RESUMO
Oxy-fuel combustion of refuse waste is gaining considerable attention as a viable CO2 negative technology that can enable the continued use of stationary combustion plants during the transition to renewable energy sources. Compared to fossil fuels, waste-derived fuels tend to be highly heterogeneous and to contain a greater amount of alkaline metals and chlorine. Therefore, experimental studies are mandatory to thoroughly elucidate refuse materials' combustion and pollutant formation behavior. This paper presents an experimental investigation on the air and oxy-fuel combustion of solid recovered fuel at a 200 kWth circulating fluidized bed facility. In the course of two experimental campaigns, the effects of combustion atmosphere and temperature on pollutant formation (i.e., NO x , SO2, and HCl) and reactor hydrodynamics were systematically studied. In contrast to air-firing conditions, the experimental results showed that oxy-fuel combustion enhanced the volume concentration of NO x by about 50% while simultaneously decreasing the fuel-specific NO x emissions (by about 33%). The volume concentrations of SO2 and HCl were significantly influenced by the absorption capacity of calcium-containing ash particles, yielding corresponding values close to 10 and 200 ppmv at 871-880 °C under oxy-fuel combustion conditions. In addition, the analysis of hydrodynamic data revealed that smooth temperature profiles are indispensable to mitigate bed sintering and agglomeration risks during oxy-fuel operation. The results included in this study provide a valuable contribution to the database of experimental information on the oxy-fuel combustion of alternative fuels, which can be applied in future process model validations and scale-up studies.
RESUMO
Due to its large reserves, coal is expected to continue to play an important role in the future. However, specific and absolute CO2 emissions are among the highest when burning coal for power generation. Therefore, the capture of CO2 from power plants may contribute significantly in reducing global CO2 emissions. This review deals with the oxyfuel process, where pure oxygen is used for burning coal, resulting in a flue gas with high CO2 concentrations. After further conditioning, the highly concentrated CO2 is compressed and transported in the liquid state to, for example, geological storages. The enormous oxygen demand is generated in an air-separation unit by a cryogenic process, which is the only available state-of-the-art technology. The generation of oxygen and the purification and liquefaction of the CO2-enriched flue gas consumes significant auxiliary power. Therefore, the overall net efficiency is expected to be lowered by 8 to 12 percentage points, corresponding to a 21 to 36% increase in fuel consumption. Oxygen combustion is associated with higher temperatures compared with conventional air combustion. Both the fuel properties as well as limitations of steam and metal temperatures of the various heat exchanger sections of the steam generator require a moderation of the temperatures during combustion and in the subsequent heat-transfer sections. This is done by means of flue gas recirculation. The interdependencies among fuel properties, the amount and the temperature of the recycled flue gas, and the resulting oxygen concentration in the combustion atmosphere are investigated. Expected effects of the modified flue gas composition in comparison with the air-fired case are studied theoretically and experimentally. The different atmosphere resulting from oxygen-fired combustion gives rise to various questions related to firing, in particular, with regard to the combustion mechanism, pollutant reduction, the risk of corrosion, and the properties of the fly ash or the deposits that form. In particular, detailed nitrogen and sulphur chemistry was investigated by combustion tests in a laboratory-scale facility. Oxidant staging, in order to reduce NO formation, turned out to work with similar effectiveness as for conventional air combustion. With regard to sulphur, a considerable increase in the SO2 concentration was found, as expected. However, the H2S concentration in the combustion atmosphere increased as well. Further results were achieved with a pilot-scale test facility, where acid dew points were measured and deposition probes were exposed to the combustion environment. Besides CO2 and water vapour, the flue gas contains impurities like sulphur species, nitrogen oxides, argon, nitrogen, and oxygen. The CO2 liquefaction is strongly affected by these impurities in terms of the auxiliary power requirement and the CO2 capture rate. Furthermore, the impurity of the liquefied CO2 is affected as well. Since the requirements on the liquid CO2 with regard to geological storage or enhanced oil recovery are currently undefined, the effects of possible flue gas treatment and the design of the liquefaction plant are studied over a wide range.
Assuntos
Dióxido de Carbono/análise , Carvão Mineral , Centrais Elétricas/normas , Ar/análise , Corrosão , Eletricidade , Monitoramento Ambiental/métodos , Monitoramento Ambiental/normas , Combustíveis Fósseis/análise , Temperatura Alta , Óxidos de Nitrogênio/análise , Oxigênio/análise , TemperaturaRESUMO
The use of cement raw meals as sorbent precursors for CO2 capture can reinforce the synergies between the cement production process and calcium looping CO2 capture technology. In this work, we measure the CO2-carrying capacity of different calcined samples of a particular marl, which were obtained under very different calcination conditions and setups (a thermogravimetric analyzer, a drop tube furnace, and an industrial calciner). We find that the reactivity toward CO2 of these calcined materials displays a strong sensitivity to the calcination conditions, in particular to calcination time. A pronounced competition between the belite (Ca2SiO4) formation reaction and the formation of free CaO needed for CO2 capture is detected. As the calcination of the raw meal approaches flash conditions (i.e., >90% calcination conversion in less than 10 s), the belite formation is shown to be minimized, leading to sorbents with CO2-carrying capacities of approximately 0.4 mol CO2/mol CaO.
RESUMO
The 1999/31 Elemental Carbon Directive sets strict rules on the disposal of untreated municipal solid waste in the European Union countries and forces a reduction of the biodegradable quantities disposed off to landfills up to 35% of the amount produced in 1995 in the coming decade. More environmentally friendly waste management options shall be promoted under the framework of the Community Waste Strategy ([96] 399 Final). In this context, the production and thermal use of solid recovered fuels (SRFs), derived from nonhazardous bioresidues and mixed- and mono-waste streams, could be a key element in a future waste management system. Within the scope of the European Demonstration Project, RECOFUEL, SRF cocombustion was demonstrated in two large-scale lignite-fired coal boilers at RWE power station in Weisweiler, Germany. As a consequence of the high biogenic share of the cocombusted material, this approach can be considered beneficial following European Directive 2001/77/EC on electricity from renewable energy sources (directive). During the experimental campaign, the share of SRF in the overall thermal input was adjusted to approximately 2%, resulting into a feeding rate of approximately 25 t/hr. The measurement campaign included boiler measurements in different locations, fuel and ash sampling, and its characterization. The corrosion rates were monitored by dedicated corrosion probes. The overall results showed no significant influence of SRF cocombustion on boiler operation, emissions behavior, and residues quality for the thermal shares applied. Also, no effect of the increased chlorine concentration of the recovered fuel was observed in the flue gas path after the desulfurization unit.
Assuntos
Eliminação de Resíduos/métodos , Carbono/análise , Carbono/química , Carvão Mineral , Cinza de Carvão , União Europeia , Alemanha , Material Particulado/análise , Material Particulado/química , Eliminação de Resíduos/instrumentação , Eliminação de Resíduos/legislação & jurisprudência , TemperaturaRESUMO
A new concept is proposed for combined fermentation (two-stage high-load fermenter) and gasification (two-stage fluidised bed gasifier with CO2 separation) of sewage sludge and wood, and the subsequent utilisation of the biogenic gases in a hybrid power plant, consisting of a solid oxide fuel cell and a gas turbine. The development and optimisation of the important processes of the new concept (fermentation, gasification, utilisation) are reported in detail. For the gas production, process parameters were experimentally and numerically investigated to achieve high conversion rates of biomass. For the product gas utilisation, important combustion properties (laminar flame speed, ignition delay time) were analysed numerically to evaluate machinery operation (reliability, emissions). Furthermore, the coupling of the processes was numerically analysed and optimised by means of integration of heat and mass flows. The high, simulated electrical efficiency of 42% including the conversion of raw biomass is promising for future power generation by biomass.
Assuntos
Biomassa , Biotecnologia/métodos , Eletricidade , Fermentação , Gases/química , Modelos Teóricos , Biocombustíveis , Dióxido de Carbono/análise , Simulação por Computador , Esgotos/química , Silagem , Volatilização , Madeira/química , Zea mays/químicaRESUMO
An important source of polycyclic aromatic hydrocarbons (PAHs) in residential areas, particularly in the winter season, is the burning process when wood is used for domestic heating. The target of this study was to investigate the particle-phase PAH composition of ambient samples in order to assess the influence of wood combustion on air quality in residential areas. PM(10) samples (particulate matter <10 mum) were collected during two winter seasons at two rural residential areas near Stuttgart in Germany. Samples were extracted using toluene in an ultrasonic bath and subsequently analysed by gas chromatography-mass spectrometry. Twenty-one PAH compounds were detected and quantified. The PAH fingerprints of different wood combustion emissions were found in significant amounts in ambient samples and high correlations between total PAHs and other wood smoke tracers were found, indicating the dominant influence of wood combustion on air quality in residential areas. Carcinogenic PAHs were detected in high concentrations and contributed 49% of the total PAHs in the ambient air. To assess the health risk, we investigated the exposure profile of individual PAHs. The findings suggest that attention should be focused on using the best combustion technology available to reduce emissions from wood-fired heating during the winter in residential areas.