Geological and geochemical characteristics of high arsenic coals from endemic arsenosis areas in southwestern Guizhou Province,China

Southwest Guizhou Province is one of the most important areas of disseminated, sediment-hosted-type Au deposits in China and is an important area of coal production. The chemistry of most of the coals in SW Guizhou is similar to those in other parts of China. Their As content is near the Chinese coal average, but some local, small coal mines contain high As coals. The highest As content is up to 3.5 wt.% in the coal. The use of high As coals has caused in excess of 3000 cases of As poisoning in several villages. The high As coals are in the Longtan formation, which is an alternating marine facies and terrestrial facies. The coals are distributed on both sides of faults that parallel the regional anticlinal axis. The As content of coal is higher closer to the fault plane. The As content of coal changes greatly in different coal beds and different locations of the same bed. Geological structures such as anticlines, faults and sedimentary strata control the distribution of high As coals. Small Au deposits as well as Sb, Hg, and Th mineralization, are found near the high As coals. Although some As-bearing minerals such as pyrite, arsenopyrite, realgar (?), As-bearing sulfate, As-bearing clays, and phosphate are found in the high As coals, their contents cannot account for the abundance of As in some coals. Analysis of the coal indicates that As mainly exists in the form of As⁵⁺ and As³⁺, perhaps, combined with organic compounds. The occurrence of such exceptionally high As contents in coal and the fact that the As is dominantly organically associated are unique observations.     

The geochemistry of tungsten in Bulgarian coals

This paper discusses the tungsten geochemistry in coal, based on the behavior of this element in 14 Bulgarian deposits. The W contents range from 0.5–4335 ppm in the ash and from 0.01–784 ppm in the coals. In four of the deposits the tungsten content proved to be 16 to 100 times higher than the Clarke value for sedimentary rocks. No correlation has been found between the W concentration and either the age of the coal-bearing strata or the coal rank. The deposits were divided in three groups on the basis of the relationship between tungsten and ash content. The role of sorption ash and terrigenous ash in tungsten binding was evaluated for each group. The correlation between tungsten and organic matter is demonstrated by the increased contents of tungsten in the ash of the low-ash coals, its concentration in the lighter coal fractions, its extraction from the coals by HF and NaOH only, and by model experiments. Sorption ash concentrates tungsten; terrigenous ash is a carrier of tungsten.Of the petrographic constituents of coal, vitrain was found to concentrate the largest amounts of tungsten.In two of the deposits richest in tungsten, there is a very distinct zonality in its vertical distribution — tungsten concentration decreases from the bottom to the top of the coal bed. This zonality might be explained by the diffusion (syngenetic or diagenetic with respect to the coal-forming process) through the coal bed of aqueous solutions enriched in tungsten.The wide range of variation of the tungsten concentrations, the considerable differences in the mean contents and the dispersions between the individual deposits show that tungsten is very sensitive to the differences of the source area.Coal deposits enriched in tungsten may be expected in the following favourable environments: (1) in areas with nitrogen-bearing thermal waters containing increased amounts of tungsten; (2) source areas with tungsten mineralizations; and (3) country rocks consisting of acid granitoids whose Clarke values of tungsten are the highest as compared to the other types of rocks.     

C-S-Fe relationships and the isotopic composition of pyrite in the New Albany Shale of the Illinois Basin,U.S.A.

The relationship between pyritic sulfur content (S_pyr) and organic carbon content (C_org) of shales analyzed from the New Albany Group depends upon C_org. For samples of <6 wt.% C_org, S_pyt, and C_org are strongly correlated (r = 0.85). For C_org-“rich” shales (>6 wt.%), no S_pty-C_org, correlation is apparent. The degree of Fe pyritization (DOP) shows similar relationships to C_org. These C-S-Fe relationships suggest that pyrite formation was limited by the availability of metabolizable organic carbon in samples where C_org < 6 wt.% and by the availability of reactive Fe for samples where C_org > 6 wt.%. Apparent sulfur isotope fractionations relative to contemporaneous seawater sulfate (Δ³⁴S) for pyrite formation average −40% for non-calcareous shales and −25%. for calcareous shales. Δ³⁴S values become smaller with increasing C_org, S_pyt, and DOP for all C_org-“poar” (<6 wt%) and some C_org-“nch” (<6 wt.%) shales. These trends suggest that pyrite formation occurred in a closed system or that instantaneous bacterial fractionation for sulfate reduction decreased in magnitude with increasing organic carbon content. The isotopic trends observed in the New Albany Group are not necessarily representative of other shales having a comparable range of organic carbon content, e.g. Cretaceous shales and mudstones from the western interior of North America (GAUTIER, 1986). Δ³⁴S values in the remainder of the C_org-rich New Albany Group shales are relatively large (−38 to −47%.) and independent of C_org, S_pyr, and DOP, which suggests that pyrite in these shales formed mostly at or above the sediment-water interface by precipitation from an isotopically uniform reservoir of dissolved H₂S.     

The role of coal petrographic characteristics in evaluating the non-coking nature of the coals of ramagundam and Kothagudem coalfields,Godavari Valley Basin,Andhra Pradesh,India

The maceral and microlithotype compositions of coals representative of the different coal seams of the Ramagundam and Kothagudem coalfields, Godavari Valley Basin, are compared with those of the Ib River, Talcher, South Karanpura, Hura, and Brahmani coalfields. The vitrite + clarite—“Intermidiates”—durite + fusite + shale (<20%) triangular diagram places these coals in the area of non-coking coals, clearly distinct from the coking and semi-coking coals. The vitrinite reflectance is low (R_ormoil^aver: 0.38–0.71%), far below the coking-coal range. Thus, based on petrographic composition and rank, these coals are of non-coking nature. A triangular diagram is proposed delineating the coking, semi-coking and non-coking coal areas for the Gondwana coals of India.     

Contact angles in CO2-water-coal systems at elevated pressures

Injection of carbon dioxide into coal seams is considered to be a potential method for its sequestration away from the atmosphere. However, water present in coals may retard injection: especially if carbon dioxide does not wet the coal as well as water. Thus contact angles in the coal-water-CO₂ system were measured using CO₂ bubbles in water/coal systems at 40 °C and pressures up to 15 MPa using five bituminous coals. At low pressures, in this CO₂/water/coal system, receding contact angles for the coals ranged between 80° to 100°; except for one coal that had both high ash yield and low rank, with a contact angle of 115°, indicating that it was hydrophilic. With increasing pressure, the receding contact angles for the different coals decreased, indicating that they became more CO₂-wetting. The relationship between contact angle and pressure was approximately linear. For low ash or high rank coals, at high pressure the contact angle was reduced to 30-50°, indicating the coals became strongly CO₂-wetting; that is CO₂ fluids will spontaneously penetrate these wet coals. In the case of the coal that was both high ash and hydrophilic, the contact angle did not drop to 90° even at the highest pressures used. These results suggest that CO₂ will not be efficiently adsorbed by all wet coals equally well, even at high pressure. It was found that at high pressures (> 2 MPa) the rate of penetration of carbon dioxide into the coals increased rapidly with decreasing contact angle, independently of pressure. Injecting CO₂ into wet coals that have both low rank and high ash will not trap CO₂ as well as injecting it into high rank or low ash coals.     

A short-term establishment of forest fen habitat during Pliocene lignite formation in the Ptolemais Basin, NW Macedonia, Greece

The intermontane basin of Ptolemais is part of a major tectonic trench, located in NW Greece and includes around 65% of Greek coal reserves. The Upper Xylite Layer (UXL) is a distinct lignite layer, being 3–6 m thick and outcropping in the upper part of the Pliocene Lignite-bearing Sequence at the Notio Field and Tomeas Eksi Mines of Ptolemais. Compared with the xylite-rich lithotypes, the matrix lithotypes within UXL contain more ash. Micropetrographic studies suggest that the Upper Xylite Layer is rich in huminite (>90%). Textinite dominates in the xylite-rich lithotypes, while attrinite dominates in the matrix lithotypes. The liptinite content is <10%, while inertinite rarely occurs. Palaeobotanical determination revealed that the xylite-rich coal originated from Coniferous vegetation, specifically from Glyptostrobus europaeus. The occurrence of G. europaeus as a coal-forming element is significant because, though this kind of vegetation was common in many Greek coals of Miocene age, this is the first time it has been recorded from the Pliocene. This study suggests that the Upper Xylite Layer is autochthonous. According to coal-facies diagrammes, peat accumulated under pure telmatic conditions in a relatively wet forest fen. Both herbaceous and arboreal vegetation contributed to peat formation.     

鄂尔多斯盆地煤的灰分和硫、磷、氯含量研究

详细阐述了鄂尔多斯盆地煤的灰分产率和硫、磷及氯含量的空间及垂向分布规律,并探讨了煤中硫。磷及氯含量的影响因素。研究结果表明,石炭-二叠纪煤以中灰煤为主,部分为高灰煤;低灰煤仅分布在局部地区,且灰分产率与全流呈负相关;延安组以特低灰—低灰煤为主,中灰煤次之,空间上灰分北高南低、东高西低;太原组以中高硫煤为主,山西组则以低硫煤为特征,空间上呈南高北低、西高车低之趋势;延安组亦以低硫煤为主。煤中形态硫以黄铁矿硫为主,有机硫次之,硫酸盐硫极少。从太原组到山西组再到延安组,煤中硫呈递减趋势,这与聚煤环境的变化密切相关。该盆地煤含磷低,少部分为特低磷煤。煤中氯的质量分数值平均为425．8×10-6,空间上中南部高、北西部低;垂向上,下部煤层中氯的含量高于中上部煤层,这可能与煤中氯的成因有关。     

Formation Environment of Main Brown Coal Seam in Xi-2 Minefield of Shengli Coalfield Based on Coal Ash Phase Analysis

The formation environment of the main coal seam in Shengli coal mine is analyzed, and the effect of coal ash parameters on the coal-forming environment is mainly discussed according to gray component parameters combined with other coal quality test analysis data. Results show that the hydrodynamic conditions of the main coal during coal accumulation have a general pattern of strong northeast and weak southwest, and lakeside swamp is generally in the retrograde process from south to north. The No.5 coal seam is a water entry cycle, and the No.5_lower coal is a water withdrawal cycle. The No.6 thick coal seam is formed in the peat swamp environment where the water is shallow and the groundwater activity is weak. The input of terrestrial debris material was most abundant in the formation period of No.5_lower coal, followed by No.5 coal, and that in No.6 coal is the least. Vertically, the peat swamp environment changed from weak reduction to weak oxidation to strong reducing environment. The ash yield was low to high to low from bottom to top. The organic sulfur is the main type of sulfur in the main coal seam. The weaker the hydrodynamic condition, the higher the organic sulfur content in the reduction environment, while lower organic sulfur content in the oxidation environment. The peat swamp water of No.5_lower coal is medium alkaline, and the peat swamp water of No.5 and No. 6 coals is weakly alkaline or acidic.     

Selenium in Chinese coals: distribution,occurrence, and health impact

Selenium (Se) is one of the volatile elements in coal. During mining and utilization of coal, Se is largely released into the environment, which influences environmental quality, and consequently impacts on human health. This paper is a review of current knowledge on the distribution, occurrence and environmental impact of Se in Chinese coals. This study includes the following aspects: distribution and abundance of Se in coals of different provinces of China, different coal-forming periods, modes of occurrence of Se in coals, formation mechanism of Se in coals, migration processes and transformation of Se during coal combustion and leaching and their environmental effects. The available data show that Se content in Chinese coals is highly variable in different coalfields, different coal-forming periods, and different coal seams from individual coalfields. The average Se content in Chinese coal is 3.91 mg/kg.     

Chemical and petrographical characterization of feed coal, fly ash and bottom ash from the Figueira Power Plant, Paraná, Brazil

The aim of the present study is the petrographic and chemical characterization of the coal at the Figueira Power Plant, Paraná, Brazil, prior and after the beneficiation process and the chemical characterization of fly and bottom ashes generated in the combustion process.Petrographic characterization was carried out through maceral analysis and vitrinite reflectance measurements. Chemical characterization included proximate analysis, determination of calorific value and sulphur content, ultimate analysis, X-ray diffraction, X-ray fluorescence, Inductively Coupled Plasma — Mass Spectrometry (ICP-MS) and Inductively Coupled Plasma — Atomic Emission Spectrometry (ICP-AES) analysis, and determination of Total Organic Carbon (TOC) content.Vitrinite reflectance analyses indicate a high volatile B/C bituminous coal (0.61 to 0.73% Rrandom). Maceral analyses show predominance of the vitrinite maceral group (51.6 to 70.9 vol.%, m.m.f). Except of the Run of mine (ROM) coal sample, the average calorific value of the coals is 5205 kcal/kg and ash yields range from 21.4 to 38.1 wt.%. The mineralogical composition (X-ray diffraction) of coals includes kaolinite, quartz, plagioclase and pyrite, whereas fly and bottom ashes are composed by mullite, ettringite, quartz, magnetite, and hematite. Analyses of major elements from coal, fly and bottom ashes indicate a high SiO₂, Al₂O₃, and Fe₂O₃ content. Trace elements analysis of in-situ and ROM coals by ICP-MS and ICP-AES show highest concentration in Zn and As. Most of the toxic elements such as As, Cd, Cr, Mo, Ni, Pb, and Zn are significantly reduced by coal beneficiation. Considering the spatial distribution of trace elements in the beneficiated coal samples, which were collected over a period of three months, there appears to be little variation in Cd and Zn concentrations, whereas trace elements such as As, Mo, and Pb show a larger variation.In the fly and bottom ashes, the highest concentrations of trace elements were determined for Zn and As. When compared with trace element concentrations in the feed coal, fly ashes show a significant enrichment in most trace elements (As, B, Be, Cd, Co, Cr, Cu, Li, Mn, Mo, Ni, Pb, Sb, Tl, and Zn), suggesting a predominantly volatile nature for these elements. In contrast, Sn is distributed evenly within the different ash types, whereas U shows depleted concentration in both bottom and fly ash samples.According to the International Classification of in-seam coals the Cambuí coals are of para/ortho bituminous rank of low grade (except for the ROM sample), and are characterized by the predominance of vitrinite macerals.     

The form,distribution and mobility of arsenic in soils contaminated by arsenic trioxide,at sites in southeast USA

Soils from many industrial sites in southeastern USA are contaminated with As because of the application of herbicide containing As₂O₃. Among those contaminated sites, two industrial sites, FW and BH, which are currently active and of most serious environmental concerns, were selected to characterize the occurrence of As in the contaminated soils and to evaluate its environmental leachability. The soils are both sandy loams with varying mineralogical and organic matter contents. Microwave-assisted acid digestion (EPA method 3051) of the contaminated soils indicated As levels of up to 325 mg/kg and 900 mg/kg (dry weight basis) for FW and BH soils, respectively. However, bulk X-ray powder diffraction (XRD) analysis failed to find any detectable As-bearing phases in either of the studied soil samples. Most of the soil As was observed by scanning electron microscopy, coupled with energy dispersive X-ray spectroscopy (SEM/EDX), to be disseminated on the surfaces of fine-grained soil particles in close association with Al and Fe. A few As-bearing particles were detected in BH soil using electron microprobe analysis (EMPA). Synchrotron micro-XRD and X-ray absorption near-edge structure (XANES) analyses indicated that these As-rich particles were possibly phaunouxite, a mineral similar to calcium arsenate, which could have been formed by natural weathering after the application of As₂O₃. However, the scarcity of those particles eliminated them from playing any important role in As sequestration.     

Advance in geochemical research on Au in coal ash北大核心CSCD

Recent researches on Au in coal ash were summarized in this paper, including the distribution law and the migration rule of gold in coal ash, as well as the influencing factors on volatility and use feasibility of Au in the progress of coal combustion. Au content in coal ash is much higher than that in the raw coal in most cases worldwide, only a small number of opposite cases are found in certain places. Occurrence of Au in coal, geological-geochemical environment of coal-forming and combustion conditions are the main factors controlling the volatility of gold in coal combustion, while the occurrence of Au in coal dominates the redistribution of Au. Through preliminary calculation, gold in coal ash is expected to have a considerable utilization potential in the southwestern Guizhou Province.     

Mineralogical composition and ash geochemistry of raw and beneficiated high sulfur coals

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.     

陕北横山矿区延安组3-1煤层Sr和Ba的分布及赋存模式

煤中微量元素Sr和Ba的分布和赋存模式对研究煤层成煤古环境和煤炭的洁净利用有重要的意义。通过对横山5个矿区24个主采煤层煤样的工业分析、元素分析、矿物组成分析,采用相关性分析和逐级化学提取实验,研究该主采煤层中Sr和Ba的分布和赋存模式。研究发现,区内超过75%煤样属于特低灰煤;约96%的煤样全硫质量分数超过1%;主要的矿物成分为高岭石、黄铁矿和方解石。超过总分析煤样75%的样品中Sr和Ba富集,且在水平方向上Sr和Ba含量北部较南部更高。煤中Sr和Ba主要负载在天青石、重晶石、菱锶矿、碳酸钡矿、方解石和文石等矿物中。煤中Sr和Ba富集的主要原因是煤层中含有负载这两种元素的矿物。      

Cold-climate, fluvial to paralic coal-forming environments in the Permian Collinsville Coal Measures, Bowen Basin, Australia

The Middle Permian Collinsville Coal Measures of the northern Bowen Basin illustrate a range of cold to cold-temperate, coal-forming environments. Cold climate is indicated by Glossopteris flora in the coal measures, and by restricted marine fauna dominated by brachiopods and bryozoa in correlative marine sequences of the Back Creek Group which contains also abundant lonestones (dropstones). Sedimentation was characterised by an overall transgression, interrupted by local fluvial and coastal progradation in a shallow, epicontinental sea during a relatively quiescent tectonic period.Six sedimentary environments are represented: fluvial, fluvio-paralic, barrier-strandplain, back-barrier, tidal flat and open marine. The basal coal formed from peat of swamps of abandoned areas of gravelly braided streams, and is massive, dull, and with high ash (20%), low sulphur (1%) contents. Overlying coals developed from peats formed in fluvio-paralic and paralic environments, and thicker seams are generally brighter, with low to moderate ash (8–17%) and moderate to high total sulphur (1–6%) contents. Seams associated with fluvial influence show splits and high ash yield, while seams associated with coastal deposits show high sulphur levels (up to 21%).In contrast to reported models of coal-forming environments, no clearly defined deltaic or inter-distributary bay-fill sequences were identified in the area studied. Rather, vast freshwater wetlands backed low-gradient, progradational coasts locally having bars and barriers. The barriers were not prerequisites for substantial peat accumulation, although may have locally assisted peatland development by raising the profile of coastal equilibrium.     

Petrological considerations for the demineralization of Rajmahal coals with <Emphasis Type="Italic">Pseudomonas mendocina</Emphasis> B6-1

The present study entails the results of the petrological coniderations for demineralization of Rajmahal Gondwana coals with Psudomonas mendocina B6-1. Inertinite group macerals are the dominant constituents of these coals, followed by vitrinite group, while liptinite occurs in low concentration. The amount of Mineral matter is moderately high. The concentration of major, minor and trace elements is high when compared with Clarke values. After the treatment of these coals with Pseudomonas mendocina strain B6-1, a significant reduction in the elemental content of oxygen, hydrogen and sulphur was observed. A gradual reduction of pyrite phase due to bioleaching was identified and its signatures were reflected in the XRD spectra and FTIR absorption bands. Over 5 % reduction in the ash content and decrease of major, minor and trace element to variable degrees were also noticed. Fe, As, and Ca positively correlate with the ash removal percentage indicating that the samples with high concentration of these elements were prone to demineralization with Pseudomonas mendocina strain B6-1 whereas Ni, Zn, Cr and Cu, negatively correlate with the ash removal percentage and shows that their enrichment impeded the process of demineralization. With increasing concentration of vitrinite the removal of major/minor/trace elements also increased which is attributed to the possible association of these elements with the mineral matter occurring as superficial mounting and superficial blanketing over the vitrinite macerals. This could facilitate the bacterial access to the elements to act upon and remove it to the variable extent. Some minerals occur intergrown with inertinites causing restricted bacterial action owing to the nonexposure of the mineral particles and less surface area available to the bacteria for bioleaching. Sulfur removal strongly relates with increase in inertinite content and decrease in liptinite content. This appears that sulfur associated with liptinites have shown difficult removal condition. The maximum removal of the trace elements like Cd, Cu, Co, Zn and Pb was observed from the ‘banded dull coal’ samples of the Rajmahal basin while maximum removal of major/minor elements like Fe, Ca and Mg was noticed from the ‘banded bright coal’ samples. However, maximum removal of Mn and As was also observed in the samples of ‘banded coal’.     

Environmental assessment of elements and polyaromatic hydrocarbons emitted from a Canadian coal-fired power plant

A detailed assessment of elements was carried out at a power plant rated at approximately 760 MW of electricity using western Canadian subbituminous coal. The concentrations of elements of environmental concern (As, Cd, Cr, Hg, Ni, and Pb) in milled coals, ashes, stack-emitted materials. Speciation of As, Cr, and Ni were determined. The polyaromatic hydrocarbons (PAHs) emitted from the stack were also measured. The rates of input of elemental input for As, Cd, Cr, Hg, Ni, and Pb were 28, 0.94, 230, 0.44, 44, and 88 kg/day, respectively; of which only 0.16, 0.01, 0.40, 0.27, 0.15, and 0.04 kg/day, respectively, were stack emitted. The total stack emission of toxic elements is 1.02 kg/day, with Cr being the highest contributor to this group with 0.4 kg/day. However, Hg at 0.27 kg/day has the highest percentage rate of emission at about 60%, while Cd has the lowest at about 1%. The electrostatic precipitator (ESP) removes a significant portion of the elements indicated by their relative enrichment (RE) ratios greater than 0.7. The results show that most of the elements in milled coal are low compared to world coals and other Canadian milled coals.Mercury is mostly ( 81%) emitted as gaseous elemental mercury (GEM), with 19% as reactive gaseous mercury (RGM). Particulate mercury is very low and averages about 0.1% of the total mercury at this station. Most of the arsenic in the milled coal is primarily associated with pyrite or as arsenate in its less toxic form of As⁺⁵ (> 95%). In both bottom and fly ashes, more than 95% of the total arsenic is present as As⁺⁵. Chromium in the milled coal and bottom ash is mostly non-toxic (Cr⁺³). The more toxic Cr⁺⁶ comprise less than 5% of the total Cr in the ESP fly ash and the stack-emitted ash. Nickel in milled coal and ashes is in the form of non-toxic Ni⁺², predominantly in coordination with oxygen.The emitted PAHs include acenapthene, fluorene, 2-methyl-fluorene, phenathrene, anthracene, fluoanthene, and pyrene; which are emitted from stack at the combined rate of 3.6 g/day. The concentrations of elements of environmental concern (As, Cd, Hg, Ni, and Pb) emitted to the atmosphere by the power plant in the zone of maximum impact at ground level are lower than those listed in the Health Guidelines of the USEPA and Canadian National Air Pollution Surveillance. This is based on stable meteorological conditions, down wind from the power plant for a maximum distance of 3 km.     

Geochemistry, mineralogy, and technological properties of the main Stephanian (Carboniferous) coal seams from the Puertollano Basin, Spain

This study is focused on the occurrence and distribution of mineral matter and major and trace elements in the high volatile bituminous coal from Puertollano (south-central Spain). The relationship between ash behaviour and inorganic composition, as well as the possible formation of fouling and slagging deposits in boilers during the conversion process, were investigated. The Puertollano coals do not exhibit plastic properties, despite their rank, probably because of their high ash and inertinite contents.The Puertollano coal has medium to low total S content (0.48% to 1.63% db, with a mean of 1.0% db) and is characterised by relatively high contents of Si, Pb, Sb, and Cs. Some elements such as As, Cd, Co, Cr, Cu, Ge, Li, Mn, Ni, W, and Zn are also present in relatively high contents. The enrichment in a number of heavy metals could be attributed to the common sulphide ores occurring near the Puertollano coal deposit.The following trace elements affinities are deduced: (a) sulphide affinity: As, Co, Cd, Cu, Ni, Sb, Tl, and Zn; (b) aluminum–silicate affinity: K, Ti, B, Co, Cr, Cs, Cu Ga, Hf, Li, Nb, Rb, Sn, Ta, Th, V, Zr, and LREE; (c) Carbonate affinity: Ca, Mg, Mn, and B; (d) organic affinity: B.The very high Si levels and the anomalous enrichment in Cs, Ge, Pb, Sb, and Zn shown by the Puertollano coals account for the high contents of these elements in the Puertollano fly ash when compared with the other Spanish coal fly ashes.The chemical composition of the high temperature ash (HTA) is consistent with the trend shown by the ash fusion temperatures (AFT) and also with the predictive indices related to slagging and fouling propensities. Thus, the ash fusion temperatures increase with high values of Al₂O₃ as well as with the decrease in Fe₂O₃, CaO, and MgO.     

Geochemistry and Mineralogy of Paleocene Coal from the Padhrar and Darra Adam Khel Coalfields of Pakistan

Pakistan is rich in coal resources, which amount to around 186 billion tons. The Paleocene Padhrar and Darra Adam Khel coalfields are located in the Central Salt Range Punjab Province and the Khyber Pakhtunkhwa Province, Pakistan, respectively. Padhrar coal has not been studied in detail and the Darra Adam Khel coalfields are newly-discovered, so no research has been done, due to security considerations. In this study, an attempt has been made to study the geochemical and mineralogical characteristics of the Padhrar and Darra Adam Khel coals, in order to learn about the coal quality, element enrichment mechanism, sedimentary medium conditions and potentially valuable elements for coal utilization. The Padhrar and Darra Adam Khel coals are low to medium ash, low moisture content, high in volatiles and high total sulfur coal. The vitrinite reflectance in Darra Adam Khel coal is higher than in Padhrar coal, indicating either a greater burial depth or the effects of Himalayan tectonism. The vitrinite content is dominant in the Padhrar and Darra Adam Khel coals, followed by inertinite and liptinite, the major minerals including quartz, clay minerals, calcite and pyrite. The trace elements Ni, As, Be Zn, Ge, Mo, Ta, W, Co and Nb, Sn, Hf, Ta, Pb, Th, Cd, In, Be, V, Cr, Zr, Ag, Li, W and Co are concentrated in some of the Padhrar and Darra Adam Khel coal samples, respectively. The Padhrar coal shows positive Ce, Eu and Gd anomalies, with most of the Darra Adam Khel coal showing negative Ce, Eu and positive Gd anomalies with high LREE. The Al2O3/TiO2 values indicate that the sediment source of the Padhrar and Darra Adam Khel coals is mostly related to intermediate igneous rocks. The Sr/Ba, SiO2 + Al2O3, Fe2O3 + CaO + MgO/SiO2 + Al2O3 and high sulfur content in the Padhrar and Darra Adam Khel coals indicate epithermal and marine water influence with a tidal flat, coal-forming environment and a deltaic coal-forming environment, respectively.     

Geochemistry of beryllium in Bulgarian coals

The beryllium content of about 3000 samples (coal, coaly shales, partings, coal lithotypes, and isolated coalified woods) from 16 Bulgarian coal deposits was determined by atomic emission spectrography. Mean Be concentrations in coal show great variability: from 0.9 to 35 ppm for the deposits studied. There was no clear-cut relationship between Be content and rank. The following mean and confidence interval Be values were measured: lignites, 2.6 ± 0.8 ppm; sub-bituminous coals, 8.2 ± 3.3 ppm; bituminous coals, 3.0 ± 1.2 ppm; and anthracites, 19 ± 9.0 ppm. The Be contents in coal and coaly shales for all deposits correlated positively suggesting a common source of the element. Many samples of the coal lithotypes vitrain and xylain proved to be richer in Be than the hosting whole coal samples as compared on ash basis. Up to tenfold increase in Be levels was routinely recorded in fusain. The ash of all isolated coalified woods was found to contain 1.1 to 50 times higher Be content relative to its global median value for coal inclusions.Indirect evidence shows that Be occurs in both organic and inorganic forms. Beryllium is predominantly organically bound in deposits with enhanced Be content, whereas the inorganic form prevails in deposits whose Be concentration approximates Clarke values.The enrichment in Be exceeding the coal Clarke value 2.4 to 14.5 times in some of the Bulgarian deposits is attributed to subsynchronous at the time of coal deposition hydrothermal and volcanic activity.