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Re-using of coal-fired fly ash for arsenic vapors in-situ retention before SCR catalyst: Experiments and mechanisms.
Li, Shuai; Gong, Hongyu; Hu, Hongyun; Liu, Huimin; Huang, Yongda; Fu, Biao; Wang, Linling; Yao, Hong.
Affiliation
  • Li S; State Key Laboratory of Coal Combustion, School of Energy and Power Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Gong H; State Key Laboratory of Coal Combustion, School of Energy and Power Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Hu H; State Key Laboratory of Coal Combustion, School of Energy and Power Engineering, Huazhong University of Science and Technology, Wuhan 430074, China. Electronic address: hongyunhu@hust.edu.cn.
  • Liu H; State Key Laboratory of Coal Combustion, School of Energy and Power Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Huang Y; State Key Laboratory of Coal Combustion, School of Energy and Power Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Fu B; State Key Laboratory of Coal Combustion, School of Energy and Power Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Wang L; School of Environmental Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
  • Yao H; State Key Laboratory of Coal Combustion, School of Energy and Power Engineering, Huazhong University of Science and Technology, Wuhan 430074, China.
Chemosphere ; 254: 126700, 2020 Sep.
Article in En | MEDLINE | ID: mdl-32334244
Arsenic is easily evaporated with coal combustion, which not only causes serious environmental issues but also leads to the deactivation of selective catalytic reduction (SCR) catalyst. This study focused on the re-using of coal-fired fly ash for arsenic vapors in-situ retention before SCR catalyst in the furnace. Experiments were carried out to estimate the effects of typical fly ash compounds (Ca-, Fe-, and Al-bearing components) as well as acid gases (SO2/NO) on arsenic capture at temperatures of high-temperature furnace stage (900 °C) or SCR system entry stage (450 °C). The results demonstrated that, regardless of collection plants, all the ash samples showed certain capacity in arsenic vapors retention and the capture performance was enhanced at 900 °C than at 450 °C. Both physical and chemical adsorptions occurred for arsenic capture at low temperature, while chemical adsorption by effective mineral components dominated at high temperature. The role of Ca-compounds was more remarkable than Fe/Al-compounds and CaSO4/calcium silicates were identified as the key calcium compounds that acted on arsenic adsorption by fly ash. Insignificant effects were found regarding the acid gases (SO2 and NO) on arsenic retention by fly ash owing to the high resistance of CaSO4 and calcium silicates to acid gases. These findings provided reference for the in-situ retention of arsenic by reusing fly ash that enriched in specific compositions.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arsenic / Coal Ash Type of study: Prognostic_studies Language: En Journal: Chemosphere Year: 2020 Document type: Article Affiliation country: China Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arsenic / Coal Ash Type of study: Prognostic_studies Language: En Journal: Chemosphere Year: 2020 Document type: Article Affiliation country: China Country of publication: United kingdom