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                {
                    "creatorType": "author",
                    "firstName": "Suprakas",
                    "lastName": "Sinha Ray"
                },
                {
                    "creatorType": "author",
                    "firstName": "Mosto",
                    "lastName": "Bousmina"
                }
            ],
            "abstractNote": "This review aims at highlighting on recent developments in preparation, characterization, properties, crystallization behaviors, melt rheology, processing, and future applications possibilities of biodegradable polymers and their layered silicate nanocomposites. These materials are attracting considerable interest in materials science research. Montmorillonite and hectorite are among the most commonly used smectite-type layered silicates for the preparation of nanocomposites. In their pristine form they are hydrophilic in nature, and this property makes them very difficult to disperse into biodegradable polymer matrices. The most common strategy to overcome this difficulty is to replace the interlayer clay cations with quarternized ammonium or phosphonium cations, preferably with long alkyl chains.\nA wide range of biodegradable polymer matrices is described in this review with a special emphasis on polylactide because of more eco-friendliness from its origin as contrast to the fully petroleum-based biodegradable polymers and control of carbon dioxide balance after their composting.\nPreparative techniques include (i) intercalation of polymers or prepolymers from solution, (ii) in situ intercalative polymerization method, and (iii) melt intercalation method.\nThis new family of composite materials frequently exhibits remarkable improvements of mechanical and material properties when compared with virgin polymers or conventional micro- and macro-composites. Improvements can include a high storage modulus both in solid and molten states, increased tensile and flexural properties, a decrease in gas permeability and flammability, increased heat distortion temperature and thermal stability, increase in the biodegradation rate, and so forth.",
            "publicationTitle": "Progress in Materials Science",
            "publisher": "",
            "place": "",
            "date": "November 2005",
            "volume": "50",
            "issue": "8",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "962-1079",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Progress in Materials Science",
            "DOI": "10.1016/j.pmatsci.2005.05.002",
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            "language": "",
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            "creatorSummary": "Bordes et al.",
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            "itemType": "journalArticle",
            "title": "Nano-biocomposites: Biodegradable polyester/nanoclay systems",
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                    "firstName": "Perrine",
                    "lastName": "Bordes"
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                    "lastName": "Pollet"
                },
                {
                    "creatorType": "author",
                    "firstName": "Luc",
                    "lastName": "Avérous"
                }
            ],
            "abstractNote": "In the recent years, bio-based products have raised great interest since sustainable development policies tend to expand with the decreasing reserve of fossil fuel and the growing concern for the environment. Consequently, biopolymers, i.e., biodegradable polymers, have been the topic of many researches. They can be mainly classified as agro-polymers (starch, protein, etc.) and biodegradable polyesters (polyhydroxyalkanoates, poly(lactic acid), etc.). These latter, also called biopolyesters, can be synthesized from fossil resources but main productions are obtained from renewable resources. Unfortunately for certain applications, biopolyesters cannot be fully competitive with conventional thermoplastics since some of their properties are too weak. Therefore, to extend their applications, these biopolymers have been formulated and associated with nano-sized fillers, which could bring a large range of improved properties (stiffness, permeability, crystallinity, thermal stability). The resulting ‘nano-biocomposites’ have been the subject of many recent publications. This review is dedicated to this novel class of materials based on clays, which are nowadays the main nanofillers used in nanocomposites systems. This review highlights the main researches and developments in biopolyester/nanoclay systems during the last decade.",
            "publicationTitle": "Progress in Polymer Science",
            "publisher": "",
            "place": "",
            "date": "February 2009",
            "volume": "34",
            "issue": "2",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "125-155",
            "series": "",
            "seriesTitle": "",
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            "journalAbbreviation": "Progress in Polymer Science",
            "DOI": "10.1016/j.progpolymsci.2008.10.002",
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                    "tag": "Biodegradable",
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                },
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                    "tag": "Biopolyesters",
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                    "tag": "Clay",
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            "creatorSummary": "Chevillard et al.",
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            "creators": [
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                    "creatorType": "author",
                    "firstName": "Anne",
                    "lastName": "Chevillard"
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                    "firstName": "Hélène",
                    "lastName": "Angellier-Coussy"
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                {
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                    "firstName": "Bernard",
                    "lastName": "Cuq"
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                {
                    "creatorType": "author",
                    "firstName": "Valérie",
                    "lastName": "Guillard"
                },
                {
                    "creatorType": "author",
                    "firstName": "Guy",
                    "lastName": "César"
                },
                {
                    "creatorType": "author",
                    "firstName": "Nathalie",
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                },
                {
                    "creatorType": "author",
                    "firstName": "Emmanuelle",
                    "lastName": "Gastaldi"
                }
            ],
            "abstractNote": "The objective of this work was to investigate the influence of clay nanoparticles on the biodegradability of wheat gluten-based materials through a better understanding of multi-scale relationships between biodegradability, water transfer properties and structure of wheat gluten/clay materials. Wheat gluten/clay (nano)composites materials were prepared via bi-vis extrusion by using an unmodified sodium montmorillonite (MMT) and an organically modified MMT. Respirometric experiments showed that the rate of biodegradation of wheat gluten-based materials could be slowed down by adding unmodified MMT (HPS) without affecting the final biodegradation level whereas the presence of an organically modified MMT (C30B) did not significantly influence the biodegradation pattern. Based on the evaluation of the water sensitivity and a multi-scale characterization of material structure, three hypotheses have been proposed to account for the underlying mechanisms. The molecular/macromolecular affinity between the clay layers and the wheat gluten matrix, i.e. the ability of both components to establish interactions appeared as the key parameter governing the nanostructure, the water sensitivity and, as a result, the overall biodegradation process.",
            "publicationTitle": "Polymer Degradation and Stability",
            "publisher": "",
            "place": "",
            "date": "December 2011",
            "volume": "96",
            "issue": "12",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "2088-2097",
            "series": "",
            "seriesTitle": "",
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            "journalAbbreviation": "Polymer Degradation and Stability",
            "DOI": "10.1016/j.polymdegradstab.2011.09.024",
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                    "tag": "Biodegradation",
                    "type": 1
                },
                {
                    "tag": "Montmorillonite",
                    "type": 1
                },
                {
                    "tag": "Nanocomposite",
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            "creatorSummary": "Monteiro et al.",
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            "version": 2,
            "itemType": "journalArticle",
            "title": "Thermogravimetric behavior of natural fibers reinforced polymer composites—An overview",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "Sergio N.",
                    "lastName": "Monteiro"
                },
                {
                    "creatorType": "author",
                    "firstName": "Veronica",
                    "lastName": "Calado"
                },
                {
                    "creatorType": "author",
                    "firstName": "Rubén Jesus S.",
                    "lastName": "Rodriguez"
                },
                {
                    "creatorType": "author",
                    "firstName": "Frederico M.",
                    "lastName": "Margem"
                }
            ],
            "abstractNote": "Natural fibers obtained from plants, known as lignocellulosic fibers are environmentally friendly alternatives for synthetic fiber, as polymer composite reinforcement. Applications of natural fiber composites are expanding in many engineering areas, from civil construction to automobile manufacturing. In recent years, a considerable number of scientific and technological works, including review papers, were dedicated to the characterization and properties of natural fibers and their composites. The mechanical behavior and the fracture characteristics are usually the most investigated and reviewed themes for the purpose of comparison to corresponding polymer composites reinforced with synthetic fibers, mainly fiberglass. The thermal behavior is also of practical interest for conditions associated with temperatures above the ambient, as in fire damage, curing or process involving heating procedures. In fact, several works also assessed distinct thermal responses, particularly in terms of thermogravimetric properties of natural fiber polymer composites. As no general review was conducted so far on the thermogravimetric (TG) behavior of these materials, this article presents an overview limited to temperature effects related to the loss of mass by means of TG analysis and the related derivative, DTG, for different polymer composites reinforced with the most common and relevant lignocellulosic fibers.",
            "publicationTitle": "Materials Science and Engineering: A",
            "publisher": "",
            "place": "",
            "date": "November 15, 2012",
            "volume": "557",
            "issue": "",
            "section": "",
            "partNumber": "",
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            "pages": "17-28",
            "series": "A Celebration of Prof. K.K. Chawla's Distinguished Contributions: Fibers, Foams, and Composites",
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            "seriesText": "",
            "journalAbbreviation": "Materials Science and Engineering: A",
            "DOI": "10.1016/j.msea.2012.05.109",
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                {
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                    "type": 1
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                    "type": 1
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            },
            "creatorSummary": "Yu et al.",
            "parsedDate": "2006-06",
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        },
        "data": {
            "key": "7JRBIBEG",
            "version": 2,
            "itemType": "journalArticle",
            "title": "Polymer blends and composites from renewable resources",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "Long",
                    "lastName": "Yu"
                },
                {
                    "creatorType": "author",
                    "firstName": "Katherine",
                    "lastName": "Dean"
                },
                {
                    "creatorType": "author",
                    "firstName": "Lin",
                    "lastName": "Li"
                }
            ],
            "abstractNote": "This article reviews recent advances in polymer blends and composites from renewable resources, and introduces a number of potential applications for this material class. In order to overcome disadvantages such as poor mechanical properties of polymers from renewable resources, or to offset the high price of synthetic biodegradable polymers, various blends and composites have been developed over the last decade. The progress of blends from three kinds of polymers from renewable resources—(1) natural polymers, such as starch, protein and cellulose; (2) synthetic polymers from natural monomers, such as polylactic acid; and (3) polymers from microbial fermentation, such as polyhydroxybutyrate—are described with an emphasis on potential applications. The hydrophilic character of natural polymers has contributed to the successful development of environmentally friendly composites, as most natural fibers and nanoclays are also hydrophilic in nature. Compatibilizers and the technology of reactive extrusion are used to improve the interfacial adhesion between natural and synthetic polymers.",
            "publicationTitle": "Progress in Polymer Science",
            "publisher": "",
            "place": "",
            "date": "June 2006",
            "volume": "31",
            "issue": "6",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "576-602",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Progress in Polymer Science",
            "DOI": "10.1016/j.progpolymsci.2006.03.002",
            "citationKey": "",
            "url": "http://www.sciencedirect.com/science/article/pii/S0079670006000414",
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                },
                {
                    "tag": "Blend",
                    "type": 1
                },
                {
                    "tag": "Composite",
                    "type": 1
                },
                {
                    "tag": "Polymer",
                    "type": 1
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                {
                    "tag": "Renewable resource",
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            "creatorSummary": "Carrasco et al.",
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            "version": 2,
            "itemType": "journalArticle",
            "title": "Kinetics of the thermal decomposition of processed poly(lactic acid)",
            "creators": [
                {
                    "creatorType": "author",
                    "firstName": "F.",
                    "lastName": "Carrasco"
                },
                {
                    "creatorType": "author",
                    "firstName": "P.",
                    "lastName": "Pagès"
                },
                {
                    "creatorType": "author",
                    "firstName": "J.",
                    "lastName": "Gámez-Pérez"
                },
                {
                    "creatorType": "author",
                    "firstName": "O. O.",
                    "lastName": "Santana"
                },
                {
                    "creatorType": "author",
                    "firstName": "M. L.",
                    "lastName": "Maspoch"
                }
            ],
            "abstractNote": "The kinetics of the thermal decomposition of processed poly(lactic acid) has been studied and compared to that of raw material. Processing consisted of two different industrial processes: 1) Injection (with or without further annealing); 2) Extrusion followed by injection (with or without further annealing). For this study, an integral method (based on the general analytical solution), differential methods (based on the first conversion derivative and on the 2nd derivative) and special methods have been used. On the other hand, a method based on the maximum decomposition rate has been considered. By doing that, the kinetic parameters (reaction order, frequency factor and activation energy) have been determined. It has been demonstrated that there was only one first-order reaction for the entire conversion range. A new equation (based on the second conversion derivative plot as a function of temperature) was developed allowing the calculation of the reaction order. This method quantifies peak areas (and not peak heights, as reported by Kissinger). It is very useful because it considers both peak shape and width. Activation energy, as determined by using the general analytical solution, was 318 kJ/mol for unprocessed poly(lactic acid) whereas it was 280 ± 5 kJ/mol for processed materials. All the processed materials had approximately the same thermal stability (T5 = 333.0–335.8 °C, at 95% confidence level), which was slightly lower than that of unprocessed materials (T5 = 337.5 °C). PLA melting (during extrusion and injection) was responsible for depolymerization reactions (the small molecules formed during melting processes can volatilize readily).",
            "publicationTitle": "Polymer Degradation and Stability",
            "publisher": "",
            "place": "",
            "date": "December 2010",
            "volume": "95",
            "issue": "12",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "2508-2514",
            "series": "",
            "seriesTitle": "",
            "seriesText": "",
            "journalAbbreviation": "Polymer Degradation and Stability",
            "DOI": "10.1016/j.polymdegradstab.2010.07.039",
            "citationKey": "",
            "url": "http://www.sciencedirect.com/science/article/pii/S0141391010003332",
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                    "tag": "Extrusion",
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                },
                {
                    "tag": "Injection",
                    "type": 1
                },
                {
                    "tag": "Kinetic models",
                    "type": 1
                },
                {
                    "tag": "Poly(lactic acid)",
                    "type": 1
                },
                {
                    "tag": "Thermal stability",
                    "type": 1
                },
                {
                    "tag": "Thermogravimetric analysis (TGA)",
                    "type": 1
                }
            ],
            "collections": [],
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