Four different kinds of filter-materials with reactive surfaces have been studied concerning their capacity to absorb heavy metals in leachate from a municipal waste deposit. The heavy metals studied were: lead, cadmium, copper, mercury, chromium, nickel and zinc. The leachate contains high levels of dissolved organic carbon (DOC) and has a high pH-value along with a high buffer capacity. These characteristics of the leachate make it difficult to remove pollutants and require efficient filters. The filters that were examined in the report are blast-furnace slag with CaO, sand covered with iron oxides, olivine and nepheline. The experiment was carried out in two sets, starting with batch experiments followed by a column study. The objective of the batch experiments was to find out how variations in pH affected the sorption capacity of the materials. The interval used during the test was from pH 5 to pH 10. The computer program VisualMinteq was used to evaluate the dominating sorption processes when the materials interacted with the solutions. Two different kinds of solutions were used in the batch experiment. One of them was the leachate, to which known concentrations of heavy metals were added (about 1 μM) and the other consisted of sodium nitrate, a solution without organic compounds, which was used as a reference. The sodium nitrate solution was also spiked with the same concentration of heavy metals as the leachate. The results from the batch experiment showed that the sorption of heavy metals was lowered if the DOC level was high. No relation between pH and sorption ability could be found for the leachate, but for some metals in the sodium solution a higher pH improved the removal of heavy metals. The two materials that showed best results in the batch experiment were the blast-furnace slag and the sand with iron oxides. These materials were used in the column study. The olivine material was somewhat better than the nepheline in the batch experiment. Four columns were used in the column study, two for each material. Leachate with heavy metals was pumped into the columns with a specific flow rate; at first a low flow rate was used and when half the experiment time had passed the flow rate was increased. The flow rates used were 0.12 m/24 h and 0.62 m/24 h. The outcome of the column experiment showed that the slag had the highest ability to adsorb metals. The metal sorption was over 60 percent for lead, cadmium and zinc, where the highest sorption was obtained for lead. No affects were noticed when the flow rate was increased. / I detta examensarbete har fyra olika reaktiva filtermaterials kapaciteter att ur deponilakvatten avskilja tungmetallerna bly, kadmium, koppar, kvicksilver, krom, nickel och zink testats. Deponilakvatten är ett avloppsvatten med höga halter organiskt material (DOC), högt pH och en hög buffertkapacitet. Dess sammansättning ställer stora krav på ett filter och närvaron av ligander påverkar sorptionprocesserna. Filtren som ingått i studien är kalciumoxiddopad masugnsslagg, järnoxidtäckt sand, olivin och nefelin. Försöken utfördes i två delar, med inledande skakförsök och därefter kolonnförsök. I båda försöken användes lakvatten med en extra tillsats av tungmetaller. I skakförsöken användes även natriumnitrat; ett referensvatten utan organiska ligander, även det spikat med tungmetaller. I skakförsöken studerades avskiljningens pH-beroende för de olika filtren, med ett pH-intervall på ca 5 – 10. Därefter modellerades resultaten i jämviktsprogrammet VisualMinteq för att fastställa vilka processer som styr avskiljningen. Skakförsöken och kolonnförsöken utfördes båda i klimatrum vid 8 ºC, för att efterlikna markens naturliga temperatur. Resultaten från skakförsöken visade att masugnsslagg och järnoxidsand gav bäst avskiljning för de flesta tungmetaller. Olivin och nefelin var sämre metallsorbenter, där olivin uppvisade något bättre resultat än nefelin. Inget tydligt pH-beroende för lakvattnet kunde utläsas, men för natriumnitratlösningen gav en pH-höjning en ökad sorption för vissa metaller. Den kemiska jämviktsmodelleringen visade att den dominerande processen i filtermaterialen var sorption på filterytorna. De två filtermaterialen som visade bäst resultat i skakförsöken (slagg och järnoxid) studerades vidare i kolonnförsök, där ett bestämt lakvattenflöde pumpades genom kolonner packade med materialen. Två olika flödeshastigheter testades (0,12 m/dygn och 0,62 m/dygn) och sorptionen av metaller analyserades. Slaggen uppvisade högst avskiljningskapacitet av de studerade filtren. De metaller som sorberades bäst var bly, kadmium och zink (över 60 % avskiljning), där den högsta sorptionen erhölls för bly. Gemensamt för både skak- och kolonnförsöken var att sorptionen försvårades då halten organiskt material (DOC) ökade, vilket beror på att DOC konkurrerar med de reaktiva ytorna på filtren om att binda den fria metalljonen. Ingen minskande avskiljningseffekt av en flödesökning kunde utläsas.

Os nefelina sienitos miasquíticos a intermediários do Maciço Alcalino Poços de Caldas (MAPC), em especial o tipo da Pedreira, possuem enclaves microgranulares félsicos e máficoultramáficos intrigantes. O nefelina sienito da Pedreira (NeS) pode ser divido em duas fácies texturais: uma de granulação média-grossa a grossa (NeS-g), outra de granulação média-fina a fina (NeS-f). O NeSg possui, mais comumente, enclaves microgranulares félsicos (EMF), de composição fonolítica. Estes enclaves podem envolver enclaves menores, máfico-ultramáficos, gerando enclaves duplos. O NeSf apresenta mais tipicamente enclaves microgranulares máfico-ultramáficos (EMM), ora com feições de rompimento em estado plástico, ora com bordas angulosas e lineares. Diques de composição fonolítica cortam o NeS-g. As rochas estudadas neste trabalho são constituídas por nefelina, feldspato alcalino e clinopiroxênio. Como fase acessória, têm-se titanita, magnetita e biotita-flogopita. Apatita ocorre também como mineral acessório, com exceção para o NeS-g. No NeS-g, no NeS-f e nos EMF, o clinopiroxênio possui duas fases texturais: uma prismática, verde (egirina-augita) que também pode ter núcleo róseo/incolor (diopsídio, mais comum no NeS-f e no EMF); outra fibrosa, também verde, porém fortemente pleocroica (egirina). Os EMM são constituídos essencialmente por diopsídio, com M(médio)~80. Quando porfirítico, o enclave possui macrocristais de diopsídio róseo/incolor (#mg~0,9) imersos numa matriz de diopsídio verde (#mg~0,8), ambos prismáticos. Magnetita dos NeS possui pouca variação, com teores baixos de Ti, diferente da magnetita dos enclaves. A assinatura química da nefelina dos EMM é equivalente à do NeS-f, com mais Fe3+ e menos K em relação ao NeS-g. Feldspato alcalino tende a ser mais potássico nos EMF e apresenta maior variação composicional nos EMM (Ab10-33Or72-80). Biotita está presente somente nos EMF e flogopita somente nos EMM. O padrão de elementos terras raras (ETR) do clinopiroxênio róseo/incolor do NeS-f é semelhante ao do EMM. Egirina-augita e egirina possuem enriquecimento em ETR pesados. Os enclaves máfico-ultramáficos são ultrabásicos, classificados como tefritos/basanitos (Le Bas et al., 1986) ou nefelinitos/ankaratritos (De La Roche et al., 1980), enquanto as rochas félsicas são intermediárias, correspondentes a fonolitos ou nefelina sienitos, dependendo da granulometria. Os diques e o NeS-f são peralcalinos, enquanto o EMF, o NeS-g e os EMM são peralcalinos/metaluminosos. As rochas ultramáficas/ultrabásicas, aflorantes na porção noroeste do Maciço Alcalino Poços de Caldas (Ulbrich et al., 2002), possuem padrões de ETR que indicam que estas rochas podem estar geneticamente ligadas aos enclaves máfico-ultramáficos. De uma forma geral, as características estruturais, texturais e químicas das rochas estudadas corroboram com a hipótese de coexistência de pelo menos dois magmas distintos: um félsico sienítico insaturado outro ultramáfico/ultrabásico, que teriam interagido e formado os os EMM e o NeSf, principalmente. Enquanto num estágio posterior de cristalização do magma, porém ainda em estado plástico, o dique teria se colocado, com parcial absorção da rocha pelos nefelina sienitos, formando os EMF. / The miaskitic to intermediate nepheline syenites of Poços de Caldas Alkaline Massif, especially the Pedreira type, have intriguing felsic and mafic-ultramafic microgranular enclaves. The Pedreiras nepheline syenite type (NeS) can be divided into two textural facies: one that is medium-coarse to coarse grained (NeS-c) and the other that varies between medium-fine to fine grained (NeS-f). It is common among the NeS-c microgranular felsic enclaves (MFE) with phonolitic composition. These enclaves may develop smaller ones maficultramafic, generating double enclaves. The NeS-f usually presents mafic-ultramafic enclaves (MME), sometimes showing disrupted features in plastic stage and sometimes angular and linear edges. Phonolitic dykes cut the NeS-c. The rocks studied in this work are formed by nepheline, alkali-feldspar and clinopyroxene. The accessory phase is characterized by titanite, magnetite and biotite-phlogopite. In exception to the NeS-c, apatite also occurs as an accessory mineral. In the NeS-c, NeS-f and MFE, the clinopyroxene presents two textural phases: a green prismatic one (aegirine-augite), which also may have a pinkish/colourless core (diopsyde, which is common in the NeS-f and MFE); the other one is fibrous, also green, however with strongly pleocroism (aegirine). Essencially, the MME are formed by diopsyde, with M(medium)~80. When porphyritic, the enclave has macrocrystals of pinkish/colourless diopsyde (with mg#~0,9) in a green diopsyde (mg#~0,8) matrix, both prismatic. In the NeS, the magnetite varies little: with low levels of Ti, differently from the enclaves magnetite. The chemical signature of the nepheline in the MME equals to the one present in the NeS-f and has more Fe3+ and less K when compared to the NeS-c. The alkaline feldspar in the MFE has more potassium in its structure and presents a higher compositional variation in the MME (Ab10-33Or72-80). It is also noticeable that biotite is a component only to the MFE, while the phlogopite occurs in the MME. The rare earth elements (REE) pattern in the pinkish/colourless clinopyroxene of the NeS-f is similar to the MME. Both aegirine-augite and aegirine present an enrichment regarding the heavy REE. The MME are ultrabasic, classified as tephrite/basanite (Le Bas et al., 1986) or nephelinite/ankaratrites (De La Roche et al., 1980), while the felsic rocks are intermediate, corresponding to phonolite and nepheline syenite, depending on the grain size. The dykes and the NeS-f are peralkaline, while the MFE, NeS-c and the MME are peralkaline/metaluminous. The ultrabasic/ultrapotassic rocks, outcropping in the northwestern portion of the PCAM (Ulbrich et al., 2002), have REE patterns wich indicate that these rocks may be genetically related to mafic-ultramafic enclaves. Generally, the structural, textural and chemical signatures of the rocks studied in this work confirm the hypothesis of the coexistence of at least two different magmas: a syenitic undersaturated felsic one and a ultramafic/ultrabasic one, and their interaction resulted in the MME and, above all, the NeS-f. While in a late stage of magma cristalization, but still in the plastic state, the dike would be placed, with partial absorption of the rock by the nepheline syenite, resulting in the EMF.

Os nefelina sienitos miasquíticos a intermediários do Maciço Alcalino Poços de Caldas (MAPC), em especial o tipo da Pedreira, possuem enclaves microgranulares félsicos e máficoultramáficos intrigantes. O nefelina sienito da Pedreira (NeS) pode ser divido em duas fácies texturais: uma de granulação média-grossa a grossa (NeS-g), outra de granulação média-fina a fina (NeS-f). O NeSg possui, mais comumente, enclaves microgranulares félsicos (EMF), de composição fonolítica. Estes enclaves podem envolver enclaves menores, máfico-ultramáficos, gerando enclaves duplos. O NeSf apresenta mais tipicamente enclaves microgranulares máfico-ultramáficos (EMM), ora com feições de rompimento em estado plástico, ora com bordas angulosas e lineares. Diques de composição fonolítica cortam o NeS-g. As rochas estudadas neste trabalho são constituídas por nefelina, feldspato alcalino e clinopiroxênio. Como fase acessória, têm-se titanita, magnetita e biotita-flogopita. Apatita ocorre também como mineral acessório, com exceção para o NeS-g. No NeS-g, no NeS-f e nos EMF, o clinopiroxênio possui duas fases texturais: uma prismática, verde (egirina-augita) que também pode ter núcleo róseo/incolor (diopsídio, mais comum no NeS-f e no EMF); outra fibrosa, também verde, porém fortemente pleocroica (egirina). Os EMM são constituídos essencialmente por diopsídio, com M(médio)~80. Quando porfirítico, o enclave possui macrocristais de diopsídio róseo/incolor (#mg~0,9) imersos numa matriz de diopsídio verde (#mg~0,8), ambos prismáticos. Magnetita dos NeS possui pouca variação, com teores baixos de Ti, diferente da magnetita dos enclaves. A assinatura química da nefelina dos EMM é equivalente à do NeS-f, com mais Fe3+ e menos K em relação ao NeS-g. Feldspato alcalino tende a ser mais potássico nos EMF e apresenta maior variação composicional nos EMM (Ab10-33Or72-80). Biotita está presente somente nos EMF e flogopita somente nos EMM. O padrão de elementos terras raras (ETR) do clinopiroxênio róseo/incolor do NeS-f é semelhante ao do EMM. Egirina-augita e egirina possuem enriquecimento em ETR pesados. Os enclaves máfico-ultramáficos são ultrabásicos, classificados como tefritos/basanitos (Le Bas et al., 1986) ou nefelinitos/ankaratritos (De La Roche et al., 1980), enquanto as rochas félsicas são intermediárias, correspondentes a fonolitos ou nefelina sienitos, dependendo da granulometria. Os diques e o NeS-f são peralcalinos, enquanto o EMF, o NeS-g e os EMM são peralcalinos/metaluminosos. As rochas ultramáficas/ultrabásicas, aflorantes na porção noroeste do Maciço Alcalino Poços de Caldas (Ulbrich et al., 2002), possuem padrões de ETR que indicam que estas rochas podem estar geneticamente ligadas aos enclaves máfico-ultramáficos. De uma forma geral, as características estruturais, texturais e químicas das rochas estudadas corroboram com a hipótese de coexistência de pelo menos dois magmas distintos: um félsico sienítico insaturado outro ultramáfico/ultrabásico, que teriam interagido e formado os os EMM e o NeSf, principalmente. Enquanto num estágio posterior de cristalização do magma, porém ainda em estado plástico, o dique teria se colocado, com parcial absorção da rocha pelos nefelina sienitos, formando os EMF. / The miaskitic to intermediate nepheline syenites of Poços de Caldas Alkaline Massif, especially the Pedreira type, have intriguing felsic and mafic-ultramafic microgranular enclaves. The Pedreiras nepheline syenite type (NeS) can be divided into two textural facies: one that is medium-coarse to coarse grained (NeS-c) and the other that varies between medium-fine to fine grained (NeS-f). It is common among the NeS-c microgranular felsic enclaves (MFE) with phonolitic composition. These enclaves may develop smaller ones maficultramafic, generating double enclaves. The NeS-f usually presents mafic-ultramafic enclaves (MME), sometimes showing disrupted features in plastic stage and sometimes angular and linear edges. Phonolitic dykes cut the NeS-c. The rocks studied in this work are formed by nepheline, alkali-feldspar and clinopyroxene. The accessory phase is characterized by titanite, magnetite and biotite-phlogopite. In exception to the NeS-c, apatite also occurs as an accessory mineral. In the NeS-c, NeS-f and MFE, the clinopyroxene presents two textural phases: a green prismatic one (aegirine-augite), which also may have a pinkish/colourless core (diopsyde, which is common in the NeS-f and MFE); the other one is fibrous, also green, however with strongly pleocroism (aegirine). Essencially, the MME are formed by diopsyde, with M(medium)~80. When porphyritic, the enclave has macrocrystals of pinkish/colourless diopsyde (with mg#~0,9) in a green diopsyde (mg#~0,8) matrix, both prismatic. In the NeS, the magnetite varies little: with low levels of Ti, differently from the enclaves magnetite. The chemical signature of the nepheline in the MME equals to the one present in the NeS-f and has more Fe3+ and less K when compared to the NeS-c. The alkaline feldspar in the MFE has more potassium in its structure and presents a higher compositional variation in the MME (Ab10-33Or72-80). It is also noticeable that biotite is a component only to the MFE, while the phlogopite occurs in the MME. The rare earth elements (REE) pattern in the pinkish/colourless clinopyroxene of the NeS-f is similar to the MME. Both aegirine-augite and aegirine present an enrichment regarding the heavy REE. The MME are ultrabasic, classified as tephrite/basanite (Le Bas et al., 1986) or nephelinite/ankaratrites (De La Roche et al., 1980), while the felsic rocks are intermediate, corresponding to phonolite and nepheline syenite, depending on the grain size. The dykes and the NeS-f are peralkaline, while the MFE, NeS-c and the MME are peralkaline/metaluminous. The ultrabasic/ultrapotassic rocks, outcropping in the northwestern portion of the PCAM (Ulbrich et al., 2002), have REE patterns wich indicate that these rocks may be genetically related to mafic-ultramafic enclaves. Generally, the structural, textural and chemical signatures of the rocks studied in this work confirm the hypothesis of the coexistence of at least two different magmas: a syenitic undersaturated felsic one and a ultramafic/ultrabasic one, and their interaction resulted in the MME and, above all, the NeS-f. While in a late stage of magma cristalization, but still in the plastic state, the dike would be placed, with partial absorption of the rock by the nepheline syenite, resulting in the EMF.

A viability study was undertaken on a farm Zandrivierspoort 210 JP, in the Pilanesberg Alkaline Complex to investigate the red syenite deposit. The red syenite deposit of interest is located in the south-western quadrant of the Pilanesberg. It is a potential source of nepheline, which is used as a flux in glass and ceramics industry. The study was aimed at establishing the demand for the material in South Africa and the market logistics related to its exploitation. Glass and ceramics manufacturers have different specifications as far as the quality and the product form is concerned. A market study conducted indicated that glass manufacturers require already beneficiated material with a low Fe content, depending on the kind of glass being manufactured. Ceramics manufactures also want material with low Fe content, but the material can be unbeneficiated as most of these factories already have facilities to remove Fe and other gangue. The common requirement is that material must be crushed and milled to a specific size. Red Syenite complies with the specifications of the ceramics manufacturer and did not comply directly with the specification of the glass manufacturer. The main reason for not non-compliance with glass specifications can be attributed to the fact that the material supplied was unbeneficiated. A major concern from the industry is the continuity of production from the deposit and an assurance of constant quality. It was also established that the availability of substitutes such as feldspar at a lower cost than nepheline results in an unwillingness of potential users to source nepheline despite its advantages. It is recommended that extensive geological studies be undertaken to confirm the resources and reserves of the entire nepheline-bearing deposits in the Pilanesberg. The mining of the deposit will be undertaken by employing a quarrying method, which will be followed by opencast to a depth of 50m. The Run-Of-Mine (ROM) will be crushed and milled to sizes specified by clients and the beneficiation process will follow. A financial investigation based on the known facts about the deposit established that capital, production rate, and selling price have the highest influence on the viability of the project. Transport and operating costs in this case showed a less significant influence on the viability of the project. / Dissertation (MSc (ESPM))--University of Pretoria, 2007. / Geology / unrestricted

The Motzfeldt centre is one of four major alkaline centres belonging to the Igaliko complex of South Greenland. The melts parental to the Motzfeldt centre are interpreted from Hf isotopes to be derived form a common mantle source which experienced subsequent isotopic contamination from older crustal components during the interval between segregation and emplacement. Magmatism within the centre commenced with the emplacement of the Motzfeldt Sø Formation at 1273 ± 8 Ma. This unit is unique within the Motzfeldt intrusion as it is characterised by a high degree of textural and mineralogical variability and hosts localised Nb, Ta, U, Th, Zr and REE mineralisation associated with pyrochlore and late-stage REE bearing carbonate phases. Biotite halogen contents show that in addition to enrichment of incompatible elements the MSF and Motzfeldt centre in general is particularly rich in F. The elevated F content is inferred to have extended the crystallisation interval of the melt and facilitated fractionation down to relatively low temperatures. The unusual enrichment of F and incompatible elements in the MSF is suggested to represent the first and most evolved melts extracted from the top of a stratified storage chamber at depth. The MSF is also characterised by pervasive subsolidus alteration, giving the rock and region a striking brick red colour. Pb-Pb pyrochlore studies indicate that alteration in the formation was effectively synchronous (1267 ± 6 Ma), with the magmatic age of emplacement. Fluid inclusion studies suggest that contemporaneous to the exsolution of juvenile, high salinity, F-rich fluids was the wholesale influx of hydrothermally convected low salinity groundwaters through the formation. The presence of pervasive late-stage hematite and calcite throughout the MSF suggests that the oxidation potential of the bulk fluid increased above the hematite-magnetite buffer during the waning stages of the hydrothermal phase. Mineralisation was promoted by this shift in fluid composition, reducing the complexing potential of fluid ligands and facilitating mineralisation within the high-levels units of the intrusion where alteration is most intense. Economic mineralisation associated with the centre is inferred to be largely sourced from the parental melts, however the role the hydrothermal phase played was particularly important in locally mobilising and concentrating incompatible elements within the high-level units of the formation.

<p>Highly polluted urban storm water from e.g. highways can contain large amounts of heavy metals that may cause harm if they are discharged into recipients. To remove the heavy metals a possible low-cost method that does not require much maintenance, could be the use of reactive filters with filter materials consisting of industrial residues or other cheap mineral based materials. Dissolved metal ions are removed by reactive filters through the processes of ions binding to active sites on the surface of the filter materials, or by formation of insoluble precipitates.</p><p>The ability of CaO-treated granulated blast-furnace slag, iron oxide coated sand, olivine and nepheline to remove seven heavy metals (Cr, Cd, Cu, Ni, Zn, Pb and Hg) from urban storm water was studied. Initially batch experiments were performed where the effect of pH, dissolved organic carbon (DOC) and dissolved ions on the adsorption efficiency was studied. The experiments were conducted with urban storm water and with a reference solution (10 mM NaNO3), both containing the same concentration of heavy metals (approx. 1 μM). The two materials with the best results were further investigated in a column study, where the capacity of the filter was tested. Chemical equilibrium calculations using the program Visual MINTEQ were performed in order to assess the role of precipitation as a mechanism for removal.</p><p>The results show that the blast-furnace slag was the most effective filter material and that it has great potential to be used as a heavy metal remover. Also the iron oxide coated sand worked satisfactory. The highest degree of removal was obtained for lead, cadmium and nickel, for which the removal efficiency exceeded 90% after a load of 300 times the water volume in the columns. For some metals, mainly copper, chromium and mercury the dissolved organic matter affected the removal negatively. The chemical mechanisms causing the removal are specific adsorption to the surfaces of the materials, and for the blast-furnace slag probably precipitation of insoluble metal sulfides.</p> / <p>Starkt förorenat dagvatten som rinner av från exempelvis motorvägar, kan innehålla betydliga mängder tungmetaller som kan orsaka skada om de kommer ut i omgivande vattendrag. En billig metod för tungmetallavskiljning, som inte kräver så mycket underhåll, skulle kunna vara att använda reaktiva filtermaterial bestående av restprodukter eller andra mineraliska lågkostnadsmaterial. Reaktiva filter fungerar som metallavskiljare genom att de lösta metalljonerna binder till ytgrupper på filtermaterialen eller att svårlösliga utfällningar bildas.</p><p>Förmågan att avskilja sju tungmetaller (Cr, Cd, Cu, Ni, Zn, Pb och Hg) ur dagvatten har undersökts för fyra mineraliska filtermaterial, kalciumoxiddopad masugnsslagg, järnoxidsand, olivin och nefelin. Studien inleddes med skakförsök där adsorptionens pH-beroende undersöktes. Försöken gjordes dels med dagvatten, dels med en referenslösning (10 mM NaNO3) med samma tungmetallkoncentration (ca 1μM). Detta gjordes för att studera effekter av löst organiskt material och andra ligander på adsorptionen. Därefter testades de material som uppvisat bäst resultat i skakförsöket i kolonnförsök, ett försök som mer efterliknar en praktisk tillämpning och där filtrets kapacitet kan studeras. Genom kemiska jämviktsberäkningar med programmet Visual MINTEQ var det möjligt att undersöka om bildningen av svårlösliga metallutfällningar bidrog till metallavskiljningen.</p><p>Resultaten visar att slaggen var det effektivaste filtermaterialet och att detta har stor potential att användas för avskiljning av tungmetaller. Även järnoxidsanden fungerade tillfredsställande. De metaller som avskiljdes bäst var bly, kadmium och nickel, för vilka avskiljningen var > 90 % i kolonnförsöket efter en belastning motsvarande 300 gånger vattenmängden i kolonnerna. För vissa metaller, främst koppar, krom och kvicksilver, försämrades avskiljningen betydligt när löst organiskt material fanns närvarande. Mekanismerna som står för avskiljningen är till störst del adsorption till grupper på filtermaterialens ytor, men bildning av svårlösliga metallsulfider är också tänkbar för slaggen.</p>

Les laves émises en domaine de subduction sont dominées par des compositions calcoalcalines à hypersthène normatif. En revanche, les inclusions magmatiques piégées dans les olivines magnésiennes (Fo ≥ 88) des basaltes d’arc présentent des compositions alcalines, à néphéline normative. Bien que leurs compositions en éléments traces incompatibles ne diffèrent pas de celles de leurs laves hôtes, ces magmas ne peuvent pas s’expliquer par les modèles classiques de formation des laves d’arc. L’étude d’inclusions magmatiques alcalines de plusieurs arcs du monde a permis de mettre en évidence leur variabilité de composition, en particulier en CaO et Sc, deux éléments compatibles dans le clinopyroxène. Le couplage de cette étude avec des modélisations thermodynamiques a aboutit à l’élaboration d’un modèle de source impliquant la contribution de clinopyroxénites à amphibole à environ 1 GPa. Les inclusions magmatiques à néphéline normative d’arc seraient ainsi les témoins de l’hétérogénéité de source à l’origine des magmas d’arc. Les expériences de fusion partielle du mélange homogène clinopyroxénite à amphibole – péridotite hydratée réalisées à 1 GPa permettent d’apporter des informations supplémentaires quant aux mécanismes de genèse des magmas d’arc sous-saturés en silice et de mieux comprendre les comportements de fusion des deux types de lithologies. Pour des proportions inférieures à ~ 50 % de pyroxénite dans la source, les magmas produits présentent des compositions à hypersthène normatif, comparables aux laves d’arc issues de la fusion de lithologies péridotitiques. Pour des proportions de pyroxénites supérieures, les magmas sont à néphéline normative et s’enrichissent en calcium, reproduisant ainsi la gamme de compositions observée pour les inclusions magmatiques. 50 % de mélange correspond à la limite de stabilité de l’orthopyroxène. Tant que cette phase est présente dans le résidu, les magmas engendrés restent à hypersthène normatif. De plus, la présence d’amphibole dans la source permet d’augmenter la sous-saturation des liquides résultants et d’expliquer ainsi les termes les plus riches en néphéline normative de certaines inclusions. Nos expériences de fusion d’une source homogène ont également permis de déterminer la composition des magmas formés par un processus de fusion plus réaliste, impliquant une source hétérogène pyroxénite-péridotite. La productivité de liquides des pyroxénites étant supérieure à celles des péridotites, les magmas générés à partir d’une source hétérogène seront donc principalement pyroxénitiques, c’est-à-dire davantage sous-saturés en silice. Ainsi, dans le cas d’un mélange de magmas issus d’une source hétérogène, la transition entre les compositions à hypersthène et à néphéline normatifs s’effectue aux alentours de 30-40 % de liquides pyroxénititiques, soit pour environ 20-25 % de pyroxénite dans la source. L’origine de ces lithologies dans le manteau sub-arc est attribuée à la délamination de cumulats à clinopyroxène + amphibole présents à la base de la croute des arcs. Les inclusions magmatiques à néphéline normative d’arc auraient enregistré plusieurs étapes de mélange entre des liquides quasi-purs de clinopyroxénites et des liquides péridotitiques. L’homogénéité de compositions des laves à hypersthène normatif traduirait en revanche, un stade de mélange et de différenciation plus avancé, atténuant ainsi la signature pyroxénitique. / Lavas erupted in subduction zones are dominated by calc-alkaline, hypersthene-normative compositions. However, melt inclusions trapped in magnesian olivines (Fo ≥ 88) from arc basalts often show alkaline, nepheline-normative compositions. Although their trace element compositions are comparable to those of their host lavas, these melt inclusions cannot be simply explained by the typical models for arc lava genesis. The study of melt inclusions from several island arcs from all over the world has emphasized their compositional variability, in particular in calcium and Sc, two elements compatible in clinopyroxene. The coupling of this study with thermodynamic modelling has led to the development of a source model involving the contribution of amphibole-bearing clinopyroxenites at about 1 GPa. Nepheline-normative arc melt inclusions thus underline the source heterogeneity at the origin of arc magmas. Partial melting experiments of amphibole-clinopyroxenite – hydrous peridotite homogeneous mixtures performed at 1 GPa have provided additional information on the origin of silica-undersaturated arc magmas, and also a better understanding of the melting behaviour of the two types of lithologies. For proportions of pyroxenite lower than 50 % in the mixed source, the derived melts show hypersthene-normative compositions that are comparable to peridotite-derived arc lavas. For higher proportions of pyroxenite in the source, the derived magmas become nepheline-normative, calcium-rich, and reproduce the compositional range of the melt inclusions. Fifty percent of mixing corresponds to the limit of orthopyroxene stability. As long as this phase is present in the residue, the generated melts are hypersthene-normative. In addition, the presence of amphibole in the source increases the silica under-saturation of liquids and thus accounts for the extreme enrichment in normative nepheline of some inclusions. Our melting experiments of a homogeneous source have allowed to determine the compositions of magmas derived from a mode realistic melting process, involving a heterogeneous source. As pyroxenites have higher melt productivity than peridotites, most melts produced from a pyroxenite-peridotite mixed source are comparable to those produced by a dominantly pyroxenitic source, i.e., they display normative nepheline compositions. Thus, in the case of mixing of magmas derived from heterogeneous source, the transition between hypersthene- and nepheline-normative compositions occurs for 30-40 % of pyroxenite melts, generated from 20-25 % of pyroxenite in the source. The origin of these lithologies in the subarc mantle is explained by the delamination of lower crustal cumulates consisting of clinopyroxene + amphibole. Nepheline-normative arc melt inclusions would record multi-stage mixing between clinopyroxenite and peridotite melts. In contrast, the compositional homogeneity of hypersthene-normative lavas would reflect a more advanced stage of mixing and differentiation, thereby reducing the pyroxenite signature in derived magmas.

Highly polluted urban storm water from e.g. highways can contain large amounts of heavy metals that may cause harm if they are discharged into recipients. To remove the heavy metals a possible low-cost method that does not require much maintenance, could be the use of reactive filters with filter materials consisting of industrial residues or other cheap mineral based materials. Dissolved metal ions are removed by reactive filters through the processes of ions binding to active sites on the surface of the filter materials, or by formation of insoluble precipitates. The ability of CaO-treated granulated blast-furnace slag, iron oxide coated sand, olivine and nepheline to remove seven heavy metals (Cr, Cd, Cu, Ni, Zn, Pb and Hg) from urban storm water was studied. Initially batch experiments were performed where the effect of pH, dissolved organic carbon (DOC) and dissolved ions on the adsorption efficiency was studied. The experiments were conducted with urban storm water and with a reference solution (10 mM NaNO3), both containing the same concentration of heavy metals (approx. 1 μM). The two materials with the best results were further investigated in a column study, where the capacity of the filter was tested. Chemical equilibrium calculations using the program Visual MINTEQ were performed in order to assess the role of precipitation as a mechanism for removal. The results show that the blast-furnace slag was the most effective filter material and that it has great potential to be used as a heavy metal remover. Also the iron oxide coated sand worked satisfactory. The highest degree of removal was obtained for lead, cadmium and nickel, for which the removal efficiency exceeded 90% after a load of 300 times the water volume in the columns. For some metals, mainly copper, chromium and mercury the dissolved organic matter affected the removal negatively. The chemical mechanisms causing the removal are specific adsorption to the surfaces of the materials, and for the blast-furnace slag probably precipitation of insoluble metal sulfides. / Starkt förorenat dagvatten som rinner av från exempelvis motorvägar, kan innehålla betydliga mängder tungmetaller som kan orsaka skada om de kommer ut i omgivande vattendrag. En billig metod för tungmetallavskiljning, som inte kräver så mycket underhåll, skulle kunna vara att använda reaktiva filtermaterial bestående av restprodukter eller andra mineraliska lågkostnadsmaterial. Reaktiva filter fungerar som metallavskiljare genom att de lösta metalljonerna binder till ytgrupper på filtermaterialen eller att svårlösliga utfällningar bildas. Förmågan att avskilja sju tungmetaller (Cr, Cd, Cu, Ni, Zn, Pb och Hg) ur dagvatten har undersökts för fyra mineraliska filtermaterial, kalciumoxiddopad masugnsslagg, järnoxidsand, olivin och nefelin. Studien inleddes med skakförsök där adsorptionens pH-beroende undersöktes. Försöken gjordes dels med dagvatten, dels med en referenslösning (10 mM NaNO3) med samma tungmetallkoncentration (ca 1μM). Detta gjordes för att studera effekter av löst organiskt material och andra ligander på adsorptionen. Därefter testades de material som uppvisat bäst resultat i skakförsöket i kolonnförsök, ett försök som mer efterliknar en praktisk tillämpning och där filtrets kapacitet kan studeras. Genom kemiska jämviktsberäkningar med programmet Visual MINTEQ var det möjligt att undersöka om bildningen av svårlösliga metallutfällningar bidrog till metallavskiljningen. Resultaten visar att slaggen var det effektivaste filtermaterialet och att detta har stor potential att användas för avskiljning av tungmetaller. Även järnoxidsanden fungerade tillfredsställande. De metaller som avskiljdes bäst var bly, kadmium och nickel, för vilka avskiljningen var &gt; 90 % i kolonnförsöket efter en belastning motsvarande 300 gånger vattenmängden i kolonnerna. För vissa metaller, främst koppar, krom och kvicksilver, försämrades avskiljningen betydligt när löst organiskt material fanns närvarande. Mekanismerna som står för avskiljningen är till störst del adsorption till grupper på filtermaterialens ytor, men bildning av svårlösliga metallsulfider är också tänkbar för slaggen.

Understanding crystallisation in magma chambers is a key challenge for igneous petrology. It is particularly important to understand the origins of layering in peralkaline rocks, e.g. the kakortokite (nepheline syenite), Ilímaussaq Complex, S. Greenland, as these are commonly associated with high value multi-element economic deposits. The kakortokite is a spectacular example of macrorhythmic (>5 m) layering. Each unit consists of three layers comprising arfvedsonite-rich (sodic-amphibole) black kakortokite at the base, grading into eudialyte-rich (sodic-zirconosilicate) red kakortokite, then alkali feldspar- and nepheline-rich white kakortokite. Each unit is numbered -19 to +17 relative to a characteristic well-developed horizon (Unit 0), however there is little consensus on their development. This project applies a multidisciplinary approach through field observations combined with petrography, crystal size distributions (CSDs), mineral and whole rock chemistries on Units 0, -8 to -11 and a phonolite/micro-nephelinolite (“hybrid”) sequence that crosscuts the layered kakortokite. Textures and compositions are laterally consistent across outcrop and indicators of current activity are rare. CSDs indicate in situ crystallisation with gravitational settling as a minor process. Chemical discontinuities occur across unit boundaries. The layering developed through large-scale processes under exceptionally quiescent conditions. The discontinuities reflect open-system behaviour; units were formed by an influx of volatile-rich magma that initiated crystallisation in a bottom layer. Nucleation was initially suppressed by high volatile element concentrations, which decreased to allow for crystallisation of arfvedsonite, followed by eudialyte, then alkali feldspar and nepheline to form each tripartite unit. The chemistry of the hybrid indicates mixing between a primitive (sub-alkaline) magma and kakortokite. Thus injections of magmas of varying compositions occurred, indicating a complex plumbing system below current exposure. The lessons learned at Ilímaussaq, which is extremely well exposed and preserved, are relevant to understanding magma chamber dynamics in the more common instances of pervasively altered peralkaline rocks.