• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 4
  • 2
  • 1
  • 1
  • Tagged with
  • 10
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

The Cambrian manganese deposits of North Wales

Bennett, M. A. January 1987 (has links)
No description available.
2

Determination of Metamorphic Grade for Two Formations of the Huronian Supergroup: Whitefish Falls Area, Ontario

Berger, Ben R. 04 1900 (has links)
<p>Samples from the Whitefish Falls Area were examined petrographically and chemically to determine the regional grade of metamorphism. Mineralogy from the Lorrain formation (quartzities) and Gowganda Formation (argillites) were apparently incongrous. The resolution of this problem formed the major part of the study.</p> <p>Mineralogically the quartzites contained a kyanitequartz paragenesis with a subordinate kyanite-chloritoidquartz paragenesis. The argillites showed a chlorite-biotite -plagioclase-calcite-quartz paragenesis with only minor epidote present. From textural evidence possible reactions were deduced which were used to set the upper and lower limits for pressure and temperature. These boundaries were 470°C and 3.9 kb., lower limit and 550°C with a variable pressure for the upper limit.</p> Chemically, whole rock analysis was used to determine the parameters for various chemographic diagrams. AFM, ACF and AKF plots for the argillites showed a very restrictive composition which excluded the almandine field and promoted the biotite field. The bulk composition of the argillites was cited as the main reason for the inhibition of high grade index minerals, thus appearing to be lower grade than their quartzite counterparts. AFM and AKF diagrams for the quartzites verified their mineralogy and proved their high grade nature. / Thesis / Bachelor of Science (BSc)
3

Variability of Elemental Abundances in the Local Neighborhood and its Effect on Planetary Systems

January 2014 (has links)
abstract: As the detection of planets become commonplace around our neighboring stars, scientists can now begin exploring their possible properties and habitability. Using statistical analysis I determine a true range of elemental compositions amongst local stars and how this variation could affect possible planetary systems. Through calculating and analyzing the variation in elemental abundances of nearby stars, the actual range in stellar abundances can be determined using statistical methods. This research emphasizes the diversity of stellar elemental abundances and how that could affect the environment from which planets form. An intrinsic variation has been found to exist for almost all of the elements studied by most abundance-finding groups. Specifically, this research determines abundances for a set of 458 F, G, and K stars from spectroscopic planet hunting surveys for 27 elements, including: C, O, Na, Mg, Al, Si, S, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Mo, Ba, La, Ce, Nd, Eu, and Hf. Abundances of the elements in many known exosolar planet host stars are calculated for the purpose investigating new ways to visualize how stellar abundances could affect planetary systems, planetary formation, and mineralogy. I explore the Mg/Si and C/O ratios as well as place these abundances on ternary diagrams with Fe. Lastly, I emphasize the unusual stellar abundance of &tau; Ceti. &tau; Ceti is measured to have 5 planets of Super-Earth masses orbiting in near habitable zone distances. Spectroscopic analysis finds that the Mg/Si ratio is extremely high (~2) for this star, which could lead to alterations in planetary properties. &tau; Ceti's low metallicity and oxygen abundance account for a change in the location of the traditional habitable zone, which helps clarify a new definition of habitable planets. / Dissertation/Thesis / Ph.D. Astrophysics 2014
4

The recovery of platinum group metals from low grade concentrates to an iron alloy using silicon carbide as reductant

Malan, Willem du Toit 12 1900 (has links)
Thesis (MEng) -- Stellenbosch University, 2014. / ENGLISH ABSTRACT: In this study, SiC reduction of Rowland and Easterns LG (Low Grade) concentrates was investigated. The purpose of the study was to investigate the feasibility of SiC as reductant with respect to metal fall, PGM grade in the alloy, slag composition, Cr solubility and overall PGM recovery. The integration of such process in the current matte-based collection process was also investigated. Currently, the matted-based collection process is most widely used for PGM recovery, but because PGM containing concentrates are becoming more enriched with UG2 (Upper Group 2) LG concentrates, it is expected to be integrated or replaced with an alloy collection process. This kind of process offers greater flexibility to the different types of ore that could be used. The process is chromium tolerant and environmentally friendly. For this purpose Rowland and Easterns UG2 LG Concentrate samples from Lonmin Western Platinum Limited were analysed with XRD, XRF and ICP-MS and it was found that SiO2 and MgO are the most abundant oxides and Pd is the most abundant element from the PGMs. Sulphide bearing minerals such as chalcopyrite were detected in low concentrations (below 1 %) and Cr2O3 concentrations are between 2 – 4 %. The FeO/SiO2 ratio was lower in Rowland LG concentrate. SiC reduction of Rowland and Easterns concentrate was done at 1600℃. Reductant to concentrate ratios for laboratory scale experiments were ranged from 2.5 to 3.5 kg SiC / 100 kg concentrate. SiC reduction of Rowland concentrate had different reduction times. The duration of reduction experiments ranged from 30 - 180 min. PGM recoveries from SiC reduction of Rowland concentrate were very poor (below 10 %) and Fe recoveries were lower than 50 %. A slag viscosity at the end of the melt of more than 4 poise was responsible for poor phase separation. SEM images revealed metal prills entrained in the slag phase instead of settling and combining to the alloy globule at the bottom of the crucible. However, PGM recoveries from SiC reduction of Easterns concentrate was significantly better. More than 85 % of Ir and Pd and almost 60 % of Pt were recovered in a test with a reductant to concentrate ratio of 3.5 kg SiC / 100 kg Easterns concentrate. Fe recovery was also the highest at 66%. Cr and Si concentrations were below 5 % in total. The slag viscosity at the end of melt was calculated to be less than 4 poise and a SEM image of a slag sample revealed few entrained metal prills. After the above findings on the importance of viscosity, it was decided to increase the FeO content in the initial concentrate charge in order to decrease slag viscosity, increase metal fall (PGM collecting phase) and further increase PGM recovery. Peirce-Smith converter slag was used for this purpose. A test was conducted with the addition of 10 kg converter slag / 100 kg Easterns concentrate. The reductant to concentrate ratio was kept at 3.5 kg SiC / 100 kg Easterns concentrate. The results revealed that Ir and Pd recoveries were more than 95%, while Pt recovery was almost 70%. Fe recovery increased to 76 %. On the basis of the results from the test, an optimum feed ratio between Easterns LG concentrate, Rowland concentrate and Peirce-Smith converter slag was calculated. Thermodynamic phase equilibrium calculations predicted that the concentrate charge should consist of 60 - 80% Easterns concentrate with a slag addition of 30 – 40 kg converter slag / 100 kg LG concentrate. SiC reduction of this optimum LG concentrate charge is expected to recover more than 90% of all PGMs. Cr and Si concentrations in the alloy will be below 1 % in total. The amount of converter slag as an addition will be however limited by final PGM grade in the alloy, furnace slag quantities recycled and slag resistivity required in the alloy furnace. The effectiveness of SiC as reductant was also compared to C reduction. C reduction of an optimum concentrate charge had a marginally higher metal fall at the same reductant to concentrate ratio than SiC reduction of an optimum concentrate charge. However, gas emissions are on average 3 times higher for C reduction of a concentrate charge and C reduction requires at least 300 MJ more to smelt 1 ton of LG concentrate than SiC reduction. This is mostly due to C reacting endothermically with FeO to produce Fe(l) and CO(g) in contrast to SiC reacting exothermically with FeO to produce Fe(l), SiO2(l) and CO(g). Integrating SiC reduction of LG concentrates into the existing smelting route at Lonmin was also proposed through a process flow diagram. From an economic point of view, it was found that SiC reduction of 1 ton of LG concentrate charge with a converter slag addition requires almost 700 MJ more than the smelting of a UG2 blended concentrate to produce a matte phase. However it must be taken into account that the sulphide rich layers in the Bushveld complex are being depleted rapidly and alternative processes such as SiC reduction and alloy collection process will be utilized faster than expected. Moreover, gas emissions from reductive smelting is considerably lower, hence it is a more environmentally friendly process. Finally, from the findings of this study, it could be said that base metals and PGMs could be recovered in an iron alloy from SiC reduction of LG concentrate with converter slag additions. Therefore integrating such a process into the matte-based collection process could be considered as a future alternative to smelting UG2 LG concentrates. / AFRIKAANSE OPSOMMING: In hierdie studie, word SiC reduksie met Rowland en Oostelikes LG (Lae Graad) konsentrate ondersoek. Die doel van die studie was om die doeltreffendheid van SiC as reduktant te ondersoek met betrekking tot metaalval, PGM graad in die allooi, slaksamestelling (spesifiek word daar gekyk na Cr oplosbaarheid) en algehele PGM herwinning. Die integrasie van die proses in die huidige mat-gebaseerde versamelingproses word ook ondersoek. Tans word die mat-gebaseerde versamelingproses die algemeenste gebruik om PGM'e te kollekteer, maar omdat PGM konsentrate al hoe meer verryk word met UG2 (Upper Group 2) LG konsentrate, word daar verwag dat dit geïntegreer of vervang gaan word met 'n allooi-versamelingproses. Hierdie tipe proses bied groter buigsaamheid om die verskillende reekse van erts wat gebruik kan word. Die proses kan ook chroom hanteer en is omgewingsvriendelik. Vir hierdie doel was Rowland en Oostelikes UG2 LG konsentraatmonsters van Lonmin Western Platinum Limited ontleed met XRD, XRF en ICP -MS en met die ontleding was daar gevind dat SiO2 en MgO die volopste oksides was en dat Pd die volopste elemente van die PGMe was. Sulfiedminerale soos chalkopiriet is in lae konsentrasies opgespoor (minder as 1%) en Cr2O3 konsentrasies is tussen 2-4 %. Die FeO/SiO2 verhouding was laer in Rowland konsentraat. SiC reduksie van Rowland en Oostelikes konsentrate is teen 1600 ℃ uitgevoer. Die reduktant tot konsentraat verhouding vir laboratoriumskaal eksperimente het gewissel van 2.5 – 3.5 kg SiC / 100 kg konsentraat. SiC reduksie van Rowland LG konsentraat het verskillende reduksie tye gehad. Die duur van die reduksie eksperimente het gewissel van 30-180 min. PGM herwinning van SiC reduksie met Rowland konsentreer was baie laag (onder 10 %) en Fe herwinning was minder as 50%. 'n Slakviskositeit aan die einde van die smelt was hoër as 4 poise en was verantwoordelik vir die swak skeiding van fases. SEM beelde het gewys dat fyn metaalstukkies opgehou was in die slakfase in plaas daarvan dat dit vestig en kombineer met die allooibolletjie aan die onderkant van die smeltkroes. In teenstelling was die PGM herwinning van SiC reduksie met Oostelikes konsentraat aansienlik beter. Meer as 85 % van Ir en Pd was herwin en byna 60% van Pt was herwin tydens 'n toets met 'n reduktant tot konsentraat verhouding van 3.5 kg SiC / 100 kg Oostelikes konsentraat. Fe herwinning was 66% en was ook die hoogste van al die eksperimente. Cr en Si konsentrasies was minder as 5 % in totaal. Die slakviskositeit aan die einde van smelt was bereken en is minder as 4 posie. 'n SEM beeld van 'n slakmonster het baie min vasgevangde metaalstukkies getoon. Na afloop van die bogenoemde bevindinge oor die belangrikheid van viskositeit, was daar besluit om die FeO inhoud van die aanvanklike konsentraat te verhoog. Dit was gedoen om die slakviskositeit te verminder, die metaalval (PGM kollektering fase) te verhoog en sodoende die PGM herwinning verder te verbeter. Vir die doel was Peirce -Smith omskakelaarslak gebruik. ʼn Toets was uitgevoer met die toevoeging van 10 kg omskakelaarslak / 100 kg Oostelikes konsentraat. Die reduktant tot konsentraat verhouding was behou by 3.5 kg SiC / 100 kg Oostelikes konsentraat. Die resultate het getoon dat meer as 95 % van Ir en Pd herwin was, terwyl byna 70 % Pt herwin was. Die Fe herwinning het toegeneem tot 76%. Op grond van die resultate van die toets, is 'n optimale verhouding tussen Oostelikes konsentraat, Rowland konsentraat en Peirce -Smith omskakelaarslak bereken. Termodinamiese modellering voorspel dat die begin LG konsentraat voer uit 60 – 80 % Oostelikes konsentraat moet bestaan, met 'n slak toevoeging van 30 – 40 kg omskakelaarslak / 100 kg LG konsentraat. Daar word verwag dat meer as 90 % van PGM'e herwin sal word vanaf SiC reduksie met ʼn optimum LG konsentraat voer. Cr en Si konsentrasies in die allooi sal minder as 1% in totaal wees. Die hoeveelheid slak wat bygevoeg kan word sal egter beperk word deur die finale PGM graad in die allooi, oond-slak hoeveelhede wat herwin kan word en slakweerstand wat benodig word in die allooi-oond. Die effektiwiteit van SiC as reduktant is ook vergelyk met C reduksie. C reduksie van ʼn optimale konsentraatvoer het 'n effens hoër metaalval wanneer dieselde reduktant tot konsentraat verhouding behou was vir SiC reduksie van 'n optimale konsentraatvoer. Gas hoeveelhede van C reduksie is gemiddeld 3 keer meer en vereis te minste 300 MJ meer om 1 ton LG konsentraat te smelt. Dit is hoofsaaklik te wydte aan C wat endotermies reageer met FeO om Fe (l) en CO (g) te produseer, in teenstelling met SiC wat eksotermies reageer met FeO om Fe (l), SiO2(l) en CO (g) te produseer. Integrasie van SiC reduksie met LG konsentrate in die bestaande smeltroete by Lonmin Western Platinum Limited is ook voorgestel deur 'n proses vloeidiagram. Uit 'n ekonomiese oogpunt, is daar gevind dat SiC reduksie van 1 ton LG konsentraatvoer met 'n omskakelaarslak byvoeging ongeveer 700 MJ meer benodig as om 1 ton UG2 gemengde konsentraat te smelt en 'n mat-fase te produseer. Dit moet wel in ag geneem word dat die sulfied ryk lae in die Bosveld-kompleks vinnig uitgeput word en dat hierdie alternatiewe prosesse soos SiC reduksie en ʼn allooiversameling proses vinniger as verwagtend benut sal word. Verder, gas hoeveelhede van SiC reduksie is laer en daarom is dit 'n meer omgewingsvriendelik proses. Ten slotte, vanaf die bevindinge van hierdie studie, kan dit gesê word dat basismetale en PGM'e in 'n ysterallooi herwin kan word deur middel van SiC reduksie met LG konsentrate en die toevoeging van omskakelaarslak. Daarom kan die integrasie van so 'n proses in die huidige mat-gebaseerde versameling proses beskou word as 'n alternatief vir die toekoms om UG2 LG konsentrate te smelt.
5

Effect of iron endpoint during Peirce-Smith converting on matte mineralogy and downstream processing of base and platinum-group metals

Thyse, Elton Llyle 12 1900 (has links)
Thesis (PhD) -- Stellenbosch University, 2014. / ENGLISH ABSTRACT: The process route for the production of base and platinum-group metals from natural sulfide ores commonly requires the conversion of high-iron furnace matte into an iron-lean converter matte. This is followed by pre-treatment through cooling of the iron-lean molten matte, physical processing of the solidified matte and hydrometallurgical metal extraction. Lonmin is the third largest producer of platinum-group metals in the world and utilizes Peirce-Smith converters for blowing high-iron furnace matte with air to a final iron concentration or endpoint. The molten matte is water granulated and solidification occurs via fast-cooling. The solidified matte is ground in a closed circuit ball mill with hydrocyclone classification and subjected to first stage atmospheric leaching. The specification of an ideal or desirable converter iron endpoint requires careful consideration. Most importantly, it must ensure the crystallization of converter matte with mineralogical qualities that are within the setpoints of the downstream unit processes and techniques. An additional consideration is for the final blown converter matte to achieve an optimum bulk concentration of the base metals Ni and Cu and platinum-group metals Pt, Pd, Rh, Ru and Ir. Mattes characteristic of variable iron endpoints were regularly produced at the Lonmin converter plant section. Uncertainty by plant metallurgists in knowing the desirable iron endpoint, particularly within the context of the Lonmin base metal refinery, and poor control has had detrimental effects on the mineralogical quality of the final matte and hence on the processing characteristics of the solidified matte particles downstream. A desirable iron endpoint required investigation, selection and implementation at Lonmin. The primary focus of this study was therefore to quantify the effect of a specific iron endpoint on the mineralogy and mineral chemistry of solidified converter matte. A fundamental examination of the solidification process upon cooling was regarded as critical to an in-depth understanding of the attained mineralogy and mineral chemistry as a function of a specific iron endpoint. It became equally important to quantify the effect of the resultant mineralogy, and hence iron endpoint, on the physical property of mineral structures in relation to downstream grinding, liberation and leaching characteristics. Despite considerable industry context, limited in-depth and coherent studies on the effect of a specific iron endpoint on fast-cooled converter matte systems were found in both industrial and scholarly literature. Previous findings in literature offered a limited quantitative understanding of the effect on mineralogy and mineral chemistry. Phase and cooling equilibria of multi-component, iron endpoint specific Ni-Cu-S matte systems were also not fully available. These would have been particularly useful in understanding the complexities of converter matte solidification as a function of iron endpoint. Physical property knowledge of converter matte mineral structures was hardly available and even less so in relation to grinding, liberation and leaching processes. A comprehensive investigation was therefore required to address these extensive knowledge gaps with respect to fastcooled converter matte systems in an industrial framework. Three Peirce-Smith converter production samples, representative of the extent in variability of iron endpoints attained at the converter plant, were used in a systematic investigation coupled to a novel combination of modern analytical techniques, computational thermochemistry and metallurgical testwork. The modern analytical techniques included the application of high resolution transmission electron microscopy and focused ion beam scanning electron microscopy tomography. Computational thermochemistry was applied through the use of MTDATA phase diagram software. Metallurgical testwork involved laboratory batch grinding at various specific energies. Closely associated leach experiments were also considered relevant to this wide-ranging investigation. The Peirce-Smith converter samples investigated were indicative of mattes that attained specific endpoints of 5.17%, 0.99% and 0.15 weight% Fe. The highest combined bulk concentration of the important base and platinum-group metals was achieved in the matte which attained a specific iron endpoint of 0.99%. The mineralogy of all three converter mattes was dominated by nickel sulfide mineral structures matched to the natural mineral of heazlewoodite. Mineral structures of copper sulfide, NiCu-alloy, spinel and OsRu-alloy were also constituents of the different converter mattes. The attainment of a specific iron endpoint was found to result in measurable mineralogical differences with respect to relative mineral abundances, external morphological characteristics and mineral chemistry. The mineralogical differences were particularly distinct between mineral structures of the high (5.17%) and low (0.99% and 0.15%) iron mattes. Subtle mineralogical differences were evident between mineral structures of the low iron mattes. The 0.99% Fe matte was characteristic of a significantly higher NiCu-alloy relative abundance, compared to the 5.17% Fe matte. The NiCu-alloy structures were found to act as the primary collectors of the economically significant platinum-group metals. Mineralogical observations were used to develop an understanding of the underlying mineralization mechanism of NiCu-alloy structures. High-fidelity color and grayscale 3D reconstructions were produced of the resultant mineralized structures. It was shown theoretically that variations in iron endpoint specific starting compositions of oxygen-free liquid matte systems alter the solidification pathway towards the eutectic. Moreover, a quantitative understanding of liquid phase solidification of the high and low iron matte systems, including oxygen, was developed to within ±2.5 oC. Most of the specific energy available for grinding was expended breaking the nickel sulfide matrix, particularly of the high iron matte. The breakage rates of copper sulfide mineral structures in the 5.17% Fe matte were calculated to be higher than in the 0.15% Fe matte at 25kWh/t specific energy. The degree of copper sulfide liberation was shown to be higher for the 5.17% Fe matte than for the 0.15% Fe matte at the same specific energy of grinding. A higher degree of Ni extraction and Cu cementation could be achieved when leaching low iron matte particles. The production of converter matte attaining a specific iron endpoint of 0.99% was found to be the most suitable with respect to endpoint selection criteria. A practical iron endpoint range of 1.6% to 1.0% was recommended for the production of converter matte with a resultant mineralogical quality within the constraints of the Lonmin base metal refinery. This study offers an integrated understanding of base and platinum-group metals production as a function of a desirable iron endpoint at Lonmin. This was not previously available in metal production literature. New technology for the monitoring and consistent control of such a practical iron endpoint range can subsequently be implemented. / AFRIKAANSE OPSOMMING: Die prosesroete vir die produksie van onedel en platinumgroepmetale uit natuurlike swawelertse vereis gewoonlik die omsetting van ’n ysterryke hoogoondmat in ’n ysterarm omsettermat. Hierna volg voorbehandeling deur die afkoeling van die ysterarm gesmelte mat, fisiese verwerking van die soliede mat, en hidrometallurgiese metaalekstraksie. Lonmin is die derde grootste produsent van platinumgroepmetale ter wêreld en gebruik Peirce-Smith-omsetters om ysterryke hoogoondmat met lug te blaas totdat dit ’n finale ysterkonsentrasie- of ystereindpunt bereik. Die gesmelte mat word met water granuleer, en solidifikasie vind deur middel van snelafkoeling plaas. Die soliede mat word in ’n geslotekringbalmeul met hidrosikloonklassifikasie gemaal en aan eerstestadium- atmosferiese loging onderwerp. Die spesifikasie van ’n ideale of gewenste ystereindpunt verg deeglike oorweging. Bowenal moet dit verseker dat die omsettermat kristalliseer met mineralogiese eienskappe wat binne die setpunte van die eenheidsprosesse en - tegnieke verder af in die prosesstroom val. ’n Bykomende oorweging is dat die uiteindelike geblaasde omsettermat ’n optimale massakonsentrasie van die onedel metale Ni en Cu en die platinumgroepmetale Pt, Pd, Rh, Ru en Ir moet bevat. Matte met die kenmerke van wisselende ystereindpunte is gereeld by die Lonminomsetteraanleg geproduseer. Die onsekerheid van metallurge by die aanleg oor die gewenste ystereindpunt – veral binne die konteks van die Lonmin-raffinadery vir onedel metale – sowel as swak beheer het ’n nadelige uitwerking gehad op die mineralogiese gehalte van die uiteindelike mat, en dus ook op die verwerkingskenmerke van die soliede matdeeltjies verder af in die prosesstroom. Die bepaling van die gewenste ystereindpunt het sorgvuldige ondersoek, seleksie en toepassing deur Lonmin vereis. Hierdie studie is dus hoofsaaklik uitgevoer om die uitwerking van ’n spesifieke ystereindpunt op die mineralogie en minerale chemie van soliede omsettermat te kwantifiseer. ’n Grondliggende ondersoek na die solidifikasieproses by afkoeling is as noodsaaklik beskou vir ’n diepgaande begrip van die verworwe mineralogie en minerale chemie as ’n funksie van ’n spesifieke ystereindpunt. Mettertyd het dit egter ewe belangrik geword om die uitwerking van die gevolglike mineralogie, en dus die ystereindpunt, op die fisiese eienskappe van minerale strukture met betrekking tot maling-, vrystellings- en loogprosesse verder af in die prosesstroom te kwantifiseer. Ondanks heelwat bedryfskonteks, het nóg bedryfs- nóg vakkundige literatuur veel diepte- en samehangende studies oor die uitwerking van ’n spesifieke ystereindpunt op snelafgekoelde omsettermatstelsels opgelewer. Vorige bevindinge in die literatuur het boonop ’n beperkte kwantitatiewe begrip van die uitwerking op mineralogie en minerale chemie getoon. Die fase- en afkoelingsekwilibriums van ystereindpuntspesifieke Ni-Cu-S-matstelsels met veelvuldige komponente was ook nie ten volle beskikbaar nie. Dít sou veral goed te pas gekom het om die kompleksiteite van omsettermatsolidifikasie as ’n funksie van ystereindpunt te verstaan. Kennis van die fisiese eienskappe van die minerale strukture van omsettermat was kwalik beskikbaar, terwyl selfs minder inligting oor maling-, vrystellings- en loogprosesse opgespoor kon word. Daarom was ’n omvattende ondersoek nodig om hierdie beduidende kennisleemtes met betrekking tot snelafgekoelde omsettermatstelsels in ’n nywerheidsraamwerk aan te vul. Drie Peirce-Smith-omsetterproduksiemonsters wat die wisselende bestek van ystereindpunte by die omsetteraanleg verteenwoordig, is in ’n stelselmatige ondersoek gebruik, tesame met ’n vernuwende kombinasie van moderne ontledingstegnieke, gerekenariseerde termochemiese bewerkings en metallurgiese toetswerk. Die moderne ontledingstegnieke sluit onder andere in hoëresolusie-transmissie-elektronmikroskopie (HRTEM) en gefokusdeioonstraalskandering-elektron-mikroskopie (FIB SEM) tomografie. Die gerekenariseerde termochemiese bewerkings is met behulp van MTDATAfasediagramsagteware uitgevoer. Metallurgiese toetswerk het die maling van laboratoriumlotte teen verskillende spesifieke energieë behels. Nou verwante loogproefnemings is ook as relevant vir hierdie omvattende studie beskou. Die bestudeerde Peirce-Smith-omsettermonsters het op matte met spesifieke eindpunte van 5.17%, 0.99% en 0.15 gewig% Fe gedui. Die hoogste gekombineerde massakonsentrasie van die belangrike onedel en platinumgroepmetale is in die mat met ’n spesifieke ystereindpunt van 0.99% gevind. Die mineralogie van ál drie omsettermatte is oorheers deur die minerale strukture van nikkelsulfied, wat met die natuurlike mineraal heazlewoodiet ooreenstem. Die verskillende omsettermatte het ook die minerale strukture van kopersulfied, NiCu-allooi, spinel en OsRu-allooi bevat. Daar is bevind dat die verkryging van ’n spesifieke ystereindpunt tot meetbare mineralogiese verskille in die relatiewe volopheid van minerale, die eksterne morfologiese kenmerke sowel as minerale chemie lei. Die mineralogiese verskille was veral duidelik te sien tussen die minerale strukture van die ysterryke (5.17% Fe) en ysterarm (0.99% en 0.15% Fe) matte. Fyn mineralogiese verskille is ook tussen die minerale strukture van die ysterarm matte bespeur. Die 0.99% Fe-mat het tipies beduidend meer NiCu-allooi as die 5.17% Fe-mat bevat. Die NiCu-allooistrukture tree oënskynlik op as die hoofversamelaars van die ekonomies belangrike platinumgroepmetale. Mineralogiese waarnemings is gebruik om ’n begrip te ontwikkel van die onderliggende mineralisasiemeganisme van NiCuallooistrukture. Die gevolglike gemineraliseerde strukture is met behulp van driedimensionele rekonstruksies met hoë kleurgetrouheid sowel as in grysskaal voorgestel. Daar is teoreties aangetoon dat variasies in ystereindpuntspesifieke beginsamestellings van suurstofvrye vloeibare matstelsels die solidifikasieroete na die eutetikum wysig. Daarbenewens is die vloeifasesolidifikasie van die ysterryke en ysterarm matstelsels, wat suurstof insluit, op sowat ±2.5 oC gekwantifiseer. Die meeste van die spesifieke energie wat vir maling beskikbaar was, is gebruik om die nikkelsulfiedmatriks te breek, veral vir die ysterryke mat. Berekeninge toon dat die breektempo’s van die minerale strukture van kopersulfied by die 5.17% Fe-mat hoër was as by die 0.15% Fe-mat teen ’n spesifieke energie van 25 kWh/t. Die mate van kopersulfiedvrystelling was hoër by die 5.17% Fe-mat as by die 0.15% Fe-mat by dieselfde spesifieke energie vir maling. ’n Hoër mate van Ni-ekstraksie en Cu-sementasie is verkry toe ysterarm matdeeltjies geloog is. Wat eindpuntseleksiemaatstawwe betref, is die produksie van ’n omsettermat met ’n spesifieke ystereindpunt van 0,99% as die mees geskikte aangewys. ’n Praktiese ystereindpuntbestek van 1.6% tot 1.0% word aanbeveel vir die produksie van ’n omsettermat met ’n gevolglike mineralogiese gehalte wat binne die perke van die Lonmin-raffinadery vir onedel metale val. Hierdie studie bied ’n geïntegreerde begrip van die produksie van onedel en platinumgroepmetale as ’n funksie van ’n gewenste ystereindpunt by Lonmin. Hierdie inligting was nie voorheen in literatuur oor metaalproduksie beskikbaar nie. Nuwe tegnologie vir die monitering en konsekwente beheer van so ’n praktiese ystereindpuntbestek kan dus op grond hiervan in werking gestel word.
6

The Relationship of Initial Flooding Depositional Facies to Global Sea Level and Climate on The Marion Plateau, NE Australia (ODP Leg 194)

Ciembronowicz, Katherine T 26 March 2007 (has links)
The Coral Sea has been the host to a variety of large carbonate platforms over the geologic past and presently hosts the world's largest system of coral reefs, the Great Barrier Reef, stretching more then 2,300 km along Australia's northeast coast. The Marion Plateau, which today is the site of 400 m deep hemipelagic sediment drifts, once supported two large carbonate platforms that were precursors to reef growth on the central and southern Great Barrier Reef. Previous work examining the growth phases, drownings and rejuvenation of these platforms is extensive. The purpose of this research is to examine the factors controlling the earliest sedimentation on the margin and how it influenced early development of the carbonate platforms. One hundred and eighty-three samples were taken from the base of Hole 1195 B, that was drilled during the Ocean Drilling Program's Leg 194. Analyses were performed using x-ray diffraction on the bulk powder and decalcified less than 2um size fraction smear slides. Four distinct sedimentary facies were defined on the basis of mineralogy and constituent grains. The initial marine transgression of the Marion Plateau was not a straightforward one where a shallow-water margin gradually transitioned into a deep-water margin. Instead, sediments record a complex history of unconformities, hardgrounds, and discrete sedimentary units. The initial flooding was complex as a result of its initially shallow depth at a time characterized by several glacio-eustatic sea-level changes. The data indicate that eustasy has been the strongest control on sediment deposition and clay mineral patterns on the Plateau. Falling sea level resulted in periods of increased detrital input and limited soil formation. Also, a decreasing kaolinite trend in the early Miocene, during a rising sea level, indicates that clays forming on land as a result of climate were not transported out onto the plateau.
7

Characterization of lunar crust with moon mineralogy mapper data

Sun, Ying 09 June 2015 (has links)
Indiana University-Purdue University Indianapolis (IUPUI) / This dissertation has three main focuses: (1) identify the distribution of a new rock type (Mg-spinel lithology) on the Moon and explore the likely petrogenesis of Mg-spinel; (2) investigate the presence of olivine in the crater central peaks and analyze the sources of olivine; (3) determine the compositional variations of lunar crust with depth, and establish a new model to describe the structure of the lunar crust.
8

Assessment of lime treatment of expansive clays with different mineralogy at low and high temperatures

Ali, Hatim, Mohamed, Mostafa H.A. 12 December 2019 (has links)
Yes / This paper examines the impacts of clay mineralogy on the effectiveness of lime stabilisation at different temperatures. A comprehensive experimental programme was conducted to track down the evolution of lime-clay reactions and their durations through monitoring the evolution of strength gain at predetermined times using the Unconfined Compressive Strength (UCS) test. The study examined clays with different mineralogy compositions comprising Na+ Bentonite and Ball (Kaolinite) clay. Four different clays were tested including 100% bentonite, 100% Ball clay and two clay mixtures with ratios of 1:1 and 1:3 by mass of bentonite to Ball clay. All clays were treated using a range of lime content up to 25% and cured for a period of time up to 672 h at two different temperatures of 20 and 40 °C. The results showed that the continuity of the fast phase (stage 1) of strength gain was dependent on the availability of lime in particular at the higher temperature. Whereas, for the same lime content, the duration of the fast phase and the kinetic of strength gain were significantly related to the clay mineralogy and curing temperature. Except for the initial strength gain at 0 h curing time, the lime-treated Ball clay specimens at 20 °C appeared to show no strength gain throughout the curing period that extended up to 672 h. However, when curing occurred at 40 °C, the no strength gain stage only lasted for 72 h after which a gradual increase in the strength was observed over the remaining curing period of time. The addition of Bentonite to Ball clay succeeded in kicking off the strength gain after a short period of curing time at both curing temperatures.
9

Petrology of Some Early Tertiary Lavas of the Kettle River Region, British Columbia

Church, Barry Neil 09 1900 (has links)
Information provided by previous workers shows a considerable diversification of lava types in the early Tertiary deposits of the Kettle River region of British Columbia. The aim of the present study is to establish, on the basis of mineralogical and chemical evidence, whether or not these lavas form a single magma series. A suitable spectrochemical technique was adapted for the determination of Sr, Ba, CaO, MgO, and FeO in rock samples and mineral extracts. A method based on the work of Shaw and Filby, using lanthanum as an internal standard for determination of Sr, Ba, and Ca, is extended to include the determination of MgO and FeO. Extension of the available chemical data was possible using a fused glass bead technique for refractive index determination of the lavas. In view of good correlation between refractive index and the most refractory constituents of the lavas CaO, MgO, and FeO, the refractive index serves as a good magmatic differentiation index. Examination of the refractive indices of three suites of samples, taken from widely separated points within the Kettle River region, shows that the lavas range from semi-basic to acid composition with intermediate types, andesites and trachyandesites, predominating. There is a marked paucity of basaltic rocks. The stratigraphic distribution of the lavas reveals no consistant trends toward either acid or basic compositions; neither is there any relation between stratigraphic position and lava types within the region concerned. In spite of close age and spatial association of the lavas, petrological evidence points to a three-fold division of these rocks (termed 'A', 'B' , and 'C' series). 'A' series is similar to the silica-enrichment 'calc-alkali' trend showing regular mineral and chemical progression from andesites to latite and rhyolite. 'B' series is characterized by a somewhat less well defined group of two-feldspar lavas, trachyandesites, and trachytes. An unusual undersaturated lava, termed 'analcite rhomb-porphyry' or 'shackanite' is thought to be genetically related to 'B' series but probably belongs to a poorly developed semi-basic alkali trend, 'C' series. A mechanism involving crystal fractionation of hornblende, or alternately, augite and plagioclase, is envisaged as the probable mode of origin for many of the rocks of 'A' series. On the other hand, Daly's view that the shackanite lavas were formed as a result of limestone assimilation is supported by field evidence as well as mineral and chemical data. The rocks of 'B' series, the trachyandesites and trachytes, are intermediate in composition to 'A' and 'C' series and have probably formed by process of crystal fractionation in consequence of normal cooling conditions and limestone assimilation. / Thesis / Master of Science (MSc)
10

O estudo da amalgama na obra Arte de los metales de Álvaro Alonso Barba e sua contribuição para o desenvolvimento da mineração na América

Oliveira, Antonio Rodrigues de 20 May 2009 (has links)
Made available in DSpace on 2016-04-28T14:16:40Z (GMT). No. of bitstreams: 1 Antonio Rodrigues de Oliveira.pdf: 545352 bytes, checksum: ac08c69a64ea40e5a486db97de237973 (MD5) Previous issue date: 2009-05-20 / Secretaria da Educação do Estado de São Paulo / This dissertation is related to the analysis of the work De Los Metales Art and its influence in improving the knowledge of mineralogy and metallurgy. As the original Spanish, this work was translated by us, based on terms used in mining at the end of the sixteenth century and early seventeenth century. This work highlighted by the disclosure and publication in several languages, bringing an improvement and development in the metallurgy, in all countries working with mining of gold and silver. With it, the newly discovered American colonies also have great influence, because at the time were the largest suppliers of gold and silver to European countries. Written by Álvaro Alonso Barba, established some relationships between texts of previous mining and contemporary to it, since he came to explain and improve points until then were not very clear. We talk about the technical work Barba, showing the improvement he succeeded in mining and in favor of silver, with greater recovery and less expense. Some aspects of social problems, political and financial that occurred between the Spanish colonies and Spain at the end of the sixteenth century are also studied with the aim of showing the environment in which this work was produced and to check its influence / Esta dissertação está relacionada com a análise da obra Arte De Los Metales e sua influência na melhoria do conhecimento da mineralogia e metalurgia. Sendo o original em espanhol, esta obra foi por nós traduzida, com base em termos utilizados na mineração no final do século XVI, início do século XVII. Esta obra destacou-se pela divulgação e publicação em vários idiomas, trazendo um aprimoramento e desenvolvimento para a metalurgia, em todos os países que trabalhavam com mineração de ouro ou prata. Com ela, as colônias americanas recém-descobertas também sofreram grande influência, pois eram na época as maiores fornecedoras de ouro e prata para países europeus. Escrita por Álvaro Alonso Barba, estabeleceu algumas relações entre textos de mineração anteriores e contemporâneos a ela, haja vista que veio explicar e melhorar pontos que até então não estavam muito claros. Abordaremos os trabalhos técnicos de Barba, evidenciando a melhoria que ele conseguiu na mineração e no benefício da prata, com maior aproveitamento e menor gasto. Alguns aspectos sobre os problemas sociais, políticos e financeiros que ocorriam entre as colônias espanholas e a Espanha no final do século XVI são também estudados com o objetivo de mostrar o ambiente em que foi produzida esta obra e para verificar sua influência

Page generated in 0.0761 seconds