FT-IR和程序升温热谱技术研究Mo/HZSM-5催化剂的制备过程  

A STUDY OF THE PREPARATION OF Mo/HZSM 5 ZEOLITE CATALYSTS BY USING FT IR AND TEMPERATURE PROGRAMMED TECHNIQUES

在线阅读下载全文

作  者:舒玉瑛[1] 徐奕德[1] 刘社田[1] 王林胜[1] 李光进[1] 郭燮贤[1] 

机构地区:[1]中国科学院大连化学物理研究所催化基础国家重点实验室

出  处:《催化学报》1996年第6期535-539,共5页

基  金:国家自然科学基金;国家博士后基金

摘  要:采用FT-IR和程序升温热谱技术研究了Mo/HZSM-5催化剂的制备过程.结果表明Mo/HZSM-5样品在合适的温度下焙烧一定时间,Mo物种与HZSM-5分子筛的酸中心(主要是强酸中心)起作用,并且一部分Mo物种会迁移到分子筛孔道内.在外表面的Mo物种和在孔道内强酸中心作用的Mo物种。Mo/HZSM 5 catalysts show high reactivity and selectivity in the activation of methane in the absence of oxygen. The catalytic performance of Mo/HZSM 5 catalysts is strongly dependent on the channel structure and acidity of the zeolite and the state and location of Mo species. Mo/HZSM 5 catalysts with Mo loading ranging from 0% to 10% were prepared by impregnation with an aqueous solution of ammonium heptamolybdate (AHM). The samples were dried at 393 K, and then calcined at different temperatures for 4 h. The interaction between Mo species and NH 4ZSM 5 zeolite was characterized by FT IR spectroscopy, differential thermal analysis (DTA), temperature programmed decomposition (TPDE) and NH 3 TPD at different stages of catalyst preparation. The results show that if Mo/HZSM 5 catalysts are calcined at a proper temperature, the Mo species will interact with strong acid sites (mainly with Brnsted acid sites) and part of Mo species will move into the channel. The Mo species in the form of small MoO 3 crystallites residing on the external surface and/or in the channel, and interacting with Brnsted acid sites may be responsible for the methane activation. The strong interaction between Mo species and the framework of HZSM 5 will occur if the catalyst is calcined at 973 K. This may lead to the formation of MoO 2- 4 species, which is much less active for, and detrimental to methane activation.

关 键 词: ZSM-5型 催化剂 程序升温热谱 FT-IR 

分 类 号:O643.36[理学—物理化学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象