文章摘要
Pt-Pd/CeO2-SiO2催化剂的稳定性研究
Study on the Stability of Pt-Pd/CeO2-SiO2 Catalysts
投稿时间:2019-02-23  
DOI:
中文关键词: 催化化学  NO氧化  Pt-Pd/CeO2-SiO2  热稳定性  耐硫性
英文关键词: catalytic chemistry  NO oxidation  Pt-Pd/CeO2-SiO2  thermal stability  sulfur resistance
基金项目:国家自然科学基金(21467010)、国家重点研发课题(2017YFC0211303)、云南省自然基金(2016F124)
作者单位E-mail
常仕英 昆明理工大学 材料工程学院, 昆明 650093
昆明贵金属研究所 昆明650106 
shiying.chang@spmcatalyst.com 
于飞 昆明贵金属研究所 昆明650106  
杨冬霞 昆明贵金属研究所 昆明650106  
王加俊 昆明云内动力股份有限公司 昆明 650224  
易健宏 昆明理工大学 材料工程学院, 昆明 650093 yijianhong@kmust.edu.cn 
摘要点击次数: 2684
全文下载次数: 1994
中文摘要:
      以浸渍法制备Pt-Pd/CeO2-SiO2催化剂(Pt-Pd/CS),与Pt-Pd/Al2O3催化剂进行耐硫和耐热稳定性对比。用比表面(BET)、X射线衍射(XRD)和高分辨率透射电镜(HRTEM)等表征催化剂,用模拟气小样方法(SGB)评价催化活性。结果表明,Pt-Pd/CS具有比Pt-Pd/Al2O3催化剂更好的热稳定性和耐硫性。780℃,10 h老化后,Pt-Pd/Al2O3性能轻微下降,而Pt-Pd/CS催化剂中CeO2与贵金属的相互作用增强,NO氧化活性提高。在SO2气氛中,两种催化剂的低温活性均显劣化,但在350℃以上时,Pt-Pd/CS的活性反而提高;Pt-Pd/Al2O3对SO2的饱和吸附时间和吸附量分别为Pt-Pd/CS的3倍以上,因此活性衰减迅速。
英文摘要:
      Pt-Pd/CeO2-SiO2 catalysts (Pt-Pd/CS) were prepared by impregnation method. Their sulfur resistance and thermal stability were compared with that of Pt-Pd/Al2O3 catalysts. The properties of Pt-Pd/CS catalysts were characterized by N2 adsorption, XRD, HRTEM. Their catalytic activity was evaluated by SGB test. The results showed that Pt-Pd/CS catalysts had better thermal stability and sulfur resistance than Pt-Pd/Al2O3 catalysts. The NO oxidation activity of Pt-Pd/Al2O3 catalysts slightly decreased after aging at 780℃ for 10 h, while the activity of Pt-Pd/CS catalysts increased after thermal aging due to the enhanced interaction between CeO2 and noble metals. In SO2-containing atmosphere, the low temperature activity of Pt-Pd/CS catalysts and Pt-Pd/Al2O3 catalysts significantly deteriorated, but the activity of Pt-Pd/CS increased when the temperature was above 350℃. The saturated adsorption time and saturated adsorption capacity of Pt-Pd/Al2O3 catalysts for SO2 were more than three times that of Pt-Pd/CS catalysts respectively, so the activity of Pt-Pd/Al2O3 catalyst decreases rapidly.
查看全文   查看/发表评论  下载PDF阅读器
关闭