Abstract
The Xinjiang lignite mined from Shaerhu coalfield (SEHc) easily causes severe fouling and corrosion because of its high sodium and chlorine contents. Therefore, it is necessary to study the migration and transformation behavior of sodium and chlorine during combustion in order to reveal the mechanisms of fouling and corrosion, and propose the effective solutions of above problems. In this study, based on the 0.4 T/D circulating fluidized bed (CFB) test system, the migration and transformation behavior of sodium and chlorine in SEHc during combustion at 950 °C was explored. The migration and transformation paths of sodium and chlorine were proposed through the chemical characterization of ash samples along the flue gas flow direction, as well as the thermodynamic equilibrium calculation by the software of Factsage 6.1. The experimental studies show the sodium and chlorine mainly in the form of NaCl crystal in raw coal underwent a series of physical and chemical changes during combustion, and subsequently distributed in bottom ash/circulating ash, fly ash and gas phase in various forms including sodium aluminosilicates, chlorides and sodium oxides. Sodium was more inclined to be resided in ash in the form of aluminosilicates through the reactions with other minerals (SiO2 and Al2O3), while chlorine was easily released into the flue gas in forms of HCl, Cl2, NaCl, etc. The Cl-based species might result in the corrosion of metal heating surfaces because of the presence of corrosion products (metal chlorides) in fly ash. As temperature decreased, the sodium or chlorine vapors would successively deposit in fly ash via physical condensation or chemical reaction. At 840∼570 °C, the sodium-based species (Na2O and NaCl) would first deposit in fly ash, then gaseous chlorine species (NaCl, FeCl3 and so on) primarily deposited at 570∼180 °C.
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