Porous MoO3-x nanobelt: synthesis, characterization and catalytic application; 多孔MoO3-x纳米带的合成、表征和催化应用
Chen JL(陈俊利) ; Li Y(李勇) ; Liu JL(刘俊龙) ; Zhan ES(展恩胜) ; Li J(李娟) ; Huang XM(黄秀敏) ; Shen WJ(申文杰)
2009-09-06
会议名称3rd international symposium on advanced micro- and mesoporous materials
会议日期2009-9-6
会议地点保加利亚
其他题名多孔moo3-x纳米带的合成、表征和催化应用
页码43/1
通讯作者申文杰
中文摘要porous moo3-x nanobelts were synthesized by hydrothermal method at 373 k with using p123 as surfactant. the synthesized nanobelts are pure orthorhombic α-moo3 structure, with the length up to more than 10 mm and width ranging from 20 to 100 nm. the chemical formula is determined to be moo2.44•0.48h2o and the average valence of mo is +5.1 by tg and xps measurements. n2 adsorption-desorption isotherms confirmed the presence of microspore and mesorpores, which is further evidenced by tem observation. raman spectra also confirmed the synthesized moo3-x present the α-moo3 structure, and these nanobelts might grow along the c axis due to the very higher vibrational intensity of mo-o-mo at 820 cm-1. detailed works on tuning the conditions of hydrothermal synthesis were performed to study the moo3-x formation mechanism. α -moo3 via acidification of na2moo4•h2o formed at first, and it will be reduced to moo3-x by p123 under hydrothermal conditions. with the hydrothermal temperature further increased up to 433 k, moo2 with monolithic structure appeared. more importantly, the moo3-x nanobelts showed quite promising activity for ethanol oxidation to acetaldehyde, with 78% conversion of ethanol and 79% selectivity of acetaldehyde at 593 k.
会议主办者保加利亚科学院
学科主题物理化学
语种中文
内容类型会议论文
源URL[http://159.226.238.44/handle/321008/113544]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
推荐引用方式
GB/T 7714
Chen JL,Li Y,Liu JL,et al. Porous MoO3-x nanobelt: synthesis, characterization and catalytic application, 多孔MoO3-x纳米带的合成、表征和催化应用[C]. 见:3rd international symposium on advanced micro- and mesoporous materials. 保加利亚. 2009-9-6.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace