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• W3000623216 abstract "The catalytic reduction of NO in the presence of CO was investigated by density functional theory calculations with consideration of the iron involved in char (Fe-adsorbed char). The quantitative information of reaction kinetics was also evaluated using canonical variational transition-state theory in the temperature range of 500-1800 K. The analysis of the associated adsorption energies indicates that the affinity of the carbon active site toward NO and CO is stronger than that at the Fe site, and the NO adsorption on the carbon site in the N-down mode is the most energetically favorable. Following the chemisorption step, the reactions proceed for N2O, N2, and CO2 desorption by different reduction mechanisms, depending on whether CO exists. The FeO group formed and transformed during the NO reduction is of significant importance for the whole catalytic process. The results show that the heterogeneous reduction of NO is promoted much more dramatically with the help of CO, which brings about a decrease in the activation energies accompanied by an increase in the reaction rate constants. The effectiveness of the Fe-adsorbed model derives from its prominent effect on NO-CO reaction and becomes more realistic than the original metal-free structure." @default.
• W3000623216 created "2020-01-23" @default.
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• W3000623216 date "2020-01-17" @default.
• W3000623216 modified "2023-10-11" @default.
• W3000623216 title "Density Functional Theory Investigation on the Catalytic Reduction of NO by CO on the Char Surface: the Effect of Iron" @default.
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• W3000623216 doi "https://doi.org/10.1021/acs.est.9b07081" @default.
• W3000623216 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31951386" @default.
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