首页> 外文期刊>Journal of Sol-Gel Science and Technology >Immobilized polyoxometalates onto mesoporous organically-modified silica aerogels as selective heterogeneous catalysts of anthracene oxidation
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Immobilized polyoxometalates onto mesoporous organically-modified silica aerogels as selective heterogeneous catalysts of anthracene oxidation

机译:将固定的多金属氧酸盐固定在介孔有机改性的二氧化硅气凝胶上,作为蒽氧化的选择性多相催化剂

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摘要

Immobilized molybdovanadophosphoric acids onto organically surface-modified silica aerogels were successfully prepared and investigated in heterogeneous catalysis of anthracene oxidation. The catalysts were obtained by supporting mono- and di-vanadium substituted molybdophosphoric acids on hybrid silica materials synthesized via the sol–gel process followed by surface amino-functionalization. The FTIR, DR UV–vis, and AA spectroscopy confirmed the loading and distribution of the polyoxometalate molecules on the surface of the aerogels. The nitrogen adsorption–desorption technique revealed a systematic decrease in the specific surface area and pore volume after the immobilization of the polyoxometalates. The application of the supported molecules as catalysts for anthracene oxidation showed 100% selectivity for 9,10-anthraquinone as opposed to the reactions conducted under homogeneous conditions. Moreover, at certain conditions, the catalytic activity of the supported polyoxometalates was greater than their corresponding free polyoxometalates with a clear effect of the surface chemical groups of the supporting silica aerogels. Additionally, the oxidant and solvent nature showed a crucial effect on the catalytic activity and selectivity of the immobilized polyoxometales. The heterogeneous catalysts were regenerated and reused over consecutive catalytic cycles reflecting a potential economic interest in these materials besides their high efficiency in heterogeneous catalysis.
机译:成功地制备了固定在有机表面改性的二氧化硅气凝胶上的钼钒钒磷酸,并研究了蒽氧化的非均相催化。催化剂是通过在溶胶-凝胶法合成的杂化二氧化硅材料上负载单钒和二钒取代的钼磷酸,然后进行表面氨基官能化而获得的。 FTIR,DR紫外可见光谱和AA光谱证实了多金属氧酸盐分子在气凝胶表面的负载和分布。氮吸附-解吸技术揭示了固定多金属氧酸盐后比表面积和孔体积的系统减少。与在均相条件下进行的反应相反,将负载的分子用作蒽氧化的催化剂显示出对9,10-蒽醌的100%的选择性。而且,在某些条件下,负载的多金属氧酸盐的催化活性大于其相应的游离多金属氧酸盐,对负载的二氧化硅气凝胶的表面化学基团具有明显的影响。另外,氧化剂和溶剂的性质对固定化的聚氧化甲醛的催化活性和选择性显示出关键作用。非均相催化剂在连续的催化循环中得以再生和再利用,这反映了这些材料除了在非均相催化中的高效率外,还具有潜在的经济利益。

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