Le reformage à la vapeur couplé à la sorption in-situ d’un composant du milieu réactionnel (sorption-enhanced steam reforming, SESR) est un procédé d’avant-garde qui permet simultanément la production d’hydrogène de très haute pureté et la capture du CO2. L'objectif principal de ce travail est le développement de nouveaux sorbants pour le CO2 applicables à hautes températures et l’étude de leur application dans SESR. Deux nouvelles méthodes de synthèse ont été proposées pour synthétiser du zirconate de lithium (Li2ZrO3), zirconate de sodium (Na2ZrO3) ainsi que des matériaux à base d’oxyde de calcium (CaO), trois catégories de sorbants capables de réagir avec le CO2 à hautes températures. L’application du Li2ZrO3 à la capture du CO2 a démontré une augmentation de l’activité du matériau produit par une nouvelle méthode de synthèse combinant un surfactant et traitement à ultrasons, comparativement au Li2ZrO3 préparé par une méthode avec surfactant seulement (sans ultrasons) ou par la méthode conventionnelle (mélange des composants en phase liquide). Néanmoins, pour des pressions partielles en CO2 inférieures à 0,75 bar, la faible cinétique de sorption du CO2 obtenue par le Li2ZrO3 limite son application au procédé SESR. En considérant l’amélioration des propriétés de sorption obtenue en appliquant la méthode combinée surfactant/ultrasons à la synthèse du Li2ZrO3, la même technique a été aussi appliquée à la synthèse du Na2ZrO3. Des résultats inattendus ont été pourtant obtenus. Le Na2ZrO3 développé par la nouvelle technique a été moins actif durant les cycles sorption/régénération que celui produit par la méthode conventionnelle, de par la faible résistance de sa structure poreuse à de très hautes températures. La nouvelle méthode de synthèse combinée surfactant/ultrasons a été aussi appliquée pour la synthèse de CaO stabilisé par du zirconium (Zr). Un rapport Zr/Ca de 0,303 a été trouvé optimal pour la production d’un sorbant présentant la meilleure stabilité et activité pour la capture de CO2. Dans les conditions sévères d’opération, les résultats ont généralement indiqué une capacité de sorption du CaO stabilisé supérieure à celle du CaO pure. Dans le but de réduire les coûts de production des sorbants, une source moins chère de CaO (calcaire naturel) a été utilisée en combinaison avec une nouvelle méthode de synthèse qui consiste dans l’acidification du calcaire par de l’acide citrique suivie par une calcination en deux étapes (argon et air). Doté d’une structure hautement poreuse, le CaO produit a révélé une stabilité nettement meilleure par rapport au calcaire, ainsi qu’une capacité accrue de sorption du CO2. La même technique de synthèse a été aussi utilisée pour développer plusieurs matériaux à base de CaO stabilisé par divers oxydes métalliques (Al, Zr, Mg et Y), afin d’améliorer la stabilité du sorbant dans les conditions opérationnelles sévères, particulièrement les hautes températures de régénération en présence de CO2. CaO stabilisé par l’aluminium (Al) ou le zirconium (Zr) a démontré une meilleure activité comparativement aux autres matériaux synthétisés, inclusivement dans des conditions sévères d’opération. L’application de ces deux types de sorbants au vaporeformage du méthane (SESMR) a été ensuite étudiée dans un réacteur à lit fixe. Pour minimiser les limitations diffusionnelles, deux matériaux hybrides sorbant-catalyseur ont été développés. NiO-CaO stabilisé par Zr, préparé par la méthode combinée surfactant/ultrasons, dont le contenu en NiO est de 20.5 % (masse) a montré une efficacité dans la production d’hydrogène de 92% lors du premier cycle de reformage, ce qui est remarquablement plus élevée que le rendement d’équilibre en H2 pour le procédé traditionnel de vaporeformage du méthane (SMR) ( 70%). La méthode acidification/calcination en deux étapes a été utilisée pour produire le deuxième matériau hybride (NiO-CaO stabilisé par Al). L’application du matériau contenant 25 % (masse) de NiO a conduit à une efficacité moyenne de production d’hydrogène de 97.3%, démontrant ainsi son grand potentiel pour le SESMR. Les résultats de ce projet de recherche ont clairement démontré que le procédé SESR est une alternative très avantageuse au procédé traditionnel de reformage à la vapeur (sans séparation in-situ de CO2) pour la production d’hydrogène de très haute pureté. Le matériau hybride sorbant-catalyseur NiO-CaO stabilisé par Al a démontré une excellente activité à long terme, en confirmant son potentiel élevé pour application dans le procédé SESMR. / Sorption-enhanced steam reforming (SESR) is a forefront technology to produce H2 clean fuel, which integrates both CO2 capture and H2 production in a single process. The main objective of this work is to develop novel high-temperature CO2 sorbents and to investigate their application in SESR operation. Special attention was given to lithium zirconate (Li2ZrO3), sodium zirconate (Na2ZrO3) and calcium oxide (CaO)-based materials, as most famous high temperature CO2 sorbents, by applying two novel synthesis techniques. The application of Li2ZrO3 in CO2 capture sorption showed an increase in activity of the material prepared by surfactant template/sonication method compared to Li2ZrO3 prepared by simple surfactant template method (without sonication) or conventional wet-mixing route. Nevertheless, porous Li2ZrO3 still suffered from slow kinetics of CO2 sorption at low CO2 partial pressure (below 0.75 bar), which can limit its application for SESMR operation. Taking into consideration the improvement of Li2ZrO3 sorption properties, the same surfactant template/sonication technique was then applied to develop porous Na2ZrO3. The behavior of the new developed Na2ZrO3 was unexpected. The samples prepared by surfactant template/sonication technique were found to be less active than the conventional Na2ZrO3 during cyclic operation, due to the low resistivity of the pore structure at the very high temperature treatment required for calcination. The same surfactant template/sonication was also applied to develop Zr-stabilized CaO sorbents. An optimum Zr/Ca ratio of 0.303 was found to maximize the stability and CO2 capture activity of the proposed Zr-stabilized CaO sorbent. The results generally showed a better CO2 capture ability of Zr-stabilized CaO sorbent in comparison with pure CaO in severe cyclic operating conditions. With the purpose of reducing the cost of sorbent production, a cheaper source of CaO (natural limestone) was also considered and a novel synthesis technique (limestone acidification by citric acid followed by two-step calcination (in Ar and air atmospheres)) was applied in order to prepare highly porous CaO structure with unique CO2 capture ability. The results revealed a much better stability and CO2 sorption activity of the developed sorbent compared to natural limestone. The same technique was employed to develop a number of metal oxide (Al, Zr, Mg and Y)-stabilized CaO sorbents in order to enhance sorbent stability in severe operating conditions, i.e., high temperature regeneration in the presence of CO2. Al and Zr-stabilized CaO showed the best activity during both mild and severe operating conditions. The performance of the developed CO2 sorbents providing the best performance in CO2 capture (Zr-stabilized and Al-stabilized CaO) were then investigated experimentally in the sorption enhanced steam methane reforming (SESMR) using a fixed-bed reactor. To minimize the diffusional limitations, a hybrid catalyst-sorbent was developed for both sorbents. The application of Zr-stabilized CaO-nickel hybrid catalyst with 20.5 wt% NiO loading, prepared by surfactant-template/sonication method, resulted in 92% H2 production efficiency for the initial SESMR cycle, which is remarkably higher than traditional steam methane reforming (SMR) equilibrium H2 yield (70 %). The second developed hybrid sorbent-catalyst (Al-stabilized CaO-NiO) was prepared using limestone acidification coupled with two-step calcination technique. The long-term application of the hybrid catalyst containing 25 wt% NiO led to an average H2 production efficiency of 97.3%, proving its high efficiency in the SESMR process. In summary, the results of this thesis show that the SESR process is as an efficient alternative of traditional steam reforming for production of highly pure H2. The Al-stabilized CaO-NiO hybrid sorbent-catalyst showed an excellent activity over long-term operation, thus confirming its very high potential for use in the SESMR process.

Compostos condutores protônicos de zirconato de bário dopado com ítrio, BaZr0,8Y0,2O3-δ, preparados por síntese de estado sólido, foram compactados e sinter izados com ZnO e B2O3 como aditivos. Os corpos cerâmicos sinter izados foram analisados por difração de raios X e espectroscopia de impedância. Superfícies polidas e atacadas termicamente foram observadas em microscópio de varredura por sonda. As medidas de densidade mostraram que a maior densificação foi obtida com óxido de zinco nas proporções de 2 e 5 peso%, atingindo aproximadamente 95% da densidade teórica. As medidas de resistividade elétrica evidenciaram a menor resistividade elétrica do composto cerâmico BaZr0,8Y0,2O3-δ, com 5 peso% de ZnO. Os aditivos de sinter ização, óxido de boro e óxido de zinco, foram eficientes para se obter compostos com menores valores de resistividade elétrica que os obtidos em compostos sinter izados sem aditivos. / BaZr0.8Y0.2O3-δ, protonic conductors, prepared by the ceramic route, were pressed and sintered with ZnO and B2O3 sinter ing aids. The sintered pellets were analyzed by X-ra y diffraction and impedance spectroscopy. Polished and thermally etched surfaces of the pellets were observed in a scanning probe microscope. The highest values of apparent densit y, 95%T.D., were obtained with 2 and 5 wt.% ZnO. The lowest value of electr ical resistivit y was obtained in BaZr0.8Y0.2O3-δ, compounds with 5 wt.% ZnO. Boron oxide and zinc oxide sinter ing aids were efficient to improve the apparent densit y as well as the electr ical conductivit y of BaZr0.8Y0.2O3-δ, protonic conductors.

Pb(Zr₀.₅₂Ti₀.₄₈)O₃ (PZT) thin films are of interest for their large dielectric permittivity, ferroelectric, and piezoelectric properties. The material has been widely studied for use in high frequency transducers, multi-layered capacitors, and ferroelectric random access memory. Copper foils are an inexpensive, flexible substrate with a low resistivity which makes them ideal for many transducer and capacitor applications. PZT thin films on copper foils were produced by RF sputtering and crystallized under reducing conditions. Causes and prevention of a cuprous oxide interlayer are discussed. The film structure was characterized by XRD, SEM, and AFM. The permittivity was low, but remanent polarization increased to as high as ~40 μC/cm² as film thickness and crystallization temperature increased. Residual stresses were measured by x-ray diffraction using the sin²ψ method. The relative permittivity of the PZT/Cu films was measured as a function of applied AC electric field. By performing a Rayleigh analysis on this data one can determine the relative contributions of the intrinsic, reversible, and irreversible components to the permittivity. The residual stress could be correlated to the reversible part of the permittivity. The first order reversal curves (FORCs), which characterize the ferroelectric switching, give indications of the defect state of the film. Cantilever energy harvesters were fabricated. Large electrodes were able to be evaporated onto the films after oxidizing pinholes and cracks on a hot plate. Devices were tested on a shaker table at < 100 Hz. A dynamic model based on Euler-Bernoulli beam equations was used to predict power output of the fabricated devices. The observed output was comparable to model predictions. Resonant frequency calculations were in line with observed first and second resonances at ~17 Hz and ~35 Hz which were also close to those predicted by the dynamic model. / Graduation date: 2013

No description available.

Yttria Stabilized Zirconia (YSZ) is the standard ceramic top coat material used for TBC application. Above 1200°C, issues such as CMAS (Calcium Magnesium Alumino Silicates) infiltration susceptibility, phase instability and high sintering rates limits its long durability. Therefore, new materials which can overcome these challenges without compromising the other requirements for TBCs are highly desirable. Gadolinium zirconate is one such material which has shown promising results for CMAS infiltration resistance. In this work, a relatively new TBC processing route, suspension plasma spray (SPS) has been employed to deposit gadolinium zirconate based TBCs. The primary aim of this study was to deposit two different coating systems (layered and composite) of gadolinium zirconate and YSZ composition using SPS technique and evaluate their thermal cyclic fatigue life performance. The layered system was a triple layered TBC with YSZ as the base layer, relatively porous GZ as the intermediate layer and dense GZ as the top layer. The blended TBC system comprised of a thin YSZ layer, an intermediate GZ+YSZ thick layer and dense GZ top layer. In the thermal cyclic fatigue test at 1100°C and 1200°C, it was observed that blended TBC had a lower thermal cyclic life than the layered TBC. It was shown that SPS is a promising technique to deposit columnar microstructure TBCs.

Compostos condutores protônicos de zirconato de bário dopado com ítrio, BaZr0,8Y0,2O3-&delta;, preparados por síntese de estado sólido, foram compactados e sinter izados com ZnO e B2O3 como aditivos. Os corpos cerâmicos sinter izados foram analisados por difração de raios X e espectroscopia de impedância. Superfícies polidas e atacadas termicamente foram observadas em microscópio de varredura por sonda. As medidas de densidade mostraram que a maior densificação foi obtida com óxido de zinco nas proporções de 2 e 5 peso%, atingindo aproximadamente 95% da densidade teórica. As medidas de resistividade elétrica evidenciaram a menor resistividade elétrica do composto cerâmico BaZr0,8Y0,2O3-&delta;, com 5 peso% de ZnO. Os aditivos de sinter ização, óxido de boro e óxido de zinco, foram eficientes para se obter compostos com menores valores de resistividade elétrica que os obtidos em compostos sinter izados sem aditivos. / BaZr0.8Y0.2O3-&delta;, protonic conductors, prepared by the ceramic route, were pressed and sintered with ZnO and B2O3 sinter ing aids. The sintered pellets were analyzed by X-ra y diffraction and impedance spectroscopy. Polished and thermally etched surfaces of the pellets were observed in a scanning probe microscope. The highest values of apparent densit y, 95%T.D., were obtained with 2 and 5 wt.% ZnO. The lowest value of electr ical resistivit y was obtained in BaZr0.8Y0.2O3-&delta;, compounds with 5 wt.% ZnO. Boron oxide and zinc oxide sinter ing aids were efficient to improve the apparent densit y as well as the electr ical conductivit y of BaZr0.8Y0.2O3-&delta;, protonic conductors.

No description available.

The upward trend in internal combustion engine efficiency is likely driven by the depletion of fossil fuels. Since no replacement in sight can deliver energy comparable to the conventional oil, there is a need to use it more rationally and effectively. Thermal barrier coatings have been seen for a long time as a solutionto increase the thermal efficiency of gas turbine engines but suffer from the lackof strong applicability in internal combustion engines. This is due to the different restrictions when comparing the environment on the gas turbines and in internal combustion engines. To overcome this problem and, at the same time, expand the application field of thermal barrier coatings, more efforts need to be devoted.In this work, different top coat materials using various deposition techniques were evaluated and categorized in three different thermal barrier coating (TBC) architectures. The first was the lamellar yttria-stabilized zirconia (YSZ) top coat deposited by atmospheric plasma spray (APS), used as a reference sample. The second architecture was a columnar suspension plasma spray (SPS) TBC with YSZ and gadolinium zirconate (GZO) top coat. The SPS process can produce avariety of microstructures, and they were, for the first time, tested in an internal combustion engine. The third architecture was an SPS top coat, with an additional layer on the top, called a sealing layer of either metallic or ceramic material, both never investigated in a diesel engine application earlier. For the thermophysical properties investigation, a combination of laser flashanalysis (LFA) and modeling with object-oriented finite element (OOF) was employed to understand the properties in all the applications. The performance of the coatings was evaluated in two different ways, by thermal cyclic tests, basedon the TBCs behavior under cyclic thermal loads and by single-cylinder engine experiment. The characterization of the coatings was done by scanning electron microscope (SEM) before and after the thermal cyclic tests.The performance properties were correlated with coatings microstructure and thermophysical properties. It was shown that a columnar TBC produced by SPS had a superior engine efficiency in the single cylinder engine experiment.

Ferroelectric materials are characterized by a reversible spontaneous polarization in the absence of an electric field. The characteristic polarization response of a ferroelectric material to an applied electric field enables a binary state device in the form of a thin film ferroelectric capacitor that can be used to store digital information. This provides opportunities for the development of high speed, low cost and low power, nonvolatile memory devices. The development of commercial ferroelectric memory devices has however been hampered by (a) several reliability issues including fatigue, leakage current, aging, time dependent dielectric breakdown, retention and imprint and (b) processing problems including the development of a low temperature thin film deposition process and the development of a patterning technology. Lead zirconate titanate (PZT) is now widely considered as the most promising material for ferroelectric memory applications as a result of its excellent ferroelectric properties and wide operating temperature range. However, it is commonly found that metal electroded-PZT capacitors (e.g., Pt/PZT/Pt) show a loss of switchable polarization with cumulative switching cycles. This phenomenon is known as fatigue and is the one of the critical problems affecting the lifetime of ferroelectric memories. This research is primarily focused on the problem of fatigue. On the basis of a quantitative model, various guidelines to minimize the degradation problem have been derived. The model attributes fatigue to domain pinning by space charge that is caused by defect (e.g. oxygen vacancy) entrapment at various interface sites such as electrode-ferroelectric interface, domain boundaries and grain boundaries. Two different approaches to minimize the problem have been outlined : (a) control of the defect density and (b) control of the interface state. The control of interface state was achieved by replacing the metal electrodes with conducting oxide electrodes such as RuO₂. The oxide electrode/PZT capacitors were characterized for their diffusion barrier properties, perovskite phase formation, interface nature and ferroelectric properties. The results indicate that these oxide electroded PZT films are good candidates for nonvolatile memory applications. However, the leakage current levels at the operating voltages are far higher than the metal counterparts. Simultaneous minimization of fatigue and leakage current in PZT films was achieved by using multilayer metal/conducting oxide electrodes (e.g., Pt/RuO₂). The control of defect density was attained by (a) donor doping to compensate for the oxygen vacancies (e.g, Nb doping in PZT) and (b) utilizing ferroelectric materials that have a low intrinsic defect concentration. As a result of the latter approach, novel ferroelectric materials belonging to the layer-structure family of oxides have been identified as excellent candidates for fatigue free nonvolatile memory applications. Laser ablated SrBi₂(Ta_xNb_{1 - x})₂O₉ (0<x<1) films showed very good hysteresis characteristics (remnant polarization value of 11 µC/cm², coercive field of 60 kV/cm), no fatigue was observed up to 10⁹ switching cycles and very low leakage current densities. Furthermore, the formation and properties of these films were characterized. It was found grain size and orientation played a major role in determining the properties of these films. C-axis oriented films were found to exhibit almost no polarization. An additional objective of this research was to identify an etching technology (process integration issue) for patterning of the ferroelectric capacitors. The etching process should provide high etch rates, good etch anisotropy, high etch selectivity and minimal post etch residues. It has been shown that a reactive ion etch process with CCl₂F₂/O₂ as the etch gas mixture can meet these requirements. A detailed process study has been conducted to determine the mechanism of etching. / Ph. D.

This paper reports a reciprocal Mach-Zehnder interferometer in a dual Sagnac ring configuration, and one of two arms in Mach-Zehnder interferometer is used for underwater optic fiber hydrophone. Two Mach-Zehnder interferometers operated in opposite sense are simultaneously induced from the underwater acoustic wave and the PZT phase modulation. Thus, at the output, four interferometric beams occur such that the intensity of interferometric beams will enhance. In general, one stage of a double Mach-Zehnder interferometer is just used as a sensor, another one for compensation. Specially, this paper presents two stages of a double Mach-Zehnder interferometer sense the measurand at the same time due to the topology structure of Sagnac ring pairs. In the other words, the characteristic is to win the affection of two beauties at the same time. Two rings in the same direction make a Mach-Zehnder interferometer. Besides, the inner ring in the clockwise direction and the outer one in the counterclockwise direction also make a Mach-Zehnder interferometer. So as to the unbalanced arms of the Mach-Zehnder interferometer, the underwater acoustic wave induces the light beam phase difference in optic fiber hydrophone interrogator to demodulate the acoustic wave signal by PGC circuit.