Study on the transformation of gaseous selenium during the cooling process of coal-fired flue gas

被引:7
|
作者
Xu, Wenting [1 ]
Song, Guochang [1 ]
Yang, Xingyu [1 ]
Song, Qiang [1 ,3 ]
Yao, Qiang [1 ,2 ]
机构
[1] Tsinghua Univ, Key Lab Thermal Sci & Power Engn, Minist Educ, Beijing 100084, Peoples R China
[2] Xinjiang Univ, Sch Elect Engn, Urumqi 830047, Peoples R China
[3] Tsinghua Univ, Dept Energy & Power Engn, Beijing 100084, Peoples R China
关键词
Selenium; Transformation; Flue gas; Adsorption; Ash; TRACE-ELEMENTS; POWER-PLANT; FLY-ASH; COMBUSTION; EMISSION; SPECIATION; BEHAVIOR; FATE; MECHANISM; CAPTURE;
D O I
10.1016/j.jhazmat.2022.130362
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Understanding the transformation of Se during the flue-gas cooling process is important for controlling Se emissions. By analyzing the thermal stability of Se in ash collected from power plant dust collectors, physical migration was found to be the main pathway by which gaseous Se transformed into ash during the flue-gas cooling process. The dynamic curves were obtained for SeO2 adsorption by ash at 200-900 degrees C. The adsorbed Se amount first decreased, increased, and then decreased with increasing adsorption temperature (400 degrees C and 600 degrees C were the two turning points). By comparing the adsorption characteristics of different ash and minerals and performing a speciation analysis of Se and an elemental distribution characterization after adsorption, the adsorption mechanism of gaseous Se was proposed. In the medium-high temperature range (above 500 degrees C), SeO2 was chemically adsorbed by ash through CaO and CaSO4, generating CaSeO3 and CaSeO4, respectively; the thermal stability of CaSeO4 was weaker than that of CaSeO3. In the low temperature range (below 500 degrees C), SeO2 was adsorbed by ash mainly through physical adsorption of unburned carbon, accompanied by a small amount of chemical adsorption of CaO.
引用
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页数:12
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