Laminar entrained flow reactor (LEFR) was used to determine the effect of temperature and residence time on the distribution of carbon, sulfur and nitrogen between gaseous and condensed phase products from low temperature pyrolysis of kraft black liquor. The operating furnace temperatures were between 400��C-600��C where the effect of condensable organic and organic sulfur compounds may be important. The residence times ranged from 0.3 to 2.0 seconds. In the evolution of carbon as gases, an oxidizer was used to convert all oxidizable components in LEFR effluent gas to carbon dioxide which was detected by an infrared carbon dioxide meter. With this, measurement of total carbon in the gas phase, the fine particles, and the char residue were made. The carbon yield in the gas phase increased as residence time increased. The higher the temperature, the higher the carbon yield as gases phase at each residence time. The carbon yield in the fine particles differed very little with temperature at residence time below 1.1 seconds. At higher temperature, the carbon yield in the fine particles is about the same at 500��C and 600��C, but lower at 400��C. The carbon yield in the char residue decreased as residence time increased. The carbon yield in the char residue at 500��C and residence time above 1.1 seconds was a little lower than at temperature 600��C, due to an apparent loss of char at 500��C. The char yield at 500��C was lower than expected based on the 400��C and 600��C data because of accumulation of larger, more highly swollen char particles at the tip of collector at this temperature. The average of the sum of carbon recovered as char residue, gases, and fine particles was 96.2% at 600��C, 88.1% at 500��C, and 95.7% at 400��C. The main reason for the poorer carbon recovery at 500��C was the loss of char particles which accumulated on the tip of the collector. When the char yield at 500��C is increased so that the carbon balance closed to 96%, the char yield, carbon yield, and sulfur yield at 500��C fell between the values at 400��C and 600��C. The sulfur yield in the char residue decreased as residence time increased. The higher the temperature, the lower the sulfur yield in the char residue. The nitrogen yield in the char residue also decreased as residence time increased. / Graduation date: 1997

In recent decades, advances in low NOₓ coal combustion and increasingly strict CO₂ reduction mandates have changed power plant boiler operations quite significantly. As a result of these necessary efforts, the characteristics of fly ash generated at many power plants have also changed. In particular, increases in unburned carbon content have been observed with detrimental implications on the utility of these fly ashes in concrete applications. Over the same time period, the combustion of biomass for energy generation has received increased attention due to the potential benefits of reducing CO₂ emissions and improved sustainability when compared to fossil fuel combustion. Biomass is directly burned, gasified, or co-fired with coal to achieve this goal. Currently, close to 120 million metric tons of coal combustion by products are produced in the U.S. annually. As with coal combustion, production of energy from biomass combustion/gasification results in significant by-product generation that must either be productively reused or geologically disposed. While much research effort has been devoted to understanding the properties and potential productive reuse alternatives for coal combustion residuals, relatively little work has been done on the by-products of biomass combustion. This study investigated the properties and engineering behavior of sixteen ash samples that were produced in eleven different power plants. Specifically, three high carbon content Class F fly ashes, eight coal and biomass co-fired ashes, three pure biomass ash samples, and two high quality, low carbon content ash samples, one of which is commercially marketed (for reference) were chosen. The various ash samples were characterized by means of: electron microscopy; laser diffraction and dry sieve particle size analysis; loss on ignition and total organic carbon analysis; specific surface area analysis; as well as x-ray fluorescence and x-ray diffraction. The ash samples were also investigated for their potential engineering application in the fired clay brick industry, as low-cost adsorptive agents, and in alkali activated geopolymer synthesis for geotechnical and geoenvironmental applications. Results from physical and chemical characterization of the ash samples show no significant differences between pure coal ash and coal co-fired with biomass ash samples from the same power plant. However, there are significant morphological, chemical, and mineralogical differences between coal ash and pure biomass ash. Unlike pure coal ash, biomass ash is not composed primarily of aluminosilicate glass cenospheres but rather consists mainly of charred, fibrous woody remnants with elevated calcite content as compared to coal ash. Bench scale fired bricks produced by partial replacement of clay material with high carbon coal ash, co-fired ash, and pure biomass ash, respectively, was successful. Physical properties of a number of the mix designs exceeded the highest ASTM weathering grade requirements. As sorptive agents, high carbon concentrates from coal and co-fired ash samples, along with all the biomass ash samples, showed significant uptake of lead. The unaltered as- received ash samples (i.e. no acid or steam activation) showed only moderate arsenic (V) and selenium (VI) sorption capacity. Finally, solidification/stabilization by geopolymerization of high carbon content, co-fired ash with as little as 3 molar NaOH in the activator solution was successful, possibly paving the way for various geotechnical and geoenvironmental applications in ground improvement and soil/ash-pond stabilization.

No description available.

Reclaimed surface mined soils in Appalachia are typically infertile and must be amended for optimum vegetative growth. Fluidized bed combustion residue (FBCR), a by-product of coal-fired power plants, has high levels of Ca, S, Zn, Fe, and Al, and 50% of the neutralizing capacity of limestone. Three treatments were applied to three replicated .81 ha reclaimed mine pastures: control (no amendment), 6760 kg FBCR/ha, and 3380 kg limestone/ha. Based on forage availability, six steers were rotationally grazed on pastures receiving each treatment. Steers were weighed and blood samples collected at 14-d intervals and all animals were sacrificed for tissue sampling at the end of the 114-d trial. Amendment with FBCR or limestone increased soil pH (P < .05) above control levels. Forage yield and steer gain were not significantly affected by treatment. Forage samples collected during the trial indicated that FBCR and limestone amendments elevated forage ash, Ca, Mg, S, Cu and Ca:P ratio (P < .05). Cellulose and NDF were depressed in forage grab samples collected from FBCR- and limestone-amended pastures. The forage sampled the following spring was lower in hemicellulose, Zn, un and Ni; and higher in ash, Ca, S, the Ca: P ratio in the FBCR- and limestone-amended pastures. Mean serum mineral levels of steers were not affected by pasture treatment. The blood packed cell volume was higher in cattle grazing FBCR-amended pastures. Liver levels of Fe, H, Hi and Na were lower in cattle on pastures amended with FBCR or limestone. Bile levels of Mn were depressed in cattle grazing FBCR~ and limestone-amended pastures. The level of Cu in the liver and serum was at deficiency levels and was not detectable in bile, regardless of treatment. Higher kidney levels of Ca, Hg and P were recorded for steers grazing FBCR- and limestone-amended pastures. Hair Zn was higher in cattle grazing the FBCR- and limestone- treated pastures. Rib Cr and long bone Cd levels were lower in animals grazing the limestone- and FBCR-treated pastures. This study suggests that FBCR amendment enhances nutrient quality of forage and mineral status of animals at least as well as limestone application to acidic reclaimed mine pastures. / Ph. D. / incomplete_metadata

Coal refuse and combustion byproducts as industrial solid waste stockpiles have become great threats to the environment. Recycling is one practical solution to utilize this huge amount of solid waste through activation as substitute for ordinary Portland cement. The central goal of this dissertation is to investigate and develop a new silica-alumina based cementitious material largely using coal refuse as a constituent that will be ideal for durable construction, mine backfill, mine sealing and waste disposal stabilization applications. This new material is an environment-friendly alternative to ordinary Portland cement. The main constituents of the new material are coal refuse and other coal wastes including coal sludge and coal combustion products (CCPs). Compared with conventional cement production, successful development of this new technology could potentially save energy and reduce greenhouse gas emissions, recycle vast amount of coal wastes, and significantly reduce production cost. A systematic research has been conducted to seek for an optimal solution for enhancing pozzolanic reactivity of the relatively inert solid waste-coal refuse in order to improve the utilization efficiency and economy benefit for construction and building materials. The results show that thermal activation temperature ranging from 20°C to 950°C significantly increases the workability and pozzolanic property of the coal refuse. The optimal activation condition is between 700°C to 800°C within a period of 30 to 60 minutes. Microanalysis illustrates that the improved pozzolanic reactivity contributes to the generated amorphous materials from parts of inert aluminosilicate minerals by destroying the crystallize structure during the thermal activation. In the coal refuse, kaolinite begins to transfer into metakaol in at 550°C, the chlorite minerals disappear at 750°C, and muscovite 2M 1 gradually dehydroxylates to muscovite HT. Furthermore, this research examines the environmental acceptance and economic feasibility of this technology and found that this silica alumina-based cementitious material not only meets EPA requirements but also shows several advantages in industrial application.

Contexte : L’exposition professionnelle aux sous-produits de combustion est répandue et peut contribuer à l'étiologie du cancer du sein. Cette étude vise à estimer l’association entre l’exposition professionnelle à certains sous-produits de combustion et le risque postménopausique de cancer du sein. Méthodes : Cette étude cas-témoins populationnelle comprenait des femmes ménopausées âgées de 47-75 ans résidant à Montréal, Québec (2008-2011). Les cas incluaient 695 femmes ayant reçu un diagnostic cancer du sein malin et 608 témoins sélectionnés aléatoirement à partir de la Liste électorale du Québec, appariés aux cas en fréquence (groupes d'âge de 5 ans). L’information sur les facteurs de risque et l'historique professionnel a été recueillie par entrevue. Des hygiénistes industriels ont évalué l'exposition à 293 agents, dont six sous-produits de combustion. Le risque de cancer du sein associé à l'exposition professionnelle à certains sous-produits a été estimé, pour l'ensemble des tumeurs et leurs sous-types moléculaires, par régression logistique inconditionnelle avec rapports de cotes ajustés (RC) et intervalles de confiance à 95 % (IC 95%). Résultats : Des associations positives suggestives ont été trouvées entre l'exposition aux hydrocarbures aromatiques polycycliques et certains sous-types moléculaires de tumeurs : toutes tumeurs, RC=1,18 (IC95%=0,80-1,76), tumeurs luminales A, RC=1,25 (IC95%=0,81-1,93) et tumeurs luminales B, RC=2,09 (IC95%=0,87-4,60). Un risque élevé a été observé avec l'exposition aux fumées de cuisson pour les tumeurs HER2-enrichies (RC=2,63, IC95%=0,98-6,40). Conclusion : L'exposition à certains sous-produits de combustion peut augmenter le risque de certains sous-types moléculaires de cancer du sein. Des études futures explorant cette association sont justifiées. / Background: Postmenopausal breast cancer is the most common cancer among women, yet little is known about its association with occupational exposures. Exposure to combustion by-products is widespread in occupational settings and may contribute to breast cancer etiology. Here, we sought to estimate the association between lifetime occupational exposure to select combustion by-products and the risk of postmenopausal breast cancer. Methods: This population-based case-control study included postmenopausal women residing in Montreal, Quebec (2008-2011). Cases comprised 695 women aged 47-75 years diagnosed with incident malignant breast cancer, and 608 controls randomly selected from the Quebec Electoral List, frequency-matched to cases (5-year age groups). Information on risk factors and employment history was collected by interview. Exposure to 293 agents, including six combustion by-products was assessed by industrial hygienists. Unconditional logistic regression was used to estimate adjusted odds ratios (ORs) and 95% confidence intervals (95% CIs) for breast cancer risk, both overall and by tumor molecular subtypes, to occupational exposure to select combustion by-products. Results: We found suggestive positive associations between exposure to polycyclic aromatic hydrocarbons and certain molecular subtypes of tumors: for all tumors, OR=1.18 (95% CI: 0.80-1.76), Luminal A tumors, OR=1.25 (95% CI: 0.81-1.93) and Luminal B tumors, OR=2.09 (95% CI: 0.87-4.60). Elevated risked were observed for exposure to cooking fumes for HER2-enriched tumors (OR=2.63, 95% CI: 0.98-6.40). Conclusion: Exposure to select combustion by-products may increase the risk of certain hormonal subtypes of breast cancer. Future studies exploring this association are warranted.