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Lanthanide doped ceria thin films as possible counter electrode materials in electrochromic devicesHartridge, Adrian January 2000 (has links)
No description available.
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Influência da cura térmica (vapor) sob pressão atmosférica no desenvolvimento da microestrutura dos concretos de cimento Portland / The influence of steam curing in development of microstructure of Portland cement concreteMelo, Aluísio Bráz de 10 March 2000 (has links)
Os investimentos iniciais em moldes na indústria de pré-moldados de concreto de cimento Portland, em geral, são altos, havendo a necessidade de utilizá-los o mais intensivamente possível entre uma e outra moldagem. A conseqüência é que a desforma pode ocorrer em instantes inadequados, comprometendo a durabilidade do produto. Isto contraria o conceito fundamental da pré-moldagem que está relacionado ao rigoroso controle de qualidade do produto. A cura térmica é uma alternativa, pois é utilizada para acelerar a resistência mecânica inicial do concreto. Esse beneficio imediato é acompanhado por uma redução na resistência final comparativamente à cura normal em câmara úmida. Esta redução é atribuída ao desenvolvimento de uma microestrutura modificada. Para investigar esse fenômeno, com base nos conhecimentos em ciência e engenharia dos materiais, desenvolve-se um estudo experimental, aplicado a pré-moldados com pequena espessura. O objetivo principal é analisar tais modificações e os compostos hidratados, formados ao longo do tempo após a cura térmica, considerando os materiais empregados e estabelecendo relações com a perda de resistência final. Leva-se em conta a influência das adições e da duração dos ciclos térmicos. A análise da microestrutura está baseada nos seguintes ensaios: porosimetria por intrusão de mercúrio, microscopia eletrônica de varredura, termogravimetria e difração de raio-X. Confirma-se com base nos resultados que a cura térmica favorece a maior formação de portlandita e também acelera a reação pozolânica. Para a composição entre cimento Portland, a escória de alto forno (30%) e a sílica ativa (10%), submetidas a ciclos térmicos longos (12 horas Tmax=61°C), observa-se a maior perda na resistência mecânica a longo prazo. Neste caso, há fortes indícios de que há formação de fases com menor desempenho mecânico. Através de micrografias, para essa amostra, sugere-se a formação da etringita secundária com maior prejuízo na interface pasta-agregado. As conclusões sugerem que para minimizar as interferências no processo de cura e garantir resistências mínimas nas desmoldagens rápidas, com poucas perdas a longo prazo, é interessante associar ciclos térmicos curtos, cimento de alta resistência inicial, sílica ativa e superplastificante. / The initial investments of molds in the industry which makes pre-cast of Portland cement concrete is usually very high, thus creating a necessity to maximize the utilization of each moldings. The consequence is that the forms can be removed at inadequate time, which compromise the durability of the product. This contradicts the fundamental concepts of the pre-castings, which is related to a severe quality control. Steam curing is an alternative treatment and is used to accelerate the initial mechanical resistance of the concrete. This immediate benefit is accompanied by the decrease on final resistance compared to normal curing in humid chamber. This reduction is attributed to the development of a modified microstructure. To investigate this phenomenon, based on knowleledge of materials science and engineering, an experimental study is developed which is applied in pre-cast wich small thichness. The main objective of this work is to analyze the microstructure modifications and the hydrated compounds formed, after a period of steam curing, taking in account the used materiaIs, also to establish a relations with the loss of final strength. The influence of additions and duration of steam cycles are considered. The analyses of microstructures are based on the following tests: mercury intrusion porosimetry, scanning electron microscope, thermogravimetry and X-ray diffraction. Based on the results it can be confirmed that steam curing favors a large formation of ponlandite and also accelerates pozzolanic reaction. For the composition of Portland cement, slag fumace blast (30%) and active silica (10%), submitted for long period of thermal cycles (12 hours, Tmax=61°C), a great loss strength was observed. In this case it is possible the formation of phases with poor mechanical performance. Through micrographs, for this sample, it is observed the formation of secondary ettringite with a large damage in the interface aggregate-paste. The conclusions suggest that to minimize the interference in the process of curing and to guarantee a minimum strength during the rapid separation of the concrete from the molds, with a minor loss in a long term, it is interesting to associate short steam cycles, high initial resistance cement, adive silica and superplasticizer.
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L’impact du séchage au jeune âge sur la carbonatation des matériaux cimentaires avec additions minérales / The impact of drying at the early age of the carbonation cementitious materials with mineral admixturesBertin, Matthieu 27 November 2017 (has links)
De nos jours, l’utilisation de liants à faible teneur en clinker est de plus en plus courante. Or la cinétique de réaction des additions minérales utilisées est plus lente que celle du clinker. Si les conditions de cure ne sont pas adaptées, le matériau aura une structure poreuse plus importante, ce qui le rendra plus sensible à la pénétration des agents agressifs extérieurs comme le CO2 ou les Cl-. La carbonatation du béton est l’un des principaux phénomènes pouvant diminuer la durée de vie d’une structure en béton armé. En effet, elle entraine une diminution du pH de la solution interstitielle qui a pour conséquence une dépassivation des armatures, puis la corrosion de ces dernières si les conditions s’y prêtent.L’objectif de cette thèse est d’étudier l’impact de la carbonatation au jeune âge sur des liants à faible teneur en clinker. Pour cela l’étude se compose de deux aspects : le premier est l’étude de l’impact de l’hydratation et de la carbonatation sur les propriétés de transport et les isothermes de sorption hydrique, et le second est l’étude de l’impact du couplage hydratation-séchage-carbonatation sur la microstructure et la structure poreuse. Pour le premier aspect, les propriétés de transport étudiées sont la diffusion de l’O2, la diffusion de la vapeur d’eau, la perméabilité à l’eau liquide qui sont des données d’entrée dans les modèles de carbonatation ainsi que la perméabilité aux gaz qui est un indicateur de durabilité. Pour le second aspect, l’impact du couplage est mesuré par ATG et DRX pour déterminer l’assemblage de phases, de plus de la porosimétrie par intrusion de Mercure et des pesées hydrostatiques sont effectuées pour détecter le changement de la structure poreuse. Les matériaux étudiés sont des pâtes de ciment et des bétons avec un rapport eau/ liant de 0,57 avec l’un des trois liants suivants : CEM I, CEM I +30% de cendres volantes et CEM I +60% de laitiers.Pour le premier aspect, les résultats montrent que pour les pâtes de CEM I le temps de cure a un faible impact sur les isothermes de sorption de vapeur d’eau s’il est compris entre 3 jours et 6 mois. Alors que, pour les pâtes de CEM I + 60% de laitier, l’augmentation du temps de cure accroit significativement la teneur en eau (pour HR=65%, tcure=3 jours et pour tcure=6 mois ) dû à une augmentation de la teneur en C-S-H. D’autre part, la carbonatation entraine une diminution de la teneur en eau de l’échantillon, ainsi que l’amplitude de l’hystérésis. De plus, le gel a une porosité plus grossière. Par ailleurs, la carbonatation entraine une augmentation de la perméabilité aux gaz des matériaux. Pour le second aspect, les résultats montrent que l’utilisation d’additions minérales diminue la résistance à la carbonatation du matériau et que cette résistance augmente avec le temps de cure si l’échantillon contient des additions. La carbonatation de la portlandite, des C-S-H et des aluminates est concomitante. De plus, pour les matériaux aux laitiers, les résultats montrent qu’ils sont plus sensibles à la carbonatation des C-S-H et des aluminates que les CEM I. En effet quand le rapport variation molaire de CaCO3 sur variation molaire de Portlandite est calculé, il vaut 1.8 pour le CEM I et environ 3.5 pour les matériaux aux laitiers. Enfin, la carbonatation entraine une diminution du degré de saturation de l’échantillon. En effet, le degré de saturation à la surface de l’échantillon passe de 50% à 35% après carbonatation pour les échantillons de CEM I et de 50% à 5% pour les échantillons de CEM I + 60% de laitiers. Cette diminution peut s’expliquer par la diminution de la surface spécifique qui est divisée par 2 après carbonatation due à la décalcification des C-S-H. Même si la carbonatation entraine une diminution de porosité cette dernière est trop faible dans ce cas pour contrer cet effet / Nowaday, low clinker content binders are used more and more often. But the kinetics reactions of the supplementary cementitious materials (SCM) are slower than this one of clinker. If the curing conditions are not adapted, material will have a bigger pore structure and becomes more sensitive to the ingress of aggressive species from the environment like the CO2 or Cl-. Carbonation is one of main phenomena which can lead to decrease the life time of reinforced concrete structure. Indeed, it leads to a decrease of pore solution pH which leads to the depassivation of rebar. Then these rebars can be corroded if the conditions are appropriate.The aim of this thesis is to study the impact of carbonation at early age for binder with a low clinker content. This study was composed of two aspects: the first one is focus on the impact of hydration and carbonation on the transport properties and the water vapour sorption isotherms (WVSI), and the second one is focus on the impact of coupling hydration – drying-carbonation on the microstructure and the pore structure. For the first aspect, the studied transport properties was O2 diffusivity, water vapour diffusivity, water liquid permeability which are inputs for carbonation modelling and the intrinsic gas permeability which is a durability factor. For the second aspect, the coupling impact was measured by TGA and DRX to determine the phase assemblage; moreover Mercury intrusion porosimetry (MIP) and hydrostatic weigh were carried out to measure the change in the pore structure. The studied materials were cement pastes and concretes with water to binder ratio of 0.57 with one of the following binders: CEM I, CEM I +30% PFA and CEM I + 60% GGBS.For the first part, results show that a curing time between 3 days and 6 months has a low impact on the WVSI for the CEM I paste. Whereas, in the CEM I +60% GGBS paste, when the curing time increases, the water content increases (for a RH=65%, tcuring=3 days and for tcuring=6 months ), this is due to the increase of the C-S-H content. Moreover, carbonation leads to decrease the water content and the hysteresis becomes flat. Additionally, carbonation leads to increase the intrinsic gas permeability. For the second part, the results show that the use of SCM decreases the carbonation resistance and this resistance increases with the curing time. Carbonation of Portlandite, C-S-H and aluminates occurs in the same time. Moreover, the CEM I +60% GGBS paste are more sensitive to the carbonation of C-S-H and aluminates than the CEM I paste. Indeed, the molar variation of CaCO3 to the molar variation of Portlandite ratio has a value around 3.5 for the CEM I +60% GGBS and 1.8 for the CEM I. Finally, carbonation leads to decrease the water saturation degree at the surface of sample. Indeed, the degree of saturation at the surface of the sample increases from 50% to 35% after carbonation for the CEM I paste and from 50% to 5% for the CEm I +60% GGBS paste. This decrease can be explained by the decrease of the BET specific surface which is divided by 2 after carbonation. It is due to the decalcification of C-S-H. Although carbonation leads to a decrease of porosity, this one is too small in this case to counter this effect
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Influência da cura térmica (vapor) sob pressão atmosférica no desenvolvimento da microestrutura dos concretos de cimento Portland / The influence of steam curing in development of microstructure of Portland cement concreteAluísio Bráz de Melo 10 March 2000 (has links)
Os investimentos iniciais em moldes na indústria de pré-moldados de concreto de cimento Portland, em geral, são altos, havendo a necessidade de utilizá-los o mais intensivamente possível entre uma e outra moldagem. A conseqüência é que a desforma pode ocorrer em instantes inadequados, comprometendo a durabilidade do produto. Isto contraria o conceito fundamental da pré-moldagem que está relacionado ao rigoroso controle de qualidade do produto. A cura térmica é uma alternativa, pois é utilizada para acelerar a resistência mecânica inicial do concreto. Esse beneficio imediato é acompanhado por uma redução na resistência final comparativamente à cura normal em câmara úmida. Esta redução é atribuída ao desenvolvimento de uma microestrutura modificada. Para investigar esse fenômeno, com base nos conhecimentos em ciência e engenharia dos materiais, desenvolve-se um estudo experimental, aplicado a pré-moldados com pequena espessura. O objetivo principal é analisar tais modificações e os compostos hidratados, formados ao longo do tempo após a cura térmica, considerando os materiais empregados e estabelecendo relações com a perda de resistência final. Leva-se em conta a influência das adições e da duração dos ciclos térmicos. A análise da microestrutura está baseada nos seguintes ensaios: porosimetria por intrusão de mercúrio, microscopia eletrônica de varredura, termogravimetria e difração de raio-X. Confirma-se com base nos resultados que a cura térmica favorece a maior formação de portlandita e também acelera a reação pozolânica. Para a composição entre cimento Portland, a escória de alto forno (30%) e a sílica ativa (10%), submetidas a ciclos térmicos longos (12 horas Tmax=61°C), observa-se a maior perda na resistência mecânica a longo prazo. Neste caso, há fortes indícios de que há formação de fases com menor desempenho mecânico. Através de micrografias, para essa amostra, sugere-se a formação da etringita secundária com maior prejuízo na interface pasta-agregado. As conclusões sugerem que para minimizar as interferências no processo de cura e garantir resistências mínimas nas desmoldagens rápidas, com poucas perdas a longo prazo, é interessante associar ciclos térmicos curtos, cimento de alta resistência inicial, sílica ativa e superplastificante. / The initial investments of molds in the industry which makes pre-cast of Portland cement concrete is usually very high, thus creating a necessity to maximize the utilization of each moldings. The consequence is that the forms can be removed at inadequate time, which compromise the durability of the product. This contradicts the fundamental concepts of the pre-castings, which is related to a severe quality control. Steam curing is an alternative treatment and is used to accelerate the initial mechanical resistance of the concrete. This immediate benefit is accompanied by the decrease on final resistance compared to normal curing in humid chamber. This reduction is attributed to the development of a modified microstructure. To investigate this phenomenon, based on knowleledge of materials science and engineering, an experimental study is developed which is applied in pre-cast wich small thichness. The main objective of this work is to analyze the microstructure modifications and the hydrated compounds formed, after a period of steam curing, taking in account the used materiaIs, also to establish a relations with the loss of final strength. The influence of additions and duration of steam cycles are considered. The analyses of microstructures are based on the following tests: mercury intrusion porosimetry, scanning electron microscope, thermogravimetry and X-ray diffraction. Based on the results it can be confirmed that steam curing favors a large formation of ponlandite and also accelerates pozzolanic reaction. For the composition of Portland cement, slag fumace blast (30%) and active silica (10%), submitted for long period of thermal cycles (12 hours, Tmax=61°C), a great loss strength was observed. In this case it is possible the formation of phases with poor mechanical performance. Through micrographs, for this sample, it is observed the formation of secondary ettringite with a large damage in the interface aggregate-paste. The conclusions suggest that to minimize the interference in the process of curing and to guarantee a minimum strength during the rapid separation of the concrete from the molds, with a minor loss in a long term, it is interesting to associate short steam cycles, high initial resistance cement, adive silica and superplasticizer.
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Renforcement d'alliages fer-aluminium ordonnés B2. Influence d'additions (Ni et B) et de la microstructureColas, David 28 September 2004 (has links) (PDF)
Nous étudions les effets d'additions (Ni et B) et de la microstructure sur le comportement mécanique d'alliages fer-aluminium contenant 40 % at. Al. Au niveau macroscopique, nous montrons que le nickel renforce les alliages FeAl sur toute la gamme de température, mais qu'il conduit simultanément à une diminution de la contrainte de clivage, accentuant ainsi la fragilité à l'ambiante de ces alliages. Nous confirmons l'intérêt du raffinement de la taille des grains, par métallurgie des poudres, pour améliorer la limite d'élasticité et la résistance à la rupture. Nous montrons alors le caractère additif de l'effet du nickel sur la limite d'élasticité par rapport au renforcement de type "Hall et Petch". Nous montrons aussi que les phénomènes de durcissement (nickel ou taille de grains) provoquent le masquage de l'anomalie de la limite d'élasticité que ces alliages présentent habituellement. L'étude des mécanismes de déformation à l'échelle des dislocations nous permet de préciser que le durcissement en solution solide (DSS) dû au nickel à basse température ne peut être expliqué par les théories classiques de DSS mais plus vraisemblablement par un effet du nickel sur la contrainte de Peierls. En outre, nous montrons que nos résultats microscopiques et macroscopiques concernant l'anomalie peuvent être pris en compte par le modèle de traînage de tubes d'APB. Enfin, nous mettons en relation l'observation en dynamique (microscopie en transmission in situ) d'un mécanisme de multiplication des superdislocations, avec la tendance au clivage des alliages contenant du nickel.
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Development and application of new chiral -amino alcohols in synthesis and catalysis : Use of 2-azanorboryl-3-methanols as common intermediates in synthesis and catalysisPinho, Pedro January 2001 (has links)
The development and application of unnatural amino alcohols,prepared via hetero-Diels-Alder reactions,in synthesis and catalysis is described.The studies are concerned with the [i]scope of the hetero-Diels-Alder reaction and preparation of important intermediates in the synthesis of antiviral agents,[ii ]application of amino alcohols in the ruthenium transfer hydrogenation of ketones,[iii ]use of similar precursors in the in situ generation of oxazaborolidines for reduction of ketones,and [iv] development and application of new chiral auxiliaries for dialkylzinc additions to activated imines, respectively. [i ]The use of chiral exo -2-azanorbornyl-3-carboxylates in the preparation of enantiopure cyclopentyl-amines is described.At the same time the scope of the hetero-Diels-Alder reaction,used in their preparation,is extended by manipulations of the dienophiles. [ii ]Application of 2-azanorbornyl-3-methanol as a very efficient ligand in the ruthenium-catalysed asymmetric transfer hydrogenation of aromatic ketones.This ligand (2 mol%)in combination with [RuCl2(p -cymene)]2 (0.25 mol%)gave rise to a very fast reaction (1.5 h)leading to the reduced products in excellent yields and enantioselectivities (up to 97%ee ). [iii ]Preparation of α-disubstituded 2-azanorbornyl-3-methanols,in situ generation of the corresponding oxazaborolidines,and use of the latter in reduction of aromatic ketones.Concentration, solvent,and temperature effects on the reaction outcome are described. [iv ]Development of two generations of chiral auxiliaries for the addition of dialkylzinc reagents to N - (diphenylphosphinoyl)imines.Studies using density functional computations allowed the rationalisation of the reaction mechanism and the development of a second generation of ligands that improved the previously reported results.Up to 98%ee could be obtained with these new ligands. Solvent effects on the outcome of the reaction and extension of the work to a larger variety of N - (diphenylphosphinoyl)imines are described.
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Thermoluminescence spectra from sulphates, fluorides and garnets doped with rare earth ionsAl-Maghrabi, Mufied Mahmoud January 2001 (has links)
Luminescence measurements have been applied to three different structures namely, sulphate, fluorides and YAG. In all cases the RE doping suppresses the intrinsic emission and results in intense luminescence characteristic of the RE dopant. Additionally, in double doped samples, or contaminated ones, the TL data show that each dopant defines a glow peak, which is displaced in temperature relative to the others. Examples of this were discussed for CaS04:Ce,Mn; YAG:Nd,Tb,Cr,Mn; BaF2:Ho,Ce and BaF2:Tm,Ce. The data are discussed in terms of an energy transfer model between different parts of extended defect complexes which encompass the RE ion and the lattice defects. Calcium sulphate doped with Dy define a TL peak near 200°C suitable for radiation measurements, but when co-doped with Ag the TL peak move to higher temperatures with minor effects on the peak sensitivity. In Ce,Mn double doped samples, the peak temperatures differ by -7°C between the Ce and Mn sites. The TL glow curves from alkaline earth fluorides are complex and contain several overlapping peaks. Curve fitting show that the peak maxima below room temperature are insensitive to the RE dopant. Additionally the host material has a modest effect on the peak positions. Above room temperature each dopant provides a TL curve specific to the added RE ion and do not show common peaks. Concentration has many effects on the resultant glow curve, and even at the lowest concentration used here (0.01%) there is evidence of cluster formation. Samples with high RE content show low values of the frequency factor consistent with the energy transfer model in that the emission from RE-RE cluster dominates over the emission from direct charge recombination within the defect complex. The effect of concentration and the TL mechanism operating below room temperature are also discussed. Luminescence signals from the near surface of YAG:Nd (via CL) were contrasted with those from the bulk material via RL. Results indicate that the outer few micron layers differ significantly in luminescence response from the bulk crystal. The differences were ascribed to result from solvents that enter the YAG lattice during the growth stage or subsequently from cleaning treatments via the dislocations caused by cutting and polishing. Additionally, the growth stage may include gases from the residual air in the growth furnace trapped into the YAG lattice. In each case there is a discontinuity in luminescence intensity and/or emission wavelengths at temperatures which mach the phase transitions of the contaminants. At the transition temperature there will be a sudden pressure change and this will induce surface expansion or bulk compression. The differences between the two cases were detected by the alternatives of CL and RL excitation, where the Nd or Er lines have moved in opposite directions. The detection of such low concentrations of solvents/trapped gases by luminescence is extremely difficult due to experimental limitations. Hence their role in luminescence generation is normally ignored.
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A first principles study of hydrogen related defects in siliconHourahine, Benjamin January 2000 (has links)
No description available.
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Interactions physico-chimiques ions-matrice dans les bétons sains ou carbonatés : influence sur le transport ioniqueSaillio, Mickaël, Saillio, Mickaël 10 May 2012 (has links) (PDF)
La carbonatation atmosphérique et la pénétration des ions chlorures sont les principales causes du déclenchement de la corrosion des armatures dans les bétons armés. Chacun de ses mécanismes a fait l'objet de nombreuses études dans la bibliographie. Pourtant les études prenant en compte en même temps les deux types d'agression sont rares. Le couplage des deux phénomènes existe cependant. La carbonatation intervient en effet dans tout ouvrage dès le décoffrage et il suffit que cet ouvrage soit aussi par exemple situé à proximité d'eau de mer pour que les embruns apportent des ions chlorures dans le matériau. L'objectif de cette thèse a été de quantifier les différentes phases de la matrice cimentaire et ses capacités de fixation des ions chlorures par le biais d'isothermes d'interactions pour des matériaux sains et carbonatés. Ces isothermes d'interactions obtenues notamment par la méthode des équilibres ont permis de voir que les matrices partiellement ou totalement carbonatées fixaient moins d'ions chlorures que les matrices saines. L'utilisation de moyens complémentaires d'analyses tels que l'analyse thermogravimétrique (ATG), la diffraction des rayons X (DRX) et la résonance magnétique nucléaire (RMN) a permis de mieux comprendre cette perte de fixation. Une diminution des sels de Friedel et des chlorures fixés par les C-S-H a été ainsi mise en évidence dans les matériaux carbonatés. Ces diminutions qui on été quantifiées sont attribuées à une modification sous carbonatation des phases capables de fixer les ions chlorures (phases aluminates, sulfo-aluminates et C-S-H). Des différences au niveau du réseau poreux ont été également mises en évidence par la porosimétrie par intrusion de mercure (diminution de la macroporosité et de la connectivité en général pour les matrices carbonatées par formation de CaCO3). L'objectif a été aussi de corréler toutes ces modifications observées avec les propriétés de transport des ions qui ont été obtenues par des tests de diffusion et migration des ions chlorures (et/ou sulfates) ainsi que des mesures de résistivité électrique. Les résultats expérimentaux ont montré que le coefficient de diffusion apparent est plus grand dans les matériaux carbonatés. Certaines expériences de diffusion faites en présence à la fois d'ions chlorures et sulfates ont aussi montré la concurrence de ces deux ions pour se fixer à la matrice cimentaire. Les matériaux cimentaires testés (bétons et pâtes) ont été formulés sans ou avec additions minérales (métakaolin, cendres volantes, laitier) et les propriétés de ces matériaux ont été observées à différents âges
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Optimisation of concrete mix design with high content of mineral additions: effect on microstructure, hydration and shrinkageKhokhar, Muhammad Irfan 14 September 2010 (has links)
The cement being used in the construction industry is the result of a chemical process<p>linked to the decarbonation of limestone conducted at high temperature and results in a<p>significant release of CO2. This thesis is part of the project EcoBéton (Green concrete) funded<p>by the French National Research Agency (ANR), with a purpose to show the feasibility of<p>high substitution of cement by mineral additions such as blast furnaces slag, fly ash and<p>limestone fillers. Generally for high percentages of replacements, the early age strength is<p>lower than Portland cement concrete. To cope with this problem, an optimisation method for<p>mix design of concrete using Bolomey’s law has been proposed. Following the encouraging<p>results obtained from mortar, a series of tests on concretes with different substitution<p>percentages were carried out to validate the optimisation method. To meet the requirements of<p>the construction industry related to performance of concrete at early age, which determine<p>their durability, a complete experimental study was carried out. Standard tests for the<p>characterization of the mechanical properties (compressive strength, tensile strength, and<p>setting) allowed to validate the choice of mix design on the basis of equivalent performance.<p>We focused on the hydration process to understand the evolution of the mechanical<p>properties. Setting time measurement by ultrasound device at different temperatures (10°C,<p>20°C and 30°C) showed that ground granulated blast furnace slag (GGBFS) and fly ash<p>delayed the setting process, while use of limestone filler may accelerate this process.<p>Calorimetric studies over mortars and concretes made possible to calculate the activation<p>energy of the different mixtures and a decrease in heat of hydration of concretes with mineral<p>additions was observed which is beneficial for use in mega projects of concrete. Scanning<p>Electron Microscopy observations and thermal analysis have given enough information about<p>the hydration process. It was observed that the hydration products are similar for different<p>concrete mixtures, but the time of their appearance and quantity in the cement matrix varies<p>for each concrete mix.<p>Last part of the thesis was dedicated to the study of main types of shrinkage. First of all,<p>deformations measured were correlated to hydration, capillary depression and porosity<p>evolution. Results allowed concluding that the use of mineral additions has an actual effect on<p>the plastic shrinkage behaviour, but its impact is not proportional to the percentage of<p>additions. Substitution of cement by the additions seems to have a marked influence on the<p>kinetics of the shrinkage without any effect on its long term amplitude. The study of<p>restrained shrinkage under drying conditions by means of ring tests showed that concretes<p>with high percentage of slag addition seem more prone to cracking than the Portland cement<p>concretes. / Doctorat en Sciences de l'ingénieur / info:eu-repo/semantics/nonPublished
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