L’objectif de cette thèse de doctorat a consisté à déterminer l’influence des conditions réactionnelles du vaporeformage de l’éthanol (ESR), de la dispersion du catalyseur et de la promotion par le potassium sur l’état de la surface. Ce travail a aussi aidé à comprendre l’influence de ces facteurs sur les propriétés catalytiques. Nous avons utilisé les catalyseurs à base de cobalt (promus et non promus par le potassium) supportés à l’oxyde de cérium et à l’oxyde de zirconium à faible et à forte dispersion. Les changements de l’état de la surface des catalyseurs pendant la réaction d’ERS ont été étudiés à travers la spectrométrie photoélectronique X (XPS), alors que les changements des produits ont été analisés en utilisant la spectrométrie de masse et la chromatographie en phase gazeuse. Le catalyseur supporté sur oxyde de cérium à forte dispersion a été caractérisé sous une basse pression (0.2-20 mbar) avec le rapport molaire eau/éthanol de 3/1 (420ºC). Les autres tests ont été faits sur tous les catalyseurs sous une pression totale de 1 atm avec les rapports molaires de 3/1, 9/1, 12/1 (420ºC). Nous avons utilisé un mélange eau/éthanol dans un rapport molaire de 12/1 pour étudier les changements de l’état de la surface de tous les catalyseurs dans le temps. Il a été démontré que la sélectivité d’ESR des catalyseurs pour produire des gaz et pour déposer le carbone est réglée par la concentration des groupes hydroxyles sur la surface. Quant aux catalyseurs promus, elle dépend aussi de la concentration Kδ+–Osurfδ-. / The aim of the thesis was determination the influence of the ethanol steam reforming (ESR) reaction conditions, catalyst’s dispersion and potassium promotion on a surface’s composition and understanding the influence of these changes on catalysts’ performance. Cobalt-based catalysts (unpromoted and promoted with potassium) with low- and high-dispersed ceria and zirconia supports were used. The changes of the surface state of catalysts during the ESR were studied by means of X-ray photoelectron spectroscopy, whereas the reaction products evolution was followed by mass spectrometer or gas chromatograph. Highly-dispersed ceria-supported catalyst was characterized under low pressure conditions (0.2–20 mbar) with the water/ethanol molar ratio equal to 3/1 (at 420ºC). The other tests were carried out over all catalysts under total pressure of 1 atm with 3/1, 9/1 and 12/1 molar ratios (at 420ºC). The water/ethanol ratio of 12/1 was chosen for studies of the surface state of all catalysts with time-on-stream. It was found that the ESR selectivity to gaseous products and carbon deposition is governed mainly by surface hydroxyl species concentration; in the promoted catalysts together with Kδ+–Osurfδ- surface sites.

Laser surface treatment of engineering ceramics offers various advantages in comparison with conventional processing techniques and much research has been conducted to develop applications. Even so, there still remains a considerable gap in knowledge that needs to be filled to establish the process. By employing a fibre laser for the first time to process silicon nitride (Si3N4) and zirconia (ZrO2) engineering ceramics, a comparison with the CO2 and a Nd:YAG lasers was conducted to provide fundamental understanding of various aspects of the laser beam-material interaction. Changes in the morphology, microstructure, surface finish, fracture toughness parameter (K1c) were investigated, followed by thermal finite element modelling (FEM) of the laser surface treatment and the phase transformation of the two ceramics, as well as the effects of the fibre laser beam parameter - brightness (radiance). Fibre and CO2 laser surface treatment of both Si3N4 and ZrO2 engineering ceramics was performed by using various processing gases. Changes in the surface roughness, material removal, surface morphology and microstructure were observed. But the effect was particularly more remarkable when applying the reactive gases with both lasers and less significant when using the inert gases. Microcracking was also observed when the reactive gases were applied. This was due to an exothermic reaction produced during the laser-ceramic interaction which would have resulted to an increased surface temperature leading to thermal shocks. Moreover, the composition of the ceramics was modified with both laser irradiated surfaces as the ZrO2 transformed to zirconia carbides (ZrC) and Si3N4 to silicon dioxide (SiO2) respectively. The most appropriate equation identified for the determination of the fracture toughness parameter K1c of the as-received, CO2 and the fibre laser surface treated Si3N4 and ZrO2 was K1c=0.016 (E/Hv) 1/2 (P/c3/2). Surfaces of both ceramics treated with CO2 and the fibre laser irradiation produced an increased K1c under the measured conditions, but with different effects. The CO2 laser surface treatment produced a thicker and softer layer whereas the fibre laser surface treatment increased the hardness by only 4%. This is inconsiderable but a reduction in the crack lengths increased the K1c value under the applied conditions. This was through a possible transformation hardening which occurred within both engineering ceramics. Experimental findings validated the generated thermal FEM of the CO2 and the fibre laser surface treatment and showed good agreement. However, a temperature difference was found between the CO2 and fibre laser surface treatment due to the difference in absorption of the near infra-red (NIR) wavelength of the fibre laser being higher than the mid infra-red (MIR) wavelength of the CO2 laser. This in turn, generated a larger interaction zone on the surface that was not induced further into the bulk, as was the case with the fibre laser irradiation. The MIR wavelength is therefore suitable for Viability and Characterization of the Laser Surface Treatment of Engineering Ceramics 3 the surface processing of mainly oxide ceramics and surface treatments which do not require deep penetration. Phase transformation of the two ceramics occurred at various stages during the fibre laser surface treatment. The ZrO2 was transformed from the monoclinic (M) state to a mixture of tetragonal + cubic (T+C) during fibre laser irradiation and from T+C to T and then a partially liquid (L) phase followed by a possible reverse transformation to the M state during solidification. The Si3N4 transformed to a mixture of α-phase and β-phase (α→ α+β) followed by α+β and fully transforms from α+β → β-phase. What is more, is a comparison of the fibre laser-beam brightness parameter with that of the Nd:YAG laser. In particular, physical and microstructural changes due to the difference in the laser-beam brightness were observed. This research has identified the broader effects of various laser processing conditions, as well as characterization techniques, assessment and identification of a method to determine the K1c and the thermal FEM of laser surface treated engineering ceramics. Also, the contributions of laser-beam brightness as a parameter of laser processing and the influence thereof on the engineering ceramics have been identified from a fundamental viewpoint. The findings of this research can now be adopted to develop ceramic fuel cell joining techniques and applications where laser beam surface modification and characterization of engineering ceramics are necessary.

Le carbonate de diméthyle (DMC) est utilisé comme intermédiaire en chimie des polymères. Actuellement, la production industrielle du DMC met en jeu un procédé polluant et dangereux. En revanche, la synthèse du DMC à partir de méthanol et de CO2 est un procédé « vert ». Cependant, la thermodynamique de la réaction est très défavorable, se traduisant par une conversion inférieure à 1%. L'objectif de cette thèse est de développer et d'étudier des catalyseurs très actifs qui, couplés à un réacteur membranaire, permettraient d'augmenter le rendement et l'activité. Ce manuscrit couvre plusieurs aspects : i) une étude de criblage de catalyseurs, ii) une étude de type structure-activité sur des séries de catalyseurs, basée sur des caractérisations structurales, texturales et de surface, iii) une étude mécanistique et iv) une étude cinétique. Un protocole de mesure d'activité adapté aux faibles conversions est développé. Le criblage catalytique met en évidence l'activité des solutions solides de cérine-zircone (CZ). Les CZ préparées par pyrolyse de flamme sont un ordre de grandeur plus actives que les CZ préparées par coprécipitation. De façon surprenante, il n'est pas possible a priori de distinguer des catalyseurs très actifs et peu actifs à partir de leurs caractéristiques structurales et texturales. Cependant, on observe que l'activité est corrélée à la densité et à la nature des espèces de surfaces méthoxides et carbonates. Le mécanisme réactionnel de l'état de l'art est affiné grâce à des mesures d'échanges isotopiques et de DRIFT. L'étude cinétique intègre des corrections thermodynamiques de l'équilibre de phases du binaire MeOH-CO2 qui constitue un liquide expansé / Dimethylcarbonate (DMC) is used in polymer synthesis as well as a fuel additive and solvent. The current industrial DMC production is a polluting and hazardous process. On the other hand, the direct carboxylation of methanol with CO2 is a green route to DMC. However, this reaction is highly limited by thermodynamics, limiting the conversion to less than 1%. The integration of a catalyst in a catalytic membrane reactor for water and DMC removal, would shift the equilibrium conversion thereby improving the DMC yield. The aim of this thesis is to develop and study highly active catalysts for DMC synthesis. This manuscript covers: (i) catalyst screening (ii) a structure-activity relationship study (iii) a mechanistic approach and (iv) a kinetic study. A protocol to measure the activity at low conversion has been developed. Catalyst screening evidenced solid solutions of ceria/zirconia (CZ) as the most active and selective. Flame sprayed pyrolysis ceria/zirconia are one order of magnitude more active than coprecipitated CZ. Interestingly, structural and textural features like crystalline and porous structure were similar regardless of the activity. Nevertheless, the activity could be correlated to the nature and the density of the methoxides and carbonates surface species. The mechanism was refined by isotopic exchange and DRIFT experiments. A kinetic study was performed in a batch reactor that integrated the physical equilibria of the gas-expanded reacting mixture

La déshydratation du glycérol en acroléine a été étudiée sur de nouveaux catalyseurs à base d'oxydes en vue de mettre au point un nouveau procédé de production de la méthionine. Ces catalyseurs performants sont des zircones niobiées et des zircones tungstées dopées à la silice. Si les catalyseurs proposés dans la littérature jusqu'à présent pouvaient être sélectifs, ils se désactivaient rapidement par cokage. Les nouveaux catalyseurs mis au point sont aussi actifs et sélectifs mais beaucoup plus stables sous flux réactionnel. Les performances des zircones niobiées sont très sensibles à la méthode de préparation; les catalyseurs ont été caractérisés par DRX, spectroscopie Raman, MET, EDX, XPS. Ces analyses ont montré qu'une partie du niobium est incorporée dans la zircone qui est recouverte d'espèces polymères de niobium. Les zircones tungstées performantes sont constituées d'une zircone recouverte de silice et de polytunsgtates. L'acido-basicité des catalyseurs a été étudiée par différentes techniques: réactions modèles de transformation du méthylbutynol et du 2-propanol, TPD-NH3, adsorption de NH3 et SO2étudiée par microcalorimétrie et adsorption de pyridine suivie par IR. Ces études ont permis de montrer que les sites basiques de la zircone sont néfastes pour les performances et que les sites acides de Brönsted avec une large gamme de force acide sont actifs et sélectifs en acroléine. Nous avons montré par microcalorimétrie que même les sites acides très faibles participent à la réaction / Glycerol dehydration to acrolein has been studied over innovative oxide catalysts in order to develop a new methionine production process. These performing catalysts are niobiate zirconia mixed oxides and tungstated zirconia doped with silicium. The catalysts proposed so far in the literature are active and selective but they show fast deactivation under reaction flow due to coke deposition. The new catalysts appear at least as active and selective but much more stable. The niobiate zirconia mixed oxides, which catalytic performances are very sensitive to the preparation method, have been characterized by XRD, Raman spectroscopy, TEM with EDX analyses and XPS. Theses analyses show that niobium cations are partially incorporated into zirconia and covered its surface as polymeric niobium oxide species. The efficient tungstated zirconia catalysts consist of zirconia cover with silicium and polymeric tungstate species. Acid-base properties of the catalysts have been studied by model reaction of methylbutynol and 2-propanol, NH3-TPD, SO2 and NH3adsorption followed by microcalorimetry and IR spectroscopy of pyridine adsorption. These studies show that the zirconia uncovered by silica or containing no niobium are unselective sites and that Brönsted acid sites of the polymeric tungstate or niobium oxide species are the selective sites in acrolein. The strength of these sites does not appear as a key parameter to acrolein selectivity and even weak sites participate to the reaction

Les principaux objectifs de ces travaux de thèse sont d'une part d'optimiser le protocole d'élaboration des barrières thermiques (BT) issues de la voie sol-gel et d'autre part de caractériser l'adhérence de ces barrières thermiques mais aussi de proposer des pistes en vue d'augmenter la durée de vie de celles-ci. Tout d'abord, une première étude a porté sur le choix et la validation d'un nouvel agent dispersant pour optimiser la formulation du sol chargé permettant la mise en forme des barrières thermiques. Ainsi, ce changement de dispersant a généré une microstructure conduisant à une augmentation significative de la durée de vie du système en oxydation cyclique mais a aussi permis de simplifier le protocole d'élaboration puisque l'étape de colmatage, jusqu'alors nécessaire, a été supprimée. L'étude paramétrique de la microstructure surfacique des barrières thermiques a montré que le réseau de microfissures formé initialement restait stable en fonction du vieillissement avec la création d'un sous-réseau microfissuré. Pour comprendre les mécanismes d'endommagement des barrières thermiques sol-gel et les confronter à ceux des barrières thermiques industrielles EB-PVD, la méthode d'indentation interfaciale a été retenue pour sonder l'interface revêtement/substrat. Ainsi des valeurs de ténacités apparentes ont pu être déterminées afin de comparer les adhérences des BTSG et des BTEB-PVD. A partir de ces résultats, des modèles phénoménologiques d'endommagement ont été imaginés. Pour les BTEB-PVD, l'initiation et la propagation de fissures restent localisées à l'interface barrière thermique/sous-couche de liaison, d'un coté ou de l'autre de l'oxyde de croissance selon les conditions, alors que pour les BTSG, l'endommagement est induit par la libération d'énergie élastique stockée dans le système qui augmente en fonction du vieillissement. / The main objectives of this PhD are first to improve and optimise the elaboration protocol of thermal barrier coatings (TBC) manufactured by the sol-gel route and then to characterise their adhesion and investigate the possibility to enhance their lifetime. A preliminary study is focused on the selection and validation of a new dispersing agent to optimise the composite sol formulation before shaping TBC. Indeed, the new dispersant induced a microstructure allowing to significantly increase the cyclic oxidation lifetime of the system but also to simplify the elaboration process as the reinforcement step was suppressed. The parametric study of TBC surface microstructure proved that the initial micro-cracks network remained stable during ageing including the formation of a crack sub-network. To understand the damage mechanisms of sol-gel TBC and to compare them to those corresponding to industrial EB-PVD TBC, the method of interfacial indentation was developed to investigate the subtrate/top-coat interface. The apparent toughness values were determined to compare both BTSG and BTEB-PVD adhesions. From these results, phenomenological models for damage mechanisms were proposed. For BTEB-PVD, crack initiation and propagation are located at the top-coat/bond-coat interface, either on one side or the other side of the thermally grown oxide (TGO) depending of the conditions. For BTSG, the damage is a consequence of the release of the elastic strain energy stored in the system, increasing with the ageing temperature.

La performance du couple prothétique tête fémorale/cupule impacte fortement la durée de vie d’une prothèse totale de hanche. Les céramiques affichent une excellente combinaison de propriétés de biocompatibilité, mécaniques et tribologiques. Les composites ZTA formés d’une matrice d’alumine renforcée en zircone sont optimisés pour offrir le meilleur compromis de dureté, stabilité chimique, ténacité et résistance mécanique. La prédiction de la performance de ces matériaux doit prendre en compte les trois principaux modes de dégradation identifiés en configuration céramique/céramique (CoC) : le choc avec décoaptation, le frottement et le vieillissement à basse température. Ces modes sont susceptibles d’être simulés in vitro à partir de tests expérimentaux, respectivement, sur une machine de chocs, un simulateur de marche et en autoclave. L’objectif de ce projet est de combiner ces tests afin de mieux résoudre l’équation in vitro = in vivo. Les chocs dominent les processus de dégradation avec la formation de bandes d’usure. Le matériau testé a montré une excellente résistance au vieillissement. La dégradation induite par le test d’usure standard sur simulateur de marche est négligeable et pose la question de la pertinence de ce test pour les couples CoC. L’importance de la prise en compte des chocs dans les tests expérimentaux a été confortée grâce à une analyse d’explants. Une transformation de phase de la zircone a été mécaniquement induite dans les bandes d’usure créées in vitro et in vivo. Un mécanisme de dégradation a été suggéré au sein de ces bandes. La réponse du matériau est en partie déterminée par la force appliquée au cours des chocs. / The performance of the prosthetic couple (femoral head/cup) influences strongly the lifetime of a total hip prosthesis. Ceramics exhibit an excellent combination of biocompatibility, mechanical resistance and tribological properties. Zirconia toughened alumina (ZTA) composites are made of an alumina matrix and well dispersed zirconia particles. They are tailored in order to offer the best compromise of hardness, chemical stability, toughness and mechanical resistance. The prediction of the performance of such materials must take into consideration the three main sources of degradation identified for Ceramic-on-Ceramic (CoC) bearings: shocks due to micro-separation, friction and low temperature degradation (LTD). Experimental tests on a shock machine, a hip-walking simulator and in an autoclave are able to simulate in vitro each of these sources of degradation, respectively. The aim of the project is to combine these tests in order to solve better the equation in vitro = in vivo. Shocks dominate the processes of degradation with the formation of wear stripes. The tested material showed an excellent resistance to LTD. The damage induced by the standard wear test on a hip-walking simulator is negligible, which raises the question about the relevance of this test for CoC couplings. An analysis of explants confirmed the decisive role of shocks in experimental tests. Zirconia phase transformation was mechanically induced within both in vitro and in vivo wear stripes. A degradation mechanism was suggested within the stripes. The material response is partly determined by the force applied during shocks.

No description available.

Les composés organiques volatils comme le formaldéhyde sont des polluants nocifs pour la santé humaine et leur décomposition en composés moins toxiques est fortement étudiée. Ainsi, différents catalyseurs à base d’oxyde métallique permettant une décomposition thermique efficace du formaldéhyde ont été développés. Dans cette optique, les catalyseurs à base d’oxyde métalliques sont souvent présentés comme des catalyseurs prometteurs. Ce travail consiste à préparer des catalyseurs à base de cobalt et/ou de manganèse supportés sur zircone destinés à l’oxydation du formaldéhyde. Les catalyseurs ont été synthétisés par imprégnation en excès de volume (méthode classique) en modifiant la solution métallique par ajout de cyclodextrines.Dans ce travail, différents paramètres tels que le précurseur métallique, la nature de la cyclodextrine et la quantité de cyclodextrines ont été étudiés. Un effet bénéfique de l’ajout de cyclodextrines sur l’activité catalytique est obtenu et le rôle des cyclodextrines lors de chaque étape de la préparation (dans la solution d’imprégnation, avant l’activation et après l’activation) a été abordé. Les interactions entre la cyclodextrine et le précurseur métallique en solution modifient le processus d’activation permettant ainsi la formation de petites particules plus actives.En complément à ce travail, les cyclodextrines ont également été utilisées pour préparer par précipitation assistée une zircone présentant une structure cristalline purement quadratique. La stabilisation de la phase quadratique ayant lieu grâce à la formation d’un précurseur nouveau composé de cyclodextrines incorporées dans le polymère d’oxohydroxyde de zirconium. Cette nouvelle méthode de synthèse a été adaptée pour préparer un oxyde mixte MnOx-ZrO2 qui s’est révélé particulièrement actif dans la réaction d'oxydation du formaldéhyde. / Volatile organic compounds, such as formaldehyde are currently health concern and their elimination into harmless compounds is of great importance. Different catalysts metal oxides have been developed to decompose formaldehyde under thermal treatments. The present work aims at developing cobalt and/or manganese oxides catalysts supported on zirconia designed for the deep oxidation of formaldehyde. The catalysts have been synthesized by classical wet impregnation method and the started metal solution has been modified by the controlled addition of cyclodextrins.The influence of different parameters, such as the metal precursor, the nature of the cyclodextrin nature and the amount of the cyclodextrin has been studied. A beneficial effect of cyclodextrins addition on the catalytic activity has been obtained and the role of the cyclodextrins at each stage of the preparation has been investigated (i.e. in impregnating solution, before activation and after activation). Interactions occurring in the aqueous phase between the cyclodextrin and the metal precursor modify the activation process leading to the formation of small particles size more active.As an extension, cyclodextrins have also been used to prepare by simple synthesis procedure of single-phase tetragonal zirconia. The stabilization of the tetragonal phase is suggested to occur via the formation of a composite material precursor composed of incorporated cyclodextrin within the polymeric zirconium hydroxide. Finally, the effect of the cyclodextrin modified zirconium hydroxide was adapted in the preparation of a very efficient mixed oxide MnOx-ZrO2 in the oxidation of formaldehyde.

Cette étude a pour finalité le développement d'une nouvelle famille de catalyseurs pour la combustion des suies Diesel afin de produire des filtres à particules (FAP) à régénération continue basse température. En effet, les régénérations périodiques des FAP actuellement commercialisés, engendrent une surconsommation plus ou moins élevée en carburant. Les catalyseurs étudiés sont des céramiques conductrices par les ions oxygènes et exempts de métal noble. L'ensemble de ces études a permis d'aboutir à plusieurs conclusions majeures. Les oxygènes actifs pour oxyder les particules de suies à basse température sont les oxygènes contenus dans le catalyseur. L'oxydation de la suie a donc lieu à l'interface solide/solide : suie/catalyseur. Un mécanisme de type électrochimique comme dans une pile à combustible mais à l'échelle nanométrique a été proposé : l'oxydation de la suie représente la réaction anodique qui se déroule aux points de contact suie / 8-YSZ, les électrons produits diffusent à travers les particules de suie vers les point triples entre les particules de suie (conductrices électroniques), la phase gaz (présence d'oxygène) et 8-YSZ (conducteur ionique) où se déroule la réaction cathodique d'incorporation de l'oxygène gazeux dans le matériau. Les paramètres clés qui gouvernent l'activité catalytique sont la surface de contact suie/catalyseur et donc la granulométrie de la poudre de catalyseur ainsi que la pression partielle d'oxygène dans la phase gaz et la mobilité de l'oxygène dans le catalyseur / This study aims to develop a new family of catalysts for diesel soot combustion to produce and optimize self-DPFs, based on ionic conducting ceramics, able to continuously burn soot particulates at low temperatures without fuel overconsumption and without the use of noble metals. The investigated catalysts are oxygen ionically conducting ceramics. Yttria stabilized Zirconia (8-YSZ containing 8 mol% of yttria) was chosen as the reference catalyst due to its high thermal and chemical stability and good ionic conductivity. A set of experiments was implemented to vary different parameters that can influence the reactivity of the reference catalyst. All of these studies have resulted in several major conclusions. Oxygen species active to oxidize soot particles at low temperature are those contained in the catalyst. An electrochemical type mechanism as in a fuel cell but at the nanoscale was proposed: the soot oxidation represents the anodic reaction which occurs at the contact points soot / 8-YSZ/O2 (gas) electrons are diffused through soot particles to triple points between the soot particles (electronic conductor), the gas phase (presence of oxygen) and 8-YSZ (ion conductor) where the cathodic reaction takes place with the incorporation of gaseous oxygen into the ceramic. The key parameters that influence the catalytic activity of 8-YSZ are soot / catalyst contact and thus the agglomerates size of the catalyst powder, the oxygen partial pressure in the gas phase and the mobility of oxygen in the catalyst

Hipótese do estudo: A hipótese do presente estudo é de que o cimento resinoso autoadesivo U200 apresente melhores valores de resistência adesiva entre os substratos zircônia Y-TZP/dentina humana, em comparação com o cimento resinoso convencional C&B Cement, utilizando dois tratamentos de superfície distintos (jateamento com óxido de alumínio e silicatização (Rocatec) na superfície da zircônia; e que o tratamento de superfície influencie positivamente os resultados de resistência adesiva. Objetivos: Avaliar por meio de teste de microcisalhamento a resistência adesiva da zircônia Y-TZP cimentada à dentina humana utilizando diferentes agentes de cimentação e tratamentos de superfície. Método: Foram utilizados 42 molares humanos recém extraídos, incluídos 2/3 de suas raízes em resina acrílica. A superfície oclusal foi desgastada até exposição da dentina média, tratada de acordo com as recomendações dos fabricantes dos cimentos. Quarenta e dois blocos de zircônia Y-TZP (10x10x3mm) foram divididos aleatoriamente em três grupos de acordo com o tratamento de superfície (sem tratamento-controle, jateamento com óxido de alumínio-Al2O3 ou silicatização-Rocatec). Todos os blocos de zircônia foram cimentados seguindo as recomendações dos fabricantes e divididos em seis grupos combinando os diferentes tratamentos de superfície e agentes de cimentação. Os espécimes foram armazenados em água destilada 37C por 24h e após este período foram submetidos ao teste de microcisalhamento em máquina de ensaios universal (Shimadzu AGX) com velocidade constante de 0,5mm/min até ocorrer fratura da interface. Os valores foram obtidos em Mpa e as superfícies de fraturas avaliadas e classificadas em: adesiva, coesiva e mista. As médias dos valores de resistência de união e a porcentagem das fraturas foram calculadas, e os valores submetidos à análise estatística, utilizando os testes Análise de Variância (two way) e pos-hoc teste T de Student, adotando p<0,05. Resultados: Quanto ao agente de cimentação os resultados obtidos para os grupos sem tratamento de superfície o cimento autoadesivo U200 apresentou melhor performance quando comparado ao cimento convencional C&B Cement; os grupos submetidos ao jateamento com Al2O3 e Rocatec não apresentaram diferença estatística entre os cimentos U200 e C&B Cement. Quanto à analise de superfície, os grupos cimentados com C&B e U200 apresentaram predominantemente falhas de natureza mista. Conclusão: Com base nos resultados encontrados no presente estudo foi possível concluir que o tratamento de superfície que melhor influenciou a resistência adesiva foi o jateamento com Al2O3, atendendo melhor os dois agentes de cimentação. Quanto ao agente de cimentação o U200 apresentou os melhores resultados sem tratamento de superfície. O C&B Cement e U200 apresentaram valores semelhantes com a superfície jateada com Al2O3. Para o Rocatec, os cimentos U200 e C&B Cement apresentaram valores semelhantes, entretanto menores do que os valores conseguidos para o Al2O3. / Study hypothesis: The hypothesis of this study is that the resin cement Self Adhesive U200 present best values of bond strength between zirconia substrates Y-TZP / dentin compared to conventional resin cement C & B Cement, using two surface treatments distinct (sandblasting with aluminum and silica coating (Rocatec) oxide on the surface of zirconia, and the surface treatment positively influence the bond strength. Objectives: To assess via microshear test the bond strength of zirconia Y-TZP cemented to dentin human using different cementing agents and surface treatments. Method:. freshly extracted human molars 42, including two thirds of its roots in acrylic resin were used the occlusal surface was worn until the middle dentin exposure, treated according to the recommendations of the cement manufacturers. Forty-two blocks of Y-TZP zirconia (10x10x3mm) were randomly divided into three groups according to the surface treatment (untreated control, blasting with aluminum oxide or silica coating-Al2O3-Rocatec). All zirconia blocks were cemented following the manufacturers recommendations and divided into six groups combining different surface treatments and cementing agents. The specimens were stored in distilled water 37 C for 24 h and after this period underwent microshear test in a universal testing (Shimadzu AGX) machine with constant speed of 0.5 mm / min until fracture occurs interface. The values were obtained in MPa and the fracture surfaces evaluated and classified as: adhesive, cohesive and mixed. The average values of union strength and the percentage of fractures were calculated, and values subjected to statistical analysis using analysis of variance tests (two way) and post-hoc Students t test, considering p <0.05. Results: Regarding the cementing agent the results for the groups without surface treatment U200 self-adhesive cement showed better performance when compared to conventional cement C & B Cement; groups subjected to blasting with Al2O3 and Rocatec showed no statistical difference between the U200 and cements C & B Cement. As for the analysis of surface groups cemented with C & B and U200 were mostly mixed nature of failures. Conclusion: Based on results of this study it was concluded that the surface treatment that best influenced the bond strength was blasting with Al2O3 to better serve the two cementing agents. As the cementing agent U200 showed the best results without surface treatment. The C & B Cement and U200 showed similar values with the surface sandblasted with Al2O3. Rocatec to the U200 and cement Cement B & C showed similar, though lower than the values obtained for Al2O3 values.