Fireside Corrosion of Heat Exchanger Materials for Advanced Solid Fuel Fired Power Plants

To address the challenge of climate change, future energy systems need to have reduced greenhouse gas emissions and increased efficiencies. For solid fuel fired combustion plants, one route towards achieving this is to increase the system’s steam temperatures and pressures. Another route is to co-fire renewable fuels (such as biomass) with coals. Fireside corrosion performance of two candidate superheater/reheater alloys has been characterised at higher heat exchanger surface temperature. Samples of the alloys (a stainless steel, Sanicro 25 and a nickel-based alloy, IN740) were exposed in fireside corrosion tests at 650 °C, 700 °C and 750 °C, in controlled atmosphere furnaces using the ‘deposit recoat’ test method to simulate superheater/reheater exposure for 1000 h. After exposure, the samples were analysed using dimensional metrology to determine the extent and distributions of corrosion damage in terms of surface recession and internal damage. At 650 °C, the stainless steel and nickel-based alloy performed similarly, while at 700 °C and above, the median damage to the steel was at least 3 times greater than for the nickel-based alloy. Optical and electronic microscopy studies were used to study samples’ damage morphologies after exposure. Intergranular damage and pits were found in sample cross sections, while chromium depletion was found in areas with internal damage. For high-temperature applications, the higher cost of the nickel-based alloy could be offset by the longer life they would allow in plant with higher operating temperatures.

Investigation of the mechanism for fireside corrosion in coal-fired boilers in South Africa

SYNOPSIS Furnace wall tubes from 600 MW subcritical boilers at three coal-fired power stations were sampled and the fireside deposits examined to determine the mechanism of fireside corrosion. This involved an in-depth investigation into the morphology and composition of the fireside deposits and the conditions of the furnace that enable this type of attack. SEM-EDS analysis revealed high concentrations of oxygen, iron, and sulphur, QEMSCAN and XRD analyses identified the presence of Fe3O4, Fe2O3, FeS, and FeS2. Differential thermal analysis showed thermal activities at temperatures of 500-600°C, 900-1100°C, and 1100-1250°C, which are associated, respectively, with FeS2 oxidation to FeS and Fe2O3, at 475-525°C, formation of aluminosilicates at 925-1100°C, and melting of FeS around 1190°C. The absence of sodium and potassium eliminates the contribution of molten alkali sulphates to the corrosion. The consistent coexistence of iron sulphide and iron oxide is indicative of the substoichiometric conditions in the furnace, while the detection of pyrite suggests that the coal is not completely combusted, which points to a poor combustion process. These observations were affirmed by gas analysis at one of the stations, where very high levels of carbon monoxide were measured at the furnace wall (> 14 000 ppm) and furnace exit (> 3500 ppm). The high CO concentrations are indicative of limited combustion caused by limited O2. These reducing conditions promote the formation of FeS-rich deposit, which is the corrosive species responsible for degradation. Keywords: fireside corrosion, sulphidation, coal-fired boiler, furnace wall tubes.