development of DESs based on a summary of the fundamental research in the field.

363 citations

Journal ArticleDOI
TL;DR: In this paper, 70 DESs were synthesized successfully based on glycerol (Gly) as the HBD with different phosphonium and ammonium salts, namely methyl triphenyl phosphono-bromide (MTPB), benzyl triphenyi-triphenyl-phosphonium bromide(BTPC), allyl triphethenyl phono-phonium (ATPB), choline chloride (ChCl), N,N-diethylethanolammonium chloride (DAC), and tetra-

353 citations

Journal Article
TL;DR: In this paper, the effects of confinement on glass transition temperature (Tg) and physical aging are measured in polystyrene (PS), poly(methyl methacrylate) (PMMA), and poly(2-vinyl pyridine) (P2VP) nanocomposites containing 10- to 15-nmdiameter silica nanospheres or 47-nm-diameter alumina nanosphere.
Abstract: The effects of confinement on glass transition temperature (Tg) and physical aging are measured in polystyrene (PS), poly(methyl methacrylate) (PMMA), and poly(2-vinyl pyridine) (P2VP) nanocomposites containing 10- to 15-nm-diameter silica nanospheres or 47-nm-diameter alumina nanospheres. Nanocomposites are made by spin coating films from sonicated solutions of polymer, nanofiller, and dye. The Tgs and physical aging rates are measured by fluorescence of trace levels of dye in the films. At 0.1–10 vol % nanofiller, Tg values can be enhanced or depressed relative to neat, bulk Tg (Tg,bulk) or invariant with nanofiller content. For alumina nanocomposites, Tg increases relative to Tg,bulk by as much as 16 K in P2VP, decreases by as much as 5 K in PMMA, and is invariant in PS. By analogy with thin polymer films, these results are explained by wetted P2VP–nanofiller interfaces with attractive interactions, nonwetted PMMA–nanofiller interfaces (free space at the interface), and wetted PS–nanofiller interfaces lacking attractive interactions, respectively. The presence of wetted or nonwetted interfaces is controlled by choice of solvent. For example, 0.1–0.6 vol % silica/PMMA nanocomposites exhibit Tg enhancements as large as 5 K or Tg reductions as large as 17 K relative to Tg,bulk when films are made from methyl ethyl ketone or acetic acid solutions, respectively. A factor of 17 reduction of physical aging rate relative to that of neat, bulk P2VP is demonstrated in a 4 vol % alumina/P2VP nanocomposite. This suggests that a strategy for achieving nonequilibrium, glassy polymeric systems that are stable or nearly stable to physical aging is to incorporate well-dispersed nanoparticles possessing attractive interfacial interactions with the polymer. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 2935–2943, 2006

347 citations