Photocatalytic isomerization of norbornadiene to quadricyclane over metal (V, Fe and Cr)-incorporated Ti-MCM-41

被引:54
|
作者
Zou, Ji-Jun [1 ]
Liu, Yi [1 ]
Pan, Lun [1 ]
Wang, Li [1 ]
Zhang, Xiangwen [1 ]
机构
[1] Tianjin Univ, Key Lab Green Chem Technol, Sch Chem Engn & Technol, Minist Educ, Tianjin 300072, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
Norbornadiene; Quadricyclane; Photocatalyst; M-Ti-MCM-41; Photoisomerization; TI-CONTAINING MCM-41; VISIBLE-LIGHT; VALENCE ISOMERIZATION; INCORPORATED MCM-41; ENERGY-STORAGE; CR; DEGRADATION; DECOMPOSITION; PHOTOOXIDATION; IRRADIATION;
D O I
10.1016/j.apcatb.2010.01.024
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photoisomerization of norbornadiene using M-Ti-MCM-41 (M = V, Fe and Cr) has been studied to develop an alternative for solar energy accumulation and high energy aerospace fuel synthesis. The photocatalysts were prepared via hydrothermal method and characterized by EDX, XRD, N-2 adsorption-desorption, TEM, UV-vis, XPS and IR. With the same Si/M ratio in starting materials, the final concentration of V in the photocatalyst is significantly lower than that of Fe and Cr. V5+ and Fe3+ ions are highly dispersed in Si-O framework with tetrahedral coordination when the metal content is low, and the ordered structure is well retained. However, some species in higher coordination and polymerized environments present with increasing metal content, and the ordered structure becomes to collapse. Cr ions are difficult to get into the framework with various species like extraframework Cr6+ and bulk Cr2O3 formed, also the ordered structure is greatly destroyed. Under UV irradiation, the transition metal ions can improve the photoisomerization activity, with the order of V > Fe > Cr. The activities of V- and Fe-Ti-MCM-41 rise with the increase of Si/M ratio, whereas the performance of Cr-Ti-MCM-41 is irregular. The photocatalysts do not exhibit any activity under visible light, regardless of their absorption in visible-light region. The activity is closely related to the extent of dispersion and local structure of metal ions, about which an indirect excitation process of Ti-O species is suggested. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:439 / 445
页数:7
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