Effect of precipitants on the catalytic activity of Co–Ce composite oxide for N2O catalytic decomposition

被引:2
作者
Yongzhao Wang
Xiaobo Hu
Ke Zheng
Hongxi Zhang
Yongxiang Zhao
机构
[1] Shanxi University,School of Chemistry and Chemical Engineering, Engineering Research Center of Ministry of Education for Fine Chemicals
来源
Reaction Kinetics, Mechanisms and Catalysis | 2018年 / 123卷
关键词
Co–Ce composite oxide; Precipitant; Precipitated precursor; N; O catalytic decomposition;
D O I
暂无
中图分类号
学科分类号
摘要
Co–Ce composite oxide catalysts have been prepared by the co-precipitation method using K2CO3 (Co–Ce–A), KOH (Co–Ce–B) and NH3·H2O (Co–Ce–C) as precipitants. The effect of different precipitants on the catalytic activity for N2O catalytic decomposition was investigated in a fixed-bed continuous flow reactor. The structure and properties of the catalysts were characterized by XRD, TEM, FT-IR, Raman, XRF, BET, EC, H2-TPR and O2-TPD. The results show that under the reaction conditions of N2O 0.1% and GHSV 10,000 h−1, the catalyst prepared by using K2CO3 as precipitant exhibits better N2O catalytic decomposition activity than that prepared by using KOH or NH3·H2O as precipitant. The XRD, TEM and BET results reveal that all the samples exist as a Co3O4 phase with the spinel structure though the precipitated precursors are different, while Co–Ce–A shows higher specific surface area and smaller crystalline size. Further characterizations results suggest that compared with Co–Ce–B and Co–Ce–C, Co–Ce–A possesses not only stronger interaction between Co and Ce species, but also higher electrical conductivity resulting from the more amount of residual K, which improves the reduction of Co3+–Co2+ and facilitates the desorption of surface oxygen species. Therefore, Co–Ce–A exhibits enhanced N2O catalytic decomposition activity.
引用
收藏
页码:707 / 721
页数:14
相关论文
共 200 条
[1]  
Li L(2014)undefined Environ Sci Technol 48 5290-5297
[2]  
Xu JH(1993)undefined Catal Today 17 277-284
[3]  
Hu JX(1999)undefined Coordin Chem Rev 187 303-327
[4]  
Han JR(2012)undefined J Catal 294 99-112
[5]  
Riley BW(2006)undefined Combust Sci Technol 178 1477-1489
[6]  
Richmond JR(2014)undefined Rsc Adv 4 29107-29119
[7]  
Trogler WC(2005)undefined J Mol Catal A 227 187-196
[8]  
Liu N(2014)undefined Chin J Catal 35 1105-1112
[9]  
Zhang RD(2014)undefined J Mater Chem A 2 5178-5181
[10]  
Chen BH(2013)undefined Ind Eng Chem Res 52 4504-450912