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[pt] Emulsões podem ser formadas durante o processo de exploração dos reservatórios de petróleo. Essas emulsões podem trazer diversos prejuízos, como mudanças nas características dos óleos e problemas no bombeamento. Diante disso, aditivos químicos capazes de promover a desestabilização de emulsões de petróleo são importantes para otimizar o processo produtivo e mitigar os problemas causados. Há diversos estudos dedicados à avaliação de substâncias para atuar como desemulsificantes. Porém, a compreensão de como a estrutura química dos aditivos está correlacionada com as características físico-químicas dos óleos e emulsões ainda é escasso. Esse trabalho tem como objetivo entender como as características dos aditivos estão relacionadas com as particularidades de óleos parafínicos e asfaltênicos. Para isso, três óleos brasileiros foram usados para preparar e caracterizar emulsões água-óleo e avaliar sua estabilidade após o uso de diferentes aditivos. As emulsões preparadas com esses óleos apresentaram grandes diferenças nas propriedades reológicas. Entre elas, a viscosidade e gelificação em um dos óleos parafínicos, o que pode impactar diretamente na eficiência de desemulsificação devido à dificuldade de incorporação dos aditivos no bulk da emulsão. A estabilidade das emulsões foi estudada por testes de envelhecimento em diferentes condições de temperatura sem e com adição de diferentes aditivos: surfactantes, polímeros, ácidos orgânicos e inorgânicos e álcoois. De forma geral, aditivos anfifílicos com grupos aniônicos apresentaram melhor eficiência desemulsificante para todos os óleos. A aromaticidade, a acidez e o volume molecular dos aditivos também foram características importantes para a desemulsificação, porém, dependem da temperatura. Confirmou-se que a escolha de um desemulsificante para emulsões de petróleo depende da composição dos óleos e das características reológicas das emulsões formadas. Para emulsões de óleos parafínicos a temperatura foi determinante na eficiência de desemulsificação, enquanto para o óleo asfaltênico, a acidez influenciou mais. / [en] Emulsions can be formed during the exploration process of oil reservoirs. These emulsions, when unwanted, can bring several losses, such as loss of oil and changes in its characteristics and problems in pumping. Therefore, the development of chemical additives capable of promoting the destabilization of oil emulsions is important to optimize the production process and mitigate the problems caused. In the literature, there are several studies dedicated to the evaluation of substances to act as demulsifiers. However, the understanding of how the chemical structure of additives is correlated with the physicochemical characteristics of oils and emulsions is still scarce. This work aims to understand how the characteristics of the substances are related to the particularities of oils and their emulsions to better understand how demulsification occurs and also to propose additives with greater efficiency for the systems studied. To this end, three Brazilian oils were used to prepare water-oil emulsions and to evaluate the demulsifying capacity of different chemical additives. The stability of the emulsions was studied by aging tests under different temperature conditions without and with the addition of the different additives: surfactants, polymers, organic and inorganic acids and alcohols. The tests were carried out under different conditions to evaluate the effect of temperature mainly due to the high paraffin content in some oils. The characterization of the emulsions (without additives) showed large differences in rheological properties between the systems prepared with oils. These include viscosity, thixotropy and gelation in one of the paraffinic oils, which can directly impact the demulsification efficiency due to the difficulty of incorporating the additives into the emulsion bulk. From the aging tests, it was generally observed that amphiphilic substances with high interfacial activity and with anionic groups showed better demulsifying efficiency for all oils. The aromaticity, acidity and molecular volume of the additives were also important characteristics for demulsification, but they are temperature dependent. Finally, it was concluded that in general, the choice of a demulsifier for petroleum emulsions depends on the composition of the oils and the rheological characteristics of the emulsions formed. For paraffinic oil emulsions, the temperature was decisive for the demulsification efficiency, whereas, for the others, the acidity proved to be more decisive.

no / The identification of proteins involved in tumour progression or which permit enhanced or novel therapeutic targeting is essential for cancer research. Direct MALDI analysis of tissue sections is rapidly demonstrating its potential for protein imaging and profiling in the investigation of a range of disease states including cancer. MALDI-mass spectrometry imaging (MALDI-MSI) has been used here for direct visualisation and in situ characterisation of proteins in breast tumour tissue section samples. Frozen MCF7 breast tumour xenograft and human formalin-fixed paraffin-embedded breast cancer tissue sections were used. An improved protocol for on-tissue trypsin digestion is described incorporating the use of a detergent, which increases the yield of tryptic peptides for both fresh frozen and formalin-fixed paraffin-embedded tumour tissue sections. A novel approach combining MALDI-MSI and ion mobility separation MALDI-tandem mass spectrometry imaging for improving the detection of low-abundance proteins that are difficult to detect by direct MALDI-MSI analysis is described. In situ protein identification was carried out directly from the tissue section by MALDI-MSI. Numerous protein signals were detected and some proteins including histone H3, H4 and Grp75 that were abundant in the tumour region were identified

Nowadays the environmental sustainability and the limitation of the energy consumption of buildings is of substantial importance in order to reduce greenhouse gases emissions and mitigate the consequences of climate change. Thermal energy storage (TES) allows to store thermal energy when available in order to use it when and where necessary. The use of insulating materials with TES capability may results in the compensation of energy absorption peaks caused by air conditioning or by space heating with a consequent reduction of energy consumption and related CO2 emissions. This work aims at the development and characterization of composite materials based on polymeric foams and containing a phase change material providing the TES capability. The production procedures were optimized in order to maximize the quality of the samples and the main properties of the resulting materials were then investigated. Different matrices were considered in this work: thermosetting, thermoplastic and elastomeric ones. As thermosetting matrix, a polyurethane foam was considered: this foam was filled, during the production process, with increasing amounts (from 10 to 40 wt%) of a microencapsulated PCM with a melting point of 24 °C. The addition of the PCM caused the disruption of the regular close cell morphology of the foams with a consequent increase of the thermal conductivity and a reduction of the mechanical properties. On the other hand, the addition of the PCM led to interesting TES properties, measured both through differential scanning calorimetry and infrared thermography (up to 54 J/g). Polyethylene was chosen as thermoplastic matrix and the technology of salt leaching was used to obtain foams without the use of chemical foaming agents. Foams containing different amounts (up to 56 wt%) of a microencapsulated PCM with a melting point of 24 °C were prepared. The addition of the PCM led to a decrease of the connectivity and porosity values of the prepared foams with a consequent decrease of the mechanical properties and increase of the thermal conductivity. Despite the rupture of a certain part of the PCM capsules due to the production process, good TES properties (up to 50 J/g) were measured. Elastomeric foams were prepared using an EPDM rubber as matrix and different foaming agents for the expansion process: foams obtained using two different commercial foaming agents were compared with foams obtained using the salt leaching technique. In the first case, a shape-stabilized PCM was added during the production process, while in the second one the foams were impregnated with a liquid PCM without the necessity of a shape stabilization. Salt leaching foams were able to retain higher PCM loads with respect to foams produced using commercial foaming agents and were therefore characterized by higher TES capability (up to 129 J/g). Infrared thermography tests highlighted that the time required to reach a reference temperature during heating/cooling cycles was three times longer for samples with a PCM amount of about 55 wt%. These foams evidenced a general decrease of the mechanical properties upon PCM addition. Moreover, a strong influence of the temperature on the mechanical behaviour of these foams was highlighted, with the PCM acting as softener above its melting point and as hardener below. In order to consider practical applications, elastomeric panels made of an ethylene propylene diene monomer (EPDM) rubber filled with a shape stabilized PCM and covered with a nitrile-butadiene rubber (NBR) envelope were prepared. It was possible to verify the absence of leakage, the uniform distribution of the PCM and the influence of temperature on the mechanical properties of the samples. From rheological tests it was also possible to observe the plasticizing effect of the PCM that hindered the vulcanization process of the EPDM/PCM compound. In the second part of this work larger samples were prepared and used for the internal insulation of wood boxes that were subjected to heating/cooling cycles, simulating thus real summer conditions in north Italy. The beneficial effect of the PCM resulted in a consistent reduction of the temperature peak with respect to a reference box insulated with elastomeric panels without PCM. Moreover, the fire behaviour of the produced samples was studied and the effect of the addition of different flame retardants was deeply investigated. The addition of a flame retardant based on ammonium polyphosphate and aluminium diethyl phosphinate as synergistic agents allowed a strong reduction of the peak of heat release rate measured through cone calorimeter tests, with a significant improvement of the fire behaviour. Fire tests allowed also to point out the significant role, in improving the fire performances of the samples, of the interactions between ammonium polyphosphate and the mineral fillers present in the EPDM/PCM compound (clay) and in the envelope (talc, kaolin and silica). A better comprehension of the combustion mechanisms and of the flame retardant efficacy was achieved through the analysis of the combustion residues. Finally, the specific enthalpy of the different systems was evaluated with respect to the cost of the raw materials used in the production stages in order to classify them on the basis of their melting enthalpy and on the economical aspects.

Le travail de recherche mené au cours de cette thèse a été effectué dans le cadre d’une collaboration industrielle et a porté sur l’étude des caractéristiques physico-chimiques d’une matrice lipidique à libération prolongée. L’originalité de cette dernière tient à sa forme galénique, des microsphères calibrées d’environ 400 µm de diamètre, fabriquées par procédé de prilling puis conditionnées en sachets.Les caractérisations entreprises au cours de cette thèse ont été menées progressivement en partant de l’étude du comportement thermique individuel des constituants (excipients lipidiques et principe actif), puis de leurs mélanges pour définir les conditions d’existence et les caractéristiques structurales des phases solides qu’ils engendrent, notamment lors du prilling. Plusieurs diagrammes d’état partiels ont été construits pour permettre de cerner l’organisation de la matrice formant le produit fini et disposer de leviers fiables pour corriger d’éventuelles déviations du procédé de fabrication. Cette analyse était également indispensable pour décrire précisément le processus de libération du principe actif et en déterminer les paramètres cinétiques. / The research conducted in this thesis, during an industrial collaboration, is focused on the study of physicochemical characteristics of a sustained release lipid matrix. The originality of this matrix is its dosage form, microspheres of 400 microns in diameter, manufactured by a prilling process and packaged in stick-packs.The characterizations conducted during this thesis have been carried out gradually starting from the study of the thermal behavior of individual components (lipidic excipients and drug) and their mixtures to define the phase formation conditions and the structural characteristics of the solid phases generated, especially during the prilling process. Partial phase diagrams were constructed to understand the final product matrix organization and to identify actions to correct any deviations in the process. This analysis was also needed to accurately describe the drug release mechanism and to determine the kinetic parameters.

O Herpesvírus equino tipo -1 (EHV-1) pertence ao gênero Varicellovírus da subfamília Alphaherpesvirinae pertencente à Família Herpesviridae. É um vírus envelopado, de DNA linear fita dupla, composto por 76 genes distintos. O EHV-1 é responsável por grandes prejuízos econômicos na equinocultura mundial. Responsável por doença neonatal fatal, mieloencefalopatia, rinopneumonite e abortamento, encontra-se amplamente distribuído pela população equina do território nacional. O objetivo do presente estudo foi o de padronizar uma reação em cadeia pela polimerase (PCR) para detecção do EHV-1 em tecidos incluídos em parafina a fim de permitir estudos retrospectivos em arquivos de amostras histopatológicas. Assim, foram inoculados experimentalmente 12 camundongos com 21 dias de idade da linhagem CH3/Rockfeller com três diferentes isolados de EHV-1, dois provenientes da Argentina e um do Brasil. Esses animais foram observados por quatro dias e, após sacrifício por sobre dose de uma associação de ketamina e xilazina, foram submetidos à necropsia e colhidos o pulmão e sistema nervoso central (SNC). Os órgãos colhidos foram divididos em duas partes aproximadamente iguais: uma mantida a -20ºC até processamento e a outra fixada em formalina 10% tamponada e posteriormente incluída em parafina. A extração foi realizada com nove fragmentos contínuos de 4µm cada, a partir do protocolo de extração com proteinase K/ fenol/ clorofórmio. Foi realizada avaliação da sensibilidade analítica da PCR com oito diluições na base 10 para os três isolados utilizados. A amplificação do DNA viral foi realizada utilizando primers direcionados para a ORF64. A fim de descartar a eventual presença de inibidores da reação de PCR e assegurar a adequada extração de DNA, foram incluídos primers direcionados para o gene da beta-actina. A PCR mostrou-se capaz de amplificar DNA viral alvo numa diluição de até 10-5, sendo positiva entre 10-1 a 10-2 DICT50/25µL. Com a PCR padronizada, foi possível detectar o DNA do EHV-1 em: a) 100% (12/12) das amostras de pulmão congeladas e 100% (12/12) das amostras de pulmão incluídas em parafina; b) em 91% (11/12) das amostras de SNC congeladas e 41% (5/12) das amostras de SNC incluídas em parafina. A aplicação da PCR padronizada em uma coleção de amostras incluídas em parafina do Laboratório de Anatomia Patológica do IB/SP, colhidas de cinco casos de abortamento em equinos, revelou que o DNA do EHV-1 foi detectado em: a) um caso em que originalmente foi possível isolar o EHV-1; b) em 4/4 amostras que revelaram-se originalmente negativas. Com base nos resultados obtidos, foi possível concluir que a PCR padronizada teve bom desempenho na detecção de DNA viral em amostras incluídas em parafina de animais experimentalmente infectados e, provavelmente, uma sensibilidade diagnóstica mais elevada que os métodos utilizados para o diagnóstico do EHV-1 na coleção de amostras de equino testada. / The equine herpesvirus type 1 (EHV-1) belongs to Varicellovírus genus, Alphaherpesvirinae subfamíly of the Herpesviridae Famíly. It is an enveloped virus, double stranded linear DNA, composed of 76 distinct genes. The EHV-1 is responsible for great losses in horsebread world. Responsible for neonatal death, mieloencephalopaty, rinopneumonite and abortion, it is widely distributed into brasilian equine population. The purpose of this study was to standardize a polymerase chain reaction (PCR) for EHV-1detection in paraffin- embedded tissues allowing retrospective studies based on the collection histopatological samples. Thus, 12 mice (CH3/Rockfeller) with 21 days of age were inoculated with 3 different isolates of EHV-1, 2 from Argentina and one from Brazil. These mice were observed for 4 days and, after sacrifice by overdose of a combination of ketamine and xylazina, it were subjected to necropsy and collected the lung and central nervous system (SNC). The collected tissues were divided into 2 approximately equal parts: 1one stored at -20ºC until processing, and another set at 10% buffering formalin and later paraffin-embedded. The extraction was performed with continuous 9 fragments of 4µm each, using the extration protocol with proteinase K/ fenol/ clorofórmio. The assessment of analytical sensitivity of PCR were determined using 8 dilutions for all 3 virus isolates. The viral DNA amplification was performed using primers targeted to ORF64. In order to rule out the possible presence of PCR inhibitors and to ensure adequate extraction of DNA, primers directed to the gene for beta-actin were included It was possible to amplify viral DNA until 10-5 dilution, corresponding to 10-1 to 10-2 DICT50/25µL. With the standardized PCR, it was possible to detect the EHV-1 DNA in: a) 100% (12/12) of lung frozen sample and 100% (12/12) of the paraffin-embedded lung; b) 91% (11/12) of the frozen CNS and 41% (5/12) CNS paraffin-embedded. Moreover, the standardized PCR was tested in a collection of paraffin-embedded specimens from Pathological Anatomy Laboratory od Biological Institute Sao Paulo State, taken 5 cases of the abortion in horses. It were possible to detect EHV-1 DNA in: a) 1 sample from a case in that originally was possible to isolate the EHV-1, b) 4/4 sample originally negative diagnosed. Based on these results, it is possible to conclude that the standardized PCR performed well for detection viral DNA in paraffin-embedded tissues of experimentally infected animals, and probably a higher diagnostic sensitivity than the methods used for diagnosis of EHV-1 in the collection samples tissues tested for equine.

Les variations de température à la surface externe d'une conduite peuvent provoquer la solidification du fluide en écoulement interne, induisant la formation de dépôts solides sur les parois en contact avec le fluide. Ces dépôts peuvent s'avérer néfastes au bon fonctionnement du système intégrant cette conduite ce qui motive l'étude de ces phénomènes physiques afin de comprendre les mécanismes qui les gouvernent et de permettre leur prévention. Ce genre de situations peuvent être rencontrées dans le domaine pétrolier, par exemple lors du transport en pipeline d'huiles chargées de paraffines, d'hydrates ou d'asphaltènes ; dans le domaine agroalimentaire pour la circulation de produits liquides dans des tubes refroidis ou bien tout simplement pour des canalisations d'eau subissant un refroidissement. Dans la majorité des cas le fluide en écoulement dans les conduites pétrolières est un matériau à changement de phase (MCP) complexe et sa composition multiple avec des interactions entre la rhéologie, la constitution et la température impactant la thermo-hydrodynamique de l'écoulement et la cinétique de transition de phase. Dans le cadre de cette thèse nous proposons de nous pencher sur ces aspects par voie de modélisation. Dans la première partie de ce travail, nous avons développé un modèle physique basé sur la méthode enthalpique pour étudier l’impact de la convection naturelle sur des écoulements et des transferts thermiques avec transition de phase solide liquide dans différentes géométries (cavité carré, cylindre, sphère, autour d’un faisceau de cylindre, …). L'effet du maillage et de l'ordre de précision des schémas numérique est aussi présenté. Le même modèle a été utilisé pour analyser la cristallisation d’un mélange de deux paraffines dans des cellules calorimétriques (Differential Scanning Calorimetry). Pour cette étude, le modèle a été validé à l’aide des résultats expérimentaux de la technique DSC. Le problème de l’écoulement d’un mélange de deux paraffines dans une conduite cylindrique a été aussi abordé afin de prédire la cristallisation du mélange sur la paroi interne de la conduite. Une étude paramétrique a été effectuée pour analyser l’influence de différents paramètres (nombre de Reynolds, concentration initiale de la solution binaire, température de la paroi, …) sur la cinétique de la cristallisation du mélange. La deuxième partie de la thèse a été consacrée à l’étude de l’écoulement avec changement de phase liquide-solide d’un brut paraffinique dans des conduites pétrolières. En effet, la cristallisation des paraffines dans les bruts engendre un équilibre phase thermodynamique liquide/solide. Un modèle thermodynamique rendant compte de cet équilibre a été développé (et validé à l’aide de résultats expérimentaux disponible dans la littérature). Ce modèle nous a permis de prédire la température de cristallisation commençante (Wax Appearance Temperature), ainsi que la quantité de paraffines cristallisées. Ce modèle thermodynamique a été couplé avec un modèle physique reposant sur les équations de conservation de la masse, de la quantité de mouvement, de l'énergie et des espèces pour décrire l’écoulement d’un brut paraffinique avec changement de phase liquide-solide dans des conduites pétrolières. Le modèle physique a été validé à l’aide de résultats expérimentaux disponibles dans la littérature. / Temperature change at the outer surface of a pipe can cause solidification of the fluid flowing internally, inducing the formation of solid deposits on the walls in contact with the fluid. This kind of phenomena can be encountered in many situations in the industrial context such as petroleum industries, for example when transporting pipeline oils with paraffins, hydrates or asphaltenes; food industry for the flow of liquids in cooled tubes or simply for water pipes undergoing cooling.The rheology of the transported fluid, its composition and temperature are among the key factors that influence the thermo-hydrodynamics of the flow and the kinetics of the formation of the deposits. The analysis of their impact is required to enhance the understanding of these mechanisms in order to avoid their undesirable effects as fouling or complete blockage of pipes.In this thesis we propose to study these mechanisms by numerical modelling. We will focus on the modelling of phase change and especially on the description of liquid-solid interfaces by models able to integrate the thermodynamics of physical phenomena such as diffuse interface methods. We seek the two-dimensional numerical resolution of the equations of flow, heat and mass transfer while taking into account the coupling between rheology, composition and temperature in the liquid phase as well as at the interface. The work will be undertaken in the basis of the in-house computational fluid dynamics (CFD) code developed in the laboratory.

Realizou-se estudo comparando o uso da reação em cadeia da polimerase à evolução clínica e painel de exames tradicionais para diagnóstico em pacientes com suspeita clínica de tuberculose cutânea e micobacteriose atípica. Observou-se sensibilidade da reação em cadeia da polimerase de 88%, especificidade de 83%, valor preditivo positivo de 82%, valor preditivo negativo de 88% e acurácia de 85% com concordância pelo teste de McNemar (p= 0,655). Os exames do painel de maior acurácia, após a reação em cadeia da polimerase, foram o teste tuberculínico com acurácia de 79% e a presença de dermatite crônica granulomatosa com reação em cadeia da polimerase positiva com acurácia também de 79%, ambos com concordância pelo teste de McNemar (p= 0,179 e p= 0,655, respectivamente) / A study was performed comparing the polymerase chain reaction and the traditional panel of exams for the diagnosis in patients with a clinical suspicion of cutaneous tuberculosis and atypical mycobacteria infection to the clinical evaluation. It was observed that the sensitivity of the PCR was 88%, the specificity was 83%, the positive predictive value was 82%, the negative predictive value was 88% and the accuracy was 85% in agreement with the McNemar test (p=0.655). The panel exams of second highest accuracy, were the tuberculin test with an accuracy of 79% and the chronic granulomatous dermatitis with positive PCR, also with an accuracy of 79%, both in agreement with the McNemar test (p=0.179 and p=0.655, respectively)

L'objectif de cette thèse était d’évaluer quelques Metal-Organic Frameworks (MOFs), choisis en fonction de leur taille de pores, de leur volume poreux et de leur stabilité thermique, en adsorption et séparation des hydrocarbures. Pour étudier le comportement général des MOFs nous avons choisi des MOFs avec des centres métalliques insaturés, des MOFs à charpente anionique et des ZIFs neutres et avons étudié leur sélectivité en séparation de trois familles d'hydrocarbures, à savoir alcanes, alcènes, aromatiques. Les MOFs à centre métallique insaturé se comportent généralement comme des zéolithes polaires, les ZIFs comme des zéolithes apolaires et/ou comme des tamis moléculaires. Les adsorbants les plus prometteurs sont testés sur des séparations d’intérêt industriel telles que la séparation des isomères de xylène, la séparation des paraffines linéaires, monobranchées et di-branchées et l’adsorption sélective du thiophène en vu de l’évaluation de ces adsorbants en désulfuration des essences. / The aim of this thesis was to evaluate several Metal Organic Frameworks (MOFs), selected based on criteria of pore size, pore volume and thermal stability, in adsorption and separation of hydrocarbons. For studying the general behavior of MOFs in hydrocarbon adsorption, we have chosen MOFs with open metal sites, MOFs with anionic frameworks and neutral ZIFs. The MOFs with open metal sites behave similar to polar zeolites, the ZIFs behave like apolar zeolites and/or like molecular sieves. Finally we selected the most interesting MOFs and tested them in several separations with industrial interest: xylene isomers, paraffin isomers and selective adsorption of thiophene for the purpose of fuel desulfuration.

This research addresses and illuminates a little understood region of miscible polymer mixtures and demonstrates a new means of separating wax from such blends. The method, termed Deformation Induced Phase Segregation potentially eliminates need of toxic processing solvents for wax removal or recovery in these types of blends. Previous theories of polymer combinations address them exclusively as solutions or as blends, two independent classes having very different behaviors. This study provides bridge connecting these two classes by identifying crossover points between them and the behaviors exhibited therein. The blends of this form were found to be semi-miscible, forming a homogenous phase in the melt but a two-phase system in the solid, with the rheological behavior influenced by the polymer's molecular weight and architecture. It also demonstrates practical promise of this regime by introducing a mechanical compression process to separate the wax phase from such a type of blend. This process potentially permits production of ultra-high molecular weight polyethylene (UHMwPE) films and fibers by melt processing, thereby obviating need of otherwise essential but expensive and environmentally unfriendly toxic solvents.