Role of coal type and rank on methane sorption characteristics of Bowen Basin, Australia coals

The effect of coal composition, particularly the organic fraction, upon gas sorption has been investigated for Bowen Basin and Sydney Basin, Australia coals. Maceral composition influences on gas retention and release were investigated using isorank pairs of hand-picked bright and dull coal in the rank range of high volatile bituminous (0.78% R_{o max}) to anthracite (3.01% R_{o max}). Adsorption isotherm results of dry coals indicated that Langmuir volume (V_L) for bright and dull coal types followed discrete, second-order polynomial trends with increasing rank. Bright coals had a minimum V_L at 1.72% R_{o max} and dull coals had a minimum V_L at 1.17% R_{o max}. At low rank, V_L was greater in bright coal by about 10 cm³/g, but as rank increased, the bright and dull trends converged and crossed at 1.65% R_{o max}. At ranks higher than 1.65% R_{o max}, both bright and dull coals followed similar trends. These competing trends mean that the importance of maceral composition on V_L varies according to rank. In high volatile bituminous coals, increases in vitrinite content are associated with increases in adsorption capacity. At ranks higher than medium to low volatile bituminous, changes in maceral composition may exert relatively little influence on adsorption capacity. The Langmuir pressure (P_L) showed a strong relationship of decreasing P_L with increasing rank, which was not related to coal type. It is suggested that the observed trend is related to a decrease in the heterogeneity of the pore surfaces, and subsequent increased coverage by the adsorbate, as coal rank increases. Desorption rate studies on crushed samples show that dull coals desorb more rapidly than bright coals and that desorption rate is also a function of rank. Coals of lower rank have higher effective diffusivities. Mineral matter was found to have no influence on desorption rate of these finely crushed samples. The evolution of the coal pore structure with changing rank is implicated in diffusion rate differences.     

Petrologic studies of terrestrial organic matter in Carpathian flysch sediments, southern Poland

In the Carpathian Flysch, coal is present either as exotics of Carboniferous coal deposits or as autochthonous, thin layers of lustrous coal. This paper present the results of the studies of coal-bearing rocks that are coeval with the enclosing flysch sediments. These coals form lenses up to 0.15 m thick. Their morphology precludes an exotic origin. The main petrographic component is collinite with admixtures of poorly fluorescing telinite. Minor components are: exudatinite, sporinite, fusinite, micrinite and sclerotinite. Mineral matter consists of framboidal pyrite clay minerals and quartz.The random reflectance of telocollinite varies from 0.38% to 0.72%, which corresponds to subbituminous and bituminous ranks. Correlation between chemical analysis, coking properties and relfectance measurements, leads to the conclusion that boundary between subbituminous and bituminous coals should be defined by the following values: C=80wt%, VOLATILES=43wt%; calorific VALUE=32.3 MJ/kg; and R^o=0.56–0.57%.Atypical properties, such as: upper C value (75–80wt%); high volatile matter contents (over 43wt%) and low random reflectance (^o about 0.38–0.57%) in subbituminous coals; low C value (about 80–82wt%); low reflectance (0.56–0.72%); and good coking properties, of the bituminous coals are attributed to quick coalification during increasing temperature as a result of tectonic stress.     

内蒙古胜利煤田0-1孔煤中微量元素地球化学特征

运用电感耦合等离子体质谱和煤质分析等技术方法,对内蒙古胜利煤田0-1号钻孔揭露的早白垩世1、2和4号煤层(共20个煤分层,1个夹矸)进行了研究。结果显示,1、2号煤层的挥发分产率大于44%,透光率小于50%,煤类为褐煤;4号煤层挥发分产率42%,透光率53%,煤类为次烟煤(长焰煤);1、2号煤层灰分和硫含量较高,4号煤层灰分和硫含量较低。与世界煤微量元素含量平均值相比,1、2和4号煤层中Sb富集,V、Zr、Nb、Hf、W等元素轻微富集,其它微量元素的含量接近或低于世界煤含量的平均值。1、2和4号煤层中稀土元素和钇(REY)含量较低,根据上地壳标准值(La/Lu)N比值,所有煤分层均显示重稀土富集类型特征,而煤中泥岩夹矸则显示轻稀土富集类型特征。     

Co-carbonization of selected American coals with commercial additives

Because of the short supply of high-quality coking coals in certain areas of the world, many methods of improving the coking characteristics of poorly coking or noncoking coals have been examined as alternatives to importing more expensive, better quality coals. Co-carbonization, or the addition of coal-derived or petroleum-derived materials to the coal charge prior to carbonization, has been used on a commercial basis in the Japanese coking industry. These additives have been used in both solid and liquid form as binders in coal briquettes or as direct additions to the coal blend.In this study three different coal lithotypes were sampled from each of three United States bituminous coal seams: (1) a marginally coking high-volatile B-rank Illinois No. 6 Seam; (2) a highly fluid, good coking quality, high-volatile A-rank Pittsburgh Seam; and (3) a strongly coking low-volatile Blue Creek Seam. Each lithotype sample was carbonized in small-scale (50 g) charges with each of three additives at 0, 2, 5, and 10% additive by weight. The additives included ASP, an asphalt pitch; KRP, a petroleum residue pitch; and SRC, a solvent-refined coal product. The different lithotypes were sampled to examine the effects of coal type as well as rank. A micro-tumbler test was used to give at least a relative coke-strength value for the cokes produced. In addition, all the cokes produced were examined microscopically to determine the effects of co-carbonization on the coke structure.The Illinois No. 6, Pittsburgh, and Blue Creek Seam coals all showed substantial strength increases when co-carbonized with 2, 5, and 10% of each of the three additives, particularly at the 5 and 10% levels. The SRC appears to be the best additive overall for the three ranks of coal, as judged by its ability to combine with the coal to make a higher strength coke. There appear to be no conclusive coke-strength differences among lithotype samples for any of the three coals, probably because of the small scale of the tests and the relatively small differences in inert maceral content among the lithotypes. Five percent by weight of additive appears to be sufficient, if properly blended with the coal charge, to produce higher strength cokes. This is also probably the maximum economically viable level, particularly in the United States coking industry. Two percent is probably the minimum additive level for adequate mixing on a commercial scale.     

Studies of the relationship between coal petrology and grinding properties

The maceral and microlithotype composition of selected coals has been investigated with respect to the grinding properties, specifically Hardgrove grindability index (HGI), of the coals. The study expands upon previous investigations of HGI and coal petrology by adding the dimension of the amount and composition of the microlithotypes. Coal samples, both lithotypes and whole channels, were selected from restricted rank ranges based on vitrinite maximum reflectance: 0.75–0.80% R_max, 0.85–0.90% R_max and 0.95–1.00% R_max. In this manner, the influence of petrographic composition can be isolated from the influence of rank. Previous investigations of high volatile bituminous coals demonstrated that, while rank is an important factor in coal grindability, the amount of liptinite and liptinite-rich microlithotypes is a more influential factor. In this study, we provide further quantitative evidence for the influence of microlithotypes on HGI and, ultimately, on pulverizer performance.     

Possibilities of the utilization of micropetrographic parameters in the scientific classification of bituminous coals

Proposals for new scientific classifications of bituminous coals are based on micropetrographic parameters, i.e. vitrinite reflectance as a criterion of the coalification and maceral composition, presupposed to express the connection between the genetic peculiarities and physical, chemical, and technological properties of the coal mass. In the case of coals with high inertinite contents, however, the utilizability of these parameters meets with difficulties resulting from the subjectivity of determining the different transitional material and from insufficient knowledge of inertinite behaviour at higher temperatures. In the case of the maceral-variable bituminous coals produced in the Ostrava-Karviná Coal Basin, these insufficiencies are not important since it is especially the expression of the variability of the properties of isometamorphic vitrinites, which has decisive effects up-on the course of the thermo-chemical transformations, that is of principal importance to the scientific classification of these coals.In the first approximation, the properties of isometamorphic vitrinites may be expressed by the parameter (H/O)_at, closely connected with fluidity. While the micropetrographic parameters reflect in particular the peculiarities in the chemical structure of the aromatic parts of coal macromolecules, the parameter (H/O)_at expresses the properties of the non-aromatic structures of vitrinite, significantly affecting the course of its thermal degradation. The experimental results show that the value of the parameter (H/O)_at, fluidity and the course of degassing the coal of a lower coalification are independent of the maceral composition and vitrinite reflectance; also that the caking and coking properties of low-rank coals are especially dependent on the parameter (H/O)_at and partially on the micropetrographic parameters. All these facts should be taken into consideration in preparing new scientific classifications of bituminous coals.     

Reactivity of semifusinite and fusinite in the view of micro-Raman spectroscopy examination

The study was performed on inertinite concentrates prepared from 19 samples of bituminous, mostly coking, coal (R_r = 0.87–1.42%) from the Upper Silesian Coal Basin of Poland. In all examined samples, total semifusinite differs from fusinite, in terms of mean values, by higher frequencies of the D1 and D4 band position and lower frequency of the D3 band position, higher G band FWHM, the A_D3/A_ALL and A_D4/A_ALL ratios (where A_ALL means the surface of all the Raman bands), and lower D1 band FWHM, the I_D1/I_G and A_D1/A_ALL ratios. Similar differences exist between reactive and non-reactive semifusinites. The diameter of coherent domains (L_a) increases in the following sequence: reactive semifusinite < non-reactive semifusinite < fusinite. The A_{D3 + D4}/A_ALL ratio reflects inertinite reactivity in bituminous coals, and decreases with the increase of mean reflectance (R_r) of semifusinite and fusinite. Using the A_{D3 + D4}/A_ALL, I_D1/I_G and A_D1/A_ALL ratios or the D3 band position it is possible to interpret thresholds dividing, in terms of mean values, total semifusinite and fusinite, coming from different coals. The results of the study suggest that the term “semifusinite” should only comprise reactive and semi-reactive components. Non-reactive semifusinite should be considered fusinite. Semifusinite from bituminous coals (of R_r ≈ 0.9–1.4%), defined in the proposed way, would be characterized by the A_{D3 + D4}/A_ALL ratio ≥ 0.35, or the I_D1/I_G ratio ≤ 1.03.     

The use of numerical simulation in predicting coalbed methane producibility from the Gates coals, Alberta Inner Foothills, Canada: Comparison with Mannville coal CBM production in the Alberta Syncline

Two medium to low volatile bituminous rank coals in the Lower Cretaceous Gates Formation (Mannville equivalent), Inner Foothills of Alberta, were cored as part of a coalbed methane exploration program. The target seams (Seam 4 and Seam 10) were intersected at 652 m and 605 m, respectively. The coals were bright banded, relatively competent and reasonably cleated, with cleat spacing between 5–20 mm. The FMI (Formation Micro-Imaging) log identified two primary fracture directions, corresponding to both face and butt cleats, which were developed almost equally in some coal intervals. The amount of shearing was limited, in spite of the presence of numerous thrust faults and fold structures in the corehole vicinity. Total gas content was high, with an average of 17.7 cm³/g (arb; 568.1 scf/t). An adsorption isotherm of the thick Seam 4 showed gas saturation levels of 90% at in-situ reservoir conditions. Methane content was 92–96% and carbon dioxide levels were less than 2%. Isotopic studies on the methane confirmed the thermogenic origin of the gas, as anticipated based on the coal rank. The coal seams were fracture stimulated using 50/50 nitrogen and fresh water along with 9 to 12 tons of 12/20 mesh sand used as a proppant. It is believed that the coals were not stimulated properly because of the small proppant volume and the complex — and often unpredictable — fracture pattern in coals, particularly in the Inner Foothills region that has high stress anisotropy. An injectivity test showed coal absolute permeability to be less than 1 mD, the skin to be −  2 (indicating a slightly damaged coal) and water saturation in the cleats to be 90%. A four-month production test was conducted; gas rates declined from 930 to 310 m³/d (33 to 11 MCFD) and water rates were low (< 5 BWD). Produced water was saline (TDS was 20,000 mg/L) and high in chloride and bicarbonate ions. Production testing was followed by history matching and numerical simulation, which consisted of numerous vertical and horizontal well development scenarios and other parameters. Simulating multiple parallel horizontal wells in the Gates coals resulted in the highest peak gas production rates, cumulative production and recovery efficiencies, in agreement with public data from the Mannville coals in the deeper part of the Alberta Syncline. The positive effect of constructive interference in depressurizing the coal reservoirs and accelerating gas production over short periods of time was demonstrated. Coal quality data from a nearby underground mine shows that drilling horizontal wellbores in the Gates coals would be challenging because of unfavourable geomechanical properties, such as low cohesion and unconfined compressive strength values, and structural complexity.     

Changes in hydrocarbon maturity indices with coal rank and type,Buller Coalfield,New Zealand

The Buller Coalfield (South Island, New Zealand) is an inverted late Paleogene Basin that contains middle Eocene bituminous coals which exhibit considerable variation in both coal rank (across-basin), and coal type (in-seam). Twenty-two fractionated bitumen extracts of Brunner Coal Measures coal samples from 12 drillholes were analyzed by GC and GC–MS to characterize the effect of coal rank and type on conventional hydrocarbon maturity indices at the beginning and end of the oil window (0.56–1.26% Ro_max).The Carbon Preference Index, pristane/phytane and isoprenoid/n-alkane ratios evolve throughout the high volatile bituminous B rank stage, while other biomarker ratios [18α(H)-22,29,30-trisnorneohopane/17α(H)-22,29,30-trisnorhopane (Ts/Tm), 18α(H),21β(H)-30-norneohopane (C₂₉ Ts)/17α(H),21β(H)-30-norhopane and C₃₀ diahopane/hopane] do not show appreciable change in value until medium volatile bituminous rank. Various aromatic based ratios appear to be more effective in delineating rank throughout the entire oil window; in particular the Methylphenanthrene Index and vitrinite reflectance are positively correlated over the entire bituminous rank range. However, subtle changes in depositional conditions (variable coal type) complicate these rank estimates. Within a given coal seam, variation in CPI, isoprenoid/n-alkane and hopane/sterane ratios appear to be related to the hydrogen content of the coal, while the homohopane index and the oleanane/hopane ratio covary with sulfur content. As with depressed vitrinite reflectance values, MPI is similarly lowered in the perhydrous samples. The mechanisms that control these hydrocarbon parameters during deposition and diagenesis are complex and convoluted, however, changes in bacterial activity and community (with marine incursion) appear to play an important role. Due to these anomalies, none of the hydrocarbon maturity indices calculated can be singularly used to constrain coal rank.     

Arsenic in coal: a review

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, As_org dominates, both being authigenic. A contribution of the terrigenic As (in silicates) is usually minor and of the biogenic As_bio (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 — As_pyr or As_org. If As_pyr dominates, an As accumulation in heavy fractions (or in high-ash coals) is observed, and if As_org dominates, it is enriched in medium-density fractions (or low- and medium-ash coals). Arsenic is in part accumulated in the inertinite vs. vitrinite (As_org ?).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 As_org, As_pyr and “shielded” As-bearing micromineral phases escape into gaseous and particulate phase and only minor part of As_clay 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 As_pyr 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.     

Quality of selected coal seams from Indiana: implications for carbonization

The chemical properties of two high-volatile bituminous coals, the Danville Coal Member of the Dugger Formation and the Lower Block Coal Member of the Brazil Formation from southern Indiana, were compared to understand the differences in their coking behavior. It was determined that of the two, the Lower Block has better characteristics for coking. Observed factors that contribute to the differences in the coking behavior of the coals include carbon content, organic sulfur content, and oxygen/carbon (O/C) ratios. The Lower Block coal has greater carbon content than the Danville coal, leading to a lower O/C ratio, which is more favorable for coking. Organic sulfur content is higher in the Lower Block coal, and a strong correlation was found between organic sulfur and plasticity. The majority of the data for both seams plot in the Type III zone on a van Krevelen diagram, and several samples from the Lower Block coal plot into the Type II zone, suggesting a perhydrous character for those samples. This divergence in properties between the Lower Block and Danville coals may account for the superior coking behavior of the Lower Block coal.     

Changes of semifusinite and fusinite surface roughness during heat treatment determined by atomic force microscopy

This study describes changes of surface roughness of semifusinite and fusinite as an indicator of structural alteration resulting from heat treatment at 400–1200 °C. Surface roughness has been investigated by atomic force microscopy of inertinite concentrates from coking coals (vitrinite reflectance R_r = 1.07%–1.41%) from the Upper Silesian Coal Basin of Poland (Namurian C — Westphalian A). Unheated fusinite has a higher surface roughness than semifusinite from the same coal. The average surface roughness of semifusinite decreases with the Swelling Index of the parent coal. Heating increases the surface roughness of semifusinite and fusinite. Increase in the average surface roughness is stronger for semifusinite than fusinite and correlates to increasing reflectance of these macerals. The surface roughness of semifusinite correlates to the relative mass loss of the inertinite concentrates during heating. After heating to 1200 °C fusinite has a lower average surface roughness than semifusinite from the same coal. Consequently, average surface roughness can be used as a measure of structural alteration of inertinite group macerals during heat treatment.     

Correlation between optical, chemical and micro-structural parameters of high-rank coals and graphite

In order to identify the parameters that best characterize the chemical and structural evolution of organic matter during coalification, the relationships between optical, chemical and micro-structural parameters in high-rank coals and natural graphite were studied. The samples include anthracites from Peñarroya–Belmez–Espiel Basin (Spain), Douro Basin (Portugal), and Alto Chicama Basin (Peru); and natural graphite from Canada, Mozambique, and Austria.Correlations between the following optical parameters were assessed: vitrinite random reflectance (R_r), Reflectance Indicating Surfaces (RIS) axis (R_MAX, R_INT and R_MIN), and RIS parameters (R_am, R_ev and R_st), as well as B_w and AI anisotropy parameters. Furthermore, the chemical parameters used were chosen according to their significant variation in coals, namely volatile matter, carbon, and hydrogen contents calculated in dry ash free basis (VM_daf, C_daf, H_daf), as well as the H/C atomic ratio. Structural organization was characterized by micro-Raman spectroscopy and XRD. Raman parameters used were the full width at half maximum (FWHM) and position of G and D1 bands on the first-order Raman spectrum, and the ID1/IG intensity area ratio. The selected XRD parameters were interlayer spacing d₀₀₂, and crystallite sizes L_a and L_c.Results show that: (i) R_MAX RIS axis seems to correlate best with chemical and micro-structural parameters; (ii) for the majority of studied samples, H_daf and H/C atomic ratio are the only chemical parameters with significant correlations with R_MAX; (iii) the FWHM of the G band of Raman spectrum shows good linear correlation with the XRD parameter d₀₀₂; and, (iv) structural organization of carbon materials, as measured by trends in their optical and crystalline parameters, is influenced by their hydrogen content (daf basis) and therefore by the H/C atomic ratio.     

A note on the characters of some Lower Gondwana coals of West Siang district in the Arunachal Himalaya and their trace element content

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.     

The lateral and vertical reflectance and petrological variation of a heat-affected bituminous coal seam from southeastern British Columbia, Canada

Thermally altered pods of coal of very high rank have been observed in a high-volatile-bituminous coal seam in the eastern side of Eagle Mountain, Elk Valley Coalfield, British Columbia. Rank changes have been measured over a strike distance of 7.5 m from 1.24% to 7.1% R_{o max}, corresponding to a rank gradient of 0.78% R_om⁻¹.Petrologically, unaltered to extremely altered vitrinite showing nongranular (basic) anisotropy, mosaic-textured liptinite and pyrolytic carbon are the most abundant components. The limited presence of mosaic on vitrinite is an indication that the coal seam may have been weathered prior to being heat-affected.Evidence points to localized temperatures as high as 1,000°C, which could have been caused by a lightning strike. The eastern side of Eagle Mountain has experienced higher temperatures than the western side, and it appears that the heat ‘front’ and zone of alteration have an irregular pattern, pointing to saturation of parts of the coal seam by water.Four types of pyrolytic carbon having distinct morphology, anisotrophy and optical path with increasing temperature were observed. Reflectance of pyrolytic carbon falls within the zone of heat-affected coals, whereas the optical path of heat-affected Seam 15 samples is different from that of fresh coal with increasing rank.Finally, the reflectance of vitrinite in heat-affected coal is higher than the reflectance of vitrinite in carbonaceous shale in the Seam 15 section.     

Nitrogen functionality in “oil window” rank range vitrinite rich coals and chars

X-ray photoelectron spectroscopy (XPS) was used to characterize organic nitrogen species in coals and chars. The coals comprise a set of vitrinite-rich samples from the Penn State Coal Bank set, ranging from vitrinite reflectance (R_r) 0.42-1.60%. Chars were obtained after coal pyrolysis under an inert atmosphere at 800 °C and fast heating rate. In the coals, pyrrolic nitrogen was the predominant form, steadily decreasing with coal rank, while pyridinic and quaternary nitrogen showed pronounced variation with rank. In contrast to the coals, the chars show much less pyrrolic and pyridinic nitrogen, and more quaternary nitrogen. The chars were also characterized by having oxidized nitrogen and nitro sub-peaks, which were not observed for the coals. Apparently the occurrence of these forms is related to the decrease in the pyridinic nitrogen.     

On the optically biaxial character and heterogeneity of anthracites

The results of the study of optical properties of 13 anthracites from different parts of the world are presented in this paper. Measurements of reflectance values were made on non-oriented vitrinite grains for a minimum of 300 points per sample. The reconstruction of Reflectance Indicating Surfaces (RIS) were made by Kilby's method [Kilby, W.E., 1988. Recognition of vitrinite with non-uniaxial negative reflectance characteristics. Int. J. Coal Geol. 9, 267–285; Kilby, W.E., 1991. Vitrinite reflectance measurement — some technique enhancements and relationships. Int. J. Coal Geol. 19, 201–218]. It was found that the use of Kilby's method for strongly anisotropic materials like anthracites did not give unambiguous results. Some improvement in Kilby's method, consisting of the division of the cumulative cross-plot into several elemental components, is suggested. Each elemental cross-plot corresponds to a textural class of anthracite, which is characterized by the values of RIS main axes R_MAX^(k), R_INT^(k) and R_MIN^(k) (k=1,2,…n; n — number of classes). The global texture of anthracite is characterized as a RIS with main axes calculated as the weighted means of , and for each class of this anthracite.The division of cumulative Kilby's cross-plot on elemental components makes possible the calculation of new coefficients H_t and H₁₀ characterizing the heterogeneity of the structure and texture of anthracites. The results of our study show that all anthracites have biaxial negative textures, but their heterogeneity varies in a wide range of H_t and H₁₀ coefficients depending upon the individual coal basin.     

A preliminary study of mineralogy and geochemistry of four coal samples from northern Iran

This study is related to four Jurassic-age bituminous coal (0.69–1.02 Ro%) samples collected from coal mines from the west, central and east of central, Alborz in northern Iran. Geological settings played key roles in determining the geochemistry and mineralogy of coals from the central Alborz region of northern Iran. The mineralogy of coals from the eastern part of the region is dominated by kaolinite; halloysite; and carbonates such as calcite, dolomite/ankerite, and siderite. The coals were deposited in a lacustrine environment. In the western part of the region, where the depositional setting was also lacustrine with volcanic input and tonstein deposition (glass shards present), the coal primarily contains kaolinite (68%) and fluorapatite (26%). In contrast, coal from the central part of the region, which was deposited in a terrestrial environment and on eroded limestone and dolomite rocks, is dominated by dolomite (98%) with little input by kaolinite. These coals have low sulphur (0.35–0.70 wt.%), which is mostly in the organic form (0.34–0.69 wt.%). Pyritic sulphur is detected only in one coal and in small quantities. The boron contents of these coals range from 9 to 33 mg/kg, indicating that deposition occurred in a fresh water environment. Coal with higher concentrations of Ba, Sr, and P contain fluorapatite and goyazite–gorceixite series [BaAl₃ (PO₄)₂ (OH)₅, H₂O] minerals, which indicates volcanoclastic input. Compared to world coal averages, these coals exhibit low concentrations of elements of environmental concern, such as As (1.3–5.9 mg/kg), Cd (< 0.02–0.06 mg/kg), Hg (< 0.01–0.07 mg/kg) Mo (< 0.6–1.7 mg/kg), Pb (4.8–13 mg/kg), Th (0.5–21 mg/kg), Se (< 0.2–0.8 mg/kg) and U (0.2–4.6 mg/kg). Two of the northern Iranian coals have concentrations of Cl (2560 and 3010 mg/kg) that are higher than world coal average.     

Coalification levels and their significance in the groundhog coalfield,North-Central British Columbia

The only significant deposits of anthracite and meta-anthracite in Canada occur in Upper Jurassic-Lower Cretaceous strata of the Groundhog coalfield in northcentral British Columbia. The coal rank in the coalfield varies from low volatile bituminous (1.70% R_{0 max}) to meta-anthracite (5.8% R_{0 max}). The main coal bearing unit, the Currier, includes up to 17 seams of anthracite and meta-anthracite most of which are less than 1 m thick. In the McEvoy unit, which overlies the Currier, up to 9 coal seams, mainly of semi-anthracite, occur that are up to 0.8 m thick. The coals are variably argillaceous, locally sheared and cut by quartz and less commonly, by carbonate veins. Coalification gradients in the coalfield vary from 0.8% to 3.0% R_{0 max} km^?1. The rank of coal within both the McEvoy and Currier units appears to increase towards the eastern edge of the coalfield.The level of coalification and the coalification gradients in the coalfield are anomalously high considering an indicated maximum depth of burial of 3500 m. From comparison with coalification models it appears that geothermal gradients in the order of 50° to 70°C/km must have existed for a period of time measured in millions of years. Studies to date suggest the coalification is pre-tectonic and thus pre-Late Cretaceous although there is some evidence for high heat flow in the Tertiary. The origin of the high heat flow may be related to intrusion accompanying collision of the Stikine terrain with the early Mesozoic margin of North America and/or high heat flux over an easterly dipping subduction zone below the Coastal volcanic-plutonic arc to the west.     

Petrographic prediction of coking properties for the Curragh coals of Australia

Curragh Queensland Mining Limited, Australia, produces a high quality medium volatile bituminous coking coal from the Orion, Pollux and Castor seams from the upper Permian Rangal Coal Measures. It is one of the lowest ash, prime hard coking coal blends produced in Australia. It is also low in sulfur and produces very strong coke when carbonized alone and in blends. Early attempts to predict coking properties of the coals from petrographic data produced predicted coke stabilities that were significantly lower than those determined from coke tests. There is some question as to how much of the ‘inertinite’ in these and other southern hemisphere coals is truly inert during carbonization and how much is reactive. The current study characterized the Curragh coals in terms of physical, chemical and petrographic characteristics and also involved the production of test oven cokes for characterization and strength testing. As part of the work effort a series of suggested techniques for improving predictions of coke strength from petrographic data were examined and a new and improved technique was developed for the Curragh coals. How broadly the technique can be applied to other coals needs to be determined.