Migmatite-Like Textures in Anthracite: Further Evidence for Low-Grade Metamorphic Melting and Resolidification in High-Rank Coals

Previous studies demonstrated that melting, initiated by supercritical fluids in the 375–400 °C range, occurred as part of anthracite metamorphism in the Appalachian Basin. Based on the known behavior of vitrinite at high temperatures and, to a lesser extent, at high pressures, it was determined that the duration of the heating, melting, and resolidification event was about 1 h. In the current study, featureless vitrinite within banded maceral assemblages demonstrates the intimate association of melted and resolidified vitrinite with anthracite-rank macerals. By analogy with metamorphosed inorganic rocks, such associations represent diadysites and embrechites, i.e., cross-cutting and layered migmatites, respectively. Even though the temperature of formation of the anthracite structures is several hundred °C lower than that seen in metamorphosed inorganic rocks, anthracites are metamorphic rocks and the nomenclature for metamorphic rocks may be appropriate for coal

Interlaboratory comparisons of petrography of liquefaction residues from three Argonne Premium coals

Three Argonne Premium coal samples, the Beulah-Zap lignite (North Dakota), the high volatile A bituminous Stockton (West Virginia), and the low volatile Pocahontas No. 3 (Virginia), were ground to three initial sizes: -20 mesh, -100 mesh, and "micronized". The samples were each subjected to liquefaction at 673 K for 30 min at a 2:1 tetralin :coal ratio and in an H 2 atmosphere at 13.79 MPa (~ 2000 psi). Polished pellets of the unconverted residues were circulated to three laboratories for a study designed to determine, albeit on a limited scale, the interlaboratory consistency in constituent identification and the problem areas in maceral/neo-maceral/mineral recognition. Within broad categories, the agreement for the Beulah-Zap and Pocahontas No. 3 residues is good. The high volatile A bituminous Stockton coal was the most plastic and most altered, resulting in a residue lending itself to more subjective interpretations. The biggest discrepancy between the laboratories is in the distinction of granular residue and mineral matter and in the transitions between "partially reacted macerals" and "vitroplast" and between "vitroplast" and "granular residue". The initial size of the feed coal appears to influence the recognition of material in the residue

Interlaboratory comparisons of petrography of liquefaction residues from three Argonne Premium coals

Three Argonne Premium coal samples, the Beulah-Zap lignite (North Dakota), the high volatile A bituminous Stockton (West Virginia), and the low volatile Pocahontas No. 3 (Virginia), were ground to three initial sizes: -20 mesh, -100 mesh, and "micronized". The samples were each subjected to liquefaction at 673 K for 30 min at a 2:1 tetralin :coal ratio and in an H 2 atmosphere at 13.79 MPa (~ 2000 psi). Polished pellets of the unconverted residues were circulated to three laboratories for a study designed to determine, albeit on a limited scale, the interlaboratory consistency in constituent identification and the problem areas in maceral/neo-maceral/mineral recognition. Within broad categories, the agreement for the Beulah-Zap and Pocahontas No. 3 residues is good. The high volatile A bituminous Stockton coal was the most plastic and most altered, resulting in a residue lending itself to more subjective interpretations. The biggest discrepancy between the laboratories is in the distinction of granular residue and mineral matter and in the transitions between "partially reacted macerals" and "vitroplast" and between "vitroplast" and "granular residue". The initial size of the feed coal appears to influence the recognition of material in the residue

Coal liquefaction process streams characterization and evaluation. Novel analytical techniques for coal liquefaction: Fluorescence microscopy

This study demonstrated the feasibility of using fluorescence and reflectance microscopy techniques for the examination of distillation resid materials derived from direct coal liquefaction. Resid, as defined here, is the 850{degrees}F{sup +} portion of the process stream, and includes soluble organics, insoluble organics and ash. The technique can be used to determine the degree of hydrogenation and the presence of multiple phases occurring within a resid sample. It can also be used to infer resid reactivity. The technique is rapid, requiring less than one hour for sample preparation and examination, and thus has apparent usefulness for process monitoring. Additionally, the technique can distinguish differences in samples produced under various process conditions. It can, therefore, be considered a potentially useful technique for the process developer. Further development and application of this analytical method as a process development tool is justified based on these results

Variations in chemistry of macerals as refl ected by micro-scale analysis of a Spanish coal

An Oligocene lignite (Ebro Basin, Spain) and its density fractions were analyzed petrographically and with microscale techniques (electron microprobe and micro-FTIR) to gain insight into differences between individual macerals of low rank high-sulfur coal. The density of the alginite-dominated fraction is below 1.26g/cm3, and that of the huminite-dominated fraction is above 1.38g/cm3. Densities within 1.26-1.38g/cm3 represent mixtures of liptinite and huminite macerals. With regard to elemental composition, alginite has the highest carbon content (75.6% on average) and the lowest oxygen content (6.1% on average). Corpohuminite is characterized by the lowest carbon content (62.3% on average) and the highest oxygen content (21.5% on average). Nitrogen contents for corpohuminite and ulminite (~1%) are similar, but are significantly lower in alginite (0.2% on average). Sulfur content is highest in alginite (13.4% on average), followed by corpohuminite (9.8%) and ulminite (7.7%). Functional group analysis documents large differences between macerals of the huminite and liptinite group, but also indicates differences between individual macerals within both the huminite and liptinite group. These ifferences are most notable in aromaticity, degree of aromatic ring condensations, and hydrocarbon potential

Notes on Contributions to the Science of Rare Earth Element Enrichment in Coal and Coal Combustion Byproducts

Coal and coal combustion byproducts can have significant concentrations of lanthanides (rare earth elements). Rare earths are vital in the production of modern electronics and optics, among other uses. Enrichment in coals may have been a function of a number of processes, with contributions from volcanic ash falls being among the most significant mechanisms. In this paper, we discuss some of the important coal-based deposits in China and the US and critique classification systems used to evaluate the relative value of the rare earth concentrations and the distribution of the elements within the coals and coal combustion byproducts

Possibilities of using silicate rock powder: An overview

This study evaluates the on use of crushed rocks (remineralizers) to increase soil fertility levels and which contributed to increase agricultural productivity, recovery of degraded areas, decontamination of water, and carbon sequestration. The use of these geological materials is part of the assumptions of rock technology and, indirectly, facilitates the achievement of sustainable development goals related to soil management, climate change, and the preservation of water resources. Research over the past 50 years on silicate rocks focused on soil fertility management and agricultural productivity. More recently, the combined use with microorganisms and organic correctives have shown positive results to mitigate soil degradation; to expand carbon sequestration and storage; and to contribute to the adsorption of contaminants from water and soil. In this article we show results obtained in several countries and we show that this technology can contribute to the sustainability of agriculture, as well as to reverse global warming. Although mineral nutrients are released more slowly from these types of inputs, they remain in the soil for a longer time, stimulating the soil biota. In addition, they are a technology to soluble synthetic fertilizers replace, since the few nutrients derived from such inputs not consumed by plants are lost by leaching, contaminating groundwater and water resources. In addition, conventional methods rely heavily on chemical pesticides which cause damage to soil's microfauna (responsible for the decomposition of organic matter and nutrient cycling) and the loss of organic carbon (in the form of dioxide), which is quickly dispersed in the atmosphere. Silicate rock powders are applied in natura, have long-lasting residual effects and reduce greenhouse gas emissions

Nano-Scale Rare Earth Distribution in Fly Ash Derived from the Combustion of the Fire Clay Coal, Kentucky

Fly ash from the combustion of eastern Kentucky Fire Clay coal in a southeastern United States pulverized-coal power plant was studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and selected area electron diffraction (SAED). TEM combined with elemental analysis via energy dispersive X-ray spectroscopy (EDS) showed that rare earth elements (REE; specifically, La, Ce, Nd, Pr, and Sm) were distributed within glassy particles. In certain cases, the REE were accompanied by phosphorous, suggesting a monazite or similar mineral form. However, the electron diffraction patterns of apparent phosphate minerals were not definitive, and P-lean regions of the glass consisted of amorphous phases. Therefore, the distribution of the REE in the fly ash seemed to be in the form of TEM-visible nano-scale crystalline minerals, with additional distributions corresponding to overlapping ultra-fine minerals and even true atomic dispersion within the fly ash glass

Water structuring and collagen adsorption at hydrophilic and hydrophobic silicon surfaces

The adsorption of a collagen fragment on both a hydrophobic, hydrogen-terminated and a hydrophilic, natively oxidised Si surface is investigated using all-atom molecular dynamics. While favourable direct protein-surface interactions via localised contact points characterise adhesion to the hydrophilic surface, evenly spread surface/molecule contacts and stabilisation of the helical structure occurs upon adsorption on the hydrophobic surface. In the latter case, we find that adhesion is accompanied by a mutual fit between the hydrophilic/hydrophobic pattern within the protein and the layered water structure at the solid/liquid interface, which may provide an additional driving force to the classic hydrophobic effect