MOE Key Laboratory of Thermo-Fluid Science and Engineering, Xi'an Jiaotong University, Xi'an, 710049, China.
MOE Key Laboratory of Thermo-Fluid Science and Engineering, Xi'an Jiaotong University, Xi'an, 710049, China.
J Environ Manage. 2020 Jun 1;263:110411. doi: 10.1016/j.jenvman.2020.110411. Epub 2020 Mar 11.
Oxy-combustion is one of the most promising technologies for carbon capture and sequestration. When CO-neutral biomass is burned under oxy-combustion conditions, named "oxy-biomass combustion" a negative CO emission can be achieved. However, the high content of potassium and chlorine in biomass results in sever ash deposition and corrosion in air fired furnaces, which are further aggravated in oxy-combustion mode due to the enrichment of corrosive species by flue gas recycle. In this paper, the hot corrosion behaviors and mechanism of two representative materials (TP347H, HR3C) used for superheaters in furnaces are studied. The effects of oxy-combustion atmosphere, KCl deposition, effect of SO, effect of water vapor, and temperature on the corrosion kinetics at the starting stage are investigated. The corrosion severity of the materials was determined using the weight gain method, and the microstructures and chemical compositions of corrosion layers were characterized by the scanning electron microscopy with energy dispersive spectroscopy, and X-ray diffraction. The results show that the hot corrosion rate is significantly sped up by KCl deposition, more than five times the gas corrosion rate under the same gas composition and temperature. HR3C with higher Cr and Ni contents is more likely to form Cr enrichment on the interface between the corrosion layer and the substrate than TP347H, resulting in stronger resistance to the hot corrosion than TP347H. When the corrosion atmosphere is changed from air-combustion to oxy-combustion, the hot corrosion rate is reduced with a denser Cr oxide film and less metal sulfides. The increase of temperature in the presence of KCl deposition significantly affects the hot corrosion rate, e.g. the corrosion rate at 650 °C is 16 times higher than that at 450 °C. Water vapor and SO concentrations have opposite influences on the hot corrosion, respectively. Compared to the dry environment, a high-humidity environment decreases the hot corrosion rate; however, a higher SO concentration facilitates the sulfation of KCl deposits, leading to stronger damage to the chromium oxide film and thereby an increased hot corrosion rate.
富氧燃烧是一种很有前途的碳捕集和封存技术。当 CO 中性生物质在富氧燃烧条件下燃烧时,即“富氧生物质燃烧”,可以实现负 CO 排放。然而,生物质中钾和氯的含量很高,导致在空气炉中严重积灰和腐蚀,而在富氧燃烧模式下,由于烟道气再循环使腐蚀性物质富集,这种情况进一步加剧。本文研究了两种用于炉过热器的代表性材料(TP347H、HR3C)在富氧燃烧气氛中的热腐蚀行为和机理。考察了富氧燃烧气氛、KCl 沉积、SO 影响、水蒸气影响和温度对起始阶段腐蚀动力学的影响。采用增重法确定材料的腐蚀程度,利用扫描电子显微镜和能谱分析、X 射线衍射分析对腐蚀层的微观结构和化学成分进行了表征。结果表明,KCl 沉积显著加速了热腐蚀,在相同的气体组成和温度下,其腐蚀速率是气体腐蚀速率的五倍以上。HR3C 由于含有较高的 Cr 和 Ni,比 TP347H 更容易在腐蚀层和基体之间形成 Cr 富集,因此比 TP347H 具有更强的抗热腐蚀性。当腐蚀气氛从空气燃烧变为富氧燃烧时,由于形成了更致密的 Cr 氧化物膜和较少的金属硫化物,热腐蚀速率降低。在存在 KCl 沉积的情况下,温度升高会显著影响热腐蚀速率,例如在 650°C 时的腐蚀速率是在 450°C 时的 16 倍。水蒸气和 SO 的浓度对热腐蚀有相反的影响。与干燥环境相比,高湿度环境会降低热腐蚀速率;然而,较高的 SO 浓度会促进 KCl 沉积物的硫酸盐化,从而对 Cr 氧化物膜造成更强的破坏,导致热腐蚀速率增加。