化学
腈
氮气
污水污泥
热解
污染物
催化作用
苯甲腈
氧化还原
有机化学
环境化学
无机化学
化学工程
污水
废物管理
工程类
作者
Yimeng Jiao,Ze Guo,Yifei Wu,Junrong Yue,Linlin Yin,Yu Tian,Jun Zhang
标识
DOI:10.1021/acssuschemeng.4c05347
摘要
The ongoing emission of gaseous pollutants from sewage sludge microwave pyrolysis poses formidable threats. This study specially elucidates the evolutional pathways between reactive and stable nitrogen-containing compounds in a novel sludge endogenous mineral-mediated microwave pyrolysis system, primarily responsible for curtailing NH3 and HCN production. NH3 and HCN yields were reduced by 33.2 and 22.0%, respectively, which are derived from the comprehensively oxidative catalysis of Al2O3, CaO, Fe2(SO4)3, FeCl3, and Fe2O3. Minerals further accelerated the conversion of 40.7% NH3 and 74.0% HCN to N2 by inducing the formation of FeNX, CaCXNy, and Ca2Fe2O5. The lowest release levels of NH3 and HCN were achieved with 20% Fe2O3 and 20% CaO at 500 °C, respectively. Additionally, 600 °C was identified as a critical threshold for minerals and microwave inhibition of NH3 and HCN formation, as higher temperatures weaken the inhibitory effect. Crucially, minerals enhanced engagement and cross-linking of nitrogenous species by attaching with proteins and occupying their redox-active sites, which directly promoted the formation of stable nitrogenous structures and ultimately hindered the formation and transformation of heterocyclic-N and nitrile-N. Minerals also imposed the transfer of reactive heterocyclic-N to stable heterocyclic-N and reactive alkyl nitrile-N to stable nitrile-N, thereby hampering the production of NH3 and HCN. This study provides a novel strategy for the in situ control of gaseous nitrogen pollutant formation using minerals and microwave technology in practical applications.
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