Citation: YANG Xin-Li, YIN An-Yuan, DAI Wei-Lin, FAN Kang-Nian. Synthesis of Highly Efficient WO3-Doped MCF Catalyst and Its Application in the Selective Oxidation of Cyclopentene to Glutaraldehyde[J]. Acta Physico-Chimica Sinica, ;2011, 27(01): 177-185. doi: 10.3866/PKU.WHXB20110105 shu

Synthesis of Highly Efficient WO3-Doped MCF Catalyst and Its Application in the Selective Oxidation of Cyclopentene to Glutaraldehyde

  • Received Date: 20 August 2010
    Available Online: 19 November 2010

    Fund Project: 国家自然科学基金(20973042, 20903035) (20973042, 20903035) 上海市科委(08DZ2270500) (08DZ2270500)高等教育博士生研究基金(20090071110011)资助项目 (20090071110011)

  • We synthesized WO3 doped mesocellular silica foam (WO3-doped MCF) catalysts with a high tungsten oxide content of 20% (w, mass fraction) directly using sodium tungstate and tetraethylorthosilicate as precursors. The catalysts showed high thermal stability after calcination at 773 K. Small-angle X-ray scattering, N2 adsorption, and transmission electron microscopy results indicated that the characteristic three dimensional mesocellular structural features of the MCFs were retained after the incorporation of tungsten oxide species. Ultraviolet-Raman and ultraviolet-visible diffuse reflectance spectroscopy data showed that isolated or lowly condensed oli meric tungsten oxide species were obtained for the WO3- doped MCF catalysts. These oxide species were stable and highly dispersed in the silica-based MCF matrix with a tungsten oxide content lower than 20% (w). We found that the nature of the tungsten species largely depended on its content and the direct synthesis method was beneficial in obtaining highly dispersed tungsten oxide species. In the selective oxidation of cyclopentene (CPE) to glutaraldehyde (GA), the 20% (w) WO3-doped MCF catalyst had a CPE conversion of 100% and a GA yield of 83.5% after reacting for 16 h. Furthermore, very stable catalytic activity after many recycling tests was apparent for the WO3-doped MCF catalyst indicating that almost no tungsten species was leached into the reaction solution. A proper amount of tungsten oxide and its high dispersion accounted for the high activity.

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