Richard David Harvey

Maceral distributions in Illinois coals and their paleoenvironmental implications

Abstract For purposes of assessing the maceral distribution of Illinois (U.S.A.) coals analyses were assembled for 326 face channel and drill core samples from 24 coal members of the Pennsylvanian System. The inertinite content of coals from the Missourian and Virgilian Series averages 16.1% (mineral free), compared to 9.4% for older coals from the Desmoinesian and older Series. This indicates there was generally a higher state of oxidation in the peat that formed the younger coals. This state probably resulted from greater exposure of these peats to weathering as the climate became drier and the water table lower than was the case for the older coals, although oxidation during allochthonous deposition of inertinite components is a genetic factor that needs further study to confirm the importance of the climate. Regional variation of the vitrinite-inertinite ratio (V-I), on a mineral- and micrinite-free basis, was observed in the Springfield (No. 5) and Herrin (No. 6) Coal Members to be related to the geographical position of paleochannel (river) deposits known to have been contemporaneous with the peats that formed these two coal strata. The V-I ratio is highest (generally 12–27) in samples from areas adjacent to the channels, and lower (5–11) some 10–20 km away. We interpret the V-I ratio to be an inverse index of the degree of oxidation to which the original peat was exposed. High V-I ratio coal located near the channels probably formed under more anoxic conditions than did the lower V-I ratio coal some distance away from the channels. The low V-I ratio coal probably formed in areas of the peat swamp where the watertable was generally lower than the channel areas.

Environmentally critical elements in channel and cleaned samples of Illinois coals

Abstract Sixteen trace and minor elements that occur in coal are listed among 189 substances identified as ‘hazardous air pollutants’ (HAPs) in the US Clean Air Act Amendments of 1990. We investigated the occurrence and cleanability of the 16 HAPs in Illinois coals, as a contribution to the discussion about the potential effect of pending environmental regulations on the future use of these coals in power generation. The average ash content of the samples of conventionally cleaned as-shipped coals is about 20% lower than that of standard channel samples. Conventional cleaning reduces the average concentrations of As, Cd, Co, Hg, Mn, Ni, Pb, Sb and Th in the as-shipped coals by more than 20% relative to channel samples. Thus, basing assessments of health risks from emissions of HAPs during coal combustion on channel samples without appropriate adjustment would overestimate the risk. Additional cleaning by froth-flotation reduces the ash content of finely-ground as-shipped coals by as much as 76% at an 80% combustibles recovery. Although the average froth-flotation cleanability for the majority of HAPs is less than that for ash, the cleanabilities in some individual cases approaches, or even exceeds, the cleanability for ash, depending on the modes of occurrences of the elements.

Agglomeration of Ash in Fluidized Beds Gasifying Coal: The Godel Phenomenon

In a bed of anthracite or bituminous coke fluidized by air at 10 to 15 meters per second at 1200� to 1400�C, molten ash forms beads on the surface of a coke particle, some exuding from its interior. The beads merge and detach them-selves to grow further as loose fluidized ash agglomerates of low carbon content.

Variation of organic sulfur in macerals of selected Illinois Basin coals

Abstract An electron microbeam technique was used to determine the distribution of organic sulfur in the main macerals of five Illinois Basin coals. On average, sporinites are the highest, inertinites the lowest, and vitrinites intermediate in organic sulfur for each coal. The observed differences are likely due to varying affinities of the different pre-maceral materials for sulfur and/or local variation in the production of H 2 S primarily during the peat stage. Investigation of molecular structures of individual macerals in relation to the findings of this study may delineate the relative abundance of organic sulfur in various organic compounds and thus lead to the development of efficient desulfurization processes.

Size and maceral association of pyrite in Illinois coals and their float-sink fractions

Abstract The amount of pyrite (FeS 2 ) removed by physical cleaning varies with differences in the amount of pyrite enclosed within minerals and of free pyrite in feed coals. A microscopic procedure for characterizing the size and maceral association of pyrite grains was developed and evaluate by testing three coals and their washed products. The results yield an index to the cleanability of pyrite. The index is dependent upon particle size and has intermediate values for feed coals, lower values for cleaned fractions, and higher values for refuse fractions; furthermore, it correlates with pyritic sulfur content. In the coals examined, the summed percentage of grain diameters of pyrite enclosed in vitrinite, liptinite, and bi- and trimacerite provides a quantitative measure of the proportion of early diagenetic deposition of pyrite.

SEM-EDX and isotope characterization of the organic sulfur in macerals and chars in Illinois Basin coals

Two samples of the Herrin (Illinois No. 6) Coal and one sample of the Colchester (Illinois No. 2) Coal from the Illinois Basin were studied to evaluate the spatial distribution of organic sulfur within macerals occurring next to pyrite grains, both in the raw coal and their chars. The chars were produced by pyrolysing the coal at 250–550°C in a nitrogen atmosphere. Representative splits of the coals and their chars were mounted in epoxy and polished for optical microscopy and scanning electron microscopy-energy dispersive x-ray spectroscopy (SEM-EDX). Determinations of organic sulfur concentrations were made at 996 locations within macerals, mostly vitrinite, around 115 grains of pyrite and at 50 locations around 5 pores in chars. The pyrite considered here is restricted to the disseminated type within macerals. On the average, the organic sulfur content increased near pyrite grains after the coals were charred at 550°C, indicating that some of the pyritic sulfur released during charring was retained within the organic matrix rather than being emitted to the atmosphere. One of the coal samples and its chars were isotopically characterized by chemically separating the pyritic and organic sulfur fractions, followed by analyzing the isotopes of the sulfur forms with a Nuclide 6–60 ratio mass spectrometer. The sulfur isotope (δ34S) data confirmed the movement of pyritic sulfur into the macerals after charring to 550°C. About 18% of the organic sulfur that remained in the 550°C char had originally been pyritic sulfur in the untreated coal.