摘要
Red mud(RM),as an alkaline waste,was recently proved to be a promising substitute for the SCR catalyst.Dealkalization could improve the acidity and reducibility of red mud,which were critical for SCR reaction.However,the dealkalization effect depended on the reaction between acid solution and red mud.In this study,we realized the directional control of the chemical state of active sites through tuning the acid pretreatment(dealkalization)process.The pretreatment endpoint was controlled at pH values of 3–5 with diluted nitric acid.When the pH values of red mud were 3 and 5(CRM-3 and CRM-5),activated catalysts showed NOx conversion above 90%at 275℃–475℃.The high initial reaction rate,Ce^(3+)/(Ce^(3+)+Ce^(4+))ratio,and surface acidity accounted for the excellent SCR performance of CRM-5 catalyst.Meanwhile,more Fe^(3+) on the CRM-3 surface improved the NH_(3) adsorption.There was a strong interaction between Al and Fe in both CRM-5 and CRM-3 catalysts.DFT results showed that the adsorption capacity of the Al-O_(3)-Fe for NH_(3) and NO is stronger than that of Fe-O_(3)-Fe,which enhanced the NOx conversion of the catalyst.However,the almandine was formed in CRM-4,consumed part of Fe^(3+) and Al^(3+),and the interaction between Al and Fe was weakened.Also,deposited almandine on the catalyst surface covered the active sites,thus leading to lower NH_(3)-SCR activity.
基金
financially supported by the National Natural Science Foundation of China(Grant No.21906090)
the National Key Research and Development Program of China(Nos.2017YFC0210200 and 2017YFC0212800)
the Primary Research&Development Project of Shandong Province(China)(Nos.2018GSF117034 and 2019JZZY020305)
The scientific calculations in this paper have been done on the HPC Cloud Platform of Shandong University(China).