A atividade industrial diversificada tem sido responsável pelo lançamento, no ambiente, de resíduos que contém materiais tóxicos e/ou de difícil degradação. Benzeno, tolueno, etilbenzeno e xilenos (BTEX) são compostos importantes, por estarem presentes em águas superficiais e subterrâneas, geralmente a partir de contaminações por derivadas de petróleo. Enquanto a degradação aeróbia de BTEX já está amplamente entendida e descrita, a aplicação de processos anaeróbios de tratamento, indicados na década de 80 ainda requer mais estudos. Reatores anaeróbios horizontais de leito fixo de bancada preenchidos com cubos de espuma de poliuretano, contendo lodo anaeróbio proveniente de diversas fontes trataram a água residuária sintética a base de proteínas, carboidratos, lipídios, contendo solução etanólica de BTEX e solução de BTEX em detergente comercial; e solução etanólica de BTEX como únicas fontes de carbono. A influência da adição de nitrato e sulfato como aceptores de elétrons na degradação anaeróbia também é discutida. Os reatores foram capazes de remover BTEX nas concentrações testadas de até 15,0 mg/L de cada composto, com tempos de detenção hidráulica de 11,4 horas e 13,5 horas. Os reatores forneceram condições excelentes para o desenvolvimento de biofilme complexo capaz de degradar BTEX, contendo organismos degradadores de BTEX, acetogênicos, acetoclásticos e hidrogenotróficos. Arqueas metanogênicas representaram menos de 0,5% do total de organismos anaeróbios na biomassa dos reatores. O modelo cinético de primeira ordem com residual foi o que melhor representou os dados experimentais e as velocidades de degradações de BTEX, estimadas neste trabalho, foram cerca de 10 a 94 vezes maiores que as encontradas na literatura, em ensaios realizados em microcosmos. / The diversified industrial activity has been responsible for discharge in the environment of toxic and/or difficult degradation compounds. Benzene, toluene, ethylbenzene and xylenes (BTEX) are important compounds present in surface and ground waters, usually from petroleum products contamination. While BTEX aerobic degradation is extensively understood and described, anaerobic treatment application, started in the eighties, associated to fundamental studies need to be improved. Bench-scale horizontal-flow anaerobic immobilized biomass reactors filled with polyurethane foam matrices, containing immobilized anaerobic biomass from various sources, treated synthetic substrate containing protein, carbohydrates, lipids, BTEX solution in ethanol and BTEX solution in commercial detergent, as well as BTEX solution in ethanol as the sole carbon source. The influence of the addition of nitrate and sulfate as electron acceptors on anaerobic degradation is also discussed. The reactors were able to remove up to 15.0 mg/L of each BTEX compound, with hydraulic detention time of 11.4 hours and 13.5 hours. The reactors provided excellent conditions for developing a complex biofilm with BTEX-degraders, acetogenic, acetoclastic and hydrogenotrophic microorganisms. Methanogenic archaea were found to represent less than 0.5% of the total anaerobic organisms in the biomass inside the reactors. Residual first order kinetic model fitted well the experimental data and the BTEX degradation rates, estimated in this work, were about 10- to 94-fold higher than those found in the literature, in microcosms studies.

Este trabalho apresenta as avaliações de desempenho, das demandas operacionais e dos fatores intervenientes no aumento da escala da unidade piloto do Reator anaeróbio Horizontal de Leito Fixo (RAHLF) no tratamento de esgoto sanitário após passagem por peneira com malha de 1 mm, durante dois anos de operação. O reator dispunha de volume total de 237,5 1, construídos com tubos comerciais de PVC de 14,5 cm de diâmetro (D), dispostos em cinco módulos horizontais em série de 2,88 m, perfazendo um comprimento total de (L) de 14,4 m e relação de total de L/D de 100. O suporte de imobilização de biomassa, espuma de poliuretano em matrizes cúbicas de 1 cm de aresta, mostrou-se adequado ao desenvolvimento do biofilme. Em partida, sem inoculação prévia, ocorreu a sua consolidação a partir de 70 dias, com predominância de morfologia semelhante a Methanosaeta sp. em relação a da Methanosarcina. Em torno de 90 dias com afluente de 350 mg/l de DQO, observe-se a melhor qualidade do efluente, com valor de 100 mg/l de DQO. Em longa operação ocorreu queda de rendimento e menor reprodutibilidade das previsões do projeto, atribuída aos constantes entupimentos e ineficácia das operações de limpeza, com o comprometimento de volume reacional verificados por estudos de hidrodinâmica. Da investigação das origens dos equipamentos observou-se tratar mais de um efeito local e qualitativamente relacionado à biomassa retida que propriamente quantitativo e extensivo ao longo de todo reator, com produção continuada de polímeros extracelulares, promovendo um efeito sinérgico com os predominantes organismos filamentosos e com os sólidos particulados retidos no leito. Diante das potencialidades desta configuração de reator apontam-se alternativas de mitigação dos entupimentos e o direcionamento dos estudos necessários para novo aumento de escala para o tratamento de esgoto sanitário. / This work evaluated the performance, the operational demands and the intervenient factors in the scale-up of the horizontal flow anaerobic immobilized biomass (HAIB) reactor pilot unit, treating domestic sewage previously screened. The operation was monitored for two years. The five- module (2.88 m length each) reactor volume was 237.5 liters and it was built with commercial PVC pipes of 14.5 cm of diameter (D), resulting in a total length (L) of 14.4 m and in a total ratio L/D of approximately 100. The immobilization support, cubic matrices of polyurethane foam (1 cm edge), showed to be suitable for the anaerobic biofilm development. During the start-up, without previous inoculation, the biofilm seemed to be consolidated after 70 days, and Methanosaeta sp. morphology predominated, in detriment of Methanosarcina. With an affluent of 350 mg COD/L, the best reactor performance was observed in about 90 days of operation (100 mg COD/L in the effluent). However, with the continuous operation, its performance decreased and the project predictions did not seem to fit anymore. These facts were probably due to the frequent cloggings ant the inefficiency of the backwashing procedures, leading to a decreasing of the operational volume. The origin of the clogging seemed to be related to the extracellular polymer production, linked to a synergic effect with the filamentous organisms and the particulate solids in the bed. Despite these operational problems, there were found alternatives to mitigate the clogging, and studies about a new scale-up methodology, in order to treat domestic sewage, were strongly recommended.

Submeteu-se um Reator Anaeróbio Horizontal de Leito Fixo (RAHLF) de bancada, ao aumento progressivo da concentração de matéria orgânica afluente, e a cargas de choque orgânicas, com o objetivo de verificar-se seu desempenho e estabilidade operacional. O RAHLF foi construído com um tubo de boro-silicato de 100 cm de comprimento, 5,0 cm de diâmetro e 1995 ml de volume total e preenchido com lodo anaeróbio imobilizado em matrizes de espuma de poliuretano. O reator foi alimentado, inicialmente, com substrato composto principalmente de carboidratos em concentrações, expressas como Demanda Química de Oxigênio (DQO) de, aproximadamente, 200, 1000 e 2000 mg/l. Posteriormente, os carboidratos foram substituídos por metanol e ácidos voláteis, em concentrações totais, aproximadas, de 2000, 3000, 4000 e 5000 mg DQO/l. Atingido o estado estacionário para cada condição operacional, foram aplicadas cargas de choque, aumentando-se em três vezes o valor da DQO afluente, durante período equivalente ao tempo de detenção hidráulica (sete horas). O sistema apresentou problemas operacionais durante os experimentos com carboidratos, quando submetido a 2000 mg DQO/l, correspondente à taxa volumétrica de carregamento orgânico de 8,77 KgDQO/m3.d. Não foi verificado qualquer problema operacional durante os experimentos com substrato contendo metanol e ácidos voláteis, e o reator apresentou eficiência de remoção de DQO superior a 90%. Para o experimento com DQO afluente igual a 2000 mg/l, os parâmetros cinéticos foram estimados a partir de modelo cinético de 1ª ordem, obtendo-se valor de k1 igual a 0,049 h-1, nos demais experimentos ajustou-se modelo cinético de 2ª ordem com valor médio de k2 equivalente a 2,0 x 10-4 l/mg.h Foram aplicadas cargas de choque orgânicas equivalentes a, aproximadamente, 17; 27; 40 e 47 kgDQO/m3.d. Os efeitos das sobrecargas orgânicas no reator foram transientes em todos os casos, tendo o reator voltado à condição inicial em, no máximo, 15 horas após o início das sobrecargas. / A Horizontal flow Anaerobic lmmobilized Sludge Reactor (HAIS) was subjected to progressively increasing concentrations of organic effluent material and to organic shock loads with the purpose of investigating its operational performance and stability. The HAIS, consisting of a 100 cm long, 5 cm diameter borosilicate tube with a total volume capacity of 1995 mL, was filled with anaerobic sludge immobilized in foam and polyurethane matrixes. The reactor was initially fed with a substrate composed mainly of carbohydrates in concentrations, expressed as Chemical Oxygen Demand (COD), of approximately 200, 1000 and 2000 mg/L. These carbohydrates were later replaced by methanol and volatile acids in total concentrations of 2000, 3000, 4000 and 5000 mg COD/L. Shock loads were applied after each operational condition became stationary, with the effluent COD tripled for a period equivalent to the hydraulic detention time (seven hours). The system presented operational problems during the experiments with carbohydrates when subjected to 2000 mg DQO/l, which corresponded to a volumetric organic load index of 8,77 Kg COD/m3.d. No operational problems were detected during the experiments with substrates containing methanol and volatile acids, and the reactor presented a COD removal efficiency of over 90%. The kinetic parameters for the COD effluent with 2000 mg/L were estimated based on a first arder kinetic model, which resulted in a k1 value of 0,049 h-1, while a kinetic model of the second order was used for the remaining experiments, with a mean value of k2 equivalent to 2,0 x 10-4 L/mg.h. Organic shock loads of approximately 17; 27; 40 and 47 kg COD/m3.d were applied. The effects of the organic overloads on the reactor were transient in every case, with the reactor returning to its initial condition at the most 15 hours after the beginning of the overloads.

Este trabalho avaliou o desempenho de um sistema que combina os processos anaeróbio e aeróbio, para tratamento de esgoto sanitário, operado de modo contínuo sem e com recirculação da fase líquida. A combinação dos processos anaeróbio e aeróbio tem como objetivo aproveitar as vantagens de cada um, minimizando seus aspectos negativos. Foi utilizado um reator, em escala de bancada, de leito fixo e fluxo contínuo de escoamento ascendente com argila expandida e espuma de poliuretano como suportes de imobilização da biomassa. O desempenho do sistema foi avaliado em três diferentes tempos de detenção hidráulica (TDH), 6, 8 e 10 horas, na fase anaeróbia, nos quais os melhores valores de remoção de matéria orgânica chegaram a 80%, com valores de DQO efluente abaixo de 150 mg/L. Com a inserção da fase aeróbia ao sistema (TDH de aproximadamente 11 horas, sendo 8 horas para a fase anaeróbia e 3 horas para a fase aeróbia), a eficiência subiu para mais de 90% com DQO efluente abaixo dos 50 mg/L. A nitrificação ocorreu perto do 15° dia operacional do sistema combinado e estava praticamente estável ao fim dessa etapa operacional. Após o 20º dia de operação as concentrações de nitrito mantiveram-se sempre baixas, o que indica equilíbrio da nitrificação. Foram obtidos ganhos quando feita recirculação do efluente tratado, principalmente em relação à remoção de matéria orgânica (95%) e remoção de nitrogênio total que foi de 75% para razão de recirculação de 1,5. O reator avaliado apresentou estabilidade operacional, alta remoção de matéria orgânica e nitrogênio sem a necessidade de adição de fonte exógena de carbono e de suplementação de alcalinidade. / This work evaluated the performance of a system that combines anaerobic and aerobic processes, for treatment of domestic sewage. The bench-scale fixed-film reactor was operated in a continuous way without and with recycle of the liquid phase. Expanded clay and polyurethane foam were used as supports for immobilization of the biomass. Initially, the system was operated under anaerobic condition and its performance was evaluated for three different hydraulic retention times (HRT), 6, 8 and 10 h. In this phase, COD removal efficiency of 80% was reached for HRT of 10 h, with effluent COD below 150 mgCOD/L. The combined anaerobic-aerobic operation (HRT of approximately 11 h, being 8 h for the anaerobic phase and 3 h for the aerobic phase) favored the organic matter removal that reached 90%, with effluent COD below 50 mgCOD/L. The operation with liquid recycle provided the best results with COD removal of 95% and total nitrogen removal of 75% under recycle ratio of 1.5. The anaerobic-aerobic fixed bed reactor, with recycle of the liquid phase, proved to be an excellent alternative for domestic sewage treatment, mainly when organic matter and nitrogen removals are required. The concomitant C and N removal without addition of exogenous source electron donor and with no additional alkalinity supplementation was the main advantage of this reactor over the conventional reactors applied for this purpose.

Um reator anaeróbio horizontal de leito fixo foi operado a escala de laboratório, visando verificar sua capacidade de degradação de fenol. O RAHLF foi construído em vidro de borosilicato com 100 cm de comprimento e 5,04 cm de diâmetro, preenchido com lodo anaeróbio imobilizado em matrizes de espuma de poliuretano. Prévio à realização do experimento o reator foi operado com substrato sintético, contendo como fontes de carbono glicose, ácido acético e ácido fórmico, atingida a estabilização da matéria orgânica para uma carga orgânica de 1028 mg/L, correspondente a uma remoção de DQO de 98%, foi iniciada a adição de fenol começando com uma concentração de 50 mg/L como única fonte de carbono. A concentração de fenol adicionada variou de 50 a 1200 mg/L e sua degradação foi avaliada através de determinação cromatográfica, utilizando cromatografia gasosa e parâmetros físico-químicos como pH, ácidos voláteis, alcalinidade e DQO. O RAHLF foi operado com um tempo de detenção hidráulica (TDH) de 12,3 horas. Com 50 mg/L, após 33 dias o reator atingiu uma remoção de fenol de 97%. Com 100 mg/L e depois de 148 dias de operação não foi detectado fenol no efluente do reator. Com 300 mg/L e após 58 dias de operação o reator apresentou 99% de remoção e uma concentração no efluente de 0,85 mg/L. Com 600 mg/L, 900 mg/L e 1200 mh/L, após 47, 29 e 7 dias de operação o reator alcançou remoções de 99%. Em todas as concentrações foi observado o predomínio de Methanosaeta, Methanobacterium e cocosmetanogênicos. Em relação à bactéria oxidadora de fenol foi observado o predomínio de coco-bacilos. As altas remoções de fenol observadas neste trabalho são devidas provavelmente à utilização de células imobilizadas. / A bench-scale horizontal-flow anaerobic immobilized biomass (HAIB) reactor was assayed aiming to verify its potential use for phenol degradation. The HAIB reactor consisted of a bore-silicate tube (100 cm long; 5.04 cm diameter) filled with polyurethane foam matrices containing immobilized anaerobic sludge. Before being subjected to phenol, the reactor was fed with synthetic substrate at the influent chemical oxygen demand (COD) of 1,028 mg/L achieving 98% of COD removal efficiency. Thereafter, phenol as the sole carbon source was added under step-increasing concentrations from 50 to 1,200 mg/L. Phenol degradation was evaluated by gas chromatographic analysis of influent and effiuent samples. Process monitoring included determinations of pH, volatile acids, alkalinity and COD. The HAIB reactor was operated at a constant hydraulic detention time (HDT) of 12,3 hours. After 33 days with 50 mg/L of phenol in the influent, the reactor achieved 97% of phenol removal efficiency. Successful phenol degradation (efficiency removal of 99%) occurred for influem concentrations of 100, 300, 600, 900 and 1,200 mg/L after 148, 58, 47, 29 and 7 days, respectively. The predominance of Methanosaeta, Methanobacterium and methanogenic cocci could be observed in all the operating conditions, besides the presence of phenol-oxidizing microorganisms as irregular rods. The results indicate that phenol degradation at very high rates can be accomplished in HAIB reactors containing acclimatized biomass.

Este trabalho avaliou o desempenho de um sistema que combina os processos anaeróbio e aeróbio, para tratamento de esgoto sanitário, operado de modo contínuo sem e com recirculação da fase líquida. A combinação dos processos anaeróbio e aeróbio tem como objetivo aproveitar as vantagens de cada um, minimizando seus aspectos negativos. Foi utilizado um reator, em escala de bancada, de leito fixo e fluxo contínuo de escoamento ascendente com argila expandida e espuma de poliuretano como suportes de imobilização da biomassa. O desempenho do sistema foi avaliado em três diferentes tempos de detenção hidráulica (TDH), 6, 8 e 10 horas, na fase anaeróbia, nos quais os melhores valores de remoção de matéria orgânica chegaram a 80%, com valores de DQO efluente abaixo de 150 mg/L. Com a inserção da fase aeróbia ao sistema (TDH de aproximadamente 11 horas, sendo 8 horas para a fase anaeróbia e 3 horas para a fase aeróbia), a eficiência subiu para mais de 90% com DQO efluente abaixo dos 50 mg/L. A nitrificação ocorreu perto do 15° dia operacional do sistema combinado e estava praticamente estável ao fim dessa etapa operacional. Após o 20º dia de operação as concentrações de nitrito mantiveram-se sempre baixas, o que indica equilíbrio da nitrificação. Foram obtidos ganhos quando feita recirculação do efluente tratado, principalmente em relação à remoção de matéria orgânica (95%) e remoção de nitrogênio total que foi de 75% para razão de recirculação de 1,5. O reator avaliado apresentou estabilidade operacional, alta remoção de matéria orgânica e nitrogênio sem a necessidade de adição de fonte exógena de carbono e de suplementação de alcalinidade. / This work evaluated the performance of a system that combines anaerobic and aerobic processes, for treatment of domestic sewage. The bench-scale fixed-film reactor was operated in a continuous way without and with recycle of the liquid phase. Expanded clay and polyurethane foam were used as supports for immobilization of the biomass. Initially, the system was operated under anaerobic condition and its performance was evaluated for three different hydraulic retention times (HRT), 6, 8 and 10 h. In this phase, COD removal efficiency of 80% was reached for HRT of 10 h, with effluent COD below 150 mgCOD/L. The combined anaerobic-aerobic operation (HRT of approximately 11 h, being 8 h for the anaerobic phase and 3 h for the aerobic phase) favored the organic matter removal that reached 90%, with effluent COD below 50 mgCOD/L. The operation with liquid recycle provided the best results with COD removal of 95% and total nitrogen removal of 75% under recycle ratio of 1.5. The anaerobic-aerobic fixed bed reactor, with recycle of the liquid phase, proved to be an excellent alternative for domestic sewage treatment, mainly when organic matter and nitrogen removals are required. The concomitant C and N removal without addition of exogenous source electron donor and with no additional alkalinity supplementation was the main advantage of this reactor over the conventional reactors applied for this purpose.

La réduction des émissions anthropiques de CO2 constitue actuellement un enjeu majeur. Parmi les technologies destinées à la production d'énergie, le Chemical Looping Combustion (CLC) présente un potentiel intéressant avec un faible coût de capture de CO2. Le CLC consiste à produire de l'énergie à partir de combustibles fossiles, en présence d’un transporteur d’oxygène solide qui fournit l’oxygène nécessaire à la combustion. Le matériau est ensuite régénéré sous air dans un deuxième réacteur. En sortie du réacteur de combustion, seuls les gaz CO2 et H2O sont émis et ainsi, après la condensation de l’eau, du CO2 quasiment pur est obtenu. La viabilité du procédé CLC à échelle industrielle dépend des performances et de la durée de vie des transporteurs d’oxygène utilisés. Au cours de cette thèse, les performances et le vieillissement d’un transporteur d'oxygène modèle (NiO/NiAl2O4), vis-à-vis de l’oxydation de CO ont été étudiées. Pour cela, des cycles d'oxydation-réduction dans un réacteur à lit fixe traversé ont été réalisés. Au cours de l’étude de l'influence des conditions de fonctionnement sur les performances du transporteur, il a été observé que la réactivité du transporteur augmente avec la température. De plus, le liant (NiAl2O4) participe également à la réaction d’oxydation du CO. Une évolution de la structure cristalline du liant au cours des cycles à haute température, a été mise en évidence à l’aide des techniques de caractérisation du solide (DRX, MEB-EDX, TPR,...). En parallèle à ces travaux, un outil numérique de simulation du lit fixe traversé a été développé afin de modéliser la réaction de réduction du transporteur d'oxygène avec le combustible CO. / Nowadays, the reduction of anthropogenic greenhouse gas emissions (especially CO2) constitutes an important challenge. Among the different technologies currently studied for the CO2 capture during energy production, the Chemical Looping Combustion (CLC) shows an interesting potential with a low cost of capture. CLC consists of producing energy from fossil fuels or biomass combustion, in the presence of an oxygen carrier (generally a metal oxide) which provides the required oxygen for combustion. The material is then reoxidized with air in a different reactor. At the combustion reactor outlet only H2O and CO2 gases are emitted, therefore after condensation almost pure CO2 can be obtained. The success of a large scale CLC application depends on finding suitable oxygen carriers with good performances and long lifetime. The objective of this work is to study the performances and the ageing of a model oxygen carrier (NiO/NiAl2O4) with CO as fuel. For this, oxidation/reduction cycles have been carried out in a fixed bed reactor. The influence of the operating conditions on its performances is also investigated. From these studies, it is observed that the reactivity of the oxygen carrier increases with temperature. Moreover, the binder used in the oxygen carrier (NiAl2O4) reacts also with the fuel CO to produce CO2. An evolution on the support’s structure during cycles at high temperature is demonstrated using solid characterization techniques (DRX, MEB-EDX and TPR). After these experimental studies, a numerical model has been developed to simulate the reduction reaction of the oxygen carrier with CO in a fixed bed reactor.

Se presenta un modelo matemático para el diseño y simulación de un reactor de lecho fijo con enzimas inmovilizadas en partículas esféricas porosas. La ecuación de diseño del reactor se ha resuelto para el caso de un sistema enzimático, con limitaciones difusionales internas, que obedece a una cinética de Michaelis-Menten reversible.La validez del modelo se ha comprobado con el sistema enzimático naringina/naringinasa, aplicable al proceso de desamargado de zumos cítricos. / A mathematical model for design and simulation of a fixed bed reactor with immobilized enzymes in spherical particles is presented. The reactor design equation is solved for an enzymatic system taking into account internal diffusional limitations. Moreover, the enzyme obeys a reversible Michaelis-Menten kinetic. The validity of the model is checked by using the enzymatic system naringine/naringinase, which is used for fruit juice debbitering processes.

Cette thèse s'inscrit dans le domaine de la catalyse hétérogène pour des applications en raffinage et enpétrochimie. Comme objet d'étude, nous avons ciblé les catalyseurs d'hydrotraitement qui permettentd'éliminer les impuretés contenues dans le pétrole comme le soufre. Ces catalyseurs d'hydrotraitementsont constitués de sulfures de molybdène supportés sur alumine et généralement promus par du nickelou du cobalt.L'enjeu de la thèse porte sur la compréhension des phénomènes mis en jeu au cours de la sulfuration etde la stabilisation (cokage, passivation, évolution de la phase sulfure) des catalyseurs pour la réactiond'hydrodésulfuration des gazoles visant à réduire sa teneur en soufre. Néanmoins, à l'heure actuelleaucune technique ne permet de caractériser le catalyseur lors de la sulfuration en phase liquide (avecou sans DMDS) et du test dans les conditions de température et de pression industrielles.La présente thèse vise le développement d'une « caractérisation operando » de ce type de réaction ens'appuyant sur la spectroscopie Raman, une des seules technique de laboratoire permettant d'effectuerdes analyses avec les contraintes précédemment citées. Une unité, composée d'un réacteur cylindriquetransparent, a donc été conçue et mise au point pour suivre par spectroscopie Raman les phases solideet liquide au cours de la sulfuration et de la réaction d'HDS. Parallèlement, une méthodologie decaractérisation et de focalisation a été développée. Ce montage et cette méthodologie ont permisd'accéder pour la première fois à des profils spatiaux et temporels sur la phase solide dans lesconditions d'activation et de réaction d'hydrotraitement des gazoles en condition d'hydrodésulfuration(30 bar, 350 °C).Malgré un signal de fluorescence probablement liée à la décomposition radicalaire du précurseur desoufre (DMDS) entre 200 et 260°C, il a été possible de suivre au cours du temps à des positions fixesla disparition de la phase oxyde, l'évolution de la phase sulfure et du coke . Ces résultats ontnotamment permis d'étudier l'impact de la charge sur la cinétique de sulfuration .Le suivi spatial, lelong du réacteur par exemple, s'avère plus délicat et nécessitera de développer des méthodes pourcompenser les variations d'intensité du signal Raman induites par le positionnement aléatoire desgrains ainsi que l'écoulement. Concernant la phase liquide, une approche multivariée utilisant desoutils chimiométriques a été appliquée afin de relier l'émission de fluorescence intrinsèque à denombreux diesels à certaines de leurs propriétés (teneur en soufre et en aromatiques, densité…). Lesmodèles ont été développés à partir de spectres acquis à température ambiante et à pressionatmosphérique, mais leurs performances satisfaisantes encouragent à étendre l'approche auxconditions réactionnelles d'HDS qui reste une perspective de ce travail / This thesis is in the field of heterogeneous catalysis for the applications in refining and petrochemistry. As an aim of this study, we have focused on the hydrotreatment catalysts that are applied to remove some of the impurities from crude oils, like sulfur. Such hydrotreatment catalysts consist of alumina supported molybdenum sulfides, being generally promoted by nickel or cobalt.The aim of this work have consisted on the understanding of the phenomena occurring during the stabilization phase (coking, passivation, evolution of the sulfide phase) during the catalysts sulfidation and under the reaction of hydrodesulfurization, HDS, aiming to reduce the diesels sulfur content. A better understanding of these phenomena would ease the development of new generations of more efficient catalysts. This thesis aims at extending the operando characterization methods to allow a spatial and temporal follow-up of liquid and catalyst during this type of reactions. A unit was designed and built to follow the solid and liquid phases during the catalysts sulfidation and under HDS reaction. The operando follow-up was done using Raman spectroscopy through a cylindrical transparent reactor. In parallel, a methodology has been developed to focus and acquire good quality spectra through the reactor..With these reactor and methodology , we were able to access for the first time to time-space resolved profiles of the solid phase during the sulfidation and the diesel hydrodesulfurization (under 350 °C and 30 bar). Temporal profiles concerns the oxide phase disappearance, sulfide phase growth and coke formation. Spatial profiles are more challenging and will require a methodology more robust to signal changes induced by the random position of pellets and flow pattern. With respect to the liquid phase, a multivariate approach based on chemometrics has gave properties of diesels at room temperature and atmospheric pressure. The good results are encouraging enough to propose to extend the approach to HDS conditions that constitutes one of the perspectives of the work

L’acylation de Friedel-Crafts est parmi les réactions les plus fondamentales et les plus utiles pour former des cétones aromatiques. Bien que la mise en oeuvre de ces réactions soit habituellement pénalisante en termes de sous produits formés, de rendement atomique et de quantité de catalyseur utilisée, cette voie est encore largement utilisée dans l’industrie de la chimie fine. Ces dernières années, la prise de conscience de l’impact des activités industrielles sur l’environnement a mené les chimistes à travailler sur de nouvelles voies, moins dangereuses et plus respectueuses de l’environnement.Nous avons considéré ici l’acylation d’un dérivé du benzofurane par un chlorure d’acyle, correspondant à une étape intermédiaire pour la fabrication d’un principe actif pharmaceutique. Dans cette étude, la première proposition a consisté à remplacer les catalyseurs classiques (FeCl3 ou AlCl3) par des catalyseurs solides réutilisables. Dans ce travail, plusieurs catalyseurs (zéolites, résines échangeuses d’ions...) ont d’abord été testés dans des conditions « conventionnelles » , c’est-à-dire en utilisant un solvant organique, afin de déterminer le plus performant, en termes de réactivité, de durée de vie et de réutilisabilité. Une zéolite Y s’est avéré la plus adaptée. Cependant, l’utilisation d’un solvant organique (ici le 1,2-dichlorobenzène) reste discutable et l’utilisation du CO2 supercritique comme solvant a donc été envisagée. Pour cela, nous avons imaginé et dimensionné un réacteur tubulaire à lit fixe de catalyseur fonctionnant sous pression et en continu. Les résultats présentés montrent la faisabilité d’un tel procédé et pose les jalons pour arriver à une ou des solutions pour une meilleure mise en oeuvre industrielle des réactions de Friedel-Crafts. / Friedel-Crafts acylation is among the most fundamental and useful reactions to yield aromatic ketones, but it is one of the less acceptable in terms of unwanted polluting by-products or atom economy because of overconsumption of catalyst which is used in stoichiometric quantities in the conventional process. This route is nevertheless still widely used in the fine chemicals industry. In recent years, awareness of the impact of industrial activities on the environment has lead chemists to work on new chemical routes, less dangerous and more environmentally friendly. We considered here the acylation of a benzofurane derivative by an acid chloride, as an intermediary step for a pharmaceutical product. In this study, one of the first alternative was to replace conventional catalysts (FeCl3 or AlCl3), by reusable solid catalysts. In this work, different catalysts (zeolites, ion-exchange resins...) were first tested in "conventional" conditions, i.e., using an organic solvent (1,2-dichlorobenzene in our case), to determine the best one, in terms of reactivity, lifetime and reusability. The zeolite Y was found the most appropriate. However, the use of an organic solvent still remains questionable and the use of supercritical carbon dioxide as the solvent was also considered. Its inherent properties include non-flammability, mild critical conditions, tuneable solubility near to the critical point and very low environmental impact. The reaction was operated using a specifically designed continuous high pressure fixed bed and results concerning yield and selectivity are presented. These results demonstrate the feasibility of such an approach, which would ultimately yield to better industrial operation of Friedel-Crafts reactions.