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  • Articles  (19)
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  • 1
    ISSN: 1432-1866
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Abundant and diverse platinum-group minerals (PGM) occur throughout the Tertiary layered intrusion on Rum, Scotland. In this paper we document the distribution of PGM within the Eastern Layered Series (ELS) on Rum, which comprises 16 alternating units of olivine-dominant feldspathic peridotite grading to plagioclase-dominant allivalite. The PGM occur in six main chrome-spinel layers in the Eastern Layered Series and are clearly associated with minor concentrations of interstitial sulphides. Common PGM phases include: Pd–Cu alloys, Pt–Fe alloys, native Pt, laurite, moncheite, sperrylite, isomertiete, cooperite and braggite along with a large number of other less common arsenide, bismuthotelluride and sulphide phases. Analyses of the discrete chromitite layers yield up to ΣPGE + Au 2618 ppb. Although present throughout the 750-m-thick ELS, there are clear stratigraphical changes in the PGM assemblage. The presence of PGM in the ELS on Rum are interpreted as being caused by mantle melting associated with the proto-Icelandic `hot spot', followed by localised concentration because of the combined effects of magma mixing, sulphide-silicate liquid immiscibility and fractional crystallisation. Most of the PGM are magmatic in origin but some grains show evidence of hydrothermal alteration.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 14 (1979), S. 448-454 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is confirmed that the loss of HO· from the molecular ion of o-nitrotoluene involves exclusively a hydrogen from the methyl group. However, in higher homologues hydrogen atoms from non-benzylic sites are also implicated. With such compounds this fragmentation mode is shown not only by the ortho but, to a lesser extent, by the meta and para isomers as well. The proportion of the total ion current borne by the [M - 17]+ ion follows the order ortho 〉 meta 〉 para, which is attributed to substituent migration around the ring with a hydroxyl radical only being lost when the groups are on adjacent ring atoms. Other ions present in the spectra point to interaction between substituents to form a new heterocyclic ring.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2018
    Description: 〈p〉Chlorite is a key mineral in the control of reservoir quality in many siliciclastic rocks. In deeply buried reservoirs, chlorite coats on sand grains prevent the growth of quartz cements and lead to anomalously good reservoir quality. By contrast, an excess of chlorite – for example, in clay-rich siltstone and sandstone – leads to blocked pore throats and very low permeability. Determining which compositional type is present, how it occurs spatially, and quantifying the many and varied habits of chlorite that are of commercial importance remains a challenge. With the advent of automated techniques based on scanning electron microscopy (SEM), it is possible to provide instant phase identification and mapping of entire thin sections of rock. The resulting quantitative mineralogy and rock fabric data can be compared with well logs and core analysis data. We present here a completely novel Quantitative Evaluation of Minerals by SCANning electron microscopy (QEMSCAN®) SEM–energy-dispersive spectrometry (EDS) methodology to differentiate, quantify and image 11 different compositional types of chlorite based on Fe : Mg ratios using thin sections of rocks and grain mounts of cuttings or loose sediment. No other analytical technique, or combination of techniques, is capable of easily quantifying and imaging different compositional types of chlorite. Here we present examples of chlorite from seven different geological settings analysed using QEMSCAN® SEM–EDS. By illustrating the reliability of identification under automated analysis, and the ability to capture realistic textures in a fully digital format, we can clearly visualize the various forms of chlorite. This new approach has led to the creation of a digital chlorite library, in which we have co-registered optical and SEM-based images, and validated the mineral identification with complimentary techniques such as X-ray diffraction. This new methodology will be of interest and use to all those concerned with the identification and formation of chlorite in sandstones and the effects that diagenetic chlorite growth may have had on reservoir quality. The same approach may be adopted for other minerals (e.g. carbonates) with major element compositional variability that may influence the porosity and permeability of sandstone reservoirs.〈/p〉
    Print ISSN: 0375-6440
    Electronic ISSN: 2041-4927
    Topics: Geosciences
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  • 4
    Publication Date: 2018-12-21
    Description: Chlorite is a key mineral in the control of reservoir quality in many siliciclastic rocks. In deeply buried reservoirs, chlorite coats on sand grains prevent the growth of quartz cements and lead to anomalously good reservoir quality. By contrast, an excess of chlorite – for example, in clay-rich siltstone and sandstone – leads to blocked pore throats and very low permeability. Determining which compositional type is present, how it occurs spatially, and quantifying the many and varied habits of chlorite that are of commercial importance remains a challenge. With the advent of automated techniques based on scanning electron microscopy (SEM), it is possible to provide instant phase identification and mapping of entire thin sections of rock. The resulting quantitative mineralogy and rock fabric data can be compared with well logs and core analysis data. We present here a completely novel Quantitative Evaluation of Minerals by SCANning electron microscopy (QEMSCAN®) SEM–energy-dispersive spectrometry (EDS) methodology to differentiate, quantify and image 11 different compositional types of chlorite based on Fe : Mg ratios using thin sections of rocks and grain mounts of cuttings or loose sediment. No other analytical technique, or combination of techniques, is capable of easily quantifying and imaging different compositional types of chlorite. Here we present examples of chlorite from seven different geological settings analysed using QEMSCAN® SEM–EDS. By illustrating the reliability of identification under automated analysis, and the ability to capture realistic textures in a fully digital format, we can clearly visualize the various forms of chlorite. This new approach has led to the creation of a digital chlorite library, in which we have co-registered optical and SEM-based images, and validated the mineral identification with complimentary techniques such as X-ray diffraction. This new methodology will be of interest and use to all those concerned with the identification and formation of chlorite in sandstones and the effects that diagenetic chlorite growth may have had on reservoir quality. The same approach may be adopted for other minerals (e.g. carbonates) with major element compositional variability that may influence the porosity and permeability of sandstone reservoirs.
    Print ISSN: 0305-8719
    Electronic ISSN: 2041-4927
    Topics: Geosciences
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  • 5
    Publication Date: 2018-05-03
    Description: The porosity and permeability of sandstone and carbonate reservoirs (known as reservoir quality) are essential inputs for successful oil and gas resource exploration and exploitation. This chapter introduces basic concepts, analytical and modelling techniques and some of the key controversies to be discussed in 20 research papers that were initially presented at a Geological Society conference in 2014 titled ‘Reservoir Quality of Clastic and Carbonate Rocks: Analysis, Modelling and Prediction’. Reservoir quality in both sandstones and carbonates is studied using a wide range of techniques: log analysis and petrophysical core analysis, core description, routine petrographic tools and, ideally, less routine techniques such as stable isotope analysis, fluid inclusion analysis and other geochemical approaches. Sandstone and carbonate reservoirs both benefit from the study of modern analogues to constrain the primary character of sediment before they become a hydrocarbon reservoir. Prediction of sandstone and carbonate reservoir properties also benefits from running constrained experiments to simulate diagenetic processes during burial, compaction and heating. There are many common controls on sandstone and carbonate reservoir quality, including environment of deposition, rate of deposition and rate and magnitude of sea-level change, and many eogenetic processes. Compactional and mesogenetic processes tend to affect sandstone and carbonate somewhat differently but are both influenced by rate of burial, and the thermal and pressure history of a basin. Key differences in sandstone and carbonate reservoir quality include the specific influence of stratigraphic age on seawater composition (calcite v. aragonite oceans), the greater role of compaction in sandstones and the greater reactivity and geochemical openness of carbonate systems. Some of the key controversies in sandstone and carbonate reservoir quality focus on the role of petroleum emplacement on diagenesis and porosity loss, the role of effective stress in chemical compaction (pressure solution) and the degree of geochemical openness of reservoirs during diagenesis and cementation. This collection of papers contains case study-based examples of sandstone and carbonate reservoir quality prediction as well as modern analogue, outcrop analogue, modelling and advanced analytical approaches.
    Print ISSN: 0305-8719
    Electronic ISSN: 2041-4927
    Topics: Geosciences
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  • 6
    Publication Date: 2013-01-05
    Description: Porous rocks in the subsurface are now used for carbon capture and storage (CCS), to help ameliorate the effects of greenhouse gas emissions. These porous reservoir rocks require a caprock to retain the CO 2 . It is important to characterize caprock quality and its stability in the presence of elevated partial pressures of CO 2 . Lower Triassic sandstones are common in the UK and NW Europe and are being considered for future CCS projects. The caprock to these sandstones is the Middle and Upper Triassic Mercia Mudstone Group. We have studied the Mercia Mudstone using mineralogy, petrology and mercury injection porosimetry to assess its caprock quality. Detrital minerals are dominated by quartz, K-feldspar, illite and chlorite; diagenetic pore-filling minerals are dominated by calcite, dolomite and gypsum. In samples with abundant clay minerals, there are only small quantities of pore-filling diagenetic cements. Porosity is broadly uniform for both clay-rich and clay-poor samples. The cleaner (clay-poor) samples had their initial pore spaces filled with early diagenetic pore-filling carbonates and gypsum. Despite the broadly uniform porosity, mean pore throat diameter displays a strong inverse correlation with clay content whereas threshold capillary entry pressure shows a strong positive correlation with clay content. The more clay-rich samples represent much better caprock than the coarser-grained samples that contain abundant pore-filling cement. The samples could support potential column heights of supercritical CO 2 between 70 and 540 m and have calculated permeabilities between 10 –20 and 10 –19 m 2 ; leakage would occur only on geological time scales, assuming that these samples are representative of the whole caprock. Because caprock quality correlates with illite content and illite will be relatively immune to elevated partial pressures of CO 2 , the Mercia Mudstone probably represents a durable caprock for future Lower Triassic sandstone CCS projects.
    Print ISSN: 0016-7649
    Topics: Geosciences
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  • 7
  • 8
    Publication Date: 2020-08-06
    Print ISSN: 1757-8981
    Electronic ISSN: 1757-899X
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Published by Institute of Physics
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  • 9
    Publication Date: 1990-03-01
    Description: The UG1 Footwall unit is a layered pyroxenite-norite-leuconorite-anorthosite sequence between the Middle Group 4 and Upper Group 1 chromitites of the Upper Critical Zone, and is c. 300 m thick at Rustenburg Platinum Mines, Union Section, where it shows an oscillatory fluctuation in whole-rock Mg/(Mg + Fe), Cr/Co, Ni/V and Fe/Ti ratios with stratigraphic height. This permits subdivision into 8 sub-cycles which match a subdivision based on cyclical variations in orthopyroxene and feldspar compositions. Constituent pyroxene grains of pyroxenites, norites and leuconorites alike contain rounded and embayed plagioclase inclusions in abundance. Sr-isotope disequilibrium prevails in some samples between the orthopyroxene and feldspar populations. Chemical and isotopic data support a model of pulsatory injection of limited volumes of a more primitive, mafic liquid into a resident column of depleted residua, from which sodic labradorite and Mg-poor bronzite were crystallizing. The depleted liquid is equated with the supernatant liquid residuum of buried cumulates (Sric. 0.7054) and the primitive liquid with magma parental to the UG1-UG2 lineage (Sri ⩾ 0.7068). The increase in leucocratic character of the 300 m column, with height, is attributed to the rising of low-density liquids enriched in the components of feldspar during separation of the pyroxenites. Deposition of the UG1 chromitite layers is attributed to mixing of a major influx of primitive liquid with a feldspathic residuum at the top of the UG1 Footwall unit. There is no evidence to indicate the participation of a discrete A-type liquid (Irvine and Sharpe, 1982) in this process.
    Print ISSN: 0026-461X
    Electronic ISSN: 1471-8022
    Topics: Geosciences
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  • 10
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