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High-intensity pyrolysis, rapid heating in an inert gas atmosphere at up to 20 atm pressure, of 6 Australian coals was examined to gain further insight into high-intensity processes such as Integrated Gasification Combined Cycles (IGCC). Experiments focussed on pyrolysis in a specially developed Wire Mesh Reactor (WMR). The particle temperature lagged that of the mesh by 0.2 seconds at a heating rate of 100??~C s -1 and was predicted by modelling. This is part of the reason the volatile yield (VY) results for 10 s hold-time at ???b1.7 wt% daf of coal, is much more reproducible than 1 s hold-time experiments at ???b4.2 wt% daf of coal. Four coals of the same rank did not behave identically when heated. Three of the coals had a pyrolysis VY the same as the proximate VM when heated to 100??~C at 1 atm but the fourth, higher inertinite coal had a 1 atm pyrolysis VY 90% of its proximate VM. All four coals of similar rank had a significant decrease in VY, between 10 and 20 wt% daf of coal, with pressure increasing from 1 to 20 atm. The two lower rank coals showed less decrease in VY with increasing pressure than the higher rank and higher inertinite coals. The lower decrease in VY with increased pressure was mostly attributed to the lower inertinite levels for both the coals of similar rank and VM, and the coals of lower rank. Char characteristics examined focussed on pore Surface Area (SA). For high intensity WMR and Drop Tube Furnace (DTF) pyrolysis experiments CO2 SA for char from a particular coal was similar but the BET SA different. This was due to the char in the WMR experiments having longer to form larger pores determined by BET N2 SA. Both the N2 and CO2 SA was more than an order of magnitude greater than for low intensity pyrolysis char. This highlights that the WMR can be used to attain char with similar CO2 SA characteristics as other high intensity pyrolysis experiments and to provide a more meaningful insight into char reactivity than low intensity chars do.

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Thesis (M.S.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 1979. / MICROFICHE COPY AVAILABLE IN ARCHIVES AND SCIENCE. / Bibliography: leaf 93. / by Ronald Alan Dictor. / M.S.

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A thesis submitted to the Faculty of Engineering and Built Environment, University of the Witwatersrand, Johannesburg, in fulfilment of the requirements for the degree of Doctor of Philosophy, Johannesburg 2017 / South Africa (SA) has an energy-intensive coal mining industry, where coal accounts for approximately 72% of total primary energy consumption in the country, particularly in the electricity sector, where 95% of total electricity generated is derived from coal. Pulverised coal combustion has been the preferred technology adopted for power generation in South Africa for many decades. These coal-fired power plants have no flue gas desulphurisation (FGD) equipment fitted at present. Therefore, these plants account for the majority of annual SO2, CO2, and NOx emissions, making them environmentally unsustainable for power generation. Such environmental issues add to the challenges for the power producer, who is required to meet not only energy demand, but also to compete with the export market for quality coals, and to ensure that electricity generation complies with ever-changing air quality standards. Circulating fluidised-bed combustion (CFBC), a technology for the combustion of coal, biomass, waste, has not been adequately explored or tested in South Africa previously. CFB combustion is currently under intense scrutiny amongst researchers evaluating its potential as an economic and environmentally acceptable technology, in particular for the burning of lowgrade coals. The main objective of this study is to undertake a case study using CFBC technology and to establish its potential for use in South Africa as a clean and cost-effective method in power generating for high-ash, low-grade coals. Experimental tests were conducted in a CFBC pilot plant in Finland, using two high ash coals, discarded coal from South Africa (SA) and a better quality coal from Russia for comparative purposes. A review was conducted of discard coals in South Africa in order to establish an inventory in support of their potential utilisation for power generation in circulating fluidised bed boilers. A further study established a comparison between pulverised coal (PC), and fluidised bed (FBC) technologies as a future benefit analysis. All four coals proved to have very high combustion efficiencies, despite significant quality differences in terms of petrographic composition and ash content. More specifically, the SA coals achieved combustion efficiencies of 99.6 %, 99.7 % and 99.8 %, where the Russian coal achieved 98.7 percent. The Russian coal was characterised as being low in ash and high in the reactive maceral vitrinite, the two South African coals possessed high ash content (35 to 45%), one with relatively high vitrinite, and the other very low vitrinite, whilst the South African discard possessed an ash content of 65-70% and extremely low reactive vitrinite content. All these factors lean towards the suitability of SA coals to the CFB technology. In terms of NOx emissions, all coals tested showed that their NOx and N2O emission meet the minimum requirements for small plants as set out by the European and SA standards, i.e. <300 ppm for a plant with generating capacity below 100 MW. This result is in agreement with data from the literature. The emission of SO2 depends on the sulphur content in the initial coal, which also has an impact on the Ca/S Ratio. SO2 emitted from the South African coals was higher than the national permitted standard, due to the low Ca/S ratio used. This was especially the case for South African discard. Vast reserves of discard coal containing from 2MJ/kg to 14 MJ/kg in calorific value have accumulated in South Africa since the last inventory of 2001, i.e. close to 1.5 billion tonnes are in existence. It is apparent that one of the looming challenges regarding discard coal is putting this ever-accumulating material to use. From the combustion results obtained in this research, it is proposed that such materials can be combusted in a CFBC boiler, and that it produces the same efficiency as other coals from South Africa and a clean coal from Europe. Ash distribution within the boiler was found to change in proportion of bed ash to fly ash, subject to the quality of the coal used. This is also likely to change the proportions of sulphur-absorbing sorbents in future. CO2 emissions from the coals under review were found to be very close, in the region of 12.8 to 13.8 percent. / XL2018

Fouling, slagging, corrosion, and emission of submicron particulate from pulverized coal combustors have been linked to vapor alkali. Size segregated fly ash samples extracted from a 17 kW down-fired pulverized coal combustor showed strong evidence of alkali vaporization. The fraction of sodium in sizes smaller than 0.65 μm (f(8A)) showed a correlation with acid soluble sodium divided by total silicates in the parent coal. Addition of silicates to coal reduced f(8A) for sodium. Potassium existing primarily in the mineral matter, did not show a similar correlation, but f(8A) for potassium did correlate with f(8A) for sodium. Bench scale experiments indicated potassium does not vaporize in the presence of Na or Cl alone, but requires both, and was only released when sodium was captured. Additional of sodium acetate to coal increased f(8A) for potassium. Equilibrium calculations, experiment, and modelling of sodium capture by silicates during pulverized coal combustion identified several important mechanisms governing alkali behavior. The mode of occurrence of alkali in the parent coal dictates its ability to vaporize, its release kinetics, and its sate as it diffuses to the char surface. Other species such as chlorine, sulfur, moisture, and other metals influence alkali stability in the vapor, its reactivity, and its condensation characteristics. Char oxidation can influence alkali vaporization, and capture by affecting included silicate surface area. Sodium reaction with silicates captures from 70 to over 95% of total sodium for typical coals. Silicate additive appears to be a viable technique for reducing the fraction of alkali in the vapor during combustion.