This review describes some recent works related to the development of the flame retardation of silicone elastomers and/or applications of silicones as flame retardant agents in other polymers. First, the thermal degradation of silicones themselves is discussed, focussing on depolymerization mechanisms, effect of structure, heating conditions, and effect of additives (i.e. less than 5 wt% fillers) on thermal degradation of silicones. Then, the influence of several types of mineral fillers (of up to 80 wt% content) as ceramization agents of silicones is presented. Finally, the introduction of (functionalized) silicones as flame retardants into other polymers is described.
International audiencePolyurethanes cover a large range of materials exhibiting various physical and mechanical properties making them useful in different applications such as elastomers or biomaterials, for instance. The introduction of ionic groups in the polyurethane backbone opens the way to new applications where the ionic groups can act as physical crosslinkers that greatly modify the final mechanical and thermal properties of the materials. Furthermore, the hydrophilicity of the chains can be enhanced by the presence of the ionic species, and so the materials can be processed as conventional dispersions even in a polar solvent such as water. As a consequence the applications are numerous; the main commercial outlets are focused on coatings and textiles industries where they can be used as waterproof coatings or substitutes for leather. But these materials can also be used in high-tech industries for shape memory materials, biomedical devices and biocompatible materials. This review summarizes the latest developments of this class of promising materials and provides the reader with the potentialities of these polymers in various areas
This work aims to understand the degradation induced by multiple injection molding cycles on numerous properties of wood flour reinforced polypropylene (PP) composites. The influence of the initial wood particle size was studied as well as the influence of the addition of polypropylene grafted with maleic anhydride (PPgma) as a coupling agent at a given rate. Biocomposite compounds (20wt% of wood flour) are produced by twin-screw extrusion. Then, multiple injection and grinding cycles were performed (up to 7 cycles) to obtain normalized samples. The evolution of the wood flour particle characteristics is first assessed by SEM observation, size measurements and nanoindentation experiments. Then, the evolution of the PP matrix microstructure is determined by SEC tests (average molecular weight measurements), rheometer tests and DSC (polymer crystallinity). Finally, material mechanical properties are measured at a macro-scale thanks to tensile tests. Our experimental results show that the composite mechanical properties remain quite stable after 7 processing cycles despite wood flour degradation and PP degradation.
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