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Synthesis, characterization and catalytic activity of SnAPO-5 in hydrogenation reaction

机译:SnAPO-5在氢化反应中的合成,表征及催化活性

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Tin containingaluminophosphate molecular sieve with AFI structure (SnAPO-5) has been synthesizedhydrothermally by using Sn(II) and Sn(IV) salts as precursors. The SnAPO-5materials have been thoroughly characterized by powder X-ray diffraction, FTIR,UV-vis spectroscopy, scanning electron microscopy, thermal analysis, N2sorption and surface area measurements, and elemental analysis using ICP. FTIRand UV-vis spectral data of calcined SnAPO-5 reveal that Sn can be substitutedfor the phosphorous sites up to 2 mole% in the framework lattices. Substitutionof Sn preferably occurs at the phosphorous sites rather than for Al at lowermetal concentration [Sn(II) or Sn(IV) ≤ 2 mole% SnO2] but higherloading leads to octahedral tin species. The calcined SnAPO-5 material exhibitsgood hydrogenation activity for the reduction of cyclohexanone to cyclohexanolusing 2-butanol as hydrogen donor molecule under the liquid-phase reactionconditions. Other metallophosphates such as CoAPO-5, MnAPO-5 and FeAPO-5 failto undergo this hydrogenation reaction under similar experimental conditions.
机译:以锡(II)和锡(IV)盐为前驱体水热合成了具有AFI结构的含锡磷酸铝分子筛(SnAPO-5)。 SnAPO-5材料已经通过粉末X射线衍射,FTIR,UV-可见光谱,扫描电子显微镜,热分析,N2吸附和表面积测量以及使用ICP的元素分析得到了充分的表征。煅烧后的SnAPO-5的FTIR和UV-vis光谱数据表明,Sn可以取代骨架晶格中高达2摩尔%的磷位。 Sn的取代最好发生在磷位点,而不是在较低的金属浓度[Sn(II)或Sn(IV)≤2摩尔%SnO2]处发生Al取代,但较高的负载量会导致八面体锡物种。在液相反应条件下,以2-丁醇作为氢供体分子,煅烧后的SnAPO-5材料具有良好的加氢活性,可将环己酮还原为环己醇。其他金属磷酸盐(例如CoAPO-5,MnAPO-5和FeAPO-5)在相似的实验条件下无法进行该氢化反应。

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