Conception et synthèse d’une matrice polymère thermoplastique pour l’obtention de matériaux composites recyclables, résistants au feu et utilisables dans l’industrie

Novel poly(methyl methacrylate) (PMMA) thermoplastic matrices which can be used in the elaboration of composite materials have been synthesized and characterized from the point of view of their glass transition temperature (by differential scanning calorimetry) and their thermal degradation (by thermogravimetric analysis and by pyrolysis combustion flow calorimetry). The strategy followed was to incorporate in the PMMA chains repeat units comprising a flame retardant phosphorous side group via a radical copolymerization of MMA with a phosphorus-containing monomer. A set of phosphorus-containing flame retardant monomers has been synthesized from 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10 oxide (DOPO) by varying the nature of the polymerizable function (styrenic, acrylic, methacrylic), the nature of the atom bound to the phophore (oxygen, carbon, nitrogen) and the length of the spacer arm. We have shown that by adapting the structure and the quantity of the phosphorus repeating units, the glass transition temperature of the material was kept close to that of the PMMA while the thermal degradation of the materials was shifted to higher temperatures. Comparatively, physical blends of PMMA and DOPO with equivalent phosphorus contents exhibited significantly lower glass transition temperaturesDe nouvelles matrices thermoplastiques à base de poly(méthacrylate de méthyle) (PMMA) pouvant entrer dans la composition de matériaux composites ont été synthétisées et caractérisées du point de vue de leur température de transition vitreuse (par calorimétrie différentielle à balayage) et de leur dégradation thermique (par analyse thermogravimétrique et par microcalorimétrie). La stratégie suivie était d’incorporer dans les chaînes de PMMA des unités de répétition comportant un groupement latéral phosphoré retardateur de flamme via une copolymérisation radicalaire du MMA avec un monomère phosphoré. Un ensemble de monomères phosphorés retardateurs de flamme ont été synthétisés à partir de l’oxyde de 9,10-dihydro-9-oxa-10-phosphaphenanthrène-10 (DOPO) en faisant varier la nature de la fonction polymérisable (styrénique, acrylique, méthacrylique), la nature de l’atome lié au phosphore (oxygène, carbone, azote) et la longueur du bras espaceur. Nous avons montré qu’en adaptant la structure et la quantité des unités de répétition phosphorées, la température de transition vitreuse du matériau était maintenue proche de celle du PMMA alors que la dégradation thermique des matériaux était déplacée vers de plus hautes températures. Comparativement les mélanges physiques de PMMA et de DOPO avec une même teneur en élément phosphore présentent une température de transition vitreuse significativement plus bass

DOPO-Based Phosphorus-Containing Methacrylic (Co)Polymers: Glass Transition Temperature Investigation

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Devic’s disease associated with anti-Ro/SSA antibodies

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Highly active zinc alkyl cations for the controlled and immortal ring-opening polymerization of ε-caprolactone

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Pas de larme pour la neuromyélite optique, une maladie de Devic associée à des anti-Ssa

info:eu-repo/semantics/publishedJournées de neurologie de langue française, Lyon Avril 201

Evaluation of Brain Morphology and Topology in Huntington's Disease: Preliminary Results

info:eu-repo/semantics/published46the Annual Meeting ASNR (New Orleans) June 200

Soil properties and growing duration determine phosphorus phyto-availability dynamics of polyphosphate versus orthophosphate fertilizers

International audiencePurpose Polyphosphate (poly-P) fertilizers were proposed to increase the low phosphorus use efficiency (PUE) of orthophosphate (ortho-P) fertilizer but empirical data is inconsistent. Our study is aimed at investigating how soil properties, application time, and growth duration affect their phyto-availability.Methods Olsen-P dynamics were monitored using six soils amended with either ortho-P or poly-P. Subsequently, two contrasting soils (sandy and loamy) were selected to estimate P availability to plants using wheat as a model plant. Mechanistic modelling was used to interpret P dynamics in these experiments.Results For poly-P amended soils, Olsen-P increased continuously, while using ortho-P fertilizer the highest values were attained right after application and then monotonously decreased afterward. Olsen-P dynamics varied greatly among soils depending on their sorption capacity and related properties. In sandy soils, Olsen-P was consistently higher for ortho-P. In highly calcareous soils, Olsen-P was higher for poly-P after three weeks. Plant experiments confirmed a greater uptake of poly-P over ortho-P in loamy soil and extended trials (4 months) but not in sandy soils or short-term trials (4 weeks). Geochemical modeling suggested that complexation of soil Ca by poly-P reduced long-term P immobilization.Conclusions Soil properties and growth duration affect the efficiency of ortho-P vs. poly-P fertilizers. In clayey soils and extended growth duration, poly-P fertilizer can enhance PUE due to its prolonged phyto-availability as compared to ortho-P. In sandy soils and short growth duration poly-P has little advantage. The complexation of Ca by poly-P may have caused the increase of P phyto-availability

Flammability of phosphorus-containing polymers

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Striatal lesions: an underestimated complication of cerebral malaria?

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