催化作用
兴奋剂
对偶(语法数字)
材料科学
化学工程
化学
核化学
矿物学
有机化学
光电子学
工程类
艺术
文学类
作者
Jinxing Mi,Hao Liu,Shan Yang,Feifan Huang,Zhen Qian,Jin Wei Yuan,Jie Qing,Chuanzhi Sun,Chang Wang,Jianjun Chen,Junhua Li
标识
DOI:10.1021/acs.est.4c14210
摘要
Designing a bifunctional catalyst to concurrently activate NO and O 2 is of fundamental importance to the simultaneous catalytic removal of NO x and VOCs. During this process, sufficient electron transfer from the catalyst surface to the antibonding π* orbitals of adsorbed NO and O 2 is necessary to facilitate the adsorption and subsequent bond cleavage. Herein, an electronic orbital coupling strategy is applied by doping praseodymium (Pr) into a CeO 2 -TiO 2 (CeTi) composite oxide to obtain a PrCeTi bifunctional catalyst, which has a strong interaction with NO to form NO +, further splitting with N 3+ production and thereby enhancing NH 3 -SCR performance following the Langmuir–Hinshelwood mechanism. Meanwhile, O 2 adsorbs on the PrCeTi catalyst surface to produce superoxide (O 2 – ) and further transforms into peroxide (O 2 2– ) which, along with increased temperature, boosts the PhCH 3 total oxidation. Finally, the coactivation of NO and O 2 over the PrCeTi catalyst contributes to its better simultaneous removal efficiency of NO x and toluene than that of the CeTi catalyst.
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