Metal oxide-facilitated transformation is likely an important degradation pathway of antibacterial agents at soil-water interfaces. Phenolic disinfectants (triclosan and chlorophene), fluoroquinolones (FQs), and aromatic N-oxides are of particular concern due to their widespread usage, potential toxicity and frequent detection in the environment. Results of the present study show that the above antibacterial agents are highly susceptible to metal oxide-facilitated oxidation. The interfacial reactions exhibit complex reaction kinetics, which are affected by solution pH, the presence of co-solutes, surface properties of metal oxides, and structural characteristics of antibacterial agents. Adsorption of the antibacterial agents to Mn and Fe oxide surfaces generally proceeds faster than oxidation reactions of these compounds by Mn and Fe oxides, especially in the case of Fe oxides. Reaction intermediates and end products are identified by GC/MS, LC/MS and/or FTIR. Structurally-related model compounds are examined to facilitate reaction site and mechanism elucidation. On the basis of experimental results and literature, reaction schemes are proposed. In general, the antibacterial agent is adsorbed to the oxide surface, forming a precursor complex. Electrons are transferred within the precursor complex from the antibacterial agent to the oxide, followed by releasing of the radical intermediates which undergo further reactions to generate oxidation products. The precursor complex formation and electron transfer are likely rate-limiting. For triclosan, phenoxy radicals are critical intermediates to form oxidation products through three pathways (i.e., radical coupling, further oxidation of the radical, and breakdown of an ether bond within the radical). The first two pathways are also operative in the oxidation of chlorophene. For FQs, oxidation generates radical intermediates that are most likely centered on the inner N in the piperazine ring. The radical intermediates then undergo three major pathways (i.e., radical coupling, N-dealkylation, and hydroxylation) to yield a variety of products. For aromatic N-oxides, a N-oxide radical intermediate is generated upon oxidation by MnO2, followed by the loss of oxygen from the N-oxide moiety and the formation of a hydroxyl group at the C-atom adjacent to the N-oxide moiety. Overall, a fundamental understanding of the reaction mechanisms between three classes of antibacterial agents and metal oxides has been obtained.

The present research work focuses on the fabrication and characterization of epitaxial heterostructures of 0.7 Pb(Mg1/3N2/3)O3 – 0.3 PbTiO3 (PMN-PT) and La0.6Sr0.4MnO3 (LSMO) using multi target pulsed laser ablation technique. Different heterostructures such as bilayered thin films with different individual layer thickness; symmetric and asymmetric superlattices of different periodicities were fabricated. Roles of individual layer thickness, elastic strain and interfaces between PMN-PT and LSMO layers on different physical properties were studied. An attempt has been made to understand the influence of the charge depleted interface states in addition to the probable strain mediated elastic coupling effect on the observed magneto-dielectric response in these engineered heterostructures. Chapter 1 provides a brief introduction to the multiferroic materials, occurrence of magnetoelectric (ME) coupling in them, their possible technological applications and the challenges involved. A short historical account of the multiferroic research is discussed to emphasize the importance of artificial multiferroics, particularly the engineered thin film heterostructures. Finally the specific objectives of the current research are outlined. Chapter 2 deals with the various experimental studies carried out in this research work. It gives the details of the experimental set up and the basic operation principles of various structural and physical characterizations of the materials prepared. A brief explanation of material fabrication, structural, micro structural and physical property measurements is discussed. Chapter 3 addresses the phase formation, structural and microstructural features of the engineered heterostructures fabricated epitaxially on single crystalline LaAlO3 (100) substrates. A thin layer of LaNiO3 used as the bottom electrode material for electrical characterizations was grown on the bare substrate prior to the fabrication of the PMN-PT/LSMO heterostructures. The structural and microstructural features of different individual layers were also studied by fabricating single layer thin films of the materials. The effects of individual layer thicknesses on the surface roughness, grain size and lattice strain of the heterostructures are discussed. Chapter 4 deals with the ferroelectric studies of the PMN-PT/LSMO epitaxial heterostructures. Polarization hysteresis (P-E), capacitance – voltage (C-V) and pulsed polarization (PUND) measurements were carried out as functions of applied voltage, frequency and delay time to characterize the ferroelectric properties of the heterostructures. All the bilayered heterostructures exhibited robust ferroelectric response and contribution of non – remnant components to their polarization behaviour were observed from the P-E studies. The symmetric superlattices did not exhibit any ferroelectricity due to high leakage current conduction. After optimizing the LSMO and PMN-PT layer thicknesses ferroelectricity was observed in the asymmetric superlattices accompanied by substantial reduction in the leakage current conduction. The P-E loops were found to be asymmetrically shifted along the electric field axis in all the superlattices indicating the presence of dielectric passive layers and strong depolarizing fields at the interfaces between PMN-PT and LSMO. Chapter 5 deals with the ferromagnetic studies of the PMN-PT/LSMO heterostructures. All the heterostructures exhibited ferromagnetic behaviour in the temperature range of 10 K – 300 K with an in plane magnetic easy axis ([100]) compared to the out of plane ([001]) direction. The magnetization behaviour of the bilayers and superlattices as a function of magnetic field strength, temperature and different individual layer thickness of PMN-PT and LSMO are discussed in terms of the oxygen deficiency, magnetic dead layers and lattice strain effects in these engineered epitaxial heterostructures. Chapter 6 addresses the magneto-dielectric response, dielectric properties and ac conduction properties of the engineered biferroic heterostructures. In order to investigate the manifestation of strain mediated ME coupling in these heterostructures their dielectric response as a function of ac electric signal frequency have been studied under different static magnetic fields over a wide range of temperatures. The appearance of magneto-capacitance and its dependence on magnetic field strength and temperature along with the magnetoresistive characteristics of the heterostructures suggested that the charge depleted interfaces between PMN-PT and LSMO can have an effect on the observed dielectric response in addition to the probable strain mediated ME coupling. Dielectric characterization of the heterostructures performed over a wide range of temperature indicated a Maxwell-Wagner type relaxation mechanism. The manifestation of Maxwell-Wagner effect and the very low activation energy of ac conductivity obtained from the ac conduction studies revealed the strong influence of the charge depleted interfaces between PMN-PT and LSMO on the dielectric properties of the heterostructures. Chapter 7 deals with the dc leakage current conduction characteristics of the heterostructures. The leakage current characterization was performed over a wide range of temperature and analyzed in the framework of different models to investigate the leakage mechanism. All the heterostructures were found to obey the power law I∝Vα over the entire range of temperature with different values of α at different applied voltages. The bilayered heterostructures exhibited ohmic conduction in the lower electric field region and space charge limited conduction was observed at higher electric fields. On the other hand the low field dc conduction behaviour of the superlattices could not be attributed unambiguously to a single mechanism. Depending on the superlattice periodicity the low field conduction behaviour was dominated by either Poole-Frenkel (PF) emission or a combined contribution from the PF effect and ohmic conduction. At higher electric fields all the superlattices exhibited space charge limited conduction. Chapter 8 gives the summary and conclusions of the present study and also discusses about the future work that could give more insight into the understanding of the engineered epitaxial biferroic heterostructures.

The aim of this study is to form a theoretical model for simulation of glass forming ability of Fe &amp / #65533 / Based bulk amorphous alloys, to synthesize Fe &amp / #65533 / based multicomponent glassy alloys by using the predictions of the theoretical study, and to analyze the influence of crystallization and solidification kinetics on the microstructural features of this amorphous alloys. For this purpose, first, glass forming ability of Fe &amp / #65533 / (Mo, B, Cr, Nb, C) &amp / #65533 / X ( X = various alloying elements, selected from the periodic table) ternary alloy systems were simulated for twenty different alloy compositions by using the electronic theory of alloys in pseudopotential approximation and regular solution theory. Then, by using the results of the theoretical study, systematic casting experiments were performed by using centrifugal casting method. The alloying elements were melted with induction under argon atmosphere in alumina crucibles and casted into copper molds of different shapes. Characterization of the cast specimens were performed by using DSC, XRD, SEM, and optical microscopy. Comparison of equilibrium and nonequilibrium solidification structures of cast specimens were also performed so as to verify the existence of the amorphous phase. Good agreement of the results of experimental work, with the predictions of the theoretical study, and the related literature was obtained.

In der vorliegenden Arbeit wurde die Methode der magnetischen Kernspinresonanz (NMR) eingesetzt, um beim Schadstoffabbau stattfindende Prozesse und geochemische Reaktionen zerstörungs- und beprobungsfrei zu untersuchen. Dies ist möglich, da die gelösten Elektronenakzeptoren Sauerstoff und Eisen paramagnetisch sind und somit einen Ein uss auf die NMRRelaxationszeiten ausüben. Der lineare Zusammenhang zwischen der gelösten Sauerstoff- beziehungsweise Eisen-Konzentration und den NMR-Relaxationsraten 1/T1 und 1/T2 wurde quantifiziert. Weiterhin wurde der bereits bekannte Einfluss der Matrixoberflächen von porösen Medien auf die Relaxation von Wasser nachgewiesen. Die paramagnetischen Zentren auf Sandoberflächen führen ebenfalls zu einer Verkürzung der Relaxationszeiten. Es wurde gezeigt, dass die kleinsten Korngrößen der verwendeten Sande den größten Einfluss auf die Oberflächenrelaxation haben. Wird die Oberflächenrelaxation berücksichtigt, ist auch in porösen Medien die ermittelte lineare Abhängigkeit der Relaxationszeiten von der Ionenkonzentration anwendbar, um den Gehalt an gelösten paramagnetischen Ionen aus Relaxationsmessungen zu ermitteln. Beispielhaft wurde der Anstieg der Eisen(III)-Konzentration in der Porenlösung von natürlichen Sanden infolge der Auflösung eisenhaltiger Mineralien von den Oberflächen zeitlich und räumlich detailliert betrachtet. Eine durchgeführte Modellierung zeigte, dass das Reaktionssystem zu Beginn der Reaktion von der Diffusion dominiert wird, am Ende dann die Reaktionsgeschwindigkeit der bestimmende Parameter ist. Die beim biologischen Schadstoffabbau auftretenden Redoxprozesse des Eisens wurden durch rein chemische Reaktionen unter Verwendung von Oxidations- und Reduktionsmitteln simuliert. Die zeitlich und räumlich detaillierte Beobachtung des Anstiegs beziehungsweise des Abfalls der gelösten Eisen(III)-Konzentration in der (Poren-)Lösung war mit NMR-Relaxometrie trotz der Schnelligkeit der Reaktionen möglich. Mit Hilfe der anschliessenden Modellierung wurde der wichtige Einfluss des pH-Wertes auf den genauen Ablauf der Reaktionen deutlich gemacht. Nur in sehr sauren pH-Bereichen (pH < 3) liegen die Eisen(III)-Ionen in Lösung vor. Weiterhin wurde der Einfluss der Mikroorganismen selbst auf die NMR-Relaxations- und Diffusionsmessungen untersucht. Im Rahmen dieser Arbeit wurde an Medien mit Lactobacillus und Penicillium eine Verschiebungen in den Relaxationszeitverteilungen hin zu kleineren Relaxationszeiten gemessen. Dies basiert auf der bereits bekannten Verringerung der Mobilität der Spins innerhalb der Biomasse. Für Bakterien von Geobacter metallireducens konnte erstmals der Verbrauch von Eisen(III)-Ionen durch Reduktion während des Wachstum anhand der ansteigenden T2-Relaxationszeit gezeigt werden.

CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico / FAPEMIG - Fundação de Amparo a Pesquisa do Estado de Minas Gerais / Muitos microorganismos desenvolveram a habilidade de adquirir ferro a partir do seu hospedeiro para seu próprio metabolismo. Toxoplasma gondii, um parasito intracelular obrigatório, produz proteinas de roptrias que são capazes de ligar ao transportador de ferro. Além disso, quelante de ferro foi capaz de controlar o parasitismo em células intestinais de rato. Logo, este trabalho teve como objetivo investigar a relação do efeito da adição ou privação de ferro na multiplicação de T. gondii e resultado da infecção quando o parasito é administrado por via oral e em cultura celular. Camundongos C57BL/6 foram infectados oralmente com T. gondii e tratados com um quelante de ferro, deferoxamina ou suplementados com ferro e o parasitismo, parâmetros imunológicos e histológicos foram analisados. Observou-se que a infecção aumentou a deposição de ferro no intestino delgado, pulmão e fígado e também sistematicamente. O tratamento com deferoxamina foi capaz de diminuir os níveis de ferro nas amostras de soro. O tratamento com deferoxamina diminuiu a carga parasitária no intestino delgado e alterações inflamatórias no órgão, preservando seu comprimento e também diminuiu o parasitismo pulmonar. Além disso, a suplementação com ferro aumentou a carga parasitária no intestino delgado, pulmão e fígado, associado com alterações inflamatórias nesses órgãos, bem como houve aumento da proliferação parasitária em cultivo celular com células Caco-2. A infecção oral modulou o perfil de expressão de marcadores de absorção de ferro, aumentando os níveis de IL-6 sistêmicos. Juntos, nossos resultados sugerem que a quelação de ferro comumente usada para tratar a sobrecarga de ferro pode ser um medicamento promissor para controlar a proliferação de T. gondii e consequentemente a inflamação causada por infecção e que o ferro é um nutriente essencial para o metabolismo de T. gondii. / Many microorganisms have developed the ability to acquire iron from their host to their own metabolism. Toxoplasma gondii, an obligate intracellular parasite, produces rhoptry proteins that are capable of binding to the iron transporter. In addition, iron chelator was able to control parasitism in rat intestinal cells. Therefore, the objective of this work was to investigate the relationship of the effect of iron addition or deprivation on the multiplication of T. gondii and the result of infection when the parasite is administered orally and in cell culture. C57BL/6 mice were orally infected with T. gondii and treated with an iron chelator, deferoxamine or iron supplemented and parasitism, immunological and histological parameters were analyzed. It was observed that the infection increased the deposition of iron in the small intestine, lung and liver and also systematically. Treatment with deferoxamine was able to decrease iron levels in the serum samples. Treatment with deferoxamine reduced parasite burden in the small intestine and inflammatory changes in the organ, preserving its length and also decreased pulmonary parasitism. In addition, iron supplementation increased parasite burden in the small intestine, lung and liver, associated with inflammatory changes in these organs, as well as increased parasite proliferation in cell culture with Caco-2 cells. Oral infection modulated the expression profile of iron absorption markers, increasing systemic IL-6 levels. Together, our results suggest that iron chelation commonly used to treat iron overload may be a promising drug to control T. gondii proliferation and consequently inflammation caused by infection and that iron is an essential nutrient for the metabolism of T. gondii. / Tese (Doutorado)

A falta de consenso na literatura acerca dos efeitos tóxicos do chumbo no sistema auditivo é notória, tanto em estudos clínicos quanto experimentais. Em adição, tem sido relatado que o ferro apresenta um efeito protetor na toxicidade cerebral causada pelo chumbo. Assim, estudos clínicos e bioquímicos têm sido realizados no intuito de compreender a relação entre o chumbo e o sistema auditivo, bem como identificar possíveis substâncias protetoras para a toxicidade deste metal. Neste sentido, no presente estudo verificou-se o processo maturacional do nervo auditivo e tronco encefálico, associado à análise proteômica da porção auditiva do tronco encefálico de ratos expostos a acetato de chumbo e suplementados com sulfato ferroso. O experimento foi realizado por seis semanas com 30 ratos (Rattus norvergicus, variedade Wistar) machos, recém-desmamados, divididos em seis grupos de cinco animais cada, sendo um controle, que recebeu água deionizada; dois grupos experimentais que receberam 100 mg/L de Pb(CH3COO)2 na água de beber, sendo administrado simultaneamente para um deles 20 mg/kg de FeSO4 a cada dois dias; dois grupos que receberam a dose de 400 mg/L de Pb (CH3COO)2 na água de beber, onde para um deles foi administrado simultaneamente 20 mg/kg de FeSO4 a cada dois dias e um grupo experimental que recebeu água deionizada e uma solução de 20 mg/kg de FeSO4 a cada dois dias. O processo maturacional do sistema auditivo foi verificado por meio da análise do Potencial Evocado Auditivo de Tronco Encefálico (PEATE) em dois momentos distintos, antes e depois da exposição ao chumbo. Os animais foram então sacrificados, coletado sangue e removido o tronco encefálico. A concentração de chumbo no sangue e tronco encefálico, apresentou um efeito dose-resposta, confirmado pela alta correlação entre a concentração nos dois compartimentos (r2=0,905, p<0,0001), tendo o sulfato ferroso reduzido a concentração de chumbo no sangue e no tecido, embora a diferença só tenha sido significativa para o sangue grupo que recebeu 100 mg/L de Pb(CH3COO)2). Com relação ao PEATE observou-se diferença estatisticamente significativa para o interpico I-II (p=0,049) nos grupos experimentais 100 mg/L Pb(CH3COO)2 e 400 mg/L Pb(CH3COO)2 e interpico I-IV, quando comparados os grupos 100 mg/L Pb(CH3COO)2 e 100 mg/L Pb(CH3COO)2 + FeSO4 (p=0,033). A análise proteômica apontou uma diminuição considerável no número de spots proteicos detectados em todos os grupos experimentais em relação ao controle, bem como uma redução na expressão do padrão proteico. Assim, o presente estudo reforça a hipótese do papel deletério do chumbo nas dosagens de 100 e 400 mg/L de Pb (CH3COO)2 na maturação do nervo auditivo e região do núcleo coclear, com possível efeito protetor do ferro. A análise proteômica do tronco encefálico de ratos demonstrou que o acetato de chumbo altera a expressão proteica desta estrutura, contudo o efeito protetor do sulfato ferroso não foi confirmado nas proteínas identificadas. / There is a lack of consensus in the literature about the toxic effects of lead in the auditory system, both in clinical and experimental studies. In addition to that, it has been reported that iron has a protective effect on brain toxicity caused by lead. Therefore, clinical and biochemical studies have been carried out to understand the relationship between Pb and the auditory function, as well as if the ferreous sulfate as an otoprotectant. In this study the maturational process of the auditory nerve and brainstem and the proteomic profile of the auditory portion of the brainstem of rats exposed to lead and supplemented with iron were evaluated. The experiment was carried out for six weeks with 30 wealing rats (Rattus norvegicus, Wistar), divided into six groups of five animals each: a control group that received deionized water; two experimental groups receiving 100 mg/L Pb(CH3COO)2 in drinking water, being given 20 mg/kg FeSO4 simultaneously to one of them every two days; two groups received 400 mg/LPb(CH3COO)2 in drinking water, where to one of them was given 20 mg/kg FeSO4 simultaneously every two days; and an experimental group that received deionized water and a solution of 20 mg/kg FeSO4 every two days. The maturational process of the auditory system was verified by analyzing the Brainstem Auditory-Evoked Potential (BAEP) at two different times, before and after lead exposure. The animals were sacrificed, their blood collected and brainstem removed. The concentration of lead in blood and brain stem showed a dose-response, confirmed by correlation between the concentration in the two compartments (rr2 = 0.905, p <0.0001). Ferreous sulfate reduced the levels of lead in blood and tissue, although the difference was only significant for blood (group receiving 100 mg/L Pb(CH3COO)2). Concerning to BEAP we observed a statistically significant difference for the interpeak I-II (p = 0.049) in the experimental groups 100 and 400 mg/L Pb(CH3COO)2 and for the interpeak I-IV, when groups 100 and 100 mg/L Pb(CH3COO)2 + FeSO4 were compared (p = 0.033). The proteomic analysis showed a considerable decrease in the number of protein spots detected in all experimental groups compared to control, as well as a reduction in the expression pattern of the proteins. Thus, the present study reinforces the hypothesis of deleterious role of Pb in dosages of 100 and 400 mg/L Pb(CH3COO)2 in the maturation of the auditory nerve and cochlear nucleus region, with a possible protective effect of ferreous sulfate. The proteomic analysis of the brainstem of rats showed that lead acetate alters protein expression of this structure. However, the protective effect of ferreous sulfate was not confirmed for the identified proteins.

O aço especial UNS S31254 (aço 254), um aço inoxidável austenítico contendo 20,1% de cromo, 18,4% de níquel e 6,42% de molibdênio foi estudado com o objetivo de ser aplicado em técnicas eletroanalíticas, tais como a potenciometria, a condutimetria e como eletrodo indicador em medidas de pH. Os estudos eletroanalíticos foram precedidos de curvas de polarização potenciostáticas e potenciodinâmicas e de ensaios não eletroquímicos (FTICR, MEV e XPS), em que se caracterizou a presença do filme passivante. Grande parte dos estudos incluíram, para efeito de comparação, os aços UNS S 31603 (aço 316 L) e UNS S31678 (aço F 138), o primeiro de largo emprego comercial e o último, aplicável em implantes ortopédicos. Os estudos, realizados a 25° C, se iniciaram com a caracterização eletroquímica dos referidos materiais imersos em meios aquosos de ácidos clorídrico, acético, nítrico, sulfúrico e galacturônico, e dos sais cloreto de sódio, sulfato de sódio e nitrato de sódio, variando-se a concentração do eletrólito. O aço 254 se mostrou passivado, na grande maioria dos meios estudados, em toda a faixa de potenciais que se estende do potencial de corrosão (Ecorr, potencial de circuito aberto estacionário) até o potencial de transpassivação (onde ocorre o rompimento do filme e, na maioria dos meios, a oxidação generalizada da superfície e a reação H2O/O2). Em meio de ácido acético a faixa de potencial em que o referido aço se mantém passivado é a mais ampla, indicando que o rompimento do filme passivo exige maior energia, em virtude do maior teor de molibdênio superficial detectado por MEV. A corrosão por pite foi observada em meios de HCI e de NaCI a potenciais mais positivos do que o de transpassivação. A caracterização da superfície por MEV mostrou que as inclusões presentes no aço são constituídas basicamente de óxidos de alumínio e de cálcio. A análise por XPS da superfície do aço 254 apenas polido e exposto ao ar revelou a presença de Mo (VI) na superfície; em meio de NaCI 0,15 mol L-1 há o enriquecimento gradual de Mo (VI) quando se varia o potencial desde o Ecorr, passando por um potencial passivo e se estendendo a um potencial 50 mV acima do potencial de transpassivação. O aço 254 pode ser empregado em substituição à platina em todas as determinações eletroanalíticas realizadas neste trabalho, envolvendo titulações potenciométricas, medidas condutimétricas e determinação de pH. Em medidas de pH em sistemas com força iônica mais baixa, entretanto, é necessário um controle mais adequado do tratamento superficial, além dos realizados neste trabalho, para que a resposta do petencial seja mais rápida. Estes estudos podem contribuir para baixar o custo de análises industriais e de experimentos que venham a ser realizados em laboratórios diáticos. / Special UNS S31254 stainless steel (254 SS), an austenitic stainless steel with 20.1% Cr, 18.4% Ni and 6.42% Mo has been studied in order to be applied in electroanalytical techniques as potentiometry, conductimetry and as a sensor in pH measurements. The electroanalytical studies were preceded of potentiostatic and potentiodynamic polarization curves. The surface characterization was made using FTCIR, SEM and XPS as techniques. The studies have included, for comparison, UNS S 31603 (316 L SS) and UNS S31678 (F 138 SS); the former is commercially employed in a large extension and the latter is applicable in orthopedic implants. The experiments were made at 25° C, beginning with the electrochemical characterization of the ferrous materiais in different aqueous media: chloridric, acetic, sulfuric, nitric and D-galacturonic acids and saline solutions of sodium chloride, sodium sulfate and sodium nitrate, changing the electrolyte concentration. SS 254 is passivated in most of the studied media, on the entire potential range analyzed (from corrosion potential to transpassivation potential). In acetic media it was observed the largest potential range where 254 SS is passivated, indicating that a higher energy is necessary to disrupt the passivant film, due to a higher Mo concentration at the surface, detected using SEM. Pitting corrosion was observed in HCl and NaCl media at potential more positive than Etr. SEM surface characterizations have shown aluminium oxide and calcium oxide inclusions. XPS analyses have indicated the presence of Mo (VI) on the polished surface and that there is a gradual Mo (VI) increasing, in solution, when the potential changes from Ecorr to E > Etr. 254 SS can be used in potentiometric and conductimetric titrations and as a sensor electrode for pH measurements. However, in biological applications a more adequate surface treatment is needed in order to obtain rapid responses. Overall the results suggest that 254 can be used as substitute of platinum in different electroanalytical techniques. This finding contributes to lower the cost of experiments to be performed in didactic laboratories and/or industrial analyses.

A liga de alumínio designada AA4006 é muito utilizada na indústria. É uma liga do sistema Al-Fe-Si, com teores (% em massa) de Si na faixa de 0,8 a 1,2% e Fe entre 0,5 e 0,8%. Apesar de ser bastante utilizada, ela foi pouco estudada. Neste trabalho foi realizado um estudo comparativo da microestrutura e da textura cristalográfica entre chapas da liga AA4006 produzidas por dois processos industriais de lingotamento: contínuo (Twin roll caster TRC) e semicontínuo (Direct chill DC). Para a caracterização microestrutural, foram utilizadas as técnicas de microscopia óptica com luz polarizada, microscopia eletrônica de varredura com microanálise química, medidas de condutividade elétrica e ensaios de dureza Brinell. A textura cristalográfica foi determinada por difração de raios X. Foram detectadas e discutidas diferenças significativas nas morfologias e distribuições de grãos e de partículas de fases intermetálicas. O estudo da textura cristalográfica foi realizado ao longo da espessura das tiras e os resultados mostraram variações significativas da textura entre as chapas ao longo da espessura. A chapa produzida por lingotamento contínuo apresentou uma típica textura de cisalhamento nas proximidades de sua superfície, enquanto nas regiões mais internas a fibra foi observada. O estudo da recristalização de chapas metálicas laminadas a frio é muito útil para a obtenção da temperatura de amolecimento do material submetido a um tratamento térmico. Tratamentos térmicos isócronos no intervalo de uma hora foram feitos em amostras das duas chapas e a chapa produzida pelo processo TRC apresentou a temperatura para 50% de recristalização em torno de 290 ºC e a amostra da chapa produzida pelo processo DC em torno de 270 ºC. A textura cristalográfica pode mudar com a recristalização e com a laminação do metal. Utilizando estas etapas de processamento do material, a orientação dos grãos de uma tira metálica pode ser otimizada, a fim de, por exemplo, melhorar a estampabilidade de chapas na obtenção de um dado produto com valor agregado. Neste trabalho as curvas de amolecimento para duas chapas produzidas por lingotamento contínuo e lingotamento semicontínuo da liga de alumínio AA4006 também foram determinadas e comparadas. Embora as diferenças detectadas entre as curvas de amolecimento tenham sido pequenas, foi possível verificar que a recristalização da chapa produzida por twin roll caster TRC ocorre em temperaturas mais elevadas do que na chapa produzida pelo processo direct chill DC. Resultados da textura cristalográfica em amostras destas chapas (laminadas e recozidas) foram obtidos utilizando difração de raios X e difração de elétrons retroespalhados EBSD. Estes resultados indicaram a presença da textura de cisalhamento na superfície e a fibra no centro da amostra laminada a frio (70% de redução) da chapa obtida por lingotamento contínuo. Na amostra da chapa obtida por lingotamento semicontínuo, a componente cubo e a fibra foram vistas na superfície e no centro. Uma textura fraca com grãos orientados ao acaso foi vista nas duas amostras (TRC e DC) recristalizadas das duas chapas, possivelmente, devido à nucleação estimulada por partículas. A fibra desapareceu nas amostras (TRC e DC) recristalizadas. / AA4006 Aluminum alloy is extensively used in industry. It belongs to the Al-Fe-Si system, with Si between 0,8 and 1,2 % mass, and Fe between 0,5 and 0,8 % mass. This alloy is less studied despite its extensive use. A comparative microstructural study has been performed in as-received AA4006 alloy strip produced by two industrial casting processes: twin roll caster (TRC) and direct chill (DC). Polarized optical microscopy, scanning electron microscopy with microanalysis, electrical conductivity measurements and Brinnel hardness tests have been used for microstructural characterization. Significant differences in the grain and intermetallic particle sizes, morphologies and distributions were detected and are discussed. Thermal treatments effects on the silicon content in solid solution were also studied. Crystallographic textures have been also determined. Textures across thickness of both sheets have been analyzed and compared. Results showed significant texture changes across thickness of the specimens. Texture analysis was carried out using X-ray diffraction technique. Twin roll caster (TRC) sheet presented the typical shear texture near the surface, while, in internal regions, the -fibre was observed. A recrystallization study of cold rolled metallic sheets is very important to obtain softening temperature for the material during annealing. After cold rolling with 70% of reduction in thickness, followed by isochronous heat treatments, the samples of the two sheets produced by TRC and DC presented a 50% recrystallization temperature around 290 ºC and 270 ºC, respectively. Crystallographic texture can change during the metal rolling and recrystallization. These processing steps can optimize the grain orientation distribution in a metal strip to improve, for instance, the stamping process, in order to obtain an aggregated value product. Softening curves were also compared and determined for the two sheets (rolled and annealed) of the AA4006 aluminum alloy produced by twin roll caster TRC and direct chill DC processes. It was detected that the recrystallization of the strip produced by TRC process occurs at a higher temperature than that for the DC process, despite the little differences in their softening curves. Crystallographic texture results, for the sheet samples, were obtained by using X-ray diffraction and electron back scatter diffraction EBSD techniques. These results indicated the shear texture presence on the surface and fiber at the center of the cold rolled (70% area reduction) sample for the sheet produced by TRC process. In the sheet sample produced by the DC process, under the same conditions, the cube component and fiber texture (at the surface and at the center) were observed. A texture with random oriented grains was detected in two deformed and recrystallized samples of the two sheets (TRC and DC). It is suggested that this texture occurs due to the particle stimulated nucleation. There was fiber absence in the recrystallized samples (TRC and DC).

La dénitrification autotrophe utilisant le fer Ferreux est un bioprocédé innovant pour l'élimination des nitrates, en même temps que l'oxydation du fer dans les eaux usées. Les dénitrifiants chimio-autotrophes convertissent le nitrate en azote gazeux et l'oxydation du Fe(II) conduit à la production de précipités de fer ferrique qui peuvent ensuite être enlevés et récupérés. La possibilité de maintenir une dénitrification autotrophe avec le fer ferreux en utilisant une culture mixte de Thiobacillus, un inoculum de boue activée et des cultures pures de la souche Pseudogulbenkiania 2002 et de T. denitrificans dans différentes conditions de pH et d'EDTA:Fe(II) a été initialement étudiée dans des essais biologiques par lots. Des ratios plus faibles d’EDTA:Fe(II) se traduisent par une efficacité et des taux d'élimination des nitrates plus élevés. La culture mixte de Thiobacillus présente le taux d'élimination de nitrate le plus élevé, égal à 1.18 mM•(g VSS•d)-1.Par la suite, la culture mixte de Thiobacillus a été ensemencée dans deux réacteurs à lit tassé à flux montant identiques. Les deux réacteurs (réacteur 1 et 2) ont reçu respectivement 120 et 60 mg / L de nitrate et une alimentation différente de Fe (II) afin de respecter un rapport molaire Fe(II):NO3- de 5:1. L’EDTA a été supplémenté à un rapport molaire EDTA:Fe(II) de 0,5:1. Le pH, le TRH et la température étaient de 6,5-7,0, 31 h et 22 ± 2 ° C. Dans le réacteur 1, le TRH a été raccourci de 31 à 24 h et la concentration de NO3- a été maintenue stable à 250 mg / L. Inversement, le réacteur 2 a été mis en fonctionnement avec un TRH décroissant et une concentration de NO3- en alimentation, maintenant ainsi un taux de charge de NO3- stable. Après environ 80 jours d'incubation, l'élimination des nitrates était de 88% dans le réacteur 1 pour un THR de 31 h. L'élimination de nitrates la plus élevée obtenue dans le réacteur 2 était de 80%. Une diminution du TRH de 31 à 24 h n'a pas affecté l'élimination du nitrate dans le réacteur 1, alors que dans le réacteur 2 l'élimination du nitrate a diminué à 64%.De plus, l'influence des métaux lourds (Ni, Cu, Zn) sur la dénitrification autotrophe utilisant du fer ferreux a été évaluée dans des essais biologiques discontinus, en utilisant les mêmes quatre cultures microbiennes différentes. L'efficacité et les taux d'élimination des nitrates les plus élevés ont été obtenus avec la culture mixte dominante de Thiobacillus, alors que la souche Pseudogulbenkiania de 2002 était la moins efficace. Cu s'est avéré être le métal le plus inhibiteur pour les cultures mixtes. Un impact plus faible a été observé lorsque le Zn a été ajouté. Le Ni présentait l'effet inhibiteur le plus faible. Une sensibilité plus élevée à la toxicité des métaux a été observée pour les cultures pures. Enfin, la caractérisation minérale des précipités obtenus pour les expériences avec du Cu, Ni et Zn a été étudiée. Chez les témoins abiotiques, l'oxydation chimique du Fe (II) a entraîné la formation d'hématite. Un mélange de différents (hydro)oxides de Fe(III) a été observé pour toutes les cultures microbiennes, et en particulier : i) un mélange d'hématite, d'akaganéite et / ou de ferrihydrite a été observé dans les précipités des expériences réalisées avec la culture mixte dominée par la présence de Thiobacillus; ii) en plus d'hématite, de l'akaganeite et / ou de la ferrihydrite, la maghémite a été identifiée lorsque la culture pure de T. denitrificans a été utilisée; iii) l'utilisation de la culture pure de la souche Pseudogulbenkiania 2002 a entraîné la formation d'hématite et de maghémite; enfin, l'enrichissement en boues activées a permis la production d'hématite et de magnétite en plus de la maghémite. Aucune différence concernant la minéralogie des précipités n'a été observée avec l'addition de Cu, alors que l'addition de Ni et de Zn a probablement stimulé la formation de maghémite. Une caractérisation minérale supplémentaire est cependant nécessaire / Ferrous iron mediated autotrophic denitrification is an innovative bioprocess for nitrate removal, simultaneously with iron oxidation in wastewaters. Chemoautotrophic denitrifiers convert nitrate to nitrogen gas and Fe(II) oxidation results in the production of ferric iron precipitates that can be subsequently removed and recovered. The feasibility of maintaining Fe(II)-mediated autotrophic denitrification with a Thiobacillus mixed culture, an activated sludge inoculum and pure cultures of Pseudogulbenkiania strain 2002 and T. denitrificans under different pH and EDTA:Fe(II) conditions was initially investigated in batch bioassays. Lower EDTA: Fe(II) ratios resulted in higher nitrate removal efficiency and rates. The Thiobacillus mixed culture resulted in the highest specific nitrate removal rate, equal to 1.18 mM•(g VSS•d)-1.Subsequently, the Thiobacillus mixed culture was seeded in two identical up-flow packed bed reactors. The two reactors (reactor 1 and 2) were fed with 120 and 60 mg/L of nitrate, respectively, and a different Fe(II) feed in order to respect a molar ratio Fe(II):NO3- 5:1. EDTA was supplemented at a EDTA:Fe(II) molar ratio 0.5:1. The pH, HRT and temperature were 6.5-7.0, 31 h and 22±2°C. In reactor 1, HRT was shortened from 31 to 24 h and NO3- concentration was maintained stable at 250 mg/L. Conversely, reactor 2 was operated with decreasing HRT and feed NO3- concentration, thus maintaining a stable NO3- loading rate. After approximately 80 d of incubation, nitrate removal was 88% in reactor 1 at HRT of 31 h. The highest nitrate removal achieved in reactor 2 was 80%. A HRT decrease from 31 to 24 h did not affect nitrate removal in reactor 1, whereas nitrate removal decreased to 64% in reactor 2.Moreover, the influence of heavy metals (Ni, Cu, Zn) on Fe(II)-mediated autotrophic denitrification was assessed in batch bioassays. The highest nitrate removal efficiency and rates were achieved with the Thiobacillus-dominated mixed culture, whereas Pseudogulbenkiania strain 2002 was the least effective. Cu showed to be the most inhibitory metal for mixed cultures. A lower impact was observed when Zn was supplemented. Ni showed the lowest inhibitory effect. A higher sensitivity to metal toxicity was observed for the pure cultures. Finally, the mineral characterization of the precipitates obtained in the experiments with Cu, Ni and Zn was investigated. In abiotic controls, the chemical Fe(II) oxidation resulted in hematite formation. A mixture of different Fe(III) (hydr)oxides was observed with all microbial cultures, and in particular: i) a mixture of hematite, akaganeite and/or ferrihydrite was observed in the precipitates of the experiments carried out with the Thiobacillus-dominated mixed culture; ii) on top of hematite, akaganeite and/or ferrihydrite, maghemite was identified when the T.denitrificans pure culture was used; iii) the use of the pure culture of Pseudogulbenkiania strain 2002 resulted in hematite and maghemite formation; finally, the activated sludge enrichment allowed the production of hematite and magnetite besides maghemite. No difference in the mineralogy of the precipitates was observed with the addition of Cu, whereas the addition of Ni and Zn likely stimulated the formation of maghemite. Further mineral characterization is however required

Le fer ajouté dans des systèmes complexes tels que les aliments induit divers problèmes comme l'oxydation des lipides ou la précipitation d’autres composés présents dans la matrice. Il s’en suit une diminution de sa biodisponibilité et des défauts de goût. L'utilisation de chélates de fer, comme le bisglycinate de fer ou l’EDTA de fer, constitue une voie intéressante : le fer ainsi protégé n’interagirait pas avec la matrice alimentaire. La stabilité des chélates de fer (bisglycinate de fer et NaFe EDTA), supposés peu réactif pour l’initiation de peroxydation, a été attestée sur des modèles d’émulsions huile dans eau stabilisées par du caséinate de sodium ou de la β lactoglobuline. Dans un second temps, le travail a consisté à vérifier la faible influence de ces complexes sur la nature de l’interface huile/eau (étude de la tension et de la rhéologie interfaciales). La stabilité du bisglycinate de fer en solution aqueuse et en présence de β lactoglobuline a également été évaluée en fonction du pH (pH 2, 3,5 et 6,5) par rayons X. Il a ainsi été montré que la nature des protéines formant l’interface huile/eau et le type de sels de fer jouent un rôle crucial sur la stabilité oxydative des émulsions enrichies en fer. L'affinité des protéines de lait pour les ions fer libres est le premier facteur qui contrôle la peroxydation des matières grasses par l’absence de transfert à l'interface huile/eau. La capacité du complexe bisglycinate à retenir les ions fer et donc à limiter la présence d’ions fer libres (ferriques ou ferreux) apparaît comme le second facteur principal à contrôler. La compétition pour les ions fer entre les groupes fonctionnels des protéines et les contre ions de chélates (glycinate ou EDTA) gouverne ainsi l'état d'oxydation du système dans des conditions acide/base proche de la neutralité. En milieu acide, l'oxydation est principalement gouvernée par l’instabilité du complexe bisglycinate de fer et par conséquent la lente libération fer ionique dans la phase aqueuse. Pour résumer, si le complexe de fer n’est pas déstabilisé et que la protéine à l’interface huile/eau ne présente pas de groupe fonctionnel ayant une forte affinité pour le fer, alors la peroxydation des lipides en émulsion est faible. Dans notre démonstration, si une protéine n’est pas phosphorylée et pour des pH proches de 7, alors l’émulsion ne sera pas peroxydée car le fer ne migre pas à l’interface huile/eau. / Iron incorporated into food systems induces oxidation and precipitation. The consequences are a reduced bioavailability and a modification of other food flavor. The iron chelates such as Fe-bisglycinate and Fe-EDTA represent a possibility to avoid side effects, since the iron is protected. The inertety of Fe bisglycinate and NaFe EDTA for lipid peroxidation has been verified in oil-in-water emulsion models stabilized by sodium caseinate or by β lactoglobulin through the following studies: i/ increase of primary and secondary products of oxidation, ii/ change of the properties of the oil/water interface (tension and interfacial rheology), iii/ the stability of the chelate iron (Fe-bisglycinate) in the aqueous phase with β lactoglobulin at different pH (pH 2, 3.5 and 6.5). The oil/water interface stabilized by proteins with phosphate groups has induced peroxidation, which was not observed with proteins containing no phosphate residue. These results demonstrate also that the type of iron salts plays a crucial role in the oxidative stability of emulsions. The ability of the complex to retain iron ion and to avoid “free” ferrous ion is the first important factor to be controlled. The affinity of milk proteins to bind these free iron ions is the second factor that controls the transfer to oil/water interface. To sum up, the competition for iron ions between functional groups of protein and salt counter ions (glycinate, sulfate or EDTA) governs the oxidation state of the system in neutral conditions. In acidic medium, the oxidation is mainly governed by the stability of the complex and the possibility to free iron in bulk.