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个人信息Personal Information
教授
博士生导师
硕士生导师
性别:女
毕业院校:大连理工大学
学位:博士
所在单位:化工学院
学科:化学工艺. 能源化工. 工业催化
办公地点:大连市凌工路2号大连理工大学西部校区化工实验楼C331室
联系方式:0411-84986355
电子邮箱:wencuili@dlut.edu.cn
The choice of precipitant and precursor in the co-precipitation synthesis of copper manganese oxide for maximizing carbon monoxide oxidation
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论文类型:期刊论文
发表时间:2012-08-01
发表刊物:JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
收录刊物:SCIE、EI
卷号:360
页面范围:35-41
ISSN号:1381-1169
关键字:Copper manganese oxide; Co-precipitation; Precursor; Precipitant; CO oxidation
摘要:Copper manganese oxides (CMOs) were synthesized using a co-precipitation method with different precursors and precipitants for carbon monoxide oxidation. The as-synthesized catalysts were characterized by powder X-ray diffraction (XRD), low temperature N-2 sorption, Fourier transform-infrared spectroscopy (FT-IR), H-2-temperature programmed reduction (H-2-TPR), and thermal gravimetric analysis (TGA). Their catalytic activities for CO oxidation were tested by temperature programmed reaction. The results showed that the activity of CO oxidation strongly depended on the combination of precipitant and precursor anions, ranking in the order (Ac- + CO32-) > (NO3- + CO32-) > (Ac- + OH-) > (NO3- + OH-). The crystalline phase of copper manganese oxides obtained using strong electrolyte (OH-) as the precipitant were mainly spinel Cu1.5Mn1.5O4, while the catalysts prepared with weak electrolyte (CO32-) as the precipitant mostly comprised of MnCO3, Mn2O3 and CuO, and showed a much higher CO oxidation activity than that of the Cu1.5Mn1.5O4. Keeping the same precipitant while changing the precursor caused a change in the H-2 consumption which influenced the CO oxidation activity. A suitable combination of precipitant and precursor resulted in the most efficient CO oxidation catalyst. (c) 2012 Elsevier B.V. All rights reserved.