Amano Fumiaki, Tanaka Tsunehiro, Funabiki Takuzo
Department of Molecular Engineering, Graduate School of Engineering, Kyoto University, Kyoto 615-8510, Japan.
Langmuir. 2004 May 11;20(10):4236-40. doi: 10.1021/la0359981.
A silica-supported, lowly loaded vanadium oxide (V2O5/SiO2) photocatalyst promotes the photocatalytic epoxidation of propene with O2 at steady state in a flow reactor system. Very little deep oxidation of propene into CO2 takes place over V2O5/SiO2, in contrast to the results obtained over a TiO2 photocatalyst in which total oxidation is the main path. With each loading, the sums of the selectivities into propene oxide (PO) and propanal (PA) at steady state were almost the same. The monomeric VO4 tetrahedral species dispersed on SiO2 yield PO under UV irradiation. The less dispersed vanadium oxide species on SiO2 promote the isomerization of PO into PA. We utilized a flow reactor system in which the short contact time reduced the isomerization and resultant decomposition of PO over the catalyst surface.
一种二氧化硅负载的低负载量钒氧化物(V2O5/SiO2)光催化剂在流动反应器系统中能在稳态下促进丙烯与O2的光催化环氧化反应。与TiO2光催化剂的结果相反,在TiO2光催化剂上丙烯主要发生完全氧化生成CO2,而在V2O5/SiO2上丙烯极少深度氧化为CO2。在每种负载量下,稳态时环氧丙烷(PO)和丙醛(PA)的选择性总和几乎相同。分散在SiO2上的单体VO4四面体物种在紫外光照射下生成PO。SiO2上分散性较差的钒氧化物物种促进PO异构化为PA。我们使用了一种流动反应器系统,其中较短的接触时间减少了PO在催化剂表面的异构化及由此导致的分解。