FUTURE AEROSOL TECHNOLOGICAL APPLICATIONS
Transcription
FUTURE AEROSOL TECHNOLOGICAL APPLICATIONS
Cite abstract as Author(s) (2007), Title, European Aerosol Conference 2007, Salzburg, Abstract T14A026 Detailed particle analysis in the hot flue gas of a municipal waste incineration plant Christian Deuerling1, Jürgen Maguhn1, Hermann Nordsieck2, Ragnar Warnecke3 and Ralf Zimmermann1,2,4 1 Institut für Ökologische Chemie, GSF-Forschungszentrum für Umwelt und Gesundheit GmbH, Ingolstädter Landstrasse 1, D-85764 Neuherberg, Germany 2 Abteilung Umweltchemie und Prozessanalytik, BIfA-Bayerisches Institut für Angewandte Umweltforschung und -technik, Am Mittleren Moos 46, D-86167 Augsburg, Germany 3 GKS Gemeinschaftskraftwerk Schweinfurt GmbH, Hafenstrasse 30, 97424 Schweinfurt 4 Analytische Chemie, Institut für Physik, Universität Augsburg, Universitätsstrasse 1, D-86159 Augsburg Keywords: Aerosol Measurement, Cascade Impactor, Combustion Particles, high temperature aerosols Normal Operation, Mass Concentration, 1st - 4th pass (mean values) Mass Concentration [g/m³] 10 1 upon travel through the flue gas duct due to agglomeration and condensation effects. The chemical composition of the particles also changes (Fig. 2) due to condensation of volatile compounds and chemical reactions. An increase of the sulphur content can be observed probably due to sulphatation of chlorides. Chemical Composition of the Particles < 1 µm in the 4 Passes (inlet content not included) 1,0 Mass Concentration [g/m³] High-temperature chlorine corrosion of super heaters is one of the main cost factors of running municipal solid waste incineration (MSWI) plants. To setup a comprehensive model for corrosion in a MSWI plant, a measurement system was developed to analyse the complex processes the waste incineration raw gas is subjected to upon travel through the flue-gas duct of a MSWI boiler. Particles from 30 nm to 3 mm were sampled off-stack, size fractionated and analysed concerning mass concentration and chemical composition. Additionally, acidic components of the gas phase were analysed. Measurements were performed in the first (900 °C) and 2nd pass (700 °C), straight behind the first two super heater blocks in the 3rd pass (500 °C) and in the 4th pass (300 °C). Because of temporal variation of the fuel composition, each measurement was carried out in parallel at the reference point (2nd pass) and at the measuring point in question by two identical measurement systems. In order to sample the particulate matter in its current state, rapid dilution of the raw gas was accomplished by a porous tube diluter positioned directly behind the inlet of the sampling probe. The probe is held at a constant temperature of 300 °C. The raw gas subsequently passes a cyclone, further diluters and enters the instruments for analysis of chemistry and morphology. 0,9 0,8 0,7 0,6 0,5 0,4 0,3 0,2 0,1 0,0 1st pass 2nd pass 3rd pass 4th pass Passes S Cl Si Na K Ca Fe Zn Pb Figure 2. Changes in chemical composition of the fine particles upon travel through the flue-gas duct Modifications of the operation conditions of the plant on corrosion parameters such as reduction of the length of the fire, changing of the rate of recirculated air, adding of sulphur to the waste and injection of SO2 were performed resulting in changes of aerosol composition. This project is funded by the Bayerisches Staatsministerium für Umwelt, Gesundheit und Verbraucherschutz within the scope of the European Regional Development Fund (ERDF). The author wishes to thank Max-BuchnerForschungsstiftung for their kind support. 0.1 0.01 0.001 0.0001 0.01 0.1 1 10 100 1000 10000 Particle Size [µm] Z1 Z1 line Z2 Z2 line Z3 Z3 line Z4 Z4 line Figure 1. Size distribution of particle mass concentration in the four consecutive passes of the waste incineration boiler. At normal operation conditions of the plant a bimodal size distribution of the particles can be observed (Fig. 1) showing growth of the particles Deuerling, C., Maguhn, J., Nordsieck, H., Reznikov, G., Zimmermann, R. & Warnecke, R. (2005). Proc. Europ. Aerosol Conf., Ghent, 373. Schroer, C. & Konys, J. (2002). Report, Forschungszentrum Karlsruhe. Maguhn, J., Karg, E., Kettrup, A. & Zimmermann, R. (2003). Environ. Sci. Technol., 37, 4761-4770.