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Maria Mastalerz

Publications and source records attributed to Maria Mastalerz.

At least 73 records · Page 4Linked to original sources

An approach toward a combined scheme for the petrographic classification of fly ash: Revision and clarification

Hower and Mastalerz's classification scheme for fly ash is modified to make more widely acceptable. First, proper consideration is given to the potential role of anthracite in the development of isotropic and anisotropic chars. Second, the role of low-reflectance inertinite in producing vesicular chars is noted. It is shown that noncoal chars in the fuel can potentially produce chars that have the potential to stretch the limits of the classification. With care, it is possible to classify certain biomass chars as being distinct from coal-derived chars.

Energy and Fuels↗

Functional groups of fossil marattialeans: Chemotaxonomic implications for Pennsylvanian tree ferns and pteridophylls

Marattialean-fossil foliage, assigned to Pecopteris Brongniart, was an important and widespread floral component in Late Pennsylvanian mires, with phylogenetic affinity to extant marattialean taxa in tropical regions. Marattialean fossil taxonomy is, however, still uncertain. Specimens from the Pilsen limnic Basin, Westphalian D, Czech Republic, represent fertile marattialean foliage of Pecopteris (Asterotheca) nyranensis and Pecopteris (Asterotheca) miltonii, and sterile foliage of Pecopteris aspidioides and Pecopteris polypodioides. Taxonomic parameters for their assignments included cuticle, stomatal morphologies (studied for the first time), and in situ reproductive organs and spores. Chemotaxonomic interpretations hinge on fidelity of preservation of compounds, or molecular fragments thereof, that were synthesized by the once-living plants. This preservation state was possibly due to the thermal history (maximum temperature of 130 ??C) in the Pilsen Basin, acidic preservation conditions, lithology and facies stability. Although subtle, the four pecopterid species are differentiable from one another by combined FTIR characteristics, supporting taxonomy. The ratio of CH2/CH3 is hypothesized to be a chemotaxonomic parameter for Pennsylvanian pteridophylls, both in seed and true ferns that have previously been studied. It will, however, be supplemented by additional biochemical markers. ?? 2004 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Vertical variations of mercury in Pennsylvanian coal beds from Indiana

Twenty-three in-situ coal sections were sampled in Indiana mines to investigate mercury (Hg) concentrations, with a special reference to in-seam vertical variations in Hg distribution. In addition to raw coal, corresponding float fractions were also analyzed to evaluate the effectiveness of Hg reduction during conventional pre-combustion washing. Hg content in Indiana coals in the locations studied averages 0.11 mg/kg, which after recalculation into equal energy units corresponds to 9.2 lb Hg/1012 Btu (???39.5 kg Hg/ 1010 MJ). Hg content is reduced after washing to 0.07 mg/kg on average, corresponding to an equal energy Hg loading of 5.2 lb Hg/ 1012 Btu (???22.3 kg Hg/1010 MJ). A large portion of Hg appears to be associated with pyrite, as in the Springfield Coal Member of the Petersburg Formation (Pennsylvanian). In the samples from the Danville Coal Member of the Dugger Formation (Pennsylvanian), Hg is associated to a larger extent with organic matter. Large differences in Hg content may exist between different portions of a coal bed in a single location, indicating that very careful, complete sampling is necessary to get representative Hg concentration data. ?? 2005 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Mercury content of the Springfield coal, Indiana and Kentucky

With pending regulation of mercury emissions in United States power plants, its control at every step of the combustion process is important. An understanding of the amount of mercury in coal at the mine is the first step in this process. The Springfield coal (Middle Pennsylvanian) is one of the most important coal resources in the Illinois Basin. In Indiana and western Kentucky, Hg contents range from 0.02 to 0.55 ppm. The variation within small areas is comparable to the variation on a basin basis. Considerable variation also exists within the coal column, ranging from 0.04 to 0.224 ppm at one Kentucky site. Larger variations likely exist, since that site does not represent the highest whole-seam Hg nor was the collection of samples done with optimization of trace element variations in mind. Estimates of Hg capture by currently installed pollution control equipment range from 9-53% capture by cold-side electrostatic precipitators (ESP) and 47-81% Hg capture for ESP + flue-gas desulfurization (FGD). The high Cl content of many Illinois basin coals and the installation of Selective Catalytic Reduction of NOx enhances the oxidation of Hg species, improving the ability of ESPs and FGDs to capture Hg. ?? 2005 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Optical properties of pseudovitrinite; implications for its origin

A set of Pennsylvanian coals from the North American coal basins, ranging in vitrinite reflectance from 0.65% to 1.75%, was examined, with special emphasis on the optical properties of pseudovitrinite. The results suggest that pseudovitrinite originates from the same material as telocollinite. Slits in the pseudovitrinite seem to have originated in situ due to low-temperature oxidation of woody material; their opening might have been facilitated by devolatilization during coalification. The dominant orientation of the slits is perpendicular to bedding. The intensity and orientation of the slits in pseudovitrinite could be important factors in predicting coalbed gas extraction from coal. ?? 2005 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

FTIR absorption indices for thermal maturity in comparison with vitrinite reflectance R0 in type-II kerogens from Devonian black shales

FTIR absorbance signals in kerogens and macerals were evaluated as indices for thermal maturity. Two sets of naturally matured type-II kerogens from the New Albany Shale (Illinois Basin) and the Exshaw Formation (Western Canada Sedimentary Basin) and kerogens from hydrous pyrolysis artificial maturation of the New Albany Shale were characterized by FTIR. Good correlation was observed between the aromatic/aliphatic absorption ratio and vitrinite reflectance R 0. FTIR parameters are especially valuable for determining the degree of maturity of marine source rocks lacking vitrinite. With increasing maturity, FTIR spectra express four trends: (i) an increase in the absorption of aromatic bands, (ii) a decrease in the absorption of aliphatic bands, (iii) a loss of oxygenated groups (carbonyl and carboxyl), and (iv) an initial decrease in the CH2/CH3 ratio that is not apparent at higher maturity in naturally matured samples, but is observed throughout increasing R0 in artificially matured samples. The difference in the CH2/CH 3 ratio in samples from natural and artificial maturation at higher maturity indicates that short-term artificial maturation at high temperatures is not fully equivalent to slow geologic maturation at lower temperatures. With increasing R0, the (carboxyl + carbonyl)/aromatic carbon ratio generally decreases, except that kerogens from the Exshaw Formation and from hydrous pyrolysis experiments express an intermittent slight increase at medium maturity. FTIR-derived aromaticities correlate well with R0, although some uncertainty is due to the dependence of FTIR parameters on the maceral composition of kerogen whereas R0 is solely dependent on vitrinite. ?? 2005 Elsevier Ltd. All rights reserved.

Organic Geochemistry↗

Thermal maturity of type II kerogen from the New Albany Shale assessed by13C CP/MAS NMR

Thermal maturity of oil and gas source rocks is typically quantified in terms of vitrinite reflectance, which is based on optical properties of terrestrial woody remains. This study evaluates 13C CP/MAS NMR parameters in kerogen (i.e., the insoluble fraction of organic matter in sediments and sedimentary rocks) as proxies for thermal maturity in marine-derived source rocks where terrestrially derived vitrinite is often absent or sparse. In a suite of samples from the New Albany Shale (Middle Devonian to the Early Mississippian, Illinois Basin) the abundance of aromatic carbon in kerogen determined by 13C CP/MAS NMR correlates linearly well with vitrinite reflectance. ?? 2004 Elsevier Inc. All rights reserved.

Solid State Nuclear Magnetic Resonance↗

Functional group and individual maceral chemistry of high volatile bituminous coals from southern Indiana: Controls on coking

The individual maceral chemistries of two Pennsylvanian, high volatile bituminous coals, the Danville Coal Member (Dugger Formation, R o=0.55%) and the Lower Block Coal Member (Brazil Formation, R o=0.56%) of Indiana, were investigated using electron microprobe and Fourier Transform Infrared Spectrometry (FTIR) techniques, with the purpose of understanding differences in their coking behavior. Microprobe results reveal that carbon contents are highest in inertinite and sporinite, followed by desmocollinite and telocollinite. Oxygen and organic nitrogen are most abundant in telocollinite and desmocollinite; sporinite and inertinite contain lesser amounts of these two elements. Organic sulfur contents are highest in sporinite, lowest in inertinite, and intermediate in desmocollinite and telocollinite. Vitrinites within the Danville and Lower Block coals are very similar in elemental composition, while Lower Block inertinites and sporinites have higher carbon, lower oxygen, and sulfur contents which, when combined with the inertinite-and sporinite-rich composition of the Lower Block seam, strongly influences its whole coal chemistry. Fourier transform infrared spectrometry revealed greater aromatic hydrogen in the Lower Block coal, along with higher CH2/CH3 ratios, which suggest that liptinites contribute considerable amounts of long-chain, unbranched aliphatics to the overall kerogen composition of the Lower Block coal. Long-chain, unbranched aliphatics crack at higher temperatures, producing tar and oily byproducts during coking; these may help increase Lower Block plasticity. Electron microprobe and FTIR results indicate that individual maceral chemistries, combined with the maceral composition of the seam, are the primary control of better coking properties of the Lower Block coal. ?? 2003 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Evaluation of coalbed gas potential of the Seelyville Coal Member, Indiana, USA

The Seelyville Coal Member of the Linton Formation in Indiana potentially contains 0.03 trillion m3 (1.1 TCF) of coalbed gas. The gas content determined by canister desorption technique ranges from 0.5 to 5.7 cm3/g on dry ash free basis (15.4 to 182.2 scf/ton). The controls on gas content distribution are complex, and cannot be explained by the coal rank alone. Ash content and the lithology of the overlying strata, among other factors, may influence this distribution. ?? 2004 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

From in-situ coal to fly ash: A study of coal mines and power plants from Indiana

This paper presents data on the properties of coal and fly ash from two coal mines and two power plants that burn single-source coal from two mines in Indiana. One mine is in the low-sulfur (<1%) Danville Coal Member of the Dugger Formation (Pennsylvanian) and the other mines the high-sulfur (>5%) Springfield Coal Member of the Petersburg Formation (Pennsylvanian). Both seams have comparable ash contents (???11%). Coals sampled at the mines (both raw and washed fractions) were analyzed for proximate/ultimate/sulfur forms/heating value, major oxides, trace elements and petrographic composition. The properties of fly ash from these coals reflect the properties of the feed coal, as well as local combustion and post-combustion conditions. Sulfur and spinel content, and As, Pb and Zn concentrations of the fly ash are the parameters that most closely reflect the properties of the source coal. ?? 2004 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Application of SAXS and SANS in evaluation of porosity, pore size distribution and surface area of coal

This paper discusses the applicability of small angle X-ray scattering (SAXS) and small angle neutron scattering (SANS) techniques for determining the porosity, pore size distribution and internal specific surface area in coals. The method is noninvasive, fast, inexpensive and does not require complex sample preparation. It uses coal grains of about 0.8 mm size mounted in standard pellets as used for petrographic studies. Assuming spherical pore geometry, the scattering data are converted into the pore size distribution in the size range 1 nm (10 A??) to 20 ??m (200,000 A??) in diameter, accounting for both open and closed pores. FTIR as well as SAXS and SANS data for seven samples of oriented whole coals and corresponding pellets with vitrinite reflectance (Ro) values in the range 0.55% to 5.15% are presented and analyzed. Our results demonstrate that pellets adequately represent the average microstructure of coal samples. The scattering data have been used to calculate the maximum surface area available for methane adsorption. Total porosity as percentage of sample volume is calculated and compared with worldwide trends. By demonstrating the applicability of SAXS and SANS techniques to determine the porosity, pore size distribution and surface area in coals, we provide a new and efficient tool, which can be used for any type of coal sample, from a thin slice to a representative sample of a thick seam. ?? 2004 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Carbon dioxide and methane sorption in high volatile bituminous coals from Indiana, USA

Samples of coals from several coalbeds in Indiana were analyzed for CO2 and CH4 sorption capacity using a high-pressure adsorption isotherm technique. Coal quality and petrographic composition of the coals were determined to study their relationships to the volume of CO2 and CH4 that could be sorbed into the coal. At the temperature of 17 ??C and 400 psi (??? 2.8 MPa), the coals can sorb (on dry ash-free basis) from 4 to 6.3 m3/ton (128-202 scf/ton) of CH4 and 19.5-24.6 m3/ton4 (624 to 788 scf/ton) of CO2. The ratio of CO2/CH4 at these conditions ranges from 3.5 to 5.3 and decreases with an increasing pressure for all coals. The coals studied are of a very similar coal rank (Ro from 0.48 to 0.62%) but of varying petrographic composition, and CO2 sorption volumes appear to be positively correlated to the content of maceral telocollinite. ?? 2004 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Chemical and isotopic properties of kukersites from Iowa and Estonia

Kukersite samples from Estonia and Iowa were analyzed for elemental composition, functional group distribution, and carbon and hydrogen stable isotope ratios. The elemental and hydrogen isotope values, together with other analytical data, suggest a higher thermal maturity for the Iowa kukersite. The wide carbon isotopic range of 9.3??? among kukersites, with unusually negative ??13C values reaching -33.2???, indicates isotopically variable carbon sources for production of biomass, and thus major paleoceanographic differences between the environments supporting biosynthesis. ?? 2003 Elsevier Ltd. All rights reserved.

Organic Geochemistry↗

Coals of the Brazil Formation (Pennsylvanian) in Indiana: Observations of correlation inconsistencies and their implications

The coals of the upper part of the Mansfield, Brazil, and the lower part of the Staunton Formations (Atokan and Desmoinesian, Pennsylvanian) in Indiana (Illinois Basin) are characteristically thin and discontinuous. As a result, problems with correlation and identification of the seams have persisted for both researchers and industry. These discrepancies affect coal exploration, mine planning, and subsequently coal-fired utilities. This study presents exploration and operational examples demonstrating some of the correlation problems associated with the coals of the Brazil Formation, and the Upper Block and Lower Block, in particular, and the surrounding upper part of the Mansfield Formation and lower part of the Staunton Formations. Based on exploration boreholes, mine scale observations, and coal quality and petrographic data, this study suggests that (1) the coal mapped as the Upper Block Coal Member of Clay County may, in fact, be the same seam as the Lower Block Coal Member of Daviess County; and (2) the Lower Block coal of Clay County is not present south of the Switz City area of central Greene County, IN. ?? 2003 Elsevier Science B.V. All rights reserved.

International Journal of Coal Geology↗

FTIR-derived characteristics of fossil-gymnosperm leaf remains of Cordaites principalis and Cordaites borassifolius (Pennsylvanian, Maritimes Canada and Czech Republic)

Cordaites principalis and Cordaites borassifolius, gymnosperm trees of the Carboniferous, are distinguished based on compression and cuticular morphology. A new distinction between them is suggested on the basis of differences in functional groups. Cuticular and compression spectra of C. borassifolius have lower CH2/CH3 ratios, suggesting more branched aliphatic chains in comparison with cuticles and compressions of C. principalis. Other differences are observed with Fourier transform infrared spectroscopy (FTIR) technique, but they vary from sample to sample of the two species to suggest other than chemotaxonomic-based sources of variations. ?? 2003 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Isotopically exchangeable organic hydrogen in coal relates to thermal maturity and maceral composition

Hydrogen isotopic exchangeability (Hex) and ??Dn values of non-exchangeable organic hydrogen were investigated in coal kerogens ranging in rank from lignite to graphite. The relative abundance of Hex is highest in lignite with about 18% of total hydrogen being exchangeable, and decreases to around 2.5% in coals with Ro of 1.7 to ca. 5.7%. At Still higher rank (Ro > 6%), Hex increases slightly, although the abundance of total hydrogen decreases. ??Dn is influenced by original biochemical D/H ratios and by thermal maturation in contact with water. Therefore, ??Dn does not show an overall consistent trend with maturity. ?? 2002 Elsevier Science Ltd. All rights reserved.

Organic Geochemistry↗

Coal quality controls of the Danville coal in Indiana (Illinois Basin, Central USA)

The Danville Coal Member (Dugger Formation, upper Desmoinesian, Pennsylvanian) is a significant economic coal resource in the Illinois Basin, central USA. Deposition of the Danville Coal (peat) was in coastal environments, varying distances from the coastline and, in turn, variable influences from saline waters. The purpose of this study is to examine the coal quality and petrography of the Danville Coal; and to discuss their relationship with depositional environment as it relates to the final coal product. A medium sulfur (1.0-1.5 wt.%) Danville Coal reserve area (northern Indiana coalfield) was compared to a low sulfur (<1.0 wt.%) Danville Coal (central Indiana coalfield) reserve area, the two being approximately 70 km apart. The medium sulfur coal resulted from the peat being deposited in a near-marine environment less protected from the influence of saline waters, whereas the low sulfur coal resulted from fine-grained, clay-dominated sediment protecting the peat from the direct influence of saline waters. Within both areas, the coal quality, coal composition, and trace element concentrations vary as a function of the proximity of the coal to the overlying Busseron Sandstone Member (Pennsylvanian). Where the Busseron Sandstone rests near or directly on the coal, the sulfur content is significantly higher in the top third of the seam. Conversely, where there is a thick section (>3 m) of finer-grained clastic sediments atop the Danville, the sulfur and trace elements contents are significantly lower. ?? 2002 Elsevier Science B.V. All rights reserved.

International Journal of Coal Geology↗

FTIR and py-GC-MS spectra of true-fern and seed-fern sphenopterids (Sydney Coalfield, Nova Scotia, Canada, Pennsylvanian)

Sphenopterid specimens from the Late Pennsylvanian of Sydney Coalfield, Canada, are investigated by FTIR and py-GC-MS techniques as part of an on-going research project into the biochemistry and chemotaxonomy of Pennsylvanian-age pteridophylls. Included in the investigation are samples of the true-fern species Oligocarpia brongniartii and Zeilleria delicatula that are preserved as naturally macerated cuticles (NMC), and the seed-fern Eusphenopteris neuropteroides that is also preserved as a compression/impression. FTIR spectra of NMC seed-fern E. neuropteroides, and fern sphenopterid O. brongniartii are very similar, except that the latter does not have aromatic bands in the 700-900 cm-1 out-of-plane region, py-GC-MS show more aromatic compounds for the seed fern than for the two true-fern sphenopterids. Another difference between seed-fern and true-fern sphenopterids is a lower ratio of CH2 to CH3 in chemically treated specimens (CTC) for the seed fern. These observations suggest slightly higher aromaticity for the seed ferns, perhaps related to some chemotaxonomic differences. Comparison of FTIR and py-GC-MS characteristics of sphenopterids and other plant groups shows that these two techniques have potential to identifying chemotaxonomic signals from Carboniferous pteridophylls in general, although more data are needed to confirm this. ?? 2002 Elsevier Science B.V. All rights reserved.

International Journal of Coal Geology↗