Sun Hong, Liu Zhigang, Wang Ying, Quan Xie, Zhao Guozhi
School of Environmental & Chemical Engineering, Dalian Jiaotong University, Dalian, 116028, China.
School of Environmental & Chemical Engineering, Dalian Jiaotong University, Dalian, 116028, China.
J Hazard Mater. 2019 Dec 15;380:120800. doi: 10.1016/j.jhazmat.2019.120800. Epub 2019 Jul 4.
A novel MnOx@MIL-125(Ti) catalyst was constructed for the selective catalytic reduction (SCR) of NOx with NH, in which MIL-125(Ti), a kind of metal-organic frameworks (MOFs), was used as the support because of the structural feature, large surface area and high thermal stability. The SCR results showed that MnOx@MIL-125(Ti) exhibited high deNOx ability and N selectivity in a wide operating temperature range. Moreover, it exhibited better SO resistance than MnOx/TiO(P25). Characterization results revealed that MIL-125(Ti) had resulted in a high dispersion of MnOx and a strong metal-support interaction for MnOx@MIL-125(Ti), which could promote the formation of the abundant Mn and surface chemical oxygen, facilitating the activation of the reactants. In situ DRIFTS results suggested that NH-SCR over MnOx@MIL-125(Ti) followed both Langmuir-Hinshelwood (L-H) and Eley-Rideal (E-R) mechanism. In addition, NO species were proved to be the important intermediates which were involved in SCR reaction.
构建了一种新型的MnOx@MIL-125(Ti)催化剂,用于NH3选择性催化还原(SCR)NOx,其中,作为金属有机框架(MOF)的一种,MIL-125(Ti)因其结构特点、大表面积和高热稳定性而被用作载体。SCR结果表明,MnOx@MIL-125(Ti)在较宽的操作温度范围内表现出高脱硝能力和N选择性。此外,它比MnOx/TiO₂(P25)表现出更好的抗SO₂性能。表征结果表明,MIL-125(Ti)导致了MnOx在MnOx@MIL-125(Ti)上的高度分散以及强烈的金属-载体相互作用,这可以促进大量Mn和表面化学氧的形成,有利于反应物的活化。原位漫反射红外傅里叶变换光谱(DRIFTS)结果表明,MnOx@MIL-125(Ti)上的NH₃-SCR遵循Langmuir-Hinshelwood(L-H)和Eley-Rideal(E-R)两种机理。此外,NO物种被证明是参与SCR反应的重要中间体。