Abstract
Pt-Pd/CeO2-SiO2催化剂的稳定性研究
Study on the Stability of Pt-Pd/CeO2-SiO2 Catalysts
Received:February 23, 2019  
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)
Author NameAffiliationE-mail
CHANG Shiying Faculty of Material Science and Engineering, Kunming University of Science and Technology, Kunming 650093, China
Kunming Sino-Platinum Metals Catalyst Co.Ltd., Kunming 650106, China 
shiying.chang@spmcatalyst.com 
YU Fei Kunming Sino-Platinum Metals Catalyst Co.Ltd., Kunming 650106, China  
YANG Dongxia Kunming Sino-Platinum Metals Catalyst Co.Ltd., Kunming 650106, China  
WANG Jiajun Kunming Yunnei Power Co.Ltd., Kunming 650224, China  
YI Jianhong Faculty of Material Science and Engineering, Kunming University of Science and Technology, Kunming 650093, China yijianhong@kmust.edu.cn 
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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.
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