Hydrogenation behaviour of coal maceral association

The influence of the intergrowth of macerals on the hydrogenation behaviour of two seam coals from the Ruhr district is investigated. Maceral concentrates of both coals were prepared. The maceral concentrates of each coal were mixed in such a manner, that the composition by macerals corresponded to that of the parent coal. Parent coals, maceral concentrates and the imitated parent coals by mixing maceral concentrates were hydrogenated under the same conditions. Feed materials and residues were characterized petrographically and chemically. Conclusions about the reactivity of the macerals itself, but also of their intergrowths could be drawn from the composition of the hydrogenation residues and of the conversion products. In spite of the same composition by macerals and identic total reflectograms of parent and imitated coals differences in portions and composition of residues were found. While the intergrowth of macerals (microlithotypes) of the low-volatile coal 2 seems to have a positive influence on the conversion of macerals, this seems to be opposite for the higher-volatile coal 1. Probably the lay open of the maceral surfaces has a positive effect on the hydrogenation of coal 2. Vitrinites and exinites proved to be very reactive as could be expected. They yield the highest portions of liquid and gaseous products. Inertinites participate in hydrogenation only with a very restricted reactivity.     

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.     

Lasers in organic petrology and organic geochemistry, II. In-situ laser micropyrolysis-GCMS of coal macerals

The development and preliminary results of a novel laser micropyrolysis-gas chromatography, mass spectrometry (LMPy-GCMS) system are described. Short exposures of near-infra red (IR) laser radiation focused through a microscope's optics onto a specific, targeted maceral within a polymaceralic organic-rich shale or coal are used to release the thermal evaporation and pyrolysis products from the maceral. The products from multiple exposures on a single maceral type are collectively analyzed online using GCMS. This technique is intended to provide a means of chemically characterizing individual, microscopic organic entities (> 25 μm) in coals and shales without the need to physically separate them from each other (e.g. density gradient centrifugation) or from their mineral matrix (e.g. bulk analysis of kerogen concentrates). Molecular characterization of individual macerals is important in predicting the technological properties of coal and the petroleum generation potential of petroleum source rocks.Different macerals respond differently when exposed to focused near-IR laser radiation due to differences in their heat capacity and heat conduction. The thermal products released during irradiation of macerals (ulminite, alginite, sporinite and fusinite) representing the huminite, liptinite and inertinite maceral groups are presented. Under the appropriate heating, collecting, and trapping conditions, the thermal products liberated are considered representative of the macromolecular structure of the macerals. Structural elucidation of macerals in coals and shales could significantly benefit from concerted efforts of this and other in-situ micro-analytical techniques.     

不同沉积环境成因煤显微组分的有机硫分布

运用扫描电镜能谱微区测试对不同沉积环境成因煤的有机显微组分进行有机硫含量的系统测定，结果表明在不同类型的煤中某一类显微组分的有机硫含量存在明显差异；同一煤中不同亚显微组分的有机硫含量也不同。综合分析发现煤显微组分有机硫含量主要受聚煤环境、组分凝胶化程度、氧化程度的影响，而聚煤环境为主导影响因素。     

Effect of maceral subtypes and mineral matrix on measured reflectance of subbituminous coals and dispersed organic matter

The variability in reflectance of huminite (texto-ulminite, eu-ulminite A and B, different types of corpohuminite) and liptinite groups of macerals in subbituminous coals was examined using reflected light microscopy. All macerals were selected from coal and interbedded carbonaceous shale and carbonate sediment samples from the 515-m-thick coal deposit No. 2 located in the Hat Creek valley of south-central British Columbia. The measurements obtained reveal that, in addition to burial depth, reflectance distribution depends on maceral subtypes and associated mineral matrix.Huminite in the coals and sediments (kerogen) consists mainly of humotelinite, with eu-ulminite B being the dominant maceral sub-type. Reflectance values determined on huminite in coals and Type IIIb kerogen increase from eu-ulminite A and phlobaphinite type 1 through eu-ulminite B and phlobaphinite type 2 to gelinite. The reflectance of all five huminite maceral subtypes studied increases with depth. However, the increase of phlobaphinite type 1 and gelinite reflectance with depth is irregular.A comparison of the reflectance values obtained for the same maceral subtype (eu-ulminite B) from the interbedded coal, shale and carbonate samples records consistent differences, implying some dependence of the reflectance (and perhaps rate of organic maturation) on the mineral matrix. Generally, the highest eu-ulminite B reflectance was recorded from carbonate rocks and the lowest from shale, whereas coal matrix produced intermediate values.At present, it is not known whether differences in reflectance of eu-ulminite found in the above lithologies are due to differential retention, efficiency of reaction products removal, thermal conductivity of the lithologies, or existence of a calcium carbonate catalyst.     

霍林河褐煤显微组分加氢液化性状的研究

对宏观煤岩类型和显微组分组成各不相同的5个褐煤煤样,进行了加氢液化和活化两组试验,通过对其转化率差别的分析,以及将活化后的残渣在普通显微镜、荧光显微镜和扫描电镜下的观察,了解了不同显微组分组和腐植组中的不同显微组分/亚组分/种的加氢液化特性和差别。这种差异表明显微组分组成不同的褐煤在加氢液化时的转化率不同,同时也显示了显微组分基本由腐植组组成的煤样转化率有差异。      

激光荧光显微探针:方法及应用

近年来研究沉积有机物的激光诱导荧光特笥和发展基于激光的荧光显微探针技术日益受到人们的重视。采用ＦＡＭＭ－９８激光荧光显微探针研究了烃源岩显微组分。研究表明,激光荧光显微探针的微束特性使 乎可以对任何显微镜下呆辨认的有机物质颗粒进行微区分析。在激光的诱导下,所有显微组分都会产生可检测到的荧光讯号。显微组分受激光束辐照最终时刻的荧光强度（Ｆ４００）以及最终荧光强度／初始荧光强度比值（Ｆ４００／Ｆo）是     

Study of petrological characteristics of coal deposits from Marki-Jhari-Jamni area,Wardha valley coalfield,Maharashtra

A detailed study of maceral composition and vitrinite reflectance of the coal deposits from Marki-Jhari-Jamni area, situated in the northwestern extremity of Wardha valley coalfield, Yeotmal district, Maharashtra has been carried out with special reference to their depositional set up. These coals have two distinct types of maceral organization, one having significantly high distribution of the vitrinite group of macerals (35–41%) and the other containing the dominance of inertinite (26–49%). Liptinite maceral group is recorded between 14 and 24%, barring a few coal bands having liptinite maceral group as high as 33–37%. The vitrinite reflectivity ranges from 0.38–0.43%. Thus, they have attained sub-bituminous C rank. Mineral matter in these coals varies between 15 and 22%. The present study suggests that the basin primarily experienced cold climate having intermittent brackish water influx with alternating dry oxidizing spells.     

Study of petrological characteristics of coal deposits from Marki-Jhari-Jamni area, Wardha valley coalfield, Maharashtra

A detailed study of maceral composition and vitrinite reflectance of the coal deposits from Marki-Jhari-Jamni area, situated in the northwestern extremity of Wardha valley coalfield, Yeotmal district, Maharashtra has been carried out with special reference to their depositional set up. These coals have two distinct types of maceral organization, one having significantly high distribution of the vitrinite group of macerals (35–41%) and the other containing the dominance of inertinite (26–49%). Liptinite maceral group is recorded between 14 and 24%, barring a few coal bands having liptinite maceral group as high as 33–37%. The vitrinite reflectivity ranges from 0.38–0.43%. Thus, they have attained sub-bituminous C rank. Mineral matter in these coals varies between 15 and 22%. The present study suggests that the basin primarily experienced cold climate having intermittent brackish water influx with alternating dry oxidizing spells.     

Investigations on the petroleum generation potential of bituminous coals from the Saar region

The Saar basin contains bituminous coals (high volatile A and B). Five coals of Westphalian and Stephanian age with distinctly varying maceral compositions were analysed by Soxhlet extraction and supercritical extraction with different solvents and microscopically. From the data obtained it is concluded that the oldest coals have a potential for oil generation, whereas the younger coals do not. This conclusion is explained by varying liptinite contents and varying adsorption capacities of different vitrinite macerals for bitumen.     

Comparison of elemental composition of macerals determined by electron microprobe to whole-coal ultimate analysis data

The elemental composition of the individual macerals in a suite of Australian coals has been determined in polished sections using light-element electron microprobe techniques. The analyses of the individual macerals in each coal were combined with data on maceral abundance to produce an inferred chemical composition for the organic matter of the respective whole-coal samples, and this was compared, for each sample, to the respective whole-coal ultimate analysis data, corrected to a dry, ash-free (daf) basis. Except for slightly lower values in some lower-rank coals, the inferred percentages of whole-coal C estimated from the microprobe data were found to be very close to the respective whole-coal C percentages as determined by conventional ultimate analysis. The proportion of O in the coals indicated by the microprobe study, however, appears to be as much as 2% higher than that derived from the ultimate analysis data, especially in the lower-rank coal samples. The difference it may represent errors in calculating the O percentages in ultimate analysis, errors in the microprobe analysis due to difficulties in calibration or measurement, or increased proportions of O in the coals due to factors such as take-up with storage of the polished sections. The percentages of whole-coal N calculated from the microprobe data are up to 0.5% (absolute) below the proportion of N determined directly by whole-coal ultimate analysis. This may reflect the inherent difficulty of dealing with a light element at low concentrations by the microprobe technique, or it may indicate that some of the N occurs in the coals in mineral form. The percentages of whole-coal (organic) S calculated from the microprobe study are close to the percentages of organic S determined for each sample by more conventional techniques. With the exception of (organic) O, which may be affected by other factors, and also possibly of N, the electron microprobe technique appears from the study to provide results that are consistent with ultimate analysis over a wide rank range.     

黄陇煤田煤中显微组分与孢粉类型的相关趋势

对陕西黄陇煤田中下侏罗世延安组４号煤进行了煤岩学和孢粉学的详细定量分析，并用计算机对显微组分与孢粉类型之间的的关系作了相关分析，结果表明，煤中显微组分与孢粉类型之间在在相关关采、这种相关关系反映了显微组分的形成与成煤植物之间存在着成因上的联系，即煤中基质状和碎屑状显微组分主要由草本植物和材蕨植物形成，而其细胞结构和条带状的显微组分主要由木本裸子植物形成，，这两种类型显微组分的比值可以反映成煤植被特征。     

中国西北侏罗纪煤系显微组分热解油生物标志物特征及其意义

从西北地区侏罗纪煤中分离出来的不同显微组分热解油生物标志物总体上比较相似,但在一些特殊生物标志物的分布上存在明显差异。藻类体、孢子体、角质体热解油Pr/Ph比值一般在1.5～2.0之间,镜质体和基质镜质体热解油Pr/Ph比值在3～4之间,但均只有相应原煤抽提物Pr/Ph比值的一半。在常规生物标志物甾烷和萜烷组成中,藻类体和孢子体含有相对丰富的C27甾烷,角质体其次,镜质体和基质镜质体C27甾烷含量很低或者基本不含C27甾烷;藻类体和角质体含有较高的伽马蜡烷,而与藻类体来自相同原煤的孢子体伽马蜡烷含量很低;镜质体和基质镜质体基本上不含伽马蜡烷;分离显微组分的原煤伽马蜡烷含量均很低。由此可见,伽马蜡烷的含量不仅与有机质沉积水体的盐度有关,与母源的成分也有关系。显微组分热解油与煤系原油生物标志物组成特征对比表明,煤系原油是藻类体、孢子体、角质体等富氢组分和相对贫氢的镜质组生成产物的混合物。不同油气藏中的原油,每一类显微组分的贡献可能不尽相同,有些原油可能主要来源于藻类体和孢子体等富氢显微组分,而有些原油除了富氢显微组分有贡献外,镜质组对其也有一定的贡献,但富氢显微组分应该是煤系含油气盆地中主要的生油显微组分。     

鄂尔多斯盆地延安组煤有机岩石学研究

鄂尔多斯盆地侏罗纪延安组煤系地层可否成为该盆地另一套油源岩的问题,历来存有争议。系统的煤岩和有机岩石学分析表明:煤中倾油性的壳质组分含量低,基质镜质体的类型也不利于生油,因此,延安组煤系有机质不大可能形成具有工业价值的煤成油藏     

中国陆相源岩显微组分的分类及其岩石学特征

本文通过对中国6个主要油田及15个煤田共三百多块陆相源岩所作的详细有机岩石学研究,提出了以全岩与干酪根为基础的分散有机质分类方案,系统总结了显微组分光性、成因及分布规律,鉴定出了我国陆相源岩中三种新显微组分。此分类不仅适用于低成熟源岩,而且还可用来划分过成熟干酪根的显微组分。     

海拉尔盆地煤及其显微组分的红外漫反射光谱特征

利用红外漫反射光谱和谱带分离技术,从海拉尔盆地煤及其显微组分的红外漫反射光谱图中,在３１００－２８００ｃｍ＾－１范围内分辨出１２或１３个峰,并确认了结构归属,同时建立了５个反映有机质化学结构组成特征的参数,讨论了煤与显微镜组分的生烃潜能。     

Micro-FTIR spectroscopy of liptinite macerals in coal

Reflectance FTIR microspectroscopy has been used to investigate the chemical structure of the liptinite macerals, alginite, bituminite, sporinite, cutinite and resinite in bituminous coals of Carboniferous to Tertiary age. In comparison with the spectra of vitrinite in the same coals, the micro-FTIR spectra of liptinite macerals are characterized by stronger aliphatic CH_x absorptions at 3000–2800 and 1460–1450 cm⁻¹, less intense aromatic C=C ring stretching vibration and aromatic CH out of plane deformation at 1610–1560 and 900–700 cm⁻¹ respectively and various intense acid C=O group absorptions at 1740–1700 cm⁻¹. The peaks at 1000–900 cm⁻¹ due to aliphatic CH₂ wagging vibrations in olefins and at 730–720 cm⁻¹ due to CH₂ rocking vibration in long chain aliphatic substances ([CH₂]_n, n≥4), are characteristic of liptinite macerals. Collectively the micro-FTIR spectral characteristics indicate that liptinite is composed of greater numbers of long chain aliphatics, fewer aromatics and a broader range of oxygen-containing groups than other macerals. Marked differences exist in micro-FTIR spectra within the liptinite maceral group. Alginite has the strongest aliphatic and least aromatic absorptions followed by bituminite, resinite, cutinite and sporinite. The aliphatic components in alginite are the longest chained and least branched whereas those in sporinite are the shortest chained and most branched. Bituminite, resinite and cutinite are intermediate. Notable differences in micro-FTIR spectra of individual liptinite macerals, such as intensities and peak locations of aromatic C=C in alginite, C=O groups in bituminite and resinite and substituted aromatic CH and C–O–C groups in cutinite and sporinite, also exist, which are attributed to differences in depositional environments or biotaxonomy.     

Splint coals of the Central Appalachians: Petrographic and geochemical facies of the Peach Orchard No. 3 split coal bed,southern Magoffin County,Kentucky

The Bolsovian (Middle Pennsylvanian) Peach Orchard coal bed is one of the splint coals of the Central Appalachians. Splint coal is a name for the dull, inertinite-rich lithologies typical of coals of the region. The No. 3 Split was sampled at five locations in Magoffin County, Kentucky and analyzed for petrography and major and minor elements. The No. 3 Split coals contain semifusinite-rich lithologies, up to 48% (mineral-free basis) in one case. The nature of the semifusinite varies with position in the coal bed, containing more mineral matter of detrital origin in the uppermost durain. The maceral assemblage of these terminal durains is dominated by detrital fusinite and semifusinite, suggesting reworking of the maceral assemblage coincident with the deposition of the detrital minerals. However, a durain in the middle of the coal bed, while lithologically similar to the uppermost durains, has a degraded, macrinite-rich, texture. The inertinite macerals in the middle durain have less distinct edges than semifusinites in the uppermost terminal durains, suggesting degradation as a possible path to inertinite formation. The uppermost durain has higher ash and semifusinite contents at the eastern sites than at the western sites. The difference in the microscopic petrology indicates that megascopic petrology alone can be a deceptive indicator of depositional environments and that close attention must be paid to the individual macerals and their implications for the depositional setting, especially within the inertinite group.     

Chemical composition of macerals in bituminous coals of the Gunnedah Basin, Australia, using electron microprobe analysis techniques

The chemical composition of the organic matter in the principal macerals of high-volatile bituminous coals from the Gunnedah Basin, New South Wales (Rv_max of telocollinite between 0.6 and 1.1%) has been evaluated from polished section specimens using an electron microprobe technique. Highest proportions of carbon occur in the inertinite macerals, especially fusinite and secretinite (formerly resino-sclerotinite), as well as in sporinite; lowest proportions of carbon occur in the different macerals of the vitrinite group. Oxygen shows the reverse trend, being most abundant in vitrinite and least abundant in the inertinite components, whereas sulphur is lowest in the inertinites and highest in the liptinite (mainly sporinite) present. Evaluations of maceral composition, using the carbon content of telocollinite as a rank indicator, show that carbon is more abundant in both sporinite and semifusinite, relative to vitrinite, in low-rank high-volatile bituminous coals. The difference decreases with increasing rank, and the proportion of carbon in telocollinite becomes essentially the same as that in sporinite and semifusinite at carbon contents of about 89 and 91%, respectively. The carbon content of fusinite and secretinite, on the other hand, does not seem to vary appreciably with rank advance. No significant difference in composition occurs in the rank range studied between the three vitrinite varieties present, desmocollinite, telocollinite and a more highly reflecting telocollinite resembling pseudovitrinite. No evidence was found to indicate a higher hydrogen content, relative to telocollinite, for the vitrinite matrix of desmocollinite.     

Tracing the origins of polymethylene moieties in coal

Many coals have been shown to contain long polymethylene segments (up to C₃₀ and longer) which crack to ethylene, propylene, butadiene and other low molecular weight hydrocarbons when the coals are pyrolyzed. The polymethylene content varies in different coals and can be 10% or more in low rank coals. Cannel coals may contain up to 20% polymethylene. Polymethylene moieties are either very low or absent in low-volatile bituminous coals and anthracite.A method of analysis for polymethylene in coals, based on liquefaction in a donor solvent followed by ¹H NMR spectroscopy has been described. With this analysis, it has been shown that polymethylene moieties are present in higher concentrations in exinite macerals than in vitrinites or inertinites. Analysis of peats also show the presence of polymethylene components at levels similar to that found in coal. Analysis of various parts of present-day plants also shows the presence of polymethylene materials in concentrations varying significantly from one kind of plant to another. Within a given plant type, some parts of the plant appear to be richer in polymethylene than others. Spores and pollen are frequently especially rich in polymethylene, accounting for the corresponding high concentration in exinite macerals in coal.Samples of Texas Eocene lignites representing a depositional time interval of 15–20 million years and three distinctly different climatic and vegetational conditions were analyzed for polymethylene contents. The differences in polymethylene levels are consistent with differences in flora and support the idea that the original plants are the sources of polymethylene components in coal.