淮北煤田煤中汞的赋存状态

系统采集淮北煤田10、7、5、4和3煤层的29个煤样品, 采用逐级化学提取方法研究了煤中汞的赋存状态, 根据提取步骤和汞的特性, 将煤中的汞分为水溶态、离子交换态、有机态、碳酸盐结合态、硅酸盐结合态和硫化物结合态, 利用Flow Injection Mercury System(FIMS)分析了样品中总汞和不同形态中汞的含量.测试结果表明, 与华北石炭-二叠纪煤、中国煤以及美国煤含量相比较, 淮北煤田煤中汞的含量明显富集.逐级化学提取实验结果和煤中汞与硫、灰分的相关分析结果表明, 岩浆的侵入对煤中汞的赋存状态有较大的影响, 不受岩浆侵入影响的10、4和3煤层煤中的汞主要以有机态和硫化物结合态存在, 受岩浆侵入影响的5和7煤层中的汞主要以硅酸盐结合态存在.      

煤矸石中汞和砷的赋存形态研究

对煤矸石中汞、砷的赋存形态进行研究,可以为煤矸石发电过程中汞、砷的脱除提供理论依据。采用逐级化学浸提法将3个不同产地煤矸石中汞、砷的赋存形态分为可交换态、碳酸盐结合态、铁锰结合态、硫化物结合态、有机结合态和残渣态。采用不同的浸提溶液得到对应结合态的测试结果。结果表明,煤矸石中汞、砷的赋存形态具有一定的相似性。煤矸石中汞、砷主要以硫化物结合态为主,其质量分数占总汞的67.66%~72.68%,占总砷的56.71%~79.36%;其次为残渣态,其质量分数占总汞的23.70%~28.06%,占总砷的11.47%~18.02%。另外在煤矸石中砷还以少量有机结合态形式存在。      

Mercury in Eastern Kentucky coals: Geologic aspects and possible reduction strategies

Mercury emissions from US coal-fired power plants will be regulated by the US Environmental Protection Agency (USEPA) before the end of the decade. Because of this, the control of Hg in coal is important. Control is fundamentally based on the knowledge of the amounts of Hg in mined, beneficiated, and as-fired coal. Eastern Kentucky coals, on a reserve district level, have Hg contents similar to the USA average for coal at mines. Individual coals show greater variation at the bench scale, with Hg enrichment common in the top bench, often associated with enhanced levels of pyritic sulfur. Some of the variation between parts of eastern Kentucky is also based on the position relative to major faults. The Pine Mountain thrust fault appears to be responsible for elemental enrichment, including Hg, in coals on the footwall side of the thrust.Eastern Kentucky coals shipped to power plants in 1999, the year the USEPA requested coal quality information on coal deliveries, indicate that coals shipped from the region have 0.09 ppm Hg, compared to 0.10 ppm for all delivered coals in the USA. On an equal energy basis, and given equal concentrations of Hg, the high volatile bituminous coals from eastern Kentucky would emit less Hg than lower rank coals from other USA regions.     

Mercury in coal and the impact of coal quality on mercury emissions from combustion systems

The proportion of Hg in coal feedstock that is emitted by stack gases of utility power stations is a complex function of coal chemistry and properties, combustion conditions, and the positioning and type of air pollution control devices employed. Mercury in bituminous coal is found primarily within Fe-sulfides, whereas lower rank coal tends to have a greater proportion of organic-bound Hg. Preparation of bituminous coal to reduce S generally reduces input Hg relative to in-ground concentrations, but the amount of this reduction varies according to the fraction of Hg in sulfides and the efficiency of sulfide removal. The mode of occurrence of Hg in coal does not directly affect the speciation of Hg in the combustion flue gas. However, other constituents in the coal, notably Cl and S, and the combustion characteristics of the coal, influence the species of Hg that are formed in the flue gas and enter air pollution control devices. The formation of gaseous oxidized Hg or particulate-bound Hg occurs post-combustion; these forms of Hg can be in part captured in the air pollution control devices that exist on coal-fired boilers, without modification. For a given coal type, the capture efficiency of Hg by pollution control systems varies according to type of device and the conditions of its deployment. For bituminous coal, on average, more than 60% of Hg in flue gas is captured by fabric filter (FF) and flue-gas desulfurization (FGD) systems. Key variables affecting performance for Hg control include Cl and S content of the coal, the positioning (hot side vs. cold side) of the system, and the amount of unburned C in coal ash. Knowledge of coal quality parameters and their effect on the performance of air pollution control devices allows optimization of Hg capture co-benefit.     

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.     

Sequential solvent extraction for the modes of occurrence of selenium in coals of different ranks from the Huaibei Coalfield, China

Forms of selenium in bituminous coal, anthracite, and cokeite (natural coke) from Huaibei Coalfield, Anhui, China, have been determined by sequential solvent extraction. The selenium content in bulk samples is 4.0, 2.4, and 2.0 μg/g in bituminous coal, anthracite, and cokeite, respectively. The six forms of selenium determined by six-step solvent extraction are water-leachable, ion-exchangeable, organic matter-associated, carbonate-associated, silicate-associated, and sulfide-associated. The predominant forms of selenium in bituminous coal are organic matter-associated (39.0%), sulfide-associated (21.1%), and silicate bound (31.8%); these three forms account for 92% of the total. The organic matter bound-selenium decrease dramatically from bituminous coal (39.0%) to anthracite (11.6%) and to cokeite (0%), indicating that organic matter bound selenium is converted to other forms during metamorphism of the coal, most likely sulfide-form. The sulfide-associated form increased remarkably from bituminous coal (21.1%) to anthracite (50.4%) and cokeite (54.5%), indicating the formation of selenium sulfide, possibly in pyrite during the transformation of bituminous coal to anthracite and cokeite. The silicate-associated selenium in bituminous coal (31.8%) is much higher than that in anthracite (16.4%) and cokeite (15.8%), indicating that silicate-associated selenium is partly converted to sulfide during metamorphism.     

Petrographic, mineralogy, and geochemistry of coals of Pabedana, Kerman Province, Central Iran

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.     

Deformation metamorphism of bituminous and anthracite coals from China

Tectonic displacement of coal seams in China has resulted in faulting parallel to coal bedding. Displacement along these faults caused significant comminution of the coal on the footwall contributing to various mining problems, the worst of which is catastrophic failure, or “outbursting” of the working face during mining. The granular texture and mostly unconsolidated nature of the coal suggests that faulting occurred relatively late in the coalification sequence, at a time of maximum tectonic stress. Coal samples taken on either side of the fault plane (normal and deformed coal layers) were obtained in an effort to establish what influence these tectonic stresses might have had on coal properties as well as what they might reveal about the influence of tectonic pressure on organic maturity. Sample sets were collected within coal beds from undisturbed and adjacent deformed layers, including 21 bituminous samples from the Pingdingshan coal field and nine anthracite samples from the Jiaozuo coal field, the Tieshenggou coal mine of the Yuxi coal field in Henan province, the Beijing Xishan coal field, the Baijiao mine of the Furong coal field in Sichuang province and the Baisha coal field in Hunan province, China. Results from vitrinite reflectance, proximate and ultimate analyses show some differences in reflectance, hydrogen content and nitrogen content of anthracite coal. No significant difference was found between volatile matter yields of normal and deformed coal specimens. GC measurements of the saturated hydrocarbon fraction of chloroform extracts from bituminous coals showed that lower molecular weight carbon fragments were concentrated in the deformed samples. Therefore, although changes in the gross chemical properties of the deformed coal were insignificant, some modification of the chemical structure is seen to have occurred as a result of exposure to tectonic pressure.     

华亭烟煤地下气化污染物分布及富集规律

煤炭地下气化为我国清洁、低碳、安全、高效现代能源建设开辟新的途径。为研究华亭烟煤地下气化污染物的富集、分布规律,以评估华亭烟煤地下气化的环境影响因素,采用地下气化模拟实验平台系统,通过不同富氧—水气化实验、不同尺度煤样的热解实验,研究煤层气化过程中焦油及气化残留物中重金属元素的富集规律。结果表明:随着烟煤的尺度（块体大小）增加,烟煤热解焦油呈增加趋势,而焦油产率呈先增加后减小的趋势;烟煤在N₂、CO₂气氛中热解时,热解焦油中主要成分为酚类、萘类以及烃类污染物;气化后残留重金属Ni、Cr、Zn、Cu、As这5种元素在氧化区最为富集、还原区次之、干馏干燥区最不富集,而Hg在氧化区富集程度最高、干馏干燥区次之、还原区最次,Pb在还原区富集程度最高、氧化区次之、干馏干燥区最次;重金属元素残留程度由高到低依次为Zn、As、Hg、Cr、Ni、Cu、Pb。针对华亭矿区,煤层气化后应重点检测重金属元素Zn、As、Hg。在后期实际煤层气化生产阶段,应结合华亭矿区煤层特征及地下水特征,在项目选址、气化工艺等方面进行污染物防控。在当前生态环境保护形势严峻的当下,研究成果对煤炭地下气化开采的污染物处置和减排具有一定的指导意义。      

The petrology of greek brown coals

Results are given in the petrography of Greek coals collected from most of the major coal-bearing basins in Greece.Rank was determined by measuring reflectances on the maceral varieties eu-ulminite A and eu-ulminite B and on the maceral textinite. Reflectances obtained from these components indicate a coalification stage of brown coal for all samples. Within this group of samples there is, however, a fairly wide scatter of reflectance values indicating for some of them the transition zone from peat to brown coal and for others a coalification stage close to the transition into bituminous coals. Reflectances obtained from eu-ulminite A and eu-ulminite B were found to correlate well with chemical rank parameters such as volatile matter and calorific value.Composition was determined by maceral analysis. The coals are in general characterized by low amounts of macerals of the inertinite group, low to intermediate amounts of macerals of the liptinite group and high amounts of macerals of the huminite group. Within the latter group densinite, attrinite, eu-ulminite and textinite make up the bulk of the samples.Typical macerals observed in the coals are illustrated by two black and white and three colour plates.Cluster analysis based on maceral distribution, mineral matter and reflectance indicates that the samples studied can be divided into three major groups. The first one is dominated by eu-ulminite and densinite with relatively high reflectances. The second is dominated by attrinite, textinite and texto-ulminite with somewhat lower reflectances. The third is represented by a single sample in which textinite and resinite are the most abundant macerals. This sample also has the lowest reflectance.     

The structural evolution of organic matter during maturation of coals and its impact on petroleum potential and feedstock for the deep biosphere

The structural evolution of coals during coalification from peat to the end of the high volatile bituminous coal rank (VR_r = 0.22–0.81%) has been studied using a natural maturity series from New Zealand. Samples were studied using a range of standard coal analyses, Rock–Eval analysis, infrared spectroscopy (IR), X-ray photoelectron spectroscopy (XPS), and pyrolysis gas chromatography (Py-GC). The structural evolution of coal during diagenesis and moderate catagenesis is dominated by defunctionalisation reactions leading to the release of significant amounts of oxygen and thereby to an enrichment of aromatic as well as aliphatic structures within the residual organic matter. Based on the evolution of pyrolysis yields and elemental compositions with maturity it can be demonstrated that oxygen loss is the major cause for increasing Hydrogen Index values or hydrocarbon generating potentials of coals at such maturity levels. For the first time, the loss of oxygen in form of CO₂ has been quantified. During maturation from peat to high volatile bituminous coal ranks ∼10–105 mg CO₂/g TOC has been released. This is equivalent to 2.50E−4 to 1.25E−3 mg CO₂ generated from every litre of sediment per year falling into the range of deep biosphere utilisation rates. Immature coals, here New Zealand coals, therefore manifest the potential to feed deep terrestrial microbial life, in contrast to more mature coals (VR_r > ∼0.81%) for which defunctionalisation processes become less important.     

Iodine in Chinese coals and its geochemistry during coalification

To determine the I distribution in Chinese coals, a nationwide survey was undertaken based on the distribution, periods of formation, rank and production yields of various coal deposits. A total of 305 coal samples were collected and their I contents were determined by catalytic spectrophotometry with pyrohydrolysis. The geochemistry of I during coalification (including both peat diagenesis and coal metamorphism) was assessed. It was found that the I contents of Chinese coals range from 0.04 mg kg^–1 to 39.5 mg kg^–1 and exhibit a lognormal distribution, with a geometric mean of 1.27 mg kg^–1. Statistical correlation analysis and the observation that I contents increase with coal rank indicate that coal I is chalcophile in nature, and not generally organically bound. When peat developed into lignite through diagenesis, 95–99.9% of the original I was lost. The composition and structure of clay minerals present in the coal were controlled by the original depositional environment. The higher the I content of coals, the more likely the original sediments were affected by a marine environment. Iodine contents increased from lignite through sub-bituminous and bituminous coals to anthracite. This indicates that coal absorbed excess I from hydrothermal fluids during metamorphism (including geothermal metamorphism and telemagmatic metamorphism). The telemagmatic metamorphism was caused by magmatic activities that depended on the specific geological structure of the region. In China, most high-rank coals were formed by telemagmatic metamorphism.     

Maceral/ microlithotype partitioning with particle size of pulverized coal: Examples from power plants burning Central Appalachian and Illinois basin coals

Pulverized coals from eleven power plants burning Central Appalachian coal blends and eight power plants burning Illinois Basin coal blends were studied in order to assess the petrographic nature of industrial-scale coal grinding. All coals were high volatile bituminous. Coals were wet screened at 100 (150 μ), 200 (75 μ), 325 (about 40 μ), and 500 (about 25 μ) mesh. Petrographic analysis of the whole coals and size fractions consisted of a combined maceral and microlithotype analysis. Microlithotype analysis, in particular, provides a reasonable approximation of the whole-particle composition at the scale of utility coal pulverization. In the size fractions, duroclarite, the most abundant trimaceral microlithotype, is most abundant in the coarsest fraction and least abundant in the finest fraction. Vitrite, the most abundant monomaceral microlithotype, exhibits the opposite trend. Duroclarite becomes more enriched in vitrinite towards the finer sizes. The partitioning of microlithotypes and the partitioning of macerals within the microlithotypes is indicative of the relative brittle nature of vitrite compared to the hard-to-grind trimaceral microlithotypes. Increased vitrinite in duroclarite is an indication that the microlithotype within the particular size fraction is more brittle than relatively vitrinite-depleted duroclarite in coarser fractions. The relative grindability of microlithotypes will, in turn, impact combustion efficiency.     

A microscopic study of the combustion residues of subbituminous and bituminous coals from Alberta, Canada

Chars produced by the combustion of a set of three coals from Alberta, Canada, were classified morphologically using reflected light microscopy. Produced chars are different in morphological features, pore thickness, anisotropy and degree of reactivity, because of differences in the vitrinite and inertinite contents.The subbituminous A coal produced the highest percentage of unreactive or slightly reactive components due to its high inertinite content (20.0%), followed by isotropic cenospheres. Isotropic cenospheres, both thin- and thick-walled, and exploded cenospheres are the characteristic chars produced by the high-voltile bituminous B coal, whereas the low-volatile bituminous coking coal produced cenospheres with granular anisotropy (mosaic) on the walls and abundant coke fragmentsOptical microscopy is useful in differentiating the performance of a series of coals during combustion based on petrographic composition and rank and can aid in understanding the relationship between ‘reactive’ and ‘non-reactive’ coal macerals to burnout performance.     

Tetrapyrrole pigments in United States humic coals

Analyses of forty-two United States humic coals have revealed a striking divergence between chlorophyll diagenesis in coals when compared to the more widely studied marine sediments, shales, asphalts and petroleums. Porphyrins of humic coals have been found to be dominated by the ETIO-series, to lack members above C-32, and, in lower ranked samples (e.g. Sub-bituminous-B, high volatile C) to exhibit mass spectral envelopes with unique even-carbon number predominances. The weighted average mass, as well as the carbon number maximum (viz. mode), of these coal porphyrin homologies has been found to decrease as rank increases. The generation of porphyrins of the ETIO-series is suggested as occurring both during early coal formation, including oxidative scission of the isocyclic ring at the phorbide stage, and later during the catagenic alteration of surviving DPEP-series porphyrins. A preliminary study of chlorophyll diagenesis in a South Florida peat partially substantiates this suggestion and has further shown that the coal porphyrins can be derived from bacterial, as well as higher plant, chlorophylls.     

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.     

Application of reflectance micro-Fourier transform infrared analysis to the study of coal macerals: an example from the late jurassic to early cretaceous coals of the Mist Mountain Formation, British Columbia, Canada

The applicability of the reflectance micro-Fourier Transform infra-red spectroscopy (FTIR) technique for analyzing the distribution of functional groups in coal macerals is discussed. High quality of spectra, comparable to those obtained using other FTIR techniques (KBr pellet and transmission micro-FTIR), indicate this technique can be applied to characterizing functional groups under most conditions. The ease of sample preparation, the potential to analyze large intact samples, and ability to characterize organic matter in areas as small as 20 μm are the main advantages of reflectance micro-FTIR. The quantitative aspects of reflectance micro-FTIR require further study.The exaples from the coal seams of the Mist Mountain Formation, British Columbia show that at high volatile bituminous rank, reflectance micro-FTIR provides valuable information on the character of aliphatic chains of vitrinite and liptinite macerals. Because the character of aliphatic chains influences bond disassociation energies, such information is useful from a hydrocarbon generation viewpoint. In medium volatile bituminous coal liptinite macerals are usually not detectable but this technique can be used to study the degree of oxidation and reactivity of vitrinite and semifusinite.     

Effect of oxidative weathering on the thermoplastic and liquefaction behaviors of four coals

Using a Gieseler plastometer to measure the thermoplastic behavior, a systematic study of the change in fluid properties with progressive oxidative weathering of three high volatile A bituminous and one low volatile bituminous coal was performed. The degree of fluidity was found to decrease rapidly with initial oxidation and then more slowly with additional oxidation. The effect of oxidation on liquefaction behavior also was studied. A level of oxidation, which significantly reduced Gieseler fluidity, had no detrimental effect on the liquefaction conversion determined as ethyl acetate soluble material, of three of the four coals tested.     

A review of coal properties pertinent to carbon dioxide sequestration in coal seams: with special reference to Victorian brown coals

This paper presents reviews of studies on properties of coal pertinent to carbon dioxide (CO₂) sequestration in coal with specific reference to Victorian brown coals. The coal basins in Victoria, Australia have been identified as one of the largest brown coal resources in the world and so far few studies have been conducted on CO₂ sequestration in this particular type of coals. The feasibility of CO₂ sequestration depends on three main factors: (1) coal mass properties (chemical, physical and microscopic properties), (2) seam permeability, and (3) gas sorption properties of the coal. Firstly, the coal mass properties of Victorian brown coal are presented, and then the general variations of the coal mass properties with rank, for all types of coal, are discussed. Subsequently, coal gas permeability and gas sorption are considered, and the physical factors which affect them are examined. In addition, existing models for coal gas permeability and gas sorption in coal are reviewed and the possibilities of further development of these models are discussed. According to the previous studies, coal mass properties and permeability and gas sorption characteristics of coals are different for different ranks: lignite to medium volatile bituminous coals and medium volatile bituminous to anthracite coals. This is important for the development of mathematical models for gas permeability and sorption behavior. Furthermore, the models have to take into account volume effect which can be significant under high pressure and temperature conditions. Also, the viscosity and density of supercritical CO₂ close to the critical point can undergo large and rapid changes. To date, few studies have been conducted on CO₂ sequestration in Victorian brown coal, and for all types of coal, very few studies have been conducted on CO₂ sequestration under high pressure and temperature conditions.     

Geochemical and mineralogical evidence for a coal-hosted uranium deposit in the Yili Basin,Xinjiang, northwestern China

The petrological, geochemical, and mineralogical compositions of the coal-hosted Jurassic uranium ore deposit in the Yili Basin of Xinjiang province, northwestern China, were investigated using optical microscopy and field emission-scanning electron microscopy in conjunction with an energy-dispersive X-ray spectrometer, as well as X-ray powder diffraction, X-ray fluorescence, and inductively coupled plasma mass spectrometry. The Yili coal is of high volatile C/B bituminous rank (0.51–0.59% vitrinite reflectance) and has a medium sulfur content (1.32% on average). Fusinite and semifusinite generally dominate the maceral assemblage, which exhibits forms suggesting fire-driven formation of those macerals together with forms suggesting degradation of wood followed by burning. The Yili coals are characterized by high concentrations of U (up to 7207 μg/g), Se (up to 253 μg/g), Mo (1248 μg/g), and Re (up to 34 μg/g), as well as As (up to 234 μg/g) and Hg (up to 3858 ng/g). Relative to the upper continental crust, the rare earth elements (REEs) in the coals are characterized by heavy or/and medium REE enrichment. The minerals in the Yili coals are mainly quartz, kaolinite, illite and illite/smectite, as well as, to a lesser extent, K-feldspar, chlorite, pyrite, and trace amounts of calcite, dolomite, amphibole, millerite, chalcopyrite, cattierite, siegenite, ferroselite, krutaite, eskebornite, pitchblende, coffinite, silicorhabdophane, and zircon. The enrichment and modes of occurrence of the trace elements, and also of the minerals in the coal, are attributed to derivation from a sediment source region of felsic and intermediate petrological composition, and to two different later-stage solutions (a U–Se–Mo–Re rich infiltrational and a Hg–As-rich exfiltrational volcanogenic solution). The main elements with high enrichment factors, U, Se, As, and Hg, overall exhibit a mixed organic–inorganic affinity. The uranium minerals, pitchblende and coffinite, occur as cavity-fillings in structured inertinite macerals. Selenium, As, and Hg in high-pyrite samples mainly show a sulfide affinity.