扫描手机二维码

欢迎您的访问
您是第 位访客

开通时间:..

最后更新时间:..

  • 石勇 ( 副教授 )

    的个人主页 http://faculty.dlut.edu.cn/sys99/zh_CN/index.htm

  •   副教授   硕士生导师
  • 任职 : Royal Society of Chemistry(RSC)会员,Journal of Physics and Chemistry of Solids;Journal of Alloys and Compounds;《环境科学与技术》,《化学反应工程与工艺》等杂志特约审稿人。
论文成果 当前位置: 中文主页 >> 科学研究 >> 论文成果
TPD and TPSR studies of formaldehyde adsorption and surface reaction activity over Ag/MCM-41 catalysts

点击次数:
论文类型:期刊论文
发表时间:2011-04-20
发表刊物:6th International Conference on Interfaces Against Pollution (IAP 2010)
收录刊物:SCIE、EI、CPCI-S
卷号:379
期号:1-3,SI
页面范围:136-142
ISSN号:0927-7757
关键字:Formaldehyde; Ag/MCM-41; Catalytic oxidation; TPD; TPSR
摘要:The adsorption and surface reaction activity of formaldehyde were studied on the Ag/MCM-41 catalysts with different silver loadings by temperature-programmed desorption (TPD) and temperature-programmed surface reaction (TPSR) methods. It appeared that the silver loading had strong influence on the adsorption and surface reaction activity of HCHO. The addition of silver active species provided new adsorption site for the HCHO at low temperature, and its desorption temperature moved to lower temperature with the increase of silver loading to 8 wt%. With the further increase of silver loading, the desorption temperature of HCHO shifted to higher temperatures, which could be due to the aggregation of silver particles on the surface of the support. Moreover the quantity of adsorbed HCHO at higher silver loading (>8 wt%) changed inversely with the increase of silver content. TPSR experiments indicated that the surface reaction activity for HCHO oxidation was proportional with the adsorption performance of HCHO over Ag/MCM-41 catalysts with different silver loadings, and 8Ag/MCM-41 catalyst showed highest surface reaction activity for HCHO oxidation. Thus it is reasonable to suggest that an appropriate silver loading and particle dispersion would be essential to obtain high catalytic activity for HCHO oxidation at low temperatures. (C) 2010 Elsevier BY. All rights reserved.

 

辽ICP备05001357号 地址:中国·辽宁省大连市甘井子区凌工路2号 邮编:116024
版权所有:大连理工大学