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1.
A quantitative 13C-NMR technique was applied to humic acids, isolated from total solvent extracts obtained from coals, varying in rank from lignite to medium volatile bituminous. The results from elemental analysis and 13C-NMR structural ratios are interpreted in the form of three distinct structural phases in the maturation of coal humic acids. These phases reflect the rank of the parent coals. A decrease in polar functional group content and corresponding increase in aromaticity is observed with increasing maturation of humic acid chemical structure. Limits are postulated for the oxygen content and level of aromaticity for humic acids derived from higher rank coals.  相似文献   

2.
D/H, 13C/12C, 18O/16O and 34S/32S ratios in the organic matrix and organic solvent extracts of Australian coals, and in the fluids and minerals associated with these coals, are reported and reviewed against similar isotopic data for coals from other regions.Where coals are immature, original isotopic differences between macrolithotypes, and between solvent extracts (lipid concentrates) and insoluble residues, are largely preserved. However, with increasing maturity these characteristic differences, particularly those between macrolithotypes, are rapidly erased. Conversely, where, as indicated by low total sulfur contents, coals of Cretaceous to Permian age were deposited under essentially freshwater conditions, δ34S values* for the organically-bound sulfur remain remarkably constant at +4 ± 3‰ relative to meteoritic sulfur. In similar, younger Tertiary coals, the organic sulfur is markedly enriched in 34S.Five distinctive isotopic patterns, which may be interpreted in terms of the environment of sulfate reduction, can be recognized from 34S/32S ratio measurements on the various forms of sulfur in Australian coals.Isotopic studies of seam gas hydrocarbons collected in situ show these to be unexpectedly strongly depleted in the heavier isotopes of hydrogen and carbon relative to natural gases from proposed humic sources. Furthermore, no pronounced increase in the 13C content in methane with increase in rank of the parent coal was observed. In addition, several sources of associated carbon dioxide have been delineated, including normal maturation processes, invasion of the seams by magnetic carbon dioxide, and interaction of the coal with intrusive magma.Isotopic exchange between free seam gases is not accepted as an explanation for some unusual isotopic fractionations seen, rather the data suggest that these gases may be formed in a state approaching isotopic equilibrium. This argument also satisfactorily explains the isotopic compositions of primary siderite and secondary calcite associated with bituminous coal seams. However, where seams are invaded and permeated with externally derived carbon dioxide, usually of magnetic origin, carbonates are frequently absent, presumably as a result of the action of carbonic acid.  相似文献   

3.
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.  相似文献   

4.
Supercritical gas sorption on moist coals   总被引：2，自引：1，他引：1  
The effect of moisture on the CO2 and CH4 sorption capacity of three bituminous coals from Australia and China was investigated at 55 °C and at pressures up to 20 MPa. A gravimetric apparatus was used to measure the gas adsorption isotherms of coal with moisture contents ranging from 0 to about 8%. A modified Dubinin–Radushkevich (DR) adsorption model was found to fit the experimental data under all conditions. Moisture adsorption isotherms of these coals were measured at 21 °C. The Guggenheim–Anderson–de Boer (GAB) model was capable of accurately representing the moisture isotherms over the full range of relative pressures.Moist coal had a significantly lower maximum sorption capacity for both CO2 and CH4 than dry coal. However, the extent to which the capacity was reduced was dependent upon the rank of the coal. Higher rank coals were less affected by the presence of moisture than low rank coals. All coals exhibited a certain moisture content beyond which further moisture did not affect the sorption capacity. This limiting moisture content was dependent on the rank of the coal and the sorbate gas and, for these coals, corresponded approximately to the equilibrium moisture content that would be attained by exposing the coal to about 40–80% relative humidity. The experimental results indicate that the loss of sorption capacity by the coal in the presence of water can be simply explained by volumetric displacement of the CO2 and CH4 by the water. Below the limiting moisture content, the CO2 sorption capacity reduced by about 7.3 kg t− 1 for each 1% increase in moisture. For CH4, sorption capacity was reduced by about 1.8 kg t− 1 for each 1% increase in moisture.The heat of sorption calculated from the DR model decreased slightly on addition of moisture. One explanation is that water is preferentially attracted to high energy adsorption sites (that have high energy by virtue of their electrostatic nature), expelling CO2 and CH4 molecules.  相似文献   

5.
实验变形煤的光性组构分析   总被引：4，自引：1，他引：4       下载免费PDF全文
三种Rmaxo分别为0.67%,3.41%和4.90%的煤样,在t=350-700℃、Pc=400-600MPa、ε=10%-30%、ε=3.63×10-4-2.59×10-5s-1条件下的变形实验表明:(1)煤光性组构的成因是芳环层片在构造应力作用下重新定向所致,重新定向的主要机制是煤化过程中芳环层片的择优成核生长,同时存在物理转动定向机制的作用;(2)芳环层片的重新定向主要发生在煤级相对较低阶段,VRI的Z轴主要反映这一阶段的构造应力方向;(3)YRI的形态特征并非仅与有限应变有关,它不能直接作为有限应变分析的标志。  相似文献   

6.
The four most abundant minerals generally found in Euramerican bituminous coals are quartz, kaolinite, illite and pyrite. These four minerals were isolated by density separation and handpicking from bituminous coal samples collected in the Ruhr Basin, Germany and the Appalachian basin, U.S.A. Trace-element concentrations of relatively pure ( 99+%) separates of major minerals from these coals were determined directly by using instrumental neutron activation analysis (INAA). As expected, quartz contributes little to the trace-element mass balance. Illite generally has higher trace-element concentrations than kaolinite, but, for the concentrates analyzed in this study, Hf, Ta, W, Th and U are in lower concentrations in illite than in kaolinite. Pyrite has higher concentrations of chalcophile elements (e.g., As and Se) and is considerably lower in lithophile elements as compared to kaolinite and illite. Our study provides a direct and sensitive method of determining trace-element relationships with minerals in coal.Mass-balance calculations suggest that the trace-element content of coal can be explained mainly by three major minerals: pyrite, kaolinite and illite. This conclusion indicates that the size and textural relationships of these major coal minerals may be a more important consideration as to whether coal cleaning can effectively remove the most environmentally sensitive trace elements in coal than what trace minerals are present.  相似文献   

7.
The Sohagpur coalfield is a remnant of the Son valley basin of Gondwana deposition and can be subdivided into three major subbasins from west to east: Rungta-Amlai, Kotma and Bijuri. Thick coal seams occur in the Barakar Formation (Lower Permian) and are being worked extensively.Petrographic, reflectance, chemical and trace-elemental studies on samples of coal representative of the coal seams of the different subbasins have been carried out, and the results are presented here. Petrographically, the coals of one subbasin are different from those of another subbasin and are mainly composed of vitrinertite I, and vitrinertite V, that alternates with fusite. Vitrite increases in proportion in the coal seams towards the eastern part of the coalfield, and sclerotinite occurs in increased proportion in coal seams towards the western part. The reflectance in oil (Romax) varies from 0.50 to 0.58% in the coals of Rungta-Amlai, 0.46–0.56% in Kotma, and 0.53–1.05% in Bijuri subbasins. Chemically, the coals belong to type High Volatile Symbol B 4 of Class Bituminous. The significant trace elements are V (20–400 ppm); Cu, Ni, Co (up to 300 ppm); Mn, Ba, Sr, Zr (up to 800 ppm); and La (up to 1200 ppm). The trace elements show a tendency to increase in proportion towards the eastern part of the coalfield.To the immediate east of the coalfield lies the Chirimiri coalfield, of which the compositional characteristics are also presented. These data clearly suggest that the coals of the Son valley are different from those of the other Gondwana basins, i.e., Mahanadi, Godavari, and Damodar valley basins.  相似文献   

8.
印度尼西亚是我国最大的煤炭进口国,本文应用电感耦合等离子体质谱、原子荧光光谱、直接测汞仪等技术分析了上海口岸31批进口印度尼西亚煤炭中的12种微量元素,结合数理统计方法研究该类煤炭中微量元素的赋存形态。结果表明,进口印尼煤炭中含有高汞煤、三级含砷煤,As、Hg的平均富集系数大于1,其迁移风险值得关注;Be、Cu、Mo、Cd、Sn、Pb含量均低于中国煤和世界煤炭的平均水平,体现出印尼煤炭低灰分的品质特征。12种微量元素和相关项目(灰分和全硫)可划分为3类:第一类归纳为黏土矿物吸附类,包括As、Be、Cr、Co、Ni、Cu、Mo、Cd、Sn、Pb、灰分;第二类归纳为硫铁矿类,包括Hg、全硫;第三类归纳为碳酸盐矿物类,包括Ba。本文研究结果对于指导进口煤炭开发、利用过程中的环境评价和洁净化处理具有一定的参考价值。  相似文献   

9.
Four lithotypes (vitrain, bright clarain, clarain, and fusain) of a high volatile bituminous Springfield Coal from the Illinois Basin were characterized using advanced solid-state 13C nuclear magnetic resonance (NMR) spectroscopy. The NMR techniques included quantitative direct polarization/magic angle spinning (DP/MAS), cross polarization/total sideband suppression (CP/TOSS), dipolar dephasing, CHn selection, and recoupled C-H long-range dipolar dephasing techniques. The lithotypes that experienced high-pressure CO2 adsorption isotherm analysis were also analyzed to determine possible changes in coal structure as a result of CO2 saturation at high pressure and subsequent evacuation. The main carbon functionalities present in original vitrain, bright clarain, clarain and fusain were aromatic carbons (65.9%-86.1%), nonpolar alkyl groups (9.0%-28.9%), and aromatic C-O carbons (4.1%-9.5%). Among these lithotypes, aromaticity increased in the order of clarain, bright clarain, vitrain, and fusain, whereas the fraction of alkyl carbons decreased in the same order. Fusain was distinct from other three lithotypes in respect to its highest aromatic composition (86.1%) and remarkably small fraction of alkyl carbons (11.0%). The aromatic cluster size in fusain was larger than that in bright clarain. The lithotypes studied responded differently to high pressure CO2 saturation. After exposure to high pressure CO2, vitrain and fusain showed a decrease in aromaticity but an increase in the fraction of alkyl carbons, whereas bright clarain and clarain displayed an increase in aromaticity but a decrease in the fraction of alkyl carbons. Aromatic fused-rings were larger for bright clarain but smaller for fusain in the post-CO2 adsorption samples compared to the original lithotypes. These observations suggested chemical CO2-coal interactions at high pressure and the selectivity of lithotypes in response to CO2 adsorption.  相似文献   

10.
The distribution of aromatic hydrocarbons and stable carbon isotope ratios of organic matter in a series of nine Miocene Embalut coal samples obtained from nine coal seams of Kutai Basin, East Kalimantan, Indonesia were studied. The rank of the Embalut coals ranged from lignites to low rank sub-bituminous coals (0.36–0.50% Rr), based on measurements of huminite reflectance. The aromatic hydrocarbon fractions of all coal samples were dominated by cadalene in the lower boiling point range and picene derivatives in the higher boiling point range of the gas chromatograms. Cadalene can be attributed to the contribution of Dipterocarpaceae and various hydrated picenes to the contribution of additional angiosperms to the coal forming vegetation. The picenes originate from alpha- and beta-amyrin. However, in some coal samples minor amounts of simonellite and retene were also detected which argues for an additional contribution of gymnosperms (conifers) to coal forming vegetation preferentially in the Middle Miocene and at the beginning of the Late Miocene. The results of stable carbon isotope ratios (δ13C) in most of the coal samples are consistent with their origin from angiosperms (δ13C between ?27.0‰ and ?28.0‰). During the Miocene the climate of Mahakam Delta was not uniformly moist and cooler than the present day climate. This would have been favourable for the growth of conifers, especially in the montane forests. The contribution of conifers to the Embalut coals might be a result of the cool Middle/Late Miocene climate during peat accumulation in the Kutai Basin.  相似文献   

11.
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.  相似文献   

12.
Samples of heat affected coal taken near two igneous intrusions (dykes) in the Victoria Tunnel Seam of the Newcastle Coalfield have been investigated by chemical analysis, petrography, Fourier transform infrared spectroscopy and solid state13C NMR spectroscopy. Visual inspection of the seam near the intrusion showed four distinct zones. These have been called, in order of increasing distance from the dyke, the massive cinder, the banded cinder, heat affected coal and apparently unaffected coal. The samples show an increase in structural change as the distance from the dyke decreases, with the samples taken from the massive cinder nearest the dyke being classified as semicokes.FTIR and13C NMR results, together with the results of dipolar dephasing NMR experiments, suggest that the predominant structural change in the heat affected zone is replacement of aromatic ethers and/or phenols with hydrogen, leading to an increase in proton aromaticity. Closer to the intrusion, bond rupture leads to a marked loss of aliphatic groups, while in the most affected region adjacent to the dyke aromatic crosslinking has also occurred to form coke-like material.  相似文献   

13.
超临界CO2对煤化学结构的改造对煤层CO2封存能力极为关键。论文开展了模拟埋深1500m （62.5℃、15 MPa）条件下4组不同变质程度煤的ScCO2-H2O体系与煤岩地球化学反应实验。通过傅里叶变换红外光谱和X射线粉末衍射实验获得了反应前后煤化学结构演化特征,探讨了煤化学结构演化的机理。结果表明:ScCO2作用后,煤中脂肪烃链长度普遍增加,仅肥煤的芳香烃丰度增大,肥煤、瘦煤和贫煤含氧基团丰度的增大主要由氢键基团含量的增加贡献,无烟煤含氧基团丰度则主要受低分子化合物溶出的影响。ScCO2引起的溶胀作用造成肥煤和瘦煤芳香层面之间交联键断裂,芳香微晶内部结构疏松,而芳香层面内CAr-CAr交联的形成提高了肥煤和瘦煤芳香性和芳香环缩合度;贫煤和无烟煤中非稠合多苯结构脱落使芳香微晶内部更紧凑,脂肪烃链长度的增加则降低了贫煤和无烟煤芳香性和芳香环缩合度。   相似文献   

14.
Mineral matter in three naturally weathered coals from Pennsylvania strip mines and in two laboratory-oxidized coals has been characterized by 57Fe Mössbauer spectroscopy, scanning electron microscopy and other techniques to determine mineralogical trasnformations that occur in coals during weathering. Pyrite was found to be the most readily oxidized mineral, forming a variety of iron sulfates initially and geethite eventually. The iron sulfates formed were different in the two laboratory-oxidized coals, despite identical oxidation treatments. Calcite disappeared from one calcite-rich coal with increasing oxidation, but was not replaced by an equivalent amount of gypsum. A severely weathered strip-mine coal was enriched in calcium, which was dispersed through the oxidized macerals. Extended X-ray absorption fine-structure spectroscopy indicated that this dispersed calcium was most likely present as salts of carboxylic acids. Siderite was suprisingly resistant to oxidation at room temperature. Less direct evidence indicates that clay minerals also take part in the alteration to some extent.The coals oxidized in the laboratory showed alteration behavior that differed in a number of respects from that of the strip-mine coals. For example, iron sulfates were much less common in the latter coals; also, the formation of geothite appeared to be controlled to a large extent by the pyrite particle size in the strip-mine coals, but not in the laboratory-oxidized coals.The oxidation of an individual pyrite grain is not only a function of general conditions (temperature, humidity, oxygen partial pressure), but also the immediate local (< 1 mm) chemistry, as a variety of iron sulfates were observed in the coals, often in close proximity. Also, assemblages of gypsum and goethite were observed in otherwise slightly oxidized coal, which indicates that the alteration of pyrite and calcite, when in close contact, proceeds most rapidly.  相似文献   

15.
With the development of deep mining in recent years, coal and gas compound dynamic disasters become increasingly serious. In this study, uniaxial and triaxial compression tests were conducted on gas-bearing coals, coal–sandstone combined bodies and coal–mudstone combined bodies and the permeabilities in the triaxial tests were measured simultaneously. The mechanical behavior and seepage characteristics of coals and coal–rock combination bodies under triaxial conditions were compared in details. The results show that the peak strength among three samples is: coal–sandstone combined body > coal–mudstone combined body > coal. If other conditions were held constant, the strength and the elastic modulus of all specimens show that tendency increases with the increment of the confining pressure or with the decrease in the gas pressure. The strength characteristics of all three specimens met the Mohr–Coulomb criterion, and the residual strength has an increasing trend with the increase in confining pressure. The permeability evolutions of gas-bearing coals and coal–rock combination bodies which are determined by the crack propagation in the coals and rocks are not exactly the same. This preliminary study is intended to deepen our understandings of the mechanisms of coal–gas compound dynamic disasters and provide theoretical bases for their predictions.  相似文献   

16.
The Tertiary North East Indian coals, classified as sub-bituminous rank, have found less industrial application owing to their physico-chemical attributes. These coals are characterized by low ash (<15%), high volatile matter (>35%) and high sulphur (2.9-4.46%). Majority of the sulphur occurs in organic form affixed to the coal matrix owing to marine influence, is difficult to remove. The coal maceral analysis shows the dominance of vitrinite (>75%) with lesser amounts of liptinite and inertinite. Reflectance measurements (Rmax) of these sub-bituminous coals fall in the range of 0.57 to 0.65. In this study, the petrographical (maceral), thermal and other physico-chemical analyses of some low rank Tertiary sub-bituminous coals from north-east India were carried out to assess their potential for combustion, liquefaction and coal bed methane formation. The petrofactor, conversion (%) and oil yield (%), combustion efficiency of the coal samples were determined. The respective linear correlations of conversion (%) of the coals with their vitrinite contents, petrofactor and oil yield values have been discussed. The relative combustion efficiency of the coals was measured from the thermo gravimetric analysis (TGA) of coals. The influence of maceral composition upon gas adsorption characteristics of these high volatile coals showed the increase in methane adsorption with vitrinite enrichment. Both the maceral and mineral matter contents were observed to have important influence on the gas adsorption characteristics.  相似文献   

17.
The density gradient centrifugation technique has recently been applied to the separation of macerals from whole coals. Sufficient quantities have been separated to permit examination of pure exinite, vitrinite and inertinite fractions by combined cross polarization and magic angle sample spinning (CP/MASS) carbon-13 NMR techniques. The similarities and differences observed in the maceral groups of two coals are discussed. Diversity in precursors or in differential chemical maturation or a combination of both of these factors can be used to account for subtle spectral differences in the two coals and macerals studied even though the gross spectral features are very similar for a given maceral type. The data show that CP/MASS is a technique that can address such interesting geochemical questions.  相似文献   

18.
低阶煤甲烷吸附特性研究对瓦斯含量预测、瓦斯抽采及危害防治有着重要意义,为此,选取陕西6个典型矿井低阶煤样,进行低温氮吸附、低压二氧化碳吸附及甲烷等温吸附实验,获得低阶煤吸附孔结构特征。利用微孔填充及单分子层吸附理论定量表征甲烷吸附特征参数与吸附孔结构参数之间的关系,明确吸附孔中甲烷吸附机理。结果表明：吸附孔的比表面积主要由微孔提供,甲烷吸附能力主要受吸附孔孔容大小控制,微孔孔容对吸附孔总孔容的贡献率在74.71%～88.97%。甲烷极限吸附量与吸附孔平均孔径呈线性负相关,与吸附孔孔容、比表面积呈线性正相关,Langmuir压力常数随吸附孔平均孔径、孔容和比表面积的增加仅在小范围内波动,无明显线性相关。6个低阶煤样的分形特征明显,综合分形维数为2.573～2.720,平均值为2.647,说明低阶煤吸附孔非均质性强,甲烷极限吸附量随分形维数增加先增加后减小,整体呈上升趋势。基于微孔填充和单分子层吸附理论可以定量表征低阶煤吸附孔结构与甲烷吸附能力之间的关系,甲烷极限吸附量计算值与实验测试值相对误差较小,长焰煤相对误差为4.47%～6.65%,不黏煤为13.77%～16.02%。研究成果可为后...  相似文献   

19.
华北南部构造煤纳米级孔隙结构演化特征及作用机理   总被引：16，自引：2，他引：14  
构造煤是在构造应力作用下,煤体发生变形或破坏的一类煤,在世界主要产煤国家皆有分布。构造变形不同程度的改变着煤的大分子结构和化学成分,而且也影响到构造煤的纳米级孔隙结构(<10 0 nm ) ,它是煤层气的主要吸附空间。通过构造煤显微组分和镜质组油浸最大反射率的测定,采用液氮吸附法对不同变质变形环境、不同变形系列构造煤的纳米级孔隙分类、孔隙结构特征进行了深入系统的研究,并结合高分辨透射电子显微镜和X射线衍射对大分子结构和孔隙结构的分析,结果表明:不同类型构造煤纳米级孔径结构自然分类,可将孔径结构划分为过渡孔(15～10 0 nm )、微孔(5～15 nm )、亚微孔(2 .5～5 nm )和极微孔(<2 .5 nm ) 4类。低煤级变形变质环境中随着构造变形的增强,不同类型构造煤过渡孔孔容明显降低,微孔及其下孔径段孔容明显增多,可见亚微孔和极微孔,过渡孔的比表面积大幅度降低,而亚微孔的却增加得较快。从脆韧性变形煤至韧性变形煤,总孔体积、累积比表面积、N2 吸附量随着构造变形的增强,这些结构参数均迅速增加,但中值半径进一步下降。非均质结构煤孔隙参数与弱脆性变形煤相当。中、高煤级变形变质环境形成的各种类型构造煤与低煤级变质变形环境相比,孔隙参数的变化基本一致。但不同类型构造煤的变化又有所区别  相似文献   

20.
Sorption and desorption behaviour of methane, carbon dioxide, and mixtures of the two gases has been studied on a set of well-characterised coals from the Argonne Premium Coal Programme. The coal samples cover a maturity range from 0.25% to 1.68% vitrinite reflectance. The maceral compositions were dominated by vitrinite (85% to 91%). Inertinite contents ranged from 8% to 11% and liptinite contents around 1% with one exception (Illinois coal, 5%). All sorption experiments were performed on powdered (−100 mesh), dry coal samples.Single component sorption/desorption measurements were carried out at 22 °C up to final pressures around 51 bar (5.1 MPa) for CO2 (subcritical state) and 110 bar (11 MPa) for methane.The ratios of the final sorption capacities for pure CO2 and methane (in molar units) on the five coal samples vary between 1.15 and 3.16. The lowest ratio (1.15) was found for the North Dakota Beulah-Zap lignite (VRr=0.25%) and the highest ratios (2.7 and 3.16) were encountered for the low-rank coals (VRr 0.32% and 0.48%) while the ratio decreases to 1.6–1.7 for the highest rank coals in this series.Desorption isotherms for CH4 and CO2 were measured immediately after the corresponding sorption isotherms. They generally lie above the sorption isotherms. The degree of hysteresis, i.e. deviation of sorption and desorption isotherms, varies and shows no dependence on coal rank.Adsorption tests with CH4/CO2 mixtures were conducted to study the degree of preferential sorption of these two gases on coals of different rank. These experiments were performed on dry coals at 45 °C and pressures up to 180 bar (18 MPa). For the highest rank samples of this sequence preferential sorption behaviour was “as expected”, i.e. preferential adsorption of CO2 and preferential desorption of CH4 were observed. For the low rank samples, however, preferential adsorption of CH4 was found in the low pressure range and preferential desorption of CO2 over the entire pressure range.Follow-up tests for single gas CO2 sorption measurements consistently showed a significant increase in sorption capacity for re-runs on the same sample. This phenomenon could be due to extraction of volatile coal components by CO2 in the first experiment. Reproducibility tests with methane and CO2 using fresh sample material in each experiment did not show this effect.  相似文献   

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