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1.
A series of hand-picked vitrinite samples from the Lower Kittanning Seam, Pennsylvania have been examined using quantitative pyrolysis-gas chromatography. These vitrinites ranged in rank from 0.59 to 1.71% reflectance, a rank range from high volatile C bituminous to low volatile bituminous. High molecular weight pyrolysis products included alkyl aromatic and phenolic compounds. Attempts have been made to correlate the pyrolysis product composition to rank parameters including vitrinite reflectance, volatile matter yield, carbon content, atomic H/C ratio and Rock-Eval determined Tmax. Total yield of phenols was found to be strongly and inversely rank related. A clear relationship between C8 alkyl-benzene yield and rank was not found for the sample set.  相似文献   

2.
Study of a series of twenty-six German high volatile bituminous B to low volatile bituminous coals of Upper Carboniferous age by recently refined analytical methods (‘flow-blending’ extraction, medium pressure liquid chromatography, HPLC, glass capillary gas chromatography and spectral fluorescence microscopy) reveals that yield and composition of soluble organic matter are strongly controlled by rank. In particular, the following points of inflection are noted in rank trends around 0.9% vitrinite reflectance: a maximum in yields of total soluble organic matter, aromatic hydrocarbons and n-alkanes; the most pronounced change in aromatic hydrocarbon composition; a trend reversal for pristane/ phytane ratios; a gradient change in the odd/even-predominance of long chain n-alkanes; appearance of a bimodal n-alkane distribution; and a sharp drop in concentration of individual n-, and isoprenoid alkanes. This discontinuity in rank trends around 0.9% Rm is interpreted to reflect a major change in reaction types, i.e. a shift from predominantly hydrocarbon generating to predominantly fragmentation reactions. Rank trends of maceral fluorescence exhibit the following pronounced changes over a similar but broader rank range: Different types of the maceral sporinite show a relatively abrupt shift of the fluorescence colour from yellow towards red between 0.8–0.9% Rm while up to about 1.0% Rm a sharp increase is recorded in the proportion of fluorescent vitrinite. This coincidence at a near-equal rank stage suggests a common cause for changes in yield and composition of the soluble organic matter and the maceral fluorescence of these coals.  相似文献   

3.
Canada's coal resources occur in 16 sedimentary basins or groups of basins and range in age from Devonian to Tertiary. The Western Canada Sedimentary Basin (WCSB), which contains the vast majority (about 90%) of the nation's coal resources of immediate interest, underlies a large area in the provinces of British Columbia, Alberta, Saskatchewan and Manitoba, extending northward to about the 62nd Parallel in Yukon and Northwest Territories. Coal deposits in the WCSB range in age from Early Carboniferous (Mississippian) to Paleocene. Rank ranges from lignite to semianthracite. About 36% of the total estimated 71,000 megatonnes of resources of immediate interest in the WCSB is bituminous coal, including a high proportion in the medium to low volatile range. Their low sulphur contents and acceptable ash levels make these medium and low volatile bituminous coals attractive 3s coking feedstocks and large quantities are mined for that purpose. The lower rank western Canadian coals are used mainly for electricity generation.Significant resources of bituminous coal occur in the coalfields of Atlantic Canada where they have been mined since 1720. Most of these coals are classed as high volatile A bituminous and most are used for power generation. Large resources of coal (lignite to anthracite) also occur in more remote regions of Canada, such as the Bowser Basin in northwestern British Columbia, and Sverdrup Basin/ Franklinian Geosyncline in the Arctic Islands. Information on distribution and compositional attributes of these frontier region coals is commonly scarce.  相似文献   

4.
n-Alkanes in the soluble organic matter extracted from a series of vitrinite and sporinite concentrates have been analysed by gas chromatography. The macerals were isolated from coals ranging in rank from 77.1% to 86.6% carbon (vitrinite: dry, ash-free), and yields of n-alkanes ranged from 10 to 580 ppm for vitrinites and from 20 to 970 ppm for sporinites. The maximum yields were found at a rank of 85.4% C from vitrinites and 86.6% C from sporinites.Distribution maxima of the n-alkanes, as shown by gas chromatography, range from C27 and C29 at lower ranks to as low as C16 at higher ranks. The distributions also show a progressive decrease in the preference of odd-carbon-number homologues with increasing rank. Virtually smooth distributions were attained in high-volatile bituminous A coals. Quantitative data show that the loss of the odd-carbon-number preference occurred, for the most part, while individual long-chain homologues increased in concentration.There is a progressive increase in the amounts of shorter-chain n-alkanes with increasing rank. It is suggested that sequential processes may have occurred whereby the rate of formation of long-chain n-alkanes in high-volatile bituminous A rank macerals becomes slower than their rate of subsequent fragmentation to shorter chain lengths. Consequently, assuming derivation from the insoluble maceral matrices, the chain-length distributions of parent n-alkyl structures within the insoluble material may retain characteristics pertaining more to the nature of the source organic matter at the time of deposition than do the extractable n-alkane patterns, especially at higher ranks.  相似文献   

5.
The effect of petrographic composition on the methane sorption capacity has been determined for a suite of coals and organic-rich shales. Subbituminous and bituminous coals were separated into bright and dull lithotypes by hand-picking. The methane sorption capacities range between 0.5 and 23.9 cm3/g at a pressure of 6 MPa. The low volatile bituminous Canmore coal and the anthracite sample have the highest capacities with the “natural coke” having the lowest. For low-rank coals there is no significant difference between bright and dull samples except for one coal with the dull sample having a greater sorption capacity than its bright equivalent. For higher-rank coals, the bright samples have a greater methane capacity than the dull samples and the difference between sample pairs increases with rank. The boghead coal samples have the highest sorption capacities in the liptinite-rich coals suite and are higher than subbituminous to medium volatile bituminous samples. Pore size distribution indicates that methane is held as solution gas in liptinite-rich coals and by physical sorption in micropores in liptinite-poor coals. These contrasting processes illustrate that liptinite-rich samples need to be independently assessed. The positive relationship between reactive inertinite content and methane sorption capacity occurs within the subbituminous to medium volatile bituminous coals because the reactive inertinite is structurally similar to vitrinite and have a higher microporosity than non-reactive inertinite. Reactivity of inertinite should be assessed in CBM studies of dull coals to provide a better understanding of petrographic composition effects on methane capacity.  相似文献   

6.
Two thermal parameters, initial volatilization temperature (IVT) and average volatilization rate (AVR), have been determined by thermogravimetric analysis in argon for 38 coal samples ranging in rank from lignite to low-volatile bituminous. Both IVT and AVR are correlated with percent volatile matter and vitrinite reflectance.The IVT values increase gradually from about 250 to 445°C with increasing rank; however, a change in slope is observed in the region of high-volatile bituminous coals (from about 340°C to about 380°C) when IVT's are plotted against percent volatile matter or percent fixed carbon. The changes in slope near 340°C and near 380°C occur at “coalification jumps” recognized on the basis of changes in the optical and chemical character of the macerals. In general, AVR values decrease gradually with increasing rank for the lignite and sub-bituminous coals and for the medium- and low-volatile bituminous coals; however, a sharp increase in AVR occurs in high-volatile bituminous coals. The change in slope of the IVT curves and sharp increase in the AVR values for high-volatile bituminous coals reflect the development of new, higher vapor pressure organic compounds produced during this stage of the coalification process.A plot of AVR vs IVT reveals three regions which correspond to: (1) lignite and sub-bituminous coals; (2) high-volatile bituminous coals; and (3) medium- to low-volatile bituminous coals.  相似文献   

7.
The structural evolution of coals during coalification from peat to the end of the high volatile bituminous coal rank (VRr = 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 (VRr > ∼0.81%) for which defunctionalisation processes become less important.  相似文献   

8.
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% Ro max) to anthracite (3.01% Ro max). Adsorption isotherm results of dry coals indicated that Langmuir volume (VL) for bright and dull coal types followed discrete, second-order polynomial trends with increasing rank. Bright coals had a minimum VL at 1.72% Ro max and dull coals had a minimum VL at 1.17% Ro max. At low rank, VL 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% Ro max. At ranks higher than 1.65% Ro max, both bright and dull coals followed similar trends. These competing trends mean that the importance of maceral composition on VL 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 (PL) showed a strong relationship of decreasing PL 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.  相似文献   

9.
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   

10.
《Organic Geochemistry》1999,30(8):985-1010
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% Romax).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.  相似文献   

11.
In the present study, petrographic and geochemical investigation of Meghalayan coal deposits have been carried out to classify these coals in terms of rank, type and grade, using Indian and International classification schemes. Based on petrographic and geochemical characteristics, an attempt has also been made to identify the potential utilization of Meghalayan coals for various industrial applications. According to the study, these coals have been classified as sub-bituminous C to high volatile bituminous in rank, vitric in type and clean to ashy in grade. Considering their hydrocarbon potential, these coals are suitable for liquefaction and gasification.  相似文献   

12.
Thermally metamorphosed Tertiary age coals from Tanjung Enim in South Sumatra Basin have been investigated by means of petrographic, mineralogical and chemical analyses. These coals were influenced by heat from an andesitic igneous intrusion. The original coal outside the metamorphosed zone is characterized by high moisture content (4.13–11.25 wt.%) and volatile matter content (> 40 wt.%, daf), as well as less than 80 wt.% (daf) carbon and low vitrinite reflectance (VRmax = 0.52–0.76%). Those coals are of subbituminous and high volatile bituminous rank. In contrast the thermally metamorphosed coals are of medium-volatile bituminous to meta-anthracite rank and characterized by low moisture content (only < 3 wt.%) and volatile matter content (< 24 wt.%, daf), as well as high carbon content (> 80 wt.%, daf) and vitrinite reflectance (VRmax = 1.87–6.20%). All the studied coals have a low mineral matter content, except for those which are highly metamorphosed, due to the formation of new minerals.The coalification path of each maceral shows that vitrinite, liptinite and inertinite reflectance converge in a transition zone at VRmax of around 1.5%. Significant decrease of volatile matter occurs in the zone between 0.5% and 2.0% VRmax. A sharp bend occurs at VRmax between 2.0% and 2.5%. Above 2.5%, the volatile matter decreases only very slightly. Between VRr = 0.5% and 2.0%, the carbon content of the coals is ascending drastically. Above 2.5% VRr, the carbon content becomes relatively stable (around 95 wt.%, daf).Vitrinite is the most abundant maceral in low rank coal (69.6–86.2 vol.%). Liptinite and inertinite are minor constituents. In the high rank coal, the thermally altered vitrinite composes 82.4–93.8 vol.%. Mosaic structures can be recognized as groundmasss and crack fillings. The most common minerals found are carbonates, pyrite or marcasite and clay minerals. The latter consist of kaolinite in low rank coal and illite and rectorite in high rank coal. Change of functional groups with rank increase is reflected most of all by the increase of the ratio of aromatic C–H to aliphatic C–H absorbances based on FTIR analysis. The Oxygen Index values of all studied coals are low (OI < 5 mg CO2/g TOC) and the high rank coals have a lower Hydrogen Index (< 130 mg HC/g TOC) than the low rank coals (about 300 mg HC/g TOC). Tmax increases with maturity (420–440 °C for low rank coals and 475–551 °C for high rank coals).Based on the above data, it was calculated that the temperature of contact metamorphism reached 700–750 °C in the most metamorphosed coal.  相似文献   

13.
The Herrin (No. 11) coal in western Kentucky is in the upper part of the Pennsylvanian (Des Moinesian) Carbondale Formation. Samples were obtained from 13 mines in Kentucky and one mine in Illinois in three equal benches from two to three channels for a total of 93 samples. The rank of the coal (as vitrinite reflectance) is high volatile C bituminous in the Moorman Syncline and high volatile A bituminous in the Webster Syncline. Reflectance does not vary between mines in in the Moorman Syncline. The percentage of total vitrinite macerals for each mine is over 85% and the percentage of togal vitrinite plus liptinite maceralsis over 89% (average over 90%) (both on dry, mineral-free basis). The variation of the two maceral percentages is only significant at the betweenbench level, the middle bench generally having the lowest vitrinite and vitrinite plus liptinite percentages.  相似文献   

14.
对福建、京西地区高煤级Ⅲ无烟煤煤样分别进行了30℃条件下的甲烷等温吸附试验。结果显示,高煤级Ⅲ无烟煤对甲烷的吸附量要低于相同条件下的烟煤和高煤级Ⅰ、Ⅱ无烟煤。通过综合分析煤样的低温液氮吸附试验结果及其孔隙特征,结合煤结构理论和前期研究成果,分析认为:高煤级Ⅲ无烟煤的孔隙发育不均衡性、比表面积与孔容极小性以及芳香度高度缩合性,导致了其对甲烷的吸附空间大大减少,对甲烷的吸附量显著降低。研究成果对于丰富完善煤吸附气体理论,指导高煤级Ⅲ无烟煤地区矿井瓦斯治理及地面煤层气勘探开发都具有重要意义。   相似文献   

15.
刘娇  吴淑琪  贾静  佟玲 《华东地质》2019,(4):309-316
文章研究了吹扫捕集-气相色谱-质谱法测定土壤中挥发酚的方法,分析了吹扫捕集各参数对挥发酚测定的影响,优化了吹扫捕集条件和气相色谱-质谱条件。通过与索氏提取技术对比,证明吹扫捕集-气相色谱-质谱法在实际样品检测中具有操作简便、分析周期短、试剂用量少、干扰小等优点,适用于测定沸点较低、溶解度较小的挥发酚,推荐选择经典的索氏提取技术测定沸点较高、溶解度较大的挥发酚。  相似文献   

16.
The research work details the maceral organization of eleven coal seams intersected at a maximum depth of 446.45 m from Bhupalpalli area of the Mulug coal belt, in Warangal district of Godavari valley. Samples for petrographic study have been collected from ten coal seams intersected between 106 m and 299 m depth range from Bore-hole No. 618 which includes, IA and its underlying I, II, Index below II, IIIB, IIIA, III, IVA, IV and Index below IV respectively. However, the coal samples from the bottom most V seam were collected from Bore-hole No. 616 encountered between 445.65 m and 446.45 m. The study has revealed that V seam is marked by vitric type and seam IVA contains coal of fusic nature. The seams I, II, Index below II, IIIB, IIIA and IV, however, are represented by mixed type of coal. Whereas, the seams IA and III have the prevalence of vitric as well as mixed coal types. IA seam has witnessed alternate oxic and anoxic moor condition and also wet moor with intermittent moderate to high flooding. All the other seams have been deposited during alternate oxic and anoxic moor conditions. The coal seams of the study area have shown a wide range of variation in vitrinite reflectance (Ro mean %). The top of III, basal part of IV and the entire Index below IV have recorded high vitrinite reflectance (Ro mean %), which ranges between 0.66-0.67% thus they have reached high volatile bituminous B stage, all the other seams show lower reflectance and therefore have attained high volatile bituminous C rank.  相似文献   

17.
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.  相似文献   

18.
Importance of the study of the influence of coal oxidability on vitrinite reflectance (VR) as a criterion of the quality of coals and indicator of paleogeothermal regime is shown. Overview of relevant concepts demonstrates that this issue remains debatable. Carboniferous coals of the Dobrudja foredeep, which belong to the class of helitolites in terms of their microcomponent composition, were studied. They were subjected to oxidation during storage outdoors. Consequently, the VR value of high volatile bituminous (long-flame and gas ranks, according to the Russian classification) coals decreased, but this parameter remained virtually unaltered for medium volatile bituminous (fat) coals. Bulgarian researchers obtained similar results for Carboniferous coals of the Dobrudja basin represented by helitolites and mixtohumolites. In our opinion, the VR decrease in the course of coal oxidation is caused by decrease in the condensation and density of aromatic structures and increase in the share of nonaromatic carbon atoms.  相似文献   

19.
《Organic Geochemistry》1999,30(8):881-889
The 13C/12C isotopic ratios for coal-derived polycyclic aromatic hydrocarbons (PAHs) from a number of processes encompassing low and high temperature carbonisation, gasification and combustion have been determined using gas chromatography–isotope ratio mass spectrometry (δ13C GC–IRMS). The results, in conjunction with those for PAHs released under controlled laboratory pyrolysis conditions, indicate that the primary control on the isotopic values of coal-derived PAHs is likely to be the extent of ring growth required to form PAHs during processing. Thus, for relatively mild conversion processes such as low temperature carbonisation where the major aromatics are alkyl substituted 2–3 ring PAHs, the isotopic signatures are similar to those of the parent coals (−24 to −25‰ for UK bituminous coals). However, the δ13C values for the PAHs become lighter in going to high temperature carbonisation (−25 to −27‰), gasification (−27 to −29‰ for old Town gas plants in the UK) and combustion (−29 to −31‰) as the extent of ring condensation increases and confirming that the PAHs are not released as primary volatiles. To demonstrate the potential of applying these differences to source apportion environmental PAHs where major inputs from coals can be expected, soil and vegetation samples taken close to a low temperature carbonisation plant (Bolsover, North Derbyshire) have been analysed. In addition to low temperature coal tar, significant inputs of PAHs from transport fuels, high temperature carbonisation and possibly combustion (coal/biomass) have been inferred from the isotopic ratios, taken in conjunction with the differences in alkyl substitution patterns.  相似文献   

20.
Several techniques including gas chromatography, petrography, nuclear magnetic resonance and infrared spectroscopy are applied to the investigation of pertrifluoroacetic acid oxidation of a series of Permian Australian bituminous coals in order to probe the effects of maturation on aliphatic structure. The occurrence of insoluble oxidation products is attributed to reagent blocking by carboxylated aromatic species. The combined influence of maturation and semifusinite content is reflected in the concentration and structural composition of functionalised long chain aliphatic oxidation products.  相似文献   

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