催化作用
煅烧
甲醛
X射线光电子能谱
化学
解吸
吸附
摩尔比
化学工程
热解
无机化学
材料科学
核化学
物理化学
有机化学
工程类
作者
Jurong Liu,Yiming Zheng,Qinyu Zhu,Yaxin Dong,Suhong Lu,Bo Peng,Yu‐Liang Chen,Shanghong Zeng,Kelun Li
标识
DOI:10.1007/s10563-020-09301-9
摘要
A series of MnOx–CeO2 with different molar ratios of Mn/Ce had been synthesized via in-situ pyrolysis of Mn–Ce-MOFs precursor. The as-prepared catalysts were applied for catalytic oxidation of formaldehyde (HCHO) and also characterized by N2 adsorption–desorption, XRD, SEM, H2-TPR, O2-TPD and XPS. The result of catalytic test indicated that MnOx–CeO2 with a Mn/Ce molar ratio of 5:5 exhibited outstanding catalytic performance, which could achieve complete oxidation of HCHO at a temperature as low as 40 °C. Moreover, MnOx–CeO2 (5:5) possessed good stability and resistance to moisture. The HCHO conversion still retained over 99.0% as adding 5% H2O to the gas feed. The studies revealed that the close contact between Mn and Ce species in the Mn–Ce-MOFs precursor enhanced the interaction between MnOx and CeO2 through the calcination. The high specific surface area, easy low-temprature reducibility, abundant surface active oxygen and rich Mn4+ species were contributed to the excellent catalytic activity of MnOx–CeO2. Therefore, the MnOx–CeO2 catalyst possessed promising application prospect in removing HCHO at ambient temperature.
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