氧化剂
焚化
氯
化学
大气(单位)
还原气氛
环境化学
废物管理
有机化学
气象学
物理
工程类
作者
Jianye Bei,Xu Xu,Mingxiu Zhan,Xiaodong Li,Wentao Jiao,Lavrent Khachatryan,Angjian Wu
标识
DOI:10.1021/acs.est.2c05830
摘要
Gasification is an effective technology for the thermal disposal of municipal solid waste (MSW) with lower dioxin emission compared to the prevailing incineration process. Nevertheless, the mechanism of dioxin formation in the reducing atmosphere during the gasification process was seldomly explored. Herein, the effects of the atmosphere, temperature, and chlorine source were systematically investigated in terms of dioxin distribution. With CO2 and H2O as gasification agents, a reducing reaction atmosphere was formed with abundant H2 which effectively suppressed the generation of C-Cl, contributing to a substantial decrease of dioxin concentration by ∼80% compared to the incineration process. The formation of dioxin was favored at temperatures below 700 °C with its peak concentration achieved at 500 °C. It was unveiled that inorganic chlorine played a dominant role in the reducing atmosphere, with a lower proportion of C-O-C/O-C═O on residual slag compared to an oxidizing atmosphere. Additionally, the generated H2 reduced the concentration of dioxins by attacking C-Cl and inhibiting the crucial Deacon reaction for dioxin formation, validated by density functional theory calculation. Eventually, the formation route paradigm and the reaction mechanism of dioxin formation from MSW gasification were revealed, facilitating and rationally guiding the control of dioxin emission.
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