[pt] Este trabalho originou-se com um problema industrial, o de recobrimento de um cabo por uma camada de verniz. A questão era modelar o processo de recobrimento de modo que este pudesse ser controlado, evitando perdas e otimizando a produção. O problema é descrito e resolvido nesta tese. Além disso, é formulada uma teoria de interfaces, como as existentes em escoamentos com fronteiras livres ou móveis, onde a tensão superficial desempenha um papel dominante. A formulação da teoria é feita com base na Mecânica do Contínuo, e a interface é modelada como um corpo bidimensional que separa e interage com corpos tridimensionais, dos quais faz parte. A teoria desenvolvida é aplicada em vários problemas com superfície livre para demonstrar a versatilidade da mesma. Uma as contribuições a destacar é o desenvolvimento de um código para o cálculo de superfícies capilares de equilíbrio. / [en] This work was originated with an industrial problem, the process of coating of rods with a enamel. The task was described mathematically the process such as it can be controlled, in order to avoid losses and to optimating the production. In this work the problem is formulated and solved. Furthermore, a theory of interfaces is formulated, like that exist in free or moving boundary flows, when the surface tension is a dominating force. The formulation of the theory is made within the continuous media mechanics point of view, and the interface is modeled as a bidimensional body separating and interacting with tridimensional bodies. Of course, the interface is a part of the bodies. The theory is developed and applied to several free boundary problems in order to show its adaptability. One of the principal goals of this work is the development of an algorithm and the computational program for computing equilibrium capillary surfaces.

AbstractAtmospheric dust is a major component of the Earth System. The optical properties of dust and their roles in cloud nucleation processes have a major impact on Earth’s radiative budget and hydrological cycle. Dusts also take part in many biogeochemical cycles in surface waters of the oceans and on land through their capacity to supply key micronutrients (e.g. Fe, P) sustaining primary production. The aim of this thesis is to improve the understanding of dust cycle by creating new and innovative methods allowing to trace the source regions of dust and quantify their respective contributions. We developed a chromatographic method to isolate and analyze six isotopic systems (i.e. Pb, Nd, Sr, Zn, Cu, Fe) widely used to trace dust source areas. We optimized a new method for single, low-mass dust samples and, in doing so, we observed that the usual rock reference materials (RM) used to calibrate isotopic analysis were not representative of dust. In fact, there is little to no RM for dust and therefore, we set out to characterize precisely the isotopic signatures of two new dust reference materials, ATD and BCR-723. The latter two are representative of natural-like and urban-like dust that we propose now as new standards for atmospheric dust studies. We also investigated dust deposition, along a 250-km transect from the NE Antarctic coastline to the Princess Elisabeth Station area. Using dust samples collected from Sigma-2 passive samplers or isolated from snow samples, we determined the morphology, size distribution and chemical composition of the dust samples at the particle-scale using an automated Scanning Electron Microscope coupled to Energy Dispersive Spectroscopy (SEM-EDS). More than 5500 particles were analysed and the results showed that the grain-size distribution was <5 μm. We also observe difference in mineralogy at the coast compared to the inland section of our transect: dominance of quartz and aluminosilicates at the coast and of Fe-Mg silicates near the Sør Rondane. Based on this discrepancy, we interpret the ‘coastal’ dust samples to come from distal source while Fe-Mg silicate rich samples were hypothesized to originate from the nearby Sør Rondane range. To trace the source of those dust samples, we analysed their REE content and developed a whole new statistical approach to trace and quantify their source(s). The idea is to correlate systematically the REE pattern of those samples with, not only, PSA REE pattern from distal and local rocks but also with all their possible mixing combinations. To do so, we used the correlation coefficient (R), Akaike and Bayesian Information Criterion (AIC-BIC) to determine whether a dust sample traces a single or a mixture of multiple PSAs. Using this numerical method, we determined that local inputs of dust from the Sør Rondane mountains dominate the inland-most section of the 250-km transect. In contrast, coastal sampling sites (up to 50 km inland) are influenced by dust coming from Puna-Altiplano, Patagonia and Southern Africa. As such, this work presents the first unambiguous geochemical evidence that Southern African dust reach North East Antarctic coast. Finally, we also revisited the REE-dataset measured in EPICA Dome-C (EDC, Gabrielli et al. [Quaternary Science Reviews 29 (2010) 265-273]) and EPICA Dronning Maud Land (EDML, Wegner et al. [Climate of the Past 8 (2012) 135-147]) ice cores in order to reconstruct the dust provenance over the last glacial-interglacial interval. Our results showed that,during the Last Glacial Maximum (before 18 kyr BP), dust in both ice cores was predominantly coming from New-Zealand (NZ) with secondary inputs from South-Central Western Argentina (S-CWA) and Patagonia. The glacial-interglacial transition (18-11.6 kyr BP) saw the decline of NZ and S-CWA inputs and the increase of contributions from Patagonia, Southern Africa and Puna Altiplano. The Holocene (after 11.7 kyr BP) is marked by dust inputs coming from Patagonia, Southern Africa and Puna Altiplano while NZ stabilized to a secondary level and S-CWA ceased to supply dust. We demonstrated that variations and relative contributions recorded in ice cores are all related to important climatic changes in source regions having an impact on their capacity to supply dust. Our REE statistical approach provide an unprecedented way to identify and quantify the dust source regions in Antarctic ice core and in doing shed new light of those ‘iconic’ archives of Earth’s climate and atmospheric circulation. / RésuméLes particules atmosphériques (PA) sont un composant majeur du système Terre. Leurs propriétés optiques ainsi que leur rôle au sein des processus de nucléation des nuages ont des impacts majeurs sur le budget radiatif et hydrologique de la terre. Les PA interviennent aussi dans de nombreux cycles biogéochimiques à la surface des océans ou sur terre grâce à leur capacité à fournir des nutriments clés (e.g. Fe, P) soutenant la production primaire. Le but de ce doctorat est d’améliorer la compréhension du cycle des PA en créant de nouvelles méthodes innovatrices permettant de tracer leurs origines et quantifier leurs contributions. Nous avons développé une nouvelle méthode chromatographique optimisée pour les PA afin d’analyser six systèmes isotopiques (i.e. Pb, Nd, Sr, Zn, Cu, Fe) largement utilisés pour tracer l’origine des PA. Afin de combler un manque crucial en terme de matériaux de référence (MR), nous avons quantifié deux nouveaux MR de PA, ATD et BCR-723 (représentatifs des milieux naturels et urbains) et nous les proposons pour toutes les futures études géochimiques de PA. Nous avons aussi étudié les dépositions atmosphériques le long d’un ‘transect’ de 250 km depuis la côte Antarctique jusqu’à la station Belge Princesse Elisabeth. Premièrement, nous avons réalisé des analyses morphologiques et chimiques à l’échelle de la particule à l’aide d’un Microscope Electronique à Balayage à dispersion d’énergie (MEB-EDS). Les analyses ont montré une distribution granulométrique <5 μm ainsi qu’une variation de composition chimique (i.e. minéralogie) depuis la côte jusqu’aux Sør Rondane. Deuxièmement, afin de mieux identifier l’origine de ces PA, nous avons analysé les terres rares (REE) et développé dans son intégralité une nouvelle approche statistique permettant d’identifier les sources ainsi que leurs contributions relatives. Grâce à cela, nous avons déterminé que les échantillons à la côte proviennent du Puna-Altiplano, de Patagonie et du Sud de l’Afrique (SAF). C’est la première fois que des apports du SAF sont formellement identifiés en Antarctique. Finalement, nous avons revisité les data-set de REE des carottes de glace du projet EPICA (EDC et EDML) afin de reconstruire les apports de PA durant la dernière transition glacière/interglaciaire. Nos résultats ont montré que durant la dernière période glaciaire les PA proviennent principalement de Nouvelle-Zélande (NZ) avec des apports secondaires provenant de la partie Sud du centre de l’Ouest Argentin ainsi que de Patagonie. Une transition est marquée entre 18 et 11.6 ka BP jusqu’à un équilibre dès l’Holocène (après 11.7 ka BP) marqué par des apports de sources variées venant de Patagonie, SAF, Puna-Altiplano et NZ. Nous avons aussi démontré que les variations des contributions relatives de sources enregistrées dans les carottes de glaces sont toutes en relation avec des changements climatiques importants au niveau des régions sources impactant leur capacité à générer des PA. Notre approche statistique exploitant les REE apporte une méthode sans précédent pour identifier et quantifier les sources de PA des carottes de glace d’Antarctique et ouvre de nouvelles opportunités sur ces archives du climat et de la circulation atmosphérique de la Terre. / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

Polymers are increasingly being used in engineering designs due to their favorable mechanical properties such as high specific strength, corrosive resistance, manufacturing flexibility. The understanding of the mechanical behavior of these polymers under both static and dynamic loading is critical for their optimal implementation in engineering applications. One such polymer utilized in a wide variety of applications from medical instrumentation to munitions is Polyetherimide, referred to as Ultem. This thesis characterizes both the static and dynamic mechanical behavior of Ultem 1000 through experimental methods and numerical simulations. Standard compression experiments were conducted on and MTS test frame to characterize the elastic-plastic behavior of Ultem 1000 under quasi-static conditions. The dynamic response of the material was investigated at very high strain rates using a custom built miniaturized Kolsky bar apparatus. The smaller Kolsky bar configuration was chosen over the conventional Kolsky device to increase the maximum capable strain rates and to reduce common experimental problems such as wave dispersion, friction, and stress equilibrium. Since a universal test standard for this apparatus is not available, the details of the design, construction, and experimental procedures of this device are provided. The results of the high strain rate testing revealed a bilinear relationship between the material yield stress and strain rate. This relationship was modeled using the Ree-Eyring two stage activation process equation.

No description available.

Recent mapping of the Eagle Lake Quadrangle, NY, coupled with whole-rock geochemistry and microscopy has offered insight into the petrogenesis of the magnetite-apatite deposits of the Hammondville mining district in the eastern Adirondack Mountains. This study provides insight into the magmatic history of the ca. 1060-1050 Ma Lyon Mountain Granite (Hammondville Pluton) which is intimately related to, and hosts the deposits in this area. Magnetite seams are commonly surrounded by well layered magnetite gneiss, which typically parallel the seams, although in some outcrops appear to be slightly truncated by them. Mineralization is generally concordant with the weak layering found throughout the rest of the pluton, and similarly lacks a pervasive metamorphic fabric. Sub-solidus deformation is recorded in some localized shear zones that occur in both the seams and host-granite indicating post-crystallization and post-mineralization deformation events. These episodes could have provided conduits for fluids responsible for growing younger zircon that past workers dated and interpreted as a separate time of mineralization. We conclude that magnetite mineralization likely occurred as separate magma, or magnetite rich fluid, injected into the Lyon Mountain Granite either as a syn-magmatic process, or while it was still a crystalline mush.

Pour la première fois, une étude par spectroscopie infrarouge à transformée de Fourrier et par microsonde ionique des minéraux majeurs de la croûte inférieure et des péridotites mantelliques a été entreprise afin de mieux caractériser les mécanismes d’incorporation et les teneurs en eau de ces minéraux nominalement anhydres, et de déterminer leurs compostions isotopiques en H, O, et Li pour retracer les échanges latéraux et horizontaux de l’eau dans la lithosphère continentale profonde. Les résultats montrent que: (1) Les minéraux nominalement anhydres, comme les pyroxènes et plagioclase, dans les granulites de la croûte inférieure contiennent de l’eau en trace essentiellement sous forme hydroxyles et accessoirement sous forme moléculaire, avec des concentrations (exprimées en poids H2O) allant de 200 à 2330 ppm pour les clinopyroxènes, de 60 à 1875 ppm pour les orthopyroxènes, de 65 à 900 ppm pour les plagioclases. Les teneurs calculées pour chaque roche totale d’après sa composition minéralogique et la teneur en eau des minéraux varient de 155 à 1100 ppm. (2) Les teneurs en H2O des minéraux majeurs et en roche totale de la croûte continentale inférieure sont manifestement plus élevées que celles du manteau lithosphérique sous-jacent, suggérant des variations verticales de la quantité d’H2O dans la lithosphère continentale profonde. Un tel contraste peut affecter de façon notable le comportement rhéologique de la lithosphère continentale. (3) Les rapports isotopiques de l’oxygène des pyroxènes étudiés, et probablement les roches totales, exprimés en [delta]18OSMOW , vont de ~ 4,5 à 12,5‰. Ceci indique la contribution de matériaux recyclés de la croûte continentale durant la pétrogenèse des échantillons ayant un TM18O élevé. (4) Les minéraux de la granulites sont caractérisés par des valeurs de élevées TMD, avec des valeurs de -80~-10‰ exprimées en [delta]DSMOW; les minéraux sont le plus souvent en équilibre les uns avec les autres lorsque l’on considère leurs compositions isotopiques moyennes. (5) Les compositions isotopiques du Lithium mesurée dans les minéraux de nos échantillons de granulites, exprimées en [delta]7Li par rapport à Lsvec, varient de -13 à +4.7 ‰. Ces valeurs sont donc pour la plus part inférieures à celles mesurées sur les MORB (2 – 6‰). La dispersion des valeurs reflètent l’hétérogénéité de la source des granulites, et les valeurs bassent resultent probablement de la perte par diffusion de Li pendant la mise en place des liquides silicatées provenant du manteau dans la croûte inférieure. (6) La grande hétérogénéité des teneurs en eau et en Lithium, et des compositions isotopiques de H-O-Li indique l’absence de circulation de fluide pervasive au travers de la croûte inférieure, qui aurait pour effet de supprimer les hétérogénéités à petite échelle et de les diminuer fortement à grande échelle / For the first time, systematic investigations of water content and H-O-Li isotopic compositions of minerals in lower crustal granulites, as well as water content of minerals in mantle peridotites, from eastern China have been carried out by Fourier transform infrared spectrometer and ion microprobe. The results show that: (1) Nominally anhydrous minerals, such as pyroxenes and plagioclase, in the lower crust generally contain trace amounts of structural water, with their content (H2O by wt.) varying from 200 to 2330 ppm for clinopyroxene, 60 to 1875 ppm for orthopyroxene, 65 to 900 ppm for plagioclase and 155 to 1100 ppm for the estimated bulk compositions. (2) Water contents of minerals in lower crustal granulites from eastern China, and their bulk values, are significantly higher than those in the underlying upper mantle, implying vertical heterogeneities of water distribution in the deep continental lithosphere; the contrast in water content even affect the rheological strength of the lithosphere. (3) The O-isotopic compositions of pyroxenes in the lower crustal granulites from eastern China are highly variable between different localities (~ 4.5 to 12.5‰, expressed in [delta]18OSMOW values), indicating variable influences from recycled crustal materials on their protoliths. (4) The H-isotopic compositions of granulite minerals from eastern China, are mostly in the range of -80 to -10‰ expressed in [delta]DSMOW values, and these minerals are usually in equilibrium with their [delta]D values. The relatively high [delta]D of granulite minerals may be related with degassing loss of H during the genesis of granulites. (5) The Li-isotopic compositions of granulite minerals from eastern China are usually in the range of -13 to 4.7‰, mostly lower than those of MORB (2-6‰). They reflect the source heterogeneity and are probably results of high-T Li diffusion during the intrusion of their original melts into the preexisting lower crust. (6) The large dispersion of Li and water contents and of H-O-Li isotopic results indicate the absence of any pervasive fluids in the lower crust

Löslighet och transport av sällsynta jordartsmetaller i Källfallsfältets gruvsandsmagasin Hugo de Campos Pereira Syftet med detta arbete har varit att kartlägga vilka mekanismer som styr lösligheten av sällsynta jordartsmetaller (eng. rare earth elements, REE) i sulfidhaltig anrikningssand vid den föredetta gruvan Källfallsfältet i Västmanland. För syftet har markvatten- och grundvattenprovtagning utförts, tillsammans med laktester och geokemisk modellering med Visual MINTEQ ver. 3.0. Resultaten visade att sulfidvittring är den främsta processen som styr pH i anrikningssanden, och därmed också indirekt REEs löslighet. Däremot är sulfidvittring ingen källa till REE i sig då ämnena inte föreligger sulfidbundna, något som oxiderat tillgänglighetstest NT ENVIR 006 visade. Istället går REE ut i lösning i anrikningssanden genom vittring av lättvittrade silikatmineral. Vanligtvis betraktas metall bunden i silikatform inte som geokemiskt aktiv. Jämförelser mellan laktester med olika jämviktstid visade att en kinetisk (tidsberoende) faktor föreligger, kopplad till nämnda silikatvittring, som påverkar pH och således också metallöslighet vid laktester på anrikningssanden. Vid jämförelse mellan laktester och halter i anrikningssandens mark- och grundvatten bör denna därmed vägas in. Det pH-statiska laktestet SIS-CEN/TS 14997 visade begränsad möjlighet att undersöka kinetik med anledning av att det utförs under förhållandevis kort tid, 48 timmar. REE- och Cu-halter vid syratitrering (de behandlingar med lägst syratillsatser) och enstegslakning (SIS-CEN ISO/TS 21268-2:2010) visade god, respektive förhållandevis god, överensstämmelse med uppmätta markvattenhalter. Detta visade att syratitrering och enstegslakning är laktest som är tillämpbara, respektive förhållandevis väl tillämpbara, för att uppskatta markvattenhalter i anrikningssanden. Specieringsmodellering med Visual MINTEQ ver. 3.0 visade att pH och DOC är de viktigaste parametrarna som styr REEs speciering i anrikningssandens mark-, grund och ytvatten. Samtliga REE bildar starka komplex med löst organiskt material, men koncentrationerna av DOC var generellt sett låga. I sura sulfatrika mark-, grund och ytvatten domineras specieringen av lösta sulfatkomplex, huvudsakligen (REE)SO4+, följt av fria hydratiserade joner som näst vanligaste förekomstform. Dessa resultat överensstämmer väl med tidigare modelleringsstudier av REEs speciering i sura sulfatrika vatten resulterande från gruvavfall. Med bakgrund av detta och av att REEs ekotoxicitet verkar överensstämma med den fria jon-modellen (eng. free ion model) förväntas REE uppvisa högre toxicitet vid låga pH-värden. / Solubility and transport of rare earth elements in the mine tailings of Källfallsfältet Hugo de Campos Pereira The mechanisms which govern the solubility of rare earth elements (REEs) in sulfide-containing tailings at the former mine site of Källfallsfältet (Västmanland, Sweden) were studied by the means of soil water and ground water sampling, leaching tests and geochemical modeling using Visual MINTEQ ver. 3.0. The results showed that weathering of sulfides is the primary process governing pH in the tailings, and thus also REE solubility. However, weathering of sulfides is no source for REE in itself since the elements are not bound in sulfides, which the oxidized availability test NT ENVIR 006 showed. Instead REE are released into solution by weathering of easily weathered silicates. Usually, metal bound in silicate form is not considered geochemically active. A kinetic (time dependent) factor, associated with the weathering of silicates, was found to affect pH and thus also metal solubility in leaching tests performed on the tailings. The standardized pH static leaching test (SIS-CEN/TS 14997) showed limitations in observing kinetic effects because of its relatively short equilibration time (48 h). Thus, in future studies with similar materials, leaching test kinetics should be taken into account when comparing leached concentrations with field measured concentrations. Acid titration and one step batch test (SIS-CEN ISO/TS 21268-2:2010) proved to be applicable and relatively well applicable to the tailings, respectively, in order to estimate soil solution concentrations. Speciation calculations using Visual MINTEQ ver. 3.0 showed that pH and DOC concentration are the most important factors which affect REE speciation in soil solution, ground water and surface water associated with the tailings. In acid sulfate rich solutions, low in DOC, speciation is dominated by sulfate complexes, mainly (REE)SO4+, followed by free dissolved ions as the second most common form. These results are in accordance with previous modeling studies of REE speciation in acid sulfate rich waters resulting from tailings. This, together with previous results showing that REE ecotoxicity seems to follow the free ion model, implies that the toxicity of the elements is expected to increase with decreasing pH value.

De två kemiskt nära besläktade metallerna niob (Nb) och tantal (Ta) räknas av Europakommissionen som kritiska råmaterial. Detta på grund av en kraftigt ökad efterfrågan och en geografiskt koncentrerad global produktion av dem. Det här arbetet utgör en del av ett större projekt som bedrivs av EuroGeoSurveys (EGS); GeoERA FRAME, som har till syfte att kartlägga förekomsten av kritiska råmaterial inom EU. Två granitpegmatitiska prov från Kolsva fältspatgruva har undersökts med avseende på deras kemi och mineralogi; dels sådana som tentativt identifierats som kolumbitmineral och dels sådana som innehåller ett samarskitliknande mineral. I arbetet har tre huvudsakliga analysmetoder använts: 1) optisk mikroskopi, 2) svepelektronmikroskopi (SEM) med energidispersiv mikrokemisk analys (EDS), samt 3) pulverröntgendiffraktionsanalys (XRD). De kemiska analyserna som genomfördes på ”kolumbit-proven” visade att de bestod av kolumbit-(Fe), med generell formel AB2O6 och med en järndominans i A-katjonposition och niobdominans i B-katjonposition. Analyserna visad även på förekomst av mineral tillhörande pyroklorsupergruppen. De samarskitartade mineralen uppvisade en partiell likhet med samarskitgruppmineral (generell formel ABO4), men med hög grad av metamiktisering, dåliga stökiometrier, låga REE-halter, samt med varierande järn- och kalciumdominans i tentativ A-katjonposition och niobdominans i B-katjonpositionen. Även aluminiumsilikater, mineral från spinellgruppen samt hematit påvisades. Uppsprickning av de metamikta och spröda samarskitartade mineralen har möjliggjort en fluidmedierad omvandling, vilket bl.a. lett till bildning av sekundär radiogen blyglans. Resultaten av undersökningarna bekräftar att Kolsvapegmatiten representerar ett lokalt niob-tantalmineraliserat system. / The two chemically related metals niobium (Nb) and tantalum (Ta) are classified by the European Commission as critical raw materials. This is due to a highly increased demand and a limited global supply situation for these metals. This work is a part of a larger project run by EuroGeoSurveys (EGS); the GeoERA FRAME, which aims to map the distribution of critical raw materials in the EU. Two granitic pegmatite samples from the Kolsva feldspar mine were studied with regards to their chemistry and mineralogy. They had been tentatively identified as consisting of a columbite mineral and a samarskite-like mineral, respectively. In the project, three main analytical methods have been used: 1) optical microscopy, 2) scanning electron microscopy (SEM) with energy-dispersive spectroscopy (EDS), and 3) powder X-ray diffraction analysis (XRD). The analyses performed on the “columbite samples” indicated that most of them were columbite-(Fe), general formula AB2O6, with an iron dominance in the A-cation position and niobium dominance in the B-cation position. The analyses also indicated the presence of minerals belonging to the pyrochlore supergroup. The analyses of the samarskite-like minerals yielded results showing a partial resemblance to the samarskite group minerals (general formula ABO4), but with a high degree of metamictisation, poor stoichiometries, low to very low REE contents, variable iron and calcium-dominance in a tentative A-cation position and niobium-dominance in the B-cation position. Aluminium silicates, minerals from the spinel group and hematite were also observed in this assemblage. Fracturing of the brittle, metamict samarskite-like minerals have enabled a fluid-mediated alteration, which a.o. led to the formation of secondary radiogenic galena. The study confirms that the Kolsva pegmatite represents a locally Nb-Ta mineralised system.

Abstract Mineralogical-mineral chemical characterisation of Nb-Ta-bearingassemblages from the Stripåsen granitic pegmatite, NorbergJens Henriksson The occurrence of Nb-Ta-bearing minerals has earlier been briefly documented inthe Stripåsen granitic pegmatite, Norberg, central Bergslagen. This report describesthe background, preparation and basic characterisation of sampled Nb-Ta-bearingmineral assemblages from this pegmatite. These comprise (Y,REE,U,Th)-(Nb,Ta,Ti)-oxides of mainly a tantalum-dominated A 2-m B 2 X 6-w Y 1-n -type, belonging to the pyrochloresupergroup. The major primary mineral is suggested to have been afluorcalciomicrolite, ideally (Ca,Na,☐) 2 Ta 2 O 6 F. In association with abundant fractureformation related to metamictisation of the microlite minerals, they are interpreted tohave been variably altered by late-stage fluids. Thus, the system has beenextensively modified after the primary crystallisation of the pegmatite melt. Besidesthese (Y,REE,U,Th)-(Nb,Ta,Ti)-oxides, monazite-(Ce) ((Ce, LREE)PO 4 ), nativebismuth (Bi) and presumably radiogenic galena (PbS) were identified. The sampleshave mainly been studied by means of scanning-electron-microscopy with energydispersive spectroscopy (SEM-EDS), utilising reflected polarised light microscopy asa complementary tool. The study was done within the framework of the EU-supported FRAME-project which is focused on a selection of metals and minerals,among others niobium (Nb) and tantalum (Ta). / Sammanfattning Mineralogisk-mineralkemisk karakterisering av Nb-Ta-förande associationerfrån Stripåsenpegmatiten, NorbergJens Henriksson Förekomsten av Nb-Ta-förande mineral har tidigare dokumenteras iStripåsenpegmatiten, Norberg, centrala Bergslagen. Här redogörs för bakgrund,provförberedelse och grundläggande karakterisering av provtagna Nb-Ta-förandemineralassociationer från denna pegmatit. Proven som undersökts innehåller(Y,REE,U,Th)-(Nb,Ta,Ti)-oxider av främst tantaldominerad A 2-m B 2 X 6-w Y 1-n -typtillhörande pyroklorsupergruppen. Den huvudsakliga primära fasen tolkas ha varit enfluorkalciomikrolit, idealiskt (Ca,Na,☐) 2 Ta 2 O 6 F. I anslutning till rikligt förekommandesprickor som är relaterade till omfattande metamiktisering har mikroliternaomvandlats i varierande grad av sena fluider. Systemet har alltså förändrats kraftigtefter den primära kristallisationen av pegmatitsmältan. Förutom (Y,REE,U,Th)-(Nb,Ta,Ti)-oxider identifierades monazit-(Ce) ((Ce,LREE)PO 4 ), gedigen vismut (Bi)och vad som sannolikt är radiogen blyglans (PbS). Provmaterialet har huvudsakligenundersökts med genom svepelektronmikroskopi med energidispersiv spektroskopi(SEM-EDS), varvid malmmikroskopi har använts som ett kompletterande verktyg.Studien gjordes inom ramverket för det EU-stödda FRAME-projektet som blandannat fokuserar på förekomster av de kritiska och konfliktrelaterade metallerna niob(Nb) och tantal (Ta).

Σκοπός της παρούσας εργασίας, είναι η διερεύνηση των υδροχημικών παραμέτρων των κοκκωδών υδροφόρων της λεκάνης του Σπερχειού, καθώς και η πιθανή τροφοδοσία τους από τα ανθρακικά πετρώματα. Για το σκοπό αυτό πραγματοποιήθηκαν μετρήσεις στάθμης, καθώς και υδροχημικές αναλύσεις κύριων στοιχείων, ιχνοστοιχείων και σπάνιων γαιών. Γεωλογικά η περιοχή, στο βορειοανατολικό και νοτιοανατολικό τμήμα της ,δομείται από τους σχηματισμούς της Υποπελαγονικής ζώνης, στο νότιο από τους σχηματισμούς της ζώνης Παρνασσού-Γκιώνας και στο δυτικό από τους σχηματισμούς της ζώνης της Πίνδου. Οι Ολοκαινικές και Πλειο-πλειστοκαινικές αποθέσεις, δομούν το πεδινό τμήμα της λεκάνης και φιλοξενούν τον κύριο υδροφόρο ορίζοντα της περιοχής. Ο ελεύθερος αυτός υδροφόρος μεταπίπτει σε υπό πίεση, εξαιτίας της παρουσίας αργιλικών σχηματισμών, στα ανατολικά της περιοχής. Στα ορεινά τμήματα της λεκάνης, εντός των ανθρακικών σχηματισμών, αναπτύσσονται σημαντικοί υδροφόροι ορίζοντες. Με βάση τον πιεζομετρικό χάρτη της περιοχής προκύπτει ότι η διεύθυνση της ροής του υπόγειου νερού, είναι κυρίως ΒΑ-ΝΑ και o προσχωματικός υδροφόρος, τροφοδοτείται πλευρικά, από τους ανθρακικούς σχηματισμούς, που βρίσκονται νότια και βορειοανατολικά του πεδινού τμήματος. Τα υπόγεια νερά της περιοχής, ομαδοποιούνται σε τρεις κύριους υδροχημικούς τύπους: Ca-HCO3, Ca-Mg-HCO3 και (Ca)-Νa-Cl-(HCO3). Ο πρώτος υδροχημικός τύπος χαρακτηρίζει τα φρέσκα νερά της περιοχής, ο δεύτερος τα νερά που παρέμειναν για μεγαλύτερο χρονικό διάστημα στον υδροφόρο και εμπλουτίστηκαν σε Μg+2, και ο τρίτος τα νερά που δέχονται την επίδραση είτε της θάλασσας, είτε των θερμών νερών από μεγαλύτερα βάθη. Από τα αποτελέσματα των υδροχημικών αναλύσεων προέκυψε ότι στην πλειοψηφία τους τα δείγματα είναι κορεσμένα σε ασβεστίτη και δολομίτη. Eπίσης σε μία ομάδα δειγμάτων, διαπιστώθηκε απεμπλουτισμός σε Na, γεγονός που αποδόθηκε σε διαδικασίες ιοντοανταλαγής. Οι αυξημένες συγκεντρώσεις Fe, Mn, αποδόθηκαν στη διάλυση των ορυκτών του φλύσχη της Πίνδου, ενώ ο Zn και τα NΟ3 σε ανθρωπογενείς παρεμβάσεις (βιομηχανικά απόβλητα και λιπάσματα). Το As το Li και το Β συνδέονται με την παρουσία θερμών πηγών. Τέλος η μεθοδολογία των σπάνιων γαιών, επαλήθευσε τα αποτελέσματα της πιεζομετρίας αλλά και τα υδροχημικών αναλύσεων, ότι δηλαδή ο προσχωματικός υδροφόρος της περιοχής, τροφοδοτείται πλευρικά από τα ανθρακικά πετρώματα της περιοχής και συγκεκριμένα από τους ασβεστόλιθους της Υποπελαγονικής ζώνης και της ζώνης Παρνασσού-Γκιώνας. / In the frames of this study the hydrochemical parameters of porous aquifers at Sperchios basin, were investigated. Moreover their possible recharge by carbonate rocks was examined. Therefore, a series of water level measurements and a sampling campaign were carried out. The samples were analysed for main, trace and rare earth elements. Regarding the area’s geological setting, its northeastern and southeastern part is comprised of formations of the Subpelagonic Zone, its southern edge of Parnassos-Giona Zone and its western part of Pindos Zone. At the lowlands these formations are overlain by Holocene and Pleistocene deposits which host the most important aquifer of the region. It is an unconfined aquifer, which at the eastern part turns into a confined one, due to the presence of clay formations. Many important aquifers have been also developed in the basin’s carbonate formations. The region’s piezometric map at the southern area indicates that the main water flow direction is NE-SE. Moreover it points out that the carbonate formations recharge the porous aquifer. According to their hydrochemical characteristics groundwater can be divided into three main types: Ca-HCO3, Ca-Mg-HCO3 and (Ca)-Na-Cl-(HCO3). The first one is typical of the region’s fresh water, the second one indicates longer residence time of the water that was enriched in Mg+2 and the third one of water that was either influenced by sea water or hot springs. The elaboration of the hydrochemical data also showed that the majority of water samples are saturated in calcite and dolomite. There is also a depletion of certain samples in Na+ which was attributed to ion exchange processes. High Fe and Mn concentrations originate from the dissolution of Pindos Flysch minerals, As, Li and B to the presence of hot springs, while Zn and NO3 were related to human impact (industrial waste and fertilizers). The rare earth elements confirmed the original hypothesis, which was based on piezometric data and hydrochemical data analysis, that the region’s porous aquifer is laterally recharged by the carbonate rock formations of Subpelagonic and Parnassos-Giona Zone limestones.