首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
Since the Carboniferous, tropical latitudes have been the site of formation of many economic coal deposits, most of which have a restricted range of mineralogical composition as a result of their depositional environment, climatic conditions, and diagenesis. Mineralogical and microscopic investigations of tropical peats from Tasek Bera, Peninsular Malaysia, were performed in order to better understand some of these factors controlling the nature, distribution and association of inorganic matter in peat-forming environments. Distribution and nature of the inorganic fraction of peat deposits give insight into the weathering conditions and detrital input into the mire system. Because the inorganic composition of peat deposits is determined by plant communities, height of water table, and climate, the results of the quantitative and qualitative analysis can be used to reconstruct palaeoclimatic conditions.Tasek Bera is a peat-accumulating basin in humid tropical Malaysia with organic deposits of low- to high-ash yield and thus representative of many ancient peat-forming environments. Clay minerals dominate the mineralogical composition of the peat and organic-rich sediments, while quartz and clays dominate the underlying siliciclastic deposits. Kaolinite is the most abundant clay mineral in the organic deposits with minor amounts of illite and vermiculite. Particle size analyses indicate that >50% of the inorganic detrital fraction is <2 μm. Most detrital quartz grains range in size from fine silt to fine sand. The fine sand fraction accounts for a maximum of 5 wt.% of the inorganic constituents. In addition, abundant biogenic and non-biogenic, Al- and Si-rich amorphous matter occur. In the ombrotrophic (low-nutrient) environment, biogenic inorganic material contributes up to >75% of the ash constituents. As a consequence, the vegetational communities make an important contribution to the inorganic and overall ash composition of peats and coals. The ash content of the often inundated peat consists on average of 10% opaline silica from diatoms and sponge spicules, while the ash of the top deposits may have up to 50% biogenic silica. Hence, Al- and Si-hydroxides and the opaline silica from diatoms and sponges represent a large repository of Al and Si, which may form the basis of mineral transformation, neoformation and alteration processes during coalification of the peat deposits. As a result, most coal deposits from paleotropical environments are anticipated to have little to no biogenic inorganic material but high amounts of secondary clays, such as kaolinite (detrital kaolinite, resilisified kaolinite, or desilisified gibbsite) or illite, and various amounts of detrital and authigenetic quartz.  相似文献   

2.
The concentrations of major and trace inorganic elements in a succession of Permian coals from the Gunnedah Basin, New South Wales, have been determined by X-ray fluorescence techniques applied to both whole-coal and high-temperature ash samples. The results have been evaluated in the light of quantitative data on the minerals in the same coals, determined from X-ray diffraction study of whole-coal samples using a Rietveld-based interpretation program ( ™), to determine relationships of the trace elements in the coals to the mineral species present. Comparison of the chemical composition of the coal ash interpreted from the quantitative mineralogical study to the actual ash composition determined by XRF analysis shows a high degree of consistency, confirming the validity of the XRD interpretations for the Gunnedah Basin materials. Quartz, illite and other minerals of detrital origin dominate the coals in the upper part of the sequence, whereas authigenic kaolinite is abundant in coals from the lower part of the Permian succession. These minerals are all reduced in abundance, however, and pyrite is a dominant constituent, in coals formed under marine influence at several stratigraphic levels. Calcite and dolomite occur as cleat and fracture infillings, mostly in seams near the top and bottom of the sequence. The potassium-bearing minerals in the detrital fraction are associated with significant concentrations of rubidium, and the authigenic kaolinite with relatively high proportions of titanium. Zirconium is also abundant, with associated P and Hf, in the Gunnedah Basin coal seams. Relationships exhibited by Ti, Zr, Nd and Y are consistent with derivation of the original sediment admixed with the seams from an acid volcanic source. Pyrite in the coals is associated with high concentrations of arsenic and minor proportions of thallium; no other element commonly associated with sulphides in coals, however, appears to occur in significant proportions with the pyrite in the sample suite. Small concentrations of Cl present in the coal are inversely related to the pyrite content, and appear to represent ion-exchange components associated with the organic matter. Strontium and barium are strongly associated with the cleat-filling carbonate minerals. Ge and Ga appear to be related to each other and to the coal's organic matter. Cr and V are also related to each other, as are Ce, La, Nd and Pr, but none of these show any relationship to the organic matter or a particular mineral component.  相似文献   

3.
The mineralogy of the high-volatile bituminous coals and associated strata from the Greta seam, Sydney Basin, Australia, has been evaluated in this study. Although the seam is not immediately overlain by marine strata, percolation of marine water into the original peat bed is indicated by the petrological, mineralogical and geochemical characteristics, which resemble those of coals with marine roof strata. The upper and lower sections of the seam have contrasting mineralogy. Pyrite typically comprises 40 to 56 wt% of the mineral assemblage in the marine-influenced upper part of the seam section. The lower part contains much less pyrite (typically <5 wt%, organic-free basis), and also relatively abundant dawsonite (up to 14 wt%, organic-free basis). The minerals within most coal plies are largely of authigenic origin. These include pyrite, siderite, clay minerals (mainly kaolinite and Na-rich mixed-layer illite/smectite), and quartz, most of which have a relatively early, syngenetic origin. Minor Ti-bearing minerals, anatase or rutile, and phosphate minerals, fluorapatite and goyazite, were probably also formed during early diagenesis. Other minerals have features that indicate late-stage precipitation. These include abundant cleat- and fracture-filling dawsonite, which may be the result of reactions between earlier-precipitated kaolinite and Na2CO3- or NaHCO3-bearing fluids. Minor albite may also be epigenetic, possibly precipitated from the same Ca–Al bearing fluids that formed the dawsonite. The most abundant detrital minerals in the Greta coals are quartz, poorly ordered kaolinite, illite and mixed-layer illite/smectite (I/S). These occur mainly in the floor, roof and other epiclastic horizons of the seam, reflecting periods of greater clastic influx into those parts of the original peat-forming environment. Detrital minerals are rare in the coals away from the epiclastic horizons, probably owing to almost complete sediment bypassing in the depositional system. Alternatively, any detrital minerals that were originally present may have been leached from the peat bed by diagenetic or post-diagenetic processes.  相似文献   

4.
The minerals and non-mineral inorganic constituents in Triassic and Tertiary low-rank coals from various coal deposits in South Australia were studied using selective chemical leaching and oxygen-plasma ashing techniques. Although gypsum may be present in some samples, most of the sodium, calcium and magnesium, as well as part of the sulphur, appears to occur as a combination of dissolved ions in pore water and exchangeable ions attached to carboxylate groups. Significant concentrations of iron and aluminium occur in acid-soluble form, probably as organometallic complexes within the hydrocarbon structure.Quartz is the dominant mineral in the Tertiary coal samples. It appears to be mainly detrital, but doubly terminated euhedral crystals suggest an authigenic origin in one of the deposits. Well crystallized kaolinite is common in the Triassic coals, while poorly crystallized kaolinite occurs in the Tertiary samples. Siderite, calcite and possibly collophane occur in the Triassic coals; sparse pyrite is present in both the Tertiary and the Triassic samples.The differences in minerals and other inorganic constituents between the Tertiary and Triassic deposits can be explained partly by variations in the composition of the pore waters permeating the strata, and partly by mobility of silica and alumina from different sources within the peat deposit. The relative mobility of the different inorganic constituents is also significant in beneficiation of the coal for use in combustion processes.  相似文献   

5.
Geochemistry and origin of elements in some UK coals   总被引：3，自引：0，他引：3  
Twenty-four UK coals ranging in rank with 4.6%–37.6% volatile matter were analysed for 46 major and trace elements. The samples were obtained from the UK Coal Bank and are representative of the major UK coal fields. The major element distributions are interpreted in terms of the mineralogical variations—quartz and kaolinite are largely responsible for the Si and Al, carbonates for Ca and Mg and pyrite for Fe. Also exerting an influence in some samples are siderite, Al-phosphate minerals and illite. Based on statistical relationships with the major elements, Rb, Cr, Th, Ce, Zr, Y, Ga, La, Ta, Nb and V are thought to be mainly present in the clay minerals, and As, Mo, Sb, Tl, Se and Bi and Pb are probably present in pyrite. Strontium and Ba are concentrated in a restricted number of samples related to the phosphate minerals. Germanium is the only element for which a major organic association can be demonstrated. Elements with an indirect association with the organic matter are Na, Cl, and Br in porefluids and possibly Te. The ash content is controlled mainly by the detrital input and the trace elements related to the ash content are therefore those elements associated with the clay minerals. Variations with rank would appear to be mainly related to the moisture content (porefluids). The trace elements associated with the quartz and clay minerals are thought to be dominantly detrital in origin. The non-detrital elements, essentially those contained in pyrite, are thought to have been incorporated in the depositional environment from waters with enhanced salinities through seawater ingress, hence there are positive relationships between S and trace element concentrations.  相似文献   

6.
The review presented covers: (a) historical introduction; (b) some analytical comments; (c) some peculiarities of the As geochemistry in environment; (d) an estimation of coal Clarke value of As; (e) some coals enriched in As; (f) mode of As occurrence in coal; (g) factors influencing the As distribution in coal matter and coal bed; (h) genetic topics; (i) some topics related to environmental impact of As by the coal combustion.The World average As content in coals (coal Clarke of As) for the bituminous coals and lignites are, respectively, 9.0±0.8 and 7.4±1.4 ppm. On an ash basis, these contents are higher: 50±5 and 49±8 ppm, respectively. Therefore, As is a very coalphile element: it has strong affinity to coal matter — organic and (or) inorganic but obligatory authigenic. The coalphile affinity of As is like that for Ge or S.There is strong regional variability of As distribution due to geologic variability of the individual coal basins. For example, bituminous coals in Eastern Germany, Czech Republic and SE China are enriched in As, whereas the coals in South Africa or Australia are very depleted compared to coal Clarke of As. In general, some relationship exists between As content and its mode of occurrence in coals. Typically, at high As content, sulphide sites dominate (pyrite and other more rare sulphides), whereas at low As content, Asorg dominates, both being authigenic. A contribution of the terrigenic As (in silicates) is usually minor and of the biogenic Asbio (derived from coal-forming plants) is poorly known.Both organic and inorganic As can exist not only as chemically bound form but also in the sorbed (acid leacheable) arsenate form. With increasing coal rank, sorbed exchangeable arsenate content decreases, with a minimum in the coking coals (German data: the Ruhr coals).Relations of As content in coal to ash yield (or its partitioning in sink–float fractions) and to coal petrographic composition are usually complicated. In most cases, these relations are controlled by main site (form) of As — Aspyr or Asorg. If Aspyr dominates, an As accumulation in heavy fractions (or in high-ash coals) is observed, and if Asorg dominates, it is enriched in medium-density fractions (or low- and medium-ash coals). Arsenic is in part accumulated in the inertinite vs. vitrinite (Asorg ?).There are four genetic types of As accumulation on coal: two epigenetic and two syngenetic: (1) Chinese type—hydrothermal As enrichment, sometimes similar to known Carlin type of As-bearing telethermal gold deposits; (2) Dakota type—hypergene enrichment from ground waters draining As-bearing tufa host rocks; (3) Bulgarian type—As enrichment resulting from As-bearing waters entered coal-forming peat bogs from sulphide deposit aureoles; (4) Turkish type—volcanic input of As in coal-forming peat bog as exhalations, brines and volcanic ash.During coal combustion at power plants, most of the initial As in coal volatilizes into the gaseous phase. At the widely used combustion of pulverized coal, most of Asorg, Aspyr and “shielded” As-bearing micromineral phases escape into gaseous and particulate phase and only minor part of Asclay remains in bottom ash. The dominant fraction of escaping As is in fly ash. Because 97–99% of the fly ash is collected by electrostatic precipitators, the atmospheric emission of As (solid phase and gaseous) is usually assumed as rather minor (10–30% from initial As in coal). However, fly ash disposal creates some difficult environmental problems because it is potentially toxic in natural waters and soils. The As leaching rate from ash disposal is greatly controlled by the ash chemistry. In natural environment, As can be readily leached from acid (SiO2-rich) bituminous coal ashes but can be very difficult from alkali (CaO-rich) lignite ashes.If the Aspyr form dominates, conventional coal cleaning may be an efficient tool for the removing As from coal. However, organic-bound or micromineral arsenic (“shielded” grains of As-bearing sulphides) are not removed by this procedure.Some considerations show that “toxicity threshold” of As content in coal (permissible concentration for industrial utility) may be in the range 100–300 ppm As. However, for different coals (with different proportions of As-forms), and for different combustion procedures, this “threshold” varies.  相似文献   

7.
Coal is one of the most available energy sources on earth. The mineralogical and geo-chemical aspects of coals are of prime importance for their utilization. The mineralogical composition, ash chemistry, and ash fusion temperature (AFT) ranges of raw and beneficiated coals are investigated in this paper. Further, the mineral matter transformation during the beneficiation processes viz. by oxidative desulfurization; alkali extraction and ultrasonication along with the relationship of the ash fusion temperature (AFT) ranges with the ash components in the coal are discussed. The major oxides present in the coal and beneficiated coal ashes include Fe2O3, Al2O3, SiO2, CaO, and MgO, which significantly affect the ash fusion temperature ranges. Initial deformation temperature (IDT) changes with the ash components and, increases with the increase in the Fe2O3 content in coal ash. With increasing concentrations of both Al2O3 and SiO2, the initial deformation temperature (IDT) also increases. The increasing and decreasing nature of the initial deformation temperature (IDT) observed is also dependent upon the CaO and MgO contents. XRD analysis of the coal samples revealed significant changes in mineral matter contents with the types of beneficiation processes adopted for coal. The minerals like chlorite, illite, montmorillonite, pyrite, calcite, aragonite, and alumina have been removed during the beneficiation processes. The FTIR spectra also indicate the presence of minerals like gypsum (G), calcite (C) aragonite (Ar), quartz (Q) and kaolinite (K) in the raw coal and their subsequent removal after the beneficiation processes.  相似文献   

8.
The Carboniferous succession in the Donets Basin hosts about 130 seams, each with a thickness over 0.45 m. Nine economically important seams from the (south)western Donets Basin are studied using organic petrographical, inorganic geochemical, and organic geochemical techniques. The main aim of the study is the reconstruction of peat facies of Serpukhovian (Mississippian) and Moscovian (Middle Pennsylvanian) coals.Formation of major coal seams commenced during Serpukhovian times. Early Serpukhovian coal accumulated in a relatively narrow shore-zone and is rich in inertinite and liptinite. Very low ash yields, low to moderate sulphur contents, and upward increasing inertinite contents suggest coal deposition in raised mires.Moscovian coal has a significantly wider lateral extension and is generally rich in vitrinite. Coal properties vary widely in response to different peat facies. Low-sulphur, low-ash k7 coal was formed in a raised mire or in a low-lying mire without detrital input. l1 and l3 seams containing several fluvial partings were formed in low-lying mires. Both seams are more than 2 m thick. Seams m2 and m3 contain high-sulphur coal, a consequence of deposition in a peat with marine influence. In contrast, syngenetic sulphur content is low in the m51 upper seam, which was formed in a lacustrine setting. The late Moscovian n1 seam, up to 2.4 m thick, accumulated in a swamp with a vegetation rich in bryophytes and pteridophytes. The properties of the n1 seam are transitional between those of Serpukhovian and other Moscovian seams. Differences in maceral composition between Serpukhovian and Moscovian coals probably reflect changes in climate and vegetation type.Tuff layers are observed in the l1, l3, and m3 seams. The l3 and m3 seams contain abundant authigenic quartz. Trace element contents are high in many seams. As contents are especially high in seams c102, k7, l3 and m3. Ash in the l3 seam contains up to 8000 ppm As. Co is enriched near the base of several seams. Maxima up to 2400 ppm occur in the ash of the k7 and l3 seams. Cd contents in ash are frequently as high as 30 or 40 ppm.  相似文献   

9.
The aim of the present study is to provide additional information about the properties and depositional environment of the Kipra lignite seam, which was deposited during the regressive stage of development of the Maritza-West basin. Petrographical and mineralogical data, along with ash yields and sulphur contents of 24 samples from a seam profile, have been used to study the vertical variation of the depositional settings during peat accumulation and subsequent coalification.The Kipra lignite is characterized by high ash yields and sulphur contents. It formed in a rheotrophic, low-lying mire with alkaline pH value. Vegetation with low preservation potential dominated within the palaeomire. During peat formation, frequent changes of the water level controlled the depositional environment. During the deposition of units 1 and 2, high water energy caused the transportation of high amounts of inorganic material into the mire, resulting in the formation of weakly gelified mineral-rich lignite. The organic matter from units 3 and 4 is characterized by enhanced gelification, which probably reflects the decreasing energy of the system. Good positive correlation between sulphur contents and the GI values was established in units 4, indicating that the gelification of the tissues was probably mainly controlled by the bacterial activity. In contrast, the gelification of the samples from unit 3 of the Kipra seam was probably governed by the redox conditions. The organic matter deposited under relatively wet conditions, in which the thermal and oxidative destruction of the tissues, was limited.A variety of major, minor and accessory minerals are present in Maritza-West lignite. The mineral composition is dominated mainly by pyrite, gypsum and calcite, and to a lesser extent limonite, quartz, kaolinite, montmorillonite, illite, chlorite and plagioclase. Jarosite, hematite, halloysite, mica, K-feldspar, aragonite, siderite, and dolomite were also determined in very low concentrations. These minerals formed syngenetically and epigenetically. The syngenetic stage is characterized mainly by the formation of pyrite, carbonates, silicates and sulphates, whereas the Fe-oxyhydroxides, partially the carbonates and almost all silicates are of detrital origin. During the epigenetic stage, carbonates, sulphates, clay minerals, pyrite, and Fe-oxyhydroxides were formed. Alteration products like gypsum, jarosite, limonite, chlorite, kaolinite, illite, mica, and calcite were generated due to the transformation of detrital and authigenic minerals.  相似文献   

10.
Contents of the rare-earth elements(REE) in two coal seams from North Shanxi Province,China,were determined using the instrumental neutron activation method.Based on the REE distribution tpatterns,and correlation analysis and cluster analysis,the main conclusions were drawn as follows.The REE contents are controlled mainly by the coal-forming environments,but might be affected by acidic solution Jeaching after peat sedimentation.The REE distribution patterns should be nearly the same in the sublayers of the same coal seam,and the occurrence of abnormal patterns might indicate the geological effect during post-sedimentation.The REE in coals are present mainly in the inorganic phase,and might be derived mainly from terrigenous detrital minerals.Some harmful elements,such as V,P,Mo,Cr,Cu,Mo,Th and Cd,might have cleaning potential during processing and dressing by washing because they are associated with REE.  相似文献   

11.
Chromium contents obtained from 20 coal and 5 associated rock samples collected from the basal part of the Eocene Chuckanut Formation, in Skagit and Whatcom counties, northwest Washington, range between 30 and 300 ppm (mean 120 ppm whole-coal basis). The lenticular coals, ranging in rank from subbituminous to anthracite, and with an ash content of 12–46%, crop out along the western flank of the Cascade Range. Results of X-ray diffraction analysis of low-temperature ash show that the mineral matter in the coal samples consists predominantly of quartz and clay (kaolinite, illite and chlorite group). However, accessory minerals, isolated from the coal samples and analyzed by X-ray diffraction, scanning electron microscope and optical methods, contain angular fragments and euhedral crystals of the spinel group (chromite, magnetite and trevorite ), kaolinite-serpentine group (antigorite and chrysotile), chlorite group, amphibole group and pyroxene group minerals (augite, diopside and enstatite), all of which are commonly enriched in chromium.Although associated primarily with the inorganic fraction of the coal, concentrations of chromium in the samples show no statistically significant correlation with ash content. Localized concentrations of chromium in the coal are the result of natural contamination from the alteration of detrital chromium-bearing mineral grains introduced into the peat-forming mires from nearby Jurassic ophiolite bodies. The coals formed in the early Eocene, in rapidly subsiding small basins that developed during the uplift and erosion of the pre-Tertiary ophiolite terrain. Scattered bodies of source rock, random distribution of chromium-bearing minerals within the coal and sample heterogeneity account for the variation in Cr contents of the samples.  相似文献   

12.
鸡西煤田是东北地区重要的炼焦煤基地，由于受成煤环境的影响，原煤灰分较高，影响了煤炭精细加工利用和环境。采用Ｘ射线衍射、红外光谱等分析方法对鸡西煤的无机地球化学特征研究显示，煤中的主要矿物为石英、方解石、粘土矿物、黄铁矿和菱铁矿等，它们分别以不同的状态赋存于有机质中。煤灰的主要成分为ＳｉＯ２和Ａｌ２Ｏ３，其主要源自流水带入泥炭沼泽的石英和粘土等同生矿物。元素分析表明，煤中硫、磷及微量元素锗和镓等含量较低。  相似文献   

13.
This paper discusses the result of the detailed investigations carried out on the coal characteristics, including coal petrography and its geochemistry of the Pabedana region. A total of 16 samples were collected from four coal seams d2, d4, d5, and d6 of the Pabedana underground mine which is located in the central part of the Central-East Iranian Microcontinent. These samples were reduced to four samples through composite sampling of each seam and were analyzed for their petrographic, mineralogical, and geochemical compositions. Proximate analysis data of the Pabedana coals indicate no major variations in the moisture, ash, volatile matter, and fixed carbon contents in the coals of different seams. Based on sulfur content, the Pabedana coals may be classified as low-sulfur coals. The low-sulfur contents in the Pabedana coal and relatively low proportion of pyritic sulfur suggest a possible fresh water environment during the deposition of the peat of the Pabedana coal. X-ray diffraction and petrographic analyses indicate the presence of pyrite in coal samples. The Pabedana coals have been classified as a high volatile, bituminous coal in accordance with the vitrinite reflectance values (58.75–74.32 %) and other rank parameters (carbon, calorific value, and volatile matter content). The maceral analysis and reflectance study suggest that the coals in all the four seams are of good quality with low maceral matter association. Mineralogical investigations indicate that the inorganic fraction in the Pabedana coal samples is dominated by carbonates; thus, constituting the major inorganic fraction of the coal samples. Illite, kaolinite, muscovite, quartz, feldspar, apatite, and hematite occur as minor or trace phases. The variation in major elements content is relatively narrow between different coal seams. Elements Sc,, Zr, Ga, Ge, La, As, W, Ce, Sb, Nb, Th, Pb, Se, Tl, Bi, Hg, Re, Li, Zn, Mo, and Ba show varying negative correlation with ash yield. These elements possibly have an organic affinity and may be present as primary biological concentrations either with tissues in living condition and/or through sorption and formation of organometallic compounds.  相似文献   

14.
One hundred twenty-two samples of Jurassic and Paleogene brown coals and 1254 peat samples from the south-eastern region of the Western-Siberian platform were analyzed for gold by the neutron-activation method. Mean content of Au in Jurassic coals is 30 ± 8 ppb, in Paleogene coals is 10.6 ± 4.8 ppb, and in peat is 6 ± 1.4 ppb. Concentrations of gold as high as 4.4 ppm were found in coal ash and 0.48 ppm in the peat ash. Coal beds with anomalous gold contents were found at Western-Siberian platform for the first time.Negative correlation between gold and ash yield in coals and peat and highest gold concentrations were found in low-ash and ultra-low-ash coals and peat. Primarily this is due to gold's association with organic matter.For the investigation of mode of occurrence of Au in peat the bitumen, water-soluble and high-hydrolyzed substances, humic acids, cellulose and lignin were extracted from it. It was determined that in peat about 95% of gold is combined with organic matter. Forty to sixty percent of Au is contained in humic acids and the same content is in lignin. Bitumens, water-soluble and high-hydrolyzed substances contain no more than 1% of general gold quantity in peat.The conditions of accumulation of high gold concentrations were considered. The authors suggest that Au accumulation in peat and brown coals and the connection between anomalous gold concentrations and organic matter in low-ash coals and peat can explain a biogenic–sorption mechanism of Au accumulation. The sources of formation of Au high concentration were various Au–Sb, Au–Ag Au–As–Sb deposits that are abundant in the Southern and South-Eastern peripheries of the coal basin.  相似文献   

15.
Chemical analyses of high-temperature coal ashes were used to establish the distribution, association and relationship between major inorganic elements such as Si, Al, Ti, Fe, Mn, Mg, Ca, Na, K, P, S and CO2 in a number of New South Wales economic coal seams and to study the composition and character of mineral matter in these coals. The methods used for the evaluation of the data were statistical analysis (univariate and bivariate), ratios, normative mineral composition and variation diagrams.The distribution of major and minor inorganic elements in coal appears to be related to the amount of mineral matter occurring in coal (determined as ash yield) and its mineralogical composition. The quantitative variations in levels of these elements can be classified as in-seam and inter-seam variations. In-seam variations are largely ash yield dependent, i.e. the levels of an element (wt.%) in coal increase along with the increase of its ash content (wt.%). The inter-seam variations are more complex and are related to both ash yield and to the mineralogical composition of mineral matter.The principal components of New South Wales coal ashes are silicon and aluminium. Silicon may be present as silica or combined with aluminium in different proportions to form clay minerals, such as kaolinite, illite, mixed-layer clay minerals, and smectite. Thus, the concentration levels of aluminium in relation to silicon in coal may give an indication about the character of clay minerals present in coal.Ratios and correlation coefficients of element pairs such as Al and Ti, Na and K, and Na and Al were used to determine differences in the chemical composition of high-temperature coal ashes of seams from various stratigraphic positions and provinces. In some seams the nature of associations of these elements is more significant than in others. This is interpreted as being a product of specific environmental conditions controlling the deposition of these seams.The nature of clay mineral content in coal is believed to be a major reason for chemical dissimilarities found between seams of various stratigraphic levels and geographic areas. For example, in some seams kaolinite, in others expandable clay minerals are dominant. The vertical distribution of these minerals has a stratigraphic significance. Within the Upper Permian Newcastle Coal Measures a trend from kaolinite-rich through to expandable minerals-rich and to kaolinite-rich assemblages can be observed from the bottom to the top. These changes are noticeably gradual.All significant variations in the clay mineral assemblages could relate to the long-term changes in the provenance of sedimentary material, weathering conditions in the source area and the rate of subsidence in the place of deposition. These changes are associated with major tectonic events controlling the history of sedimentation within the paralic Sydney and Gunnedah Basins during the Permian.  相似文献   

16.
The stratigraphic and regional variation of petrographic and chemical properties within the coals of the Upper Carboniferous Tradewater Formation and surrounding rocks in the Western Kentucky coal field were analyzed with the intent of constructing a depositional model for the occurrence of these low sulfur coals. Cores were megascopically described, and coal samples were analyzed for maceral, ash, and sulfur contents. These data were then analyzed to determine regional variation within the study area, as well as vertical variation within single coal columns.Sedimentological data from core logs indicate that the majority of the Tradewater rocks consist of irregularly distributed, coarsening-upward, fine-grained detrital material that was deposited in shallow bodies of water. Fossiliferous shales and limestones indicate a marine influence. Less common coarse-grained, fining-upward sequences appear to represent deposits of meandering or braided channels.Like the detrital rocks, the coal seams are irregularly distributed and exhibit substantial variation in petrographic and chemical properties which reflect changes in the Eh and pH of the coal swamp waters. These individual swamps were relatively limited in extent and probably occupied a low-lying coastal area. The relatively high vitrinite content of most of the coals suggests a reasonable degree of preservation of decaying plant materials. The study of benched samples from surface mines suggests a distinct dichotomy between swamps that were in more or less continuous contact with sulfate-rich marine or brackish water and those in which peat accumulated in a dominantly fresh-water setting. Most of the latter show a pattern of upward increasing sulfur content and decreasing vitrinite content, indicating increasing influences of oxygenated water that would encourage microbial action and which would degrade the peat and increase the tendency for sulfide precipitation. The high sulfur coals do not display this variability. The high rates of lateral variability encountered in the data suggest that future study should concentrate on smaller areas where variation can be completely documented.  相似文献   

17.
The clays and other minerals in a succession of Late Permian coals of high-volatile bituminous to semi-anthracite rank have been identified, using low-temperature oxygen plasma ashing and X-ray diffraction, and evaluated to identify the relative roles in mineral matter formation of detrital input, early diagenesis in the peat swamp and late diagenesis associated with rank advance. Although well-ordered kaolinite of probable early diagenetic origin is abundant throughout the succession, the uppermost and lowermost seams of the sequence, regardless of rank, contain relatively abundant illite and/or interstratified illite/smectite, along with a small but significant proportion of chlorite. These clays are thought to be essentially of detrital origin, washed or blown into the peat deposit in relative abundance during the establishment and subsequent overwhelming of an extensive and long-lived swampy environment. Quartz is also abundant in the lower seams of the sequence, especially close to the regional sediment source area. Illite is unusually abundant in the topmost seam in both high- and low-rank parts of the succession, and thus appears to represent detrital input from a particular source material. Although significant changes are reported in the clays of the associated strata due to rank advance, the principal effect of rank advance on the minerals in the coal itself appears to be the development of an ammonium illite, and possibly some additional fine-grained chlorite, in the semi-anthracite material. Isolation within the organic matter of the coal is thought to have inhibited access for ions such as K+, which might otherwise have become involved in metamorphic reactions and given rise to mineralogical changes commonly found in non-coal sedimentary successions.  相似文献   

18.
Leaching processes are believed to be responsible for the unusually low-ash content (sometimes less than 1%) of the thick (up to 35 m) Cretaceous coals located in the Greymouth coalfield, South Island, New Zealand. Although leaching of inorganics in peat is a generally accepted process, little is known about leaching after burial. The “Main” and “E” seams in the Greymouth coalfield show good correlation between low ash and bed thickness. The ash content, however, is often less than 1%, which is lower than most known modern analogues (i.e. peat). There are several lines of evidence that suggest that mineral matter may have been removed from the coal not only in the peat stage but also after burial. For example, etching features found in quartz grains and clay aggregates indicate that some leaching processes have taken place. In addition, liptinitic material (e.g., bitumen) in the cleat networks supports the conclusion that there has been some movement of solutions through the coal after burial. These solutions may have helped to remove some of the inorganics originally within the Greymouth coals.  相似文献   

19.
In Part 1 of the present investigation, 37 representative Eocene coal samples of Meghalaya, India were analyzed and their physico-chemical characteristics and the major oxides and minerals present in ash samples were studied for assessing the genesis of these coals. Various statistical tools were also applied to study their genesis. The datasets from Part 1 used in this investigation (Part 2) show the contribution of major oxides towards ash fusion temperatures (AFTs). The regression analysis of high temperature ash (HTA) composition and initial deformation temperature (IDT) show a definite increasing or decreasing trend, which has been used to determine the predictive indices for slagging, fouling, and abrasion propensities during combustion practices. The increase or decrease of IDT is influenced by the increase of Fe2O3, Al2O3, SiO2, and CaO, respectively. Detrital-authigenic index (DAI) calculated from the ash composition and its relation with AFT indicates Sialoferric nature of these coals. The correlation analysis, Principal Component Analysis (PCA), and Hierarchical Cluster Analysis (HCA) were used to study the possible fouling, slagging, and abrasion potentials in boilers during the coal combustion processes. A positive relationship between slagging and heating values of the coal has been found in this study.  相似文献   

20.
Lower Gondwana coal from Garu-Gensi area in the West Siang district of Arunachal Pradesh in the Eastern Himalayas have been characterized with respect to their maceral constituents, mineral matter, ash composition, sulphurand trace-element contents. These are low-rank bituminous coals (V0 = 0.64) and their vitrinite content is about 60%. A first hand data with respect to twenty one trace-elements are reported. Our data indicate that these Lower Gondwana coals of extra-peninsular region are richer in terms of their trace-element content when compared with their counter parts of peninsular India.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号