个人信息Personal Information
教授
博士生导师
硕士生导师
任职 : 大连理工大学成都研究院院长
性别:男
毕业院校:中科院大连化学物理研究所
学位:博士
所在单位:化工学院
学科:化学工艺. 物理化学. 功能材料化学与化工
办公地点:大连理工大学西部校区化工综合楼A401室
联系方式:辽宁省大连市高新区凌工路2号,邮编116024
电子邮箱:changhai@dlut.edu.cn
Solid-State Method Toward PdO-CeO2 Coated Monolith Catalysts for Oxygen Elimination Under Excess Methane
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论文类型:期刊论文
发表时间:2014-12-01
发表刊物:CATALYSIS LETTERS
收录刊物:SCIE、EI
卷号:144
期号:12
页面范围:2052-2064
ISSN号:1011-372X
关键字:PdO-CeO2; Solid-state method; Oxygen elimination; Methane oxidation; Monolithic catalysts
摘要:Nanocrystalline PdO-CeO2 oxides were prepared by solid state grinding method, and then thermal treated at elevated temperatures. XRD, BET, Raman, XPS and TEM were employed to investigate the relationship between physicochemical characteristics and catalytic performances for the oxides. Homogeneous solid solutions are structurally stable up to 700 A degrees C whilst segregation of Pd particles occurs at higher temperature. Monolith catalysts were obtained by wash-coating oxides onto cordierites, attempting to eliminate the scarce oxygen mixed in methane through methane oxidation reactions. Oxides calcined at 800 A degrees C exhibited a higher activity during the first light-off experiment. However, activities improved dramatically for the other catalysts after the first ignition. It is apparent that small Pd particles at ceria surface were responsible for the activation of reactants at lower temperature, whereas well-dispersed Pd in ceria or solid solutions attributed to the total conversion of oxygen. Mars-van Krevelen mechanism was proposed with oxygen activation as the rate-limiting step on the PdCe-500 catalysts.
PdO-CeO2 catalysts, prepared by solid-state method and wash-coated onto cordierites, exhibited a high activity for oxygen elimination under excess methane. Metallic Pd on the surface was regarded as the active sites for ignition while Pd2+ in the lattice was responsible for total oxygen conversion.