Niobium oxides and niobates physical properties

Niobium oxides have been pointed as an alternative to tantalum in the production of solid electrolytic capacitors, with advantages regarding the dielectric constant, density and price. In this work, it is intended to create a new family of niobium oxides based capacitors, adapting the technology and production line currently used with tantalum. Despite the known potentialities of niobium oxides, and many types of niobates, in several technological applications, the understanding of these oxide systems is still noticeably insufficient. Hence, a careful bibliographic review is shown, which evidences the complexity of these materials, the difficulty in identifying of their different phases and polymorphs, as well as in the interpretation of their properties. In this context, several fundamental studies on niobium oxides are presented, namely structural, microstructural, optical and electrical characterizations, which allow not only to contribute in an important way for the general knowledge of the physical properties of these materials, but also to advance to a sustained development of the niobium oxides based solid electrolytic capacitors. Several processing parameters were studied, clearing the way towards the creation of a prototype. It was also decided to perform a preliminary study on the synthesis and characterization of other oxide systems based in niobium, namely rare-earth orthoniobates (RENbO4), which interest has been related to their optical properties and protonic conductivity. Hence, single and polycrystalline samples of RENbO4 were synthesized and characterized structural, optical and electrically, leaving open an interesting future work.

Genesis of the brecciated rocks from mid atlantic ridge hydrothermal systems : Lucky Strike (37º50’N) and Menez Gwen (37º50’N)

Tese de doutoramento, Geologia (Metalogenia), Universidade de Lisboa, Faculdade de Ciências, 2014

Contributo da geoquímica e da sedimentologia na caracterização de influências antropogénicas em ambientes estuarinos

Tese de doutoramento, Geologia (Geoquímica), Universidade de Lisboa, Faculdade de Ciências, 2016

Projeto e seleção de materiais magnéticos permanentes

Os materiais magnéticos permanentes têm sido utilizados em dispositivos eletromagnéticos há mais de 100 anos mas, devido aos progressos recentes das suas características magnéticas e a disponibilidade a custos acessíveis, a sua aplicação é atualmente transversal a uma vasta gama de áreas tecnológicas. A introdução dos ímanes de terras raras nos finais da década de 60 do século passado revolucionou a engenharia de projeto, conduzindo a uma reconfiguração dos dispositivos com fatores de escala anteriormente impraticáveis, elevando ainda o rendimento daqueles, ao eliminar as perdas associadas à criação de campos magnéticos baseados em densidades de correntes. Este trabalho descreve as principais classes dos materiais magnéticos permanentes com relevância comercial e fornece as linhas gerais do projeto magnético, com especial relevo para os materiais baseados em terras raras.

Efeitos de ordenamento chiral em supercondutores e sistemas magnéticos desordenados

Este trabalho apresenta uma investigação experimental sobre as propriedades magnéticas e de transporte elétrico de sistemas caracterizados por desordem e frustração. Tais sistemas são amostras granulares do supercondutor de alta temperatura crítica YBa2Cu3O7-δ e amostras do tipo vidro-de-spin e reentrantes das ligas magnéticas diluídas AuMn 8at% e AuFe xat% (x = 8, 12, 15, 18 e 21). No supercondutor granular foram estudados os efeitos de flutuações termodinâmicas na magnetocondutividade nas proximidades da transição supercondutora e a linha de irreversibilidades magnéticas. A transição para o estado de resistência nula é um processo que ocorre em duas etapas. Inicialmente, a transição de pareamento estabiliza a supercondutividade no interior dos grãos. A transição de coerência ocorre em temperaturas inferiores e ativa ligações fracas entre os grãos através de um processo do tipo percolação. O regime que antecede a transição de coerência é caracterizado por flutuações na fase do parâmetro de ordem. A linha de irreversibilidades magnéticas, estudada a partir da magnetoresistência e magnetização DC, revela um comportamento do tipo Almeida-Thouless em baixos campos magnéticos aplicados, seguido de um crossover, em µ0H = 0.1 T, para um comportamento do tipo Gabay-Toulouse. A linha de irreversibilidades é interpretada como sendo uma manifestação experimental de uma transição de vidro chiral. As ligas magnéticas diluídas foram estudadas através do efeito Hall extraordinário. Os resultados mostram claramente que dois termos de sinais contrários contribuem para este efeito nestes sistemas. Em particular, é observada uma anomalia no coeficiente de Hall extraordinário em temperaturas próximas à temperatura de ordenamento dos vidros-de-spin e de “canting” dos reentrantes que não é prevista por nenhuma teoria convencional de efeito Hall. A interpretação dos resultados é feita em termos do modelo de vidro chiral, mostrando a importância de uma contribuição de origem puramente chiral. Esta é a primeira vez que a chiralidade, uma propriedade intrínseca de sistemas desordenados e frustrados, é observada experimentalmente de modo direto.

Geologia e geoquimica do complexo cambaizinho, sao gabriel - RS

Mapeamentos geológicos feitos pelo autor na região do Arroio Cambaizinho - são Gabriel/RS, resultaram na definição do Complexo Cambaizinho, representado pelas seqüências meta-sedimentar e máfica-ultramáfica, intimamente associadas ao longo de toda a extensão da associação supracrustal. A seqüência meta-se dimentar é constitu1da por gnaisses quartzo-feldspáticos dominan tes, anfibolitos bandados e quartzitos subordinados, derivados de sedimentos areno-pelítico-carbonatados estruturados, de forma ritmica em ambiente subaquoso. Niveis composicionais de ocorrência restrita contendo estaurolita, definem o grau metamórfico (médio) para esta região. Intercalações de serpentinitos, xistos magnesianos variados e anfibolitos a granulação fina, na forma de camadas e/ou lentes interestratificadas nos meta-sedimentos indicam suas derivações a partir de derrames e/ou intrusões , ígneas de pequena profundidade de composição básica-ultrabásica. Este juntamente com níveis de sedimentos qu1micos intercalados e corpos de gabros, constituem a seqüência máfica-ultramáfica. O complexo, representa o segmento norte de um cintu rão supracrustal polideformado de forma geométrica aproximadamente linear, com orientação NNE, que se extende desde a localidade de Passo do Ivo, situado mais a sul, até a região objeto deste trabalho. Quatro fases de deformação dúcteis foram das para a área, estando as duas primeiras (Dl e D2) identifica associadas xx aos eventos metamórficos regionais Ml e M2. O metamorfismo mais antigo (Ml), assinalado por paragêneses diagnósticas em metapelitos alcançou o fácies anfibolito (zona da estaurolita), estando representado em outras litologias pela ocorrência de olivina metamórfica em paragênese com tremolita e/ou talco (meta-serpentinitos) e hornblenda mais oligoclásio/andesina em meta-básicas. O M2, mais jovem, atingiu o fácies xistos verdes, cujas assembléias mineralógicas se associam à foliação S2, de distribuição ir regular ao longo do cinturão. As condições fisicas de Ml foram de média P/T, similares às do metamorfismo Dalradiano. Intrusões graniticas na forma de lâminas (corpos ta bulares) durante a segunda fase de deformação D2, datados pelo mé todo Rb/Sr em 661 :: 29 Ma e agrupados sob a denominação de Granatóides Sanga do Jobim, fornecem idades mínimas para o complexo. Os vários grupos composiciconais da seqüência máfic~ -ultramáfica, individualizados com base em critérios petrográf~ cos e conteúdo de elementos maiores correspondem a: serpentinitos e olivina-talco ultramafitos (cumulados komatilticos); xis tos magnesianos à talco e clorita e anfibólio xistos (komatiitos); clorita-hornblenda xistos (basaltos komatiiticos), litos e metagabros (basaltos e gabros tolelticos). anfibo Estes vários tipos litológicos foram originados através de diferentes graus de fusão parcial do manto como indicado pelo hiato composicional de MgO (11 à 17%) e os diferentes padrões de ETR existentes entre os anfibolitos/metagabros (toleitos) e os serpentinitos/xistos magnesianos (komatiltos).As variações composicionais no interior de cada grupo, foram controladas pelo fracionamento (acumulação ou extração) de olivina e pouco ortopiroxênio (serpentinitos e olivina-talco ultramafitos)clinopiroxênios (clorita e anfibólios xistos, clorita hornblenda xistos), clinopiroxênio e plagioclásio (anfibolitos e metagabros). As abundâncias e os padrões de ERTL (elementos terras raras leves) enriquecidos, juntamente com os baixos valores das razões A1203/Ti02 e CaO/Ti02 das amostras de xistos magnesiinos das camadas A e B sugerem derivações deste material a partir de baixas percentagens de fusão de um manto enriquecido em mentos incompatíveis. As anomalias negativas de Ce e Eu na ele maio ria das rochas da seqüência máfica-ultramáfica indicam que protólitos ígneossofreram alterações em ambiente submarino.

Metodologia Samário/Neodímio : uma abordagem analítica simplificada e alguns exemplos aplicativos

O presente trabalho discorre sobre o desenvolvimento de uma nova técnica para análise isotópica de Sm-Nd com uso de um traçador combinado de Nd145/Sm149 e de somente a coluna primária, que envolve apenas razões que não requerem correção por interferência isobárica. O trabalho divide-se em duas partes: (i) na primeira parte está apresentado um breve histórico da aplicação da metodologia Sm/Nd e a sua prática rotineira nos laboratórios de geocronologia; (ii) na segunda parte, a nova metodologia Sm/Nd proposta envolvendo calibrações de um traçador combinado de Nd145 e Sm149 e os resultados obtidos nas análises de 3 amostras pré-selecionadas, incluindo uma amostra de referência (BHVO-2) e um teste da validade da técnica de se traçar uma amostra em alíquota. A razão Sm147/Sm149 e as razões de Nd (Nd143/Nd145, Nd143/Nd146 e Nd145/Nd146) nas amostras foram analisadas simultaneamente utilizando um arranjo triplo de filamento (Ta, Re, Ta). A presença de outros ETR não interferiu na eficiência de ionização, sendo as emissões do Sm e do Nd praticamente simultâneas. Esse fato implica que para corrigir o fracionamento observado na razão Sm147/Sm149 pode ser usada a razão Nd143/Nd146 = 0,7101232. A correção de fracionamento, como é empregado no método convencional, reduz os erros nos cálculos das concentrações de Sm e Nd. A razão Nd143/Nd144 normalizada, necessária para idades modelo ou isócrona, é derivada da multiplicação da razão Nd143/Nd145 obtida na amostra natural normalizada para Nd145/Nd146 = 0,482620 por um fator constante de 0,348404. Esse valor de normalização estabelecido é baseado em 45 análises independentes em duas amostras de referência laboratorial (SPEX e Johnson Mattey) obtidas no modo dinâmico de análise utilizando um espectrômetro de massa da VG Sector equipado com 9 coletores A razão Nd143/Nd144 calculada e a idade modelo TDM são plenamente concordantes quando comparadas aos valores obtidos pelo método convencional. Algumas restrições podem surgir quando os valores de Sm e Nd obtidos nas alíquotas forem comparados com os resultados obtidos da amostra total. Pequenas discrepâncias, provavelmente atribuíveis à não homogeneização da solução final, podem ser irrelevantes, uma vez que as razões Sm147/Nd144 e Nd143/N144d derivada estão dentro dos erros experimentais (2s). Para laboratórios de geocronologia com um espectrômetro de massa equipado com pelo menos 5 coletores e com o método Rb/Sr implementado, a nova metodologia proposta para o método Sm/Nd constitui-se em uma alternativa de aplicação quase imediata, desde que a solução de traçador combinado Nd145 e Sm149 esteja bem calibrada e a coluna de resina catiônica tenha resolução adequada para eficiente separação dos elementos terras raras.

Obtenção de óxidos a base de níquel e cobalto para reação de oxidação parcial do metano

Nickel-based catalysts supported on alumina have been widely used in various reactions to obtain synthesis gas or hydrogen. Usually, higher conversion levels are obtained by these catalysts, however, the deactivation by coke formation and sintering of metal particles are still problems to be solved. Several approaches have been employed in order to minimize these problems, among which stands out in recent years the use of additives such as oxides of alkali metals and rare earths. Similarly, the use of methodologies for the synthesis faster, easier, applicable on an industrial scale and to allow control of the microstructural characteristics of these catalysts, can together provide the solution to this problem. In this work, oxides with spinel type structure AB2O4, where A represents divalent cation and B represents trivalent cations are an important class of ceramic materials investigated worldwide in different fields of applications. The nickel cobaltite (NiCo2O4) was oxides of spinel type which has attracted considerable interest due to its applicability in several areas, such as chemical sensors, flat panel displays, optical limiters, electrode materials, pigments, electrocatalysis, electronic ceramics, among others. The catalyst precursor NiCo2O4 was prepared by a new chemical synthesis route using gelatine as directing agent. The polymer resin obtained was calcined at 350°C. The samples were calcined at different temperatures (550, 750 and 950°C) and characterized by X ray diffraction, measurements of specific surface area, temperature programmed reduction and scanning electron microscopy. The materials heat treated at 550 and 750°C were tested in the partial oxidation of methane. The set of techniques revealed, for solid preparations, the presence of the phase of spinel-type structure with the NiCo2O4 NixCo1-xO solid solution. This solid solution was identified by Rietveld refinement at all temperatures of heat treatment. The catalyst precursors calcined at 550 and 750°C showed conversion levels around 25 and 75%, respectively. The reason H2/CO was around 2 to the precursor treated at 750°C, proposed reason for the reaction of partial oxidation of methane, one can conclude that this material can be shown to produce synthesis gas suitable for use in the synthesis Fischer-Tropsch process

Síntese e caracterização de catalisadores nanométricos de LaSrNiO4 para aplicação em dessulfurização de tiofeno

The mixed metal oxides constitute an important class of catalytic materials widely investigated in different fields of applications. Studies of rare earth nickelates have been carried by several researchers in order to investigate the structural stability afforded by oxide formed and the existence of catalytic properties at room temperature. So, this study aims synthesize the nanosized catalyst of nickelate of lanthanum doped with strontium (La(1-x)SrxNiO4-d; x = 0,2 and 0,3), through the Pechini method and your characterization for subsequent application in the desulfurization of thiophene reaction. The precursor solutions were calcined at 300ºC/2h for pyrolysis of polyester and later calcinations occurred at temperatures of 500 - 1000°C. The resulting powders were characterized by thermogravimetric analysis (TG / DTG), surface area for adsorption of N2 by BET method, X-ray diffraction (XRD), scanning electron microscopy (HR_SEM) and spectrometry dispersive energy (EDS). The results of XRD had show that the perovskites obtained consist of two phases (LSN and NiO) and from 700ºC have crystalline structure. The results of SEM evidenced the obtainment of nanometric powders. The results of BET show that the powders have surface area within the range used in catalysis (5-50m2/g). The characterization of active sites was performed by reaction of desulfurization of thiophene at room temperature and 200ºC, the relation F/W equal to 0,7 mol h-1mcat -1. The products of the reaction were separated by gas chromatography and identified by the selective detection PFPD sulfur. All samples had presented conversion above 95%

Influência do método de síntese e caracterização de pós compósitos de NiO- Ce1-xEuxO2-δ para anodos catalíticos de células a combustível

Fuel cells are electrochemical devices that convert chemical energy into electricity. Due to the development of new materials, fuel cells are emerging as generating clean energy generator. Among the types of fuel cells, categorized according to the electrode type, the solid oxide fuel cells (SOFC) stand out due to be the only device entirely made of solid particles. Beyond that, their operation temperature is relatively high (between 500 and 1000 °C), allowing them to operate with high efficiency. Another aspect that promotes the use of SOFC over other cells is their ability to operate with different fuels. The CeO2 based materials doped with rare earth (TR+3) may be used as alternatives to traditional NiO-YSZ anodes as they have higher ionic conductivity and smaller ohmic losses compared to YSZ, and can operate at lower temperatures (500-800°C). In the composition of the anode, the concentration of NiO, acting as a catalyst in YSZ provides high electrical conductivity and high electrochemical activity of reactions, providing internal reform in the cell. In this work compounds of NiO - Ce1-xEuxO2-δ (x = 0.1, 0.2 and 0.3) were synthesized from polymeric precursor, Pechini, method of combustion and also by microwave-assisted hydrothermal method. The materials were characterized by the techniques of TG, TPR, XRD and FEG-SEM. The refinement of data obtained by X-ray diffraction showed that all powders of NiO - Cex-1EuxO2-δ crystallized in a cubic phase with fluorite structure, and also the presence of Ni. Through the characterizations can be proved that all routes of preparation used were effective for producing ceramics with characteristics suitable for application as SOFC anodes, but the microwave-assisted hydrothermal method showed a significant reduction in the average grain size and improved control of the compositions of the phases

Estudo das propriedades magnéticas e estruturais do composto (Sm1 - xMMx)2Fe17 e seus nitretos

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Geologia, Geocronologia, Geoquímica e Petrogênese das Rochas Ígneas Cretácicas da Província Magmática do Cabo e suas Relações com as Unidades Sedimentares da Bacia de Pernambuco (NE do Brasil)

The area studied forms a thin NNE-directed belt situated south of Recife town (Pernambuco state), northeastern Brazil. Geologically, it comprises the Pernambuco Basin (PB), which is limited by the Pernambuco Lineament to the north, the Maragogi high to the south and the Pernambuco Alagoas massif to the west, all of them with Precambrian age. This thesis reports the results obtained for the Cabo Magmatic Province (CMP), aiming the characterization of the geology, stratigraphy, geochronology, geochemistry and petrogenesis of the Cretaceous igneous rocks presented in the PB. The PB is composed of the Cabo Formation (rift phase) at the base (polymictic conglomerates, sandstones, shales), an intermediate unit, the Estiva Formation (marbles and argillites), and, at the top, the Algodoais Formation (monomictic conglomerates, sandstones, shales). The CMP is represented by trachytes, rhyolites, pyroclastics (ignimbrites), basalts / trachy-andesites, monzonites and alkali-feldspar granite, which occur as dykes, flows, sills, laccoliths and plugs. Field observations and well descriptions show that the majority of the magmatic rocks have intrusive contacts with the Cabo Formation, although some occurrences are also suggestive of synchronism between volcanism and siliciclastic sedimentation. 40Ar/39Ar and zircon fission tracks for the magmatic rocks indicate an average age of 102 r 1 Ma for the CMP. This age represents an expressive event in the province and is detected in all igneous dated materials. It is considered as a minimum age (Albian) for the magmatic episode and the peak of the rift phase in the PB. The 40Ar/39Ar dates are about 10-14 Ma younger than published palynologic ages for this basin. Geochemically, the CMP may be divided in two major groups; i) a transitional to alkaline suite, constituted by basalts to trachy-andesites (types with fine-grained textures and phenocrysts of sanidine and plagioclase), trachytes (porphyrytic texture, with phenocrysts of sanidine and plagioclase) and monzonites; ii) a alkaline suite, highly fractionated, acidic volcano-plutonic association, formed by four subtypes (pyroclastic flows ignimbrites, fine-to medium-grained rhyolites, a high level granite, and later rhyolites). These four types are distinguished essentially by field aspects and petrographic and textural features. Compatible versus incompatible trace element concentrations and geochemical modeling based on both major and trace elements suggest the evolution through low pressure fractional crystallization for trachytes and other acidic rocks, whereas basalts / trachy-andesites and monzonites evolved by partial melting from a mantle source. Sr and Nd isotopes reveal two distinct sources for the rocks of the CMP. Concerning the acidic ones, the high initial Sr ratios (ISr = 0.7064-1.2295) and the negative HNd (-0.43 to -3.67) indicate a crustal source with mesoproterozoic model ages (TDM from 0.92 to 1.04 Ga). On the other hand, the basic to intermediate rocks have low ISr (0.7031-0.7042) and positive HNd (+1.28 to +1.98), which requires the depleted mantle as the most probable source; their model ages are in the range 0.61-0.66 Ga. However, the light rare earth enrichment of these rocks and partial melting modeling point to an incompatible-enriched lherzolitic mantle with very low quantity of garnet (1-3%). This apparent difference between geochemical and Nd isotopes may be resolved by assuming that the metasomatizing agent did not obliterate the original isotopic characteristics of the magmas. A 2 to 5% partial melting of this mantle at approximately 14 kbar and 1269oC account very well the basalts and trachy-andesites studied. By using these pressure and temperatures estimates for the generation of the basaltic to trachy-andesitic magma, it is determined a lithospheric stretching (E) of 2.5. This E value is an appropriated estimate for the sub-crustal stretching (astenospheric or the base of the lithosphere?) region under the Pernambuco Basin, the crustal stretching probably being lower. The integration of all data obtained in this thesis permits to interpret the magmatic evolution of the PB as follows; 1st) the partial melting of a garnet-bearing lherzolite generates incompatible-enriched basaltic, trachy-andesitic and monzonitic magmas; 2nd) the underplating of these basaltic magmas at the base of the continental crust triggers the partial melting of this crust, and thus originating the acidic magmas; 3rd) concomitantly with the previous stage, trachytic magmas were produced by fractionation from a monzonitic to trachy-andesitic liquid; 4th) the emplacement of the several magmas in superficial (e.g. flows) or sub-superficial (e.g. dykes, sills, domes, laccoliths) depths was almost synchronically, at about 102 r 1 Ma, and usually crosscutting the sedimentary rocks of the Cabo Formation. The presence of garnet in the lherzolitic mantle does not agree with pressures of about 14 kbar for the generation of the basaltic magma, as calculated based on chemical parameters. This can be resolved by admitting the astenospheric uplifting under the rift, which would place deep and hot material (mantle plume?) at sub-crustal depths. The generation of the magmas and their subsequent emplacement would be coupled with the crustal rifting of the PB, the border (NNE-SSW directed) and transfer (NW-SE directed) faults serving as conduits for the magma emplacement. Based on the E parameter and the integration of 40Ar/39Ar and palynologic data it is interpreted a maximum duration of 10-14 Ma for the rift phase (Cabo Formation clastic sedimentation and basic to acidic magmatism) of the PB

Petrologia do magmatismo tardi-brasiliano no Maciço São José de Campestre(RN/PB), com ênfase no Plúton Alcalino Caxexa

The area studied is located on the north-easternmost portion of the Borborema Province, on the so-called São José de Campestre Massif, States of RN and PB, Northeast Brazil. Field relations and petrographic, geochemical and isotope data permitted the separation of five suites of plutonic rocks: alkali-feldspar granite (Caxexa Pluton), which constitutes the main subject of this dissertation, amphibole-biotite granite (Cabeçudo Pluton), biotite microgranite, gabbronorite to monzonite (Basic to Intermediate Suite) and aluminous granitoid. The Caxexa Pluton is laterally associated to the Remígio Pocinhos Shear Zone, with its emplacement along the mylonitic contact between the gneissic basement and the micashists. This pluton corresponds to a syntectonic intrusion elongated in the N-S direction, with about 50 km2 of outcropping surface. It is composed exclusively of alkali-feldspar granites, having clinopyroxene (aegirine-augite and hedenbergite), andradite-rich garnet, sphene and magnetite. It is classified geochemically as high silica rocks (>70 % wt), metaluminous to slightly peraluminous (normative corindon < 1%), with high total alkalis (>10% wt), Sr, iron number (#Fe=90-98) and agpaitic index (0.86-1.00), and positive europium anomaly. The Cabeçudo Pluton is composed of porphyritic rocks, commonly containing basic to intermediate magmatic enclaves often with mingling and mixing textures. Petrographically, it presents k-feldspar and plagioclase phenocrysts as the essential minerals, besides the accessories amphibole, biotite, sphene and magnetite. It is metaluminous and shows characteristics transitional between the calc-alkaline and alkaline series (or monzonitic subalkaline). Its REE content is greater than those ones of the Caxexa Pluton and biotite microgranite, and all spectra have negative europium anomalies. The biotite microgranites occur mainly on the central and eastern portion of the mapped area, as dykes and sheets with decimetric thickness, hosted principally in orthogneisses and micashists. Their field relationships as regards the Caxexa and Cabeçudo plutons suggested that they are late-tectonic intrusions. They are typically biotite granites, having also sphene, amphibole, allanite, opaques and zircon in the accessory assemblage. Geochemically they can be distinguished from the porphyritic types because the biotite microgranites are more evolved, peraluminous, and have more fractionated REE spectra. The Basic to Intermediate rocks form a volumetrically expressive elliptical, kilometric scale body on the Southeast, as well as sheets in micashists. They are classified as gabbronorites to monzonites, with the two pyroxenes and biotite, besides subordinated amounts of amphibole, sphene, ilmenite and allanite. These rocks do not show a well-defined geochemical trend, however they may possibly represent a monzonitic (shoshonitic) series. Their REE spectra have negative europium anomalies and REE contents greater than the other suites. The aluminous granitoids are volumetrically restricted, and have been observed in close association with migmatised micashists bordering the gabbronorite pluton. They are composed of almandine-rich garnet, andalusite, biotite and muscovite, and are akin to the peraluminous suites. Rb-Sr (whole rock) and Sm-Nd (whole-rock and mineral) isotopes furnished a minimum estimate of the crystallization (578±14 Ma) and the final resetting age of the Rb-Sr system (536±4 Ma) in the Caxexa Pluton. The aluminous granitoid has a Sm-Nd garnet age similar to that one of the Caxexa Pluton, that is 574±67 Ma. The strong interaction of shear bands and pegmatite dykes favoured the opening of the Rb-Sr system for the Caxexa Pluton and biotite microgranite. The amphibole-plagioclase geothermometer and the Al-in amphibole geobarometer indicate minimum conditions of 560°C and 7 kbar for the Cabeçudo Pluton, 730°C and 6 kbar for the microgranite and 743°C and 5 kbar for the basic to intermediate suite. The Zr saturation geothermometer reveals temperatures of respectively 855°C, 812°C and 957°C for those suites, whereas the Caxexa Pluton shows temperatures of around 757°C. The Caxexa, Cabeçudo and microgranites suites crystallized under high fO2 (presence of magnetite). On the other hand, the occurrence of ilmenite suggests less oxidant conditions in the basic to intermediate suite. Field relations demonstrate the intrusive character of the granitoids into a tectonically relatively stable continental crust. This is corroborated by petrographic and geochemical data, which suggest a late- or post-collisional tectonic context. It follows that the generation and emplacement of those granitoid suites is related to the latest events of the Brasiliano orogeny. Finally, the relationships between eNd (600 Ma), TDM (Nd) and initial Sr isotope ratio (ISr) do not permit to define the precise sources of the granitoids. Nevertheless, trace element modelling and isotopic comparisons suggest the participation of the metasomatised mantle in the generation of these suites, probably modified by different degrees of crustal contamination. In this way, a metasomatised mantle would not be a particular characteristic of the Neoproterozoic lithosphere, but a remarkable feature of this portion of the Borborema Province since Archaean and Paleoproterozoic times.

Petrologia do plúton Serra da Macambira, neoproterozóico da faixa seridó, província Borborema (NE do Brasil)

The final stage of Brasiliano/Pan-African orogeny in the Borborema Province is marked by widespread plutonic magmatism. The Serra da Macambira Pluton is an example of such plutonism in Seridó Belt, northeastern Borborema Province, and it is here subject of geological, petrographic, textural, geochemical and petrogenetic studies. The pluton is located in the State of Rio Grande do Norte, intrusive into Paleoproterozoic orthogneisses of the Caicó Complex and Neoproterozoic metassupracrustal rocks of the Seridó Group. Based upon intrusion/inclusion field relationships, mineralogy and texture, the rocks are classified as follows: intermediate enclaves (quartz-bearing monzonite and biotite-bearing tonalite), porphyritic monzogranite, equigranular syenogranite to monzogranite, and late granite and pegmatite dykes. Porphyritic granites and quartz-bearing monzonites represent mingling formed by the injection of an intermediate magma into a granitic one, which had already started crystallization. Both rocks are slightly older than the equigranular granites. Quartz-bearing monzonite has K-feldspar, plagioclase, biotite, hornblende and few quartz, meanwhile biotite-bearing tonalite are rich in quartz, poor in K-feldspar and hornblende is absent. Porphyritic and equigranular granites display mainly biotite and rare hornblende, myrmekite and pertitic textures, and zoned plagioclase pointing out to the relevance of fractional crystallization during magma evolution. Such granites have Rare Earth Elements (REE) pattern with negative Eu anomaly and light REE enrichment when compared to heavy REE. They are slight metaluminous to slight peraluminous, following a high-K calc-alkaline path. Petrogenesis started with 27,5% partial melting of Paleoproterozoic continental crust, generating an acid hydrous liquid, leaving a granulitic residue with orthopyroxene, plagioclase (An40-50), K-feldspar, quartz, epidote, magnetite, ilmenite, apatite and zircon. The liquid evolved mainly by fractional crystallization (10-25%) of plagioclase (An20), biotite and hornblende during the first stages of magmatic evolution. Granitic dykes are hololeucocratic with granophyric texture, indicating hypabissal crystallization and REE patterns similar to A-Type granites. Preserved igneous textures, absence or weak imprint of ductile tectonics, association with mafic to intermediate enclaves and alignment of samples according to monzonitic (high-K calcalkaline) series all indicate post-collisional to post-orogenic complexes as described in the literature. Such interpretation is supported by trace element discrimination diagrams that place the Serra da Macambira pluton as late-orogenic, probably reflecting the vanishing stages of the exhumation and collapse of the Brasiliano/Pan-African orogen.

Obtenção in situ do compósito alfa-SiAlON-SiC

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