La vaste gamme de combinaisons possibles de cations et anions, ainsi que les excellentes propriétés intrinsèques des liquides ioniques (LIs) peuvent être considérées comme les principaux facteurs qui ont conduit au développement d’une recherche utilisant des LIs comme additifs des matériaux polymère. Ainsi, l'objectif principal de ce travail est d'explorer le rôle de la nature du cation et/ou du anion du LI sur les propriétés des matériaux basées de poly (méthacrylate de méthyle) (PMMA). Dans une première partie, des LIs de type imidazolium et ammonium ont été incorporés au PMMA et des caractérisations morphologiques et structurales ont été effectuées afin de comprendre leur impact sur les propriétés thermiques, viscoélastiques et mécaniques des matériaux résultants. Dans la section suivante, la capacité de ces LIs à base d'imidazolium et d'ammonium en tant qu’agents interfaciaux à la surface de la silice a été évaluée. Sub-micro et nanoparticules de silice, ainsi que les LIs, ont été incorporées dans une matrice de PMMA afin de préparer des composites. L'amélioration des propriétés des matériaux ont été discutées en fonction du degré auquel chaque LI influence la compatibilité entre les particules et la matrice polymère. De plus, ces composites ont été exposés au dioxyde de carbone en état supercritique (scCO2) pour utiliser celui-ci comme agent moussant et ainsi produire des matériaux expansés. Le rôle du LI et des particules de silice pour structurer les matériaux expansés a été analysé. Dans la dernière partie de cette étude, le scCO2 est utilisé comme milieu de réaction pour la modification chimique par greffage de la surface des nanoparticules de silice par des LIs de type imidazolium, contenant également des groupes hydrolysables et différentes chaînes alkyles. Le rôle de la pression et la quantité de LI ajoutées au milieu de réaction, ainsi que la longueur de la chaîne alkyle des LIs se sont avérées essentielles pour contrôler le degré de fonctionnalisation des nanoparticules. Enfin, ces nanoparticules modifiées ont été incorporées dans une matrice PMMA. Des analyses de morphologie ont été utilisées pour évaluer la dispersion des particules dans la matrice et les propriétés physico-chimiques de ces matériaux ont été également étudiées. / The large array of cation/anion combinations, and the excellent intrinsic properties of ionic liquids (ILs) open a large range of possibilities in their use as additives to polymer materials. Thus, the main objective of this work is to explore the role of both the cation and anion of a series of ILs on the properties of poly(methyl methacrylate) (PMMA)-based materials. In a first approach, low amounts of imidazolium and ammonium-based ILs were incorporated as additives to PMMA in the molten state. Morphological and structural characterizations were developed in order to understand the impact of the presence of such ILs on the thermal and mechanical properties of the resulting materials. Then, in the following section, the ability of the same imidazolium and ammonium-based ILs as physical modifiers of silica surface was evaluated. In such an approach, ILs were supposed to act as interfacial agents. Sub-micron and nanosize silica particles were used to prepare PMMA composites. Thus, the extents of each IL improve the interfacial interaction between PMMA and silica particles were discussed. In addition, supercritical carbon dioxide (scCO2) was used as foaming agent to produce foamed PMMA-based composites. In such a case, the combined effect of the presence of ILs and silica particles was analyzed regarding the morphology of the foamed structures. In the last section, scCO2 was used as reaction medium, in an environmental friendly approach, to chemically modify silica nanoparticles using a series of imidazolium IL-functionalized silanes (with different alkyl chain lengths). Thermogravimetric analysis (TGA) was used to highlight the effect of the working pressure and the content of such ILs in the reaction medium. The effect of the alkyl chain length on the grafting density of the resulting nanoparticles was also discussed. Finally, novel PMMA-based nanocomposites were prepared by the incorporation of such grafted nanoparticles. Transmission electron microscopy (TEM) and small-angle neutron scattering (SANS) analyses were used to evaluate the state of dispersion of the particles into the polymer matrix. Moreover, the thermal, rheological and mechanical properties of the materials were studied.

Le contexte environnemental actuel conduit les constructeurs automobiles à diminuer les émissions globales de CO2. Afin de répondre à cet objectif, plusieurs voies sont accessibles mais l’allègement de la structure du véhicule apparaît comme la solution la plus prometteuse grâce à la substitution des pièces métalliques par des matériaux composites et plus particulièrement des composites thermoplastiques à matrices acryliques. Cette étude s’est donc intéressée à développer et caractériser plusieurs formulations à base acrylique afin d’identifier les différents leviers (choix du monomère / condition de polymérisation) permettant d’atteindre une polymérisation rapide (< 3 à 5 min) adaptée aux hautes cadences de l’industrie automobile. Le moulage par transfert de résine (RTM) ayant été choisi comme procédé de mise en œuvre, une seconde étape de travail a été de caractériser l’évolution de la viscosité au cours de la polymérisation. En disposant des mesures cinétiques et rhéologiques, il a aussi été possible, par modèle inverse, de proposer un suivi in-situ de la polymérisation via la corrélation des données par des mesures diélectrométriques. Puis, dans une optique d’amélioration de la tenue chimique du PMMA, la synthèse d’un polymère réversible présentant alternativement une structure tridimensionnelle et une structure linéaire a été réalisée. Ainsi, grâce à la préparation d’un comonomère présentant des fonctions Diels-Alder, il a été possible d’obtenir un polymère ayant la capacité d’emprunter les propriétés de résistance chimique des réseaux thermodurcissables tout en conservant l’aptitude à la transformation des thermoplastiques. Enfin, une dernière étude s’est portée sur le renforcement du PMMA par mélange avec différents polymères. Ainsi, grâce à un choix judicieux de polymères présentant des caractéristiques physico-chimiques intéressantes, il a été possible d’améliorer significativement la tenue en température mais également la résistance au choc de la matrice acrylique développée. / Nowadays, polymer matrix composites are widely used for aerospace, automotive, railway and sport industries. For similar structural properties, these materials coul be very attractive since they could be 30 to 40% lighter than metallic counterparts. In the current context of environmental development issues, thermoplastic-based composites, (in our case acrylic matrix based one), can be considered as they can be easily recycled as opposed to thermoset-based ones. Furthermore, they could exhibit good mechanical properties, i.e. stiffness and impact resistance, enabling them to be relevant for many applications. Manufacturing structural composites requires to produce parts without defects having complex geometries. For this purpose Resin Transfer Molding (RTM) has been selected to process such composites. Indeed, it corresponds to a low temperature closed-mold process allowing for manufacturing complex continuous fiber-based-reinforced parts. However, it requires precursors with a very low viscosity (η < 1 Pa.s) to ensure a good impregnation of the dry preform. To be cost effective, fast reactive systems have also to be selected. Thermoplastic polymers which own a very high viscosity in molten state cannot be directly used. Our strategy is to design an acrylic-based reactive formulation exhibiting a very low initial viscosity, i.e. about 100 mPa.s and which can subsequently polymerizes via a free radical mechanism once the mold is filled and the preform fully impregnated. Therefore, our main objective is to optimize curing conditions (especially thermal initiator ratios and temperature) of RTM-compatible acrylic-based reactive formulations to lead to suitable composite parts with high conversion rate, low residual monomer content and relevant process cycles.

GONÇALVES, Fabrício Mota. Evapotranspiração e coeficientes de cultivo (KC) da cana-de-açúcar irrigada por gotejamento subsuperficial. 2010. 64 f. : Dissertação (mestrado) - Universidade Federal do Ceará, Centro de Ciências Agrárias, Departamento de Engenharia Agrícola, Programa de Pós-Graduação em Engenharia Agrícola, Fortaleza-CE, 2010. / Submitted by demia Maia (demiamlm@gmail.com) on 2016-06-28T16:59:16Z No. of bitstreams: 1 2010_dis_fmgonçalves.pdf: 3900094 bytes, checksum: 1ad79acf1432c0de09bcbdf52cb0f8c3 (MD5) / Approved for entry into archive by demia Maia (demiamlm@gmail.com) on 2016-06-28T16:59:48Z (GMT) No. of bitstreams: 1 2010_dis_fmgonçalves.pdf: 3900094 bytes, checksum: 1ad79acf1432c0de09bcbdf52cb0f8c3 (MD5) / Made available in DSpace on 2016-06-28T16:59:48Z (GMT). No. of bitstreams: 1 2010_dis_fmgonçalves.pdf: 3900094 bytes, checksum: 1ad79acf1432c0de09bcbdf52cb0f8c3 (MD5) Previous issue date: 2010 / Sugar cane is one of the crops with the highest level of water consumption, with a high evapotranspiration demand throughout most of its cycle. Knowledge of the sugar cane water demand, the time that irrigation should be applied, and how to irrigate the crop are becoming increasingly important for the sustainable development of irrigated sugar cane cultivation, especially in areas of low water availability, as it is the case in northea stern Brazil. The experiment was carried out at the Curu Experimental Field (property of the Embrapa Tropical Agroindustry), located in the Curu-Paraipaba Irrig ation Project, city of Paraipaba-CE (3 ° 29 '20''S, 39 ° 9' 45''W and elevation 30m), in order to determine the evapotrans piration and crop coefficients (Kc) of sugarcane (Saccharum L. officinarium), subsurface drip-irrigated. It was used the SP 6949 sugar cane variety, planted in a spacing of 1.8 m between double rows and 0.4 m between rows within the double row. As to t he irrigation, we used one lateral water line for each double row, buried at a depth of 0.15 m, w ith self-compensating drip emitters, with a flow rate of 1 L h-1, spaced 0.5 m on the water line. The crop was irrigated daily and there were three fertigations per week. The irrigation de pth was periodically adjusted, keeping the soil water potential between -8 kPa to -20 kPa. The crop evapotranspiration (ETc) was determined using a wei ghing lysimeter with a surface area of 2.25 m 2. The reference evapotranspiration (ETo) was estimated by the FAO Penman-Monteith method. The durations of the phenological stages of cane sugar were estimated through analysis of soil cover, with the use of digital images. Durations of 31, 49, 237 and 118 days were observed, respectively for initial, crop development, mid-season and late season stages. The yields achieved within and outside the lysimeter were respectively 144.4 and 108.8 t ha -1 . The total ETc observed during the cycle of the sugar cane was 1074.1 m m, with maximum values of 6.6 mm d-1 during the mid-season stage. Observed Kc values for initial, mid-season and late season stages were respectively 0.23, 1 .03 and 0.50. In the crop development stage, the relationship between Kc and the (crop) soil cover was represented with good accuracy by a negative quadratic model. / A cana-de-açúcar é uma das culturas com maior consumo de água, apresentando uma alta demanda evapotranspirativa ao longo da maior parte do seu ciclo. O conhecimento das necessidades hídricas da cana-de-açúcar, do momento de aplicação da água requerida pela mesma e a forma de aplicação torna-se cada vez mais importante para o desenvolvimento sustentável da sua produção irrigada, principalmente em regiões de pouca disponibilidade hídrica, como é o caso da região Nordeste do Brasil. O experimento foi conduzido no Campo Experimental do Curu, pertencente à Embrapa Agroindústria Tropical localizado no Perímetro Irrigado Curu-Paraipaba, município de Paraipaba-CE (3° 29’ 20’’ S, 39° 9’ 45’’ W e altitude de 30 m), com o objetivo de determinar a evapotranspiração e os coeficientes de cultivo (Kc) da cana-de-açúcar (Saccharum officinarium L.), irrigada por gotejamento subsuperficial. Utilizou-se a variedade de cana SP 6949, plantada no espaçamento de 1,8 m entre fileiras duplas e 0,4 m entre linhas dentro da fileira dupla. Na irrigação utilizou-se uma linha lateral para cada fileira dupla, enterrada na profundidade de 0,15 m, com gotejadores autocompensantes, com vazão de 1 L h-1, espaçados de 0,5 m na linha. A cultura foi irrigada com freqüência diária e foram realizadas três fertirrigações por semana. A lâmina de irrigação foi ajustada periodicamente, mantendo-se o potencial de água no solo entre -8 kPa e -20 kPa. A evapotranspiração da cultura (ETc) foi determinada utilizando-se um lisímetro de pesagem com área superficial de 2,25 m2. A evapotranspiração de referência (ETo) foi estimada pelo método FAO Penman-Monteith. As durações das fases fenológicas da cana-de-açúcar foram estimadas por meio da análise da cobertura do solo pela cultura, determinada com o uso de imagens digitais. Foram observadas durações de 31, 49, 237 e 118 dias, para as fases inicial, de desenvolvimento, intermediária e final, respectivamente. A produtividade alcançada dentro e fora do lisímetro foi de 144,4 e 108,8 t ha-1, respectivamente. A ETc total observada durante o ciclo da cana-de-açúcar foi de 1.074,1 mm, com valores máximos da ordem de 6,6 mm d-1 durante a fase intermediária. Foram observados valores de Kc iguais a 0,23, 1,03 e 0,50, para as fases inicial, intermediária e final, respectivamente. Na fase de desenvolvimento vegetativo a relação entre o Kc e a cobertura do solo pela cultura foi representada com bastante exatidão por um modelo quadrático negativo.