The optical features and hydrocarbon-generating model of “barkinite” from Late Permian coals in South China

Leping coal is known for its high content of “barkinite”, which is a unique liptinite maceral apparently found only in the Late Permian coals of South China. “Barkinite” has previously identified as suberinite, but on the basis of further investigations, most coal petrologists conclude that “barkinite” is not suberinite, but a distinct maceral. The term “barkinite” was introduced by (State Bureau of Technical Supervision of the People's Republic of China, 1991, GB 12937-91 (in Chinese)), but it has not been recognized by ICCP and has not been accepted internationally.In this paper, elemental analyses (EA), pyrolysis-gas chromatography, Rock-Eval pyrolysis and optical techniques were used to study the optical features and the hydrocarbon-generating model of “barkinite”. The results show that “barkinite” with imbricate structure usually occurs in single or multiple layers or in a circular form, and no definite border exists between the cell walls and fillings, but there exist clear aperture among the cells.“Barkinite” is characterized by fluorescing in relatively high rank coals. At low maturity of 0.60–0.80%R_o, “barkinite” shows strong bright orange–yellow fluorescence, and the fluorescent colors of different cells are inhomogeneous in one sample. As vitrinite reflectance increases up to 0.90%R_o, “barkinite” also displays strong yellow or yellow–brown fluorescence; and most of “barkinite” lose fluorescence at the maturity of 1.20–1.30%R_o. However, most of suberinite types lose fluorescence at a vitrinite reflectance of 0.50% Ro, or at the stage of high volatile C bituminous coal. In particular, the cell walls of “barkinite” usually show red color, whereas the cell fillings show yellow color under transmitted light. This character is contrary to suberinite.“Barkinite” is also characterized by late generation of large amounts of liquid oil, which is different from the early generation of large amounts of liquid hydrocarbon. In addition, “barkinite” with high hydrocarbon generation potential, high elemental hydrogen, and low carbon content. The pyrolysis products of “barkinite” are dominated by aliphatic compounds, followed by low molecular-weight aromatic compounds (benzene, toluene, xylene and naphthalene), and a few isoprenoids. The pyrolysis hydrocarbons of “barkinite” are mostly composed of light oil (C₆–C₁₄) and wet gas (C₂–C₅), and that heavy oil (C₁₅⁺) and methane (C₁) are the minor hydrocarbon.In addition, suberinite is defined only as suberinized cell walls—it does not include the cell fillings, and the cell lumens were empty or filled by corpocollinites, which do not show any fluorescence. Whereas, “barkinite” not only includes the cell walls, but also includes the cell fillings, and the cell fillings show bright yellow fluorescence.Since the optical features and the hydrocarbon-generating model of “barkinite” are quite different from suberinite. We suggest that “barkinite” is a new type of maceral.     

Petrologic and geochemical characteristics of “barkinite” from the Dahe mine, Guizhou Province, China

Although “barkinite” has long been studied by many geologists, its geochemical characteristics and environment of deposition are still not known in detail. In order to study the petrography and geochemical characteristics of “barkinite”, coal samples from two Permian coal seams were taken from the Dahe mine, Guizhou Province. The samples were separated into maceral fractions, and then analyzed by microscopical, isotopic, Rock-Eval, and geochemical methods. The microscopical results indicate that “barkinite” occurs as four main types. According to their relationship to other maceral groups, “barkinite” is ostensibly formed under variably dry–wet or oxidizing–reducing conditions. The extract yield, isotope data and Rock-Eval values of “barkinite” are different from other macerals. Microscopical and geochemical results indicate that “barkinite” forms part of the liptinite group.     

Properties of thermally metamorphosed coal from Tanjung Enim Area, South Sumatra Basin, Indonesia with special reference to the coalification path of macerals

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 (VR_max = 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 (VR_max = 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 VR_max of around 1.5%. Significant decrease of volatile matter occurs in the zone between 0.5% and 2.0% VR_max. A sharp bend occurs at VR_max between 2.0% and 2.5%. Above 2.5%, the volatile matter decreases only very slightly. Between VR_r = 0.5% and 2.0%, the carbon content of the coals is ascending drastically. Above 2.5% VR_r, 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). T_max 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.     

Striking liptinitic bark remains peculiar to some Late Permian Chinese coals

An unusual liptinite coal component has been reported in the Chinese literature over the past sixty years. It has been described as a maceral in the Chinese National Standard (1991), but it has not been named internationally. In Chinese literature it is called “barkinite”, on the basis of its morphological features and because it is believed to have originated as bark tissue.“Barkinite” occurs in Late Permian, marine-influenced coals and is best represented in the Changguang, Leping and Shuicheng Basins of southern China.The material originates from plant periderm or the bark of higher plants. However, “bark” contains a variety of substances, including resin and suberin, which are recognised as the precursors of the resinite and suberinite macerals. “Barkinite” is distinguished by (i) its thickness; individual pieces can be more than ten cells thick and several centimetres long and (ii) it fluoresces strongly at 0.6% vitrinite reflectance and loses its fluorescence at about 1.1% vitrinite reflectance.The reporting of “barkinite” from only Chinese coals may be due to its origin from Lepidodendron and Psaronius flora, which was common in the Northern Hemisphere during the Carboniferous, but which was isolated to China by the Late Permian. It is proposed that the remnant flora evolved into unique forms in China by the Late Permian. Lepidodendron and Psaronius remains, coupled with a strongly marine-influenced, peat-forming environment have given rise to “barkinite” and to its restricted distribution.     

Organic Geochemical and Petrographic Characteristics of the Coal Measure Source Rocks of Pinghu Formation in the Xihu Sag of the East China Sea Shelf Basin: Implications for Coal Measure Gas Potential

Coal measure source rocks, located in the Xihu Sag of the East China Sea Shelf Basin, were analyzed to define the hydrocarbon generation potential, organic geochemistry/petrology characteristics, and coal preservation conditions. The Pinghu source rocks in the Xihu Sag are mainly gas-prone accompany with condensate oil generation. The coals and shales of the Pinghu Formation are classified from "fair" to "excellent" source rocks with total organic carbon(TOC) contents ranging from 25.2% to 77.2% and 1.29% to 20.9%, respectively. The coals are richer in TOC and S1+S2 than the shales, indicating that the coals have more generation potential per unit mass. Moreover, the kerogen type of the organic matter consists of types Ⅱ-Ⅲ and Ⅲ, which the maturity Ro ranges from 0.59% to 0.83%. Petrographically, the coals and shales are dominated by vitrinite macerals(69.1%–96.8%) with minor proportions of liptinite(2.5%–17.55%) and inertinite(0.2%–6.2%). The correlation between maceral composition and S1+S2 indicates that the main contributor to the generation potential is vitrinite. Therefore, the coals and shales of the Pinghu Formation has good hydrocarbon generation potential, which provided a good foundation for coal measure gas accumulation. Furthermore, coal facies models indicates that the Pinghu coal was deposited in limno-telmatic environment under high water levels, with low tree density(mainly herbaceous) and with low-moderate nutrient supply. Fluctuating water levels and intermittent flooding during the deposition of peat resulted in the inter-layering of coal, shale and sandstone, which potentially providing favorable preservation conditions for coal measure gas.     

Brecciated and mineralized coals in Union County, Western Kentucky coal field

Coals from the D-2 and D-3 boreholes in the Grove Center 7 1/2 min quadrangle, Union County, KY, have been found to be highly brecciated and mineralized. The mineralization is dominated by a carbonate assemblage with minor sulfides and sulfates. Included among the secondary minerals is the lead selenide, clausthalite. Overall, the emplacement of secondary vein minerals was responsible for raising the rank of the coals from the 0.6–0.7% R_max range found in the area to as high as 0.95–0.99% R_max.A 1.3-m-thick coal found in one of the boreholes is unique among known Western Kentucky coals in having less than 50% vitrinite. Semifusinite and fusinite dominate the maceral assemblages. The coal is also low in sulfur coal, which is unusual for the Illinois Basin. It has an ash yield of less than 10%; much of it dominated by pervasive carbonate veining. The age of the thick coal in core D-2 is similar to that of the Elm Lick coal bed, found elsewhere in the Western Kentucky coalfield. The coals in D-3 are younger, having Stephanian palynomorph assemblages.     

The petroleum generation potential and effective oil window of humic coals related to coal composition and age

A worldwide data set of more than 500 humic coals from the major coal-forming geological periods has been used to analyse the evolution in the remaining (Hydrogen Index, HI) and total (Quality Index, QI) generation potentials with increasing thermal maturity and the ‘effective oil window’ (‘oil expulsion window’). All samples describe HI and QI bands that are broad at low maturities and that gradually narrow with increasing maturity. The oil generation potential is completely exhausted at a vitrinite reflectance of 2.0–2.2%R_o or T_max of 500–510 °C. The initial large variation in the generation potential is related to the original depositional conditions, particularly the degree of marine influence and the formation of hydrogen-enriched vitrinite, as suggested by increased sulphur and hydrogen contents. During initial thermal maturation the HI increases to a maximum value, HI_max. Similarly, QI increases to a maximum value, QI_max. This increase in HI and QI is related to the formation of an additional generation potential in the coal structure. The decline in QI with further maturation is indicating onset of initial oil expulsion, which precedes efficient expulsion. Liquid petroleum generation from humic coals is thus a complex, three-phase process: (i) onset of petroleum generation, (ii) petroleum build-up in the coal, and (iii) initial oil expulsion followed by efficient oil expulsion (corresponding to the effective oil window). Efficient oil expulsion is indicated by a decline in the Bitumen Index (BI) when plotted against vitrinite reflectance or T_max. This means that in humic coals the vitrinite reflectance or T_max values at which onset of petroleum generation occurs cannot be used to establish the start of the effective oil window. The start of the effective oil window occurs within the vitrinite reflectance range 0.85–1.05%R_o or T_max range 440–455 °C and the oil window extends to 1.5–2.0%R_o or 470–510 °C. For general use, an effective oil window is proposed to occur from 0.85 to 1.7%R_o or from 440 to 490 °C. Specific ranges for HI_max and the effective oil window can be defined for Cenozoic, Jurassic, Permian, and Carboniferous coals. Cenozoic coals reach the highest HI_max values (220–370 mg HC/g TOC), and for the most oil-prone Cenozoic coals the effective oil window may possibly range from 0.65 to 2.0%R_o or 430 to 510 °C. In contrast, the most oil-prone Jurassic, Permian and Carboniferous coals reach the expulsion threshold at a vitrinite reflectance of 0.85–0.9%R_o or T_max of 440–445 °C.     

Properties, origin and nomenclature of rodlets of the inertinite maceral group in coals of the central Appalachian basin, U.S.A.

Resin rodlets, sclerenchyma strands and woody splinters, which are collectively called rodlets, were studied by chemical, optical petrographic, and scanning-electron microscopic (SEM) techniques. A study was made of such rodlets from the bituminous coal beds of the central Appalachian basin (Pennsylvanian; Upper Carboniferous) of the United States. Comparisons were made with rodlets from coal beds of the Illinois basin, the Southern Anthracite Field of Pennsylvania, the St. Rose coal field of Nova Scotia, and European and other coal fields. In order to determine their physical and chemical properties, a detailed study was made of the rodlets from the Pomeroy coal bed (high volatile A bituminous coal; Monongahela Formation; Upper Pennsylvanian) of Kanawha County, West Virginia. The origin of the rodlets was determined by a comparative analysis of a medullosan (seed fern) stem from the Herrin (No. 6) coal bed (high volatile C bituminous coal; Carbondale Formation) from Washington County, Illinois. Rodlets are commonly concentrated in fusain or carbominerite layers or lenses in bituminous coal beds of the central Appalachian basin. Most of the rodlets examined in our study were probably derived from medullosan seed ferns. The three types of rodlets are distinguished on the basis of cellularity, morphology and fracture.The resin rodlets studied by us are noncellular and appear to be similar in properties and origin to those found in coal beds of the Middle and Upper Pennsylvanian of the Illinois basin. The resin rodlets extracted from the Pomeroy coal bed exhibit high relief and high reflectance when polished and viewed in reflected light; they are opaque in transmitted light. In cross section, the resin rodlets are oval to round and have diameters ranging from 60 to 450 μm. Many are solid, but some have vesicles, canals or cavities, which are commonly filled with clay, probably kaolinite. Typically, they have distinct fracture patterns (“kerfs”) in longitudinal and cross sections and many are characterized by dense (probably oxidized) rims. The orientation and amounts of void space and mineralization of resin rodlets in coal have resulted in much confusion in their recognition and classification. The resin rodlets are petrographically recognized as sclerotinites of the inertinite maceral group. We here propose that resin rodlets be assigned to the maceral variety of sclerotinites termed “resino-sclerotinite” because of their presumable resinous origin. Other investigators have confused some fusinitized resin rodlets with fungal masses, which have different morphological properties and which probably have different chemical properties. We here propose that such fungal masses be assigned to the maceral variety of sclerotinites termed “fungo-sclerotinite.”The sclerenchyma strands examined in our study are cellular, thick-walled, and crescent-shaped in cross section. They exhibit high reflectance and high relief and belong to semifusinite and fusinite of the inertinite maceral group. Sclerenchyma strands are commonly associated with resin canals in Medullosa and related seed-fern genera, which are common in coal balls of the Illinois basin. We here propose adoption of the maceral varietal terms “sclerenchymo-fusinite” and “sclerenchymo-semifusinite” for these bodies.The woody splinters in the Pomeroy coal bed are cellular and thin-walled and have scattered pits as much as a few microns in diameter. They are dark brown to black in transmitted light and commonly have a lower reflectance than the resino-sclerotinite and sclerenchymo-fusinite of the Pomeroy coal. The woody splinters belong to semifusinite and fusinite of the inertinite maceral group. The maceral varietal terms “xylemo-semifusinite” and “xylemo-fusinite” are here proposed for these bodies.Elemental chemical data for the resin rodlets of the Pomeroy coal bed of the central Appalachian basin indicate that resin rodlets have significantly lower atomic H/C and O/C ratios than do sclerenchyma strands and woody splinters. The lower atomic H/C and O/C ratios of the resin rodlets correlate with the highest reflectance. In the coal ball medullosan seed-fern stem from the Herrin (No. 6) coal bed of the Illinois basin, the reflectances of the resin rodlets, woody splinters and sclerenchyma strands are similar and comparable to those of associated vitrinite in the coal ball stem and in the attached coal. However, resin rodlets and sclerenchyma strands in the attached coal have significantly higher reflectances, similar to those of the Pomeroy coal.     

Hydrocarbon—Generating Characteristics of Barkinite—Rich Colas from Late Permian Longtan Formation ,South China

Leping coal (including barkinite-rich coal) is a unique kind of coal,which is widely distrbuted in the Late Permian Longan Formation,South China,In this paper,ROck-Eval,Py-GC and simulation experiment via an open-system were used to study the hydrocarbon-generating potential,hydrocarbon composition.and hydrocarbon-generating model of barkiniterich coals from the shuicheng coal field of Guizhou Province,Southwest China.The results show that barkinite-rich coals have high hydrocarbon-generating potential,with S1 S2 being 211-311mg/g,and can produce large amounts of hydrocorbon at the high-maturity stage,mostly within the temperature range of 420-450℃(corresponding to VR0 1.1-1.5%);barkinite-rich coal is one of the better oil sources and light hydrocarbon and wet gas are the major hydrocarbon components,which account for 45% and 33% of the total hydrocarbons.respectively.These characteristics are of importance for exploring oil and gas resources in the Late permian Longtan Formation coals,southwest China.     

Predicted CO2 emissions from maceral concentrates of high volatile bituminous Kentucky and Illinois coals

A large collection of well-characterized coals, documented in the Center for Applied Energy Research's (CAER) database, was used to estimate the CO₂ content of maceral concentrates from Kentucky and Illinois high volatile bituminous coals. The data showed no correlation between CO₂ versus coal ranks and between CO₂ versus maceral content. Subsequently, eight sets of low-ash density-gradient centrifugation (DGC) maceral concentrates from five coal beds were examined, spanning in the high volatile rank range. Heating value was not determined on the concentrates, but instead was calculated using the Mott–Spooner formula. There was a good correlation between predicted CO₂ and maceral content for the individual iso-rank (based on vitrinite reflectance, analyzed on whole (parent) coal) sets. In general, the predicted CO₂ increases from liptinite-rich through vitrinite-rich to inertinite-rich concentrates (note: no “concentrates” are absolutely monomaceral).     

Analysis and characterization of samples from sedimentary strata with correlations to indicate the potential for hydrocarbons

The Rock-Eval pyrolysis and TOC analysis have been widely used to evaluate the source rock quality. The atomic H/C ratio of kerogen, however, has been overlooked in source rock evaluation. In this study, coal and carbonaceous samples, including 26 from northwestern Taiwan, 12 from China, and 4 from the United States were analyzed, and integrated with 157 published data, to explore the significance of atomic H/C ratio as a parameter of source rock evaluation. Two different linear trends were observed in the cross-plot of S ₁ versus S ₂. Field outcropped shale or C-shale exhibits a steeper slope compared to that of coal samples which can be attributed to the compositional difference in their organic material. A rather strong positive correlation for H% versus S ₂ illustrates the contribution of H-containing macerals, especially exinite. Organic matters in the samples studied are of type II/III kerogen based on the relationship between HI and T _max. The H/C ratio, as well as the HI, S ₁, and S ₂, generally decreases with the maturity increasing. The H/C ratio decreases slightly from 1.1 to 0.7 with the maturity increasing from R _o 0.55 to 0.85%. Samples with H/C ratio in this range show significant change in certain other geochemical parameters (e.g. HI, S ₁, S ₂, S ₁ + S ₂, S ₁/(S ₁ + S ₂), S ₁/TOC, (S ₁ + S ₂)/TOC, T _max). The (S ₁ + S ₂)/TOC ratio (defined as QI) was used as an indicator of the hydrocarbon potential. The QI, HI, and H/C ratio show a certain correlation, all increasing accordingly. The QI of the samples analyzed in this study is approximately 100–380 (mgHC/gTOC), similar to that of most humic coals for oil and gas generation. Samples with R _o value lower than 0.55% always show significant variation in their HI, ranging from 80 to 520 mgHC/gTOC. It is inferred that hydrocarbon potential started from R _o 0.55% and atomic H/C ratio 1.1 in this study.     

Applications of microscopy to coke making

A Canadian perspective of the petrographic, thermal rheological and grade of metallurgical coals required to make coke with high strength and strength after reaction (CSR) properties is presented. The development of automated microscopic techniques to obtain reproducible and reliable petrographic data to predict coke quality is discussed. The amount of “altered vitrinite” in the microscopic coke textures has been used as a reference to quantifiy in situ coal oxidation. Relationships between coke microscopy, coal petrography and thermal rheological data show that FSI can be used to estimate the amount of oxidized vitrinite plus petrographic inert contents of coal. Plastic temperature ranges determined from microscopic examination of the coal/coke transformations for Appalachian and Canadian coals show that standard thermal rheological tests underestimate the plastic range for high inertinite coals.     

A new approach to interpreting Rock-Eval S2 and TOC data for kerogen quality assessment

A simple method for application in source potential mapping is used to assess the original oil and gas potentials in source rock horizons based upon Rock-Eval potential (S₂) and total organic carbon (TOC) values. The method assumes that kerogens consist of mixtures of end-members with assigned hydrogen index values. Based on suggested algorithms, the average amounts of oil-prone, gas-prone and inert organic material over source rock intervals are determined in TOC units. The method uses regression lines from plots of remaining hydrocarbon potentials (S₂) versus total organic carbon (TOC), and “quick-look” transparent overlays are used to read the appropriate kerogen mixture.Mineral matrix effects during pyrolysis, when strong, can cause erroneous results. This effect which occurs for oil-prone kerogens and adsorptive minerals can cause problems particularly for lean samples (S₂ = 0–3 mg HC/g rock) whilst the errors for richer samples are less.The method is applied on three sections of Upper Jurassic organic-rich rocks from the Danish North Sea sector, which are at different maturity stages. One of these sections is dominated by gas-prone material, one is dominated by oil-prone material and the third section contains a mixture of oil- and gas-prone material.The method has been compared with other methods that split kerogens in oil and gas generating potential and has given reasonable results.Experience using the method and a presented example suggest that sedimentological, system tract information may be derived from S₂ to TOC cross-plots. A constructed modelling example suggests that the end-member concept used in this approach may be used in forward type source rock prediction models when combined with sedimentological models. The resulting S₂–TOC plots can be used in order to check the forward modelling results against observed values.     

Petrology, rank and evidence for petroleum generation, Upper Triassic to Middle Jurassic coals, Central Alborz Region, Northern Iran

Upper Triassic to Middle Jurassic coals from the Alborz region of northern Iran were analyzed by reflected light-fluorescence microscopy and Rock Eval 6® pyrolysis to evaluate their regional rank variation, degree of hydrothermal alteration, and petroleum generative potential. The coal ranks in the region range from a low of 0.69%Ro_R in the Glanddeh-Rud area to a high of 1.02%Ro_R in the Gajereh area. T_max (°C) values (Rock Eval 6 pyrolysis) also increase progressively with increasing vitrinite %Ro values, however T_max is suppressed lower than would be expected for each rank ranging from 428 °C for the Glandeeh coal to 438 °C for the Gajereh coal. T_max suppression may be caused by maceral composition and soluble organics within the coal. Moderately high hydrogen indices, persistent and oily exudations from the coals during UV exposure, and traces of hydrocarbon fluid inclusions suggest that liquid petroleum was likely generated within some of the coals.     

Methane and CO2 sorption and desorption measurements on dry Argonne premium coals: pure components and mixtures

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 (VR_r=0.25%) and the highest ratios (2.7 and 3.16) were encountered for the low-rank coals (VR_r 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.     

Liquid hydrocarbon generation potential from Tertiary Nyalau Formation coals in the onshore Sarawak, Eastern Malaysia

Tertiary coals exposed in the north-central part of onshore Sarawak are evaluated, and their depositional environments are interpreted. Total organic carbon contents (TOC) of the coals range from 58.1 to 80.9 wt. % and yield hydrogen index values ranging from 282 to 510 mg HC/g TOC with low oxygen index values, consistent with Type II and mixed Type II–III kerogens. The coal samples have vitrinite reflectance values in the range of 0.47–0.67 Ro %, indicating immature to early mature (initial oil window). T _max values range from 428 to 436 °C, which are good in agreement with vitrinite reflectance data. The Tertiary coals are humic and generally dominated by vitrinite, with significant amounts of liptinite and low amounts of inertinite macerals. Good liquid hydrocarbons generation potential can be expected from the coals with rich liptinitic content (>35 %). This is supported by their high hydrogen index of up to 300 mg HC/g TOC and Py-GC (S ₂) pyrograms with n-alkane/alkene doublets extending beyond C₃₀. The Tertiary coals are characterised by dominant odd carbon numbered n-alkanes (n-C₂₃ to n-C₃₃), high Pr/Ph ratio (6–8), high T _m /T _s ratio (8–16), and predominant regular sterane C₂₉. All biomarkers parameters clearly indicate that the organic matter was derived from terrestrial inputs and the deposited under oxic condition.     

Facies and genesis of Carboniferous coal seams of Northwest Germany

In order to get detailed information about the facies and genesis of Upper Carboniferous coal seams of Northwest Germany, maceral analyses of complete seam profiles (Westphalian B-D, mainly Westphalian C) were carried out. Four main facies and twelve subfacies could be distinguished. The main facies are:

1. (1) The sapropelic-coal facies, consisting of fine-grained inertinite and liptinite, which forms from organic sediments deposited at the bottom of moor lakes.

2. (2) The densosporinite facies which is high in inertinite and liptinite and low in vitrinite. Syngenetic pyrites, clastic layers, thick vitrains and fusains do not occur. This facies originates from peats of ‘open mires’ with higher groundwater table and herbaceous vegetation. The ‘open mire’ was situated in the centre of extensive swamps. Consequently, clastic sedimentation did not affect this swamp type and nutrient supply and pH values were low.

3. (3) The vitrinite-fusinite facies, which is high in vitrinite. This is the result of abundant vitrains. Under the microscope, fusains were mostly identified as fusinite. The vitrinite-fusinite facies originates from a forest mire. More or less abundant seam splits and clastic layers show that rivers flowed in the neighbourhood of this area.

4. (4) The shaly-coal facies, which represents the most marginal part of the former swamp frequently affected by clastic sedimentation.

Within the Carboniferous of the Ruhr Region it seems unlikely that the thin coal seams of the Namurian C and Westphalian A1 contain a densosporinite facies. The swamps were situated in the lower delta plain where they were often affected by marine influences. Consequently, coals are high in minerals and sulfur and they are thin and discontinous. The best conditions for the formation of extensive swamps, with open mires (densosporinite facies) in their central parts, prevailed during Westphalian A2 and B1 times. Low contents of sulfur and minerals and high content of inertinite are typical for these coals. Sedimentation mainly took place in the transitional zone from the lower to the upper delta plain. During the Westphalian B2 and C fluvial sedimentation dominated. Within the coal seams minerals, sulfur and pseudovitrinite increase while inertinite decreases. This is the consequence of coal of the densosporinite facies occurring with increased rarity. The coal seams of the Westphalian C2 contain no densosporinite facies because peat formation was restricted by increasing fluvial sedimentation and by a better drainage. As a consequence, extensive swamps with ‘open mires’ in the centre were no longer formed after the formation of the “Odin” seams. Above the “Odin” seams coal of the vitrinite-fusinite facies contains thick-walled torisporinites. Variations and lowering of the groundwater table caused mild oxidative influences during peat formation. This is documented by an increase in pseudovitrinite, the occurrence of torisporinites and the absence of spheroidal sideritic concretions. Sulfur content increases in the absence of the low-ash and low-sulfur coal of the densosporinite facies.In Upper Carboniferous coal seams of the Ibbenbüren Region the inertinite and telocollinite contents are higher than in those of the Ruhr Region. Therefore, variations of the groundwater table have been more pronounced and resulting oxidative influences must have been more severe. Seldom occurring marine and brackish horizons and a higher fusinite (fusain) content indicate a slight elevation of this area. From Early Westphalian D times onward, peat formation was no longer possible because of the better drainage. This resulted in severe oxidative conditions which excluded peat formation.     

Solid bitumen reflectance and Rock-Eval Tmax as maturation indices: an example from the “Nordegg Member”, Western Canada Sedimentary Basin

Marine, organic-rich rock units commonly contain little for vitrinite reflectance (VR₀) measurement, the most commoly used method of assessing thermal maturity. This is true of the Lower Jurassic “Nordegg Member”, a type I/II, sulphur-rich source rock from the Western Canada Sedimentary Basin. This study examines the advantages and pitfalls associated with the use of Rock-Eval T_max and solid bitumen reflectance (BR₀) to determined maturity in the “Nordegg”. Vitrinite reflectance data from Cretaceous coals and known coalification gradients in the study area are used to extrapolate VR₀ values for the “Nordegg”.T_max increases non-linearly with respect to both BR₀ and extrapolated VR₀ values. A sharp increase in the reflectaance of both solid bitumen and vitrinite occurs between T_max 440–450°C, and is coincident with a pronounced decrease in Hydrogen Index values and the loss of solid bitumen and telalginite fluorescence over the same narrow T_max interval. This T_max range is interpreted as the main zone of hydrocarbon generation in the “Nordegg”, and corresponds to extrapolated VR₀ values of 0.55–0.85%. The moderate to high sulphur contents in the kerogen played a significant role in determining the boundaries of the “Nordegg” oil window.A linear relationship between BR₀ and extrapolated VR₀, as proposed elsewhere, is not true for the “Nordegg”. BR₀ increases with respect to extrapolated VR₀ according to Jacob's (1985) formula (VR₀=0.618×(BR₀)+0.40) up to VR₀≈0.72% (BR₀≈0.52%). Beyond this point, BR₀ increases sharply relative to extrapolated VR₀, according to the relatioship VR₀ = 0.277 × (BR₀) + 0.57 (R² = 0.91). The break in the BR₀−VR₀ curve at 0.72%VR₀ is thought to signifiy the peak of hydrocarbon generation and represents a previously unrecognized coalification jump in the solid bitumen analogous to the first coalification jump of liptinites.     

Oil-generating coals of the San Juan Basin, New Mexico and Colorado, U.S.A.

Coal beds of the Upper Cretaceous Fruitland Formation in the San Juan Basin of northwestern New Mexico and southwestern Colorado have significant liquid hydrocarbon generation potential as indicated by typical Rock-Eval Hydrogen Indexes in the range of 200–400 mg hydrocarbon/g organic carbon (type II and III organic matter). Small, non-commercial quantities of oil have been produced from the coal beds at several locations. The oils are characterized by high pristane/phytane (ca 4) and pristane/n-C₁₇ ratios (ca 1.2), abundant C₂₁₊ alkanes in the C₁₀₊ fraction with a slight predominance of odd carbon-numbered n-alkanes, abundant branched-chain alkanes in the C₁₅₊ region, and a predominance of methylcyclohexane in the C₄----C₁₀ fraction. The oils are indigenous to the Fruitland Formation coals and probably migrated at thermal maturities corresponding to vitrinite reflectance values in the range 0.7–0.8%. Although the oils found to date are not present in commercial amounts, these findings illustrate the potential of some coals to generate and expel oil under conditions of moderate thermal heating.     

Characteristics of hydrocarbon generation from organic macerals in Jurassic coal measures, Xinjiang, China

The Jurassic coals of the Junggar and Turpan-Hami basins, Xinjiang, China, are characterized by abundant vitrinite. Microscopic analysis of Junggar coal samples indicates that they contain desmocollinite and hydrogen-rich vitrinite with a low reflectivity. The hydrocarbon-generating potential of various macerais follows the decreasing order of exinite > vitrinite > inertinite. However, desmocollinite is a principal maceral for hydrocarbon generation in this area because the content of vitrinite is higher than that of exinite. Data from simulating experiments and infrared spectra show that the hydrocarbon-generating process occurred primarily at the lower-mature stage in the Middle-Lower Jurassic coal measures. Generally, crude oil from the Qigu oilfield has a close similarity in hopanoid distribution to the vitrinite and exinite from the Jurassic strata with C₂₃-C₃₂ pentacyclic triterpanes and γ-lupane being present. The distribution of steranes is also similar. C₂₉-sitostane is dominant and Q₂₇ ergostane is subordinate. Only a trace amount of cholestane is present. All this suggests that the crude oil from the Qigu oilfield was derived from Jurassic coal measures.