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发表时间：2022-10-09

发表刊物：化学学报

卷号：77

期号：8

页面范围：758-764

ISSN号：0567-7351

摘要：A series of bimetallic MOF-74-CoMn catalysts with different metal ratios have been successfully synthesized by hydrothermal method and applied in selective catalytic reduction of NO with CO (CO-SCR). The experimental procedure for the preparation of MOF-74-CoMn catalyst is as follows:The reaction solution was a 3.28 mmol mixture of Co(NO3)(2)center dot 6H(2)O and Mn(NO3)(2)center dot 6H(2)O, 1.09 mmol 2,5-dihydroxyterephthalic acid (H4DOBDC) and 90 mL ethanol-DMF-water. The molar ratio of mixture (Co/Mn) was 1:0, 1:1, 1:2, 1:4, 1:6, respectively. The reactant solution was ultrasonically stired for 30 min until homogeneous. Then, the mixture was transferred into a 100 mL Teflon autoclave then kept in an oven at 100 degrees C for 24 h. Finally, after purified with DMF and methanol, the products were dried in a vacuum oven at 80 degrees C for 24 h to obtain a purple MOF-74-CoMn catalyst, which were stored in vacuum or an inert atmosphere. The prepared sample is referred to as MOF-74-Co1Mnx, where x represents a molar ratio of Co to Mn is 1 :x (x= 0, 1, 2, 4, 6). The SCR catalytic activities were carried out in a fixed-bed flow reactor in gas stream. The experimental results show that the NOx conversion rate of bimetallic MOF-74-CoMn catalyst is generally higher than that of single metal MOF-74-Co catalyst, and their reaction temperature window is wider. Especially, MOF-74-Co1Mn2 exhibited the highest selective catalytic reduction of NO with CO (CO-SCR) performance which is close to 100% with a temperature range from 175 to 275 degrees C. Further, the bimetallic MOFs catalysts were characterized by X-ray powder diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), N-2 adsorption/desorption, X-ray photoelectron spectroscopy (XPS), Hydrogen-temperature programed reduction (H-2-TPR) and Infrared spectroscopy (FTIR) techniques. The results showed that the synergistic effect between Co and Mn metals could obviously promote the formation of unsaturated metal sites and oxygen vacancies, thereby promoting their catalytic reduction efficiency of selective catalytic reduction of NO with CO (CO-SCR).

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